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VOL XII., No. i. 


JANUARY 1914. 


IRevtew 

OF 

neurology $ Ifts^cbtatrs 

(Founded by the late Dr Alexander Bruce) 


Editor 

A. NINIAN BRUCE 

M.D., D.Sc., M.R.C.P.E., F.R.S.E. 


Assistant Editors 


CHAS. MACFIE CAMPBELL 

M.D., B.Sc., M.R.C.P.E. 


S. A. KINNIER WILSON 

M.D., B.Sc. Edin., M.R.C.P. Lond. 


J. D. ROLLESTON 

M.A., M.D. 


Supported by 


J. SHAW BOLTON, Wakefield 
J. MICHELL CLARKE, Bristol 
Sir THOMAS CLOUSTON, Edinburgh 
C. C. EASTERBROOK, Dumfries 
Sir DAVID FERRIER, London 
HENRY HEAD, London 
WALTER K. HUNTER, Glasgow 
JOHN MACPHERSON, Edinburgh 
HAMILTON C. MARR, Edinburgh 


F. YV. MOTT, London 
RISIEN RUSSELL, London 
Sir E. A. SCHAFER. Edinburgh 
C. S. SHERRINGTON, Oxford 

G. ELLIOT SMITH, Manchester 
PURVES STEWART, London 
ALDREN TURNER, London 

YV. B. WARRINGTON, Liverpool 
R. T. WILLIAMSON, Manchester 



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THE REVIEW OF NEUROLOGY AND PSYCHIATRY contains 
original articles, as well as digests, abstracts, reviews and bibliography 
of the most recent neurological and psychiatrical literature. 

Each Contributor of original articles will receive fifty reprints of 
his paper. 

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CONTENTS. 

•■I«INAL ARTICLES s— rioa 

The Nuoleus Intercalate of Staderini. LEONARD J. KIDD, M.D. 1 

ABSTRACTS l— 

Aa atomy x— 

(1) A Note on the Sulcus Poet-Centralis Superior. 

GEOFFREY JEFFERSON 21 

(2) On the Microscopic Structure of the Otic Ganglion. 

CARLO RIQUIER 22 

(3) Contribution to the Knowledge of the Membranous Labyrinth. On a 

Fourth Crista Acustica. C. B. BENJAMINS 22 

Ptyekalogy i— 

(4) Experimental Production in Mammals of the Pineal Precocious Macro- 

Genito-Somatic Syndrome. SARTESCHI, U. 23 

(5) Studies on Pellagra—I. The Influence of the Milling of Maize on the 

Chemical Composition and the Nutritive Value of Maize Meal. 

CASIMIR FUNK 24 

Pathology s— 

(6) On the Structure of the Myelin Sheath and its Alteration in Secondary 

Degeneration. FERUCCIO GUIDI 25 

(7) Contribution to the Pathology of Paralysis Agitans. 

HASKOVEC and BASTA 25 

(8) A Peculiar Form of Nodular Hyperplasia of the Liver Associated with 

Brain Changes. 

YUGO YOKOYAMA and WALTHER FISCHER 26 
(0) Histological Observations on the Nervous System of the Progeny of 

Animals Subjected to Chronic Alooholic Poisoning. M. FERRARI 26 

Clinical Neurology x— 

(10) The Investigation of the Higher Nervous Functions. I. PAWLOW 27 
(Kr)- A'Biogene.tic Principle. • E. LUGARO 28 

(12> The IdiopcthicvVafteties of Myoclonus, MOUIZ 28 

(13T Traumatic Intramuscular Ossification. JOHN MORLEY 29 

.(14). Absence of the Oc»*lo-Cardiac Reflex in Tabes. 

M. LOEPBR and A. MOUGEOT 29 

(15) ' Oh-the Incomplete Formsof Recklinghausen’s Disease. P. BERTEIN 30 

(16) The Meningeal Form of Poliomyelitis. ARNOLD NBTTER 30 

(17) Meningeal Syndrome of the Poliomyelitis Type. 

E. JOLTRAIN and P. ROUFFLAC 30 

(18) Meningitis after Follicular Tonsillitis. E. SIEMKRLING 31 

(19) Hypertrophic Cervical Meningitis. 

BABIN SKI, JUMENTIE, and JARKOWSKI 31 

(20) A Case of Meningitis Purulenta Aseptica after Intr&nasal Interference. 

LEOPOLD REISCHIG 31 

(21) A Meningo-Cerebellar Symptom-Complex in Febrile Diseases occurring 

in Tuberculous Individuals. FOKRSTBR 32 

(22) Typhoid Cerebro-Spinal Meningitis in an Infant. L. LAGANE 32 

(23) On the Spinal Cord Phenomena of Typhoid Fever, and especially 

Metatyphoid Myelitis. G. GAUTHIER 33 

(24) On Post-Diphtheritic Abducens Paralysis. C. ROTHER 33 

(25) A Further Contribution to the Subject of Traumatic Hasraatomyelia. 

BERNHARDT 34 





REVIEW OF 

NEUROLOGY AND PSYCHIATRY 




REVIEW 


of *... • : - **.: •' 

NECROLOGY and PSYCHIATRY 

(Founded by the Late Dr ALEXANDER BRUCE) 


Editor 

A. N INI AN BRUCE 

M.D., D.Sc., M.R.C.P.E., F.R.S.E. 


Assistant Editors 

CHAS. MACFIE CAMPBELL S. A. KINNIER WILSON 

M.D., B.Sc., M.R.C.P E. M.D., B.Sc., F.R.C.P. (Lond.) 

J. D. ROLLESTON 


Supported 

J. SHAW BOLTON, Wakefield 
J. MICHELL CLARKE, Bristol 
Sir THOMAS CLOUSTON, Edinburgh 
C. C. EASTERBROOK, Dumfries 
Sir DAVID FERRIER, London 
HENRY HEAD, London 
WALTER K. HUNTER, Glasgow 
JOHN MACPHERSON, Edinburgh 
HAMILTON C. MARR, Edinburgh 


BY 

F. W. MOTT, London 
RISIEN RUSSELL, London 

Sir E. A. SCHAFER, Edinburgh 
C. S. SHERRINGTON, Oxford 

G. ELLIOT SMITH, Manchester 
PURVES STEWART, London 
ALDREN TURNER, London 

W. B. WARRINGTON, Liverpool 
R. T. WILLIAMSON, Manchester 


VOLUME XII. 



EDINBURGH 

OTTO SCHULZE & COMPANY 

20 SOUTH FREDERICK STREET 
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PRINTED AT 
THE DARIEN PRESS 
EDINBURGH 



Contents 


ORIGINAL ARTICLES 

pa<;E 

The Nucleus Intercalates of Staderini. Leonard J. Kidd, 

M.D..1 

The Arcuate Nucleus in Man, the Anthropoid Apes, and 

the Microcephalic Idiot. A. Ninian Bruce, M.D. - 51 

The Parietal Area. Geoffrey Jefferson, M.S. (Lond.), F.R.C.S. 04 

Notes of a Case of Recurrent Paralysis of the Third 
Cranial Nerve. Robert A. Fleming, M.D., F.R.C.P. 

(Edin.) ------- 58 

Labyrinth Suppuration. (A Review.) J. S. Fraser, M.B., 

F.R.C.S. (Edin.).87 

Iscovesco’s Experimental Researches on Lipoids of Organs. 

(A Review.) Leonard J. Kidd, M.D. - - 100 

The Neural Atrophy of the Muscles of the Hand, with¬ 
out Sensory Disturbances. J. Ramsay Hunt, M.D. - 137 

On the Technique of Nerve Palpation by Nerve “Fric¬ 
tion.” Edgar F. Cyriax, M.D. - - - - 148 

On the Mechanism of some Cases of Manic-Depressive Ex¬ 
citement. C. Macfie Campbell, M.D., B.Sc., M.R.C.P.E. 175 

The Nature and the Treatment of the So-called “ Genuine 

Epilepsy.” G. C. Bolten (The Hague, Holland) - 231 

Notes on a Case of Pellagra. D. Maxwell Ross - - 244 

Babinski’s “ Second Sign ” of Organic Hemiplegia in Hemi- 

CHOREA, AND ITS BEARING ON THE ORGANIC NATURE 

- of Chorea. Arthur F. Hertz - 250 

A Case of Amaurotic Family Idiocy. W. E. Hume (New- 

castle-on-Tyne) - - - - - - 281 

V 


315603 



vi CONTENTS 

PAUE 

The Action op Adrenalin and Epinixe on the Pupil in 

Epilepsy. R. M. Stewart .... 287 

Drop-Methods of Counting the Cells of the Cerebro¬ 
spinal Fluid—The Relation of the Cell-Count to 
the W asserhann Rbaction. R. Donald, B.Sc. (N.Z.), 

D.P.H. (Oxf.).333 

The Alleged Sensory Cutaneous Zone of the Facial Nerve 

of Man. Leonard J. Kidd, M.D. - 393 

The Mechanism of Periodic Mental Depressions as shown 
in Two Cases, and the Therapeutic Advantages of 
such Studies. L. Pierce Clark, M.D. (New York City) 433 

The Pyridine-Silver Method. With a Note on the Affer¬ 
ent Spinal Non-Mrdullated Nerve Fibres. S. Walter 
Ranson, Ph.D., M.D. ..... 467 

The Significance of the Unconscious in Psychopathology. 

Ernest Jones, M.D., M.R.C.P. (Lond.) - - 474 

Studies in Neurological Technique.— No. 2 : Indication and 
Method for the Use of the Electrical Re-enforce¬ 
ment for the Elicitation of the Absent Reflexes. 

Walter B. Smith, M.D. (Boston, Mass.) - - - 507 



■Review 

of 

IReurolocjE ant> pe^cbiatrg 


Original Hrticles 


THE NUCLEUS INTERCALATUS OF STADERINI. 

By LEONARD J. KIDD, M.D. 

1. Introductory Historical Remarks. 

2. Morphological and Experimental Evidence. 

3. Summary and Conclusions. 

4. References. 


1. Introductory Historical Remarks. 

In the year 1894 Rutilio Staderini 1 described for the first time a 
nucleus of small cells in the medulla oblongata of the rabbit, 
situated between the hypoglossal nucleus and the dorsal vagus 
nucleus. In 1895 he found it in the dog, and in 1896 in man 
and the monkey. Although to him unquestionably belongs the 
great credit of having been the first writer to describe this nucleus, 
it is held to be probable that Stilling actually saw it some seventy 
years ago, but failed to identify it as a definite cell-group. It 
was also pointed out by Van Gehuchten 2 in 1898 that the cell- 
mass which Gierke 3 in 1873 took to be the dorsal vagus nucleus 
was really the nucleus intercalate: a reference to one of Gierke’s 
figures shows that Van Gehuchten interpreted this point correctly. 
Many modern works on neurology and anatomy figure Staderini’s 
nucleus intercalate, but there seem to be still very few careful, 
detailed studies of it in existence. All writers are agreed that 
its cells are small, and that in the lower half of the floor of the 
fourth ventricle a transverse section shows it intercalated between 


i 






LEONARD J. KIDD 


.2:'.;-. 

the hypoglossal nucleus and the dorsal vagus nucleus. So far as 
the upper half of the medulla oblongata is concerned, most authors 
describe and figure the nucleus intercalatus as being anatomically 
continuous with the cells of the dorsal triangular vestibular 
nucleus without any break whatever. This description un¬ 
doubtedly applies to many human and some other mammalian 
brains, but not to all, as I shall show presently. So much has this 
anatomical continuation with the dorsal vestibular nucleus entered 
into the minds of descriptive neurologists that there is a wide¬ 
spread but rather surprising belief that the nucleus intercalatus 
of Staderini is connected with the eighth pair of nerves. 

2. Morphological and Experimental Evidence. 

One of the most illuminating papers dealing with the cell- 
groups and surface markings of the floor of the fourth ventricle is 
that by Streeter 4 (1903). I hope to show in this paper, more 
fully than I attempted to show in 1910 in my paper on the dorsal 
vagus nucleus, that Streeter arrived correctly at the true morpho¬ 
logical position of the nucleus intercalatus of Staderini. Streeter 
made a careful study of the surface markings of the floor of the 
fourth ventricle in many human and some other mammalian 
brains. He showed that in the lower half of the floor of the 
fourth ventricle in man the trigonum hypoglossi consists of (1) 
a narrower median field which overlies the frontal end of the 
hypoglossal nucleus, and (2) a lateral field, the area plumiformis 
of Retzius, which overlies the nucleus intercalatus of Staderini. 
It is vital to note that a definite sulcus separates these two fields. 
Streeter’s text-figure 1 of a Weigert preparation, made by Weigert 
himself, shows beautifully the neuroglial partitions which separate 
the ventro-mesially situated hypoglossal nucleus from the ventro- 
laterally situated nucleus intercalatus, and the latter nucleus from 
the dorso-laterally placed dorsal vagus nucleus, and also the 
latter from the dorsal median vestibular nucleus. The three sulci 
which separate respectively each two of the adjoining nuclei of 
this series of four nuclei are as follows:—(1) The sulcus lateralis, 
i.e., the surviving embryonic sulcus limitans of His, which separates 
the dorso-laterally situated dorsal vagus nucleus from the ventro- 
laterally situated nucleus intercalatus of Staderini; (2) the sulcus 
dorsalis, which separates the dorso-laterally situated dorsal vagus 



THE NUCLEUS INTERCALATE OF STADERINI 3 


nucleus from the dorsally situated dorsal median vestibular nucleus; 
(3) the sulcus ventralis, which separates the ventro-laterally 
situated nucleus intercalatus of Staderini from the ventro-mesially 
situated hypoglossal nucleus. I think we cannot doubt that these 
sulci are primitive and fundamental, and that they separate 
morphologically and physiologically distinct cell-groups. Thus, 
in the lower half of the floor of the fourth ventricle, the four 
primitive, fundamental subdivisions of the brain are represented 
as follows:—(1) The ventro-mesial cell-column, developed in the 
ventral lamina of the neural tube, the hypoglossal nucleus, somatic 
motor; (2) the ventro-lateral cell-column, developed probably in 
the ventral part of the embryonic schalt-stiick of His (the pars 
intercalaris of the neural tube), the nucleus intercalatus of Staderini, 
visceral motor for unstriped muscle; (3) the dorso-lateral cell- 
column, developed probably in the dorsal part of the schalt-stiick 
of His, the dorsal vagus “ nucleus,” visceral afferent for unstriped 
muscle [the visceral afferent endoneural vagus ganglion of Kidd 14 
(1910)]; (4) the dorso-mesial cell-column, developed in the dorsal 
lamina of the neural tube, the dorsal vestibular nucleus, an afferent 
reception-nucleus, somatic afferent I have attempted to show 
these points diagrammatically in Figs. 1 and 2. 

In the upper half of the floor of the fourth ventricle, i.e., the 
region of the striae acousticae, which is just above the upper limit 
of the dorsal vagus nucleus, the somatic motor column of the 
brain is not represented, the reason being, of course, that in exist¬ 
ing vertebrates there is no somatic motor nucleus between the 
abducens and the hypoglossal nuclei. In this region we have 
the following arrangements:—(1) Mesially situated the nucleus 
funiculi teretis, which I have previously suggested (1910) is a 
median central sympathetic nucleus of unknown connections: 
this nucleus is sometimes, at any rate, separated by a neuroglial 
partition from (2) the nucleus intercalatus of Staderini, as is well 
seen in Streeter's Fig. 2; and the nucleus intercalatus is (3) 
similarly separated from the dorsal vestibular nucleus by a 
neuroglial partition. It will be remembered that Streeter sug¬ 
gested in 1903 that the nucleus intercalatus of Staderini may be a 
central sympathetic nucleus, an opinion which I adopted in 1910 
as almost certainly correct. I believe, therefore, that the cell- 
groups of the upper half of the floor of the fourth ventricle at the 
level of the striae acousticae are arranged morphologically as 



4 


LEONARD J. KIDD 


follows:—(1) Somatic motor column not represented in existing 
vertebrates. (2) Visceral motor column probably doubly repre- 



Sulcus Dorsalis. 

Sulcus Lateralis Limitans of His. 


Sulcus Ventralis. 


Firs. 1 .—Diagram of the Four Primitive, Fundamental, Morphological, 
and Physiological Subdivisions of the Neural Tube. 

1. Ventro-raesial cell-column, somatic motor. 2. Ventro-lateral cell-column, 
visceral motor. 3. Dorso-lateral cell-column, visceral afferent. 4. Dorso-mesial 
cell-column, somatic afferent. Of these cell-groups, 1 is developed in the ventral 
lamina of the neural tube ; 4 in the dorsal lamina; and 2 and 3 probably in the 
ventral and dorsal parts respectively of the schalt-stiick of His (the pars inter- 
calaris). The depth of the three sulci is purposely exaggerated. 

sented, viz., by (a) the nucleus funiculi teretis, (?) a median 
sympathetic nucleus, and ( b ) the nucleus intercalate of Staderini, 



Floor of Fourth Vkntbici.k. 

1. Ventre-mesial hypoglossal nucleus, somatic motor. 2. Ventro-lateral 
nucleus intercalatus of Staderini, visceral motor. 3. Dorso lateral dorsal vagus 
“nucleus,” visceral afferent (Kidd, 1910). 4. Dorsal vestibular nucleus, somatic 

afferent. 


a lateral sympathetic nucleus. (3) Visceral afferent column not 
represented (as the level of the section is above the upper limit 




THE NUCLEUS INTERCALATE OF STADERINI 5 


of the dorsal vagus “ nucleus (4) Somatic afferent column, 
the dorsal vestibular nucleus. Fig. 3 illustrates these points 
sufficiently clearly, I think. 

Now it is quite true that these neuroglial septa, described 
by Streeter, are not seen in all human brains, and they are also 
absent in some specimens of some other brains. And it is also 
true that there is often unbroken continuity between the cells of 
the upper part of the nucleus intercalatus and those of the dorsal 
vestibular nucleus; this was the condition found by Stokes* in 
his recent study of the acoustic-complex in the opossum (Didelphys 
virginiana). A very well-marked sulcus ventralis is sometimes 
seen on the ventricular border of the lower half of the fourth 
ventricle between the hypoglossal nucleus and the nucleus inter¬ 
calatus of Staderini: this is extremely well seen in one of Cajal’s 


Dorsal Vestibular Nucleus. 
Nucleus Intercalatus of Staderini. 


I-— Nucleus Funiculi Teretis. 

Fig. 3.—Diagram of Cell-Groups of Upper Half of Floor 
of Fourth Ventricle, in Region of Strias Acoustic m. 

Columns 1 and 3 are absent in this level. 2' is the nucleus funiculi teretis, 
(?) a median sympathetic nucleus (Kidd). 2 is a lateral sympathetic nucleus. 
4 is a somatic afferent reoeption-nucleus. 

figures reproduced in Quain’s “ Anatomy,” 1908, vol. iii., Part I., 
p. 135: the sulcus here appears to be about one-seventh the 
depth of the nucleus intercalatus itself. There appear to be but 
few published studies of the exact extent of the nucleus inter¬ 
calatus, but Streeter found, after an examination of many human 
brains, that its length is 11 ram. and its greatest width 22 mm. 
It will be noticed that its extent is very nearly the same as that 
of the dorsal vagus nucleus which Streeter found to be 135 mm. 
in length and 2 mm. in average width. It seems to me possible 
that the greater width of the nucleus intercalatus may just about 
balance the slightly greater length of the dorsal vagus nucleus: 
in any case there can hardly be very much difference between 
them in absolute bulk. The former extends, of course, a little 

# J. H. Stokes, Amer . Joum . of A not ., vol. xii., 1912, p. 434. 




6 


LEONARD J. KIDD 


higher cephalad than the latter, but not quite so far caudad. In 
their general structure the cells of the nucleus intercalatus 
resemble closely those of the dorsal vagus nuoleus and those of 
the intermedio-lateral cell-column of the thoracic spinal cord; so 
far as I know, the nucleus intercalatus does not contain such a 
large number of spindle-shaped cells as the dorsal vagus nucleus 
does: but I make this statement with much reserve, for it seems 
that we need a careful histological examination of its cells by the 
best and newest methods. The small size of the cells of Staderini’s 
nucleus suggests that they are connected with the innervation of 
unstriped muscles: they certainly do not resemble either somatic 
motor or somatic afferent nerve-eells. 

In my opinion there are some very strong objections to the 
view that the nucleus intercalatus is connected with the eighth 
pair of nerves. Thus, no one has brought forward any experi¬ 
mental evidence in its favour, whereas there is plenty of evi¬ 
dence that the dorsal vestibular nucleus is one of the afferent 
reception-nuclei of the vestibular nerve. But let us, for the sake 
of argument, admit for a moment the identity of these two nuclei: 
to what conclusion would such a hypothesis inevitably lead us ? 
We should have to teach that the upper part of the nucleus 
intercalatus, a somatic afferent reception-nucleus, becomes lower 
down in the bulb a visceral motor nucleus! The only alternative 
would be to say that the nucleus intercalatus is really a complex 
of two morphologically and physiologically distinct nuclei, viz., 
an upper somatic afferent and a lower visceral motor nucleus 
Now, who can point to any instance in any vertebrate of a somatic 
afferent nucleus of reception being anatomically continuous with 
a visceral motor nucleus? I believe that the mistake hitherto 
made by writers, with the exception of Streeter, has been that 
they have failed to see that there is evidence in some human and 
other mammalian brains of the existence of a neuroglial septum— 
one of Weigert’s “ Kielstreifen ” or tracks left by embryonic sulci 
—separating off the nucleus intercalatus from the dorsal vesti¬ 
bular nucleus. We know that there are considerable variations 
in the bulb of the degree of development of the three sulci which 
separate the various cell-groups from one another. It may be 
objected that in the primitive mammal, the opossum, Stokes failed 
to find any trace of a septum separating the nucleus intercalatus 
from the dorsal vestibular nucleus; but that would not of itBelf 



THE NUCLEUS INTERCALATE OF STADKU1XI 7 


prove its non-existence in even higher mammalian forms. We 
know that even highly specialised groups of animals may show, in 
certain respects, characters of greater antiquity than even other 
groups which are in most respects much more primitive. Thus, 
in teleosts, which are a highly specialised group of fishes, we see 
in their ontogeny certain features of great antiquity which are 
not present in the selachians, which are on the whole a much 
more ancient group. I may point especially to the extensive 
studies of Calderwood, who has shown that many of the deep-sea 
teleosts off the Scottish coasts reveal features of great antiquity. 
There is also Ross 6. Harrison’s embryological study on the salmon, 
which shows that the exoneural dorsal root ganglia are developed 
from migrated endoneural afferent neuroblasts, a feature of great 
antiquity. 

We may now ask the question: If the nucleus intercalatus of 
Staderini be really a visceral motor, lateral sympathetic nucleus, 
how do its axons pass out from the central nervous system, and 
round the cells of what sympathetic ganglion or ganglia do they 
end ? One thing seems clear, viz., that they do not pass either 
up the brain-stem or down the spinal cord to enter any cranial 
nerve from the glossopharyngeal forwards, or any spinal nerve 
from the first cervical nerve backwards; my reason for saying 
this is that experimental sections made either just above or just 
below the level of the nucleus intercalatus have never given any 
retrograde chromolysis of its cells. There remain, then, only two 
other possibilities, viz., the axons of its cells might enter (1) the 
hypoglossal nerve, or (2) the vagus nerve. In the year 1898 
Ossipow 6 found changes in the cells of the nucleus intercalatus 
and also in the dorsal part of the hypoglossal nucleus—as well as 
in both dorsal vagus nuclei—in two rabbits which survived ninety 
and ninety-one days respectively after unilateral vagotomy, and 
also in one dog which survived six months and three weeks after 
bilateral vagotomy. I am not certain as to the exact situation of 
Ossipow’s section of the vagus nerve. His work is briefly summar¬ 
ised by both Van Gehuchten 2 and Molhant 7 ; and in the German 
abstract of Ossipow’s Russian paper it is stated that he divided 
the cervical part of the vagus, rather a vague statement, which 
leaves one in doubt whether the section was made above the 
ganglion nodosum or not; but that it probably was so I gather 
from the further statement in the German abstract that Ossipow 



8 


LEONARD J. KIDD 


connects the “ root-bundles ” of the vagus nerve with the nucleus 
intercalatus of Staderini. Although Ossipow’s work was of 
interest from the point of view of the connections and nature of 
that nucleus, it obviously required repetition on more scientific 
lines. This was supplied in 1903 by Tricomi-Allegra* who * 
“performed unilateral avulsion of the vagus nerve above the 
ganglion nodosum in the cat and rabbit: the method of Nissl 
showed constant chromolysis in the cells of the dorsal vagus 
nucleus and also in those of the ventral vagus nucleus (the nucleus 
ambiguus). In addition, he observed chromolysis in the cells of 
a very small grey column situated outside and behind the central 
canal at the limit of the white and grey matter, and even in the 
caudal part of the hypoglossal nucleus. By the Marchi method 
he found evident signs of degeneration in the solitary bundle and 
its nucleus, the dorsal vagus nucleus, the nucleus intercalatus of 
Staderini, the hypoglossal nucleus, and the commissural ganglion 
of CajaL” The changes which Tricomi-Allegra found in the 
hypoglossal nucleus are attributed by Van Gehuchten, doubtless 
correctly, to damage done at the operation to some of the fibres 
of the hypoglossal nerve; for there is abundance of experimental 
evidence by Van Gehuchten 2 and others which proves that all the 
axons of the cells of the hypoglossal nucleus pass out by the 
hypoglossal nerve. Tricomi-Allegra held that the nucleus inter¬ 
calatus of Staderini is connected with the vagus nerve. But 
Molhant 7 states that in 1898 Van Gehuchten failed to obtain any 
chromolysis of the cells of that nucleus after section of the vagus 
nerve in the rabbit. [I am not quite certain, from Molhant’s 
description, and from Van Gehuchten’s own description 2 in 
another paper, whether the latter observer divided the vagus 
above or below the ganglion nodosum.] We may, I think, take 
it as definitely established by the experiments of Molhant, Van 
Gehuchten, and at least twenty other experimentalists, that section 
of the vagus nerve below the ganglion nodosum does not give 
retrograde chromolysis of any of the cells of the nucleus inter¬ 
calatus of Staderini. Therefore if that nucleus be really the 
visceral motor nucleus for the innervation of the unstriped muscle 
supplied by branches of the vagus nerve—as I believe it to be—it 
is clear that its pre-ganglionic axons do not end round the cells of 

* My account of his work is taken from Van Gehuchten (1903). a It is also 
mentioned by Molhant (1911). 7 



THE NUCLEUS INTERCALATE OF STALER INI 9 


any of the ganglia of the terminal plexuses in the organs of the 
vagus nerve, such as the pulmonary, cardiac, and myenteric, but 
must end round cells of either the ganglion nodosum or the 
ganglion jugulare vagi. 

But before I discuss the nature of the ganglion nodosum it is 
essential, for a proper understanding of the nature of the nucleus 
intercalate of Staderini, to attempt to show why the currently 
accepted doctrine, that the dorsal vagus nucleus is visceral motor 
for the unstriped muscle of the vagus nerve, is erroneous. Quite 
twenty experimentalists, from the work of Dees 8 (1889) up to the 
truly admirable exhaustive study of Molhant 7 (1911), have proved 
that the dorsal vagus nucleus gives origin to centrifugal fibres; 
and some of these twenty observers have further proved that it 
gives origin to centrifugal fibres exclusively, so that we must now 
reject the belief that it is in part an afferent reception-nucleus. 
There are three definite periods in the history of the “ nucleus ” : 
—(1) Until the time of Dees 8 (1889) all writers held that it was 
an afferent reception-nucleus for one or more of the vagus group 
of nerves; (2) the second period extends from 1889 to 1910: it 
may be called the motor period; and (3) the third began and 
ended in 1910 with my attempt 14 to prove that all the cells of 
this “ nucleus ” are afferent, and that it is the endoneural afferent 
ganglion of the vagus nerve; but after three years I am still in a 
minority of one in holding this opinion. Now it is obvious that 
all the twenty experimentalists from the time of Dees to Molhant, 
and over thirty descriptive writers who have specially written on the 
dorsal vagus nucleus, have taken it for granted that the ganglion 
nodosum and jugulare vagi are exclusively afferent root-ganglia, 
and also that the only sympathetic ganglia of the vagus nerve are 
the terminal ganglia situated in its peripheral organs; and they 
have also assumed that the peripheral processes of the cells of the 
dorsal vagus “ nucleus ” are interrupted in those peripheral vagus 
terminal ganglia. There is, however, not an atom of evidence in 
favour of any of these assumptions on which alone they base their 
opinion that the dorsal vagus nucleus is motor. It is obvious that 
the requisite crucial experiment cannot be performed; for we 
want to divide all the nerve-fibres on the peripheral side of these 
peripheral terminal vagus plexuses, and that is impossible. But I 
believe that, if we could do this, we should still get chromolysis in 
the cells of the dorsal vagus nucleus, as its peripheral processes all 



10 


LEONARD J. KIDD 


pass, I believe, uninterruptedly from the medulla oblongata into 
the unstriped muscle (and glands and blood vessels also probably) 
of all those vagus organs which contain unstriped muscle. 
Molhant performed his various experiments on the vagus nerve 
and its branches in the rabbit at the following levels: (1) for the 
stomach he divided the gastric branches of the vagus close up to 
the cardia; (2) for the trachea he divided the recurrent laryngeal 
branch at a point peripheral of the point at which its laryngeal 
branches are given off: he had previously proved histologically 
that at the point of his section the recurrent laryngeal nerve con¬ 
tains exclusively small nerve-fibres which go to the trachea (and 
in man to the oesophagus also, but not in the rabbit, whose 
oesophagus contains no unstriped muscle); (3) for the other 
organs he divided cardiac branches and the thoracic vagus, and 
attempted extirpation of one lung. Thus, when he found chromo¬ 
lysis of the cells of the dorsal vagus nucleus after these operations 
he concluded quite rightly that that nucleus innervates exclusively 
those vagus organs which contain unstriped muscle: but he 
assumed that it is motor, and that its pre-ganglionic axons end 
round cells of peripheral terminal vagus ganglia. But he seems 
to have forgotten that, so far as we know, there is no group of 
sympathetic ganglion cells interposed between the trachea and the 
point of his section of the peripheral part of the recurrent 
laryngeal nerve. If there be really no such ganglion cells, then 
we cannot escape the conclusion that those fibres which come 
from the dorsal vagus nucleus to enter the tracheal unstriped 
muscle must pass the whole way without interruption. Now it is 
important to note that when Molhant concluded from his study 
that the dorsal vagus nucleus is motor to unstriped muscle— 
instead of contenting himself, as he should scientifically have done, 
with saying that it gives origin exclusively to centrifugal fibres for 
unstriped muscle—he was really sinning against the light; for, at 
the outset of his historical summary, on p. 144, he writes these 
words concerning the earlier view of the nature of the dorsal 
vagus nucleus, held up to the year 1889, that it is an afferent 
reception-nucleus:—“ Its situation dorsally of the sulcus limitans 
of the ventricle all the more justified this opinion, the embryo- 
logical researches of His having established in fact that this 
sulcus separates the sensory grey masses from the motor grey 
masses." So that Molhant, in concluding that the “ nucleus ” is 



THE NUCLEUS INTERCALATE OF STADERINI 11 


motor merely because it gives origin to centrifugal fibres, in effect 
throws the established “fact” of Wilhelm His, sen., overboard, 
and thus teaches, along with over thirty other writers, that a cell- 
group, situated always entirely dorsally of the more or less persist¬ 
ing embryonic sulcus lateralis limitans of His, is motor. Clearly, 
if the thirty be right, then His and I are wrong; but if His and I 
be right, the thirty must cry “ peccavimus.” I must here add that 
Molhant, in his beautifully planned and executed experimental 
study of the nucleus ambiguus in the rabbit, has proved that it 
innervates exclusively striped muscles. Therefore it cannot be 
the motor nucleus for the unstriped muscle of the organs of the 
vagus nerve. Now if the dorsal vagus nucleus be not the motor 
nucleus for these unstriped muscles, there are only three alterna¬ 
tive bulbar cell-groups left to us; these are (1) the hypoglossal 
nucleus, (2) the small-celled nucleus of Roller, and (3) the small- 
celled nucleus intercalatus of Staderini. We exclude the hypo¬ 
glossal nucleus because all its axons enter the hypoglossal nerve; 
and we exclude Roller’s nucleus because section of the vagus nerve 
either below the ganglion nodosum, or above it or the ganglion 
jugulare, does not give any chromolysis of its cells. There remain 
only the nucleus intercalatus; it is the motor nucleus, and the 
only one, for the unstriped muscles supplied by the vagus nerve. 

I must now attempt to show that the ganglion nodosum, and 
possibly also the jugulare, is a ganglionic-complex, partly visceral 
afferent, and partly a sympathetic ganglion. It will be remembered 
that in 1886 and in 1889 Gaskell 9 suggested that the ganglion 
nodosum x., ganglion petrosum ix., and the ganglion geniculatum 
viL, are sympathetic ganglia. In the year 1912 Mollgaard 10 stated 
that in an earlier paper of his own—published in what I take to 
be either the Danish or some Scandinavian language—he showed 
that the broncho-motor innervation of the vagus nerve is in¬ 
terrupted in the ganglion nodosum. We know that the ganglion 
nodosum, petrosum, and geniculatum are of epibranchial origin. 
Now, Mollgaard has traced, in the selachian, Acanthias vulgaris, 
nerve-fibres passing from the medulla oblongata and ending round 
cells of the branchio-gastricus ganglion: he homologises this 
ganglion with the ganglion nodosum of higher vertebrate forms. 
In his 1912 paper 10 he gives a detailed account of an experiment 
in which he destroyed the dorsal vagus nucleus of a cat by a 
2 mm. deep incision in the bulb: he found later a few degenerated 



12 


LEONARD J. KIDD 


nerve-fibres ending round cells of the ganglion nodoBum and none 
peripheral of that ganglion. But unfortunately he overlooked the 
fact that of necessity his incision severed some, at any rate, of the 
axons of the nucleus intercalate of Staderini, bo that it was a 
mere guess on his part that all the degenerated fibres came from 
the damaged dorsal vagus nucleus. He concluded that that 
nucleus is partly a motor nucleus whose axons end round cells of 
the ganglion nodosum, and partly an afferent reception-nucleus. 
But we must reject both conclusions. For we have the evidence 
of some twenty experimentalists that all the “axons” of the 
dorsal vagus “ nucleus ” pass through the ganglion nodosum with¬ 
out interruption. I need hardly say, however, that I regard 
Mollgaard’s finding of prime importance, when taken in conjunction 
with the findings of the twenty experimenters just mentioned, and 
also with the findings of Tricomi-Allegra.® For it goes a long way 
towards the proof of the accuracy of my opinion of the nature of 
the nucleus intercalatus: thus, it tends to show that some, at any 
rate, of its axons end round cells of the ganglion nodosum, and 
that the latter gives origin to all the post-ganglionic motor fibres 
for the innervation of the unstriped muscle of the organs of the 
vagus nerve. Mollgaard also made the important histological 
discovery that the ganglion nodosum contains a few multipolar 
cells. It is interesting in this connection to note, on the other 
hand, that in 1911 L. R. Muller 11 found a few multipolar cells in 
the ganglion jugulare but none in the nodosum. I may add that 
Mollgaard’s view that the dorsal vagus nucleus is partly visceral 
motor and partly visceral afferent (reception) is not likely to gain 
adherents; it seems to me a decidedly bizarre morphological 
curiosity, and it would be difficult, I think, for anyone to point to 
any known instance, in any vertebrate, of such a strange complex. 
It is evident also that, as his incision in the medulla oblongata of 
the cat divided only some of the axons of the cells of the nucleus 
intercalatus, the latter nucleus must send many more axons to 
end round cells of the ganglion nodosum than the number of 
degenerated fibres found by him would indicate. 

I believe that not only is the ganglion nodosum in part a true 
motor sympathetic ganglion, but that it is not improbable that so 
also is the ganglion jugulare. I have been led to this belief partly 
by the histological evidence of Muller 11 that the ganglion jugulare 
vagi contains some multipolar cells, but even more by the study 



THE NUCLEUS INTERCALATE OF STADERINI 13 


of the admirable comprehensive embryological researches of 
Kuntz 18 on the development of the sympathetic nervous system of 
vertebrates from fishes to mammals. Kuntz has shown that the 
vago-sympathetic system is almost certainly the most ancient 
part of the whole autonomic-sympathetic system; he has shown 
that the embryonic sympathetic nervous system is composed of 
two distinct sets of nerve-elements, viz., (1) cells which migrate 
out from the cerebro-spinal ganglia and neural crest, and (2) cells 
which wander out from the ventral part of the neural tube; both 
sets of cells enter the anlagen of the sympathetic ganglia. In the 
case of the vagus nerve, cells migrate from the two vagus ganglia, 
and from the wall of the rhombencephalon: the earliest cells pass 
peripherally to the peripheral organs and enter the anlagen of the 
peripheral terminal vagus plexuses (the vago-sympathetic plexuses 
of Kuntz), viz., the pulmonary, cardiac, and the myenteric and 
submucous plexuses of the digestive tube. It is only at a later 
date that these plexuses receive a fresh accession of cells from the 
thoracic sympathetic system. In his valuable paper on the evolu¬ 
tion of the sympathetic system Kuntz discusses the question of 
the existence of a sympathetic system in Petromyzonts, and con¬ 
cludes, almost certainly rightly, that the earliest sympathetic 
system, the vago-sympathetic, in which is probably to be included 
nerve-elements belonging to the facialis nerve, was primarily 
concerned with the innervation of the blood vessels of the 
branchial apparatus. Now it seems to me that it is highly 
probable that some of the neuroblasts which migrated out from 
the rhombencephalon were arrested in the two vagus ganglia, or 
at any rate the nodosum, and thus formed ultimately the persisting 
proximal motor sympathetic ganglia of the vagus nerve. But I 
go further than this: I believe that all the neuroblasts which 
originally wandered down the vagus nerve into its terminal 
plexuses, and were of two kinds, afferent and motor, formed 
ultimately the only part of the vagus-sympathetic system which 
is truly autonomic or independent of all impulses passing down the 
vagi nerves. I have for many years rejected unconditionally the 
teaching of Langley that the autonomic-sympathetic system is 
entirely or mainly motor; it is, I believe, exactly the other way 
round, being probably quite 60 per cent, afferent and only 40 per 
cent, motor. It is probable, I think, that the terminal vagus 
plexuses (I exclude for the moment the fibres which reach them 



14 


LEONARD J. KIDD 


from the thoracic sympathetic) consist of both afferent and motor 
migrated cells and that they are interconnected by nerve-processes 
to form a local, independent-, autonomic, reflex nervous mechanism. 
I admit of course that some of these points are difficult to establish, 
but the last-named probability is suggested by the recent histo¬ 
logical study by Kuntz 12 (1913) of the local innervation of the 
digestive tube. The point that has always astonished me in the 
adherents of the entirely or mainly motor character of the 
sympathetic-autonomic system is the fact that these are the very 
observers who for a long period of years have accepted unques- 
tioningly the genesis of the sympathetic system entirely from the 
neural crest. Now the neural crest gives origin—mainly, if not 
entirely—to afferent nerve-elements. One would have supposed 
that a sympathetic system derived from the neural crest alone 
would have become exclusively afferent, or nearly so. But the 
researches of Kuntz (1909,-10,-11) have shown the falsehood of 
the exclusively neural crest theory of the origin of the sympathetic 
system; at the same time a careful detailed study of all his nine 
papers has convinced me that the majority of the nerve-elements 
of the sympathetic system are afferent; the number of elements 
which migrate from the ventral wall of the neural tube is in all 
vertebrate classes smaller than the number of those which come 
from the neural crest and the cerebro-spinal ganglionic anlagen. 

3. Summary and Conclusions. 

The main reasons why the nucleus intercalatus of Staderini has 
been hitherto misunderstood by most writers appear to me to be 
the following:—(1) Failure to study its morphological position; 
(2) failure to remember that, if histological structure and the size 
of the nerve-cells of a nucleus be any guide whatever in the 
determination of its function and morphology, then the nucleus of 
Staderini is a visceral nucleus; (3) failure to see the morphological 
inadmissibility of the motor view of the dorsal vagus “ nucleus ”; 
(4) failure to grasp the ganglionic-complex nature of the ganglion 
nodosum vagi; (5) failure to study the bearing of embryological 
researches on the nature of both the ganglion nodosum and the 
peripheral terminal vagus ganglia and plexuses. In order to 
attempt to run these questions to earth it has been necessary 
for me to enter on a rather lengthy discussion. Let us now see 



THE NUCLEUS INTERCALATE OF STADERINI 15 


what we have learnt from it all. We have a well-defined, small- 
celled nucleus situated in the floor of the fourth ventricle of 
many mammals up to that of man ; its total bulk is, so far as we 
can judge by Streeter’s careful measurements, very nearly the same 
as that of the dorsal vagus nucleus; in the lower half of the 
ventricular floor it is obviously always situated in the primitive 
ventro-lateral cell-column of the brain; it is therefore visceral 
motor for unstriped muscle. In the upper half of the floor of the 
fourth ventricle it is also situated in the same ventro-lateral cell- 
column, as I have attempted to show; it is evident that Streeter 4 
grasped this truth also, for he suggested that it might be a 
central sympathetic nucleus. And it is also apparently true to¬ 
day that he and I are the only two writers who have yet grasped 
this truth. By a process of exclusion I have further shown that 
the axons of the nucleus of Staderini do not pass either up the 
brain-stem or down the spinal cord; they do not enter any 
cranial nerve except the vagus; they do not end round cells of 
any of the peripheral terminal vagus ganglia (pulmonary, cardiac, 
Bubmucous, myenteric). Therefore, if, as other evidence proves to 
be the case, the nucleus intercalate of Staderini be really the 
visceral motor vagus nucleus for unstriped muscle, its axons must 
end round cells of one or both of the vagus ganglia (nodosum 
certainly, jugulare possibly). In favour of the correctness of the 
view expressed by Gaskell, 9 so long ago as the year 1886, that the 
ganglion nodosum is sympathetic in character, we have:—(1) The 
fact that it contains some multipolar cells; (2) the morphological 
studies of Mollgaard 10 in Acanthias vulgaris', (3) his further 
finding that, after a section 2 mm. deep made in the medulla 
oblongata of a cat in the region of the dorsal vagus nucleus and 
nucleus intercalatus—which incision of necessity served some of 
the axons of the latter nucleus—some degenerated nerve-fibres 
could be traced downwards and be found to end round cells of the 
ganglion nodosum, and to be in addition absent in the vagus nerve 
below that ganglion. And to these points I may add my own 
suggestions, based on a study of the splendid series of embryo- 
logical and histological researches of Kuntz. 12 The careful 
experimental work of Molhant 7 (1912) has shown that the 
nucleus ambiguus of the rabbit innervates striped muscles 
exclusively. Here again I have shown by a process of exclusion 
that the motor nucleus for the unstriped muscles supplied by 



16 


LEONARD J. KIDD 


branches of the vagus nerve is not the hypoglossal nucleus, not 
Roller’s nucleus, and not the dorsal vagus V nucleus.” The only 
possible remaining cell-group which could be the required motor 
nucleus is Staderini’s nucleus; and the experimental evidence in 
favour of this has also been given here. It would he difficult to 
point to anything stranger in the history of neurology than the 
truly surprising way in which writers, who up to the year 1889 
accepted the afferent reception-nucleus nature of the dorsal vagus 
“nucleus,” then suddenly veered round to the teaching that it 
was motor, and all, forsooth, because it was then proved that it 
gives origin to centrifugal fibres, and they could not grasp the 
conception of a centrifugal fibre being afferent. And yet, had 
they studied their comparative neurology, they would have recog¬ 
nised that evidence had been in existence since the year 1877 
which proved the existence of what I called in 1910 the “endo¬ 
neural afferent ganglionic system.” Then again a few years ago 
J. B. Johnston* showed that such a system exists in Amphioxus, 
which is in some respects one of the most ancient of existing 
vertebrates; and further he traced the dendrites of these endo¬ 
neural afferent ganglionic cells into the skin. And Ross G. 
Harrison f showed that the peripheral afferent root ganglia of the 
teleost Salmo mlar are developed from migrated endoneural 
afferent neuroblasts. And from this we learn that in at least one 
ancient vertebrate form the endoneural afferent ganglionic system 
is more ancient than the exoneural ganglionic, and actually gives 
origin to it. 

On the question as to the constitution of the nerve-elements 
of the peripheral terminal vagus ganglionic plexuses, we must 
recognise definitely that they are formed of two genetically 
distinct parts, viz., (A) a part derived from the vagus nerve, vago¬ 
sympathetic, and (B) an ontogenetically and phylogenetically 
younger part derived from the sympathetic system. And each 
part consists of two parts, an earlier and a later. Thus, I believe 
the vago-sympathetic system to be composed of (1) the earliest 
formed elements, derived from the earliest migrated neuroblasts 
which passed down the vagi from the hind-brain and the vagus 
ganglia; these neurones of the terminal peripheral vagus plexuses 
are entirely independent of all nerve-influences passing down the 

* Biological Bulletin, Vol. i. f 1905. 

t Archiv. fur Mikroa. Anat., Vol. lvii., 1901. 



THE NUCLEUS INTERCALATE OF STADERINI 17 


vagi; they are composed of both afferent and motor nerve-cells, 
and they thus form a local peripheral, independent, autonomic reflex 
mechanism for the unstriped muscle of heart, bronchi, lungs, and 
digestive tube. [An interesting piece of experimental work by 
Cannon and Burket 13 tends, I think, to support my view. These 
authors have studied the question of the endurance of anaemia by 
the nerve-cells of the myenteric plexus; they produced complete 
compression of parts of the alimentary canal of cats, and found 
evidence of the continued existence, both physiologically and 
histologically, of the nerve-cells of the myenteric plexus after 
three hours of complete anaemia, i.e., two hours longer than happens 
in the case of the sympathetic ganglia. They are thus “ the most 
hardy nerve-cells thus far found in the body.”] But it is also true 
that the peripheral terminal vagus ganglionic plexuses give passage, 
without any cell-connection, to two sets of vagus fibres shown 
diagrammatically in Fig. 4; (a) the post-ganglionic motor axons 
rising in cells of the visceral motor part of the ganglion nodosum, 



Fig. 4.—Diagram or Constitution or Vagus Supply to Unstriped 
Musclb, including Cardiac. 


N.LS., Nucleus Intercalatus of Staderini. D. V.N., Dorsal Vagus “ Nuoleus.” 
The local peripheral reflex vago-sympathetic ganglionic plexus is figured: it 
hows two afferent cells and two motor cells, also a post-ganglionic motor axon 
and a dorsal vagus ganglionio dendrite passing through the plexus without cell- 
oonnection. The sympathetic part of the plexuses is omitted. The arrows 
indicate the direction of physiological impulses. 


2 



18 


LEONARD J. KIDD 


and ( b ) the peripheral processes (dendrites) coming from the cells 
of the dorsal vagus “ nucleus,” i.c., endoneural afferent fibres. 

B. The part of these terminal vagus plexuses, which is geneti¬ 
cally derived from the sympathetic system, likewise consists of (a) 
an older, independent, truly autonomic part, and ( b ) a younger, which 
depends functionally on motor and afferent impulses which re¬ 
spectively reach it from and pass from it to the sympathetic 
system. There are thus at least four great groups of neurones in 
these vago-sympathetic terminal plexuses. I am very much in¬ 
clined to believe that (1) all the afferent fibres of the vagus nerve 
which go to organs containing unstriped muscle (and the heart) 
are either processes of the independent, afferent nerve-cells of the 
terminal plexuses or else come from the dorsal vagus “ nucleus ”; 
and (2) that the afferent fibres of the vagus nerve which rise in 
cells of the ganglion nodosum and jugulare pass wholly to skin 
of ear, dura mater of posterior fossa, muscles of pharynx and 
larynx, and mucous membrane of pharynx and larynx. But it is 
a very difficult matter to prove or to disprove. For, if it be found 
that section of a branch of the vagus nerve which is distributed to 
an organ containing unstriped muscle is followed by chromolysis 
of some of the cells of the ganglion nodosum or jugulare, this could 
be interpreted in two separate ways. Thus those who deny that 
the ganglion nodosum contains any visceral motor cells would 
naturally conclude that the chromolysed cells are visceral afferent; 
whereas those who hold to the partly sympathetic nature of the 
ganglion nodosum (and possibly also jugulare) would say that these 
affected cells could theoretically be afferent, or motor, or both 
motor and afferent. And I don’t at present see how anyone is 
going to solve this problem. In conclusion, we need a careful 
renewed experimental inquiry in order to place the question of the 
nature and connections of the nucleus intercalatus of Staderini on 
a sound basis. The chief thing to be done is to perform experi¬ 
mental section of the vagus nerve between the ganglion nodosum 
and the ganglion jugulare; the animals ought to be kept not 
longer than from four to six days. If we find chromolysis of all 
the cells of the nucleus intercalatus of Staderini, we should con¬ 
clude that all its axons end round cells of the ganglion nodosum, 
and none round those of the jugulare. If, however, a few cells of 
Staderini’s nucleus escape chromolysis, we should attempt to per¬ 
form vagotomy above the ganglion jugulare. [One writer confesses 



THE NUCLEUS INTERCALATE OF STADERINI 19 


that he failed to do this in the rabbit; so one would suggest some 
other animal for this purpose.] If we found then a total chromo¬ 
lysis of Staderini’s nucleus we Bhould conclude that some of its 
cells end round cells of the ganglion jugulare. If positive results 
were obtained by one or other of these operative procedures, we 
could resort in another series of animals to Van Gehuchten’s 
indirect Wallerian method. The animals must be kept for from 
thirty to fifty days, and it should then be possible to trace by 
Marchi’s method degenerated fibres passing down from Staderini’s 
nucleus to one or both vagus ganglia. One would greatly welcome 
a histological study by the best modern methods of the cell- 
characters of the nucleus intercalatus of Staderini; and to this 
might well be added a careful study of the medulla oblongata of 
sub-mammalian vertebrates; for Staderini’s nucleus, or some cell- 
group corresponding to it in position and cell-characters, ought to 
be found in some of them at any rate, i.e., if it be really, as I have 
here claimed to show, the visceral motor nucleus for the innerva¬ 
tion of all the unstriped muscle of the vagus organs, with the 
exception of that part of this musculature which is innervated by 
the truly autonomic part of the peripheral terminal vagus ganglia. 
The formal conclusions may be stated thus:— 

1. The nucleus intercalatus of Staderini consists of small cells 
of visceral type, is situated in the ventro-lateral primary cell- 
column of the hind-brain, is a central lateral sympathetic nucleus, 
is the motor nucleus for the unstriped muscles supplied by the 
vagus nerve, and has no morphological nor physiological connec¬ 
tion with any part of the eighth cranial nerve. That nerve is 
exclusively a somatic afferent nerve. 

2. The axons of the cells of Staderini’s nucleus end round cells 
of the ganglion nodosum, and possibly also the jugulare. The 
ganglion nodosum certainly, and the jugulare possibly, are really 
ganglionic complexes, i.e., some of their cells are visceral afferent, 
some visceral motor. 

3. The dorsal vagus “nucleus” is the “endoneural afferent 
ganglion " (Kidd, 1910) for the unstriped muscle supplied by the 
vagus nerve; all its cells are afferent; it is not, even in part, an 
afferent reception-nucleus. 

4. The peripheral terminal vagus plexuses consist of four 
distinct sets of elements, two of vagus origin, and two of sym¬ 
pathetic origin, (a) The older part of the vago-sympathetic 



20 


LEONARD J. KIDD 


system consists of independent, truly autonomic, afferent and 
motor neurones which form a local independent reflex mechanism; 
(&) the younger part consists of nerve-fibres which are dependent 
on influences passing by them from and to the vagi nerves, viz., 
(1) the post-ganglionic motor fibres which rise in the motor part 
of the ganglion nodosum, and (2) the endoneural afferent fibres 
(dendrites) which pass down the vagus nerve from the dorsal 
vagus “ nucleus ”; (3) the older part of the sympathetic portion 
of the peripheral terminal vagus plexuses is independent, and 
forms a local reflex mechanism; (4) the younger part depends on 
motor and afferent impulses passing respectively from and to the 
sympathetic system. 

5. A renewed experimental and comparative histological study 
of the nucleus intercalatus of Staderini is needed. 

I am indebted to Dr A. Ninian Bruce for his kindness in re¬ 
drawing my diagrams to my design. 

4. References. 

1 Stadkrini, R— 

1894. Monitort. Zod. Ilal., Anno ▼., No. 8. 

1895. Arch. Hal. de Bid., Vol. 23, p. 41. 

1895. Internal. MonaUchr. /. A not. u. Phytid., Vol. 12, p. 220. 

1896. Ibid., Vol. 13, pp. 326, 337. 

* VAN GSHtrCHTXN, A.— 

1898. /own. de Neurd. , VoL 3. 

1903. Lt Nivraxe, VoL 5, p. 296. 

* Gram*— 

1873. PJlilgtr’t Arehiv.f. Phytid., Vol. 7, p. 583. 

4 Strut**, G. L.— 

1903. Amer. Joum. qf Anal., Vol. 2, p. 299. 

* Ossipow, W. P. — 

1898. Nevrologitechesky Wjeetnik., Vol. 6 (Russian language). 

(Abstract in Neurd. Centroid., VoL 17, 1898, p. 697.) 

* Tricomi-Allxgra, G.— 

1903. Rivista. di Paid. Nerv. e. Mentale. 

7 Molhant, M.— 

1911. Lt Nivraxe, Vol. 11, p. 131 (Dorsal vagus nucleus). 

1912. Ibid., Vol. 12, p. 221 (Nucleus ambiguus). 

* Dus, O.— 

1889. Arch./. Peychiatr. it. Nerven-Krankh., Vol. 20, p. 89. 

* Gaskkll, W. H.— 

1886. Joum. of Phyeid., VoL 7, p. 71. 



ABSTRACTS 


21 


19 Mollqaard, H.— 

1912. Skandinav. Arch./. Physiol. , Vol. 26, p. 315. 
u Muller, L. R.— 

1911. Deutsch. Arch./. Klin. Med., Vol. 101, p. 421. 

11 Kuntz, A.— 

1909. Anal. Ameiger, Vol. 35, p. 381; Anal. Record , Vol. 3, p. 458. 

1910. Joum. Comp. Neurol. , Vol. 20, p. 211 (Mammals); Vol. 20, p. 283 

(Birds). 

1911. Amor. Joum. o/ Anal., Vol. 11, p. 279 (Reptiles). 

1911. Joum. Comp. Neurol. , Vol. 21, p. 177 (Fishes); p. 215 (Evolution of 
the Sympathetic Nervous System); p. 397 (Amphibia). 

1913. Ibid., Vol. 23, p. 173 (The innervation of the digestive tube). 

11 Cannon, W. B., and Burket, I. R.~ 

1913. Amor. Joum. o/Physiol ., VoL 32, p. 347. 

14 Kidd, L. J.— 

1910. Rev. o/ Neurol, and Psychiatry, Vol. 8, p. 673 (The dorsal vago¬ 
glossopharyngeal nucleus). 

[A full list of references to the literature of the dorsal vagus nucleus will be 
found in the papers by Molhant 7 (1911) and by Kidd. 14 The only additional 
reference known to the writer now is the paper by Niedzvietzky (Bull. Soc. Imp. 
des Naturalistes de Moscov ., Ann6e 1896, No. 3, 1897, p. 515); he is one of about 
twenty experimentalists who proved that the dorsal vagus nucleus gives origin 
to oentxifugal fibres: his work was done on four rabbits.] 


abstracts. 

ANATOMY. 

A NOTE ON THE SULCUS POST-CENTRALIS SUPERIOR. 

(l) Geoffrey Jefferson, Anat. Anxeig., 1913, xliv., Juni 12, S. 91. 

The sulcus “ interparietalis ” of animals lower than anthropoids is 
identical with the sulcus post-centralis of man, and should be 
called by that name. The so-called sulcus post-centralis superior 
of pithecicUe lies within the sensory area, and cannot therefore 
really be “ post-centralis ” in function. It should be called sulcus 
prse-parietalis as a distinguishing mark. The sulcus post-centralis 
superior of man is a composite sulcus, and consists of three separate 
parts, not all of which can be identified in any given case. The 
sulcus cinguli has an arcus cinguli (mihi) thrown round its outer 
end. Every deep sulcus is thus bounded by an arcus (e.g., parieto- 




22 


ABSTRACTS 


occipital, calcarine). The arcus cinguli is bounded by a sulcus, to 
which I have given the name of sulcus paracinguli. This sulcus is 
frequently continuous with the sulcus post-centralis superior. To 
this fact is largely due the variety of form which the latter sulcus 
displays. It is advisable to distinguish limiting sulci as being of 
the first and second degree, according as they separate areas of 
totally different function and structure, or merely specialised parts 
of one great area from one another ( e.g ., the parietal area). 

A. Ninlan Bruce. 


ON THE MICROSCOPIC STRUCTURE OF THE OTIC GANGLION. 
(2) (Sulla fine struttura del ganglio otiro.) Carlo Riqjjier, Riv. di 
Patol. nerv. e ment., 1913, xviii., p. 609. 

The otic ganglion has been studied in this paper in preparations 
made from the ox and the human subject. The type of cell in 
the otic ganglion in both cases was found to resemble the cells 
occurring in ganglia of undoubted sympathetic nature. The 
differences that may be observed between the otic and the sympa¬ 
thetic ganglia are mainly those of gross structural form, or of 
distribution and size of the cellular elements. F. L. Golla. 


CONTRIBUTION TO THE KNOWLEDGE OF THE MEMBRAN- 
(3) OUS LABYRINTH. ON A FOURTH CRISTA AOUSTICA. 
(Beitrag zur Kenntnis des L&utigen Labyrinthes. Uber dine 
vierte Crista Acustica.) C. E. Benjamins, Zttckr. /. Ohrenheilk ., 
1913, lxviii., May, S. 101. 

The author first of all defines the difference between the crista 
ampullaris and the macula acustica. The crista lies on a fold of 
the membranous wall, has long hairs united to a cupula, and lacks 
otoliths; the macula, on the contrary, lies spread out flat, has short 
hairs, and is always covered by otolithic crystals. He now gives a 
description of the crista quarta as occurring in fishes, reptiles, and 
mammals. A detailed description is given in the case of the eel. 
The crista quarta is found on the floor of the so-called sinus 
posterior utriculi, which runs between the ampulla posterior and 
utriculus. It consists of an epithelial hillock of slightly lower 
height than that of the crista ampullarum, and of a characteristic 
round shape. It sits on an elevation of the membranous wall. 
A little bundle of long hairs stretches into the lumen of the sinus 
and is connected with a cupula. Otoliths are absent. The nerve 
supply comes as a twig from the branch of the eighth, which 



ABSTRACTS 


23 


supplies the posterior ampulla. Eighteen varieties of fish were 
examined; the crista was found in all except the flat fish and 
syngnatlivs acus. In the frog a sensory epithelial hillock with long 
hairs is found in a recess of the upper sacculus wall. The author 
thinks this probably is the homologue of the crista quarta. In 
the adder the crista is found in the lower part of the utriculus, 
close to the entrance of the ampulla posterior. In the pigeon it 
lies close to the crista ampullaris posterior. In birds a consider¬ 
able reduction in size of the crista quarta is noticeable. The 
mole, hedgehog, rabbit, mouse, pig, cat dog, Tarsius spedruvi, and 
man were examined. In all of these the crista quarta is found in 
the sinus posterior utriculi, near the ampulla of the posterior canal. 
In the rabbit it was not found, but is probably present. It varies 
from 90 p to 120 /x broad, and from 40 /x to 60 /x high. 

Retzius had noticed the structure in fishes, and named it the 
macula acustica neglecta. This name should be changed to crista 
quarta. 

A chapter is devoted to embryology. In bony fishes the crista 
quarta is developed from the epithelium of the macula sacculi. In 
mammals and fishes it develops from a high round layer of 
epithelium on the lateral wall of the utriculus, which becomes 
smaller and confines itself to the sinus posterior utriculi, becoming 
differentiated into a round structure at the entrance of the hori¬ 
zontal canal, and the crista quarta. Some suggestions are thrown 
out as to physiological significance which must be small in animals. 
The article is illustrated with very fine micro-photographs. 

Raymond V£rel. 


PSYCHOLOGY. 

EXPERIMENTAL PRODUCTION IN MAMMALS OF THE PINEAL 
(4) PRECOCIOUS MACRO GENITO-SOMATIC SYNDROME. (La 
Sindrome epifisaria macrogenitosomia precoce ottenuta speri- 
mentalmente nei Mammiferi) Sartkschi, U., Pathologica., 1913, 
v., Dec. 1, p. 707. 

Sarteschi has produced, by means of pineal extirpation, the same 
bodily overgrowth, hypertrophy of the testes, and premature 
sexual development in very young rabbits and puppies which 
Foa did in cockerels (1912). Sarteschi attempted pinealectomy 
also in very young kittens, but with constantly fatal results. He 
used the operative method of Lomonaco, and by ligature of the 
stalk obviated the risk of haemorrhage; a temporary ligature of 
the carotid artery gives an anaemic field of operation. Out of 



24 


ABSTRACTS 


23 rabbits operated on at the age of about 45 days, 3 survived; 
a small remnant of the pineal body was found adherent on 
autopsy, and the testes were greatly hypertrophied; the animals 
had grown much more than the controls of the same age. One 
doe gave birth to young, and one buck became a father. All the 
organs and internal secretory glands were normal. Sarteschi 
concludes that in rabbits pinealectomy, whether it be complete or 
incomplete, determines a great bodily development, sexual 
precocity, and notable enlargement of the testes. In puppies, the 
operation is more difficult: out of 27, 5 survived: operation took 
place at the age of 2 months. The same results were obtained as 
in the rabbits: one male puppy copulated completely several 
times at the age of 6 months, but without fertilisation until he 
was nearly 7 months old. It was noted that after each sexual 
act he lost flesh, but his general health and nutrition remained 
good; his testes were of adult size before he was 5 months old; 
on autopsy they were histologically normal. Another male puppy 
showed at the age of 5 months great size and adiposity, with 
enlarged testes; but his sexual functions were not tested. 
Sarteschi “ accepts Pellizzi’s hypothesis that the pineal body 
exercises a moderating action on genito-somatic development.” 
Four figures illustrate the testicular hypertrophy and the large 
size of the fat puppy here mentioned. Leonard J. Kidd. 


STUDIES ON PELLAGRA—I. THE INFLUENCE OF THE MILLING 
(ft) OF MAIZE ON THE CHEMICAL COMPOSITION AND THE 
NUTRITIVE VALUE OF MAIZE-MEAL. Casimib Funk, 
Joum. Physiol 1013, xlvii., p. 389. 

The chemical investigation of the different fractions of the maize 
grain obtained during the milling renders it extremely probable 
that the localisation of vitamines is closely analogous to that of 
rice. There are four distinct layers which give on analysis 
different results, and it would seem probable that the vitamines 
are distributed in the external layers of the grain. This explains 
why, according to the mode of preparation of maize-meal in 
different countries, the manifestations of pellagra vary from mild 
to severe forms. We are not able to say at the present moment 
which of the three external layers is more likely to contain the 
bulk of the vitamines. Besides vitamines the grain is deprived 
during the process of milling of a great quantity of salts, proteins, 
fat, and lipoids. The result of this investigation is that for the 
present moment it would be advisable to abandon the present 
mode of milling, since only the whole grain, including the skin, 
can be regarded as a complete food. A. N ini an Bruce. 



ABSTRACTS 


25 


PATHOLOGY. 

ON THE STRUCTURE OF THE MYELIN SHEATH AND ITS 
(6) ALTERATION IN SECONDARY DEGENERATION. (Sulla 
itruttura della guaina mielinica e eul suo comportamento nelli 
degeneration! secondarie con nn nuovo metodo dlndagine.) 
Fkbuccio Goidi, Riv. di Patol. nerv. e ment., 1913, zviii., p. 638. 

Thr method used is that of Besta, which is thus summarised:— 

1. Blocks of nervous tissue are fixed in a solution of 20 per 
cent, formalin with 2 per cent, acetic aldehyde. 

2. They are washed for twenty-four hours in frequently 
changed water. 

3. Removed to 4 to 5 per cent, ammonium molybdate for forty- 
eight hours. 

4. Celloidin blocks prepared (alcohol, alcohol ether, ether, soft 
celloidin, hard celloidin), and sections cut. 

5. Sections of 20 to 30 /t stained for some hours in Mallory’s 
phosphotungstic hsematoxylin at 40° C„ washed for some minutes 
in water, differentiated by the method of Pal, and mounted in balsam. 

By this method a preparation is obtained showing a well- 
marked reticular appearance in normal nerve fibres both in 
longitudinal and cross section. 

In cross section it is seen that the reticulation is confined to 
the sheath, and the axis is uncoloured. 

In the process of secondary degeneration the alveolar reticular 
structure becomes irregular, and later, granular in appearance; 
finally the sheath appears to be uniformly clear'and structureless. 

The first signs of degeneration are met with twenty-four hours 
after the initial lesion. F L. Golla. 


CONTRIBUTION TO THE PATHOLOGY OF PARALYSIS AGITANB. 

(7) Haskovxc and Basta, Nouv. Icon, de la SalpStriire, 1913, March- 
April, p. 127. 

In two advanced cases of paralysis agitans the authors have found 
that along the axones of the white matter of the central nervous 
system a neuroglial network is often to be seen, and similarly a 
network inside the nerve sheaths of the peripheral nerves. They 
also noted regressive pigmentary changes in the nerve cells, more 
advanced, in their opinion, than can be accounted for by the age 
of the patients. They think the changes in the peripheral nerves 
may explain the tremor. 

They also noted changes in the thyroid, and venture the 
suggestion that these are primary to the alterations of the 
neuroglia and of the medullary sheaths of the peripheral nerves. 



26 


ABSTRACTS 


Without further descriptions of the condition of the central 
nervous system (basal ganglia, regio subthalamica, &c.), any 
attempt to explain the pathogeny of the disease in this indeter¬ 
minate fashion is unsatisfactory. S. A. K. Wilson. 

A PECULIAR FORM OF NODULAR HYPERPLASIA OF THE 

(8) LIVER ASSOCIATED WITH BRAIN CHANGES. (Uber eine 
eigenartige Form knotiger Hyperplasie der Leber, kombiniert 
mit GeMmverftnderungen.) Yuoo Yokoyama and Walthkr 
Fischer, Virckouft Archiv ., 1913, cci., S., 305. 

Authors describe a case of a woman, set. 24, who at the age of 
19, without any obvious cause beyond a fright, liegan to develop 
curious mental symptoms. She lost the power of speech, and 
became incapable of work of any kind. The reflexes were normal 
but the gait spastic. Eventually she became unconscious, and 
developed gangrene of the lower extremities. Post mortem, the 
main changes were found in the liver and in the brain. The liver 
showed numerous knob-like projections on the surface. On 
section, yellow areas of liver tissue were found with intervening 
bands of fibrous tissue. The brain showed slight lepto-meningitis 
to the naked eye. Microscopically the liver showed areas of focal 
necrosis, also bands of fibrous tissue dividing the liver substance 
into areas varying much in size. There was well-marked prolifera¬ 
tion of the small bile ducts. 

In the brain a gliosis was found in the cortex of the frontal 
lobes. The vessels were increased in number and their walls 
thickened. In other parts of the cortex a similar increase of 
neuroglia was found, but in a less marked degree. There was 
degenerative changes in the basal ganglia, with similar overgrowth 
of neuroglia. 

The authors regard the condition as probably toxic in origin, 
the poison producing changes in the liver similar to those found 
in subacute yellow atrophy, and in the brain degeneration followed 
by overgrowth of neuroglia. As to the nature of the toxin, they 
do not consider that they can make a positive statement ( v . Revieio, 
1913, xi., p. 167). James Miller. 

HISTOLOGICAL OBSERVATIONS ON THE NERVOUS SYSTEM 

(9) OF THE PROGENY OF ANIMALS SUBJECTED TO 
CHRONIC ALCOHOLIC POISONING. (Riserche istologiche del 
sistema nervoso centrole in discendenti di animali cronicamente 
alcoolizzati.) M. Ferrari, Clinica Medica Italiana, 1911. 

The lesions produced in the nervous system of guinea-pigs sub¬ 
jected to prolonged alcoholic poisoning can be transmitted to their 



ABSTRACTS 


27 


offsprings. Lesions are found in the meninges, the vessels, and 
the nerve cells. The cells are most frequently and severely 
damaged in the spinal cord. In some cases epileptic convulsions 
occurred both in mother and offspring. F. L. Golla. 


CLINICAL NEUROLOGY. 

THE INVESTIGATION OF THE HIGHER NERVOUS FUNCTIONS. 

(10) I. PxWLOyr, Brit. Med. Jowrn ., 1913, Oct. 18, p. 973. 

The outlines are here given of twelve years of work upon the 
mechanism of the formation of new reflexes and the mechanism of 
the analysers. These reflexes of recent formation are termed 
“ conditional reflexes,” from their great dependence on a multitude 
of conditions. Ordinary reflexes may be termed “ unconditional 
reflexes.” To study conditional reflexes the salivary glands were 
used. The fundamental condition for the formation of a con¬ 
ditional reflex is that whatever indifferent stimulus is chosen for 
the purpose of the reflex which it is desired to build up, it is given 
at the same time as the food or acid is introduced into the mouth. 
After a few such sittings it will be found that this formerly in¬ 
different stimulus alone is now capable of calling forth a secretion 
of saliva, e.g., the usual result of painful stimuli is that the animal 
either defends itself against it or attacks it. If electrical stimula¬ 
tion of the skin be accompanied by feeding of the animal, after a 
time even the strongest electrical stimuli applied to the skin gives 
rise merely to the feeding reaction, i.e., to secretion of saliva and 
to no symptoms of fright or pain. Even cutting or burning the 
skin merely causes symptoms of the keenest appetite. The im¬ 
pulse, which formerly went to a particular region, is now directed 
to a different one, and one of the most important functions of the 
highest parts of the central nervous system is the dispersion of 
such impulses. These reflexes are subject to inhibition, which 
may be spontaneous, external, internal, or conditional. In an 
animal from which the cerebral hemispheres have been completely 
removed it is impossible to form any “conditional reflexes” at 
all. It appears, therefore, that the cerebrum is the organ for the 
analysis of sensations and for the construction of new reflexes and 
new connections. It represents that part of the animal organism 
which is specialised for the purpose of retaining the animal always 
in a state of equilibrium with the outer world, i.e., it is the organ 
which is above all others necessary for the unimpeded evolution of 
the organism. It is perhaps not rash to think that some of the 
newly-formed conditional reflexes can be transmitted hereditarily 



28 


ABSTRACTS 


and become unconditional thereby. During all this work the 
author has never been able to turn to psychological conceptions for 
help, or to use explanations founded on these conceptions. Such 
help as psychology gives are mere examples of undetermined 
thought, e.g., the animal has remembered, or desired, or thought, 
&c. A. Ninian Bruce. 


A BIOOBNBTIO PRINCIPLE. (Un Prindpio Biogenetivo: la molti- 
(11) plic&zione degli effetti utili indirettL) £. Luoaeo, Riv. dt 
Patol. nerv. e ment., 1913, xviiL, p. 129. 

The study of the “ thinking horses ” of Krall leads the author to 
the conclusion that the structure of the central nervous system is 
such as to render possible under appropriate stimuli association 
complexes which would never be developed during normal life. 

F. L. Golla. 


THE IDIOPATHIC VARIETIES OF MYOCLONUS. (Myoclonies 
(12) essentielles.) Mouiz, Nouv. Icon, de la SalpStriere , 1913, March- 
April, p. 85. 

This is an excellent paper on a vexed subject and repays perusal 
Mouiz distinguishes symptomatic from idiopathic myoclonus. 
In the former group his classification is:— 

1. Infective myoclonus, in toxi-infective conditions. Included 
in this section is Dubini’s disease. 

2. The myoclonus of hemiplegia. 

3. Syphilitic myoclonus. 

4. Hysterical myoclonus. 

5. The myoclonus of degenerates (including Brissaud’s “ vari¬ 
able chorea ”). 

6. Epileptic myoclonus, subdivided into— 

(a) Intermittent epileptic myoclonus. 

(b) Familial epileptic myoclonus—Unverricht’s disease. 

(c) Nystagmus-myoclonus (Lenoble and Aubineau). 

In the latter group are:— 

1. Idiopathic fibrillary myoclonus, inclusive of the myokymia 
of Kny and Schultze and the fibrillary chorea of Morvan. 

2. Paramyoclonus multiplex of Friedreich, in which as a rule 
the muscular contractions do not produce displacement of the 
limbs; and 

3. Myoclonus with big movements (“ & grand displacements ”). 
The author’s paragraphs on diagnosis are very good, but he 



ABSTRACTS 


29 


cannot enlighten our ignorance of the etiology and pathogenesis of 
idiopathic myoclonus. There is a valuable bibliography. 

S. A. K. Wilson. 

TRAUMATIC INTRAMUSCULAR OSSIFICATION. John Mobley, 

(13) Brit Med. Joum., 1913, Dec. 6, p. 1475. 

"Traumatic intramuscular ossification (‘myositis ossificans’) is 
due to migration of osteoblasts into adjacent contused muscle and 
blood clot, after destruction of the periosteum and loss of its 
function as limiting membrane to the growth of bone. It is 
essentially the same process as callus formation. The condition 
may be produced experimentally in animals by reproducing the 
same mechanical conditions by an aseptic open operation. In a 
case of difficulty in diagnosis from sarcoma, open exploration is 
advisable. Simple excision is usually, but not invariably, followed 
by recurrence. Conservative treatment condemns the patient to 
a long period of disability, which may occasionally be permanent. 
Excision, combined with grafting of deep fascia on to the denuded 
surface of bone, gives the best prospect of rapid and complete 
recovery, and is urged for all cases not complicated by ossifying 
periarthritis. Osteoblasts and chondroblasts are the same cells 
under different conditions of nutrition.” A. Ninian Bruce. 

ABSENCE OF THE OCULO CARDIAC REFLEX IN TABES. 

(14) (L’absence dn rdflexe oculo-cardiaque dans le tabes.) M. Loepee 

and A Mougeot, Prog. M6L, 1913, Dec. 27, p. 675. 

In normal persons compression of the eyeballs is followed, after an 
interval of at most two or three seconds, by a slowing of the 
cardiac rhythm by about eight pulsations per minute: on cessation 
of the compression the pulse-frequency returns to its normal. 
The afferent limb of the arc is in the trigeminus nerve, the motor 
limb in the vagus. The writers have carefully examined for this 
reflex in twenty-one tabetics, also the knee and ankle jerks, 
corneal reflexes, Argyll Robertson pupil, the sensibility of the 
eyeballs on deep pressure, and the presence or absence of aortic 
lesions. A table gives particulars of all these points in all the 
cases. The oculo-cardiac reflex was abolished on both sides in 
nineteen out of the twenty-one cases. The authors believe that 
abolition is the rule in tabes; abolition may also occur in some 
cases of exophthalmic goitre, diabetes, and plumbism. All the 
twenty-one cases showed the A. R. pupils. The authors regard the 
loss of the oculo-cardiac reflex in tabes as due to a mesencephalic 
lesion ; it is analogous to the A. R. pupil, and is a sign of upper 
tabes. Leonard J. Kidd. 



30 


ABSTRACTS 


ON THE INCOMPLETE FORMS OF RECKLINGHAUSEN’S 
(15) DISEASE. (Contribution & l’dtude dea formes firnstes de la 
mal&die de Recklinghausen.) P. Bebtbin, Gas. d. Hop., 1913, 
lxxxvi., p. 2093. 

A soldier, aged 22, was admitted to hospital with multiple skin 
tumours and pigmentation. There were no tumours along the 
nerves. The condition had been present since childhood; at the 
age of 5 years a large tumour had developed on the shoulder, 
shortly after it had been injured by a cart wheel. Examination 
of the tumours removed showed an absence of nerve fibres, but 
Bertein regards this absence as apparent rather than real, and 
thinks that the fibromatosis was a true neuro-fibromatosis with 
exclusive localisation in the terminal cutaneous nerves. 

J. D. Rolleston. 


THE MENINGEAL FORM OF POLIOMYELITIS. Arnold Netter, 

(16) Brit. Joum. Child. Dit., 1913, x., p. 531. 

Poliomyelitis with meningeal onset has recently been remarkably 
frequent in France, not only in Paris and the suburbs, but also in 
the provinces ( v. Review, 1910, viii., pp. 35, 537, and 1911, ix., pp. 
75-6). In other countries the meningeal form of poliomyelitis has 
been less frequent, though cases have been recorded in Norway, 
Sweden, Austria, Germany, Holland, and England. The confusion 
between poliomyelitis and epidemic cerebro-spinal meningitis used 
frequently to be made, and was the more excusable as the two 
diseases might appear in epidemic form at almost the same time 
and in the same countries, but the progress of bacteriology and 
experimental pathology now renders the error avoidable. In the 
diagnosis of the condition Netter attaches great importance to the 
examination of the knee jerks, which are lost at an early stage, and 
to the presence of pains in the limbs, which is more marked than 
in other forms of poliomyelitis. J. D. Rolleston. 

MENINGEAL SYNDROME OF THE POLIOMYELITIS TYPE. 

(17) (Syndrome mfoingl k type de poliomyllite.) E. Joltrain and 
P. Rouffiac, Bull, et mim. Soc. mid. Hop. de Paris , 1913, xxxvl, 
p. 473. 

A youth, aged 18, was admitted to hospital with well-marked signs 
of meningitis. Previous attacks of bronchitis and the insidious 
onset of the disease suggested tuberculous meningitis. There 
were marked weakness of the lower limbs and loss of knee and 
ankle jerks. Lumbar puncture gave issue to a clear fluid under 
marked hypertension, containing a large quantity of albumin and 



ABSTRACTS 


31 


abundant lymphocytes, but no microbes. Wassermann negative. 
Within a week the symptoms subsided, and the reflexes returned, 
first the ankle jerks and then the knee jerks. 

Convalescence was slow, but there was no definite paralysis. 

J. D. Rolleston. 

MENINGITIS AFTER FOLLICULAR TONSILLITIS. (Meningitis 

(18) nach follilmlttrer Angina.) E. Siemerling, Deut. Med Wchnschr., 
1913, xxxix., p. 2287. 

A case of serous meningitis in a boy aged 15 years successfully 
treated by repeated lumbar puncture and unguentum cinereum. 
An unusual feature was the abundance of cellular elements, 
especially lymphocytes (300 in 2 c.c.). Wassermann negative. 

J. D. Rolleston. 

HYPERTROPHIC CERVICAL MENINGITIS. Babinski, JumentiS, 

(19) and Jabkowski, Nouv. Icon, de la Salpetriere, 1913, Jan. -Feb., p. 10. 

In this case the clinical symptoms were those of a slowly pro¬ 
gressive quadriplegia, with bilateral atrophy of the shoulder girdle 
musculature, spasticity, paralysis and contracture of the legs, but 
with remarkably little sensory disturbance. The pathological 
condition was a markedly thickened arachnoid in the cervical 
region of the cord, of syphilitic nature, compressing the cord. 
There was, however, little or no evidence of degeneration in the 
spinal paths below or above the lesion. Similarly, the anterior 
and posterior roots were less destroyed than might have been 
expected. S. A. K. Wilson. 

A CASE OF MENINGITIS PURULENTA ASEPTIOA AFTER 

( 20 ) INTRANASAL INTERFERENCE. (Bin Fall von Meningites 
purulenta aseptica nach einem intranasalen Eingriff.) Leopold 
Rsischig, Zttchr. /. Ohrenheilk , 1913, lxix., August, S. 78. 

The patient, a boy aged 7, suffered from nasal discharge coming 
from the left ethmoid and antrum. The left middle turbinal 
was removed and the anterior ethmoidal cells opened; the 
antrum was punctured and washed out. The nose was lightly 
plugged with iodoform gauze. Next morning the temperature 
was 38 9, and the plug was removed. Two days later typical 
symptoms of meningitis were developed; vomiting; slow, irregular 
pulse, 54-60; temperature, 37‘8 ; distinct stiffness of the neck, and 
Kemig’8 sign. Patellar reflexes were not increased, and Babinski 
negative. 30 c.c. cloudy flocculent fluid were removed by lumbar 
puncture, which gave on standing for an hour a green-yellow 



32 


ABSTRACTS 


deposit of pus. No bacteria were seen in fibres, and no growth 
got on culture. After the lumbar puncture improvement set in, 
and in ten days the patient was recovered. He received treatment 
also by urotropin. The author, discussing the cause of infection, 
thinks it probably spread by the lymph paths, accompanying a 
bundle of the olfactory nerve, which, according to Bonninghaus, 
extends on the lateral wall of the nose as far as the middle 
• turbinal. Raymond V£rbl. 

A MBNINGO CEREBELLAR SYMPTOM-COMPLEX IN FEBRILE 

(21) DISEASES OCCURRING IN TUBERCULOUS INDIVIDUALS. 
(Der meningo-zerebellare Symptomencomplex bei fieberhaften 
Erkrankungen tuberkulSser Individuen.) Fokrsteb, Neurol. 
Centralbl 1913, Nov. 16, p. 1414. 

In tuberculous children suffering from such affections as broncho¬ 
pneumonia, pneumonia, bronchitis, pleurisy, &c., the author has 
noted the frequent development of definite and unmistakable 
meningeal and cerebellar symptoms, as a rule with the disappear¬ 
ance of the febrile condition. Sometimes the nervous symptoms 
have continued for weeks or months, sometimes they have been 
of brief duration. They, too, always clear up. He is unable to 
say whether the febrile process lights up a latent meningeal 
tuberculosis, or whether there is a simple toxic meningeal irrita¬ 
tion, with internal hydrocephalus, or whether there is possibly an 
encephalitic process. S. A. K. Wilson. 

TYPHOID CEREBRO SPINAL MENINGITIS IN AN INFANT. 

(22) (Mdningite ctfrtfbro-spinale k bacilles d’Eberth chez un nourisson.) 
L. Lagane, Le Novriston , 1913, L, p. 360. 

A male infant, aged 23 months, was admitted to hospital for a 
febrile state of six days’ duration. There were no typical symp¬ 
toms of typhoid fever, but an incomplete meningeal syndrome was 
present, consisting of slight rigidity in the lower limbs and marked 
vaso-motor troubles. Lumbar puncture gave issue to a turbid 
greenish fluid under hypertension. Antimeningococcic serum was 
at once injected, but no improvement resulted, and death took 
place four days after admission. No necropsy. Examination of 
the cerebro-spinal fluid during life showed numerous typhoid 
bacilli and polymorphonuclears. A blood culture showed typhoid 
bacilli, but cultures of the cerebro-spinal fluid remained sterile. 
The agglutinating power of the cerebro-spinal fluid was intense, 
even in dilution of 1 in 300, while that of the blood, though 
definite, was less marked (c/. Review, 1913, xi., p. 632). 

J. D. Rollkston. 



ABSTRACTS 


33 


ON THE SPINAL COED PHENOMENA OF TYPHOID FEYEB AND 
(83) ESPECIALLY METATYPHOID MYELITIS. (Contribution k 
l’dtude des accidents mddullaires survenant an cours de la fibvre 
typhoids et en particulier de la mydlite metatyphoidique.) Q. 
Gauthier, Thitet de Parte, 1913-14, No. 42. 

Gauthier's main conclusions are as follows:— 

1. Paralysis in typhoid fever due to well-marked myelitis is 
infinitely rarer than paralysis due to neuritis. But cases of 
incomplete myelitis are relatively frequent. The severity of the 
attack of typhoid fever and the age of the patient have no 
influence on the appearance of the spinal cord symptoms. They 
seem, however, to be more frequent in convalescence. 

2. Autopsies in well-marked cases of myelitis show diffuse 
lesions, which are parenchymatous, vascular, and interstitial, the 
grey substance being more affected than the white. The 
parenchymatous lesions appear predominant. 

3. typhoid fever does not give a specific character to the 
special phenomena occurring in the disease. 

4. The prognosis is very grave in well-marked myelitis, and 
less grave in the abortive forms, but it is possible that these acute 
toxi-infections play a part in the production of various chronic 
processes of spinal sclerosis. 

5. Before making a diagnosis of myelitis a minute examination 
of the vertebral column is necessary to exclude the possibility of 
typhoid spine. 

The thesis contains the histories of eighteen cases, one of 
which is original (</. Eevievj, 1909, vii., pp. 660-61, and 1913, 
xi., pp. 489 and 493). J. D. Rolleston. 


ON POST-DIPHTHERITIC ABDTJOENS PARALYSIS. (Tiber post 
(24) diphtherische Abduzensiahmung.) C. Rotheb, Inaugural-Disser¬ 
tation, Breslau, 1912. 

The thesis is based on the study of thirty-four cases observed in 
the Hamburg-Eppendorf Hospital. The writer’s conclusions are as 
follows:— 

1. Abducens paralysis is relatively uncommon in diphtheria. 
It occurred in 1 per cent, of Rother’s cases. 

2. The average date for its appearance was the thirty-fifth day. 

3. Males were chiefly affected, especially boys from five to 
fifteen, in whom the affection was twice as frequent as among 
girls of the same age in whom diphtheria was almost as frequent. 

4. Abducens paralysis was not isolated, but was always associ¬ 
ated with other palsies. 

3 



34 


ABSTRACTS 


5. The left abducena was affected three times more frequently 
than the right. A bilateral affection was the least frequent 
event. 

6. No family disposition to abducena paralysis was observed. 

7. The prognosis was good. Complete recovery occurred in all 
cases but one, who still had slight weakness of the right abducens 
nine months after discharge from hospital. 

J. D. Rolleston. 


A FURTHER CONTRIBUTION TO THE SUBJECT OF TRAUMATIC 
(25) TT JBMATOMYELIA. Bernhardt, Neurol. Centralbl ., 1913, Feb. 

1, p. 147. 

The chief point of interest in this case of hsematomyelia, develop¬ 
ing after a fall of 27 feet, is that the phenomenon of myotonia 
appeared in the muscles of the right lower extremity—the lesion 
was in the lumbar cord mainly—and the myotonic electrical 
reaction was readily obtained. Myotonia has already been noted 
in syringomyelia (Handelsman and others). It is worth re¬ 
membering that in the cases originally described by Kny and 
Schultze as myokymia or myoclonus fibrillaris multiplex, the myo¬ 
tonic electrical reaction was found. In the present case, in the 
somewhat atrophic affected muscles of the right leg, more or less 
constant fascicular or fibrillar muscle twitching was present. 

S. A. K. Wilson. 


REMOVAL OF INTRATHECAL TUMOUR FROMLUMBAR REGION 
(26) OF SPINAL CORD. J. Michbll Clarke and C. A. Morton, 
Brit. Med. Joum ., 1913, May 3, p. 932. 

A woman, aged 52, with no suspicion of syphilis, began to suffer 
from “ rheumatic pains ” in the right thigh in 1909. In 1912 they 
became worse, sharp and shooting in character, and the right leg 
became weak and later numb. A month later it became quite 
paralysed. Loss of power then developed in the left leg, and in 
July she was paraplegic, had a feeling of tightness around the 
lower abdomen, and occasional incontinence. She was examined 
with difficulty on account of the great pain when moved or 
touched. The right leg could not be moved, the left could be 
drawn up slightly and bent at the knee. The paralysis was of 
the flaccid type. The muscles below both knees were markedly 
wasted, and the reaction of regeneration present. Sensation was 
affected below the knees, and there was an indefinite zone of 
hyperesthesia on the left lower lumbar region. Knee-jerks and 



ABSTRACTS 


35 


ankle-jerks were present, with marked ankle clonus on right side, 
not on left. X-ray and cerebro-spinal fluid normal. The diag¬ 
nosis was an extramedullary tumour at the level of the fourth and 
fifth lumbar and first sacral root, chiefly on the right side. At the 
operation a small fibroma was found about an inch in length 
opposite the body of the twelfth dorsal vertebra. There was no 
shock, and a good and uneventful recovery resulted. 

A. Ninian Bruce. 


THE SURGICAL TREATMENT OF CORD TUMOURS. Rotstaot, 
(27) Aouv. Icon, de la SalpStrUre, 1913, Jan.-Feb., p. 36. 

Three cases are described in some detail One point of diagnostic 
value is emphasised by the author: the association of a pleocytosis 
in the cerebro-spinal fluid, with marked increase in the albumin 
content of the same, is very suggestive, if not pathognomonic, of 
compression by a tumour. Nonne also has observed this associa¬ 
tion in six cases of spinal cord tumour. S. A. K. Wilson. 


CHANGES IN THE SPINAL CORD IN TUMOURS OF THE 
(28) POSTERIOR CRANIAL FOSSA (Les modifications dans la 
moelle dpini&re an cours des tumours silgeant dans la fosse 
postdrienre dn crane.) Raimistb and Nkiding, Aouv. Icon, de la 
Salpitriere, 1913, May-June, p. 246. 

In three cases of posterior fossa tumonr (in none were the knee- 
jerks lost) the authors found, mainly in the dorsal cord, swollen and 
cedematous fibres in the intramedullary part of the anterior and 
posterior roots, specially the former. This change was most 
marked when the roots entered the pia mater. No cellular changes 
were found, and no systemic degenerations in the cord. Further, 
in their three cases the writers also noted vascular engorgement, 
mainly in the cord but also in the meninges. There was also a 
dilatation of the perivascular lymphatics, especially in the lumbar 
region. 

The explanation they offer is that increase of pressure in the 
cerebro-spinal fluid impedes lymph circulation in the dorsal cord, 
and that the fluid itself penetrates between the intramedullary 
root fibres; hence lymph stasis and dilatation of lymphatics. At 
the same time the increased pressure leads to venous stasis, and 
these, combined, produced the structural modifications already 
noted, which may go on to actual degeneration. 

S. A. K. Wilson, 



36 


ABSTRACTS 


CONGENITAL FACIAL PARALYSIS. (Angeborene F&zuOis 
(29) lahmnng.) Aloysio de C astro, Neurol. Centra Ibl., 1913, Dec. 1, 
p. 1474. 

Apart from obstetrical causes, congenital facial palsy is a rarity; 
when it occurs it is usually of the infantile Kemschvmnd type. 
The case here reported, however, is one of the even rarer cases 
due to congenital agenesis of the petrous portion of the temporal 
bone. The patient, in addition to having a typical peripheral 
facial paralysis, was completely deaf on the same side : the pinna 
was awanting, and a small pin’s-head canal was present at its 
site, ending blindly. S. A. K. Wilson. 


REPORT OF TWO OASES EXHIBITING LESIONS OF SPECIAL 
(30) INTEREST FOR THE LOCALISATION OF APHA8I0 DIS¬ 
ORDERS. La Salle Archambault, Albany Med. Annals, 1913, 
xxxvi., March, p. 126. 

Case I. A man, aged 70, right-handed, had suffered for ten years 
from postero-lateral sclerosis, for which he was under observation. 
Lobar pneumonia in February 1910 was followed by a right 
hemiplegia of unevenly distributed intensity. He gradually 
rallied, but died 2nd June 1910. He was submitted to all the 
tests usually employed for the detection of aphasic disorders, but 
no deficit could at any time be demonstrated. At the autopsy, 
the posterior third of the ascending frontal convolution was 
completely destroyed, with slight involvement of the inferior third 
of the ascending frontal convolution. 

Case II. A woman, aged 54, right-handed, was suddenly seized 
one day with motor aphasia and agraphia. This was complete 
for one week, and gradually passed off. From this time on, for 
three years, severe convulsions, followed by motor aphasia of one 
to three days’ duration, occurred, with almost the periodicity of 
true epilepsy at intervals of about six weeks. Then a severe 
attack of right hemiplegia and complete motor aphasia occurred. 
The paralytic symptoms cleared up slowly. There was no 
dysarthria nor sensory aphasia. Her vocabulary never became 
large, and if she used a wrong word, she was aware of the fact. 
Spontaneous speech was not much in evidence. She still continued 
to have severe convulsions at fairly regular intervals, with motor 
aphasia for one or two days. At the autopsy three cerebral lesions 
were found. The largest was of three months’ standing, and 
completely destroyed the posterior two-thirds of the outer segment 
of the lenticular nucleus, and the corresponding part of the external 
capsule, the claustrum and sub-cortex of the island of ReiL The 
second was small, and lay in the middle segment of the superior 



ABSTRACTS 


37 


frontal convolution. The inferior frontal convolution was intact. 
The third lesion was in the angular gyrus, at its junction with the 
base of the second temporal convolution. A. Ninian Bruce. 

CONTRIBUTION TO THE STUDY OF THE LOCALISATIONS 

(31) IN APHASIA. (Contribution & l’6tude des localisations do 
l’aphasia.) La Salle Abchambatjlt, JVouv. Icon, dc la SalpStrtere, 
1913, Jan.-Feb., p. 20. 

In the case of an old man of 70, with slight right facial weakness, 
and a monoplegia of the right arm, and with no aphasia, it was 
discovered subsequently that the posterior end of the third left 
frontal gyrus was destroyed by a softening which slightly invaded 
the corresponding part of the precentral gyrus. The patient was 
right-handed. Although the descriptions from both the clinical 
and the pathological side are somewhat meagre, the author is 
perhaps justified in claiming this as a case in support of Pierre 
Marie’s contentions. 

In a second case, in a woman of 54, a lesion was found in¬ 
volving the posterior two-thirds of the outer segment of the 
lenticular nucleus, and the corresponding part of the external 
capsule, claustrum, and the island of Reil. There were also 
lesions in the first frontal convolution, and the angular gyrus 
of the same (left) hemisphere. The author says, in his considera¬ 
tion of the case, that the main lesion was sufficient “ k elle seule k 
determiner une aphasie motrice k la fois tr&s marquee et per- 
manente.” It does not appear, however, in his description of the 
clinical symptoms, that the patient’s “ motor aphasia ” was either 
typical or severe. She was evidently able to say a good deal in 
response to questions, and after the ictus she “ continua k enrichir 
quelque peu son vocabulaire pendant environ huit semaines.” She 
was able to repeat words which she could not say spontaneously. 
The author “ is convinced that the projection fibres from the 
inferior frontal gyrus were not caught in the lenticular lesion.” 

In this paper Figs. 1 and 2 are presumably interchanged. 

S. A. K. Wilson. 

A LEFT PREFRONTAL GLIOMA WITH APHASIA (Glioma pre 

(32) frontale sinistio con afasia.) G. Pellacani, Riv. dc Patol. nerv. 
t merit., 1913, xviii., p. 512. 

The patient died soon after admission to an asylum, to which he 
had been sent on account of mental depression culminating in an 
attempt at suicide. He was found to have paresis of the right 
arm, but no aphasia. Two days after admission he had a right¬ 
sided fit, followed by aphasia, lasting for three hours. A right 



38 


ABSTRACTS 


hemiplegia with motor aphasia developed in the coarse of the 
next few days, and the patient rapidly sank into a semi-comatose 
state, and died. A glioma was found extending from the foot of 
the superior frontal convolution to the beginning of its upper 
third, and involving a portion of the middle frontal Whilst 
superficially the area of Broca appeared to be intact, microscopical 
examination of Weigert Pal preparations revealed the presence 
of marked degeneration. F. L. Golla. 

HAEMORRHAGE INTO THE LEFT SUPRAMARGINAL AND 

(33) ANGULAR GYRL (Enorragia nel giro sopramarginali e nel giro 
angolare dis sinistra.) E. Ciabla, Riv. di Patol. nerv.« ment., 
1913, xviiL, p. 473. 

The patient presented periods of lucidity, alternating with periods 
of confusion, partial auditory aphasia associated with dysarthria. 
There was slight left facial and brachial paresis. Clonic contrac¬ 
tions of the neck muscles and the limbs occurred, chiefly localised 
to the left, but sometimes generalised. During a generalised 
attack there was conjugate deviation of the head and eyes to the 
right There were occasional tremors of the left quadriceps and 
choreiform movements of both upper extremities. No disturbances 
of objective sensation, and no apraxia. The cerebro-spinal fluid 
was yellowish. The homolateral motor discharges could not be 
explained by non-decussation of the pyramidal tracts, as these 
were found to decussate normally. It was noted that softening 
from the cortical lesion had extended inwards sufficiently to 
involve some of the cortico-callosal fibres. To irritation of these 
fibres causing discharges from the right cortex the author ascribes 
the homolaterality of many of the fits. Another point insisted on 
is the absence of apraxia, although the left supramarginal gyrus 
was in great part destroyed. F. L. Golla. 

CLINICAL OBSERVATIONS ON TUMOURS OF THE PIA MATER. 

(34) (Osservazioni clinichs ed anatomo patolgiche sopra i tumori della 
pia cerebrals.) Ciurrmi, Riv. di PatoL nerv. e ment., 1913, xviii. 
p. 709. 

The author adds a fifth case to the four previously described of 
this rare condition. 

The cerebro-spinal fluid contained large round cells with 
granular protoplasm which allowed him to make the diagnosis 
of a tumour affecting the meninges. Post mortem, an endothelioma 
of the pia was found, which occupied the greater portion of the 
cerebral convexity, and compressed, without infiltrating, the 
subjacent cerebral cortex. F. L. Golla. 



ABSTRACTS 


39 


A CASE OF “ IDIOPATHIC HYDROCEPHALUS" IN THE FORM 

(35) OF WEBER’S SYNDROME: RAPID CURE BY LUMBAR 
PUNCTURE. (Uber einem Fall von “Hydrocephalus idio- 
pathicus” outer der Maske des Weber’schen Symptomen- 
komplexes. Sofortige Heilung durch Lumbalpunktion.) Conto, 
Neurol. Centralbl 1913, Jan. 1, p. 20. 

The patient was a man of 24, who for a month had suffered from 
headache, giddiness, vomiting, and in whom a left hemiplegia and 
a right oculomotor palsy had gradually developed. (The condition 
of the optic discs is unfortunately not specified.) Within twenty- 
four hours of a lumbar puncture, in which no fewer than 35 c.c. 
were withdrawn, the patient’s condition showed a phenomenal 
change for the better. A second lumbar puncture was made, 20 
c.c. being withdrawn, and in a short time the patient left hospital, 
every symptom having disappeared. 

Unilateral symptoms in serous meningitis are rare, nevertheless 
they occur: they are still rarer in idiopathic hydrocephalus. The 
author imagines in his case that hypersecretion of the right 
choroid plexus produced pressure symptoms, the hydrocephalus 
increasing the tension especially where the plexus surrounds the 
cerebral peduncle. S. A. K. Wilson. 

A CASE OF TUMOUR OF THE PITUITARY BODY. A. L. Taylor, 

(36) Lancet, Nov. 22,1913. 

The case was that of a married woman, aged 48, with a history of 
five years’ illness. The outstanding symptoms were mental apathy 
passing into profound dementia, amaurosis, epileptic fits, and 
vomiting: there were no dystrophic symptoms. 

Death took place from cerebral compression after a sequence 
of fifteen fits. The autopsy showed a spindle-celled sarcoma, 
4'5 cm. x 6 cm., occupying the middle third of the anterial cranial 
fossa, and arising from the sella turcica. No actual invasion of the 
adjacent parts was present, but a deep hollow between the frontal 
lobes was the result of the growth. Attention is drawn to the 
pressure on the frontal lobes producing dementia; two other 
similar cases are mentioned. Author’s Abstract. 


HYPOPHYSEAL INFANTILISM. Souqurs and Chauvet, Nouv. 
(37) Icon, de la Salpetribre, 1913, March-April, p. 69. 

When the patient, whose case is described at length, came under 
observation, he was 27 years old. Since the age of 8 he had 
entirely ceased to grow, and at that age he had begun to show the 
early symptoms of intracranial tumour. From the age of 8 to 18 



40 


ABSTRACTS 


he remained in a stationary condition. Then slight improvement 
set in, of a temporary kind. When seen and examined by the 
authors his whole appearance was typically infantile, without any 
adiposity at all. His height was 1 m. 27, his weight was 29£ 
kg. His body was well proportioned, with no hair in axillae or on 
the pubis; the external genitalia were infantile. His voice had not 
“broken.” The pupils were inactive to light, there was double 
optic atrophy, and vision was nil. The urine was normal; so was 
the cerebro-spinal fluid. An X-ray showed considerable enlarge¬ 
ment of the sella turcica. 

In an interesting discussion, with references to analogous cases 
in the literature, the author leans to the opinion that the 
symptoms are due in this case to a hypo-function of the anterior 
lobe of the pituitary body. S. A. K. Wilson. 


THREE CASES OF DYSPITUITARISM. A. W. Falconeb, Edin. 
(38) Med. Joum., 1913, xi., Dec., p. 487 

Case I. —Female, aged 16£, with dwarfism, sexual infantilism, 
emaciation, marked diminution of carbohydrate tolerance, 
abnormally small sella turcica, left homonymous hemianopia, 
with double optic atrophy, and history of polyuria: subject of 
congenital syphilis, and Wassermann reaction strongly positive. 

Case II. —Male, aged 21, with definite acromegalic features, 
sexual infantilism, and characteristic type of adiposity. 

Case III. —Male, aged 18, with feminine type of adiposity, 
maxillary prognathism, high carbohydrate tolerance, slightly 
enlarged sella turcica, and fits of “ dreamy ” type (associated with 
irritation of uncinate lobe). Fits disappeared on glandular 
feeding. A. Ninian Brucb. 


DOES ACHONDROPLASIA CORRESPOND TO A PARTIAL HYPO 
(39) PITUITARISM? (L’achondroplasie rdpond-elle k one uuraflisance 
hypophysaire partielle 7) Baumel and Mabgarot, Nouv. Icon, de 
la SalpHriere, 1913, May-June, p. 202. 

Apropos of a case of achondroplasia the authors suggest as syndromes 
of pituitary insufficiency the following:— 

1. Defect of anterior lobe :— 

Total —ateleiosis (Hastings Gilford). 

Partial —achondroplasia: periosteal dystrophy. 

2. Defect of posterior lobe:— 

Total— -dystrophia adiposo-genitalis (Frohlich). 

Partial —adiposity without genital hypoplasia: genital 
hypoplasia without adiposity. 



ABSTRACTS 


41 


It may be remarked that it is very far indeed from demonstrated 
that ateleiosis is due to defect of anterior lobe function, and the 
association of partial anterior hypopituitarism with achondroplasia 
is purely hypothetical. Nor is it certain that genital hypoplasia 
without adiposity is linked to partial defect of posterior lobe 
function. S. A. K. Wilson. 


ACHONDROPLASIA AND CH0NDR0HYP0PLA8IA. Ravenna, 
(40) Nouv. Icon, de la Salpitriere , 1913, May-June, p. 157. 

The author is concerned with those by no means rare atypical 
cases of achondroplasia, in which the condition is limited in its 
somatic distribution. He refers, among others, to the cases of 
humeral micromely of Regnault, and Stannus and Wilson. His 
own two cases are interesting, inasmuch as they present only 
slight signs of what is commonly called achondroplasia, and illus¬ 
trate the extreme difficulty of determining where that condition 
begins and ends. S. A. K. Wilson. 


A FRESH CONTRIBUTION TO THE STUDY OF ACHONDRO- 
(41) PLASIA. Parhon and Schunda, Nouv. Icon, de la Salpctriere, 
1913, May-June, p. 185. 

Four cases are described, one of which came to autopsy. The 
main findings were sclerosis of the thyroid and also of the 
pituitary. The patient, however, was 57 years old. 

S. A. K. Wilson. 


THE NERVOUS VARIETIES OF A NEW FORM OF TRYPANO- 
(42) S0MIA8IS—CHAGAS’ DISEASE. (Lee formes nerveuses d’une 
nouvelle trypanosomiase—Maladie de Chagas.) Carlos Chagas, 
Nouv. Icon, de la Salpctriere , 1913, Jan.-Feb., p. 1. 

The author describes the symptoms of a new form of trypano¬ 
somiasis produced by the Trypanosoma Cruzi, which reaches the 
human body through the bite of the intermediate host, Triatoma 
magista, one of the hemiptera. The disease occurs with remark¬ 
able frequency in Brazil: more than 200 cases have come under 
the author’s notice. From the neurological standpoint the clinical 
picture of the acute cases is that of a rapidly fatal diffuse meningo¬ 
encephalitis ; the chronic cases are of the diplegic type, sometimes 
with cerebellar symptoms. The trypanosome has been found in 
all the regions of the brain, both in grey and in white matter, 



42 


ABSTRACTS 


and the foci in which it occurs are found to bear no relation to 
the vascular system. Not a few of the cases which survive, and 
become chronic, show the symptoms of pseudobulbar palsy, and 
often their mental condition becomes reduced to one of idiocy. 

S. A. K. Wilson. 


TWO FAMILIES WITH SEVERAL MEMBERS IN EACH 8UFFER- 
(43) ING FROM OPTIC ATROPHY. Jambs Taylor and Gordon 
M. Holmes, Trans. Oph. Soc. of the U.K. , Vol. xxxiii., 1913, p. 95. 

The first family consisted originally of nine, six males and three 
females. Three of four surviving males had optic atrophy; the two 
surviving sisters had good vision. The visual condition was very 
similar in all three; in two practically no other symptoms were 
present; in the third, in which there was also a history of lues, 
absent in the other two, definite symptoms of tabes were present. 

In the second family of ten children the affection was similar 
but more widespread. Of six males, three showed the condition 
under discussion, and one had been operated on for cataract. The 
four females are healthy, the eldest married and had seventeen 
children, of whom six died, one of orbital tumour. The mother 
had three sisters and two brothers, one of whom was nearly blind. 
Of the sisters, one had healthy descendants, another had three male 
children, all with bad vision, and four females. 

In all the cases the same type of visual affection occurred, 
namely, central scotoma with more or less peripheral restriction 
of the field of vision, in this particular differing from Leber’s 
atrophy, which it resembled in its mode of onset. The disease 
was transmitted by the females, and appeared only in the males, 
affecting the younger members of a family, in which there was 
more than one case, at an earlier age than the elder. 

The paper is illustrated by charts and a pedigree. 

H. M. Traquair. 


NERVOUS SYMPTOMS ASSOCIATED WITH OPTIC ATROPHY OF 
(43) THE FAMILIAL TYPE Jambs Taylor and Gordon Holmes, 
Trans. Oph. Soc. of the U.K., VoL xxxiii., 1913, p. 116. 

Seven cases are described which presented visual conditions re¬ 
sembling those found in Leber’s disease in association with nervous 
symptoms, the most common of which were absence or diminution 
of the deep reflexes, especially the ankle and knee jerk. Numb¬ 
ness and tingling in the limbs, together with some anaesthesia and 
analgesia, were also present. 



ABSTRACTS 


43 


In regard to the relation of these cases to Leber’s disease, two 
possibilities are considered. They may belong to Leber’s type, 
differing only in the coexistence of some organic nervous trouble, 
or they may represent another type of familial degeneration 
only related to Leber’s atrophy by the similarity of the visual 
affection. While inclining towards the first of these alternatives, the 
authors point out that the question can only be decided by the 
investigation of a large number of undoubted cases of familial 
optic atrophy. 

Charts and a pedigree illustrate the paper, and a bibliography 
is appended. H. M. Traquaib, 


VASCULAR AND OTHER RETINAL CHANGES ASSOCIATED 

(45) WITH GENERAL DISEASE. Jamjes Taylob, Trans. Oph. Soc. 
0 / the U.K., VoL xxxiil, 1913, p. 1. 

This paper deals mainly with so-called embolism of the central 
artery of the retina, and with those cases which are characterised 
by thrombosis of the retinal veins with effusion and haemorrhages. 
In regard to the first group the author points out that cardiac 
changes are not always present, and that some of the cases are 
undoubtedly due to thrombosis. In eight cases of the second 
group, seven had either cardiac hypertrophy or albuminuria, one 
had neither. 

Thrombosis of the retinal veins, therefore, while not of such 
serious import as albuminuric retinitis, nearly always indicates 
grave visceral disease. H. M. Traquaib, 

EFFECT OF THE ADMINISTRATION OF ALCOHOL ON WAS8ER- 

(46) MANN’S REACTION. (Effetto della somministnudone di alcool 
sulla reazione di Wassermann.) A. Rkzza, Eiv. ital. di Neuro- 
patol., Psychiat. ed Elettroter., 1913, vi, p. 464. 

As the result of his study of nine cases, Rezza concludes that 
the administration of alcohol in doses, recommended by previous 
observers as sufficient to modify Wassermann’s reaction, does not 
in any way affect the reaction in syphilis whether complicated or 
not by nervous symptoms. J. D. Rollsston. 

SPASMOPHILIA AND EPILEPSY. Gbaztz, Neurol. Centralbl., 1913, 

(47) Nov. 1, p. 1366. 

The relations between epilepsy and infantile convulsions are not 
clear; some authors deny, though the majority assert, a definite 
association between the two: any differences are in degree, not 



44 


ABSTRACTS 


in kind. Included in infantile convulsions are so-called eclampsia 
infantum, tetany with convulsions, &c. Some light is thrown 
on this important question by a consideration of the signs of 
spasmophilia: it is a constitutional defect characterised by (1) 
increased excitability to anodal stimulation ; (2) the occurrence of 
Chvostek’s sign: (3) direct muscular irritability—with “ tumour 
formation on percussion: (4) hypertonus of the arteries from 
overaction of the vaso-constrictors: (5) alteration in the blood 
state—presence of Pappenheim’s leucoblasts (nucleus tending to 
polymorphism, with basophil cytoplasm), and increase in large 
mononuclears. 

The author has examined a series of cases of genuine idio¬ 
pathic epilepsy from these standpoints, and finds that almost all 
show these definite signs of spasmophilia, although the clinical 
symptoms were not present. It' is remarkable to note the in¬ 
creased electrical excitability in some of the author’s cases, AOC 
being obtained with 2 ma. and KOC with 3 ma. It is worth 
remembering, also, that in more than 80 per cent, of 138 
epileptics examined by and Long, muscle tumour formation 
was obtained by direct percussion. In some cases of tetany from 
removal of the parathyroids with the thyroid, Esser found a blood 
condition analogous to that mentioned above, which the author 
also obtained in five out of seven cases of epilepsy. 

S. A. K. Wilson. 


THE BRADSHAW LECTURE ON HYSTERIA IN SOME OF ITS 
(48) ASPECTS. T. R. Glynn, Brit. Med. Jowrn ., 1913, Nov. 8, p. 1193. 

A general review of this condition, with an account of a large 
number of interesting cases. A. Ninian Bruce. 


A CASE OF HYSTERICAL MONOPLEGIA FOLLOWING ELECTRIC 
(49) SHOCK. Puevxs Stewart, Brit. Med. Joum., 1913, Dec. 20, 

p. 1680. 

A case of typical hysterical paralysis in a tall muscular young 
man, in which the exciting psychical trauma was an electric shock. 
The left upper limb dangled helpless and flail-like by his side. 
There was total cutaneous amesthesia and analgesia of the limb up 
to the level of the shoulder-joint, bounded by a sharp “ amputation¬ 
line.” This anaesthesia was observed by the patient himself, and 
was not suggested to him by any of the various physicians whom 
he had consulted. There was no evidence of a sexual clement, 
although psycho-analysis had not yet been tried. Suggestion, after 
one month, had produced no result. A. Ninlan Bruce. 



ABSTRACTS 


45 


ON A CASE OF POLYNEURITIS OF PREGNANCY WITH 

(50) SYMPTOMS OF GRAVES’ DISEASE. (Sopra un caso di 
polineurite gravidic* unit* a morbo di Plaiani-Basedow.) 
Pebbebo v. Fenoglietto, Riv. di Patol. nerv. e meat ., 1913, 
xviii., p. 649. 

The history is that of a case of pregnancy in which symptoms of 
exophthalmic goitre developed towards the beginning of the fourth 
month, followed by severe pains in the limbs. A premature birth 
in the eighth month of pregnancy was succeeded by an aggravation 
of the thyroid symptoms, and when examined four months later 
the patient was found to be suffering from multiple neuritis. For 
three months there was some fever, and then the condition 
slowly improved. The case is discussed at some length, and from 
the fact that the patient improved during the administration of 
Moebius’ serum, the author concludes that the whole syndrome is 
referable to hyperthyroidism. F. L. Golla. 

GRAVES’ DISEASE IN THE MALE SEX. (Die Basedowsche Krank 

(51) belt beim Manns.) Mendel and Tobias, Neurol. Centralbl., 1913, 
Dec. 1, p. 1477. 

Ah interesting revue d'ensemble. 

From a large number of cases in the literature the authors 
obtained the following figures: 9 3 cases in women to 1 in man, 
in proportion: the majority of male patients were between the 
ages of 20 and 40. The symptomatology does not vary much 
in the two sexes, except that as a rule the more purely nervous 
symptoms are more marked in the male. The prognosis is worse, 
as a rule, with men, according to the consensus of recorded 
opinion, but the authors have not found it so in their own cases, 
which number 282, observed during the last ten years. 

S. A. K. Wilson. 


GRAVES’ DISEASE AND SOLERODERMIA. Mabinesco and 
(52) Goldstein, Nouv. Icon, de la Salpetriere, 1913, July-Aug., p. 272. 

In this case the typical syndrome of Graves’ disease was accom¬ 
panied by the presence of some twelve or fourteen plaques of 
sclerodermia, more or less symmetrically placed on the lower 
extremities below the knee. The authors go fully into the question 
of the association of sclerodermia with diseased conditions of the 
ductless glands, and admit its most frequent occurrence where 
the thyroid is involved. They do not believe, however, that this 
association is found in every case, and incline to the view that the 
essential lesion is to be found in the centres for the innervation of 
the ductless glands in the sympathetic system. S. A. K. Wilson. 



46 


ABSTRACTS 


A CASE OF SOLEBODERMIA AND ITS RELATIONS TO THE 
(53) SYNDROME OF PROFIOHET. (Etude radiologique d'un cm 
de Scllrodermie. Analogies de la Sclfoodermie avec le syndrome 
de Proflchet.) Bjertolotti, Now. Icon, de la Salpttri&re, 1913, 
July-August, p. 291. 

This is an interesting paper, raising many questions of importance. 
The patient was a woman of 36, presenting unmistakable signs 
of hypothyroidism, with sclerodermia more or less generalised, but 
reaching a maximum in the extremities: there were also acro¬ 
cyanosis and local asphyxia of the fingers, and localised muscular 
atrophy. There were signs of muscular induration, with contrac¬ 
tures, from interstitial myositis, but the atrophied muscles of the 
neck and shoulders were not hard, and resembled those of a 
myopathy. Further, in the neighbourhood of the sclerodermatous 
areas were small, hard, calcareous nodules (syndrome of Profichet: 
“ pierree de la peau ”): there was also a generalised bronzing of 
the skin. 

The author discusses the various points of interest in the case: 
he thinks the nodules are secondary to the sclerodermia, which 
in its turn is associated with the thyroidal atrophy. 

S. A K. Wilson. 


A CASE OF GRAVES’ DISEASE SUCCESSFULLY TREATED WITH 
(54) THE MILK OF A THYROIDECTOMISED WOMAN. (Ein 
erfolgreich mit Milch einerthyroidektomierten Frau behandelten 
Fall von Morbus Basedowii.) Pychlau, Deut. Med. WocK., 1913, 
xxxix., p. 2299. 

A woman, aged 37, who had been suffering from Graves’ disease 
for some years and had been unsuccessfully treated with rodagen, 
antithyroidin and other preparations, showed rapid improvement 
after being given the milk of her sister who had been thyroidecto- 
mised for Graves' disease two years previously. 200 c.c. of the 
milk was given daily, and the treatment was continued for four 
months. Within a month the thyroid became smaller, and within 
two months the exophthalmus disappeared, there were further 
diminution of the goitre and marked improvement of the cardiac 
action. This treatment had to be discontinued, as the sister 
became pregnant and the milk dried up. J. D. Rollkston. 


THE RELATION OF THE THYROID TO ANTITOXIN. Rufkkt 
(55) F arrant, Lancet, 1913, clxxxv., Dec. 27, p. 1820. 

“ Certain diseases, and especially certain toxaemias, cause hyper¬ 
plasia of the thyroid gland in man and animals. Among these 



ABSTRACTS 


47 


diphtheria toxin has been examined especially, and it is found 
that a small dose is sufficient to elicit hyperplasia in a susceptible 
animal, but that as immunity is acquired the thyroid no longer 
undergoes hyperplasia under the toxin. The hyperplasia thus 
decreases as the antitoxic value of the serum increases. The 
thyroid gland, in other words, is protected from the action of the 
toxin by the presence of antitoxin in the serum. There is no 
reason to suppose that any special relation exists between antitoxin 
formation and the thyroid gland—for example, the latter is not 
antitoxic itself. 

“ In some cases commercial antidiphtheritic serum fed to rabbits 
caused death, with the same symptoms as thyroid feeding; this 
may be due to the serum of partially immunised horses containing 
an unusual amount of thyroid secretion from the hyperplasia. 
But this could not be controlled, as the amount of iodine in pure 
serum was too small for accurate estimation. The pure antitoxic 
serum does not appear to contain any estimable increase of iodine/' 

A. Ninian Bruce. 

A CASE OF EPILEPSIA ALTEBNANS. Db Vries, Neurol. Centralbl., 
(56) 1913, March 16, p. 341. 

A bot of 5 suddenly developed an encephalitis at the age of 2£, 
and from that time onwards he suffered from slight hemiparesis 
of the left face, arm, and leg, with horizontal mystagmus in the 
right eye only, and from attacks of tonic contraction of the left 
face, arm, and leg, with forced tonic conjugate deviation of the 
head and eyes to the right. The attacks lasted about three 
minutes, and recurred some twenty or thirty times in the 
twenty-four hours. Consciousness was never lost in them, and 
there was no clonic twitching anywhere, except slightly of the 
left face. There was an extensor response on the left side, with 
exaggerated tendon reflexes, and very slight ataxia of the left 
arm. 

The author expressly notes that during the attacks the patient 
was perfectly able to innervate and move the tonically contracted 
left limbs, though slowly. For this reason he concludes that the 
lesion did not involve the pyramidal tracts. The tonic cramps 
were not of pyramidal origin. From a consideration of a few rare 
cases of similar sort recorded in the literature, the author places 
the lesion in the upper part of the right side of the pons, above 
the level of the fifth cranial nerve, so situated as to involve the 
cortico-pontine path for deviation of the head and eyes after it 
has crossed to the right. On transverse section, he places the 
lesion in the tegmentum, i.e., posteriorly. 

He discusses briefly the fact of the tonic nature of the con- 



48 


ABSTRACTS 


vulsions, and holds that stimulation of “ subcortical centres ” 
produces tonic contraction, while typical clonic contractions are 
of cortical origin. S. A. K. Wilson. 


PSYCHIATRY. 

THE TREATMENT OF GENERAL PARALYSIS WITH SODIUM 
(57) NUOLEINATE AND SALVAR8AN. (Uber Behandlungs- 
▼ersnche mit Natrium mtclemicnm und Salvaraan bei progressiver 
Paralyse, Ac.) Jolowioz, Neurol. Centralbl., 1913, Feb. 15, p. 210. 

Twenty-five cases of general paralysis were treated with intra¬ 
muscular injections of sodium nucleinate, at intervals of from 
eight to fourteen days, followed by intravenous administration of 
salvarsan. In none of the cases was any definite or permanent 
amelioration obtained. The cerebro-spinal fluid, examined in 
sixteen cases, showed no special alterations after treatment. 

S. A. K. Wilson. 


THE ALTERATIONS OF THE CELLS OF THE BULB FOUND IN 
(68) A CASE OF DEMENTIA PR-ffiCOX. (Alterazioni delle cellule 
gangliari del bulbo in un caso di demenza precoce con morte im- 
provista.) A. Rezza, Riv. de Patol. new. e ment., 1913, xviii., 
p. 426. 

Portions of the bulb were examined in a case of dementia prsecox, 
death having been due to accidental causes. The autopsy was 
performed twelve hours after death. The author found constantly 
in the cells examined extensive vacuolation which was not only 
obvious in the cell body, but could be demonstrated in its proto¬ 
plasmic processes. . F. L. Golla. 


THE PSYCHOSIS OCCURRING IN TYPHOID FEVER. (Delli 

(69) psicose nel duoroo del tifo.) Moissey Kobyunsky Riv. di Patol. 
new. e ment ., 1913, xviii., p. 633. 

The writer distinguishes three types of psychosis occurring in 
typhoid fever. 

1. States of acute confusion (amentia and delirium) that 
resemble acute mania, and are prefebrile. 

2. States of hallucinatory confusion with prevalent occupation 
delirium. 

3. States of maniacal depressive insanity which often simulate 
the commencement of a katatonic form of dementia prsecox. 

F. L. Golla. 



REVIEW 


49 


THE MEIOSTAGMINE REACTION IN SOME CASES OF MENTAL 
(60) DISEASE (La re&zione meiostagminica sul Bangui di alcuni 
malati di mente.) F. Benioni, Riv. di Patol. nerv. e merit., 1913, 
xviil, p. 92. 

The surface tension of the blood of a number of cases of goitre, 
cretinism, and idiocy was observed when the serum was tested 
with antigens derived from neoplasm and thyroid glands. The 
results are inconclusive. F. L. Golla. 


TREATMENT. 

THE HIGH FREQUENCY CURRENT IN THE TREATMENT 
(61) OF HIGH BLOOD PRESSURE. H. van Rensselaer, Albany 
Med. Annals, 1913, xxxvi., Feb., p. 77. 

The underlying causes of most cases of high blood pressure is 
metabolic, from faulty digestion of food. The hypertension usually 
precedes renal, cardiac, and arterio-sclerotic changes. By proper 
treatment with high frequency currents the general condition, 
and especially the metabolic processes, are improved. If the 
hypertension be recognised early the initial stages may be cured. 
The actual development of Bright’s disease may be prevented, 
and if renal or cardiac lesions are already present, their rapid 
advance may be checked, and life thus prolonged. At a later 
stage the resistance to the enfeebled heart may be lessened, and 
the risk of apoplexy diminished. A. Ninian Bruce. 


■Review. 

INDUSTRIES FOR THE FEEBLE-MINDED AND IMBECILE. A. 

(62) Bickmork, pp. vi.+66. 1913. Adlard & Son, London. Price2s.net 

Mr Bickmore, who, for the past ten years, has been Craftsmaster 
and Clerk of the Works at Darenth Industrial Colony, an institution 
for feeble-mined and imbecile patients of all ages, gives here a 
brief but most practical account of some of the principal industries 
which may be taught to the feeble-minded. He first gives a short 
history of Darenth Industrial Colony, and then devotes a few pages 
to each of the following trades:—Carpentering, book-binding, brush¬ 
making, basket-making, shoemaking, fibre mat-making, wool rug- 

4 



50 


BOOKS AND PAMPHLETS RECEIVED 


making, tinsmith, tailoring, upholstering, printing, needlework, 
house-painting, building, and wood-chopping. There are numerous 
illustrations. The book is one which cannot but prove of value to 
all those interested in the important question of the training of 
the feeble-minded. A. Nenlln Bruck. 


BOOKS AND PAMPHLETS BBOBIVBD. 

Bickmore, A “ Industries for the Feeble-minded and Imbecile.” Pp. 
vi.+66, illustrated, 1913. Adlard & Son, London. Pr. 2s. net. 

Clark, L. Pierce. “A Clinical Contribution to the Irregular and 
Unusual Forms of Status Epilepticus” (Amer. Joum. Insanity, 1913, lxx., 
Oct, p. 336). 

Clark, L. Pierce. “Newer Aspects of the Treatment of Epilepsy” 
(Med. Record, 1913, Aug. 2). 

Dana, Charles A. “Mental Tests” (Med. Record, 1913, Jan. 4). 

Dana, Charles A, and Berkeley, Wm. N. " The Functions of the Pineal 
Gland” (Med. Record, 1918, May 10). 

Eulenburg, A “Kinder- und Jugendselbstmorde” ( Sammlung Hocke, 
1914, x., H. 6. Pr. M. 1). 

Liepmann, H. “ Die ‘ freie Selbstbestimmung ’ bei der Wahl des Aufent, 
haltsortes nach dem Reichgesetz fiber den Unterstfitznngswohnsitz ” 
(Sammlung Hocke, 1913, x., H. 5. Pr. M. 1.20). 

Rybakow, Theodore. “ La cyclophrdnie,” Moscow, 1914. 

Scholz, L. “Die Gesche Gottfried. Eine kriminalpaychologische 
Studie.” S. Karger, Berlin. 

“ The Psychoanalytic Review.” Vol. 1, No. 1, November 1913. Issued 
quarterly. $6.00 per volume. 

“ Internationale Zteckr. f. Antlicke Psychoanalyse .” 1913, I., H. 6, 
Nov. Jahrlich 6 Hefte. M. 18, =K. 21.00. 

“State Hospital Commission.” Twenty-fourth Annual Report Oct 1, 
1911, to Sept 30,1912. State of New York. 

“ The Training School.” 1913, x., December. 



■Review 

of 

IReurolog^ anb lP>8pcblatn> 


©rigtnal Hrticles 


THE ARCUATE NUCLEUS IN MAN, THE 
ANTHROPOID APES, AND THE MICRO- 
CEPHALIC IDIOT. 

By A. NINIAN BRUCE, M.D., Edinbubou. 

(With Plates 1 and 2.) 

The arcuate nucleus is a small flattened mass of grey matter 
situated on the ventral surface of the medulla oblongata im¬ 
mediately above the decussation of the pyramids. In the higher 
levels of the medulla oblongata, where the open part of the 
medulla is reached, this grey mass shifts its position, and comes 
to lie upon the mesial aspect of the pyramid, and thus constitutes 
the immediate boundary of the antero-median fissure. At the 
upper end of the medulla the arcuate nuclei usually increase in 
size, fuse together across the middle line, and become continuous 
with the grey matter of the ventral part of the pons. Large 
numbers of the anterior superficial arcuate fibres sweep out from 
the antero-median fissure, and end in this nucleus, whilst others 
take origin within it. Many of the anterior arcuate fibres, how¬ 
ever, pass continuously over its surface, and bind it down to the 
pyramid (Cunningham, “ Text-Book of Anatomy,” 1902, p. 460). 

The exact position of the arcuate nuclei in man is well shown 
in Fig. 1, which is taken from a section through the upper part 
of the medulla oblongata of a human adult. Examination of 
similar sections from other adult brains shows that the actual 


5 



52 


A. NINIAN BRUCE 


amount of grey matter which composes this nucleus is subject 
to considerable variation. In some brains it forms a continuous 
narrow strip extending along the surface of the medulla oblongata 
from the lower level of the inferior olive, to fuse with the pontine 
nuclei above. In other brains the greater mass of the grey 
matter is found about the middle of the inferior olive, and rapidly 
tapers off above and below. In other cases it is not continuous 
with the pontine nuclei. It also shows considerable variation in 
shape, in some cases being roughly triangular in outline, in others 
spreading over the greater part of the ventral part of the corre¬ 
sponding pyramids. In many cases it is broken up into a number 
of smaller, more or less isolated, patches scattered irregularly over 
the ventral and ventro-lateral surface of the medulla oblongata. 

The development of the arcuate nuclei has been recently 
described by Essick (Amer. Joum. Anal., 1912, xii., p. 25). They 
arise from the “ rhombic lip ” of His in common with the inferior 
olivary and pontine nuclei—“ the nuclei pontis being formed by 
a migration through a restricted pathway, the corpus ponto- 
bulbare; the nuclei arcuati along with part of the olive by a 
superficial migration over the ventral surface of the medulla” 
( loc . cit., p. 54). In the human embryo, about the beginning of the 
second month, an intramedullary migration of cells takes place 
from the rhombic lip to make up the inferior olive. Towards 
the end of the month this path of migration becomes more and 
more superficial, until many of the cells cross the raphe before 
passing into the medulla. In the lower mammals, where the 
arcuate nuclei are absent, the comparatively simple olivary com¬ 
plex soon acquires its allotment of cells, and when production 
of olivary neuroblasts ceases, those on the surface soon find their 
way into the anterior. In man, however, beforo the olive has 
received all of its cells, and while the migration from the rhombic 
lip is still proceeding actively, neuroblasts which cannot be dis¬ 
tinguished from those destined for the inferior olive begin to 
appear upon the surface. These elements stop on the ventral 
surface near the raphe, and constitute the anlage of the arcuate 
nucleus. At first the pyramidal tract is found to be covered 
from the cervical flexure to the pontine nuclei by this super¬ 
ficial layer of cells, but this uninterrupted sheet of nuclear 
matter becomes later broken up by the formation of the external 
arcuate fibres, and the growth of the pyramidal tract. The crossing 





Plate 1. 



Fn;. 1. 

Transverse .section of Medulla 
Oblongata of Human Adult. 
To show |K)sition of the arcu¬ 
ate nuclei. 


i 






Plate 2. 


Fkl 4. 

Transverse section of Medulla 
Oblongata of Orang. To 
show absence of l>oth arcuate 
nuclei. 


Fid. f>. 

Transverse section of Medulla 
Oblongata of (JhinifKiiizee. To 
show absence of both arcuate 
nuclei. 


Fid. (i. 

Transverse section of Medulla 
Oblongata of Microeephalie 
I<liot (Robert Lindsay). To 
show absence of both areuate 
nuclei. 



THE ARCUATE NUCLEUS IN MAN, ETC. 


53 


of the arcuate axones in the raphe begins to push the main mass 
of the nuclei to each side of the middle line, but the further 
separation into two separate masses is brought about by the 
constant interstitial addition of pyramidal axones. This results 
in a further separation of the inferior olivary nuclei as well as of 
the arcuate nuclei. The arcuate nuclei, being situated on the 
surface, are drawn away from each other, often, however, leaving 
a small amount of grey matter in the form of a connecting bridge. 

The point to which I wish to draw attention in this paper is 
that the arcuate nuclei are absent in the anthropoid apes. This 
fact was well known to the late Professor Cunningham, who 
always referred to it in his lectures upon the structure of the 
nervous system. The sections from which the accompanying four 
figures were taken are from the brains of the gorilla (Fig. 2), gibbon 
(Fig. 3), orang (Fig. 4), and chimpanzee (Fig. 5). The original 
sj>ecimens were made by the late Professor Cunningham, and 
formed part of his collection in the Anatomical Department of 
the University of Edinburgh. It will be easily seen from them 
that the arcuate nuclei are absent. In the case of the chimpanzee, 
the whole medulla oblongata had been cut serially; in the orang 
the series was also very complete. In the gibbon and gorilla the 
series was not so complete, but there were sufficient sections to 
make quite certain that the arcuate nuclei were absent. 

It is also interesting to note that the arcuate nucleus is also 
absent in the true microcepbalic idiot (Fig. 6). The case from 
which this section was taken was that of Robert Lindsay, and will 
be described later in full. His was a very typical case of the 
condition, and the whole of the central nervous system was 
examined. The medulla oblongata was cut serially from end to 
end, and a careful examination revealed a complete absence of both 
arcuate nuclei. 

I am indebted to the Trustees of the Carnegie Trust who 
awarded a grant to provide the illustrations. 



54 


GEOFFREY JEFFERSON 


THE PARIETAL AREA. 

By GEOFFREY JEFFERSON, M.S. (Lond.), F.R.C.S. 

In two recent papers, 1 - 2 the writer has advanced some new 
views on the anatomy and development of the parietal and post- 
central areas of man. These views are based on the modern 
conception of the origin and cause of the cerebral sulci put forward 
by Elliot Smith. A brief account of this work of the last named 
will be found in the new Cunningham’s “ Text-Book of Anatomy,” 
and especially in the paper by him referred to below. 

Difference of structure of the various parts of the cortex is the 
principal factor in the causation of sulci. And with this difference 
of structure we may assume a difference of function. From this 
we may argue that as we trace the mammalian scale upwards we 
shall find that with evolution new sulci will appear to limit or 
infold the cortical areas with which the newly acquired functions 
are associated. There can be few functions, however, that are 
totally unrepresented on even the lowest brains. So that what 
probably happens in the anthropoids is this: the very high 
development of those cortical areas which are represented but 
Blightly in the lowest animals. In such cases some of the ap¬ 
parently new sulci of the former will be merely exaggerations of 
slight puckerings on the cortex of the latter, whilst the remaining 
sulci will be quite new, being due to a differentiation of which 
there is no trace in lower brains. 

Since the cerebral sulci are called into being by the specialisa¬ 
tion of the cortex into areas, it follows that the sulci will be 
identical in different brains only if the structure of the brains is 
identically the same. It is the slight difference of structure, with 
the corresponding slight differences in the shape and disposition 
of the sulci, that causes brains to be so different in appearance, 
even though belonging to animals of the same species. The more 
highly evolved any two brains are, the more dissimilar will they 
be; for now cortical specialisation will be reaching its highest 

1 ‘‘ The Morphology of the Sulcus Interparietalis, B.N.A.,” Journal of 
Anatomy, July 1913. 

3 “A Note on the Sulcus Poet-centralis Superior,” Anaiomiechtr Anzieger, 
1913, xlir. 



THE PARIETAL AREA 


55 


forms, and the newer the area the more liable it is to slight 
variation. In the second paper, referred to above, the writer has 
stated: “I am fully aware that the sulci cannot be taken as the 
rigid boundaries of specialised areas, as was pointed out long ago 
by Sherrington. But at the same time, I cannot conceive of sulci 
being far removed from such boundaries, seeing that it was 
specialisation of cortex which produced them.” 

The more primitive a sulcus is, and the more primitive the 
area which it limits, then the more constant in position and shape 
does it appear to be, though it may often be modified or obscured 
by the confluence of newer sulci produced by the more recently 
specialised areas. On the most primitive brains the sulci which 
either limit or are infolded in the areas differentiated for loco¬ 
motion and general and special sensation are the only outstanding 
furrows. On the anthropoid brains these furrows are much less 
salient; their outlines are obscured by the appearance of a vast 
number of sulci which have arisen with the new areas which 
are characteristic of the higher brains. To take an example: 
Evidence is adduced in the papers above referred to, for believing 
that the parietal association area with the characteristic furrows 
crossing it appears for the first time in the anthropoids, and is not 
present in animals lower than they. This area widely separates 
the areas of vision and common sensation from one another, and 
its most characteristic feature in man is the great development of 
its lower part, i.e., the angular and supra-marginal gyri. The 
rudiment of a parietal area is present in apes as low as pithecidae, 
but it is not at all similar in structure to that of man. In the 
latter it consists most characteristically of four structurally different 
quadrants. These are separated from one another by the furrows 
which their differentiation has produced. Thus, the separation of 
the area into upper and lower portions of different structure gives 
rise to the sulcus parietalis horizontalis (ramus horizontalis of the 
intraparietal sulcus of Turner in the old terminology). Then the 
differentiation of each upper and lower portion into anterior and 
posterior structurally different areas, leads to the formation of the 
superior and inferior parietal sulci, which are, of course, vertically 
directed. It seems likely that the changes in the lower parietal 
area occur later in evolution than those in the upper. For the 
pithecidse have a parietal cortex, small though it is, which some¬ 
what resembles that of the superior parietal cortex of man. But 



56 


GEOFFREY JEFFERSON 


they have nothing comparable with the structure of the angular 
and supra-marginal gyri (lower parietal lobule). 

It will be realised from the foregoing remarks that the typical 
parietal furrows can only appear in animals whose cortical 
structure resembles that of man. Thus, no sulcus parietalis 
horizontalis can arise until the parietal field is differentiated into 
upper and lower portions. So that homologues between the 
parietal furrows of man and those say of cercopithecus whose 
parietal cortex is of uniform structure cannot truly be found. 
Yet the more horizontal part of the oblique furrow on the retro- 
central cortex of the last named is commonly urged to be homo¬ 
logous with the sulcus parietalis horizontalis of man. Which is 
absurd. For everything points to the sulcus parietalis horizontalis 
being a new furrow in the anthropoids, in whom for the first time 
there is a specialisation of the parietal area into upper and lower 
fields. 

The sulcus parietalis horizontalis is frequently superficially 
confluent with the sulcus post-centralis inferior. Each of these 
furrows has a separate cause and origin, but as cortical development 
proceeds, the two tend to run into one another. This confluence 
has led anatomists to regard these two really perfectly independent 
sulci as parts of a system of furrows to which the name “ Intra- 
parietal sulcus of Turner ” has been given. This system is com¬ 
pleted by the addition to it of Wilder’s sulcus paroccipitalis. The 
whole thus well merits Eberstaller’s epithet of Furchen conglomerat. 
Such a grouping together of furrows can only lead to confusion. 
In the papers referred to, the individuality of each sulcus has been 
insisted upon and the simple names already alluded to applied to 
each—this in the hope of a speedier recognition of their nature 
and origin. 

There is one further point not referred to previously. There 
are three arching gyri in this region commonly described in 
anatomical text-books as belonging to the inferior parietal area. 
These are the supra-marginal, angular, and post-parietal gyri, and 
they are said to be wound around the upturned ends of the lateral 
fissure (Sylvius), the superior temporal, and the middle temporal 
sulcus respectively. 

There is some excuse for retaining the terms supra-marginal 
and angular gyri as they do actually correspond to definite areas, i.e., 
the anterior and posterior inferior parietal areas. Each gyrus is 



THE PARIETAL AREA 


57 


of homogeneous structure throughout its extent. On the other 
hand, it is quite uncommon to find a well-formed post-parietal 
gyrus. Usually it is absent The sulcus that it is said to be 
thrown around is not the end of the commonly much broken up 
middle temporal sulcus, but the anterior occipital. This last is a 
limiting sulcus with a cortex of different structure in front of and 
behind it. It is obvious, therefore, that the post-parietal can 
never be as constant as the other two arching gyri for the reason 
that it could not be homogeneous in structure. The anterior 
occipital sulcus is the boundary line between the parietal area and 



Description op Figure. 

Scheme showing how the sulci separate different areas. The s. post- 
oentrales, sup. et inj ., separate the general sensory area from the parietal associa¬ 
tion area, whilst this last is divided into four quadrants by its own special sulci. 
In the inferior parietal area it will be noted that there are two sulci. Of these, 
one, the s. pariet. inf., is a limiting sulcus separating the anterior and posterior 
parts of the inferior parietal area, whilst the other, the ramus ascendens of the 
sup. temporal sulcus, is an axial furrow infolded in the area of black triangles. 
The figures used to denote the different areas have no special significance (after 
Brodmann). 



58 


ROBERT A. FLEMING 


the peri-striate (Brodmann) 1 or the rather indefinite area parieto- 
occipitalis (Elliot Smith). 2 What the true anatomical boundary, if 
any, of the occipital lobe should be may well be open to argument. 
But the whole area for vision maps out the arbitrary text-book 
occipital lobe fairly accurately. At the worst the mapping out of 
precise boundaries for the occipital lobe is an extremely un¬ 
important point, as it passes into the parietal and temporal lobes 
without break of surface. If a boundary must be found for it, it 
should be the limits of the peristriate area of Elliot Smith, visuo- 
psychic of Bolton and others. 

1 K. Brodmann, “ Lok&liaation der Groeahirnrinde,” Jotum. fur Ptychologie 
und Neurologic, Leipzig, 1906-7. 

* Elliot Smith, “New Topographical 8urvey of Cortex,” Jonm. of A not., 
July 1907. 


NOTES OF A CASE OF RECURRENT PARALYSIS 
OF THE THIRD CRANIAL NERVE. 

By ROBERT A. FLEMING, M.D., F.R.C.P. Edin. 

C. C., aet. 12, school girl, was admitted to my wards on the 4th 
March 1913, complaining of double vision and consequent vertigo. 

There is no family history of alcoholism, epilepsy, or any 
nervous disease, and no family predisposition to migraine attacks. 
Her father, a rubber worker, is alive and healthy, her mother has 
been several times in the ward, suffering from chronic interstitial 
nephritis. The patient has six brothers and five sisters, all alive 
and healthy. Her home is fairly comfortable, and there is always 
a sufficiency of good food. 

The previous illnesses include measles, abscess of both ears, 
whooping-cough, and chicken-pox. She has frequently complained 
of pain over the left mastoid, but at present there is no discharge 
from either ear. 

Her first attack of recurrent paralysis of the third nerve dates 
from winter, three years ago, and commenced, according to the 
mother’s account, with twitching or shaking of her head. This 
went on for some days, and was followed by a sudden pain in her 
left eye. The pain was very severe, and lasted over a week, 
greatly interfering with sleep. The shaking ceased when the pain 
began, and about two days after the pain started the left eye 



NOTES OF A CASE OF RECURRENT PARALYSIS 59 


closed, and the patient could only lift the lid with her finger, and 
when she did so found she had double vision, and complained of 
giddiness. The paralysis, which presumably, from her description, 
was the same as that seen on the present occasion, gradually 
passed off. 

After an interval of eight months the patient had a second 
attack, commencing much in the same way, with head-shaking or 
twitching, followed by severe headache and pain especially referred 
to the left eye, and ending in paralysis of the third nerve on the 
left side. 

Each of these two attacks was completely recovered from, the 
double vision and ptosis completely disappearing. 

The present—and third —attack began three days before ad¬ 
mission, and was preceded by a certain amount of head-twitching 
or shaking and severe headache, mostly confined to the region of 
the left eye. When I saw the patient there was marked ptosis of 
the left eye, and complete paralysis of all the muscles, internal and 
external, supplied by the third nerve on the left side. The pupil 
was dilated, and the patient was unable to accommodate with the 
left eye. 

On the day after admission the paralysis had already begun 
to pass off, and disappeared completely within a week. All the 
affected muscles appeared to regain perfect functionating power. 

The sight of each eye is $. 

There is nothing else worthy of note as regards the nervous 
system, and excepting that the child’s chest development is 
somewhat unsatisfactory for her height, there is no other ab¬ 
normality. After admission to the ward there was no evidence 
of any twitching or shaking of the head, similar to what the 
mother stated had always preceded each of the three attacks, 

The mother considers that excessive mental overstrain at 
school was the cause of each attack. 

It should be pointed out that eight months elapsed between 
the first and second attacks, and two years and four months 
between the second and third attacks, and that there has been no 
increase in the severity of the attacks, and certainly no tendency 
to periodicity, which is believed to be so common in these cases. 
There is no neuropathic family history. The girl’s description of 
her headache resembled migraine, only it has never been associated 
with vomiting. 



60 


ABSTRACTS 


I again saw the patient in July of 1913, when she looked in 
the best of health, and much better coloured than she was after 
leaving the ward. There had been no recurrence of the paralysis. 

In many cases of recurrent or periodic paralysis the lesion 
is limited to one or other division of the third nerve, or even a 
single muscle. There is often more definite migraine-headache 
followed by vomiting, and there is a tendency for the attacks to 
recur at ever shortening intervals of time, and with greater and 
greater severity. 

Whatever the explanation may be, it is impossible to suppose 
that either a new growth, or a plastic exudate, or other gross 
morbid process, could explain the paralysis in this case. Vascular 
spasm, inhibiting the flow of blood, or paralysis of vasomotor 
nerves might cause distension of vessels, and so compress the third 
nerve in whole or in part. Strzeminski distinguishes a functional 
and an organic type, and would, of course, consider the present 
instance functional. Luzenberger thinks that the cavernous sinus 
may periodically swell or distend, while Plavee believes that the 
hypophysis is to blame. Knapp states that there is rarely 
complete recovery between the attacks, and obviously this would 
imply the presence of some gross organic lesion. Other cranial 
nerves are also occasionally affected, such as the fourth and sixth 
nerves supplying the other eye muscles, and the seventh nerve. 

No treatment was adopted in my case, nor was any necessary, 
so rapidly did the symptoms disappear. 


Hbstracts. 

PHYSIOLOGY. 

EXPERIMENTAL RESEARCHES ON CEREBELLAR FUNCTION. 

(63) Andr6 Thomas and Durupt, L'Encephale , July 10,1913, p. 21. 

The authors made small unilateral cortical lesions in the cerebellum 
of Macacus rhesus in two instances. The first lesion was in the 
right quadrilateral lobe, involving slightly the semilunar; the 
central grey nuclei and the vermis (subsequently examined) were 
untouched. After the operation the animal showed typical 
dysmetria of the right upper limb, and nothing else. After about 
ten days this dysmetria disappeared. The second lesion destroyed 



ABSTRACTS 


61 


a much larger part of the quadrilateral and semilunar lobes, and 
impinged on the right side of the vermis: the subjacent white 
matter was much involved. The posterior part of the right corpus 
dentatum was destroyed. The right superior cerebellar peduncle 
was subsequently found to be degenerated. The animal had 
constant falls to the right, sometimes preceded by oscillations 
of the head and trunk. These defects of equilibrium and the 
shaking movements soon disappeared. Discontinuity of movement 
and dysmetria were strongly marked in both upper and lower 
limbs on the right side, and these symptoms persisted. The 
defect of equilibrium in the second animal is to be associated with 
the slight involvement of the vermis. The dysmetria, practically 
identical in the two animals, was especially well seen in the 
attitude of the hand and foot in the act of grasping. It may be 
that the behaviour of the animal’s limbs immediately after the 
lesion—apparent indifference to abnormal attitudes—is to be 
linked to a transient defect of deep sensibility. Little that is 
certain is known of the relation of the cerebellum to sensation. 

The authors go fully into the question of whether the 
distribution of the lesions in the two cases may not explain the 
presence of dysmetria in the inferior extremity in the second ape 
and its absence in the first. They discuss the question of localisa¬ 
tion in the cerebellar cortex and nuclei. Their results tend to 
confirm Rothmdnn’s views, that in the quadrilateral lobe is a 
centre for regulating the motility of the upper limb, in the 
semilunar, of the lower limb. S. A. K. Wilson. 


CONSIDERATIONS ON THE PHYSIOLOGICAL PATHOLOGY OF 
(64) CONTRACTURE. (Considerazioni sulla flsiopatologia della 
contrattura.) Augusto Ott, Riv. de Patol. new. e merit., 1913, 
xviii., p. 429. 

The author criticises severely the theory of contracture propounded 
by Buscaino, who attributes this condition to the effect on the 
muscle of the accumulation of katabolic products due to imperfect 
circulation in the paralysed muscle substance. The objections 
advanced by Ott are as follows: (1) There is not sufficient 
evidence of circulatory disturbance in the paralysed muscles. 
(2) Though ligature of veins and also arteries may produce an 
augmentation of muscular tone, there is no parallelism between the 
experimental condition and that produced by paralysis. (3) There 
is no direct relation between paresis and muscular rigidity, move¬ 
ment often being only slightly impaired in cases exhibiting great 
spasticity. (4) The explanation of Buscaino does not account for 
the flexor type of contracture that predominates in the arm. 



62 


ABSTRACTS 


According to the author, the position assumed in contracture is 
in reality a reproduction of the conditions that prevail during 
intrauterine life and in the new born. The return to this primitive 
posture of the limbs occurs when cerebral influence is interfered 
with. Hypertonus is sharply separated from the mechanism of 
contracture and attributed to cerebellar influence. 

F. L. Golla. 


ON THE FUNCTIONAL RELATION BETWEEN THE CORTICAL 
(65) AND SUBCORTICAL CENTRES OF TONUS. (Sui rapporti 
funzion&li tra i centri corticali ed i sottocorticali tonici dell’uomo 
in condizioni normal! e patologiche.) V. M. Buscaino, Riv. de 
PatoL nerv. t merit., 1913, xviii., p. 441. 

A reply to the criticisms of Ott on the author’s theory of con¬ 
tracture. It is pointed out that the foetal posture varies when 
the position in the uterus is not a normal one, and hence is 
determined by external conditions and not by a nervous mechanism, 
absence of control over which is, according to Ott, the cause of the 
assumption of the foetal flexion of the limbs in contracture. The 
author maintains his theory of the toxic origin of contracture. 

F. L. Golla. 


THE EXPERIMENTAL PRODUCTION OF REFLEX IRIDOPLEOIA. 
(66) (Uber experimentelle reflektorische Pupillenstarre.) Karplus 
and Kbeidl, Neurol. Centralbl., 1913, Jan. 16, p. 82. 

Experimenting on cats and apes, the authors have traced the 
course of the fibres in the optic tract that are reflexly concerned 
with the reaction of the pupils to light. They find that all along 
the optic tract, except when it enters the external geniculate body, 
electrical stimulation produces contraction of the pupils, and these 
pupil-controlling fibres can be followed, millimetre by millimetre, 
along the superior brachium and the anterolateral edge of the 
superior corpus quadrigeminum almost to the middle line. Cutting 
through these fibres anywhere on this route electrical stimulation 
of the central end always produced contraction of the pupil. 
After bilateral section of the superior brachium the reaction of the 
pupils to light is absent, and the authors have, in an ape, pro¬ 
duced bilateral Argyll Robertson pupil in this fashion, which has 
remained unchanged eight months after the operation. They do 
not assert, however, that in the Argyll Robertson pupil in man the 
lesion is necessarily at the same spot where they have been able 
to produce it experimentally, but the data are of considerable 



ABSTRACTS 


63 


importance. A fuller account of their experiments is recorded in 
Pfinger's Archiv, vol. cxlix. S. A. K. Wilson. 


THE LOCAL ACTION OF NICOTINE ON THE DOG’S BIGHT 
(67) CARDIAC AURICLE. (Action locale de la nicotine sur 
l’oreillette droite da cceur chez le chien.) L£on Fkedericq, 
Arch. Intemat. de Physiol., 1914, xiv., Jan. 31, p. 195. 

These experiments were performed on the surface of the living 
dog’s heart: destruction of Flack’s sino-auricular node by cold 
was effected by a metal bar frozen by immersion in liquid air 
or oxygen. Conclusions :—“The eardio-inhibitory action of the 
cervical vagi is not abolished by (1) mechanical or thermal (heat 
or cold) destruction of Flack’s node; by (2) thermal destruction 
of the superficial portion of the centre of Marchand and Meyer 
(the accessible portion of the dorsal aspect of the right auricle); 
by (3) thermal destruction of the whole extent of the surface of 
the two auricles directly accessible to the action of the heated 
glass rod. The abolition of the eardio-inhibitory action of the 
vagi which follows the application of nicotine to the region of 
Flack’s node, or to Marchand and Meyer’s centre, is due, in at 
any rate some instances, to diffusion of the poison to other parts of 
the heart. Some fibres of the right vagus penetrate the heart in the 
right auricle and act on it. Likewise the left vagus contains some 
fibres exclusively destined for the left heart. This experimental 
fact is against the notion of a single intra-cardiac moderating 
centre in which the total number of the inhibitory fibres of 
the vagi terminate.” Leonard J. Kidd. 


A DIRECTLY EXCITABLE REGION IN THE HUMAN ENDO- 
(68) 0ARDIUM (Sur one region endoc&rdique directement excitable.) 

R. Argaud, Compt. Pend. d. 1. Acad, des Sciences , 1913, clvi., p. 1787. 

Argaud observed a spontaneous contraction of the exposed heart 
of a man, aged 20, forty-five minutes after decapitation: from this 
time the heart did not contract unless it were stimulated 
mechanically: the stimulus was most effective over the right 
auricle: these contractions were evoked mechanically about every 
ten seconds up to the fifty-second minute: they then lessened and 
became more and more capricious, being sometimes auricular, 
sometimes ventricular, and often there was even a slight inco¬ 
ordinate fibrillation. At the sixty-second minute the heart was 
not mechanically excitable, and electrical stimulation of its surface 
gave neither contraction nor fibrillation. The heart was now 
opened; electrical stimulation of the endocardium of the right 



64 


ABSTRACTS 


ventricle and of the whole of the left heart failed to evoke con¬ 
traction; but stimulation of the right auricular endocardium 
evoked contraction of the whole heart. From the seventy-second 
to the seventy-fifth minute three induction shocks were needed 
for this, and at the eighty-third minute after decapitation the 
heart was inexcitable. The most excitable region of all corre¬ 
sponded with the taenia of His, the Keith-Flack node, and the 
valve of Thebesius, i.e., the region most rich in nerve-ganglia. 
Argaud has often found nerve-ganglia in the substance of the 
Thebesian valve of man and other mammals. He suggests that 
in cardiac massage, instead of the usual continuous ventricular 
massage, we should apply light taps by the tips of the fingers to 
the right auricle at intervals, and watch, as far as possible, for the 
myocardial response. Leonard J. Kidd. 


HTPOPHYSBCTOMY AND GENITAL ATROPHY : AN EXPERI- 
(69) MENTAL CONTRIBUTION TO THE STUDY OF THE ADI 
POSO-GENITAL SYNDROME. (Hypophysectomie et atrophie 
glnitale: Contribution explrimentale k l’ltude du syndrome 
adiposo genital.) J. Camus and G. Roussy, Soc. de Neurol, de 
Paris, Dec. 4,1913. ( Revue Neurol ., 1913, Dec. 30, p. 770.) 

The authors showed five dogs, young and old, on which they had 
performed hypophysectomy, more or less complete, by the palatine 
route: only two showed any trophic genital changes: in one of 
these the cauterisation of the pituitary region by a red-hot needle 
had caused neighbouring lesions, as was shown by the presence of 
disturbances of co-ordination and equilibration: in the other dog 
the authors purposely produced a basal cerebral lesion which was 
rapidly followed by a large polyuria and testicular atrophy. 
They conclude tentatively that it is the basal lesion, rather than 
the pituitary lesion, which causes genital atrophy. Adiposity is 
not indissolubly connected with the genital atrophy, for they may 
be dissociated, as in the case of their second dog, which showed, 
after a total or almost total hypophysectomy, an enormous adi¬ 
posity combined with perfect integrity of genital organs and 
sexual functions. They suggest that the adiposo-genital syndrome 
may be due to lesions of separate centres which, though often 
affected simultaneously by the same processes, can be dissociated. 
As to the exact sites of these centres, we must wait for a detailed 
histological examination. (For a further account of the authors’ 
experiments on these dogs, and two other dogs on which a dummy 
operation was done without any consecutive polyuria resulting, 
see the Compt. Bend. Soc. de Biol., (a) Dec. 5, 1913, p. 483, and (b) 
Dec. 26,1913, p. 628). Leonard J. Kidd. 



ABSTRACTS 


65 


n. T HE PH Y8IOLOQIOAL ACTIVITY OF THE ADRENAL OF 
(70) THYROIDE0T0MI8ED ANIMALS. (Valent physiologique de 
la gl&nde ■nrr^nale dee anim&uz dthyroldfo.) E. Olby, Arch. 
Internal, dc Physiol ., 1914, xiv., Jan. 31, p. 175 (18 figs.). 

Conclusions :—(1) “ Adrenal extract of thyroidectomised dogs or 
rabbits, dying two to thirty-five days after operation, is quite as 
active, to judge by the cardio-vascular action of the adrenalin 
it contains, as normal adrenal extract. (2) Adrenal extract of 
rabbits rendered myxcedematous by thyro-parathyroidectomy is 
either as active, or a little less active, than that of normal animals; 
but in these cases the animals have been in a state of general 
organic cachexia on account of their malady, and one has been 
unable to see in it a specific effect due to loss of an influence 
normally existing and continuously exercised by the thyroid on the 
adrenals. (3) The adrenals of thyroidectomised rabbits, either 
sacrificed during the course of the cachexia thyreopriva or dying 
from it, are notably hypertrophied and loaded with fat: this 
hypertrophy is by no means a sign of hyperfunction.” 

Leonard J. Kidd. 


CONTRIBUTION TO THE STUDY OF HUMORAL INTER- 
(71) RELATIONS.—I. THE ACTION OF THYROID EXTRACT 
AND OF ORGANIC EXTRACTS IN GENERAL ON ADRENAL 
SECRETION. (Contribution A l’6tude des interrelations humorales. 
Action de 1’extrait thyroldien et an gdndral des extraits d’organes 
sur la sdcrdtion surrdnale.) K Glby and A. Quinquaud, Arch. 
Intemat. dc Physiol ., 1914, xiv., Jan. 31, p. 152 (21 figs.). 

These experiments were performed in each instance on two dogs: 

(1) a rather large one which supplied the adrenal blood, and 

(2) a smaller one into which the collected blood of the first was 

injected. Conclusions :—(1) “Extracts of pancreas, liver, thyroid, 
testes, kidneys, and probably of other organs also, can increase the 
amount of adrenalin which flows in the blood of the adrenal vein. 
(2) Thyroid extract is not more active than the others in this 
respect; it is less active than hepatic extract. (3) These experi¬ 
ments testify directly against the hypothesis of reciprocal 
functional relationships between the adrenals and the thyroid, or 
—more exactly—against the hypothesis of the reciprocal action of 
the secretory products of these glands.” The mechanism, by which 
the organic extracts determine this augmentation of adrenalin, is 
to be studied in new researches. Leonard J. Kidd. 



66 


ABSTRACTS 


OBSERVATIONS AND EXPERIMENTS ON GOITRE (SO-CALLED 
(72) THYROID CARCINOMA) IN BROOK TROUT (Salveltaus 
fontlnalla). David Marine, Joum. Exp. Med., 1914, xix., Jan., 
p. 70. 

Goitre in fish is a non-infectious, non-contagious, symptomatic 
manifestation of a fault of nutrition, the exact biochemical nature 
of which has not been determined. Feeding the highly artificial 
and incomplete diet of liver is the major etiological factor in 
bringing about this fault of nutrition, which is at once corrected 
by feeding whole sea fish. Water plays no essential part in the 
etiology, transmission, or distribution of the disease in the fish of 
this hatchery. A. Ninian Bruce. 


PSYCHOLOGY. 

THE MENTAL MANIFESTATIONS OF EPILEPSY. N. S. Yawger, 
(73) Joum. Abnorm. Psychol ., 1913, Feb.-March. 

In this paper the author discusses in a lucid manner the various 
mental states met with in epilepsy and expresses the opinion that 
the development of the well-known epileptic character and tem¬ 
perament may be produced by mismanagement of these persons by 
their families. H. de M. Alexander. 


A PSYCHO-ANALYTIC STUDY OF A SEVERE CASE OF HYSTERIA 

(74) L. E. Emerson, Joum. Abnorm. Psychol., 1913, Feb.-March, April- 
May. 

A detailed description of a protracted psycho-analysis in a case 
of hysteria. H. de M. Alexander. 


A CASE OF SYNESTHESIA Isador U. Coriat, Joum. Abnorm. 
(76) Psychol., 1913, April-May. 

In this subject the colour blue in its various shades was distinctly 
suggested by sounds. Coloured thinking, and to a less extent taste 
synesthesia, was also present. There was no familial tendency 
and the synesthesia, though present in a psycho-neurotic subject, 
antedated the psychoneurosis by a number of years. 

H. de M. Alexander. 


AN UNUSUAL TYPE OF SYNESTHESIA Isador H. Coriat, 
(76) Joum. Abnorm. Psychol., 1913, Juue-July. 

This occurred in an intelligent woman of 40 years in whom from 
childhood pain had produced a sensation of colour, but only when 



ABSTRACTS 


67 


the pain was severe and persistent. Each type of pain produced 
its individual and invariable colour. The duration of the colour 
and the pain synchronised; and the individual colours produced 
emotional associations of a depressing or soothing nature. The 
synesthesia could be produced artificially by peripheral stimuli. 

H. de M. Alexander. 


THE ANALYSIS AND I NTER PRETATION OF DREAMS BASED 
(77) ON VARIOUS MOTIVES. Meyeb Solomon, Joum. Abnorm. 

Psychol., 1913, June-July. 

From an analysis of some dreams the author is of the opinion 
that:— 

1. The law of determinism applies as certainly to dream life 
as it does to all other mental states. 

2. The content of the dream may depend only or mainly on 
our more recent experiences. 

3. Dreams do not necessarily depend on our infantile or child¬ 
hood experiences. 

4. Dreams are merely the continuation of our waking life, 
but are not so logical or orderly on account of the lessened 
activity of clear consciousness. 

5. Symbolism does not necessarily play any rdle in the dream- 
content—this is determined by our fears as well as our wishes. 

6. The underlying motives of dreams vary considerably—any 
of our instincts (fundamental or otherwise) alone or in combina¬ 
tion, may be the driving force of the dream. 

H. de M. Alexander. 


PATHOLOGY. 

ANATOMICAL EXAMINATION OF A CASE OF MULTIPLE 
(78) SCLEROSIS FROM DISSEMINATED SYPHILITIC MYELITIS. 

B£rikl and Dklachanal, L’Enc4phale, April 10,1913, p. 301. 

The patient was a man of 33, whose case clinically was diagnosed 
as ascending syphilitic myelo-encephalitis: the Wassermann re¬ 
action was positive both in the blood and in the cerebro-spinal 
fluid. Pathologically, two sorts of lesions were found: (1) diffuse 
inflammation of roots, meninges, and cord, typically syphilitic; 
and (2) inflammatory foci and plaques of sclerosis. There could 
be no doubt as to the occurrence of every intermediate stage of 
sclerosis-development: the evolution of the plaques was definitely 
in association with different degrees of the fundamental patho¬ 
logical process. 

6 



68 


ABSTRACTS 


The case may be considered in three ways:— 

1. The plaques are of syphilitic origin. The possibility of 
syphilis producing ordinary disseminated sclerosis has been 
accepted by a few observers. 

2. Syphilis may produce a disease allied to disseminated 
sclerosis, but distinct from it. This view has something in its 
favour. 

3. The association of plaques of sclerosis and disseminated 
syphilitic lesions is accidental. 

The authors are greatly inclined to favour the first hypothesis, 
and express their surprise that hitherto it has not gained much 
credence, for not a few cases are now on record which undoubtedly 
support it. They lay stress, further, on other cases where dis¬ 
seminated sclerosis, so called, has been indistinguishable anatomic¬ 
ally from disseminated myelitis of known toxic or infective origin, 
and therefore are disposed to deny any specificity to the lesions of 
classic disseminated sclerosis. S. A. K. Wilson. 


ON CHANGES IN THE HYPOPHYSIS IN EXPERIMENTAL 
(79) DIPHTHERIA, (tfber die VerSndemngen der Hypophyse bei 
der experimentellen Diphtherie.) S. Abramow, Virchovft Arckiv, 
1913, ccxiii., p. 408. 

From experiments on guinea-pigs Abramow had previously found 
that in diphtheritic intoxication exhaustion of adrenalin secretion 
occurs at a very early stage (first to second day). He now shows 
that the absence of adrenalin is compensated for by an increased 
secretion of the hypophysis, which occurs as soon as the suprarenal 
medulla is exhausted. Exhaustion of the hypophysis occurs 
considerably later than that of the suprarenals (fourth to fifth 
day). Thus fifteen guinea-pigs in whom death due to acute 
diphtheritic intoxication occurred within fifteen to twenty-seven 
hours showed no changes in their hypophysis except a high degree 
of hypersemia. On the other hand, twenty guinea-pigs in which 
the intoxication was less acute, showed in addition to marked 
hypersemia of the capillaries a large number of cells which had 
been exhausted by a great increase in their secretory activity. 

Abramow concludes that diphtheria toxin does not exercise 
a direct influence upon the secretion of the hypophysis, but that 
this increase of secretion is due to a correlation between the 
functions of the hypophysis and those of the other glands of internal 
secretion, especially the suprarenals. J. D. Rolleston. 



ABSTRACTS 


69 


HISTOLOGICAL RESEARCHES OH THE H7P0PHTSIS OF P8YOHO- 

(80) PATHS. Laigkel-Lavastink and Jonnesco, L'EndpkaU, Jan. 10, 
1913, p. 26. 

The authors have examined thirty-two cases of mental disease, 
but come to no very definite conclusions as to the condition of the 
pituitary. They distinguish, however, the “general paralytic” 
hypophysis as characterised by vaso-dilatation, and the “senile 
dement" hypophysis by perivascular sclerosis. 

S. A. K. Wilson. 

FATS, STEABINE8, AND LIPOIDS IN THE NORMAL AND 

(81) PATHOLOGICAL CENTRAL NERVOUS SYSTEM. (Grass!, 
sterine e lipoidi nil sistema nervoso central! in condition! nor¬ 
mal!, sperimentali e patologiche.) Buscaino, Riv. de Patol. nerv. 
e ment., 1913, xviii., p. 673. 

Three methods were used: Examination by polarised light, by 
specific fat stains, and by fractional extraction of the fatty matter. 

In the walls of the cerebral vessels of healthy subjects minute 
globules of neutral fats and non-saturated phosphatids were found, 
together with traces of other lipoids insoluble in acetone and 
petroleum ether. 

In one case of cerebral degeneration large masses of fatty 
matter were found in the vicinity of the areas of softening, and in 
this case cholesterin was also found. The other cases appeared to 
have a normal distribution of ether-extractable matter. The 
yellow pigment of the cells of the normal cerebral cortex was 
found to consist essentially of saturated phosphatids and some 
other acetone insoluble lipoids. F. L. Golla. 

THE GALAGT08IDE8 OF THE BRAIN.— L Otto Rosenheim, 

(82) Biochtm. Joum., 1913, vii., Dec., p. 604. 

A new method for the preparation of galactosides from the brain 
by means of pyridine is described. Evidence is brought forward 
to show that the galactosides exist in the brain in the preformed 
condition. A. Ninian Bruce. 

CLINICAL NEUROLOGY. 

PHYSIOLOGICAL MECHANISM OF THE KNOCK-OUT. (M<can- 

(83) !sme physiologique du knock-oat) H. Somen, Paris mid., 1913-14, 
iv., p. 54. 

Somen gives the following explanation of the knock-out which has 
met with Babinski’s approbation, as well as that of certain medical 
boxers. 



70 


ABSTRACTS 


The knock-out is essentially due to auricular irritation analogous 
to M£ni&re’s vertigo. A blow on the chin is transmitted to the 
glenoid cavity by the condyle of the inferior maxilla, the internal 
ear and semicircular canals receive a violent shock, and there 
results a bulbar cerebral and cerebellar reflex which produces all 
the symptoms of the knock-out. 

This theory also explains why a blow on the side of the chin 
is more effective in producing a knock-out than a blow aimed at 
the centre of the maxilla. A lateral blow produces a shock on 
the glenoid cavity of the opposite side only, while a blow on the 
centre of the chin is transmitted to both glenoid cavities at once, 
and its effect is thus deadened. Further, the disturbance of 
equilibration is more considerable when the irritation affects the 
semicircular canals of one side only than when it is bilateral. 

J. D. Rolleston. 


METALLIC POISONS AND THE NERVOUS SYSTEM. Gxorgk A. 
(84) Molekn, Arrur. Joum. Med. Set., 1913, cxlvi., No. 6, Dec. 

Tuf.se cases are briefly presented showing the effects of lead 
intoxication, one of arsenic, and one probably of mercury. 

The arsenical case was unusual, owing to the fact that the 
patient had an optic nerve atrophy attributable to the arsenic. 

The author’s conclusions are as follows:— 

1. A wide variation exists in individual susceptibility to all 
metallic poisons. 

2. In those susceptible, if the nervous system is attacked, the 
peripheral nervous system is the most vulnerable, and more 
especially the extensor supplies. 

3. There is with lead poisoning, in all probability, an early 
lymphocytosis of the cerebro-spinal fluid, and probably coincident 
with or succeeding upon the basophilic granulation of the red 
blood cells. 

4. Non-inflam matory degenerations of any portion of the 
peripheral system should suggest the metals as a possible cause. 

5. In the absence of skin evidences of arsenic and the blue line 
of lead, the urine, the blood, and finally artificial abscesses may be 
induced and examined for the metals; this procedure should lend 
itself as a diagnostic as well as a therapeutic aid. 

6. A positive Wassermann reaction would not seem to exclude 
especially lead in favour of syphilis in primary nerve or tract 
degenerations. 

7. The source of the poison may not be detectable until long 
after the presence of the metal as a cause has been established. 

D. K. Henderson. 



ABSTRACTS 


71 


A CONTRIBUTION TO THE STUDY OF HEREDITARY DE 
(85) GENERATION. Cabl D. Camp, Amer. Joum. Med. Set., 1913, 
cxlvi., No. 6 , Nov. 

A cask of pseudohypertrophic muscular dystrophy is reported in 
a child of 3 years, one of whose parents and a grandparent had 
the spinal type of progressive muscular atrophy. The author has 
not been able to find a similar case of heredity in the literature. 

Another case is reported in a boy of 10 years who showed a 
combination of Friedrich’s ataxia with a pseudohypertrophic 
muscular dystrophy. 

A third case was that of a boy 8 years old who in combina¬ 
tion with a pseudohypertrophic muscular dystrophy had an optic 
neuritis. D. K. Henderson. 


THE THEORY OF MYOTONIA. Gregor and Schilder, Neurol. 
(86) Centralbl., 1913, Jan. 16, p. 86. 

In a brief preliminary communication the authors show, by 
electrical methods and the string galvanometer, that in Thomsen’s 
disease the essential lesion is not in the muscles. 

S. A. K. Wilson. 


THE NERVOUS SYMPTOMS OAUSED BY SUBCLAVIAN 
(87) ANEURYSM. (Oontribnto alio studio delli sindromi nervosa 
determinate dagli aneurismi dell’arteria succlavia.) Paolo 
Magaudda, Riv. de Patol. nerv. e mmt., 1913, xviii., p. 83. 

Trophic disturbances evidenced by muscular atrophy may be found 
in muscles of the shoulder joint, arm, and hand, caused by lesions 
involving one or all of the branches of the brachial plexus. 

Paralytic disturbances, varying from a slight paresis to complete 
paralysis with muscular atrophy may occur. The muscles 
supplied by the ulnar nerve are most often affected. 

Subjective and objective disturbances of sensation are frequent. 
Clubbed fingers are occasionally observed in the hand of the 
affected limb. F. L. Golla. 


COMBINED COLUMN-DISEASES OF THE SPINAL CORD. (Zur 
(88) Frage der kombinierten Strangerkrankungen des Riicken- 
marks.) Rothmann, Neurol. Centralbl., 1913, Nov. 1, p. 1363. 

Rothmann, in a short paper, explains the difference between 
combined “ Systemerkrankungen ” and “ Strangerkrankungen,” 
apropos of subacute combined degeneration of the cord. He holds 



72 


ABSTRACTS 


that in the latter disease there is no systematised tract affection, 
but a combined column affection. In his experimental work on 
dogs he was able to produce, by continued injection of pyridin 
over several months, a profound anaemia associated with degenera¬ 
tion in the anterior and lateral and posterior columns of the cord, 
comparable to what is found in subacute combined degeneration. 
In experimental anaemia of the cord produced by clamping the 
abdominal aorta, the short tracts of endogenous fibres in the 
antero-lateral ground-bundles were more affected than the rest of 
the cord—the reverse of what obtains in subacute combined. 

S. A. K. Wilson. 


TWO OASES OF TABES COMPLICATED BY HEMIPLEGIA. 

(89) Marinesco and Noica, L'EncJphale, May 10,1913, p. 413. 

Thb authors draw an interesting comparison between two cases of 
tabes with hemiplegia. In the case with advanced tabes a slight 
pyramidal lesion was sufficient to produce severe muscular 
atrophy, and to aggravate the hypotonia and ataxia: in the case of 
mild tabes a much more severe pyramidal lesion failed to produce 
so much impairment of function. Reference is made to experi¬ 
ments by Marinesco and Minea, and by Parhon and Goldstein, in 
which previous section of the sciatic nerve rendered more intense 
the alterations produced in the anterior horn cells of the cord by 
experimental destruction of the Rolandic zone or pyramidal path 
than those in control animals whose sciatic nerves were intact. 

S. A. K. Wilson. 


ON THE TREATMENT AND NATURE OF DIPHTHERITIC 
(90) PARALYSIS. (Bsitr&ge zur Behandlung und sum Wesen der 
Diphtherieiahmung.) Rosier und Viekeck, Cmtralbl . /. Bakt ., 
1913, lvil, Ref. Beiheft, p. 104. 

The following views are current as to the influence of antitoxin 
on diphtheritic paralysis. 1. Antitoxin has not only no effect in 
preventing paralysis, but it even favours its occurrence. 2. Whether 
paralysis will occur or not in no way depends on the injection of 
antitoxin. 3. Antitoxin has a prophylactic action on paralysis. 
4. Antitoxin is effective even when paralysis has actually developed. 

The writers, from experiments with diphtheria toxin on guinea- 
pigs, give the following answers to the above views. As regards 
(1) the favouring action of antitoxin is apparent rather than real. 
Experiments showed that acute lethal intoxication could be con¬ 
verted into sublethal intoxication with subsequent paralysis. As 
regards (2) and (3) antitoxin is by no means without influence on 



ABSTRACTS 


73 


the subsequent occurrence of diphtheritic paralysis. If given at 
the right time it renders mild what would otherwise have been 
severe paralysis, and under suitable conditions prevents the occur¬ 
rence of any paralysis at all. As regards (4) when once paralysis 
has occurred, antitoxin has no therapeutic influence whatever 
{cf. Review, 1907, v., p. 862). 

Investigation of various diphtheria toxins as regards their 
content of paralysis-producing toxin gave the greatest differences. 
All attempts to separate toxin from toxone failed, and the writers 
regard a final decision as to the nature of the paralysis-producing 
toxin as at present impossible. J. D. Rolleston. 

THE NERVOUS COMPLICATIONS OF VARICELLA. R. Miller 

(91) and J. A Davidson, Brit. Joum. Child. Die., 1913, xi., p. 16. 

The writers record the following case of encephalitis complicating 
varicella and review the other examples of nervous complications 
in the literature. 

A boy, aged 2£ years, on the fifth day of a mild attack of 
varicella was found unable to stand or to speak distinctly, and to 
show a tremor of the limbs, head, and tongue. The cranial nerves 
and reflexes were normal. The tremor gradually diminished in a 
few days, and in a month from the onset had entirely disappeared. 
The character of the tremor and the general appearance of the 
child were exactly similar to those seen in cases previously 
described by Miller, under the title of "acute tremor” {Brain, 
1909, xxxii., p. 54), in which the lesions were situated in the 
cerebello-rubro-spinal system. 

The other nervous complications reported after varicella in¬ 
clude examples of poliomyelitis and peripheral neuritis, convul¬ 
sions, intracranial complications of otitis media such as meningitis, 
cerebral and cerebellar abscess and lateral sinus thrombosis, 
optic neuritis, haemorrhagic internal pachymeningitis, disseminated 
sclerosis, neuromyositis, chorea and tuberculous meningitis {cf. 
Review, 1907, v., p. 564; 1908, vi., p. 618; and 1909, vii., p. 206). 

In discussing the occasional association between varicella and 
herpes zoster, the writers suggest that focal lesions similar to those 
which apparently occur in the central nervouB system may 
originate in the posterior root ganglia, thus producing a herpetic 
eruption. J. D. Rolleston. 

SYRINGOMYELIA: WITH AUTOPSY FINDINGS IN TWO CASES. 

(92) Oskab Rlotz, Amer. Joum. Med. Sci., 1913, cxlvi., No. 6, Nov. 

Two cases of syringomyelia are reported clinically and patho¬ 
logically owing to their indicating the mode of origin of their 



74 


ABSTRACTS 


cavities, in the one case with and in the other without the 
presence of a tumour. 

The first case is that of a married woman, 38 years, who had a 
complete paraplegia which came on suddenly and lasted for about 
seven months. Anaesthesia was complete to all forms of sensation 
over the surfaces below a transverse line 3 cm. above the 
umbilicus. The reflexes were abolished below the waist-line, 
there were marked trophic disturbances, and loss of control of 
bladder and rectum. 

The anatomical diagnosis was acute softening of the cord, 
syringomyelia, chronic pachymeningitis. The cord destruction 
gave no indication of a true myelitis, nor was there evidence of 
new growth. Cavities containing a necrotic material and outlined 
by irregular walls extended in both directions of the cord, and 
there was no evidence that the spinal canal was in any way 
involved or associated with the cavities. The cavity formation 
involved mainly the white matter of the posterior columns. 

The second case was that of a man, 25 years, who had a 
complete motor and sensory paralysis below the level of a line 
situated about midwav between the nipple and umbilicus. The 
anaesthesia was complete to all forms of sensation. There was 
loss of control of sphincters. 

The autopsy showed that between the seventh and eighth 
dorsal nerves there was an area of extensive softening which 
extended in both an upward and downward direction. The 
anatomical diagnosis was: glioma of the cord with softening, 
syringomyelia. 

Cavities developed in the new growth by a process of degenera¬ 
tion. Under the following conditions cavities may be present in 
the spinal cord : (1) neuro-epithelioma glimatosis; (2) diverticula 
of central canal; (3) anomalies of closure of the posterior sulcus; 
(4) degeneration of gliomas; (5) primary syringomyelia. 

D. K. Henderson. 

ETIOLOGY OF HERPES IN CEREBRO SPINAL MENINGITIS. 
(93) (Presence of the meningococcus in the vesicles.) [Etiologie de 
iherpto dans la mdningite cdrdbro-spinale. (Presence du mlnin- 
gocoque dans les vfaicules.)] P. Durand, Lyon mid.> 1913, cxxi., 
p. 920. 

The patient was a woman, aged 34, who recovered after injection 
of anti-meningococcic serum. An abundant eruption of facial 
herpes appeared during the first few days of the disease. Cultures 
of the vesicles showed meningococci associated with the Diplococcus 
crassti#, a frequent saprophyte of the mouth and nose. Drigalski 
is the only other observer who has succeeded in finding meningo- 



ABSTRACTS 


75 


cocci in the vesicles of herpes in cerebro-spinal meningitis. Durand 
is in favour of a haematogenous rather than of a nervous origin 
for the herpes in cerebro-spinal meningitis, and refers to the cases 
of meningococcal septieiemia reported by Bovaird (v. Review, 1909, 
viii., p. 419), Monziols and Loiseleur (ibid., 1910, viii., p. 304), 
Pissavy, Kichet fils, and Portret (ibid., p. 486), in which herpes 
appeared without any nervous manifestation. 

J. D. Rollestox. 


TUBERCULOUS MENINGITIS WITH ASSOCIATION OF THE 
(94) MENINGOCOCCUS. (Mfaingite tuberculeuse avec association 
da mdniogocoqae.) L B£riel and P. Durand, Lyon mdd., 1913, 
cm, p. 913. 

This association is rare. After reference to the cases reported by 
Combe (v. deview, 1910, viii., p. 432), Lutaud (ibid., p. 622), and 
others, the writers record a case of a youth, aged 16, admitted 
to hospital with meningitis. The cerebro-spinal fluid was turbid 
and rich in albumin, polymorphs, and meningococci. Cerebro¬ 
spinal meningitis was therefore diagnosed. The necropsy, how¬ 
ever, showed general miliary tuberculosis, including involvement of 
the basal meninges. A small tubercle was also present in the 
cerebellum. Histological examination and injection of a guinea- 
pig confirmed the diagnosis of tuberculosis, which was in this case 
the primary infection. J. D. Rollestox. 


PRIMARY PNEUMOCOCCAL CEREBRO SPINAL MENINGITIS. 
95) (Des mdningitM cdrdbro-spinales primitives A pneumocoques.) 

H. Guichot, Them de Lyon, 1912-13, No. 19. 

Guichot’s main conclusions are as follows:— 

1. Primary pneumococcal meningitis is fairly frequent both in 
a sporadic and in an epidemic form. 

2. Epidemics differ from those of meningococcal meningitis in 
being less extensive and not appearing regularly in successive 
years. 

3. The course of pneumococcal meningitis is generally more 
rapid than that of meningococcal meningitis. 

4. The only certain mode of diagnosis is by lumbar puncture. 
Fairly frequent (in nine out of twenty-seven cases), a paradoxical 
formula is present, viz., absence of leucocytic reaction and 
abundance of microbes. 

5. The prognosis is graver than in meningococcal meningitis, 

the mortality being 75 per cent. J. D. Rollestox. 



76 


ABSTRACTS 


PAROTITIS COMPLICATED WITH MENINGITIS. Q. N. Acker, 
(96) Amer. Joum. Dis. Child., 1913, vL, p. 399. 

A record of two cases with a review of the literature. 

Case I. —Boy, aged 11 years. The meningeal symptoms occurred 
during the acute stages of mumps, and were accompanied by 
orchitis. Lumbar puncture, which was not performed till more 
than a month after the onset, showed a normal cerebro-spinal fluid. 
Recovery took place. 

Case II. —Boy, aged 3 years. Meningeal symptoms developed 
five days after the onset of mumps. Convulsions were frequent 
and lasted till death, which occurred ten days later. The cerebro¬ 
spinal fluid showed marked hypertension and lymphocytosis, but 
no micro-organisms. Post mortem basilar meningitis was found. 
There were no signs of tuberculosis. J. D. Rolleston. 


ON MENINGO-TYPHOID. (Contribution & l’tftude do mdningo- 
(97) typhus.) H. Pacaud, Thiset de Lyon, 1912-13, No. 48. 

The term meningo-typhoid applies to cases of typhoid fever with 
an acute onset, resembling cerebro-spinal meningitis, and in which 
the intestinal symptoms appear later. 

In comparison with the frequency of nervous and meningeal 
symptoms in typhoid fever, meningo-typhoid is rare. Its 
frequency in former times has been over-estimated, because several 
of the cases so described were really examples of paratyphoid fever 
in which a meningeal onset is not uncommon (v. Review , 1911, ix., 
pp. 326-7; Ibid., 1913, xi., p. 278). 

Meningo-typhoid must be distinguished from meningitis occur¬ 
ring in the course of typhoid fever. Although typhoid meningitis 
without intestinal lesions may be classified under the heading of 
meningo-typhoid, it aborts without presenting the intestinal phase 
of meningo-typhoid properly so called. 

The clinical diagnosis of meningo-typhoid is often very difficult, 
and will chiefly rest upon the sudden onset, discordance between 
the pulse (100) and the temperature (104* F.), and the evolution 
of the disease. The cerebro-spinal fluid varies ; it is usually clear 
and genei'ally under hypertension. Cytological examination is 
frequently negative, but sometimes shows a variable degree of 
lymphocytosis or a mixed formula (polymorphs and lymphocytes). 

In exceptional cases the fluid contains typhoid bacilli and 
sometimes may give a positive Widal’s reaction. 

The meningeal stage lasts only a few days and is then replaced 
by the ordinary symptoms of typhoid fever. 

The prognosis depends upon the condition of the meninges, the 
state of the intestine, and the degree of septicaemia. Death may 



ABSTRACTS 


77 


occur at the beginning of the second week or earlier. Meningo- 
typhoidis more frequently accompanied by complications or followed 
by nervous sequelae than the ordinary form of typhoid fever. 
Previous causes of meningeal irritance, especially tuberculosis and 
syphilis, are important factors in the etiology. 

J. D. Rolleston. 


RESPIRATORY FORM OF THE ENCEPH ALOMENINGEAL 
(98) REACTIONS IN TYPHOID FEVER IN THE CHILD. (Forme 
respiratoire des reactions enclphalo-mlniiigtos au cours de la 
flfcvre typholde chez l’enfant.) Nob£oourt and F. Mebcier, Paris 
mM., 1913-14, iv., p. 32. 

A record of two cases published in exienso in Caux’s thesis in 
girls aged 10 and 12 years respectively. In both during the 
second week of an ordinary attack of typhoid fever the respiration 
was unequal, sighing and occasionally Cheyne-Stokes in character. 
In both the cerebro-spinal fluid showed hypertension; in one 
there were no leucocytes, in the other a few lymphocytes. Both 
recovered. J. D. Rolleston. 


RESP IRATO RY DISORDERS OF NERVOUS ORIGIN IN TYPHOID 
(99) FEVER. (Los troubles respiratoires d’origine nerveuae dans la 
flbvre typholde.) P. Caux, Theses de Paris, 1913-14, No. 59. 

Anomalies of respiratory rhythm without obvious pulmonary or 
renal lesions, and sometimes accompanied by a very slight 
meningeal reaction, may occur in the course or at the onset of 
typhoid fever. 

These phenomena are most frequently found in children, and 
the existence of a neuropathic state predisposes thereto. The 
following classification may be adopted:— 

1. Accelerated respiration which is often superficial and some¬ 
times irregular. This form is constantly found in the toxic and 
adynamic forms of typhoid. 

2. Irregular, unequal, or sighing respiration. 

3. Cheyne-Stokes respiration. This may occur at a late 
stage of the disease, when it is usually associated with a severe 
attack, and is accompanied by a semi-comatose condition. But it 
is most likely to occur at the onset of typhoid, and then doeB not 
affect the prognosis, though it is often associated with symptoms 
of meningeal reaction, and may lead to the mistaken diagnosis of 
tuberculous meningitis. 

The cerebro-spinal fluid, as a rule, shows no leucocytosis, or only 
a slight and transitory lymphocytosis. 



78 


ABSTRACTS 


The respiratory anomalies of typhoid fever appear to be due 
to functional disturbances of the bulbar centres or of the cortical 
centres governing the bulbar functions by toxins, among which the 
typhoid toxin plays the principal part (cf. Review, 1907, v., p. 860). 

The thesis contains the histories of fourteen cases, two of 
which are original Ten relate to children and four to adults. 

J. D. Rollkston. 

THROMBOSIS OF THE CEREBRAL SINUSES AFTER MEASLES. 

(10 i) (Trombosi dei seni cerebral! dopo il morbillo). C. Pizzata, Gazz. 
internal, di med , chir., dec., 1914, p. 34. 

A male infant suffering from broncho-pneumonia following 
measles presented signs of meningitis. Lumbar puncture gave 
issue to a blood-stained fluid under hypertension. Cytological 
examination was negative. Death took place in a convulsion. The 
necropsy showed sub-arachnoid suppuration in the left temporo- 
sphenoidal region and thrombosis of the straight sinus, torcular 
Herophili, veine of Galen, and veins of the left temporo-sphenoidal 
lobe. 

The paper also contains brief histories of ten other cases of 
nervous phenomena following measles in children, aged from 11 
months to 6 years observed in Concetti’s clinique between 1895 and 
1903. They include examples of spastic and flaccid hemiplegia, 
palpebral tic, spinal paralysis, disseminated sclerosis, and facial 
palsy. J. D. Rollkston. 

SYNDROME H£MI BULBAIRE, Ac. Duhot, L’Encdphale, Aug. 10, 

(101) 1913, p. 132. 

This is an excellent clinical example of thrombosis of the right 
posterior inferior cerebellar artery, but the author seems to be 
unaware of much of the literature bearing on this definite and 
well established syndrome. S. A K. Wilson. 

CONCLUSIONS DERIVED FROM FARTHER EXPERIENCE IN 

(102) THE SURGICAL TREATMENT OF BRACHIAL BIRTH 
P AL SY (Erb’s Type). A. S. Taylor, Amer. Jou m. Med. Set., 1913, 
cxlvi., No. 5, Dec. 

In 1905 Clark, Taylor, and Prout published “ A Study on Brachial 
Nerve Palsy.” The clinical portion of the study was based on 
seven operative cases. Since that time thirty-six additional cases 
have been operated upon, making forty-three altogether. These 
have varied in ace from 4 weeks to 19 years. 

It is probable that both extraspinal and intraspinal lesions 



ABSTRACTS 


79 


occur in different roots of the same plexus. The damage nearly 
always extends from above downwards in the order of the roots, 
and involves from one to all the roots. 

When the lesion is intraspinal, or when the cicatrix involves 
the root well into the intervertebral canal, operation as at present 
performed offers little prospect of improvement. 

Following permanent interference with nerve function, certain 
secondary pathologic changes develop which have a decided bearing 
upon determining at what age surgical interference should be 
insisted upon. The bones of the extremity do not develop 
normally. The clavicle is small, the scapula is small, the coracoid 
process is often drawn downward and forward, forming a beak 
which interferes with free mobility of the joint, and the glenoid 
process maintains its infantile form. 

The upper end of the humerus remains infantile, and this, 
together with a similar process in the glenoid cavity, renders easy 
the posterior dislocation seen in a certain proportion of these caseb. 

The great majority of the cases are of the “ upper arm type,” 
in which the injury involves the fifth and sixth roots. 

The usual picture in the new-born child is that of a complete 
flaccid paralysis of the extremity, which lies close along the side 
with the elbow and wrist straight and the fingers somewhat flexed. 
There is marked inward rotation of the entire extremity with 
pronation of the hand. Careful palpation of the region of the 
fifth, sixth, and seventh transverse processes invariably makes out 
a characteristic induration which is always sensitive to pressure. 

Prognosis is exceedingly bad in brachial injuries; complete 
spontaneous recovery is rare. 

Operation should be performed at the earliest feasible moment 
considering the general condition of the child and the local 
resistance. Seldom will it need to be postponed beyond three 
months. 

After operation the head and shoulders must be held in 
approximation for weeks by a steel brace fitted before operation. 
One illustrative case is reported. D. K. Henderson. 


TWO OASES OF POST OPERATIVE HEMIPLEGIA. A. Webb 
(103) Jones, Lancet , 1914, Jan. 10, p. 103. 

Hemiplegia as a post-operative complication is rare. 

Case 1.—Egyptian woman, aged 40, was operated upon for a 
large uterine fibroid complicated by a tubo-ovarian abscess. The 
operation lasted two hours and was very difficult. Complete loss 
of power and sensation in the right arm and leg developed next 
morning. Recovery was slow. 



80 


ABSTRACTS 


Case 2.—Old woman with ruptured ovarian cyst, evidently 
malignant. Operation simple and cyst removed. Next day right 
hemiplegia with aphasia developed, succeeded by coma and death. 
Post mortem no sign of haemorrhage could be found: the entire 
left cerebral hemisphere showed white softening. 

A. Ninian Bruce. 


CLINICAL AND METABOLIC STUDIES OF A CASE OF HYPO 
(104) PITUITARISM DUE TO CYST OF THE HYPOPHYSIS, WITH 
INFANTILISM OF THE LORAIN TYPE D* Witt Stkttbn and 
J. Rosenbloom, Amer. Joum. Med. Set., 1913, cxlvi., No. 6, Nov. 

The patient was a male, 22 years old, who was operated upon in 
the hope of improving his eyesight and relieving his headaches. 

The cyst was evacuated, the headache was relieved, but no 
improvement has occurred in the eyesight; the right eye is blind, 
while with the left eye the patient can see movements of the hand, 
and the pupil reacts normally. 

The patient was placed on Folin’s diet which approximately 
contains 119 gm. protein, 148 gm. fat, 225 gm. carbohydrate, 
yielding 2,787 calories. 

Examination showed a marked perversion of some metabolic 
process leading to high and abnormal percentages of the neutral 
sulphur and undetermined nitrogen of the urine. 

D. K. Henderson. 


RETROGRESSIVE INFANTILISM. (Infantilisme rtgresaif) Skringes, 

(105) Joum. de mAd. de Bordeaux , 1913, lxxxiv., p. 842. 

The patient had been healthy up to the age of 25, when he had 
his left testis tom off in a carriage accident. The wound healed 
well, but his right testis rapidly diminished in size, his penis 
atrophied, his hair fell out, sexual appetite disappeared, and 
erections, hitherto normal, became incomplete and rarer, and were 
never followed by ejaculation. J. D. Rolleston. 

THE NOGUCHI LUETIN REACTION IN SYPHILIS. George B. 

(106) Foster, Amer. Joum. Med. Set., 1913, cxlvi., No. 5, Nov. 

The test was applied to seventy-five persons, seventy of whom 
at the time were or had been infected with syphilis, while the 
remaining five individuals were used as normal controls. The 
technique recommended by Noguchi was carefully followed in 
applying the tests. In forty-eight cases the reactions were noted 
daily for a period of ten days, and subsequently at periods of two 



ABSTRACTS 


81 


to four days. In the remaining cases the reactions were examined 
three to five days. All cases were under observation for from 
three to five weeks. 

The percentage of positive reactions among the thirteen 
treated cases of secondary lues was 77 per cent.; of five tertiary 
cases 80 per cent, reacted positively; while among the fifty-two 
cases in the latent stage 88 per cent, gave a positive reaction. Of 
the five apparently normal individuals used as controls, one case 
developed a typical papular reaction. It is supposed that this 
positive reaction may be explained from the fact that the maternal 
grandmother had been luetic. D. K. Henderson. 

SYPHILITIC FACIAL PARALYSIS. (Paralysis facials gyphilitique.) 

(107) P. A Prbl, Thises de Lyon, 1912-13, No. 20. 

Prel’s conclusions are as follows: Syphilitic facial paralysis is 
most likely to occur in the early stage of syphilis, especially in 
the secondary period. It then yields very readily to treatment, 
but cure is very difficult when the paralysis appears at a later 
stage. Specific treatment is the most important element in the 
diagnosis, and should be applied in every case of facial paralysis 
of doubtful origin. Definite cicatricial lesions may occur in the 
nerve, in which case mercury is almost useless, and after failure 
of potassium iodide the treatment for ordinary facial paralysis 
should be employed. The thesis contains the histories of fifteen 
cases, one of which is original. J. D. Rolleston. 

LOCAL TREATMENT OF VINCENT'S ANGINA WITH SAL- 
flOS) VARS AN. J. D. Rolleston, Practitioner , 1913, xcl, p. 847. 

A record of a case in a man, aged 20, in whom the local applica¬ 
tion of salvarsan to the ulcerated area, after failure of other 
methods, produced a rapid cure. There was no history or evidence 
of syphilis, and Wassermann’s reaction was negative. A review 
of the literature is given, and reference is made to other conditions 
in which local application of salvarsan has been successful. 

Author’s Abstract. 

CHRONIC TROPHCEDEMA AND THE END00RIN0-8YMPATHETI0 
(109) SYSTEM. Ayala, L'Enctphale, April 10,1913, p. 319. 

Apropos of a case of chronic trophcedema of the left leg, in a man 
of 51, the author advances arguments to suggest that chronic 
trophcedema is a dystrophy determined either by a congenital 
defect of the endocrino-sympathetic system, or, in acquired cases, 
by some lesion of that system. S. A. K. Wilson. 



82 


ABSTRACTS 


THE UREA CONTENT OF THE SPINAL FLUID, WITH SPECIAL 

(110) REFERENCE TO ITS DIAGNOSTIC AND PROGNOSTIC 
SIGNIFICANCE: A SERIES OF NINETY-SEVEN CASES. 

Willard B. Soper and Selma Qrand, Archive* Intern. Med., 
1914, xiii., Jan., p. 131. 

A spinal fluid urea content higher than 0 2 per cent, indicates a 
severe uraemia and a rapidly fatal termination. A content between 
01 per cent, and 0'2 per cent, means a rapidly fatal termination in 
the majority of cases of nephritis. A content between 0*05 per 
cent, and 01 per cent, does not permit of any definite conclusions 
either as regards diagnosis or prognosis. Such a content is, how¬ 
ever, suggestive of severe urea retention, and must be taken into 
consideration in the diagnosis of the condition. The authors 
believe that the determination of the presence or absence of urea 
retention in the body fluids will go far to clear up certain difficult 
problems where the question of uraemia enters into consideration. 

A. Ninian Bruce. 

A CASE OF APHASIA FROM A LESION IN THE LEFT HEMI- 

(111) SPHERE IN A LEFT-HANDED INDIVIDUAL : CROSSED 
APHASIA AND DISSOCIATED APHASIA. Long, L'Enct- 
phale , June 10, 1913, p. 520. 

Clinically: Right hemiplegia and aphasia in a woman of 55. 
Disappearance of the hemiplegia after one month; complete 
aphasia for one fortnight, passing into a typical sensory aphasia; 
little modification during the three remaining years of life. 

Pathologically: Embolic softening in the left hemisphere, in¬ 
volving the posterior end of the second frontal gyrus, the third 
frontal, the lower end of the precentral, a great part of the island 
of Reil, external capsule, claustrum, and part of the putamen, as 
well as the uncinate, arcuate, and occipito-frontal association bundles. 
There are three features of peculiar interest in this case. 

(1) Absence of motor aphasia. The difficulty resolved itself 
when the author found that the patient had been definitely left- 
handed, although she wrote with the right hand. 

(2) Absence of areas of softening posterior to the precentral gyrus, 
although the patient had word-deafness, word-blindness, paraphasia, 
alexia, and agraphia. It is known, however, that an Inselaphasie 
of itself will produce somewhat analogous symptoms, while inter¬ 
ruption of the association paths between the angular gyrus and 
temporal lobe and the frontal lobe will have the same effect. 

(3) The localisation of the sensory part of the function of 
speech in the left hemisphere in a left-handed individual. This is 
an anomaly which is difficult to explain. “ Crossed aphasia ” may 
occur in both right-handed and left-handed people. As a rule the 



ABSTRACTS 


83 


whole function of speech is located in the hemisphere contralateral 
to the predominant “ handedness ” of the individual. 

In Long’s case, however (as in an almost identical one recently 
reported by Leipmann, and in an earlier one of Byrom Bramwell’s), 
there seems to have been an undeniable division of the function of 
language between the two hemispheres. The explanation is 
uncertain: the facts are extremely important. Probably similar 
instances occur more frequently than is usually supposed. There 
are evidently individual variations. For this physiological variant 
Long proposes the name of “ dissociated aphasia.” 

S. A. K. Wilson. 

A CASE OF PROGRESSIVE LENTICULAR DISEASE. (Ein Fall 
(112) von progressiver Linsenkeraerkr&nkung. ) Cassirer, Neurol. 

CentralbL, 1913, Oct. 16, p. 1284. 

The case described by Cassirer is that of a youth of 17, who since 
boyhood had suffered from a certain awkwardness of movement of 
the right hand, especially in writing. Very gradually the condition 
progressed; speech became a little slovenly and indistinct. The 
previous history revealed no outstanding features beyond this 
progressive awkwardness of the limbs and dysarthria. When the 
patient came under observation it was noted that the facies was 
somewhat expressionless; the patient’s attitude as a whole was 
stiff; facial movements were slow and somewhat impaired; fine 
tongue movements were slow and performed with difficulty. 
Speech was slow, scanning, with a slight nasal intonation. There 
was also some difficulty in swallowing. Saliva escaped from the 
mouth. All voluntary movements were accompanied by irregular 
trembling of the limb involved : sometimes there were “attacks ” 
of generalised tremor, lasting a few minutes, of a “ shivering ” or 
“ shuddering ” type. The patient was quite unable to make move¬ 
ments quickly, and on passive movement it was easy to detect 
resistance both in flexor and extensor groups. The legs were less 
affected than the arms. There was some flexor contraction in the 
legs. Occasionally associated movements were noted. Sensi¬ 
bility was normal The reflexes, deep and superficial, were 
normal. There was no actual paralysis anywhere. 

The author emphasises as the cardinal features of this case the 
tremors, stiffness and slowness of voluntary movement, the 
dysarthria, and the absence of all signs of pyramidal affection. He 
points out that it presents the closest analogies to the disease 
described by the reviewer as “ progressive lenticular degeneration,” 
and an excellent analysis and comparison of the two are given. 
Cassirer draws attention to the “pseudosclerosis” group, pointing out 
certain differences (mental condition, epileptiform attacks) between 

7 



84 


ABSTRACTS 


it and his own case, which he includes in the Wilson’s type, 
although he agrees it may not be an etiologically identical case. 
In the reviewer’s opinion Cassirer’s case is more closely allied to 
Wilson’s disease than to the type described by Vogt, in which 
athetoid movements predominated. S. A K. Wilson. 

PROGRESSIVE EPILEPTIC MYOCLONUS. (Type Unvenicht-Lund- 

(113) borg.) Jacquin and Mabchand, L'Enctphale, March 10, 1913, 
p. 205. 

A girl of 19 suffered from infantile convulsions at the age of 3, 
developed epilepsy at the age of 10, and myoclonus made its 
appearance when she had reached the age of 15. The myoclonic 
attacks were quick, sudden, painless, non-systematised: they were 
localised chiefly in the arms, and disappeared during sleep. The 
patient died, set. 20, from pulmonary tuberculosis. There were 
general cortical sclerosis, reaching as deeply as the pyramidal 
layer, atrophy of the pyramidal cells and degeneration of tan¬ 
gential fibres. The glial sclerosis was extremely dense and fine, 
and astrocytes were not seen. S. A K. Wilson. 

PERIPHERAL NEURITIS FROM ISCHEMIA Dtthot, Pikeeet, 

(114) and Vzehaeghe, VEnctphalc, Feb. 10,1913, p. 137. 

A revue d'ensemble in which the authors draw attention to 
histological changes in the peripheral nerves, both parenchymatous 
and interstitial, occurring in the course of ischaemia from disease 
of the vasa nervorum, and in this way explain some of the 
symptoms of Volkmann’s paralysis and of arteriosclerosis, 
intermittent claudication, &c. S. A K. Wilson. 

NEUROSES AND SEXUALITY. Ladame, L'EnctphaU , Jan. 10,1913, 

(115) p. 51, and Feb. 10,1913, p. 157. 

These articles may be strongly recommended to the attention of 
all who have followed the Freudian movement in recent years. 
It is impossible to abstract them satisfactorily. It may be said, 
however, very briefly, that their critical and common-sense scrutiny 
of some of the pretensions of the Freudian School is eminently 
calculated to sober the enthusiasm of those Athenians of to-day 
who run after every new thing. S. A. K. Wilson. 

THE TEACHING OF FREUD AND HIS SCHOOL. Rtois and 

(116) Hesnaed, VEnctphale, April, May, and June 1913, pp. 356, 446, 
and 537. 

This long critical review is deserving of the attention of the 
neurologist and psychiatrist. Its viewpoint is scientific, not 



ABSTRACTS 


85 


sentimental: it is a reasoned, unbiassed, sober, and by no means 
unsympathetic discussion of Freud’s teaching. It does not lend 
itself to summarising, but we may translate some of the closing 
sentences. 

“Freud’s teaching is attractive, but extremely hypothetical, 
mainly because it is a medico-philosophical system, and because it 
brings into association an enormous amount of data inadequately 
or not at all controlled. It should not, however, be therefore 
misunderstood or condemned. On the contrary, its study should 
be continued, provided it is always regarded as a provisional 
and partial theory. . . . Freud may be pardoned for basing his 
system merely on daring hypotheses as long as it is considered 
simply as an attempt at a pathogeny for the psychoneuroses.” 

There is a very extensive bibliography attached. 

S. A. K. Wilson. 


PSYCHIATRY. 

SUPBABENAL APOPLEXY IN GENERAL PABALY8I8. SUDDEN 

(117) DEATH. (Apoplexie surrfaale chez une paralytique gfafrale. 
Mort subite.) Di Tbtssibu, Gaz. hebd. des Set. mid. de Bordeaux, 
1913, xxxiv., p. 586. 

The patient was a woman, aged 48, in the early stage of general 
paralysis. In addition to the characteristic findings in the brain, 
the necropsy showed a considerable haemorrhage into the right 
suprarenal. J. D. Rolleston. 

ON THE EEFliEXBS IN DEMENTIA PBABOOX. (Contribution t 

(118) l’Atude det reflexes dans la ddmence prdcoce.) A Borel, Thises 
de Paris, 1913-14, No. 68. 

From an examination of twenty-three cases Borel came to the 
following conclusions:— 

1. In two-thirds of the cases the tendon reflexes were 
exaggerated, and the cutaneous reflexes diminished. 

2. With the exception of Pilcz’s sign, which was present in 
78 per cent., the oculo-pupillary reflexes were too inconstant to 
be of any value. 

3. In 82 per cent. Leri’s reflex was negative or asymmetrical. 

4. Disturbances of the reflexes in dementia praecox do not 
depend upon the clinical variety of the disease, but occur 
indifferently in every form of it, and do not appear to be affected 
by states of depression and of excitement. 

5. Similar disturbances of the reflexes do not occur in mania 
or melancholia. 

6. Disturbances of the reflexes in dementia prsecox seem to 



86 


ABSTRACTS 


haimonise with the probability of the lesions being situated in the 
higher nerve centres, lesions which have been observed by 
numerous authors. 

7. The presence of Pilcz’s sign and the absence of Leri’s reflex 
in association with the disturbances of the reflexes mentioned 
(vide 1) may be of considerable value in the diagnosis of dementia 
prjecox. J. D. Rolleston. 

RESEARCHES ON THE GENITAL GLANDS IN DEMENTIA PR.® 

(119) 00X. Obrbgia, Parhon, and Urechia, L'Enetphale, Feb. 10 
1913, p. 109. 

From a histological examination of the testes and ovaries in 
several cases of dementia pnecox, the authors conclude that 
the development of the disease cannot be attributed to a disturb¬ 
ance of the internal secretion of the sexual glands. They have 
noted absence of spermatogenesis in some instances, and this, with 
other facts, such as alteration in the blood, suggests that dementia 
praecox is a generalised pathological condition, not limited to the 
brain. S. A. K. Wilson. 

ACHONDROPLASIA WITH MANIC-DEPRESSIVE PSYCHOSIS. 

(120) (Una alienata acondroplasica.) G. C. Befani, Raxsegna di Studi 
Psichiat., 1913, iii., Nov.-Dee., p. 468. 

A case of achondroplasia in a woman, aged 21, in whom the 
condition was very marked in the lower limbs. The mental 
condition was one of manic-depressive psychosis. The author 
thinks that the mental state of such cases is “ hypomanic,” and 
that such patients have a peculiar psychical vulnerability. They 
are not, however, more liable to mental disease than normal people, 
and when these do occur they are not in any way distinctive. The 
author is inclined to think that on account of this peculiar mental 
vulnerability these patients have an exaggeration of their usual 
psychical phenomena, which is in the direction of the manic- 
depressive psychoses (v. Review, 1918, xi., p. 557). 

A. Ninian Bruce. 


BOOKS AND PAMPHLETS RECEIVED. 

Braun, Alfred, and Friesner, Isidore. “ The Labyrinth : An Aid to the 
Study of Inflammations of the Internal Ear,” pp. 250. Rebman Ltd., 
London, 1913. Pr. 17s. 6d. net. 

Franz, S. Ivory. “ Psychological Factors in Medical Practice ” ( Inter¬ 
state Med. Joum., 1914, xxi.). 

Turrb, JR. “Les Origines de la Connaissance.” Felix Alcan, Paris, 
1913 . Pr. Fr. 5. 



■ftevnew 

of 

IReurologp anb jp>s£cbtatti> 


Original Hrticles 


LABYRINTH SUPPURATION. 

(.A Review.) 

By J. 8. FRASER, M.B., F.R.C.8., Edinburgh. 

Development and Anatomy of the Labyrinth. 

The membranous labyrinth is developed from the otic vesicle— 
a hollow ingrowth of epiblastic neuro-epithelium, which sinks into 
the mesoblast. Later the otic vesicle becomes differentiated into 

(1) the Pars Superior, or Static Labyrinth, consisting of the 
saccule, utricle, and the three membranous semicircular canals: 
to this part is attached the vestibular nerve and its ganglion. 

(2) The Pars Inferior, or Membranous Cochlea, to which the 
cochlear nerve and its spiral ganglion are attached. From the 
point of view of comparative anatomy the static labyrinth is con¬ 
siderably older than the auditory labyrinth. 

1. Pars Superior .—The three membranous canals communicate 
with the utricle by five openings—the superior and posterior 
vertical canals having a common opening (crus commune) at their 
non-ampullated ends. The three canals lie in the three dimensions 
of space: each canal is dilated at one end into an ampulla which 
contains a small mound of neuro-Qpithelium called the crista. 
This mound is capped by the cupola, and is supplied by a branch 
from the vestibular nerve. The utricle itself shows a layer of 
8 




88 


J. S. FRASER 


epithelium on the inner side of its external wall; the neuro¬ 
epithelium of the saccule is placed on the antero-internal wall of 
the cavity at right angles to the plane of the sensory epithelium 
in the utricle. The utricle and saccule each give off fine ducts 
which join to form the endolymphatic duct; this again ends in 
the endolymphatic sac between the layers of the dura on the 
posterior surface of the petrous pyramid. The utricle and saccule 
are supplied by tbe vestibular nerve and its ganglion in the 
internal auditory meatus. 

2. The Pars Inferior, or Membranous Cochlea, is a blind tube 
(somewhat triangular on section), coiled round a central stem or 
modiolus. In the floor of this tube, which is wider at the apex 
than at the base of the cochlea, lies Corti’s organ—a small mound 
of neuro-epithelium supplied by the cochlear division of the 
eighth nerve and its spiral ganglion, which is situated in the 
modiolus. In the embryo, and probably also in the adult, the 
narrowest part of the cochlea is connected to the saccule by means 
of a fine duct (canalis reunions ). 

The Bony Labyrinth .—In the early embryo the membranous 
labyrinth is surrounded by a layer of meBoblast, which develops 
into a hollow capsule of cartilage. This, later on, becomes con¬ 
verted into dense bone and embedded in the petrous temporal; 
the cartilage bone capsule of the labyrinth can, however, always 
be distinguished from the stirrounding lamellar bone, with its 
marrow spaces. If this cartilage bone capsule be artificially cut 
out by a skilled workman, it will be found to consist of (a) the 
bony semicircular canals, which contain the membranous canals, 
and open into ( h ) the bony vestibule, which contains the utricle 
and saccule, and communicates in front with ( c ) the bony cochlea, 
which encloses the membranous cochlea. On the outer wall of 
the vestibule we have the oval window, which is closed in the 
living by the footplate of the stapes and the annular ligament. 
The bony cochlea resembles the shell of a snail, and lies with its 
base towards the internal auditory meatus. From the central 
stem or modiolus of the cochlea the bony spiral lamina projects 
into each coil of the bony cochlea. To the edge of the bony 
spiral lamina the membranous cochlea is attached. The outer 
surface of the membranous cochlea is attached to the outer wall 
of the bony cochlea. In this way each coil of the bony cochlea 
is divided into three parts: (1) the scala vestibuli above, which 



LABYRINTH SUPPURATION 


89 


communicates with the vestibule; (2) the scala tympani below, 
which begins at the round window; and (3) the membranous 
cochlea with its spiral lamina, which lie between (1) and (2). 
At the apex of the cochlea the scala vestibuli and the scala 
tympani become continuous with one another at the helicotrema. 
The membranous labyrinth is filled with fluid (endolymph), and 
is surrounded more or less by fluid (perilymph), which separates 
it from the endosteal lining of the bony labyrinth. 

The best way to understand the anatomy of the labyrinth is 
to think of a tunnel driven through a small hilL If a section be 
made through this hill, the cut end of the tunnel will be seen, and 
round it the stonework forming the wall of the tunnel The hill 
corresponds to the petrous bone; the stone walls of the tunnel to 
the dense cartilage bone which forms the true capsule of the 
labyrinth. The cavity of the tunnel corresponds to the hollow 
space within the bony labyrinth. If we further suppose that 
the tunnel contains a train, and that both tunnel and train are 
flooded with water, we find that the water in the train corresponds 
to the endolymph, the train itself to the membranous labyrinth, 
and the fluid between the train and the walls of the tunnel to the 
perilymph. 

The outer wall of the bony labyrinth is a party wall, ie., it is 
also the inner wall of the middle ear. For this reason the oval 
and round windows, the external or horizontal canal, and the 
promontory, which contains part of the cochlea, are exposed to 
infection in cases of otitis media. The oval window communicates 
with the perilymph space of the vestibule, while the round window, 
which lies at the top of a deep niche, communicates with the 
perilymph space of the cochlea. Vibrations of the perilymph, 
set up by movement of the footplate of the stapes in the oval 
window, pass up the scala vestibuli of the cochlea to the apex, 
and then through the helicotrema down the scala tympani to the 
round window. Occasionally the bony labyrinth is almost entirely 
surrounded by air cells which communicate with the tympanic 
cavity and mastoid antrum, and form part of the middle ear cleft. 

On the inner wall of the mastoid antrum we find a series of 
small veins—the remains of an important foetal vein—which pass 
through the fossa subarcuata beneath the dome of the superior 
canal, to reach the posterior surface of the petrous pyramid, and 
there to open into the superior petrosal sinus. Infection may pass 



90 


J. S. FRASER 


along this route and give rise to extradural abscess and meningitis. 
This mode of infection has nothing to do with labyrinthitis. 

The lymphatic system of the labyrinth is divided into two 
parts—endolymph and perilymph. The endolymph system ends 
in the saccus endolymphaticus already mentioned. The perilymph 
communicates directly with the subarachnoid space of the posterior 
cranial fossa by means of the cochlear aqueduct, which opens out of 
the scala tympani of the cochlea in the region of the round window. 

The membranous labyrinth and its capsule of cartilage bone 
are supplied by the internal auditory artery—a branch of the 
basilar—which enters at the internal auditory meatus. The 
veins, on the other hand, leave the labyrinth along the aqueducts 
of the vestibule and of the cochlea. 

Physiology. 

From the physiological point of view the internal ear is divided 
into (1) the auditory labyrinth, and (2) the static labyrinth. 

1. The blind tube of the membranous cochlea commences 
within the vestibule, and coils round the central stem or modiolus 
as described above. At its beginning within the vestibule the 
cochlear duct is narrow, and at this part the highest tones are 
appreciated. At the apex of the cochlea the duct is wider, and 
here the lowest tones are heard. The range of hearing of the 
human cochlea extends from sixteen double vibrations per second 
up to about eighteen thousand—at least in young subjects. The 
auditory apparatus is tested by means of the voice (spoken and 
whispered), the watch, or akoumeter, a series of tuning forks 
ranging from C. 16 up to C. 4,096 double vibrations per second. 
Above this the upper tone limit is best tested by means of tbe 
monochord—an instrument on the principle of the violin string, 
which can be made to vibrate transversely (lower tones, 4,000-6,000 
D.V.S.) or longitudinally for the higher tones, 7,000-18,000 D.V.S. 
It is unnecessary to describe these tests further. In order to 
establish the presence of complete unilateral deafness (as in cases 
of labyrinth suppuration) B&rdny has invented the clockwork 
noise apparatus: this instrument is inserted into the patient’s 
good ear, and, when in action, fully occupies the attention of this 
ear, so that any sounds which the patient hears must be appreci¬ 
ated by the diseased ear. Syringing the healthy ear or rubbing 



LABYRINTH SUPPURATION 


91 


(he auricle with the hand serve the same purpose as the noise 
apparatus. 

2. The Static Labyrinth (BArAny).—Movements of the endolymph 
in the membranous canals act on the cristse and cupulae, and the 
stimuli so created pass by way of the vestibular nerve to the vesti¬ 
bular nuclei at the base of the brain: from these nuclei fibres 
radiate (a) to the nuclei of the motor nerves of the eye muscles 
(giving rise to nystagmus), (b) to the motor neurones of the spinal 
cord (giving rise to the irregular gait characteristic of vestibular 
lesions), and (c) to the cerebellum. Ewald showed, by experiments 
on pigeons (application of pressure to an artificial fistula in the 
horizontal canal), that movement of the endolymph in the right 
horizontal canal, from the smooth end towards the ampulla, caused 
horizontal nystagmus to the right, while movement in the opposite 
direction produced a weaker horizontal nystagmus to the left. In 
the external canal, movement of the endolymph from the smooth 
end to the ampulla is therefore the more effective movement. 
Vestibular nystagmus is of the following type: Horizontal 
nystagmus to the right consists of a quick twitch of the eyes to 
the right and a slower movement to the left—it is a rhythmic 
associated movement. Vestibular nystagmus is always most 
distinct when the patient is made to turn his eyes in the direc¬ 
tion of the rapid twitch; on the other hand, the nystagmus will 
be lessened or abolished when the patient looks in the direction of 
the slow component. It is important to remember that the slow 
movement of the nystagmus is the real vestibular component;' 
the quick twitch is voluntary, and is abolished when the patient 
is under chloroform. 

The functions of the utricle and saccule are not definitely 
known. It is believed, however, that they enable us to appreciate 
passive movement in a straight line when the eyes are closed or 
when we are in the dark, just as the canals enable us to appreciate 
passive rotation. It has also been suggested that the saccule may 
enable us to hear noises as distinguished from musical tones. 

Clinical Methods of Testing the Vestibulab 
Apparatus (BArAny). 

It is first necessary to test the patient for spontaneous 
nystagmus, as some normal people have slight but equal nystagmus 
on looking to the extreme right or left. 



92 


J. S. FRASER 


Botation .—The patient is placed in a turning chair with his 
head upright, and is rotated at the rate of ten complete revolutions 
in twenty seconds. At the end of the tenth turn the rotation is 
suddenly stopped, and the duration of the resulting nystagmus 
is measured by a watch: if opaque spectacles are worn by the 
patient the nystagmus is rendered more marked. When the head 
is in the erect position the rotation affects only the two horizontal 
canals, as they alone are in the plane of rotation. At the beginning 
of rotation to the right the endolymph in the right canal, in virtue 
of its fluid inertia, flows towards the ampulla, relatively speaking: 
in the left canal the fluid flows away from the ampulla. As the 
rotation is continued, the endolymph catches up with the movement 
of the canal wall until it rotates at the same rate. If now the 
rotation of the individual be abruptly stopped, the movement of 
the endolymph will continue, but its flow relative to the ampulla 
will be in the reverse direction to what it was at the beginning of 
rotation. In order to understand the movements of the endolymph 
and cristse, we have only to think of what oocurs in an Edinburgh 
tram car—especially on a wet day. When the car starts suddenly, 
all the passengers are violently jerked backwards, but, as the car 
goes on, they again assume an upright position, and maintain it 
until the car stops suddenly, when they are all jerked forwards. 
The cristae of the membranous canals correspond to the passengers. 

Nystagmus produced by suddenly stopping the rotation of a 
patient is known as “ after-nystagmus.” The average duration of 
the horizontal “ after-nystagmus ” in a normal individual, due to 
rotation with the head erect, is from fifteen to thirty seconds. By 
bending the head in various directions it is possible to investigate 
the remaining canals; this, however, is of little practical im¬ 
portance. We must remember that the posterior canal on the 
right side is on a plane parallel to that of the superior canal on 
the left side; the same thing, of course, holds with regard to the 
posterior canal on the left side and the superior canal on the 
right side (Crum-Brown). 

The laws of nystagmus are as follows: I. Each pair of canals 
induces nystagmus in its own plane. II. Nystagmus, due to rota¬ 
tion, corresponds to the line of intersection of the horizontal 
plane with the cornea. 

Caloric Nystagmus .—If a patient with normal vestibular 
apparatus has his right ear syringed with cold water when his 



LABYRINTH SUPPURATION 


93 


head is erect, horizontal and rotatory nystagmus to the left is 
produced. If warm water (116° F.) be used, the nystagmus is 
rotary to the right (the reader must distinguish between rotary 
nystagmus and nystagmus due to rotation). The explanation of 
caloric nystagmus is as follows: When the head is upright, the 
summit of the superior canal is the highest point in the labyrinth, 
while its ampulla lies lower down, near the outer labyrinthine 
wall. If one cools down the outer wall of the labyrinth by 
syringing cold water against it, a downward current is set up 
which acts on the crista of the superior and horizontal canals, and 
gives rise to nystagmus. In the same way warm water causes an 
ascending current: if the fluid used be at body temperature there 
is, of course, no reaction. If the vestibular apparatus be destroyed, 
or the vestibular nerve paralysed, nystagmus cannot be induced by 
syringing that ear. The caloric method has this advantage over 
rotation that we can, by syringing, test each ear separately. 

When nystagmus to the left is produced in a normal person, 
he tends to fall to the right if he stands with his feet together and 
eyes shut, i.e., he falls in the direction of the slow component of 
nystagmus. If his head be turned ninety degrees to the left he 
falls forwards; if turned ninety degrees to the right he falls 
backwards. 

Galvanism may be used to test the vestibular apparatus. 
When the cathode is applied to the right ear we get rotary 
nystagmus to the right; when the anode is applied we get 
nystagmus to the left. Galvanism, however, causes nystagmus even 
if the labyrinth be destroyed, as it acts on the vestibular nerve. 
For this reason it is not of great practical importance, except in 
cases of cerebello-pontine angle tumour. 

Fistula Symptom .—An olivary ear piece—attached by rubber 
tubing to a Politzer bag—is fitted tightly into the external 
auditory meatus. If the bag be now squeezed so as to raise the 
air-pressure in the external meatus, nystagmus is produced to the 
affected side (typical fistula symptom). Occasionally we get a 
reversed fistula symptom, i.e., compression produces nystagmus to 
the opposite side. The fistula symptom is only obtained in cases 
in which a fistula exists in the bony wall between the middle and 
inner ear, and in which the vestibular apparatus is more or less 
intact. 

Pointing Test .—The patient shuts his eyes, closes his hand 



94 


J. S. FRASER 


(palm downwards), and extends his index iinger to meet the index 
finger of the examiner. He is then told to slowly flex the hand at 
the wrist joint, and then to raise it again to meet the examiner’s 
finger. Any pointing error present is in the direction of the slow 
component of the nystagmus. A spontaneous error in the pointing 
test is usually due to a lesion in the posterior fossa, such as a 
cerebellar or extradural abscess. 

Pathology of Labyrinthitis (Braun and Friesuer: Ruttin). 

Infection of the inner ear occurs once in every hundred cases 
of purulent otitis media—usually as the result of an acute exacer¬ 
bation in a chronic case. 

Labyrinthitis may be—(1) circumscribed , or (2) diffuse. 

1. The circumscribed form may affect only the bony capsule 
(para-labyrinthitis), or it may have invaded the perilymph space 
(peri-labyrinthitis). These two forms may be combined. 

Within the vestibule there is a fibrous septum (Alexander), 
which divides the utricle and canals on the one hand, from the 
saccule and cochlea on the other. In this way labyrinthitis 
may remain for a period confined to one set of structures. The 
perilymph spaces of the ampullae of the canals are almost com¬ 
pletely shut off from the vestibule by septa of connective tissue. 
Peri-labyrinthitis may, in this way, be further limited. 

In the cochlea labyrinthitis may be limited to the lower half 
of the basal coil, whether the infection passes by way of the round 
window or oval window. The lower half of the basal coil of the 
cochlea remains the lowest portion of the cochlear cavity in every 
position of the head (Ruttin). 

2. Diffuse labyrinthitis occurs in two forms: (a) Empyema of 
the labyrinth (combined inflammation of the peri- and endo¬ 
lymphatic spaces), and (b) pan-labyrinthitis, in which the bony 
capsule is affected in addition. 

Circumscribed and diffuse labyrinthitis may be acute, sub¬ 
acute, or chronic. 

Labyrinthitis may also be classified according to the causal 
disease or organism, e.g., scarlatinal, cholesteatomatous, tubercular, 
pneumococcic, &c. Fracture of the base of the skull and injury 
with a pointed instrument, such as a knitting needle, may give 
rise to a traumatic form of labyrinthitis. 

Lastly, labyrinthitis may be classified according to the route 



LABYRINTH SUPPURATION 


95 


of infection: (1) Meningeal, as in cerebro-spinal meningitis: from 
15 to 50 per cent, of cases of cerebro-spinal meningitis are followed 
by deafness; (2) Tympanic, as in suppurative otitis media; and 
(3) Metastatic, as in mumps. 

1. Meningeal cases. —From the meninges the labyrinth may be 
infected through (a) the aqueduct of the cochlea from the 
subarachnoid space, (6) along the internal auditory meatus, (c) by 
necrosis of the inner bony wall in cases of extradural abscess. 

2. Tympanic. —From the middle ear the infection may pass to 
the labyrinth by way of (a) the oval window; (6) the round 
window; (c) fistula of the external canal; and ( d ) fistula through 
the promontory. If, for example, we take a case in which the 
prominence of the external canal is gradually absorbed by pressure 
of a mass of cholesteatoma in a case of chronic middle ear 
suppuration, we find that in time the bone is worn through so 
that the cholesteatoma is now in direct contact with the endosteum 
lining the canaL A little fibrinous exudation may occur in the 
canal in the region of this fistula ( circumscribed labyrinthitis). 
The condition present in such a case corresponds to that in 
Ewald’s experiment on the pigeon. If the air pressure in the 
external meatus and middle ear be now artificially raised, pressure 
will be exerted through the fistula on the labyrinthine fluid, and 
therefore on the crista of the external canal; giddiness and 
nystagmus are thus produced (fistula symptom). The hearing 
power is not affected, except by the otitis media already present. 
If now an acute exacerbation of the otitis occur, the feeble barrier 
remaining may be broken down so that the labyrinth becomes 
generally infected. At first the inflammatory exudation is sero¬ 
fibrinous, with only a few round cells ( diffuse serous labyrinthitis), 
and if the process stops at this stage the labyrinth may almost 
entirely recover. Such a mild attack may occasionally follow the 
radical mastoid operation. On the other hand, if the inflamma¬ 
tory process continues, the labyrinthine fluid becomes definitely 
purulent {manifest diffuse purulent labyrinthitis): in this condition 
the patient suffers severely from giddiness, vomiting, and loss of 
balancing. He is absolutely deaf, but does not usually complain 
much of tinnitus. Within a few days (three to fourteen) the mem¬ 
branous labyrinth is entirely destroyed, and the condition passes 
into the stage of latent diffuse purulent labyrinthitis. This stage may 
last for several months, while granulation tissue and new bone are 



96 


J. S. FRASER 


formed in the labyrinth. Finally, the hollow spaces of the inner 
ear become filled with connective tissue and new bone, and the 
case passes into the stage of spontaneous cure of labyrinth suppura¬ 
tion with compensation. 

The inflammatory process may extend from the labyrinth— 

(1) By way of the aqueduct of the cochlea to the subarachnoid 
space of the posterior fossa, and give rise to lepto-meningitis. 

(2) The infection may spread to the internal auditory meatus 
along the subarachnoid sheath of the cochlear nerve, or along the 
nerve to the saccule or utricle, and give rise to lepto-meningitis. 

(3) In rare cases pus accumulates in the endolymphatic sac 
(empyema of the saccus). (4) The pus in the labyrinth may burst 
inwards, usually through the posterior or superior canals, and give 
rise to extradural abscess. 

Folitzer has pointed out that an abscess may form in the 
fundus of the internal meatus, and may destroy not only the 
nerve fibres but also the labyrinthine artery: this results in 
necrosis of the membranous labyrinth, and of a large part of its 
cartilage bone capsule. 

The endosteum which lines the bony labyrinth is the most 
resistant of all the labyrinthine structures. In those cases of 
labyrinthitis in which spontaneous cure occurs, the organisation 
of the pus in the labyrinth proceeds from this membrane: osteo¬ 
blasts pass in to the granulation tissue which fills the labyrinth 
and form new bone until, eventually, the hollow spaces of the 
labyrinth are entirely obliterated. 

It will be seen that labyrinthitis may end in (1) return to 
normal, in cases of mild serous labyrinthitis; (2) spontaneous 
cure with slight permanent changes; (3) spontaneous cure with 
destruction of the labyrinthine function; (4) extension to the 
intracranial structures. If labyrinthitis extends to the cranial 
cavity it usually gives rise to lepto-meningitis; more rarely it 
leads to extradural abscess, cerebellar abscess, or sinus thrombosis. 
The most frequent path of infection, in cases of meningitis, is the 
perilymphatic or cochlear aqueduct; if it were not that this canal 
is very narrow, and that in some cases swelling of its lining 
membrane completely shuts off the perilymph in the cochlea from 
the subarachnoid space, otitic meningitis would be even more 
frequent than it is. 



LABYRINTH SUPPURATION 


97 


Thb Clinical Aspect and Treatment of Labyrinthitis 

(Ruttin). 

1. Circumscribed Labyrinthitis, and Labyrinth Fistula. 

In this condition the patient complains of attacks of dizziness, 
with occasional vomiting, especially on stooping or turning quickly. 
Spontaneous nystagmus may or may not be present; if present, 
it may be to the healthy side, to the diseased side, or even to 
both. The caloric reaction is usually diminished. With the 
noise apparatus in the healthy ear, the patient can, as a rule, 
hear fairly well. The fistula symptom is present (normal or 
reversed). 

Treatment .—The radical operation should be performed, but 
great care must be taken not to interfere with the fistula. If, as 
sometimes happens, the attacks of dizziness, from which the 
patient suffers, interfere with his work, the labyrinth operation 
may be performed (see page 98). 

2. Diffuse Serous Labyrinthitis. 

This condition occupies an intermediate position between 
circumscribed labyrinthitis and manifest diffuse purulent laby¬ 
rinthitis. 

Symptom of Diffuse Serous Labyrinthitis .—The patient com¬ 
plains of deep-seated pain in the ear, tinnitus, and deafness. The 
vestibular symptoms (dizziness, vomiting, and loss of balancing) 
are more important. The patient lies on the sound side and looks 
towards the diseased side as, in this position, the nystagmus and 
giddiness are less. The patient complains that external objects 
appear to move from the sound to the healthy side. The tem¬ 
perature is not raised. With the noise apparatus in the sound 
ear the patient is not absolutely deaf. If the lesion be on the 
left side, spontaneous nystagmus to the right is present; when 
standing with eyes shut the patient tends to fall to the side of 
the lesion, ie., in the direction of the vestibular component of the 
nystagmus—in this case to the left. The vestibular reaction to 
rotation and syringing are, as a rule, still present, though 
diminished. The fistula symptom may be present, but is usually 
absent. 

Treatment .—If the patient can still hear with the affected ear, 
the labyrinth operation should not be performed. If, on the other 



98 


J. S. FRASER 


hand, the diseased ear be quite deaf and the vestibular reaction 
absent, the labyrinth must be opened and drained at the time of 
the radical mastoid operation; in other words, if we cannot 
diagnose between diffuse serous and diffuse purulent labyrinthitis, 
we must treat the case as one of the more dangerous variety. 

3. Manifest Diffuse Purulent Labyrinthitis. 

This condition lasts only from three to fourteen days. During 
this period the patient suffers from intense giddiness, vomiting, 
and loss of balancing. The vomiting is accompanied by nausea, 
and is not of the effortless cerebral type. Complete deafness is 
present when the noise apparatus is going in the sound ear. 
Marked spontaneous nystagmus is present to the sound side, and 
the caloric reaction is absent on the diseased side. Spontaneous 
pointing and falling are to the affected side. The fistula symptom 
is not present, because the membranous labyrinth is destroyed. 
The patient is too ill for the rotation test. 

Treatment .—If there are no urgent symptoms, such as severe 
pain, fever, or signs of intracranial trouble, it is permissible to 
wait in order that a barrier may form. If, on the other hand, 
interference is called for, a free radical mastoid operation should 
be at once performed, so as to expose the promontory and the 
two windows. The dura of the posterior fossa over the sinus 
should then be laid bare with a blunt gouge. The dura is then 
separated from the bone of the posterior fossa in an inward 
direction by means of a blunt dissector, and protected from injury 
with a small flat spoon or Stacke’s protector. The petrous bone 
is now removed with the gouge and hammer in an inward and 
forward direction, until the posterior and external canals have 
been freely opened up behind the facial nerve. The vestibule is 
now opened from behind by tracing up the smooth end of the 
external canal Finally, the vestibule should be opened in front 
of the facial nerve by two or three blows with a fine gouge, 
removing the outer wall of the promontory, and joining the 
oval and round windows. At the present time the general 
opinion is that the cochlea should not be further interfered with 
unless meningitis be present. In the latter case the inner wall of 
the vestibule should be opened up and the subarachnoid space of 
the internal meatus drained (trans-labyrinthine drainage of West 
and Scott). 



LABYRINTH SUPPURATION 


99 


4. Latent Diffuse Purulent Labyrinthitis. 

At the end of from three to fourteen days the manifest stage 
passes into that of latent diffuse labyrinth suppuration. The 
labyrinth is now entirely destroyed. In this latter stage the 
patient will, if carefully questioned, give a history of recent 
dimness, vomiting, and loss of balancing. These symptoms have, 
however, now passed off. 

Symptoms in the Latent Stage .—There is complete deafness in 
the affected ear. Spontaneous nystagmus is usually absent, but 
there may he a slight rotary twitch to both sides. The caloric 
reaction is absent in the diseased ear. On rotation, there is a 
marked difference in the duration of the “ after-nystagmus,” 
depending on the direction of the rotation, e.g., if the patient have 
a latent labyrinthitis on the right side, and if we rotate him to 
the right (thus mainly testing the left or healthy labyrinth), he 
will get horizontal nystagmus to the left of almost normal 
duration—say twenty seconds. When, however, we rotate him 
to the left (thus mainly testing the right or diseased labyrinth), we 
only produce very slight nystagmus to the right of from four to 
ten seconds duration. 

Treatment .—If the radical operation is called for, the labyrinth 
operation, described above, must also be performed. If this be 
not done the patient runs a grave risk of getting meningitis as 
the result of the mastoid operation alone. 


5. Healed Labyrinthitis with Compensation. 

This condition is probably present at a period of six months 
and upwards after the attack of purulent labyrinthitis. The 
patient is quite deaf in the affected ear, and the caloric reaction is 
absent. Rotation, however, to the right and also to the left, 
produces an equal duration of “ after-nystagmus,” because compen¬ 
sation has been established, and the external canal on the healthy 
side reacts equally to both directions of rotation. In such a case, 
even if the radical mastoid operation be called for, Alexander holds 
that it is not necessary to do the labyrinth operation, as there is no 
fear of infection spreading from the inner ear to the meninges. 
Other otologists, however, consider that it is impossible to be 
quite sure that the labyrinth is filled with new bone. They 



100 


LEONARD J. KIDD 


believe that pus may still be present, and that, for this reason, it 
is safer to do the labyrinth operation at the time when the 
radical mastoid operation is performed. 

References. 

BArXny. —“ Physiologic and Pathologic des Bogeng&ng- Apparatus.’' Vienna, 
1907. 

Braun and Friksnrr.— “ The Labyrinth.” London, 1913. 

Ruttin. —“ Klinih der Seroaen und Eitrigen Labyrinth Entzundungen.” 
Vienna, 1912. 


ISCOVESCO’S EXPERIMENTAL RESEARCHES 
ON LIPOIDS OF ORGANS. 

(A Review.) 

By LEONARD J. KIDD, M.D. 

Henri Iscovksco's researches on this subject have been pursued 
for at least four or five years; but his most recent work, embodied 
in the ten papers now under review, is of special interest in 
several directions, and brings out some new facts that bear closely 
on some of our present beliefs as to the functions of organs. 
These papers are published in the Compt. Bendus Soc. de Biol., 
(a) lxxv., 1913-14, pp. 361, 393, 445, 450, 510, 548, 681; (b) lxxvi., 
1914, pp. 34, 74, 117. Iscovesco’s mode of extraction of the 
lipoids, several varieties of which are contained in each organ, is 
described; and to each lipoid specially tested he gives a number. 
A uniform procedure has been adopted, the special lipoid having 
been injected, usually in an oily solution, hypodermically into the 
loose cellular tissue of the neck in rabbits every day or two for a 
period of months; the animals, and also the controls of the same 
age, are weighed at the beginning of the treatment: later on, 
autopsy includes weighing of the body and all the important 
viscera, and tables are given of the relative weights in the treated 
and untreated animals. In many of these studies Iscovesco has 
injected these lipoid solutions into man. 

The thyroid lipoid (II. Ba), when injected daily in a dose of 
1 to 2 eg. per kg. of the rabbit’s body-weight, causes at 



RESEARCHES ON LIPOIDS OF OROAKS. : i<3t 

the end of two months a hypertrophy of the thyroid and 
heart, tachycardia, and a true exophthalmos: it stimulates (i.e., 
increases the weight of) the adrenals, ovaries, uterus, and testes; 
the female heart more than the male, the spleen slightly, the 
kidneys only in males, and the thyroid very markedly, but more in 
females. This lipoid also regularises the increase of weight and 
the bodily growth in young animals, but, on the contrary, 
diminishes the body-weight of adults. 

Out of the many lipoids of the ovary the most important is 
the fifth (V. Dc): when injected regularly for three months it 
leads to utero-ovarian hypertrophy: this lipoid is the same one 
whether it comes from cow, mare, or sow. To obtain the results, 
the animals and the controls must be virgin and aged about three 
months. Injected every two days for three months, it acts almost 
exclusively on the uterus, ovary, and thyroid, and either not at all 
or to a trifling extent on the adrenals, heart, liver, spleen, and 
kidneys. It regularises and accelerates bodily growth in young 
animals. 

The lipoid (II. Bb) extracted from the testes was injected 
into adult rabbits aged 8 months, and into young ones aged 7 
weeks, in an oily solution. In the adults 1 eg. per kg. of body- 
weight injected every two days for three months led to great 
hypertrophy of the testes; it increases the weight of the kidneys 
slightly (unlike the ovarian lipoid), and the thyroid slightly, but 
less than the ovarian lipoid does. The body-weight of these adults 
was increased: the animals became very excited, and the phe¬ 
nomena of rut were greatly accentuated. Iscovesco thinks the 
testicular hypertrophy is probably due to a selective action on 
the genital spinal cord centres. In very large doses (5 eg. per 
kg.) and also in very young subjects it leads to wasting; and 
if it be pushed, paraplegia follows: this, however, disappears 
on stoppage of the injections. In the young rabbits, aged 7 
weeks, a daily injection of 1 eg. per kg., continued for sixty days, 
gave a more regular and rapid bodily growth than in controls 
(100 v. 57). Iscovesco says that a daily dose of 2 eg. in man 
confirmed his results. 

The lipoid (II. Bd) extracted from the anterior lobe of the 
pituitary gives these results when injected daily in a £ eg. 
dose per kg. of body-weight: (1) Agitation, continual restless¬ 
ness, and pugnacity: these changes occur usually after four to six 





w;-'*:: : LEONARD J. KIDD 

• < • • • • • 

weeks of treatment; (2) increased renal secretion, with increase 
of the urea, chlorides, and phosphorus of the urine; (3) increase 
of appetite; (4) active increase of bodily growth in young but not 
in adults; (5) increased weight of adrenals, heart, and kidneys, 
but not of the genital organs in either sex. Hypodermic injection 
into man of a daily dose of 2 to 5 eg. gives at the outset a 
temporary acceleration of pulse, slight diuresis, increased appetite, 
and—in asthenic patients—a manifestly increased power of work. 
Finally, in myocarditis a rise of arterial pressure is seen after a 
certain time, and the cardiac movements are regularised. 

The lipoid (II. Bd) of the adrenal cortex gives these results 
when injected every two days, for 130 days, into rabbits aged 
135 days, in a £ eg. dose per kg. of body-weight: (1) Marked 
hypertrophy of adrenals, almost entirely confined to their cortex; 
(2) stimulation of kidneys slightly, but more in males; (3) also of 
liver; (4) markedly also of cutaneous glands. This lipoid has 
no action on heart (unlike the medullary adrenal lipoid); powerfully 
stimulates the growth of the fur; has an insignificant action on 
bodily growth and weight. Hypodermic injection of 2 to 5 eg. 
into man gives early acceleration of pulse, with a fall of arterial 
tension: after a few hours both phenomena return to normal. 
Abundant sweating follows in 60 per cent, of cases, and lasts for 
many hours, even up to twenty-four: it is chiefly nocturnal. 
Iscovesco thinks this is parallel with the stimulation of the hair- 
system in his rabbits, and he suggests that the night-sweats of 
phthisis may be explained by cortical adrenal stimulation, for he 
finds on autopsy in these cases, and also in other infectious, that 
there is evidence of lesions, or signs of stimulation of the adrenal 
cortex. Finally, he finds that a daily injection of even only 1 
or 2 eg. of this lipoid solution into man is followed by an 
increase of strength and a feeling of euphoria which may be turned 
to good therapeutic account in cachectic states. 

The lipoid (II. Bd) of the adrenal medulla seems to have been 
injected exclusively into female rabbits: treatment was continued 
for sixty days: six does, aged 14 months, received daily a dose of 
J eg. per kg. of body-weight: all were in perfect health when 
sacrificed on the sixtieth day. The treated animals had gained 
2*5 per cent, of their initial body-weight, the controls only 1*4 per 
cent. This lipoid stimulates the adrenals, but to a very much less 
degree than does the cortical adrenal lipoid, and its effect is mainly 




RESEARCHES ON LIPOIDS OF ORGANS 


103 


on the adrenal medulla: it stimulates the heart so much that 
after sixty days’ treatment the heart weighs 3*80 g. per kg. of 
body-weight, as against only 2*69 in controls. Its action on other 
organs is mostly insignificant or nil ; yet there is an increase of 
weight of the ovary (135 v. 90 of controls) which “is not 
negligible ”; the uterus, however, weighs only 80 v. 128 of controls’ 
uterus; atheroma was absent, and the aorta was normal. Daily 
injection, into many, of 2 or 3 eg. slows the pulse and increases 
the arterial pressure and the power of work. Isoovesco thinks 
that in Addison’s disease the asthenia and the cardio-vascular 
disturbances are due to lesions of the medulla, but that the 
pigmentation and cutaneous manifestations are always to be 
connected with the primary or secondary irritation of the adrenal 
cortex. (In the Reviewer’s opinion, this is a rather disappointing 
paper. We need to know the effects of this lipoid on male rabbits, 
and also whether, if a larger series of does were used, the uterus 
would be found to be constantly smaller than in controls. 
Curiously, Iscovesco does not say whether the six does were virgin 
or not) 

The lipoid (II. Bd) of the pancreas was injected into rabbits, 
aged 135 days, every other day for 131 days, in a dose of 1 c.c. 
of a 2 per cent oily solution. At the end of this period they 
showed the very large increase of 51 per cent, of their initial 
body-weight, as against only 32 per cent, in the controls: the 
treated animals had the better appetite. Autopsy showed heavier 
adrenals than those of controls, lighter thyroids, and only in¬ 
significant changes in other organs for the most part. But the 
weight of the liver was greatly increased (47 v. 36 of controls): 
it was not fatty. No other lipoid has given Iscovesco so great an 
effect on the liver. The histological changes in liver and pancreas 
are reserved for a future paper. Daily injection into man of 
1 or 2 eg. for a certain time gives: (1) Slight increase of 
arterial pressure, and (2) a constant increase of body-weight. In 
one case of diabetes an increase of sugar of 30 to 60 g. daily 
followed; but in another case the sugar diminished and dis¬ 
appeared very quickly. Iscovesco concludes that this special 
pancreatic lipoid aggravates hyper-hepatic diabetes, but rapidly 
benefits the hypo-hepatic variety. 

The liver is very rich in lipoids, e.g., in the horse, 20 g. of 
lipoids in 100 g. of dried liver; and in the ox, 16 per cent. 

9 



104 


LEONARD J. KIDD 


Iscovesco isolated a special lecithide from the ox liver, which, 
when injected in oily solution into young rabbits every two days 
for 132 days in doses of 1 eg. per kg. of body-weight, led to the great 
increase of 62 per cent of body-weight over their initial body- 
weight ; and yet this occurred in spite of the unfavourable season 
(December to February). This increase was more than double that 
of the controls (29 per cent.). Autopsy showed that this hepatic 
lecithide has no action on adrenals, heart, genitals, or thyroid; 
but it stimulates the liver and spleen slightly, and favours very 
strongly the development of the lungs. It is the only pulmonary 
stimulant substance yet discovered by Iscovesco, with the single 
exception of a lecithide extracted by him from commercial cod- 
liver oil: the latter lecithide has exactly the same pulmo-stimulant 
action as the former. In the last paper of his series of ten, he 
shows that a special lipoid (II. Bd) can be extracted from the liver 
after the special hepatic lecithide has been eliminated from the 
liver. When this lipoid is given to young rabbits aged about 
4£ months, every two days for a period of 132 days in a 
1 eg. dose hypodermically in oil, it gives no effect on body-growth 
nor on lung development, thus differing from the special hepatic 
lecithide. But it stimulates the heart (3*80 v. 2*68 of controls), 
the liver (41’93 v. 41 - 60), and kidneys slightly but much less than 
does the hepatic lecithide. Iscovesco has obtained encouraging 
therapeutic results, especially in children, in chronic pulmonary 
tuberculosis and tuberculous adenitis by hypodermic injections of 
a 2 per cent, oily solution of the hepatic lecithide, or by rather 
larger doses by mouth. In all these patients he observed increased 
weight, increased urea excretion, and improvement of appetite. 
His paper on the cod-liver oil lecithide (p. 34, 1914, lxxvl) is 
well worth study. He experimented on groups of rabbits by means 
of (1) commercial cod-liver oil alone; (2) by ditto after depriva¬ 
tion of its lecithide; (3) by olive oil; (4) by the special lecithide 
solution extracted from cod-liver oil. Of these, Nos. 4 and 1 gave 
the greatest effect on growth and the lungs; and Iscovesco found 
that rabbits bear animal oil better than vegetable oil 

Doubtless we shall in the near future learn about other organic 
lipoids from Iscovesco; meanwhile it is helpful to summarise his 
researches as follows: (1) Bodily growth in young animals is 
increased and accelerated by special lipoids extracted from the 
pancreas, thyroid, ovary, testis, anterior pituitary lobe, and cod- 



RESEARCHES ON LIPOIDS OF ORGANS 105 


liver oil, and in rabbits aged 14 months by the adrenal medullary 
lipoid; (2) the thyroid is hypertrophied by the lipoids of the 
thyroid and the ovary, and slightly by testis; (3) the heart by 
the thyroid, anterior pituitary, medullary adrenal, and the II. Bd 
hepatic lipoid; (4) the ovary by the ovarian, thyroidal, and 
medullary adrenal; (5) the uterus is hypertrophied by the ovarian 
and thyroidal, and was diminished in weight (in six rabbits) by 
the medullary adrenal; (6) the kidneys are either hypertrophied 
or show increased activity by the use of the thyroidal (males 
only), testis slightly, anterior, pituitary, cortical adrenal (chiefly 
in males), the hepatic lipoid (II. Bd) slightly, but by the hepatic 
lecithide much more; (7) the liver by the pancreatic, anterior 
pituitary, cortical adrenal, and special hepatic lipoid (II. Bd); 
(8) the adrenals by the cortical adrenal (markedly), medullary 
adrenal (slightly and mainly its medulla); (9) the skin, fur, and 
cutaneous glands strikingly by the cortical adrenal (sweating also 
in man); (10) the appetite is increased by the pancreatic, anterior 
pituitary, and the special hepatic lecithide which is identical, 
chemically, physiologically, and therapeutically, with the leci¬ 
thide extracted from commercial cod-liver oil; (11) the testes 
are hypertrophied by the thyroidal lipoid and testis lipoid; (12) 
the lungs by the pulmo-stimulant lecithides of (a) liver and (b) 
cod-liver oiL Changes in other organs, such as the spleen or 
rectum, &c., are either slight or nil, so far, at any rate, as their 
post-mortem weights are concerned. There are certain outstand¬ 
ing features of extreme interest and importance in Iscovesco’s 
careful studies: (1) The production in rabbits of a veritable 
Graves-Basedow disease (not to be distinguished from the human 
disease) by means of a thyroidal lipoid; (2) the absence of any 
genital changes in either sex from the use of the anterior pituitary 
lipoid. That the posterior pituitary lobe is not responsible 
for the production of the testicular atrophy of the adiposo-genital 
syndrome was proved by the striking case published by Maranon 
(1911) of a haemorrhagic focus which microscopical examination 
showed had destroyed the anterior pituitary lobe and had entirely 
spared the posterior lobe. But the absence of genital changes in 
either sex after prolonged use of Iscovesco’s anterior lobe lipoid in 
rabbits is on all fours with the recent experiments of Camus and 
Roussy on dogs (C. R. Soc. de Biol., lxxv., 1913, pp. 483, 628), and 
undoubtedly helps us to accept the provisional conclusion of those 



106 


ABSTRACTS 


two writers that the genital atrophy (and the polyuria) of the 
adiposo-genital syndrome of man is probably not due at all to a 
lesion of the pituitary, even when—as often happens—a pituitary 
lesion is unquestionably present, but depends rather on neighbour¬ 
ing parapituitary basal lesions which injure centres or paths, 
situated near the pituitary body, which are intimately connected, 
physiologically, in a way at present unknown to us, with the 
nutrition of the genital organs, and especially the testes and 
ovaries. It might be objected to this that Iscovesco merely failed 
to prove genital changes by the use of his II. Bd anterior lobe 
lipoid, and that there may conceivably be others that may give 
them; but we can hardly believe that after all these years of 
careful chemical, physiological, and therapeutic investigations, 
Iscovesco would have failed to isolate these genito-dystrophic or 
hypertrophic pituitary lipoids if they really had any existence. 
These inspiring and illuminating researches of his are full of 
therapeutic hints, csj., the possible value of the cortical adrenal 
lipoid in such conditions as myxoedema, dry skin, ichthyosis, &c. 
&c. Such positive studies as those of Iscovesco are infinitely more 
valuable and less misleading than many of the inexact methods 
beloved by experimentalists, such as organ removals, &c. 


abstracts. 

ANATOMY. 

ON THE BULBAR NUCLEI, WITH SPECIAL REFERENCE TO 
(121) THE EXISTENCE OF A SALIVARY CENTRE IN MAN. 

Anthony Feiling, Brain, 1913, xxrvi., p. 225. 

A miner, who had injured his neck, suffered from paralysis of the 
left side of the tongue and of the left sterno-mastoid and upper 
part of left trapezius, together with loss of taste in the whole of 
the back of the tongue, especially on the left side, paralysis of the 
left side of the palate, although no anaesthesia could he detected, 
aphonic speech, and loss of power of swallowing even for liquids. 
He died seventy-one days later from broncho-pneumonia. At the 
autopsy a fracture of the posterior fossa of the skull was found, 
involving the jugular foramen with injury to the trunks of the 
vagus, glosso-pharyngeal, spinal accessory, and hypoglossal nerves, 
without any injury to the brain itself. 



ABSTRACTS 


107 


Degeneration was found in the cells of origin of the spinal 
accessory nerve in the cervical cord, and in the whole length 
of the nucleus ambiguus, with partial degeneration in the dorsal 
nucleus of the vagus and in the hypoglossal nucleus, and marked 
fatty change in the solitary bundle. In addition, scattered de¬ 
generated cells were found in the grey matter just dorsal to the 
inferior olive and slightly neutral to the facial nucleus. It is 
suggested that these cells represent cells of origin for the secretory 
fibres which pass out with the glosso pharyngeal nerve, and 
which, by means of its tympanic branch, become distributed to 
the parotid gland. No clinical evidence as to the presence of any 
disturbance of salivary secretion was made. 

A. Ninian Bruce. 


THE VAGUS NERVE: ANATOMICAL AND EXPERIMENTAL 
(122) STUDY. PART III.-THE PERIPHERAL VAGUS GANGLIA: 
LOCALISATION OF THE SENSORY GANGLIA AND PERI¬ 
PHERAL DISTRIBUTION OF THEIR ISSUING FIBRES. 
(Le nerf vague : 4tude anatomique et expdrimentale. Troisidme 
partie. Les ganglions plriphlriques du vague: localisation des 
noyaus de sensibility et distribution pbriphdrique des fibres qui 
en dmanent.) M. Molhant, Le Ntvraxe , 1913, sir., xv., Dec. 30, 
pp. 521-679 (54 figs.). 

Chapter I .—Histological examination of the cells of the rabbit's 
ganglion nodosum by Cajal’s reduced silver method shows that 
unipolar cells, large, medium, and small, markedly preponderate. 
Molhant failed to find any multipolar cells of the type described 
by Cajal for the spinal ganglia of man and animals, but he found 
round some of the large cells of the ganglion nodosum a perisomatic 
plexus similar to that found by van Gehuchten and many other 
authors round spinal ganglion cells. He concludes that the ganglion 
nodosum is a cranial homologue of the spinal ganglia. 

Chapter II.—Structure and distribution of the sensory fibres 
of the vagus. —Molhant divided intracranially all the root fibres 
of the 9th, 10th, and 11th nerves so as to eliminate all the 
motor vagus fibres, of bulbar origin, contained in its trunk and 
branches. By keeping his animals for seven months he succeeded 
in doing this: all trace of active degeneration of vagus fibres had 
then disappeared. Almost all the large fibres and a good number 
of the small fibres had then disappeared, and only the medium¬ 
sized fibres were unchanged: these, then, are the sensory vagus 
fibres. The large majority come from the jugulare and nodosum 
ganglia, the minority from spinal ganglia via the anastomotic 
filaments of the intervago-recurrential sympathetic plexus. The 



108 


ABSTRACTS 


proper vagus sensory fibres are found in the pharyngeal branch of 
the vagus and the middle laryngeal nerve (rabbit), the superior 
laryngeal, the depressor nerve of Cyon, the nervus recurrens, and 
the thoracic vagus. 

Chapter III.—Ganglionic origin of the sensory fibres of the 
various branches of the vagus .—Molhant used the chromolysis 
method, keeping his animals for eight or ten days. His experi¬ 
mental sections were made at the following levels: (1) Below 
ganglion nodosum, respecting the superior laryngeal and the nerve 
of Cyon; (2) section of superior laryngeal; (3) of nerve of Cyon; 
(4) vagotomy 2£ cm. below origin of nervus recurrens; (5) section 
of nervus recurrens; (6) ablation of upper and middle lobes of 
right lung; (7) section of superior cardiac filaments of vagus; (8) 
violent avulsion of left vagus at level of gastric cardia; (9) section 
of pharyngeal branch of vagus. Conclusions: (1) The ganglion 
nodosum gives origin to almost all the sensory fibres of the cervical 
vagus, the ganglion jugulare to very few; (2) large cells in the 
upper pole of the nodosum give origin to the sensory fibres of the 
superior laryngeal nerve; (3) small cells in the zone adjoining 
the external border of the upper pole of the nodosum to those of 
the nerve of Cyon; (4) the middle and lower part of nodosum to 
those of the thoracic vagus; (5) the sensory cesophago-tracheal 
fibres of the nervus recurrens rise in cells situated diffusely, without 
clear limits, between the upper extremity of the nodosum and its 
swollen middle part; the laryngeal fibres of the nervus recurrens 
rise in cells of the ganglion jugulare: Molhant could not determine 
their exact localisation: “ It is probable that the notable distance 
between the ganglion and the site of nervus recurrens interruption 
led to too feeble a cell-reaction ”; (6) the fibres of the right, upper, 
and middle pulmonary lobes rise in cells situated diffusely in the 
outer parts of the middle and lower segments of the nodosum: “ if 
we admit that the sensory fibres of the pulmonary lower lobe rise 
in the same zones of the ganglion, as is probably the case, we may 
conclude that the pulmonary sensory ‘nucleus’ of the vagus is 
situated in this segment ”; (7) the sensory fibres of the nerve of 
Cyon and of the superior cardiac vagus filaments seem to rise in 
the intermediary zone between the base of the upper tapering 
part of the nodosum and its middle dilated portion; (8) the sensory 
gastric vagus fibres rise in the swollen middle of the nodosum, and 
also in the zone adjoining the convex border of its lower extremity; 
(9) the sensory fibres of the pharyngeal branch of the vagus (and of 
the rabbit’s middle laryngeal nerve which springs from it) rise in cells 
of the ganglion jugulare, but this “ nucleus ’’ represents only a small 
fraction of that ganglion’s cells. Molhant finds that the rabbit’s 
ganglion jugulare is usually intimately fused with the ganglion 



ABSTRACTS 


109 


jugulare ix. Unfortunately, he made no attempt to determine the 
ganglionic origin of the nervus auricularis x, nor of the meningeal 
branch of the vagus; and in his intracranial vagus root section he 
did not apparently try to trace the normal undegenerated laryngeal 
muscle afferenta from the ganglion jugulare into the four muscles 
supplied by the laryngeal fibres of the nervus recurrens. He does 
not even mention the possibility that the ganglion nodosum may 
be, in part, a motor sympathetic ganglion for unstriped fibres of 
the vagus. Leonard J. Kidd. 

STRUCTURE OF THE ROOTS, TRUNK, AND BRANCHES OF 
(123) THE VAGUS NERVE. M. R. Chase and S. W. Hanson, 
Joum. CompU Neurol ., 1914, xxiv., Feb., p. 31 (20 figs.). 

Tine chief study was on the dog’s vagus, but that of man, rabbit, 
cat, and rat was included. “ Most of the material was cut into 
serial sections. In this way all branches of the vagus and con¬ 
nections with the sympathetic could be followed accurately. This 
is especially important in the study of vagus roots, and of the 
relations of the vagus and sympathetic. Some material was fixed 
in ammoniated alcohol, and stained by the pyridine-silver technique 
of Ranson; some fixed in Miiller, and stained by Weigert method; 
some fixed and stained in 1 per cent, osmic acid.” The new fact 
is brought out that enormous numbers of non-medullated axons 
are present in the vagus rootlets. “ Molhant saw them in the 
vagus trunk, and Gaskell inferred their presence here, basing his 
inference on the unstained areas in osmic acid preparations. 
Their presence in the rootlets shows that those found in the trunk 
are not sympathetic fibres as Molhant maintained. They belong 
properly to the vagus.” In the dog the so-called internal branch 
of the spinal accessory has no existence; this agrees with the 
findings of Van Gehuchten and Molhant in man and rabbit. 

Leonard J. Kidd. 


A STUDY OF THE ANATOMY AND THE VASOMOTOR PHENO- 
(124) MENA OF THE SYMPATHETIC NERVOUS SYSTEM IN THE 
TURTLE. D. J. Edwards, Amer. Joum. Physiol., 1914, xxxiii., 
p. 229. 

An examination of the arrangement of the second, third, and 
fourth cervical ganglia in five different species of turtles confirms 
the view that these ganglia generally exist separately. The 
abdominal and the cervical sympathetic systems are connected 
by a small trunk, which extends from the fourth ganglion across 
the necks of the first and second ribs to the first abdominal 



110 


ABSTRACTS 


ganglion. Sympathetic fibres pass from the main sympathetic 
trunk to the viscera in two groups—a small anterior and a larger 
posterior splanchnic group. A sympathetic nervous control over 
the blood vessels in the viscera was shown by the injection 
of adrenalin into the vessels supplying this area. A vaso¬ 
constriction may be produced by stimulation of the fibres of the 
anterior splanchnic, or of the posterior splanchnic group. A 
greater rise in blood pressure results from stimulation of the 
latter group: the average rise in blood pressure thus produced was 
between 5 and 6 mm. Hg. The right posterior splanchnic 
possesses a greater vaso-constricting power than the left. The 
more common rhythmic variations in blood pressure are in¬ 
dependent of the respiratory movements. A. Ninian Bruce. 


PHYSIOLOGY. 

THE ALL-OR-NONE PRINCIPLE IN NERVE. R D. Asian, Journ. 

(125) PhytioL , 1914, xlvii., Feb. 27, p. 490. 

When a nerve is narcotised and stimulated at a point central to 
the narcotised area, the strength of stimulus necessary to affect 
the muscle does not rise gradually, but remains approximately 
constant until conduction fails. This indicates that the ability 
of the propagated disturbance to pass a region of decrement does 
not depend upon the strength of stimulus which sets it up. In 
other words, in each nerve fibre there would seem to be an all-or- 
none relation between the strength of the stimulus and the size of 
the propagated disturbance which follows it. A. Ninian Bruce. 

HYPOPHYSECTOMY AND EXPERIMENTAL GLYCOSURIA. 

(126) (Hypophysectomie et glycosuria experimental*) J. Camus 
and Q. Roussv, Compt. Rend. Soc. de Biol., 1914, lxxvi., Feb. 27, 
p. 299. 

Glycosuria was found in only six out of forty-five dogs in which 
operations on the pituitary, or its neighbourhood, had been per¬ 
formed. When it exists it is seen during the first few hours after 
operation, and is transient. Glycosuria and polyuria are not 
neoessarily associated; the latter is much the commoner pheno¬ 
menon. The kind of food taken by dogs before operation does 
not appear to influence the appearance of glycosuria; the same is 
true of age, sex, and gestation. In cats glycosuria is commoner 
than in dogs: it occurred four times out of nine partial operations 
on the two pituitary lobes. Glycosuria in dogs is not related to 
partial or total hypophysectomy. The authors attribute it to 
damage done to basal nerve-centres situated near the pituitary; 



ABSTRACTS 


111 


for, out of six of their cases in which a lesion or temporary 
irritation of the base of the brain was present, glycosuria occurred 
in four. They cannot say where these centres are situated, nor 
whether it is their stimulation or inhibition that provokes 
glycosuria. Leonard J. Kidd. 

THE INFLUENCE OF THE ADRENALS ON GROWTH. (Sur l’in- 

(127) fluence exerde par les capsules surrfinales sur la croissance.) 
Ferreira dr Mira, .ArcA. Internal, de Physiol., 1914, xiv., Jan. 31, 
p. 108 (6 figs.). 

The preliminary paper on this subject was abstracted in the 
Review (1912, x., p. 526); Figs. 2 and 3 of the present full paper 
bring out well the differences between a dog, which had undergone 
unilateral adrenalectomy, and a control animal. 

Leonard J. Kidd. 

STUDIES ON BERI-BERL VIII.—THE RELATIONSHIP OF BERI- 

(128) BERI TO GLANDS OF INTERNAL SECRETION. Casdor 
Funk and Mackenzie Douglas, Joum. Physiol., 1914, xlvii.,Feb. 27. 

Eight beri-beri pigeons were examined, and notes of the 
conditions found on examination of the thymus, pituitary, thyroid, 
suprarenal, ovary, testis, liver, kidney, pancreas, and spleen. All 
showed a great diminution in size in every case. Microscopically 
there was a marked degenerative change of the cells with higher 
functions. In most cases the marked atrophy was due to a 
disappearance of the cells, the framework of the gland alone 
remaining. The most marked change was in the disappearance 
of the thymus. A. Ninian Bruce. 


PSYCHOLOGY. 

THE HORSES OF ELBERFELD ONCE MORE. Ed. Clapar£de, 
(129) Archiv. de Ptyehol., 1913, Sept, p. 244 

Professor Clapar&de here gives an account of a second visit paid 
by him to the learned horses of Elberfeld. This time he limited 
his investigation to the attempt to solve the simple question, Can 
the horses read numbers of one and two digits ? His results were 
negative; the horses gave few correct responses, and he was 
unable to decide whether it was a case of could not or would not. 

The psychology of the controversy, which has arisen regarding 
the abilities of the horses, seems to interest M. Claparede as much 
as the establishment of the actual facts, and the greater part of 
his article is devoted to an account of the recent literature on the 
subject. 



112 


ABSTRACTS 


At the last international Congress of Zoology certain well- 
known German scientists circulated a “protest” regarding the 
calculating horses of Elberfeld. M. Clapar&de gives this protest 
in full, and then proceeds to make what we cannot but feel is a 
very just counter-protest against the document as an unsuitable 
and irrational method of taking part in a scientific inquiry. 

Margaret Drummond. 

AN ARITHMETICAL PRODIGY. J. M. Lahy, Archiv. de Psychol, 

(130) 1913, Sept, p. 209. 

An experimental study of an exceptional figure memory. The 
subject of this study is Uranie Diamandi, sister of the lightning 
calculator, Pericles Diamandi. After a detailed investigation of 
her heredity and mental powers, the writer comes to the conclusion 
that her marvellous figure faculty does not arise from any innate 
disposition, but is rather the result of a deliberate self-training. 

Margaret Drummond. 

PATHOLOGY. 

VITAL STAINING OF NERVE CENTRES BY MALACHITE 

(131) GREEN. (But la coloration vitale des centres nerveux.) 

P. Salmon, Compt. Bend. Soc. de Biol., 1914, lxxvi., Feb. 20, p. 265. 

Intravenous injection of malachite green into mice is rapidly 
fatal: only the brain and testis are coloured green. In rabbits 
1 eg. of this per 2 kilos, of body-weight gives the same elective 
staining of brain: but, unlike methylene blue, it gives definite 
symptoms, viz., a kind of cerebral cry, salivation, and characteristic 
oculomotor signs—sometimes exophthalmos, more often closure 
of eyelids and gradual narrowing of pupils to pin-points. Autopsy 
shows that mainly the grey matter is stained, the white matter 
and nerves at base of brain remaining unstained. These oculo¬ 
motor signs are temporary, and are reproduced on each re-injection. 
According to Wendelstadt and Fellmer malachite green is active 
against the trypanosomic infection of nagana. Salmon finds it 
inactive in the sleeping sickness of mice (virus of Mesnil), and in 
the spirillosis of recurrent fever. Leonard J. Kidd. 

A CONTRIBUTION TO THE PATHOLOGY OF MYASTHENIA 

(132) GRAVIS. Sydney Kuh and Morris Braude, Joum. Nerv. and 
Ment. Dis., 1913, xl., Oct. 

A case is reported in which it was noted that passive movements 
as well as active ones would cause a sensation of fatigue in the 
affected muscles. 



ABSTRACTS 


113 


The authors conclude, from a very thorough anatomical ex¬ 
amination of the case, that:— 

1. Myasthenia gravis is a disease probably of neurogenic rather 
than myogenic origin. 

2. Certain peculiar vascular changes in selected regions of the 
central nervous system may account for the distribution of its 
symptoms and the usual mode of death. 

3. These vascular changes consisted in the presence of minute 
polymorphonuclear thrombi, mostnumerous in the pons and medulla, 
thus accounting for the preponderating bulbar symptoms of the 
disease. 

4. An aberrant bundle of fibres was found in the cervical 

region of the cord. D. K. Henderson. 


CLINICAL NEUROLOGY. 

THE RELATION OF THE MYOPATHIES. William Q. Spiller, 
(133) Brain, 1913, xxxvi., p. 75. 

This paper consists of a critical review of this subject, together 
with several new cases. The subject is discussed under the 
heading of amyotonia congenita, its relation to the Werdnig- 
Hoffmann type of atrophy, the distal type of myopathy, myotonia 
atrophica, and hypertrophia musculorum vera, a somewhat 
questionable type. A. Ninian Bruce. 


A CASE OF MYATONIA CONGENITA (OPPENHEIM). J. W. 

(134) Courtney and H. B. Eaton, Boston Med. and Burg. Joum ., 1914, 
clxx., Jan. 22, p. 117. 

The case is that of a boy of five and a half years of age. He was a 
seventh month child, and it was noticed from the moment of birth 
that the head tended to fall backward on the shoulders, and that 
the muscles were “ like jelly.” A. Ninian Bruce. 


HERPES ZOSTER OTIOUS. A CRITICAL REVIEW, WITH RE- 
(136) PORT OF A CASH Virginius Dabney, N.Y. Med. Joum., 1914, 
xcix., Feb. 7, p. 272. 

The patient was a woman, aged 68, who complained of sudden 
deafness and tinnitus in her left ear. Several days later pain 
developed, but it was not until a month after this that vesicles 
appeared and the diagnosis could be made. The post-herpetic 
neuralgia was severe and persistent, lasting for over four months 



114 


ABSTRACTS 


after the healing of the last vesicle, the pain of which was only 
temporarily relieved by high frequency electricity. The vesicles 
appeared mostly singly, and not in crops as is usual in other 
cases. A. Nlnian Bruce. 


CAN HERPES ZOSTER EVER OCCUR TRAUMATIC ALLY? 

(136) H. G. Lanowill, Clinical Jovm ., 1913, xlii., p. 569. 

Langwill records two cases of herpes zoster suggestive of a trau¬ 
matic origin. 

1. A sailor, aged 46, violently twisted and wrenched his right 
arm while clinging to a rope to save himself falling into the water. 
He suffered severe pain below the armpit, and a few days after¬ 
wards was admitted to hospital with extensive zoster of the fourth, 
fifth, and sixth dorsal segmental areas. 

2. A man, aged 28, fell through a hole in the floor of a loft, 

but was caught by his left axilla catching on the edge. A week 
later burning pains came on in the left scapular region, and in four 
days’ time herpes appeared in the fifth and sixth left spaces and 
below the left axilla. J. D. Rolleston. 


ACUTE GENERALISED INFECTIVE PARALYSIS IN ADULTS. 

(137) W. B. Warrington, Liverpool Medico-Chir. Jovm., 1914, Jan 

The author relates cases of acute toxic polyneuritis, acute 
generalised poliomyelitis, Landry’s paralysis, and acute ascendiug 
myelitis. 

He gives a table of differential diagnosis. Both cases of 
Landry’s paralysis recovered, and it was noteworthy that the 
electrical reactions were normal throughout the illness. The 
cause of ascending myelitis was in all probability a sequela of 
mumps. Author’s Abstract. 


INTRACRANIAL SEROUS EFFUSIONS OF INFLAMMATORY 
(138) ORIGIN. MENINGITIS OR EPENDYMITIS SEROSA— 
MENINGISM. WITH A NOTE ON “ PSEUDO-TUMOURS ” 
OF THE BRAIN. W. B. Warrington, Quart. Joum. Med ., 
1914, vii., Jan., No. 26. 

The author considers the question, how far intracranial serous 
effusions of inflammatory origin are the cause of grave cerebral 
symptoms. 

He considers that there is no essential difference between 
meningism, serous meningitis (or ependymitis), and purulent 



ABSTRACTS 


115 


meningitis (or ependymitis), that they are each the result of toxic 
processes, but that the important point is the recognition of the 
fact that the inflammation may become arrested in the serous 
stage. When this is so, he believes that toxins, and not micro¬ 
organisms, unless of very low virulence, penetrate the barrier of the 
dura mater, and excite an inflammatory reaction. 

Under etiology, he considers sepsis, notably otitic sepsis, tuber¬ 
culosis, the specific fevers, injuries to the skull and inanition. 
Clinically, he discusses, with examples, the acute cases resembling 
more fulminating meningitis, and the chronic cases resembling 
cerebral tumour. 

He concludes by a brief reference to certain cases of “ pseudo¬ 
tumour,” in which symptoms of intracranial pressure of improved 
pathology are present. 

These he divides into— 

1. Cases chiefly in children in which all symptoms of intra¬ 
cranial pressure disappear for an indefinite time, perhaps perma¬ 
nently, without any special treatment. 

2. Cases in which recovery, partial or complete, rapidly follows 
a decompression. 

3. Cases in whioh death occurs, the naked eye appearances 
are normal, but microscopical examination has revealed a lesion. 

4. A few cases in which no lesion has been found, even with a 
microscopic examination. 

A considerable bibliography is given. 

The general conclusions of the writer are:— 

1. The effusion may be the important pathological fact, and 
the prognosis and treatment depend upon a recognition of this. 

2. The progress of an inflammatory effusion within the skull 
may be arrested at the serous stage. 

3. The primary cause is commonly a near or distant focus of 
septic infection; the toxins formed by this, but not the micro¬ 
organisms, stimulate the vessels of the meninges, brain, or ependyma 
and the choroid plexuses to the formation or excessive fluid. 

4. The primary cause may also be toxins, generated by non- 
pyogenic organisms, and in rarer cases the excessive fluid results 
from causes other than toxins of microbic origin. 

5. The symptoms in the acute or chronic condition respectively 
may stimulate the gravest form of brain disease. 

6. The diagnosis is suggested when there is reasonable evidence 
that the symptoms are those of increased intracranial pressure, if 
other well-known conditions can be excluded, and it is strengthened 
by the recognition of the primary cause. 

Author’s Abstract. 



116 


ABSTRACTS 


ON THE OHBONIO POEM OF EPIDEMIC CEREBRO SPINAL 

(139) MENINGITIS. (Contribution k l’&ude do In mlningite 
cdrfebro-spinale Ipidlmique k forme chroniqne.) B. Despujolb, 
Theses de Lyon, 1912-13, No. 28. 

The chronic form always succeeds the acute. It is characterised 
clinically by (1) a conglomeration of trophic, psychical, and sphincter 
troubles; (2) superadded and variable disorders such as febrile 
attacks, and sensory and motor phenomena; (3) involvement of 
the special senses. Anatomically the lesions are constant and 
consist in diffuse pachymeningitis most marked in the cranial 
meninges, pus in the ventricles and hydrocephalus, and lesions in 
the nerve centres, roots and peripheral nerves. The chronic form 
is most frequently found in young persons, and in subjects with 
tuberculous antecedents, especially if the anti-meningococcic serum 
treatment has been inadequate or used late. Examination of the 
cerebro-spinal fluid hardly ever throws light on the diagnosis. 

The prognosis is very gloomy; in cases that recover there are 
usually sequelae, especially involving the special senses. 

Intraspinal injections are chiefly preventive, intraventricular 
injections have proved curative. Surgical treatment, i.e., crani¬ 
ectomy, is required in cases in which cerebral hypertension is marked 
and no improvement follows lumbar puncture or trephining. 

The thesis contains the histories of twenty-one cases, one of 
which is original. J. D. Kolleston. 

DIPLOCOCCUS CRASSUS SEPTICAEMIA WITH GEREBRO SPINAL 

(140) LOCALISATION. (Un cas de septicdmie k Diplococcus crassus 
avec localisation cfr&ro-spinale.) Biscons, Paris mid., 1913-14, 
iv., p. 211. 

A soldier, aged 23, had a long febrile illness starting with articular 
symptoms and an erythematous rash which were followed by 
signs of meningeal involvement. Lumbar puncture gave issue to 
a turbid fluid under hypertension showing abundant polymorphs, 
but no micro-organisms. The Diplococcus crassus, a saprophyte of 
the naso-pharynx, was isolated in pure culture almost from the 
onset and persisted throughout the disease, its vitality diminishing 
as the symptoms abated. Recovery took place, but convalescence 
was slow. J. D. Rolleston. 

ON THE DIFFERENTIAL DIAGNOSIS OF SYPHILITIC AND 

(141) TUBERCULOUS MENINGITIS IN THE ADULT. (Mtaingite 
syphilitique et m&iingite tuberculeuse chez l’adulte (essai de 
diagnostic differential).) L. Petit, Theses de Paris, 1913-14, No. 30. 

Although the classical form of tuberculous meningitis is 
sufficiently characteristic to be readily diagnosed, numerous sources 



ABSTRACTS 


117 


of error may arise from the various forms assumed both by 
tuberculous and syphilitic meningitis. One of the most important 
clinical signs of tuberculous meningitis is the dissociation between 
the pulse and the temperature which rarely occurs in syphilitic 
meningitis. Vaso-motor troubles, convulsions and contractures 
are more in favour of tuberculous than of syphilitic meningitis, 
without being absolutely pathognomonic. A similar importance 
attaches to the headache of syphilitic meningitis which is 
characterised by long duration, intensity and nocturnal exacerba¬ 
tions. Psychical disturbance, disorders of sensation and of the 
special senses, and paralyses are found in both affections. The 
Argyll Robertson pupil is characteristic of syphilis, but is often 
absent in syphilitic meningitis. 

The most valuable laboratory methods are the examination for 
the tubercle bacilli in the cerebro-spinal fluid and Wassermann’s 
reaction. The luetin reaction may be useful in latent syphilis, 
but it must not be forgotten that tuberculous meningitis may occur 
in a syphilitic individual, and that therefore this reaction is not 
sufficient by itself for the diagnosis of syphilitic meningitis. 

The thesis contains the histories of six cases, two of which are 
original. J. D. Rolleston. 


THE NERVOUS COMPLICATIONS OF MUMPS IN THE CHILD. 
(142) (Contribution & l’ltude des oreillons chez l’enfimt, et de certaines 
complications nerveuses qui penvent s’y observer.) E. Missimilly, 
Theses de Montpellier, 1912-13, No. 71. 

The thesis contains the histories of seven cases, the following three 
of which are original:— 

1. A boy, aged 5 years, a few days after mumps complicated by 
orchitis, developed poliomyelitis, manifested by complete loss of 
power in the lower limbs. In the course of the next few months 
the paralysis entirely disappeared in the right lower limb, but per¬ 
sisted in the muscles of the left thigh, which became atrophied 
and showed R.D. 

2. A girl, aged 3 years, on the sixth day of mumps, developed 
meningeal symptoms which lasted for four days and then rapidly 
subsided under treatment by baths, ice, and purgatives. 

3. A boy, aged 10 years, on the eighth day of his disease, de¬ 

veloped meningeal symptoms which Tasted for forty-eight hours 
and then rapidly disappeared. In none of the cases was lumbar 
puncture performed. J. D. Rolleston. 



118 


ABSTRACTS 


ACUTE POLYARTICULAR RHEUMATISM LOCALISED TO A 
(143) LIMB AFFECTED WITH RECENT PARALYSIS OF THE 
BRACHIAL PLEXUS. (Rhum&tisme polyaxticulaire aigu 
localise but on membre attaint d’une paralysis r&ente da plexus 
brachiaL) Q. Gulllain and S. Dubois, Bull, et mtm. Soc. med. 
H6p. de Paris, 1914, xxxvii., p. 90. 

The patient was a man, aged 50, who had had a generalised 
attack of acute articular rheumatism fifteen years previously. In 
November 1913 he dislocated his right shoulder, causing paralysis 
of the brachial plexus, and about ten days later developed acute 
articular rheumatism in the fingers and elbow of the same side. 
Recovery followed in ten days after treatment by aspirin. 

J. D. Rollbston. 

ON THE PATHOGENY AND SYMPTOMATOLOGY OF POST- 
044 ) DIPHTHERITIC POLYNEURITIS. (Uber die Pathogenese and 
Symptomatology der Polyneuritis postdiphtberica.) A. Niekans, 
Inaugural-Dissertation, Kiel, 1912-13, No. 19. 

The thesis contains a record of a case of generalised paralysis in 
a youth aged 17, preceded by precocious paralysis of the palate 
( v . Review, 1906, iv., p. 608). J. D. Rollbston. 

TYPHOID SPINE. WITH REPORT OF A CASE COMPLICATED 
(146) BY THROMBO PHLEBITIS OF THE LEFT FEMORAL VEIN. 

C. B. Conklin, Med. Record ’, 1914, Ixxxv., p. 157. 

A man, aged 25, in convalescence from a typical attack of typhoid 
fever complicated by intestinal haemorrhage, but without nervous 
symptoms, began to complain of pain and stiffness in the lumbar 
region with painful twitchings of the thigh muscles. A month 
later he had tenderness over the left inguinal region followed by 
swelling of the thigh. 

The pain was relieved by the thermo-cautery along the spinal 
muscles, and immobilisation and support were afforded by adhesive 
plaster strapping. After five months recovery took place. 

J. D. Rollbston. 


FEAR AND ATAXIA. W. J. M. Malonby, Joum. Nerv. and Ment. 
(146) Dis., 1913, xl., Nov. 

The author states that the effect of fear upon tabetic symptoms 
cannot be overestimated. Several cases are reported in which a 
slight injury was supposed to have been the cause of the onset of 
the ataxia, but conclusive reasons are given by the author showing 
that fear was really the predominant factor. D. K. Henderson. 



ABSTRACTS 


119 


REPORT OF A CASE OF JUVENILE TABES. C. E. Riggs, Joum. 

(147) Nerv. and Ment. Die., 19131, xl., Nov. 

A boy, 7£ years old, who since the age of 10 months had been 
subject to vomiting spells at short intervals; these attacks usually 
lasted about three days. Later he showed difficulty in walking 
and complained of pains in his legs. Athetoid movements were 
seen in the right hand, and there was some intention tremor of 
both hands. The knee and Achilles jerks were absent, there was 
a marked ataxia of both legs, and a mild hypotonia in the muscles 
of the lower extremities. 

The pupils reacted to light and on accommodation, and the 
eye-grounds were normal. The blood serum and spinal fluid both 
gave a positive Wassermann reaction. D. K. Henderson. 

THE RELATION TO THE BLOOD OF THE VIRUS OF EPIDEMIC 

(148) POLIOMYELITIS. Paul F. Clark, Francis R. Fraser, and 
Harold L. Amoss, Joum. Exp. Med., 1914, xix., March, p. 223. 

Specimens of human blood taken during the paralytic stage of 
poliomyelitis and post mortem have proved not to be capable of 
infecting Macacus monkeys. Specimens of monkey blood taken at 
various stages of experimental poliomyelitis have not proved 
capable of infecting monkeys (except in one case). When 
suspensions of the spinal cord from a paralysed monkey have been 
injected into the brain, or simultaneously into the brain and spinal 
canal, the blood removed from one to forty-eight hours later failed 
to cause paralysis after intracerebral injection. When large 
volumes of active filtrate are injected into the circulation the blood 
remains infective for seventy-two hours at least, but may be no 
longer infective after ten days, when the paralytic symptoms first 
appear. When, however, the filtrate is injected in smaller amount, 
or when a filtrate of a less active virus is employed in large 
' quantity, the blood either fails to convey infection or conveys it 
irregularly. It is only when overwhelming quantities of an active 
virus are injected into the blood that paralysis results. The 
injection of moderate doses is not followed by paralysis, although 
the virus may still be detected in a blood sample twenty-four hours 
after the injection. The existence of a mechanism capable of 
excluding the virus within the blood from the central nervous 
organs is therefore inferred. Infection is accomplished far less 
readily through the circulation than by means of the more direct 
lymphatic and nervous channels of communication with the central 
nervous system. 

Several series of feeding experiments conducted with the biting 
stable fly (Stomoxys calcitram) resulted negatively. 

A. Ninian Bruce. 


io 



120 


ABSTRACTS 


THE BdLE WHICH HEREDITY PLAYS IN INDUCING BPI- 
(149) LEP8Y IN CHILDREN SUFFERING FROM INFANTILE 
CEREBRAL PALSY. L. Pierce Clark and E. A. Sharp, Joum. 
Nerv. and Ment. Dit ., 1913, xl., Oct. 

In the so-called idiopathic type of genuine epilepsy heredity 
plays a very important rdle in the causation; it is present 
perhaps in 70 per cent, of cases. In this study a comparison 
is made of the heredity history between infantile cerebral palsy 
associated with epilepsy, and the so-called idiopathic cases. 

The data consisted of 443 cases of palsy with epilepsy, and 
443 suffering from the genuine disorder. In a little less than one- 
third of the hemiplegia epileptics there was no record of hereditary 
influences; in 70 per cent, a definite record of hereditary in¬ 
fluence was found. Epilepsy and convulsions occurred in 115 
instances: alcoholism was mentioned 110 times; insanity 46 times; 
idiocy and feeble-mindedness in 10 instances; fainting spells, 
hysteria, and apoplexy were also mentioned. 

In the epileptics without hemiplegia the heredity presented 
an almost similar picture. D. K. Henderson. 


CHANGES IN THE SPINAL CORD FOLLOWING PERIPHERAL 
(150) OR CEREBRAL LESIONS, ISOLATED AND COMBINED. 
(Modificazioni spinale consecutive a lesioni periferiche o cerebrale, 
isolate e combinate.) G. d’Abundo, Riv. Ital. di Neuropatol., 
Psichiatr. ed Elettroter., 1913, vi., p. 481. 

The author carried out the following three series of experiments 
on new-born animals (dogs or cats within the first twenty-four 
hours of life). 

1. He disarticulated a limb and examined the nerve centres, 
two, four, six, and seven months later. 

2. He removed portions of the motor cortex on one side and 
subsequently examined the grey substance of the spinal cord. 

3. Besides disarticulating a hind limb, he removed the motor 
cortex on the opposite side to the disarticulated limb. 

The results of the first series of experiments were as follows:— 

1. Disarticulation of a hind limb in new-born dogs and cats 
causes a defective development of the corresponding half of the 
spinal cord, most marked in the lumbar enlargement. 

2. In the hemi-hypotrophic grey substance the anterior horn 
shows an obvious diminution of nerve cells. 

3. As one passes from the middle of the lumbar enlargement 
to the dorsal region of the cord, the defective development becomes 
less evident in the anterior horn, and more marked in the posterior 
horn. 



ABSTRACTS 


121 


4. While a deficiency of unilateral development is found 
throughout the white substance of the spinal cord, it is in the 
posterior column, corresponding to the disarticulated limb, that 
the deficiency is most marked. 

5. All the nerve cells representing the disarticulated limb do 
not disappear, but some survive, being intimately connected with 
the rest of the spinal cord by dynamic associations and functional 
spinal automatism. 

6. Regenerative activity of the nerve trunks cut in disarticula¬ 
tion of the limb is the patent demonstration of the survival of a 
considerable number of motor cells for the muscles of the disarticu¬ 
lated limb. 

7. Although a division of labour exists in the functions of the 
spinal cord, there is a very marked collective synergic solidarity 
in these functions, whereas in the cerebral cortex there is a 
decorticalisation of function better suited for a division of labour. 

The results of the second series of experiments were as follows : 
Removal of parts of the motor cortex caused a rapid and marked 
hypotrophy in the corresponding posterior horn of the spinal cord; 
whereas hypotrophy was hardly manifested at all in the anterior 
horn on the opposite side to the cortical lesion, at least during the 
first thirty-six days of life. 

The third series confirmed the results of the first two, but the 
author found that the disappearance of the nerve cells of the 
spinal grey substance corresponding to the disarticulated limb 
was much more marked than in the first series. He adds, how¬ 
ever, that before drawing conclusions it is necessary to keep the 
animals alive for at least six or seven months, as was done in the 
first series of experiments. J. D. Rolleston. 


GLIOMA OF THE CAUDA EQUINA. REPORT OF A CASE WITH 
(151) SECONDARY GLIOSIS OF THE SPINAL CORD. William 
M. Leszvnsky, N. Y. Med. Joum., 1914, xcix., Feb. 21, p. 360. 

A woman, aged 49, twelve years ago slipped and fell, striking 
herself violently on the buttocks, but was apparently uninjured. 
She remained well for three years, and then developed pain in the 
left lumbar region. Four years later the right side became 
similarly affected. Then numbness of both feet and toes followed, 
with atrophy of the muscles of both lower limbs, and she became 
unable to walk or stand, and suffered from incontinence. 

The twelfth dorsal, first and second lumbar spines and laminae 
were removed, and the whole spinal canal was filled by a large 
grey-brown tumour. This was left for extrusion. She died three 
months later, and at the autopsy a tumour mass of a fibro-hyaline 



122 


ABSTRACTS 


structure was found loosely adherent to the dura. In the centre 
a longitudinal cavity was to be seen about one inch and a half long 
lying in the anterior portions of the posterior columns. It proved 
to be a glioma. A. Ninian Bruce. 

A CASE OF CONGENITAL HEMIATROPHY. (Un c&a d*Mmi- 

(152) atrophia congtaitale.) J. Lkvy-Valensi, Paris mid., 1913-14, iv., 
p. 215. 

The patient was a woman, aged 54, in whom not only the face 
but also the trunk and limbs on the left side were affected. The 
condition is attributed to intrauterine encephalitis or to an arrest 
of development of the right hemisphere. J. D. Rolleston. 

SENSORY CHANGES IN FRIEDREICH’S DISEASE P. W. Saunders, 
(163) Brain, 1913, xxxvi., p. 166. 

Twenty typical cases of Friedreich’s disease were examined, and 
it was found that the elements of sensibility which it is assumed 
are conducted through the dorsal columns of the cord are more or 
less constantly and characteristically affected. The loss, especially 
in the early stages of the disease, falls most heavily on the lower 
extremities, i.e., on the regions innervated by the spinal segments 
that are earliest affected, and tends to spread higher and higher 
over the body, and to become more profound as the disease 
advances. The frequency with which these sensory changes occur 
would seem to justify their inclusion in the clinical picture of the 
disease as an integral, not as an exceptional, feature. 

A. Ninian Bruce. 

CEREBRAL PALSIES WITHOUT DEMONSTRABLE ANATOMI- 

(154) CAL FINDINGS. J. H. W. Rhein, Journ. Nerv. and Ment. Dis., 
1913, xl., Oct 

A review of the literature is given, and two cases are reported 
in which no anatomical findings could be found to account for the 
clinical picture. 

The author feels that one must look for the explanation in 
some quality of nerve cell or fibre which cannot by our present 
methods be demonstrated. D. X. Henderson. 

CEREBRAL HAEMORRHAGE IN CHRONIC MYELOID LEUCA2MIA. 

(155) (Sur un cas d’hlmorrhagie ctolbr&le au cours d’une leuclmie 
myelolde chronique.) C. Laubry, Arch, dct mol. du cceur, 1914, 
vii., p. 25. 

Contrary to what is stated in some text-books, cerebral haemor¬ 
rhage is a rare termination of chronic myeloid leucaemia. The 



ABSTRACTS 


123 


present case is that of a man aged 32. The blood pressure 
taken on several occasions was normal and some improvement 
was taking place under X-ray treatment, when he developed left 
hemiplegia and died in coma within twenty-four hours. There 
was no necropsy, but lumbar puncture gave issue to a bloody fluid 
whose clot gave a formula identical with that of the blood. 

J. D. R0LLK8T0N. 


CASE OF CEREBELLAR EMBOLISM. L. Casamajob, Med. Record, 

(156) 1914, lxxxv., p. 38. 

A woman who had aortic disease following acute endocarditis in 
childhood, at the age of 29 suddenly began to suffer from dizziness 
and instability of gait and station. The knee and ankle jerks were 
absent, and there was horizontal and rotary nystagmus. Wasser- 
mann’s reaction in the spinal fluid was negative. 

J. D. Rolleston. 

ENCEPHALIC PUNCTURE BY THE ORBITAL ROUTE. ITS 

(157) CLINICAL AND THERAPEUTICAL INDICATIONS. (La 
ponction encdphalique par la voie orbitaire. Ses applications 
diniques et thdrapeutiques.) L. B£riel (de Lyon), Bull, et m/m. 
Soc. med. H6p. de Paris, 1914, xxxiL, p. 157. 

The method consists in penetrating into the cranial cavity by 
the outer end of the sphenoidal fissure. It may be used for re¬ 
moval of cerebro-spinal fluid, cerebral biopsy, or introduction of 
drugs, such as salvarsan in general paralysis or serum in cerebro¬ 
spinal meningitis or tetanus. An anaesthetic is not required, but 
B6riel has only used this method with general paralytics or coma¬ 
tose subjects. The operation is as easy as lumbar puncture, the 
only drawback being the subsequent ecchymosis, which causes a 
“ black eye ” for a few days. J. D. Rolleston. 

ADIPOSITY DUE TO A JUZTA PITUITARY SARCOMA (Obdsitd 

(158) par sarcome juxta-hypophysaire.) Laignel-Lavastihe and L. 
Boudon, Bull, et m/m. Soc. m/d. des H6p. de Paris , 1914, xxx., Feb. 
19, p. 283. 

A woman of 41 developed an enormous adiposity simultaneously 
with intracranial hypertension and blindness, due to a sarcoma 
of the base of the skull. The writers attribute the adiposity to 
secondary pituitary disturbances caused by the compression of 
the tumour. The adiposity was universal, but there was normal 
growth of hair on head, axillae, and pubes; here, then, only the 
adiposity of the adiposo-genital syndrome was present. The 
anterior pituitary lobe, although atrophied, showed histological 



124 


ABSTRACTS 


evidence of its functioning, while the posterior lobe appeared to 
be more damaged. The writers raise the question “ whether the 
various parts of the pituitary may not be united together physio¬ 
logically as well as anatomically; in this way one can conceive 
that a lesion which involves one lobe may react upon another lobe 
which is seemingly intact.” They draw attention to the fact that 
the adiposo-genital syndrome is often dissociated. They attribute 
the adiposity in their case to a “ secretory or excretory insufficiency 
of the posterior pituitary lobe.” Leonard J. Kidd. 

FAMILIAL ADIPOSITY WITH ENDOCRINAL DISTURBANCES. 

(159) (Oblsitl famili&le avec perturbations endocrines.) Laignel- 
Lavastine and Pitulbsco, Bull, et Mini. Soc. Mid. da H6p. dt 
Parity 1914, xxx., Feb. 19, p. 290. 

Two adult brothers and two adult sisters of a Jewish family 
showed an adiposo-genital syndrome, with evidence of thyroid 
involvement; the males showed small genitals, sexual feebleness, 
and perversions, with infertility; the females delayed or absent 
menses, and limited or no fertility. One sister showed an 
adiposity like the diffuse form of Dercum’s disease (figured), with 
psychical changes; the adiposity was less marked in the others. 
There is only one descendant of these four patients ; he is fat and 
tall. Ovarian, luteal, thyroidal, and pituitary opotherapy was 
useless. All the patients were tall; their adiposity had no 
relation to dietetic habits. The possibility of syphilis is admitted, 
but the Wassermann reaction was not tested. Leonard J. Kidd. 

A CASE OF PROGRESSIVE LENTICULAR DEGENERATION. 

(160) James E. H. Sawyer, Brain, 1913, xxxv., p. 222. 

The case is that of a man now aged 36. The first symptoms of 
the disease appeared at the age of 19, and consisted of tremor 
and jerky movements, which gradually became worse. The case 
was examined by Dr S. A. Kinnier Wilson, who pointed out that 
the combination of tremors, rigidity, and true hypertonicity, 
dysarthria, contracture-attitudes, the absence of any sign of 
pyramidal involvement, and the state of the reflexes, establish 
the case as essentially one of extra-pyramidal motor disease, 
and that the lesions must involve the corpus striatum and sub¬ 
thalamic region on both sides. 

The case differs from those already described as progressive 
lenticular degeneration (v. Review, 1913, xl, p. 167) in the age of 
the patient, the long duration of the disease, the absence of 
emaciation and of contracture, the fact that the tremor was not 
constant, and that the dysarthria was a long drawn-out, almost 
staccato, utterance. A. Ninian Bruce. 



ABSTRACTS 


125 


SYPHILITIC BONE DISEASE OF THE SKULL. M. S. Gkegory 
(161) and M. J. Karp as, Joum. Nerv. and Ment. Die., 1913, zl., Oct. 

Tub case reported is of interest, not only because of the rarity of 
syphilitic bone disease of the skull, but also because the clinical 
picture simulated that of a cerebello-pontine tumour. 

D. K. Henderson. 


DEATH FOLLOWING TWO INJECTIONS OF NEOSALVAB8AN 
(162) AT THE ONSET OF SYPHILIS. (Un cas de mort & la suite de 
deux injections de ndo salvarsan au dlbut de la syphilis.) E. 
Joltrain, Bull, et m<hn. Soc. med. U6p. de Paris, 1914, xxxvii., 
p. 120 ; Milian, ibid., p. 124 ; Sicard, ibid., p. 124. 

The patient was a robust man, aged 20. About three weeks after 
the appearance of the chancre, when Wassermann’s reaction was 
definitely positive, he received three injections of cyanide of 
mercury. Four days after the first injection he was given, at his 
own request, 0'30 eg. of neosalvarsan, which was followed by 
Herxheimer’s reaction on the third day. A week later 0 20 eg. 
was given. He passed a restless night, but continued at work till 
three days later, when he was seized with vomiting and diarrhoea, 
rapidly followed by convulsions and coma. Lumbar puncture 
gave issue to a clear fluid under hypertension, containing a large 
quantity of albumin and lymphocytes. Death took place three 
and a half days after the injection. No necropsy. 

In the subsequent discussion Milian attributed the death to a 
special intolerance for the drug, which could be combated by 
prophylactic injections of 1 mg. of adrenalin. 

Sicard drew attention to the fact that in all severe or fatal 
cases following injections of salvarsan, Wassermann’s reaction 
was positive, and suggested that the conflict between the spirochaetes 
and the drug was the cause of the disastrous results. 

J. D. Rolleston. 


FEVER AS SOLITARY SYMPTOM OF LATENT SYPHILIS. 
(163) (Fieber als einziges Symptom latonter Lues.) H. Kraus, Wien. 
Klin. Wock., 1913, xxvi., p. 2030. 

A record of four cases in adults, aged from 25 to 40, all character¬ 
ised by obstinate fever of different types persisting for months, 
inefficacy of all antipyretic treatment, absence of typical symptoms 
of syphilis, history of infection confirmed by Wassermann’s reaction, 
exclusion of any other organic disease, and rapid disappearance of 
fever after antisyphilitic treatment. J. D. Rolleston. 



126 


ABSTRACTS 


HAVE THE EARLY CLAIMS OF 8ALVARS AN BEEN REALISED ? 

(164) C. Morton Smith, Boston Med. and Surg. Joum., 1914, clxx., Feb. 
19, p. 269. 

The early hope of curing syphilis with a single massive injection 
of salvarsan has not been realised. It is a potent remedy in heal¬ 
ing all manifestations on the skin or mucous membranes. It is 
more efficacious than mercury in changing a positive to a negative 
Wassermann reaction. Its prompt action on early moist lesions 
has a decided effect in limiting the spread of contagion. The early 
fears of damage to the cranial nerves appear to be groundless. 
When given in proper amounts at proper intervals it is practically 
devoid of danger. A Ninian Bkuce. 

PARALYSIS OF THE NERVOUS SYSTEM. James MTntosh and 
(166) Paul Fildes, Henry Head and E. G. Fearnsides, Brain, 1913, 
zzxvi, p. 1. 

Parasyphilis of the nervous system is a purely clinical conception. 
It is a diseased state that may affect any part of the brain or 
spinal cord; the manifestations of tabes dorsalis and dementia 
paralytica can only be erected into two clinical divisions by an 
arbitrary selection of signs and symptoms. Some forms of 
progressive muscular atrophy, lateral and combined sclerosis, 
primary optic atrophy, and periodic epileptiform attacks may be 
equally definite manifestations of parasyphilis. Parasyphilis is 
slightly, if at all, amenable to antisyphilitic treatment with 
compounds of arsenic and mercury, probably because these bodies 
do not enter the essential structures of the central nervous 
system. Parasyphilitic states are peculiarly liable to arise after 
mild syphilitic infection. 60 per cent, of cases of tabes have 
suffered from at most a primary sore, and in many instances the 
whole course of the initial infection was run under cover of a 
gonorrhoea. In dementia paralytica and in active, untreated 
cases of tabes dorsalis and tabo-paresie, the cerebro-spinal fluid 
yields a positive Wassermann reaction, often of great strength. 
With acute or chronic syphilis of the nervous system, other than 
parasyphilis, the behaviour of the cerebro-spinal fluid depends upon 
the extent to which the spinal cord and its membranes, including 
those of the brain-stem, are affected. Thus most cases of 
meningomyelitis show a strong positive reaction in the cerebro¬ 
spinal fluid, whilst cerebral lesions tend to give a weakly positive 
or even a negative reaction. But in cases of parasyphilis no 
obvious change occurs in consequence of such treatment within 
any comparable period. 

Parasyphilis of the nervous system depends on an atrophy of 
the nerve fibres and cells, associated with a cellular infiltration 



ABSTRACTS 


127 


of the meninges and adventitial sheaths of the vessels, and 
proliferation of the neuroglia. All infections lead to a change in 
the character of the reaction of the tissues to the poison—they 
may respond less and less (hypoallergic) until they cease to respond 
altogether (anergie), or they may respond quicker and more 
violently (hyperallergie), finally culminating in anaphylactic 
shock. This hypersensitiveness (hyperallergie) of the central 
nervous system is produced by the passage of the spirochaetes or 
their toxins up the lymphatics of the nerves from the skin and 
mucous membrane during the secondary period, or from a slight 
“ encephalitis ” during the stage of infection. In consequence of 
this hyperallergie reaction in the tissues, a renewed activity of 
the spirochsete rapidly causes death of any set of fibres or cells 
attacked and proliferation of the neuroglia. The clinical 
manifestations of “ parasyphilis ” are an expression of the reaction 
and necrosis of hypersensitised areas of the nervous system evoked 
by reappearance of the Spirochccta pallida, and this reaction is as 
truly syphilitic as the production of gummata. The difference 
merely lies in the nature of the tissues participating in the 
reaction. In tertiary syphilis the connective tissue is capable 
of repair, and the focus is readily reached by the remedial agents. 
In “ parasyphilis ” reaction of the essential nerve elements leads 
to their death, and antisyphilitic remedies cannot readily reach 
the spirochaite. A. Ninian Bruce. 

THE WASSEEMANN REACTION AND ITS APPLICATION TO 
(166) NEUROLOGY. Paul Fildes and James McIntosh, Brain , 1913, 
xxxvi., p. 193. 

In this paper the present state of our knowledge of the Wasser- 
mann reaction in all particulars which bear directly upon 
neurology is renewed. This is discussed under the headings of (1) 
the technique of the Wassermann reaction ; (2) the occurrence of 
the Wassermann reaction; and (3) the effect of antisyphilitic 
treatment upon the Wassermann reaction. Before estimating the 
value of a report upon the Wassermann test, the physician should 
be acquainted with the methods and general results of the 
serologist who gives the report. 

The following general conclusions may be drawn: (1) In 
general diagnostic work, exclusive of nervous conditions, a positive 
reaction is so constant in active syphilis that such a diagnosis is 
doubtful if the reaction be negative. (2) A positive reaction in the 
cerebro-spinal fluid indicates a syphilitic lesion of the central 
nervous system. (3) In active untreated cases of dementia 
paralytica, tabes dorsalis, and cerebro-spinal syphilis, the reaction 
is positive both in the serum and cerebro-spinal fluid. In cerebral 



128 


ABSTRACTS 


syphilis, without involvement of the spinal cord, the cerehro-spinal 
fluid is usually negative. (4) The reaction is apt to be negative in 
the serum or cerebro-spinal fluid in cases of hemiplegia, non¬ 
progressive tabes dorsalis, and old lesions of the nervous system, 
especially in cases of stationary congenital syphilis. It is also 
usually negative in the serum, particularly in very recent nerve 
lesions of the late secondary period, and in the cerebro-spinal fluid, 
particularly in treated cerebro-spinal cases. (5) The occurrence of 
a positive reaction in one of the test fluids when the other is 
negative is so common that a reaction found negative in one 
fluid only is insufficient to exclude syphilis. (6) Pure “para- 
syphilitic” lesions do not respond satisfactorily to treatment, 
as shown by the slight effect upon the reaction in the 
cerebro-spinal fluid. Cerebro-spinal lesions react very readily to 
treatment. The celerity with which the reaction in the cerebro¬ 
spinal fluid responds to treatment is an index of the “para- 
syphilitic” or “ syphilitic ” nature of the case. (7) The positive 
reaction in the serum is rapidly made negative by treatment in 
acute syphilis ; but in chronic syphilis this effect is produced very 
slowly. In the cerebro-spinal fluid, on the other hand, the rate of 
reduction of the reaction does not depend upon the duration of the 
infection. Thus, in gummatous lesions of the central nervous 
system, as also in acute secondary cerebro-spinal syphilis, the effect 
of treatment upon the reaction in the cerebro-spinal fluid is rapid. 
(8) The “provocative” injection of salvarsan for the purpose of 
exciting an exacerbation of the reaction has some, but probably an 
exaggerated, diagnostic value. A. Ninian Bruce. 

METHODS OF INCREASING THE ACCURACY AND DELICACY 
(167) OF THB WASSERMANN REACTION. Francis H. Thiele 
and Dennis Embleton, Lancet , 1914, clxxxvi., Feb. 21, p. 626. 

The method is : 1. To diminish the amount of complement used 
to one and a half times only that which will cause complete 
hieinolysis of the system adopted. 2. To use large amounts, half 
a cubic centimetre or more, of inactivated syphilitic serum. 3. To 
use 50 to 100 units of the antigen. By this method purely anti- 
complementary phenomena do not play a part. Anti-complementary 
effects being rendered obvious in the control, true complement 
fixation, even when minimal, can be readily demonstrated. In 
this way (1) cases which would otherwise give a slight reaction, 
so slight as to be doubtful on the ordinary reaction, give a full 
fixation; (2) cases which otherwise give a negative can be made 
to give a full reaction, thus bringing in a large number of latent 
cases: and (3) no fallacious results with other diseases have been 
obtained. A. Ninian Bruce. 



ABSTRACTS 


129 


THE CEREBROSPINAL FLUID AND A SPECIAL METHOD OF 

(168) TREATMENT OF ESSENTIAL EPILEPSY. Alfred Gordon, 
N.Y. Med. Joum ., 1914, xcix., Jan. 17, p. 110. 

One drop of blood drawn from the finger of one patient with 
epilepsy was dropped on the centre of the surface of fifteen drops 
of cerebro-spinal fluid taken from another patient, and vice versa, 
and complete haemolysis took place. A drop of blood from each 
patient brought into contact with his own cerebro-spinal fluid, 
remained coagulated for days in the tubes. Each patient thus 
had in his blood poisonous substances which were antagonistic to 
the other’s blood, but not to his own. 

Four patients were accordingly treated on this principle, 
namely, subcutaneous injections of cerebro-spinal fluid taken from 
another epileptic, and it was found that striking improvement 
occurred, not only in regard to the severity of the attacks, but also 
in their frequency. A. Ninian Bruce. 

THE BRAIN OF A MACROCEPHALIO EPILEPTIC. J. Wiolesworth 

(169) and George A. Watson, Brain, 1913, xxxvi., p. 31. 

* 

The patient was a man, aged 37, a piano-tuner. There was no 
history of insanity or epilepsy in the family. He was bright and 
intelligent as a child, although of a nervous, excitable disposition, 
and early showed signs of great musical ability. At the age of 
9 he had an attack of petit mal, but the first fit did not occur until 
he was 16, and from then onwards they occurred at variable 
intervals. About 27, gradual mental deterioration set in, and he 
had to be removed to an asylum a year later on account of 
delusions. He became dull and weak-minded, the fits increased 
in number, his memory and intelligence failed, and he died from 
broncho-pneumonia. 

The brain, unstripped of membranes, was found to weigh 
2,130 grms. (average weight being about 1,400 grms.). The 
cerebral hemispheres were of good general shape and appeared to 
be normally constituted, their great size and weight not being 
accounted for by the slight increase in neuroglia and thickening of 
the vessels which was found. The convolutional pattern was 
exceedingly complex, but showed little that could be regarded as 
definite marks of inferiority. It is described at considerable 
length. The microscopic changes found also do not at all 
necessarily bear upon the question of cerebral hypertrophy, being 
merely those usually present in the brains of chronic epileptics. 
There were, however, in the cerebral hemisphere many signs, 
apart from their large size, of a formative activity much greater 
than that usually seen. But this increased developmental activity 



130 


ABSTRACTS 


has proceeded on regular lines, and on the whole the departures 
from the ordinary in the convolutional pattern are in the 
direction of superiority. On the other hand, the tendency to 
insulation of areas of cortex, and the marked spurring and forking 
of certain sulci, such as is seen particularly in the left temporal 
region, may probably be looked upon as indications of formative 
activity on irregular or aberrant lines. With this greatly in¬ 
creased developmental activity, whether in the direction of 
superiority or of aberrancy, it seems likely that there would be 
a tendency to instability. This patient was neither idiotic nor 
imbecile, but was originally of average general intelligence, and it 
would appear that even when the minute structure of the brain 
appears to be normally constituted, the usual size of the brain, 
apart from its increased complexity of pattern, cannot be largely 
exceeded without introducing a condition of instability, which 
renders its possessor liable to suffer from some form of nervous 
breakdown, and especially from epilepsy. A. Ninian Bruce. 

ANTERIOR CRURAL NEURITIS. C. M. Byrnes, Joum. Nerv. and 
(170) Ment. Dit., 1913, xl., Dec. 

This is the first part of an article which will be concluded in the 
next number. 

The anatomy of the anterior crural nerve is briefly considered, 
and the various etiological factors and the importance of correct 
differentiations of the neuritic condition are emphasised. 

All cases in which one or both nerves has been the seat of 
an inflammatory state, consequent upon internal or medical 
diseases, as well as those of a so-called idiopathic nature, are dis¬ 
cussed. Those forms dependent upon distinctly local or surgical 
conditions have been excluded. 

In this paper 136 cases are analysed, and are grouped accord¬ 
ing to their etiology in the following order:— 

Metabolic diseases, infectious diseases, septic conditions and 
intoxications, local conditions in which circulating toxins may 
have been a factor, and primary idiopathic neuritis. 

Under metabolic diseases, cases are described as occurring in 
goutj, rheumatic, diabetic, and pentosuric conditions. 

In regard to infectious diseases, cases have been reported as 
occurring in typhoid fever, in tuberculosis, and in syphilis. Cases 
in the other groups are ascribed as having been due to chronic 
suppuration, alcohol, appendicitis, prolonged surgical anaesthesia, 
obstetrical conditions, exposure, and occupation and over-exertion. 

The author has collected the records of eight cases in which 
the anterior crural nerve has been the seat of an idiopathic in¬ 
flammatory condition. D. K. Henderson. 



ABSTRACTS 


131 


SUBACUTE TETANUS CUBED BT ANTITETANIO SEBUM. 
(171) (Tltanos It Evolution snbaiguB gu6ri par le slrum antitBtanique.) 
L. Jacqubt and Debat, Bull, et mim. Soc. mid H6p. de Paris, 1914, 
xxxvii., p. 190. 

The source of infection was not definitely ascertained, but the 
patient, who was a farmer, had numerous cracks on his hands. 
300 c.c. were given in thirteen injections of 30 c.c. each and four 
injections of 10 c.c. There was no opisthotonos, the contractures 
being confined to the limbs, jaws, and neck. Recovery took place, 
but flaccid paralysis of the anterior muscles of the left leg ensued 
with diminution of cutaneous sensibility. Paralysis is a rare 
sequel of tetanus in man, but is not infrequent in the horse. 

J. D. Rolleston. 


NOTES ON SUNLIGHT AND FLASHLIGHT REACTIONS, AND 
(172) ON CONSENSUAL AMTOSIS TO BLUE LIGHT. A. Mykbson 
and E. E. Eversolk, Journ. New. and Ment. Dis., 1913, xl., Nov. 

The authors have made a systematic comparison of the pupillary 
reaction when stimulated by flashlight (pocket flashlight) and 
daylight. They found no case where, with proper technique, 
daylight did not bring a reaction where the flashlight did, but 
they did find cases, especially in general paralysis, where, with no 
reaction obtainable by the use of the flashlight, daylight brought 
about a smaller pupil, although in some cases the movement itself 
could not be observed. 

The question arose whether there were specific colour qualities 
in daylight which might be specific in their stimulating power. 
A determination of the properties of three colours, red, green, and 
blue, in bringing about reflex responses of the pupil was attempted. 

The results are summarised as follows:— 

The consensual pupil reacts in a selective manner to the 
colours red, green, and blue, in the order mentioned. If there is 
disease the blue disappears first, the green probably next. 

D. K. Henderson. 


PSYCHIATRY. 

AN ANALYSIS OF THE EBBOBS IN DIAGNOSIS IN A SERIES 
(173) OF SIXTY OASES OF PARESIS. S. T. Obton, Journ. New. 
and Ment. Dis., 1913, xL, Dec. 

In nine out of sixty cases the clinical diagnosis of general paralysis 
could not be confirmed at autopsy. D. K. Henderson. 



132 


ABSTRACTS 


TRANSVESTISM B. S. Talmey, N. Y. Med. Joum ,, 1914, xcix., Feb. 

(174) 21, p. 362. 

The author describes here four cases of “ transvestism ” or “ cross 
dressing,” all being men who dressed as women. 

A. Ninian Bruce. 

THE CATATONIC SYNDROME AND ITS RELATION TO MANIG- 

(175) DEPRESSIVE INSANITY. George H. Kirby, Joum. Nerv. and 
Ment . Die., 1913, xl., Nov. 

According to Kraepelin, all non-organic cases with catatonic 
symptoms belonged to the dementia preecox group, and such 
manifestations were looked upon as significant of a deterioration 
process. Kraepelin, of course, admits that about 13 per cent, of 
the catatonics appear to recover, but the permanency of these 
recoveries he regards as unsettled, and inclines to the view that 
they are probably only remissions. Wilmans later reviewed 
Kraepelin’s own Heidelberg cases, and found that catatonic 
symptoms, as evidence of a deterioration process, had been greatly 
overrated. 

The catatonic syndrome is not a clinical unit, and it is prob¬ 
able that deteriorating and non-deteriorating catatonic cases 
represent fundamentally different reaction types. A review of a 
large material has shown that in acutely developing catatonic 
states, when not preceded by any ominous prodromal symptoms, 
recovery, with few exceptions, takes place, and in some instances 
after a duration of several years. 

The possible relation of these acutely developing catatonic 
states in relation to manic-depressive insanity is discussed, because 
the subsequent history of such cases shows not infrequently manic 
attacks. Four such cases are described. The most reliable prog¬ 
nostic data in all these cases is gained from a close study of the 
personality, and the mode of development of the psychosis. 

The author believes that Kraepelin overvalued catatonic 
manifestations as evidence of a deteriorating psychosis, and that 
many such cases have served to unduly swell the dementia praecox 
group. D. K. Henderson. 


TREATMENT. 

NOTES ON THE TREATMENT OF SCIATICA. John J. Grace, 
(176) Lancet , 1914, Jan. 10, p. 102. 

The author records six cases which have greatly improved by the 
use of the 500 candle-power lamp and static electricity, twenty 
minutes being devoted to each application. A. Ninian Bruce, 



REVIEWS 


133 


IRevievps. 

THE HIST0B7 OF THE PRISON PSTCHOSES. By Dra Paul 
(177) Nitsche, Dresden, and Karl Wilmanns, Heidelberg. Anthorised 
Translation by Francis M. Barnes, Jun., M.D., and Bernard 
Glueck, M.D., Government Hospital for the Insane, Washington, 
D.C.; with an Introduction by William A. White, M.D. “ Nervous 
and Mental Disease Monograph Series,” No. 13. New York: The 
Journal of Nervous and Mental Disease Publishing Company, 1912. 

This admirably translated monograph is a critical review of the 
principal German literature from 1853 to the present day on the 
subject of the psychoses occurring in prisoners. The authors’ object 
is in the main to set forth the evidences as to the influence of 
imprisonment, and particularly of solitary confinement, in producing 
insanity, and to determine whether the forms of insanity met with 
amongst the criminal classes have any distinguishing characteristics 
as compared with the classical types which are recognised as 
occurring in ordinary free life. The literature has been divided 
into three periods. The first embraces the observations chiefly of 
the early prison physicians. The second deals with the relation 
of the prison psychoses to the work of Kraepelin, while the third 
reviews the later literature written under the influence of the 
Magnan-Mobius ideas on degeneracy. It may be said for the 
workers in the first period, called by the authors the “ old school,” 
that many of the conclusions are evidently based upon the most 
accurate observations of competent and enlightened prison 
physicians, whose ideas are none the less worthy of notice because 
the authors were not obsessed by the multiplicity of psychological 
terms which have led later observers to the difficult task of fitting 
the mental abnormalities of prisoners into the prevailing classifica¬ 
tions. Indeed the groundwork of the whole subject is to be found 
in the observations of the old school that certain forms of insanity 
met with in prison are a later stage in processes that have arisen 
before imprisonment, and that acute forms of insanity may develop 
in prison as elsewhere, aided or not in their causation by the 
particular circumstances of the environment. Much of the 
diversity of opinion expressed in this period is not only a testimony 
to the excellence of the observations, but, as the authors point out, 
is due to the varied nature of the material studied according as the 
prisoners were already undergoing long sentences, recently sentenced, 
or awaiting trial. Much stress is laid throughout upon the effects 
of solitary confinement in producing insanity, and attention is 
drawn to the description, particularly by Kirn, of two varieties 
of psychoses which are said to be characteristic of solitary confine¬ 
ments, viz : The acute hallucinatory melancholia and the acute 



134 


REVIEWS 


hallucinatory paranoia. In comparing these observations with 
the occurrence of similar conditions at a later date, it must be 
remembered that the circumstances that were said to have pro¬ 
duced these conditions must have materially changed. Those acute 
conditions are very frequently met with at the beginning of a term 
of imprisonment where the solitary confinement has not been of 
any duration, and some cases of mild melancholia based upon the 
affective disturbances due to the prisoner’s outlook are, if they are not 
associated with a too strong neurotic predisposition, often quickly 
cured by the quietude (combined in these cases with observation 
and treatment) that results from the modified form of seclusion 
that is now applied to prisoners. There is probably, however, in a 
great majority of cases a strong neurasthenic basis, and although 
in many of these there is the hysterical element in any hallucina¬ 
tory symptoms to be taken into account, it is necessary, and that 
at once, to substitute in such conditions hospital treatment for the 
seclusion. In these cases the cure, although immediate, is rarely 
permanent, in that if returned to prison conditions the symptoms 
reappear. In regard to the contention that acute hallucinatory 
melancholia is not a common disease of free life but characteristic 
of the effects of solitary confinement, it may be noted that in 
many prisoners, probably all neurotic, this condition develops 
often a very considerable time after imprisonment as a late post¬ 
alcoholic state, which would certainly not have been allowed to 
occur in free life, but is not therefore due to the seclusion. 

The second period is very briefly discussed in the authors’ 
conclusions. Here it is noted that all psychoses occurring in 
prison assume a characteristic type, and show a certain outward 
resemblance because of the particular environment—the prison 
complex. A study of insane prisoners associated together in a 
curative establishment might lead an observer to say that this 
prison complex is much more an outcome of the characteristic 
criminal disposition, for penal systems and prison regulations vary 
much more than does this too-little noted temperament. In this 
period also it is noted that much is added to the knowledge of the 
prison psychoses because of the wider recognition that much 
criminality and mental disease appearing in prison are processes 
in a slowly developing dementia praecox. 

The third period deals with the light thrown upon the prison 
psychoses by the theories of degeneracy. Thus it was established 
that the majority of the prison psychoses are not of pure 
endogenous origin, but rather reach their development from the 
reciprocal effect of the physically diseased constitution, and the 
“ manifold physical and psychical traumata of person.” Again, the 
“physically diseased constitution” as the predisposing cause 
obscures the question of a psychological basis—the criminal mind, 



REVIEWS 


135 


as much an evidence of degeneration as the other. Here special 
attention is directed to the work of Siefert, who specifically 
’ classified the forms of insanity met with and differentiated between 
the acute psychoses arising as in ordinary free life and those 
which were produced by an unsuitable environment—the prison— 
acting upon a predisposition—degeneracy. 

The authors’ conclusions are rendered in a truly critical and 
scientific spirit, and a wise eclecticism leads them to begin and 
end with a plea for “ more light,” which, it is interesting to note, 
ia specially levelled at prison physicians, the modern representatives 
of the old school. 

A diffuse but highly scientific monograph, it is supported by 
a preface in a somewhat rhetorical vein. Few prison physicians 
will probably wholly subscribe to the preface in its description of 
the mental state of the prisoner convicted of a serious offence 
against the person. J. P. S. 

THE LABYRINTH: AN AID TO THE STUDY OF INFLAMMA- 
(178) TION8 OF THE INTERNAL EAR. By Alfred Braun, M.D., 
and Isidore Fribsner, M.D. Pp. 250, illustrated. Rebman 
Limited, London. Price 17s. 6d. net. 

For some years a want has been felt by men interested in the 
labyrinth, as up till the present there has been no book in 
the English language which contains the more recent work on the 
physiology and pathology of the labyrinth. It has been necessary 
hitherto to consult isolated works by German writers to acquire the 
desired knowledge. This want has been ably filled by the book here 
reviewed. It commences with a description of the anatomy of the 
labyrinth, in which the fullest details of both macroscopic and 
microscopic structures are described. This is followed by a section 
on the eighth nerve and its central connections. The physiology 
and methods of examination of the cochlea and vestibular apparatus 
are explained in such a way as to render the comprehension of the 
various complex reaction movements comparatively easy. The 
clinical tests for localising the seat of trouble are carefully described 
and their relative advantages and fallacies fully discussed. The 
paths of infection and pathological changes have a chapter to 
themselves, with numerous illustrations. The last chapter in the 
book is devoted to indications for treatment and operative methods. 
Finally, several pages are devoted to the bibliography of the 
subject. In conclusion, one may say that although the illustrations 
in many respects are not all that might be desired, the book forms 
an excellent risuwtf of all the recent work on the labyrinth, and 
is indispensable to the otologist who wishes to keep up to date, 
and is worthy of perusal by most neurologists. 

J. K. Milne Dickie. 


ii 



136 


BOOKS AND PAMPHLETS RECEIVED 


PATHOLOGICAL INEBRIETY: ITS CAUSATION AND TREAT 
(179) MENT. J. W. Astley Cooper. With Introduction by Sir David 
Ferries. Crown 8vo., pp. xvi and 151. Baillifcre, Tindall, <fe Cox, 
London, 1913. Pr. 2a 6d. net. 

This little book is to be regarded as an attempt to convey to the 
rank and file of the medical profession, and to those of the general 
public who are interested in temperance reform, some knowledge 
of the causation and the scientific and rational treatment of 
pathological, chronic, and periodic drunkenness, and to show how 
mistaken has been the attempt to cure inebriety by penal methods, 
and how essential to proper treatment is adequate legal control. 

It begins with short chapters upon the nature, forms, and 
causes of pathological inebriety. This is followed by a description 
of the complications, preventive treatment, and treatment by the 
combined method. A few pages are also devoted to inebriety and 
temperance societies. The psychical treatment and methods used 
to establish and develop the power of self-control are of special 
interest. 


BOOKS AND PAMPHLETS RECEIVED. 

Amoss, Harold L. “A Note on the Etiology of Epidemic Poliomyelitis ” 
( Joum. Exp. Med L, 1914, xix.). 

Clark, Paul F., and Amoss, H. L. “ Intraspinous Infection in Experi¬ 
mental Poliomyelitis” (Joum. Exp. Med., 1914, xix.). 

Clark, Paul F., Fraser, Francis R., and Amoss, H. L. “The Relation 
to the Blood of the Virus of Epidemic Poliomyelitis” (Jou m. Exp. Med., 
1914, xix.). 

Flexner, Simon, Clark, Paul F., and Amoss, H. L. “A Contribution to 
the Pathology of Epidemic Poliomyelitis” (Joum. Exp. Med., 1914, xix.). 

Flexner, Simon, Clark, Paul F.,and Amoss, H. L. “A Contribution to 
the Epidemiology of Poliomyelitis” (Joum. Exp. Med., 1914, xix.). 

Lamar, Richard V. “ Chemo-immunological Studies on Localised In¬ 
fections” (Joum. Exp. Med., 1914, xix.). 

Rybakow, Th. “La Cyclophr4nie (la psychose circulaire)” (Travaux 
de la clin. psyckiat. de VUniversity de Moscoii, 1914, No. 2). 



IRevnew 

of 

fleurologs anb flte^cbiatrs 


©rtginal Hrticles 


THE NEURAL ATROPHY OF THE MUSCLES OF 
THE HAND, WITHOUT SENSORY DISTURB 
ANCES 1 

A Further Study of Compression Neuritis of the Thenar 
Branch of the Median Nerve and the Deep Palmar Branch 
of the Ulnar Nerve. 

By J. RAMSAY HUNT, M.D., 

Associate Professor of Nervous Diseases, Columbia University, New York. 

(With Plates 3 and 4.) 

Atrophic paralysis of the small muscles of the hand occupies & 
position of peculiar importance in symptomatology, because of 
the great variety of pathological conditions in which it may 
occur as an important and often early symptom. It may follow 
involvement of the spinal cord, the anterior roots, the brachial 
plexus, and of the ulnar and median nerve. As a rule, the 
associated sensory disturbances or the absence of sensory symptoms 
play an important and often determining rdle in the topographical 
localisation of the lesion, indicating its neural, plexus, radicular, 
or medullary origin, as the case may be. 

The types of neural atrophy of the hand to which I shall refer 
have already been described in previous communications, 2 and are 

1 Read at a meeting of the New York Neurologioal Society, Jan. 1914. 

9 Ramsay Hunt, "Occupation Neuritis of the Deep Palmar Branch of the 
Ulnar Nerve," Joum. of Nerv. and Ment. Die., 1909, and “ The Thenar and Hypo- 
thenar Types of Neural Atrophy of the Hand," Am. Jour, of the Med. Sci., 
1911, Feb. 


12 



138 


J. RAMSAY HUNT 


characterised by a strictly neural distribution with complete 
absence of those disturbances of sensibility which usually 
accompany lesions of the median and ulnar nerves. For this 
reason they may resemble more or less closely certain of the 
myelopathies and myopathies beginning in the small muscles of 
the thenar, hypothenar, or interosseous regions of the hand. 

This peculiar form of neural atrophy results from a neuritis or 
compression of purely motor branches of the ulnar and median 
nerves, and may be divided into a thenar and hypothenar type. 

In the thenar group the atrophy is limited to the muscles of 
the thenar eminence supplied by the median nerve, and is the 
result of compression of the thenar branch as it passes beneath 
the anterior annular ligament of the wrist. 

The hypothenar group is characterised by paralysis with atrophy 
of all the small muscles of the hand supplied by the ulnar nerve, 
and results from compression of the deep volar branch as it passes 
between the tendons of origin of the short abductor and the short 
flexor of the little finger. 

Both of the compressed nerves are purely motor in character, 
which explains the occurrence of neural atrophy without disturb¬ 
ances of sensibility in their respective distributions. 

In my previous papers, the separation of these two types of 
neural atrophy from the other forms of occupation palsy was 
discussed in detail. In the present communication I wish to 
emphasise more particularly the points of differentiation from 
certain of the spinal atrophies of the Aran-Duchenne type. 


Cask I. 

A Typical Case of the Hypothenar Type of Neural Atrophy 
without Sensory Disturbances. 

Patient is a man, 32 years of age. His occupation consists of 
“ cutting, pressing, and ironing clothes.” There is no history of 
lues, and he is moderate in the use of alcohol. 

He was referred to the Vanderbilt Clinic, Department of 
Nervous Diseases, in November 1910, on account of weakness 
and atrophy of the muscles of the right hand. The weakness 
was first noticed about six months previously, and the atrophy 
had gradually followed. He has had no pain and no parasthesise 



Plate 3. 



. 1, Cask I.—The Hypothenar Type of Neural Atrophy without 
Sensory Disturlwinces. Posterior View, showing Atrophy of 
Interossei and Inability to Extend the Fingers. Compression 
Neuritis of the Deep Palmar Nerve. 



2, Cask I.—Hypothenar Type. Palmar Aspect, showing Atrophy 
of Hypothenar and Interossei. Note Prominence of the Thenar 
and the Sharp Border formed by the External Head of Flexor 
Brevis Pollicis. Compression Neuritis of Deep Palmar Branch. 






NEURAL ATROPHY OF THE HAND 


139 


in the hand, and has continued his occupation, but not without 
great difficulty and inconvenience. 

Physical Examination, November 1913.—The right hand is 
the seat of paralysis and atrophy, which is strictly limited to the 
ulnar distribution of the small muscles of the hand, i.e., the 
hypothenar interossei and the adductor pollicis. The general 
appearance of the hand suggests the main en griffe, with extension 
of the basal and flexion of the middle and distal flanges (Fig. 1). 
There is distinct prominence of all the metacarpal bones, with 
marked wasting on the palmar aspect of the hand and flattening 
of the hypothenar, which is in marked contrast to the thenar 
group, which stands out prominently and is well preserved (see 
Fig. 2). There is complete paralysis of the abductor, opponens.. 
and flexor brevis minimi digiti, the interossei, and the adductor 
pollicis. The functions of the flexor carpi ulnaris and of the 
palmaris brevis are preserved. An effort to abduct the little finger 
produces the typical contraction of the palmaris brevis (see Fig. 3); 
pressure over the pisiform bone also produces the usual contrac¬ 
tion of this muscle. The movements of the thenar muscles and 
those of the forearm and upper arm are normal. No fibrillary 
twitchings were noted at any time. 

The objective sensibility of the hand is normal to touch, pain, 
and temperature. Digital pressure of the ulnar nerve in the 
groove at the bend of the elbow produces the usual tingling 
sensation, which is a little more active in the paralysed than in 
the unaffected hand. There is no tenderness of the nerve trunks. 

Electrical Reactions .—Faradic and galvanic stimulation of the 
ulnar nerve at the elbow produces contractions in the flexor carpi 
ulnaris and in the palmaris brevis, hut no response in the intrinsic 
muscles of the hand supplied by the ulnar nerve. Direct faradic 
stimulation of the hypothenar group, interossei, and adductor 
pollicis produces no contractions; direct galvanic stimulation of 
these muscles elicits a slow vermicular response with reversal of 
the polar formula (complete reactions of degeneration). The 
muscles of the thenar region supplied by the median nerve (abduc¬ 
tor, opponens, and flexor brevis pollicis) yield normal electrical 
reactions. 

The general physical examination is negative. The man shows 
good muscular development without signs of atrophy or weakness. 

Pupils are equal and react promptly to light and accommodation. 



140 


J. RAMSAY HUNT 


There is no tremor of the hands. Both knee jerks and both 
Achilles jerks are present and equaL The arm reflexes (biceps, 
triceps, and supinators) are normal and of equal intensity on the 
two sides. The plantar, abdominal, and cremaster reflexes are 
normal. 

There is no lead-line on the gums. The urine is free from 
albumen and sugar. The Wassermann reaction of the blood is 
negative. The X-ray for cervical rib is negative. 

Diagnosis .—The hypothenar type of neural atrophy without dis¬ 
turbances of sensibility; compression neuritis of the deep volar 
branch of the ulnar nerve. 

Remarks on the Hypothenar Type. 

Including those previously reported six cases of this type have 
come under my personal observation, all of which were unilateral 
and identical in symptomatology with the case just recorded. In 
all there was a complete paralysis of the intrinsic muscles of the 
hand supplied by the ulnar nerve, without sensory disturbances. 
In two of the cases in which this symptom was investigated the 
function of the palmaris brevis muscles was preserved. This 
peculiarity is explained by the anatomical distribution; the filament 
supplying this small subcutaneous muscle is given off from the 
superficial palmar branch of the ulnar nerve, and so escapes injury 
in the compression of the deep palmar branch. 

Complete reactions of degeneration were observed in all of 
the cases, strictly limited to the ulnar distribution in the hand. 

The seat of the lesion in this hypothenar group may be localised 
with practical certainty. As the functions of the flexor carpi 
ulnaris, the palmaris brevis, and of the sensory branches are 
preserved, the compression must take place at a lower level, viz., 
the deep palmar branch. And as all the muscles supplied by 
this nerve are paralysed, the injury must occur before the nerve 
is broken up into its various muscular branches. This short 
section of the nerve trunk corresponds to its passage between the 
tendons of origin of the abductor minimi digiti and the floor 
brevis minimi digiti, sometimes piercing the latter structure. 
Immediately after its passage between these two muscles it comes 
in close relationship to the hook-like process of the unciform bone. 

The degree of neural atrophy varies with the duration of the 
paralysis. If the case is recent and is seen in the early stage t 



Kics. 3, Cask I. Hypolhenar Type; showing Ulnar Fluxion of the Wrist and 
Wrinkling of Skin over the lkise of Hypothenur due to Contraction of the 
Puimari* BrtvU Muscle. 



Fro. o, Cask II.—The Thenar Type. Lateral Aspect, showing Atrophy of 
Thenar Eminence and Sharp Edge of the Metacarpal Hone. 







NEURAL ATROPHY OF THE HAND 


141 


wasting of the muscles is but slightly marked, but gradually 
atrophy supervenes, and at this period may simulate a progressive 
tendency. It, however, does not progress beyond the limits of the 
ulnar distribution. The thenar eminence of the median innerva¬ 
tion always stands out sharply defined in the otherwise atrophic 
hand. 


Case II. 

The Thenar Type of Neural Atrophy without Disturbances of 

Sensibility. 

A man, aged 49, was admitted to the Neurological Division of 
the Vanderbilt Clinic in March 1913, with weakness and atrophy 
of the muscles of the ball of the left thumb. 

He denies lues, and is moderate in the use of alcohol. His 
occupation has been the same for some years, and consists in doing 
the general cleaning work of a large store, which includes sweeping, 
washing, and scrubbing floors, polishing brasses, and other work of 
a similar rough character. On an average he works from ten to 
twelve hours a day. There has been no exposure to lead intoxica¬ 
tion, and there is no evidence of the lead-line on the gums. 

Six months previously he states that the right thumb was 
injured by a blow from a heavy bar of iron, which caused some 
pain and swelling of both joints. He continued his work, however, 
but doing as much as possible with the left hand. Thus a great 
deal of work which had previously been performed with the right 
hand was done by the left hand. 

The history of his malady is as follows:— 

About five weeks before coming under observation, he noticed 
while working that the movements of the left thumb were weak, 
and that he was unable to use this member as effectually as before. 
This localised weakness appeared to increase for the next two or 
three days, since which time it has remained stationary. There 
was at no time the slightest evidence of pain or panesthesia in 
the affected hand. The disease was one purely of weakness, with 
no other subjective symptoms in the left upper extremity. 

Physical Examination, March 25th, 1913.—The left hand 
shows beginning atrophy of the muscles of the thenar eminence 
corresponding to the abductor pollicis and the opponens pollicis. 
No fibrillary twitchings are observed. There is a total paralysis 



142 


J. HAMS AY" HUNT 


r of these muscles, and a decided weakness in the movements of the 
I flexor brevis pollicis. All the other intrinsic muscles of the left 
hand are perfectly normal in volume and in function. There is 
complete preservation of the function of the adductor pollicis. 

Electrical Reactions. —Strong faradic and galvanic stimulation 
of the median nerve fails to produce any contraction in the 
paralysed movements of the thenar eminence. 

Direct faradism of the left thenar region elicits no response in 
the alxluctor or opponens pollicis. The inner portion of the flexor 
brevis pollicis and of the adductor pollicis yields good contractions. 

Direct galvanism produces a slow vermicular contraction of 
the paralysed muscles (abductor and opponens pollicis and 
external portion of the flexor brevis pollicis) with reversal of the 
polar formula. Quick, normal contractions of the inner head of 
the flexor brevis pollicis and adductor pollicis are elicitable. All 
other intrinsic muscles of the left hand, the interossei, and those 
of the hypothenar give normal electrical responses. 

The objective sensibility of the left hand and fingers is normal 
to touch, pain, and temperature. There is no tenderness along 
the course of the median nerve or where it passes beneath the 
annular ligament. 

The Eight Hand. —The phalangeal joints of the right thumb are 
still enlarged and swollen, the result of trauma some months 
previously, but are free from pain and tenderness. All the 
intrinsic muscles of the hand are normal in function. 

General Examination. —A careful study of the general muscula¬ 
ture of the body was made for evidences of weakness, atrophy, or 
fibrillary twitchiugs, with negative results. The muscles of the 
forearm, upper arm, and shoulder girdle are well developed and 
normal. The spinal column is normal in movements and contour. 

The pupils are unequal, right is larger than the left. They do 
not respond to light. Keaction to accommodation is absent on the 
right, active on the left. 

The tendon reflexes of both upper extremities ( supinator , biceps 
and triceps jerks) are of normal intensity, and are equal on the two 
sides. 

The masseter reflex is present. Both knee jerks are present 
and active, and equal on the two sides. The Achilles jerks are 
present and equal. The plantar reflex shows a flexor response on 
both sides. The abdominal and cremaster reflexes are normal. 



NEURAL ATROPHY OF THE HAND 


143 


The general sensation of the body is normal except in the 
mammary region, where spots of analgesia and hypalgesia are 
present. 

Heart is negative. Urine: no albumen; no sugar. 

Note .—On inquiry, the patient states that at rare intervals he 
has had occasional lancinating pains in the lower extremities. 
These are infrequent and not at all severe. 

There is no vesical trouble, no dysarthria, no crisis, and no 
paresthesia. 

Re-examination, 24 th November 1913.— 

The thenar atrophy on the left side is more pronounced, so that 
a distinct scooped-out appearance is produced, limited on the outer 
side by the border of the first metacarpal bone, and on the inner 
side by the internal head of the flexor brevis pollicis (Figs. 4 and 5). 
The paralysis and atrophy as well as the reactions of degeneration 
are strictly limited to the distribution of the thenar branch of the 
median nerve. No fibrillations have been noted at any time. The 
other muscles of the left hand are normal in function and in 
electrical reactions. The musculature of the right hand and both 
forearms and upper arms is normal in function and volume. 

The objective sensibility of the left hand and fingers is normal. 

The pupils are unequal, the right is greater than the 
left. Both are rigid to light, and the left only responds to 
accommodation. 

The arm jerks are all present and equal. The knee jerks are 
present and unequal, the right being a little less than the left. 
The Achilles jerks are equal. On plantar stimulation there is a 
flexor response on both sides. 

Patient has occasional lancinating pains in legs, not severe or 
frequent, but typical in character. 

The sphincters are normal. The mammary zone shows areas 
of analgesia and hypalgesia. 

Examination, January 1914.—In spite of advice to the 
contrary, the patient persists in his occupation, working about 
twelve hours a day. 

The atrophy of the left thenar is still present, and is limited 
strictly to the thenar distribution of the median nerve. 

Electrical reactions of degeneration are still present, and are 
limited to the median distribution of the thenar eminence. The 
function, appearance, and electrical responses of the other intrinsic 



144 


J. RAMSAY HUNT 


muscles of the left hand are all normal, including the adductor 
pollicis and the inner head of the flexor brevis pollicis. No fibrilla¬ 
tions. Sensibility in the median distribution remains normal. 

Pupillary responses are as noted at previous examinations. 

Responses of the upper extremities are present, and equal on 
both sides. Knee jerks are present and unequal, the left is less 
active than the right. The Achilles jerks are present and equal. 
The plantar reflexes are normal. The abdominal and cremasteric 
reflexes are normal Wassermann reaction is negative. Spinal 
puncture not performed. X-ray examination for cervical rib is 
negative. 

Diagmsis. —Incipient tabes and the thenar type of neural 
atrophy. 

Remarks on the Thenar Type. 

Including those previously described, four cases of this type 
have come under my observation, in two of which the atrophy was 
unilateral and in two it was bilateral. In all four cases, including 
those in which the atrophy was bilateral, the clinical features were 
identical, viz., paralysis with atrophy of the muscles of the thenar 
eminence innervated by the median nerve, with reactions of 
degeneration and complete preservation of sensibility in the dis¬ 
tribution of the median nerve. Fibrillary twitchings were absent, 
and a central affection was excluded. One of these cases made a 
complete recovery, one a considerable improvement, and in one the 
atrophy has persisted and remained stationary over a period of 
nineteen years, while one case has been under observation for a 
year and has not progressed. 

The symptoms in this group of cases are purely motor in 
character and are strictly limited to the thenar distribution of the 
median nerve, and can only be interpreted as resulting from a 
lesion of the thenar branch of the median as it passes beneath the 
anterior annular ligament of the wrist. This theory of compres¬ 
sion by the annular ligament, which I expressed some years ago, 1 
would seem to have received confirmation from a recent patho¬ 
logical study by Marie and Foix, 2 in which compression neuritis 

1 “Compression Neuritis of the Thenar Branch of the Median Nerve: A 
well-defined Clinical Type of Atrophy of the Hand/’ 7'ransactions of the 
American Neurological Association , 1909. 

* 2 “Atrophie iaotee de l’eroinenoe thenar d’origine nevritique. Role du 
ligament annulaire dans la pathogenie de la lesion,” Btime Neurologtque , 1913, 
xxi., Nov. 30, p. 647. 



NEURAL ATROPHY OF THE HAND 


145 


of the median nerve was found localised beneath the anterior 
annular ligament of the wrist in a case of double thenar atrophy. 

The neural atrophy in the thenar as in the hypothenar group 
comes on gradually, following in the wake of the paralysis, and 
in this way a certain progressive tendency may be manifested in 
the earlier months, which may be very suggestive of a beginning 
spinal atrophy of the Aran-Duchenne type. There are, however, 
no fibrillary twitchings, and the atrophy and reactions of degenera¬ 
tion are strictly limited to the median distribution of the thenar 
eminence. (Abductor, opponens, and the outer head of the flexor 
brevis pollicis.) 


Remarks on Diagnosis. 

The differentiation of the thenar and hypothenar types of 
neural atrophy of the hand from the other groups of compression 
neuritis, professional palsies and occupation atrophies occurring 
in the hand, have been discussed at length in my previous studies 
of this subject. Briefly stated, the essential points of difference 
are, the absence of sensory symptoms in the affected neural 
distribution and the complete paralysis of all the intrinsic muscles 
of the hand supplied by the thenar nerve (thenar type) and 
the deep palmar nerve (hypothenar type). 

A complete paralysis in an entire neural distribution with 
degenerative reactions would rule out conclusively those forms 
of occupation palsy which have been ascribed to degeneration of 
the peripheral motor terminals by muscular compression (Gessler), 1 
as well as those professional atrophies assumed to be of royositic 
or myopathic origin. 

Certain types of spinal atrophy beginning in the small muscles 
of the hand may cause uncertainty in diagnosis in the earlier stage 
when atrophy is just beginning. But the absence of a sharply 
defined limitation to a neural distribution and the progressive 
tendency, the presence of fibrillary twitchings and the later 
involvement of the other muscles of the forearm, with alterations 
of the tendon reflexes, serve very effectually to indicate its 
medullary origin. 

1 “Eine eigenartige form von Progressive Muskei Atrophie bei Gold- 
PolirinneIl. ,, Med. Correspondent, Blatt. des Wurtemberg , Ant. Land., Vertin *, 
Bd. lxvi., No. 36. 



146 


J. RAMSAY HUNT 


In a recent study of this subject Marie and Foix 1 have 
described a curious type of spinal atrophy affecting the intrinsic 
muscles of the hand, which remains strictly limited to this region 
and shows no tendency to progress to the other muscle groups of 
the upper extremity. This affection is extremely slow in its 
evolution, the atrophy gradually increasing over a period of years. 
In the two recorded cases with autopsy, the atrophy of the small 
muscles of the hand was diffuse, involving chiefly the thenar but 
also the hypothenar and interosseous region of the hand. The 
electrical reactions of degeneration were present in the atrophic 
muscles. In both cases clinical and pathological evidences of 
syphilis were present. 

The pathological lesions underlying this curiously limited and 
non-progressive atrophy of the hand were found in a corre¬ 
sponding focal atrophy of the anterior horn. The grey matter and 
cellular structures of the anterior horn were found shrunken and 
atrophic in a small area of the cord corresponding in level to the 
8th cervical segment, and encroaching slightly upon the adjacent 
7th cervical and 1st dorsal segments. The cause of this focal 
wasting of the anterior horn or tephro-rnalacia-anterior, as it has 
been termed by the authors, is an endo-periarteritis of the ante- 
rioles nourishing the affected region, which diminishes the calibre 
of the vessels, with a consequent gradual shrinking of the grey 
matter. As the vessels were not thrombosed, the gradual and 
insidious wasting of the hand muscles was caused by the slow 
diminution of the blood supply in this restricted area. 

Such a clinical picture may from its non-progressive course 
resemble very closely the thenar and hypothenar types of neural 
atrophy. In the neural atrophy, however, the paralysis is more 
rapid in its development and from the first occupies the complete 
neural distribution of the compressed nerves. 

Complete reactions of degeneration are also present at an early 
period, likewise including the entire distribution of the compressed 
nerves. 

As the paralysed muscles gradually undergo atrophy, the 
limitation of the wasting to the distribution of the compressed 
nerves is even more apparent. In the thenar type the atrophic 

1 “ L’atrophie isolee non progressive des petits muscles de la main. Tephro- 
malacia-anterior.” Marie efc Foix, Novv. 1 conograph it de la Salpttribre, 1912, 
xxv., p. 353. 



NEURAL ATROPHY OF THE HAND 


147 


area presents a punched-out appearance, due to the well-defined 
border of the internal head of the JleoMr brevis pollids, while in 
the hypothenar type a veritable main en griffe may develop, with 
complete preservation of the rounded prominence of the thenar 
eminence. 

While admitting that focal medullary affection, such as the 
tephro-malacia-anterior, may simulate rather closely such a neural 
picture, the difficulty in diagnosis is more theoretical than real; 
so that in the thenar case with incipient tabes, reported in this 
paper, I would exclude the tephro-malacia-anterion', as well as the 
more diffuse forms of spinal atrophy, even in the presence of 
syphilis, for the reasons stated above. 

The persistence of the thenar atrophy in these cases is not 
without interest, and by no means excludes the neural origin. In 
one of my cases it had lasted through a period of nineteen years. 
An explanation of this is to be found in the slight degree of dis¬ 
ability produced by the thenar palsy, so that the occupation is 
continued which had originally caused the compression. Under 
those conditions, the causative factor not being removed, regenera¬ 
tion of the nerve does not take place. 

The same may be true of the hypothenar type, but in my 
experience the disability being greater in this group of cases, the 
occupation is usually abandoned, thus relieving the nerves from 
further compression, and permitting regeneration to take place. 

As the prelude to treatment, therefore, the particular move¬ 
ments of the hand instrumental in the production of the com¬ 
pression should be interdicted. 

It is possible that with advancing years the annular ligament 
may become more rigid and less elastic, and thus render 
compression of the thenar nerve more likely in the thenar cases. 
Under these circumstances, surgical relief of pressure might be 
given consideration. 


Concluding Remarks. 

Atrophic paralysis of the intrinsic muscles of the hand, without 
disturbances of sensibility, may be of myopathic, myelopathic, or 
neural origin. 

Neural atrophy of the hand may occur as two well-defined 
clinical groups, both due to a compression lesion of a motor branch 
of the median and ulnar nerves respectively. 



148 


EDGAR F. CYR1AX 


The hypothenar type : This term indicating the seat of the com¬ 
pression lesion at the base of the hypothenar eminence and its 
relationship to the ulnar nerve (compression neuritis of the deep 
palmar nerve). 

The thenar type: This also indicating the seat of the com¬ 
pression at the base of the thenar eminence, and its relationship 
to the median nerve (compression neuritis of the thenar nerve). 


ON THE TECHNIQUE OF NERVE PALPATION BV 
NERVE “FRICTION.” 

By EDGAR F. CYRIAX, M.D., London. 

When the method of ordinary palpation is employed in order to 
determine the position, shape, and size of nerves, a great deal of 
information can thus be obtained. But this method is neither 
so reliable nor so perfect as that which has been designated nerve 
“ friction,” a procedure which not only gives information on these 
points with greater precision and accuracy, but can frequently 
reveal them when ordinary palpation entirely fails to do so. 
This method of nerve friction, which is really more a therapeutic 
than a diagnostic agent, is an improvement on the old nerve 
pressings or vibro-pressings of the Ling school of medical gym¬ 
nastics ; its existence in its present form we owe to H. Kellgren. 
In order to understand the method it will be necessary minutely 
to describe the technique. 

The part of the body in which the nerve lies should be easy 
of access, and the muscles, fasciae, &c., that lie superficial to the 
nerve should be relaxed. It is, however, not essential, though in 
most cases preferable, that the part be denuded of clothing. 1 The 
position of the medical man and the patient is simply that which 
allows the friction to be most perfectly carried out, and the 
relative positions of his digits, hand and forearm to the patient 
will vary accordingly. The exact site of the nerve sought is 

1 Nebel (Schmidts Jahrb ., 1891, ccxxx., 195) and Reibmayr (Die Massage uud 
ihre Venoerthung , 1893, 16) both stated that it was impossible to detect nerves 
by the sense of touch through ordinary clothing. How these two authors 
failed to feel, say, the cords of the brachial plexus through thin clothing is 
difficult to understand. 



TECHNIQUE OF NERVE PALPATION 


149 


located either through knowledge of topographical anatomy, or 
by means of actually feeling it by palpation: the medical man 
then places one or more digits on or near the nerve to be examined. 
Either the nail itself, or the nail together with the soft part, or 
the soft part without the nail, of the forefinger or second finger, 
less commonly of the thumb, is the actual part employed. The 
friction is then executed by drawing the tip of the digit, together 
with the superficial structures, across the nerve at right angles 
to its long axis, a certain amount of pressure being applied 
meanwhile. The amount of pressure should be the lightest 
compatible with the effect desired; for example, a friction applied 
to the facial nerve as it winds round the ascending ramus of the 
jaw with a pressure equivalent to about one ounce, is sufficient in 
many cases to enable the operator clearly to define the position 
and size of the nerve, and to produce, from the patient’s point of 
view, a mild but distinctly stimulatory effect. As soon as the 
nerve has been traversed, the pressure is relaxed. The digit may 
then either execute a friction in the reverse direction or be 
brought back to its original position, and execute another in the 
same direction. A certain amount of speed is necessary; on the 
average it may be said that a single friction occupies from one- 
fifth to one-half a second. 

Care should be taken to avoid:— 

1. Applying the pressure too long before beginning the friction, 
and not relaxing it immediately after completing it. 

2. Applying too great a pressure. 

3. Executing the friction too slowly. 

Each of the three above faults results in a dull aching sensation, 
quite unlike the stimulatory one that results if the friction is 
correctly executed. 

4. Not locating the nerve. The mere causing of pain is not 
an indication that the main nerve has been reached. 

5. Moving across the superficial structures, not together with 
them across the nerve. 

From the purely physical point of view, the following major 
effects are induced by nerve frictions when correctly executed. 
Changes arise in the length, thickness, shape, and anatomical 
position of the nerve thus treated, followed by a rapid return to 
the normal; this return may in some cases give rise to a sound 



150 


EDGAR F. CYRIAX 


which can be heard both by patient and operator. (As an example 
of the last mentioned may be cited the facial nerve.) 

1 now pass on to a list of the more important nerves in the 
human body, whose position, size, and shape can be detected by 
nerve friction, mentioning in each case the spot at which these 
frictions can most advantageously be applied, and the direction 
in which this preferably should be done. 


Name. 


Site for Application of 
the Friction. 


Direction in which the 
Friction is to be Applied. 


Supraorbital nerve— 

(a) Before the notch - 

(b) In the forehead 
Supratrochlear nerve 
Nasal nerve - 
Infratrochlear nerve 

Cutaneous branches of 
the lachrymal nerve 

Infraorbital nerve - 

Auriculo-temporal nerve 

Mental nerve - 


Orbital plate of the frontal 
bone 

Forehead - 

Nasal process of the 
superior maxilla 

Lower border of the nasal 
bone 

Nasal process of the 
superior maxilla below 
the supratrochlear nerve 

Anterior edge of the ex¬ 
ternal surface of the 
malar bone 

Across the infraorbital 
foramen 

Half an inch in front of 
the tragus 

Across the mental fora¬ 
men 


Transversely in either 
direction. 

Transversely in either 
direction. 

Above downwards. 

Behind forwards. 

Above downwards. 


Above downwards. 


Above downwards or 
laterally. 

Behind forwards. 

Transversely in either 
direction. 


Facial nerve— 

| (a) Behind the lower jaw 1 

(6) Over the zygoma 1 - 

! Superior laryngeal nerve— 
(a) Internal branch - 


(b) External branch - | 

Recurrent laryngeal nerve! 

Cervical plexus - 

Great occipital nerve— 

(a) As it becomes cut¬ 
aneous 


Posterior border of the 
ascending ramus 

Posterior half of the 
zygoma 

Interval between the hyoid 
bone and the thyroid 
cartilage 

On the alae of the thyroid 
cartilage 

Side of the trachea low 
down 

Anterior edge of the tra¬ 
pezius 

Below the superior curved 
line one inch from the 
middle line 


Above downwards. 
Behind forwards. 

Behind forwards. 

Behind forwards. 
Behind forwards. 
Before backwards. 

Without inwards. 


1 Photographs showing these frictions have been published in Intern . Clin» % 
1912, xxii. S. f i. 41-57. 






TECHNIQUE OF NERVE PALPATION 


151 


Name. 


(6) In the scalp - 
Cervical portion of the 
brachial plexus 
Pudic nerve - 

Suprascapular nerve 

Brachial plexus in the 
axilla 

Median nerve— 

(а) In the axilla - 

(б) In the upper arm * 

(c) At the bend of the 
elbow 

Ulnar nerve— 

(а) In the axilla - 

(б) Upper part of the 

upper arm 

(c) Lower part of the 

upper arm 

(d) At the internal con¬ 

dyle 

Musculo-spiral nerve 

I 

Great sciatic nerve— 

| (a) As it lies between j 

1 the tuber ischii and [ 

the great trochanter | 
(6) In the thigh - - | 

Internal popliteal nerve - | 

Posterior tibial nerve - | 

Internal plantar nerve as 
it lies between the first 
and second metatarsals 
External popliteal nerve 


Site for A implication of 
the Friction. 


Direction in which the 
Friction \» to be Applied. 


Parietal bone - 
Angle formed by the 
clavicle and acromion 
External to the spine of 
the ischium 

Either side of the supra¬ 
scapular fossa 
To either side of the cords 


As for the brachial plexus 


Without inwards. 

Before backwards. 

Transversely in either 
direction. 

Transversely in either 
direction. 

Transversely in either 
direction. 

Transversely in either 
direction. 

Behind forwards. 


Behind inner border of the 
biceps 

Anticubital fossa - - j Within outwards. 


As for the brachial plexus 

As for the median nerve * 

Inner surface of the trioeps 

To either side of the groove 
or just above or below it 
To either side of the groove 

To either side of the nerve 

Either side of the nerve • I 
Either side of the nerve - \ 
Either side of the nerve - j 
Either side of the nerve - j 


Anterior crural nerve 


. i 


Inner side of the biceps 
tendon 

Either side of the nerve, 
just below Poupart’s liga¬ 
ment 


Transversely in either 
direction. 

Transversely in either 
direction. 

Behind forwards. 

Transversely in either 
direction. 

Transversely in either 
direction. 

Transversely in either 
direction. 

Transversely in either 
direction. 

Transversely in either 
direction. 

Transversely in either 
direction. 

Transversely in either 
direction. 

Within outwards. 

Within outwards. 


Before concluding, I should like to make the observation that 
a considerable amount of practice is necessary before becoming an 
adept with the above methods, and that failure at first attempts 
aocurately to define the nerves given in the above list is merely 
another proof of the rule that practice makes perfect 






152 


ABSTRACTS 


Hbstracts. 

ANATOMY. 

ON THE COLLOIDAL STRUCTURE OF NERVE CELLS. (Snr la 
(180) structure colloldale des cellules nerveuses et ses variations it 
l’6tat normal et pathologique.) O. Marinrsco, Joum. dt Neurol ., 
1913, ziii. and xiv., p. 242. 

There can be no doubt that the ultra-microscope is modifying many 
of the accepted views as to the structure of nerve cells. In the 
above important paper, the author shows that Nisei's corpuscles 
are never seen in fresh cells, but can be produced at will by 
various reagents, including metallic salts, acids, and alcohol. 
Fresh cells contain very fine granulations, which vary in colour 
and luminosity according to the locality from which they are 
obtained, and the age of the patient. The absence of Brownian 
movements of these granulations, and the behaviour of the cells 
when treated by solutions of different concentrations show that 
the substance of the cell is of a colloidal nature. The author 
leaves open the question whether the neuro-fibrillar network is 
present before fixation of the cell, but thinks that it possibly may 
be so present. W. D. Wilkins. 


PHYSIOLOGY. 

REGENERATION OF MEDULLATED NERVES IN THE ABSENCE 
(181) OF EMBRYONIC NERVE FIBRES, FOLLOWING EXPERI¬ 
MENTAL NON-TRAUMATIO DEGENERATION. Elbkrd 

Clark, Joum. Comp. Neurol., 1914, xxiv., Feb., p. 61. 

Degeneration of medullated nerve fibres was produced in fowls by 
prolonged feeding on polished rice, and regeneration by a return to 
an adequate nutritive diet. 

In such fowls all traumatic and inflammatory effects produced 
by cutting the tissues or tying the nerve are obviated and the 
possibility of an ingrowth of fibres from other nerves into the 
regenerating nerve is eliminated. The process can also be stopped 
at any stage or greatly prolonged, and several stages of degeneration 
are seen in different fibres of the same nerve. 

Ten to twenty per cent, of the medullated fibre of the nervus 
ischiadicus showed a complete fatty change in their medullary 
sheaths into globules of degenerated myelin and a segmentation or 



ABSTRACTS 


153 


granulation of their axis cylinders. No multiplication of the nuclei 
of the neurilemma sheath could be observed. The fibres merely 
attained new axis cylinders and the medullary sheaths returned 
to normal. By prolonging the degenerative process, proliferation 
of the nuclei of the neurilemma sheath resulted. When this 
occurred the degenerated myelin quickly disappeared from the 
fibre and thus the author thinks the proliferation of the neurilemma 
sheath aids the absorption of degenerated myelin. In regeneration 
a new axis cylinder was attained by outgrowth and in the absence 
of neurilemma proliferation, and grew dowp the old medullary 
sheath which still contained large globules of degenerated myelin 
and fragments of the old axis cylinder. 

No indications of degeneration were observed in the fibres of 
the spinal cord. A. Ninian Bruce. 


PSYCHOLOGY. 

80MB NOTES ON “ TRANSFERENCE.” Smith Ely Jelliffe, Joum. 
(182) Abnorm. Psychol, 1913-1914, Dec., Jan. 

In this paper some observations are made on the forms in which 
transference was revealed to the author, what it taught him to do, 
and what not to do, and how it may be utilised for the purposes of 
furthering the treatment of the patient, or of recognising that for 
this or that patient the situation is not propitious so far as the 
immediate examiner is concerned. “ In this latter case one should 
see one’s duty and retire before an injury is done to the patient's 
belief in psychoanalysis.” The patient may then be able to 
establish a rapport with someone else whose personality fits better 
with his own. H. de M. Alexander. 


THE CASE OF LOUIS BONAPARTE, KINO OF HOLLAND. Ernest 
(183) Jones, Jowm. Abnorm. Psychol , 1913-1914, Dec., Jan. 

The author reviews the life history of Louis Bonaparte, and is of 
the opinion that Louis’ lack of co-operation with Napoleon over a 
period of some seventeen years, extending from a short time 
antecedent to Louis’ short Dutch reign until the end of the 
Empire, as opposed to his enthusiastic support of Napoleon both 
before these years and after them, can be explained on the thesis 
that Louis, though he never became a true paranoiac, certainly 
exhibited definite paranoid tendencies against which (as well as 
the homosexuality from which they sprang) he struggled all his 
life. H. de M. Alexander. 

13 



154 


ABSTRACTS 


CLINICAL NEUROLOGY. 

BULLET WOUND OF THE SPINE. A Case of Medico-Legal 
(184) Interest. W. H. Battle, Lancet, 1914, clxxxvi., Jan. 3, p. 20. 

A man and woman were found shot in a London hotel in October 
1913. The woman was not much hurt. The man showed a round 
bullet wound on the left side just below the nipple, which had 
penetrated the chest through the intercostal space. There was no 
wound of exit. He had retention and complete anaesthesia below 
the waist with loss of all reflexes. The X-rays showed a bullet at the 
level of the body of the seventh dorsal vertebra. It was thought 
to be lying in the spinal canal and laminectomy showed it to be 
situated between the dura mater and the vertebra. It was not 
fixed and easily removed. There was no sign of injury to the bone, 
and as there was no autopsy (the patient dying from cystitis 
after catheterism) it was not possible to say how it reached this 
position. A. Ninian Bruce. 

BILATERAL OCULOMOTOBIUS PALSY FROM SOFTENING IN 
(186) EACH OCULOMOTORIUS NUCLEUS. William Q. Sfillsr, 
La Nevraxe, 1913, xiv.-xv., Dec., p. 126. 

The patient was an officer, aged 52, who developed bilateral oculo- 
motorius palsy in an apoplectic attack. The origin was syphilitic, 
and every muscle supplied by the oculomotorius in each eye was 
implicated. The cause was bilateral softening of two separate 
lesions confined to the nuclei of these nerves. None of the other 
cranial nerves were affected, except the optic, and there were no 
other symptoms except preceding mental disturbance, convulsions, 
and some change in the patellar reflexes, and succeeding dorsal 
extension of each big toe from plantar irritation. 

A. Ninian Bruce. 

TABES AGGRAVATED BY “606” (Tabes aggravd par le “606.") 

(186) Ganeau and Giroux, Ann. da Mai. v4n6r., 1913, viii., p. 297. 

A case of tabes incipiens in a woman aged 38, in whom intra¬ 
venous injections of salvarsan caused amblyopia, malaise and 
transient exacerbations of the lightning pains. 

J. D. Rolleston. 

THE DIAGNOSIS OF TABES DORSALIS. Gordon Holmes, Brit. 

(187) Med. Jovm.y 1914, March 14, p. 673. 

The author discusses the symptoms and physical signs of tabes, 
and concludes that the characteristic subjective and objectively 



ABSTRACTS 


155 


demonstrable disturbances of sensation are usually the earliest, the 
most important, and the most unequivocal clinical signs of tabes 
dorsalis; that they are frequently associated with loss of certain 
of the deep reflexes, especially of the ankle-jerks and knee-jerks, 
and with pupillary, ocular, and other less frequent symptoms and 
physical signs; and that modern serological, cytological, and 
chemical methods can supplement and confirm the clinical 
diagnosis based on these clinical signs, and make the positive or 
negative diagnosis of tabes as certain as anything can be certain 
in clinical medicine. A. N ini an Bruce. 

TABES WITH UNUSUAL DISTRIBUTION OF DEEP-PAIN LOSS. 

<188) Tom A. Williams, Practitioner , 1913, xci., Sept, p. 426. 

Two cases are described in which the perception of deep pain was 
intact in the tendo Achilles and leg, but greatly impaired in the 
thigh, i.e., in the distribution of the upper lumbar roots. 

A. Ninian Bruce. 

THE FIRST OBSERVED CASES OF FRIEDREICH'S ATAXIA IN 

(189) AMERICA. J. H. Kellogg, Med. Record, 1914, lxxxv., March 7, 
p. 431. 

Friedreich first described this peculiar affection in 1863, and 
later in 1864, 1876, and 1878. He regarded it at first as a 
hereditary form of locomotor ataxia. The author points out that 
he published an account of this condition in two brothers in 1875. 
Both died two or three years later. This appears to be the first 
observations of the disease in America. A. Ninian Bruce. 

TONGUE-CHEWING. Bernard Myebs, Brit. Journ. Child. Dis., 1914, 

(190) xi., p. 111. 

Myers records four cases of this hitherto undescribed neurosis, 
and gives the following summary of his paper:— 

“ Tongue-chewing is first noticed about the second year of life 
and persists until middle age, or, perhaps, throughout life. It 
tends to be less noticeable with advancing years. Either sex may 
suffer from it. It occurs, apparently, in healthy families, in which 
certain members suffer from habit-spasms. Several members of 
one family may suffer from it. The habit is inherited, as far as 
one can see, and not copied. The same side of the tongue is 
always chewed in the same individual. The mental condition 
is quite normal, and the general health is not interfered with in 
any way. Bromides stop the tongue-chewing, but in time, after 
leaving off the drug, the habit recommences.” 


J. D. Rolleston. 



156 


ABSTRACTS 


▲ NOTE ON THE ETIOLOGY OF EPIDEMIC POLIOMYELITIS- 

(191) Harold L. Amoss, Joum. Exp. Med., 1914, xix., p. 212. 

The globoid bodies, or minute micro-organisms, cultivated from 
the central nervous organs of human beings and monkeys that 
have succumbed to poliomyelitis, may be detected in the incubated 
brain tissues of infected monkeys in forms indicating post-mortem 
multiplication. Incubating the poliomyelitic tissues in kidney- 
ascitic fluid culture medium, and then crushing them, is a more 
certain method for obtaining cultures of the organism. 

Identical bodies have been detected in blood films prepared on 
the twelfth day of the acute attack from a paralysed poliomyelitic 
monkey inoculated intraspinously. The same organism has been 
cultivated from the blood of a monkey that had received intra¬ 
venously a large dose of a Berkefeld filtrate of poliomyelitic virus. 

No other micro-organisms were detected either in the sections 
of the brain or in film preparations of the blood. These observa¬ 
tions tend to confirm the etiological relationship between the 
minute micro-organism and epidemic poliomyelitis suggested by 
the successful cultivation and inoculation experiments reported 
by Flexner and Noguchi (v. Review, 1913, xL, p. 596). 

A. Ninian Bruce. 


A CONTRIBUTION TO THE EPIDEMIOLOGY OF POLIOMYELITIS. 

(192) Simon Flexner, Paul F. Clark, and Harold L. Amoss, Joum. 
Exp. Med., 1914, xix., p. 195. 

A strain of the poliomyelitic virus was propagated in monkeys 
for four years, during which time it displayed three distinct 
phases of virulence, 'file several phases covered different periods 
of time. At the onset the virulence was low, but by animal 
passages it quickly rose to a maximum; this maximum was 
maintained for about three years, when without known changes in 
the external conditions, a diminution set in and increased, until at 
the expiration of a few months the degree of virulence about 
equalled that present at the beginning of the passages in monkeys. 
The cycle of changes in virulence is correlated with the wave-like 
fluctuation in epidemics of the disease, which also consist of a rise, 
temporary maximum, and fall in the number of cases prevailing. 
And an explanation of epidemics of disease is inferred in variations 
or mutations among the micro-organismal causes of disease affecting 
chiefly the quality of their virulence. A. Ninian Bruce. 



ABSTRACTS 


157 


▲ CONTRIBUTION TO THE PATHOLOGY OF EPIDEMIC POLIO 

(193) MYELITIS. Simon Flexnrb, Paul F. Clark, and Harold L. 

Amoss, Joum. Exp. Med.., 1914, xix., p. 206. 

The virus of poliomyelitis is neurotropic, and localises, and prob¬ 
ably is capable of multiplying, in the extramedullary parenchy¬ 
matous nervous organs. It has been demonstrated by inoculation 
tests in the intervertebral, Gasserian, and abdominal sympathetic 
ganglia. 

All the ganglia show histological lesions, more or less severe, 
similar to those of the spinal cord and brain. The severest occur 
in the intervertebral ganglia, those next in severity in the 
Gasserian, while the mildest appear in the abdominal sympathetic 
ganglia. The interstitial lesions predominate over the parenchy¬ 
matous, and in preparalytic stages the intervertebral ganglia show 
interstitial lesions, especially pronounced at the pial covering. 

Epidemic poliomyelitis is a general disease of the nervous 
system, although the most prominent and important symptoms 
are those following injury to the motor neurones of the spinal cord 
and brain. 

The virus of poliomyelitis is highly resistant to glycerin, in 
which it survives for more than two years; to 05 per cent, 
phenol, in which it survives for more than one year; while it 
succumbs after having been kept frozen constantly for several 
months. It is unsafe to employ phenol to modify the virus of 
poliomyelitis for the purpose of active immunisation. 

The cerebro-spinal fluid of convalescents tends to be devoid of 
the neutralising immunity principles for the virus of poliomyelitis, 
although they may exceptionally be present within this fluid. 
Doubtless the immunity principles are not produced locally in 
the nervous tissues, but elsewhere in the body, and are carried to 
the nervous organs by the blood. A. Ninian Bruce. 

INTRASPINOUS INFECTION IN EXPERIMENTAL POLIO- 

(194) MYELITIS. Paul F. Clark and Harold L. Amoss, Joum. Exp. 

Med., 1914, xix., p. 217. 

By intraspinous injections of specimens of poliomyelitic virus of 
suitable virulence, infection can be caused regularly in Macaco* 
rhesus monkeys. The virus passes from the subarachnoid spaces 
into the nervous tissues in which it multiplies, and into the blood. 

The constant involvement of the pia-arachnoid membranes in 
poliomyelitis, even when no paralysis occurs, and the fact that 
infection can readily be produced by intraspinous inoculation, 
suggests anew that in the pathogenesis of poliomyelitis the inter¬ 
stitial tissue changes within the meninges, blood vessels, and 
ground substance play a determining part. 



158 


ABSTRACTS 


While the virus injected into the subarachnoid spaces can be 
demonstrated there by inoculation tests forty-eight hours after the 
injection, it can no longer be detected on the fifth day, at a time 
when the first symptoms of infection make their appearance. The 
failure of the cerebro-spinal fluid from human and experimental 
cases of poliomyelitis to produce the disease when inoculated into 
monkeys is due to the fact that the virus is either fixed by the 
nervous tissues or passes into the blood. A. N ini an Bruce. 


UNUSUAL MANIFESTATIONS OF POLIOMYELITIS. F. E. Batten, 

(195) Brit. Journ. Child. Dit 1914, xi., p. 97. 

An illustrated record of seven cases:—1. Athetosis of left arm 
and left side of face, flaccid paralysis of left leg and some flaccid 
paralysis of right leg. 2. Poliomyelitis with rigid extension of 
the legs at the hips. 3. Poliomyelitis with flaccid palsy of the 
right arm and left leg with rigidity of the right leg in the 
flexed position. 4. Poliomyelitis of right arm and left leg 
occurring during intra-uterine life. 5. Poliomyelitis and ataxia 
probably due to involvement of cerebellum. 6 and 7. Poliomyelitis 
and toxic neuritis. J. D. Rolleston. 


ENCEPHALITIS IN MUMPS. (Encephalitis bei Mumps.) O. Bien, 

(196) Verhandl. d. Getelltch.f. KinderheHk 1914, xxx., p. 288. 

A previously healthy girl, aged 8 years, had a mild attack of mumps 
at the same time as her brother. Eight days later she suddenly 
had a convulsive attack and lost consciousness. Death took place 
in twenty-four hours. The necropsy revealed an acute lepto¬ 
meningitis and encephalitis. J. D. Rolleston. 

A CASE OF OTITIC MENINGITIS AND CESEBELLAB AB80E8S, 

(197) WITH RECOVERY. A. E. Barnes and W. S. Kerr, Brit. Med. 
Joum., 1914, March 14, p. 587. 

Recovery in otitic meningitis is not very common. The present 
case is that of a girl, aged 17, who suffered from severe occipital 
headache, together with an offensive discharge from the right ear. 
This was followed by delirium, high fever, and head retraction. 
Under anaesthesia a few drops of turbid cerebro-spinal fluid were 
obtained with difficulty. A radical mastoid operation was per¬ 
formed, and a large extra-dural collection of pus was evacuated 
from the posterior fossa. The next day the right external rectus 
was seen to be paralysed, and she continued to improve until five 
days later, when the headache returned and a fresh evacuation 



ABSTRACTS 


159 


of pus was made. The vomiting continued until the drainage 
tube was removed, but she left hospital cured about four months 
after the operation, the paralysis of the external rectus having 
passed off. The organisms found were staphylococci, streptococci, 
Gram-positive diplococci, and a Gram-negative motile bacillus 
resembling B. pyocyaneus. A. Ninian Bruce. 

SYPHILITIC BASAL MENINGITIS FIVE MONTHS AFTER IN- 
098) FBOTION. (Syfilitisk Basalmeningitis 5 Maaneden after 
Infektionen.) C. Rasch, Hoepitalstidende , 1914, IviL, p. 127. 

A man, aged 20, developed a urethral chancre in November, his first 
and only coitus having taken place in September. He was treated 
with mercurial inunctions, of which he had forty-three between 
December and the beginning of February, an intravenous injection 
of 50 cgm. salvarsan and an intramuscular injection of 50 cgm. 
salvarsan. At the end of February he developed extreme giddiness 
and facial paralysis. The cerebro-spinal fluid contained an excess of 
albumen and a well-marked lymphocytosis. Wassermann negative 
both in blood and in cerebro-spinal fluid. The diagnosis of basal 
meningitis with neuritis of vii. and viii. was made. The symptoms 
disappeared in a month’s time under treatment with mercurial 
inunctions, sarsaparilla, and hectin. J. D. Rolleston. 

B RAIN ABSCESS DUE TO THE BACILLUS COLI COMMUNIS. 

(199) E. P. Bernstein, Med. Record , 1914, lxxxv., p. 249. 

A case of abscess in the posterior part of the left temporo- 
sphenoidal lobe in a woman, aged 24, secondary to purulent otitis 
media. B. coli was found in the pus from the ear during life, and 
in the abscess post mortem. The mode of transmission of the 
germ must have been by the lymphatics, as no thrombosis of the 
petrous sinus was found at the necropsy. J. D. Rolleston. 

A CASE OF RECKLINGHAUSEN’S DISEASE. (Uncas de maladie de 

(200) Recklinghausen.) J. Rebattu and J. Martin, Lyon mid., 1914 , 
cxxii., p. 19. 

The patient was a man, aged 68, free from syphilis or tuberculosis 
and with no family history. He presented at least 2,500 cutaneous 
tumours and very numerous pigment patches which had first 
appeared after the age of 30. There were no tumours on the 
nerves and no nerve tissue was found in the tumours. The 
mental faculties were much below normal, but it was difficult to 
say if this deficit was recent or congenital. There were no skeletal 
deformities nor signs of disturbance of the glands of internal 
secretion. J. D. Rolleston. 



160 


ABSTRACTS 


A 0A8B OF TYPHOID SPINE. (XJn cas de spondylite typhique.) 

(201) Philibert, Rev. cCOrthop&lie, 1918, 3 a6r., v-, p. 409. 

A boy, aged 14| years, had an attack of typhoid fever with a 
severe relapse. Five days after the temperature had become 
normal, he began to suffer from severe lumbar pain radiating into 
the right buttock and great trochanter, and an angular cyphosis 
appeared involving the second, third and fourth lumbar vertebrae. 
The X-rays showed the changes described by Bonhoure (®. Review, 
1913, xi., p. 281). The patient was immobilised in a plaster jacket, 
and recovery took place in about two months. 

J. D. Rolleston. 

VENESECTION IN CEREBRAL HAEMORRHAGE, WITH REPORT 

(202) OF OASES. A. Macfarlane, Med. Record, 1914, lxxxv., p. 112. 

A record of four cases:— 

1. Man, aged 44, excessive smoker and hearty eater. Gradual 
onset of left hemiplegia. Blood pressure, 235 mm.; 12 oz. of blood 
removed from right arm with marked improvement. The next 
day 1| pints were drawn from a varicose vein in the leg, and on 
the following day 10 more oz. The blood pressure dropped to 
180 mm., ana gradually rose to 200 mm. In eight weeks he was 
able to walk without assistance. 

2. Woman, aged 54. Had had two seizures during the last 
two years, one said to be uraemic, and the other slight cerebral 
haemorrhage, from which she had recovered without paralysis. 
Sudden onset of left hemiplegia rapidly followed by coma. 12 oz. 
of blood were drawn from arm, and blood pressure sank from 
260 mm. to 185 mm. within an hour, but without improvement in 
the comatose condition. Death occurred in a few days. 

3. Woman, aged 65. Cerebral congestion without vascular 
rupture. Blood pressure, 260 mm.; fell to 175 mm. after vene¬ 
section, and recovery took place. 

4. Man, aged 70. Weakness of one side, which quickly 

developed into hemiplegia. Rapid improvement after removal of 
3 pints of blood from median basilic. He lived several years after 
this attack. J. D. Rolleston. 

A FAMILY WITH CEREBELLAR ATAXIA. C. A. Sprawson, 

(203) Brit Med. Jowm., 1914, Jan. 3, p. 23. 

A Eurasian male, aged 35, complained of tremors on standing 
and giddiness of about three and a half years’ duration. His 
father was similarly affected, the symptoms developing about the 
age of 50, and three brothers also suffered from the same condition, 
although their children are apparently healthy, but are still all 
below puberty. A genealogical table of the family is given. 

A. Ninian Bruce. 



ABSTRACTS 


161 


A GA8B OF HEREDITARY ATAXIA WITH PARAMYOCLONUS 
(SOI) MULTIPLEX. (Ataxto h<r6ditaire avec paramyoclonus multi* 
plex type Unverricht.) Gaktano Boschi, Joum. de Neurol., 1913, 
viii, p. 142. 

A full clinical account of a case that combined the symptoms of 
hereditary ataxia with those of paramyoclonus multiplex, and had 
also attacks of an epileptic character. The author accepts the 
view that hereditary ataxia is a clinical entity, Friedreich’s ataxia 
and the cerebellar heredo-ataxia of Marie being sub-varieties, often 
merging one into the other. The case described emphasises this 
point, as the patient differed from the Friedreich type in that his 
knee-jerks were exaggerated, and he had no nystagmus and no 
deformities. On the other hand, he did not present the ocular 
symptoms characteristic of Marie’s type. 

The patient also presented the symptoms of the second disease 
associated with the name of Friedreich, viz.: Paramyoclonus 
multiplex, but as the myoclonus was of a familial character and 
was associated with epilepsy, the author considers that the case 
falls under the category of the type described by Unverricht, and 
characterised by this triad of symptoms. It is interesting to note 
that a brother of the patient suffered from Friedreich’s type of 
hereditary ataxia, and a second from Marie’s type, the patient 
himself presenting symptoms from each type. 

W. D. Wilkins. 

FAMILIAL FORMS OF WILSON’S LENTICULAR DBGENERA- 
(206) TION AND WESTPHAL-STRttMPELL’S PSEUDOSCLEROSIS. 
(Zur Klinik famili&rer Formen der Wilsonschen Lenticularde- 
generation und der Westphal-Striimpellschen Pseudosklerose.) 

H. Higibb, Zttchr. f. d. get. Neurol, u. Psychiat ., 1914, xxiii (Orig.), 
S. 290. 

Thk author discusses these two diseases and considers that they 
are closely allied to one another, both being familial, rarely 
hereditary, and both being accompanied by liver changes. Both 
may be present in the same family. A. Ninian Bruce. 

FURTHER NOTE UPON A CASE OF HYSTERICAL MONOPLEGIA 
<206) FOLLOWING ELECTRIC SHOCK. Pobvbs Stewabt, Brit. Med. 
Joum., 1914, March 7, p. 626; Proe. Boy. Soc. Med., 1914, vii., Feb. 
(Neurol. Sect.), p. 41. 

This case has already been abstracted (t\ p. 44). The paralysed 
left upper arm showed no improvement from suggestive treatment, 
strong electrical stimulation, cutaneous irritants, or psycho-therapy. 
He was then given ether and nitrous oxide with plenty of air so 



ABSTRACTS 


H)2 

as to prolong the stage of excitement. The normal arm was 
bound to the trunk by a bandage, and the paralysed left arm was 
allowed to hang free. Within a few seconds, while the anaesthetic 
was being administered, the patient began to make slight move¬ 
ments of the paralysed arm, amounting shortly to violent fighting 
movements, in which he tried to snatch the mask out of the hands 
of the amesthetist. The anaesthesia was stopped and he remained 
in a hypnotic state, during which voluntary movements were 
normally performed in response to verbal commands. He has 
since remained well. A. Ninian Bruce. 

A CASE OF PITUITARY TUMOUR AND SELLAR DECOM- 
(207) PRESSION. Wilfred Harris and Cecil Qkaham, Lancet , 1913, 
clxxxv., Nov. 1, p. 1251. 

The symptoms produced by a tumour of the pituitary body may be 
divided into three groups: (1) Those produced by pressure on 
neighbouring structures, especially the optic chiasma and optic 
nerves, causing gradual failure of vision due to optic atrophy, 
central scotoma, bitemporal hemianopia, &c. (2) Those produced 

by general rise of intracranial pressure, c.g., hemiplegia, slow pulse, 
torpor, failing memory or optic neuritis. (3) Those due to inter¬ 
ference with the secretion of the gland itself, e.g., acromegaly, 
gigantism, infantilism, &e. 

The case here recorded is that of a woman, aged 38, who 
suffered from persistent headache, sleepiness, apathy, and gradual 
loss of vision. The right eye was found to be blind and the left 
showed temporal hemianopia, the left plantar reflex was extensor. 
Skiagram of the skull showed an enlarged and boat-shaped sella 
turcica. As she became more and more torpid, decompression was 
decided on through the base of the sphenoid into the sella turcica 
by the intranasal route. The operation is described at length and 
the different steps clearly indicated. It was successful, as the 
patient recovered consciousness, rapidly improved and left the 
hospital to stay with some friends in the country, apparently 
relieved of all her symptoms. Ever since the operation, however, 
she had suffered from great thirst and polyuria. Three weeks after 
leaving the hospital the headache and drowsiness returned. A second 
operation was performed, and a piece of growth of a papillomatous 
nature removed, but she suddenly collapsed thirty hours later. 

At the autopsy an encapsulated growth the size of a small golf 
ball was found in the position of the infundibulum in the floor of 
the third ventricle distorting the optic tracts and raising the basal 
ganglia. The fossa contained a markedly compressed pituitary 
gland, but no more growth was found in the fossa. Microscopically 
it was diagnosed as a perithelioma. A. Ninian Bruce. 



ABSTRACTS 


163 


A OASE OF DIABETES INSIPIDUS. W. P. Herring ham, Lancet , 

(208) 1914, clxxxvi., Jan. 3, p. 16. 

A case in a boy, aged 20, is recorded. On an ordinary diet he 
passed about 8 litres of urine, the specific gravity of which 
was 1,002 or 1,003. Sugar and albumen were lioth absent. Re¬ 
moval of salt from the diet produced no diminution in this amount. 
Restriction in the amount of fluid taken lessened the output of 
urine, but produced also loss of weight, great thirst, and loss of 
appetite, and had to be discontinued. Codeine resulted in a steady 
diminution until only about 4 litres were passed daily 

A. Ninian Bruce. 

A OASE OF MOTOR IMBECILITY. (Un cas d’insufflsance motrice.) 

(209) Decroly and E. Henrotin, Joum. de Neurol ., 1913, x. and xv., 

p. 181. 

The child described in this paper was at first looked upon as an 
imbecile of the usual type, but careful study showed that the 
delayed mental growth was due almost entirely to an inco¬ 
ordination of the muscles, especially of the tongue, eyes and neck, 
but also affecting the limbs, which resulted in an inability to make 
use of the impressions received in childhood. The authors 
contend that it is not uncommon for such cases to be passed over 
as simple cases of imbecility or idiocy, whereas they should be 
looked upon as a form of imbecility due to deprivation of the 
motor functions, analogous to that due to deprivation of the special 
senses. The inco-ordination was probably due to an infantile 
pseudo-bulbar paralysis. W. D. Wilkins. 

TERTIARY SYPHILITIC FEVER AND SYPHILITIC POTT’S 

(210) DISEASE. (Febbre sifllitica terziaria e morbo di Pott sifllitico.) 
G. Cappkllo, Gazz. d. osp ., 1914, xxxv., p. 201. 

A record of two cases in women, one of whom showed syphilitic 
spondylitis and periostitis of the tibia. The fever in both was of 
an intermittent type, and rapidly subsided under anti-syphilitic 
treatment. J. D. Rolleston. 

THE TREATMENT OF SYPHILIS OF THE NERVOUS SYSTEM 

(211) BY INTRATHECAL INJECTIONS. Harry Campbell, Brit. 
Med. Joum., 1914, March 14, p. 577. 

Ten cases are briefly described (five being tabes, two tabo-paresis, 
one general paralysis, and two interstitial syphilis). They were 
given 0*9 gram neosalvarsan intravenously. After a week this was 
repeated, and two hours later 4 oz. of blood were drawn off from a 
vein and placed in a jar containing 1 in 20 carbolic solution. 



164 


ABSTRACTS 


After twelve hours sufficient serum had separated for injection. 
It was then injected by lumbar puncture in the usual way. Im¬ 
provement resulted, in some of the cases being very marked. 

A. Ninlan Bruce. 




NEOSALVARSAN. LATE 

(212) Hdmipldgie tardive. Mort) 

p. 282. 


PLEGIA. DEATH. (NSo-salvarsan. 

Carle, Ann. de mal. vinir., 1913, viii., 


A man and his wife were injected intravenously the same day with 
0*45 gr. neosalvarsan. The woman, who had been infected by her 
husband, was of a nervous disposition, but not hysterical or 
epileptic. She had had four years regular treatment with mercury 
and potassium iodide, but had suffered frequently from intermittent 
headache at night The man bore the injection well, but the 
week following the injection the wife’s headache got worse, and 
six weeks later she developed right hemiplegia. Rapid improve¬ 
ment followed injections of benzoate of mercury, but left hemi¬ 
plegia subsequently occurred, and death took place six months 
after the injection of neosalvarsan. J. D. Rolleston. 


INFLAMMATION OF THE LABYRINTH AFTER INJECTION OF 

(213) NEOSALVARSAN. (Labyrinthite aprts injections de ndo- 
salvarsan.) Meneau, Gaz. held. d. Set. mid. de Bordeaux , 1914, 
xxxv., p. 79. 

Meneau has collected three cases:— 

(1) De Asna’s case. A man, aged 26, suffering from severe 
syphilis and tuberculosis, suddenly developed bilateral deafness 
on the day following the third injection of neosalvarsan. Im¬ 
provement occurred after the fourth, and still more so after the 
fifth injection. The deafness was regarded as a manifestation of 
nerve syphilis. 

(2) Sommer Greco’s case. A man, aged 25, after the fourth 
injection of neosalvarsan, had a rise of temperature and loss of 
hearing in the right ear. 

(3) Gray’s case (v. Review, 1913, xi., p. 339). 

J. D. Rolleston. " 


WAS8ERMANN POSITIVE AFTER FORTY-SIX YEARS OF 

(214) SYPHILIS. SYPHILITIC VARICOSE ULCERS. (Wasser- 
mann positif aprds quarante-six axis de syphilis. Ulc&res vari- 
queux syphilitiques.) Meaux Saint-Marc, Ann. dee Mai. vinir., 
1913, viii., p. 289. 

The patient was a man, aged 63, who had contracted syphilis at 
17, for which he had undergone regular treatment. 

J. D. Rolleston. 



ABSTRACTS 


165 


THE TECHNIQUE OF THE WAB8ERMANN REACTION. With 
(216) special reference to the use of antigens containing cholesterin. 
Carl H. Browning, Lancet , 1914, cixxxvi, March 14, p. 740. 

Accuracy and delicacy in performing the Wassermann reaction 
may be attained by attention to the following points:— 

1. The accurate measurement of the amount of complement 
absorbed by the mixture of (heated) serum and of antigen, 
estimated in haemolytic doses, and controlled by an estimation of 
the amount of complement inhibited by each component separately. 

2. Complement is not an invariable quantity. Not merely do 
different guinea-pigs yield serum with varying haemolytic power 
for sensitised blood corpuscles, but the deviability of two comple¬ 
ment-containing sera with the same haemolytic dose may show a 
wide difference. To control these variations known negative and 
positive sera, whose behaviour has been determined in previous 
tests, should be included in every series. An average specimen 
of complement can be obtained with some degree of certainty by 
using the pooled serum of ten to twelve guinea-pigs. 

3. The test corpuscles should be sensitised to the maximal 
degree by the addition of at least five doses of specific immune 
serum (from the rabbit). 

4. The “ antigen ” should itself possess little haemolytic or anti¬ 

complement action. Antigens which are highly satisfactory in 
these and in other respects can be obtained by employing alcoholic 
mixtures of cholesterin with certain other tissue lipoids. Choles¬ 
terin possesses a remarkable specific action in the presence of 
syphilitic sera together with certain tissue lipoids, and thus has 
proved of great practical value in eliciting the Wassermann 
reaction. A. Ninian Bruce. 

VARIETIES OF FACIAL SPASM AND THEIR TREATMENT. 

(216) E. Farquhar Buzzard, Practitioner, 1913, xci., Dec., p. 746. 

From a pathological point of view, spasms of the face may be 
divided into three main classes: (1) psychogenic, (2) cortical, and 
(3) peripheral. These are briefly discussed, attention being 
specially paid under the third heading to chronic facio-spasm 
(which may be treated by alcohol injection into the facial nerve), 
post-paralytic contracture and “ fibrillo-tonic facial spasm ” (a rare 
manifestation of cerebro-spinal syphilis). A Ninian Bruce. 

THE PATHOLOGY OF MIGRAINE J. R. Chablss, Practitioner, 1913, 

(217) xci., Sept, p. 414. 

The author considers that the clinical features of migraine may 
be explained satisfactorily as due to periodical enlargement of the 



166 


ABSTRACTS 


pituitary gland. He explains the headache, nausea, and vomiting 
as the result of increased intracranial pressure, the disturbance of 
vision (mainly hemianopia) from pressure, and the fortification 
figures, &c., from irritation of the optic tracts, the vasomotor 
phenomena from increased secretion from the posterior lobe, or 
from pressure on sympathetic fibres, and the sensory and motor 
symptoms from pressure on the crus. A. Ninian Bruce. 

ST HILDEGABD. C. Singer, Proc. Roy. Soc. Med., 1913, viL (Section of 

(218) Hist. of Med.), p. 1. 

The medical interest of this twelfth-century nun lies in the fact 
that much of the text of her book “ Scivias ” is presented in the form 
of visions. The illustrations show that the physical basis of these 
visions were migraine or scintillating scotoma, typical fortification 
figures, stare and coloured spots being represented. In some 
cases a shimmering concentric appearance occupies the whole field 
of vision. There is also evidence from her writings that Hildegard, 
who in spite of her active life had very poor health, suffered from 
migraine. J. D. Rolleston. 

MEASUREMENT OF THE BLOOD-PRESSURE IN ALCOHOLISM 

(219) AND FUNCTIONAL NEUROSES EXCLUDING CIRCULATORY 
DISTURBANCES. (Blutdruckmessungen bei Alkoholikem und 
functionellen Neurosen mit Ausschluss von Kreislaufstdrungen.) 
K. Raff, Deut. Arch.f. klin. Med., 1913, cxii., p. 209. 

Alcoholism. —Forty-one cases of chronic alcoholism in which the 
heart and kidneys were normal were examined with Reckling¬ 
hausen’s tonometer, with the following results:— 

1. A considerable rise of the systolic blood-pressure in the first 
few days of total abstinence in hospital. 

2. An almost constant level of the diastolic blood-pressure 
throughout the whole period of observation so that the increase 
in pulse-pressure was obviously due to a rise of the systolic 
pressure. 

3. This feature of the blood-pressure is so constant that in 
doubtful cases it is of diagnostic value. 

Functional Neuroses .—Fifteen cases of hysteria and five of 
neurasthenia were examined with the following results:— 

1. In hysteria lability of the systolic and diastolic blood- 
pressures predominates, and is the only constant change in the 
blood-pressure in this disease. 

2. In neurasthenia a tendency to hypertension of the systolic 

pressure predominates, and the diastolic pressure shows only slight 
variations. J. D. Rolleston. 



ABSTRACTS 


167 


CA8E WITH COMMENTS. EFFECT ON THE MENTAL STATE OF 

(220) MINOR AND MAJOR ATTACKS IN EPILEPTIC INSANITY. 

S. J. A. H. Walshb, Practitioner , 1913, xci., Nov., p. 715. 

The patient was a man, aged 25, who had suffered from epilepsy 
since the age of 7. He never had an aura, but the attacks were 
preceded by delusions. These delusions were of two kinds, slight 
delusions which lasted for from one to four days, and culminated 
in one or two attacks of petit mal ; and delusions which lasted a 
fortnight or longer and terminated in an attack of grand mal, or if 
the delusional state had been prolonged sufficiently a second 
major attack was necessary. If a major attack were deferred a 
maniacal outburst usually occurred. The epileptic seizures thus 
seemed to act as a safety-valve to the mental state to which the 
patient was at times subjected. A. Ninian Bruce. 

ADDISON’S DISEASE IN A BOY, WITH CALCIFICATION OF THE 

(221) ADRENALS, WITH REMARKS. H. D. Rolleston and £. J. 
Boyd, Brit. Jowrn. Child. Die ., 1914, xi., p. 105. 

A boy, aged 12f years, showed general bronzing of the skin, 
especially round the nipple, umbilicus, and pudenda. There was 
a pigmented scar in the right groin, but on the right side of the 
abdomen and thorax there were pale scars exactly like those left 
by herpes zoster. The systolic blood-pressure ranged between 
64 and 84 mm. Hg, and the boy was listless, sleepy, and sunken¬ 
eyed. The X-rays showed very definite calcareous particles in the 
region of the last rib and suprarenal on the right, and less definite 
ones on the left side. There were discrete opacities at the hilum 
of the lungs suggesting calcified nodules. Adrenalin chloride 
solution by mouth, and later sandwiches containing raw adrenal 
glands, were followed by an increase in the pigmentation. 
Rolleston suggests that the absence of pigmentation in the 
herpetic scare was due to impaired innervation, and regards this 
as an argument in favour of the view that the bronzing of the 
skin in Addison’s disease is due to nerve irritation. 

J. D. Rolleston. 

ETIOLOGY OF ENDEMIC CRETINISM, CONGENITAL GOITRE, 

(222) AND CONGENITAL PARATHYROID DISEASE. Robert 
M'Carrison, Lancet, 1914, clxxxvi., March 21, p. 817. 

As the results of experiments upon rats, the author concludes:— 
1. Of the offspring of goitrous parents a small percentage are 
born cretins; approximately 63 per cent, are born with congenital 
goitre, 32 per cent, with congenital parathyroid disease, and 33 
per cent, are bom with normal thyroid and parathyroid glands. 



168 


ABSTRACTS 


2. Cretinism and congenital goitre are due to the action of toxic 
substances derived from the intestines of the goitrous mother on 
the foetal thyro-parathyroid mechanism. Cretinism represents 
the maximum, and comparatively rare, effect of these toxins, 
congenital goitre their minimum, and comparatively common, 
effect. 3. Congenital parathyroid disease is due to the action on 
the foetal gland of the toxic products of organisms, present in the 
intestine of the goitrous mother, which are capable of growth 
under anaerobic conditions. A. Ninian Bruce. 

THE PATHOLOGY OF PELLAGRA. S. A. Kinkier Wilson, Proc. 

(223) Roy. Soc. Med., 1914, vil, Feb. (Neurol Sec.), p. 31. 

This preliminary paper is based on thirteen cases of pellagra. 
Abundant pathological evidence was found of a widespread 
generalised toxaemia of the peripheral and central nervous system. 
Pellagra is readily distinguishable from the trypanosome diseases. 
The histological changes are not those of an infection of blood- or 
lymph-stream. Special attention is drawn to the presence of the 
ir granules of Reich in the peripheral nerves. These are collec¬ 
tions of minute granules or flakes, all small, which stain brilliant 
violet-red with thionin blue. According to Reich, they consist of 
protagon, and are special products of the metabolism of myelin. 
They do not stain with osmic acid. It is difficult to say when a 
toxaemia of the peripheral nerves becomes a true neuritis, but in 
some cases at least parenchymatous and interstitial neuritis occurs, 
but whether these changes precede or succeed the changes in the 
cord is uncertain. Probably an ascending toxic lymph-stream 
invades the cord via the lumbar and dorsal posterior roots, and that 
the effects of the toxsemia appear either simultaneously in the 
nerves and cord, or previously in the former. Possibly the toxin 
is of alimentary origin, and there is no pathological evidence to 
disprove this. 

There is no single pathological feature of itself pathognomic of 
pellagra, the pathological process being essentially diffuse and 
unsystematised. A. Ninian Bruce. 

ZEISM OR PELLAGRA? P. A. Nightingale, Brit. Med. Joum., 1914, 

(224) Feb. 7, p. 300. 

Beri-beri, scurvy, pellagra, and zeism form a group of diseases 
almost by themselves. “ Zeism ” is a disease found in the Victoria 
Gaol, Rhodesia, and the author has examined forty cases. It was 
found that prisoners fed on mealie meal developed this disease, 
while those fed on rapoko meal did not. The difference between 
these two meals is that the rapoko is hand-milled and contains 



ABSTRACTS 


169 


the whole husk, while the mealie meal is steam-milled to a fineness 
which allows 75 per cent, to pass through a 30-inch mesh sieve, 
and thus a large proportion of the husk must be discarded. This 
discarded husk is of great nutritive value and is used for feeding 
cows. Prisoners who had been fed on mealie meal and contracted 
the disease invariably improve under rapoko meal. Zeism closely 
resembles pellagra in its alimentary symptoms, but differs consider¬ 
ably from it in its cutaneous, and bears no relationship at all to 
its nervous symptoms. The prognosis is good. The etiology 
appears to be directly opposed to any insect-borne theory, and if 
the view that pellagra is insect-borne be correct, zeism would not 
appear to be the same disease. A. Ninian Brxjce. 

THE ANALYSIS OF NYSTAGMUS. Adolphe Abrahams, Lancet , 
(225) 1913, May 31. 

This paper, which is an abstract of the author’s thesis for the 
degree of M.D. Cantab., deals firstly with the history of previous 
work in nystagmography, and then with the special instruments 
and methods employed by the author himself. A specially 
designed cinematograph camera made by the Kinrora Company of 
London was used. 

Charts are given of the movements in cases of post-rotation 
nystagmus and spontaneous nystagmus of non-vestibular origin. 

Miners’ nystagmus proved impossible to analyse by this 
method, as the movements are too small and too rapid for cinemato¬ 
graphy. The paper closes with a short note on the varieties of 
nystagmus and extensive bibliography. H. M. Traquair. 


PSYCHIATRY. 

THE SEBUM AND GEBEBBO-SPINAL FLUID BEAOTIONS AND 
(226) SIGNS OF GENEBAL PARALYSIS. George M. Robertson, 
Joum. of Mental Sci., 1914, Jan., p. 1. 

An eminently useful and practical statement of the present 
position of the clinical methods now in use for the diagnosis of 
general paralysis. The author describes in detail how the serum 
and cerebro-spinal fluid may be obtained and examined, and dis¬ 
cusses the importance, both actual and relative, of each of the six 
methods employed by him. His opinion is in agreement with 
that of the majority of clinicians in that he ascribes paramount 
importance to the presence of the Wassermann reaction in the 
cerebro-spinal fluid, and uses the other tests for confirmatory 
evidence. 

These reactions are also present in cerebral syphilis, but this 


i4 



170 


ABSTRACTS 


can be distinguished by the administration of salvarsan, which 
rapidly renders the reactions negative, whereas it has little or no 
effect on the reactions in cases of general paralysis. 

W. D. Wilkins. 

SUDDEN DEATH FROM BULBAE HAEMORRHAGE IN A CASE 

(227) OF DEMENTIA PRJSCOX. (Morte improvisa per emorragie 
bnlbari in on caso di demenza precoce.) Vincknzo Scarpxni, 
Rattegna di Studi Ptichiat., 1914, iv., Marzo-Aprile, p. 307. 

The author records the presence of a large number of haemorrhages 
in the medulla oblongata below the floor of the fourth ventricle in 
a case of dementia praecox, which died suddenly and unexpectedly. 
These also involved the nucleus of the vagus. The author 
emphasises their importance. A. N ini AN Bbuce. 

THE TREATMENT OF SYPHILITIC PSYCHOSES. (Essai da traite- 

(228) ment des psychoses d’origine syphilitiqne.) H. Damayb, Arch. 
Intemat. dc Neurol., 1914, xxxvi., March, p. 142. 

A detailed account is given of two cases treated with encouraging 
results; in both there were cardiac and renal lesions present. 
Damaye sums up his principles of treatment of syphilitic psychoses 
thus: In the first stage improve the general state by raw meat, 
taw eggs, iodised antiscorbutic syrup, guaiacolised cod-liver oil, and 
arsenic by large doses of cacodylate of soda. This treatment 
greatly improves the mental state. In the next stage, when the 
physical condition has become satisfactory, continue raw meat and 
eggs and super-alimentation, and begin antisyphilitic treatment, at 
first injections of atoxyl or hectine, and then mercurials. The 
previous stage of super-alimentation enables the patient to tolerate 
mercurial treatment. One can alternate the periods of arseuical 
and mercurial treatment ; at the same time some iodide of 
potassium is given. When thus carried out, the treatment of 
syphilitic psychoses, of whatever type they may be, gives always 
good and sometimes excellent results. One can thus arrest the 
evolution of the meningo-encephalitic or encephalitic lesions, and 
obtain their recovery either entirely or as nearly so as is possible. 

Leonard J. Kidd. 

ON THE STRUCTURE OF THE BRAIN AND THE INTERPRE- 

(229) TATION OF MENTAL PHENOMENA IN RELATION TO 
THE LAW. M. Pazzi, Rattegna di Studi Ptichiat., 1913, iii, 
Maggio-Guigno, p. 200. 

The author deplores the fact that, under the present laws, 
infanticide ranks at the same level as the common crimes. 
Pregnancy produces psychical reactions which show a diminution 
of the inhibitory influences of the cerebral cortex and a relative 



ABSTRACTS 


171 


functional autonomy of the lower centres; infanticide is a result 
of this paralysis of inhibition. When such an act has occurred, 
it is for the physician to judge how far the mother is to be 
regarded as accountable for the act. As the psychology of 
pregnancy is only to be understood by woman, movement in this 
direction must come from her. A. N ini an Bruce. 

the albumen in the CEREBROSFINAL fluid IN CASES 

(230) OF MENTAL DISEASE H. D. MacPhail, Joum. of Mental Set., 
1914, Jan., p. 73. 

The quantity of albumen in the cerebro-spinal fluid was estimated 
in cases of the principal mental diseases, including some arising 
from gross brain lesions and plumbism. The author states that if 
the amount of albumen is 1 per cent, or over the case is almost 
certainly one of general paralysis, and that in other cases the 
amount of albumen is a fair criterion of the amount of damage 
done to the cerebral tissue. W. D. Wilkins. 

THE CLINICAL VALUE AND SIGNIFICANCE OF LEUOOCYTOSIS 

(231) IN MENTAL DISEASE D. J. Jackson, Joum. of Mental Sci., 
1914, Jan., p. 66. 

The author has made daily leucocyte counts in cases of the chief 
mental diseases, and has found remissions or recoveries to be 
usually accompanied by a leucocytosis, especially of the polymorphs. 
This is most typically found in the acute confusional states, but is 
also well marked in manic-depressives. In general paralysis it 
was found that whilst remissions were accompanied, as before, by 
a polynucleocytosis, seizures were heralded by a lymphocytosis. 
Epileptics showed an increase in the polymorphs just before a fit, 
and a diminution between the fits. 

The author considers that artificial leucocytosis produced by 
the injection of terebene has had a favourable influence in several 
cases, and that remissions in general paralysis may be prolonged 
by the use of tuberculin. 

It is remarkable that many of the convalescent cases retained 
the abnormally high number of 27,000 leucocytes per c.mm. for 
weeks before discharge, and apparently showed no signs of a return 
to a more normal percentage. W. D. Wilkins. 

VACCINE TREATMENT IN ASYLUMS. W. Ford Robertson, Joum. 

(232) of Mental Sci., 1914, Jan., p. 17. 

The author discusses the vaccine treatment of many of the common 
ailments and diseases to which asylum patients are liable, and 
contends that it might be much more extensively practised than 
is at present the case. He gives full particulars of the prepara- 



172 


ABSTRACTS 


tion and dosage of autogenous vaccines, and gives the indications 
for their employment. 

Stress is laid upon the secondary infections in general paralysis 
and tabes, especially by bacilli of the diphtheroid type, and support 
is given to the view that these infections may determine the onset 
of general paralysis in a syphilitic subject. W. D. Wilkins. 

THE VILLA OS COLONY SYSTEM FOB THE CABE AND TREAT 

(233) MENT OF CASES OF MENTAL DISEASE T. E. Knowles 
Stansfield, Joum. of Mental Set., 1914, Jan., p. 30. 

A strong plea in favour of the villa type of asylum, as exem¬ 
plified by the author’s experience at Bexley Asylum, and by his 
knowledge of German and American institutions. He states that 
he is able at Bexley to have about 170 male patients on complete 
parole of the asylum estate, and that the number of escapes is 
negligible. He claims that the patients are happier, work better, 
and are more contented, and that a greater variety of treatment 
can be given, ranging from the close supervision of acute cases to 
the almost complete parole for convalescent patients. He also 
claims that the first cost is less, and the difficulties of administra¬ 
tion are no greater than with the barrack system. 

W. D. Wilkins. 

THE WEIGHT OF THE PANCREAS IN THE INSANE. (Recharches 

(234) ponddrales but le pancreas chez les alidnds.) C. Parhon, di 
Jassy, and G. Zuoravu, Arch. Intemat. de Neurol., 1914, xxxvi., 
March, p. 137. 

The authors examined the weight of the pancreas in 240 adult 
cases of insanity; it was found to be heavier in the male sex. 
Testut gives the average as 70 gr. for man and 66 for women. 
The average weights in the various psychoses were as follows: 
in alcoholism 79*37, mental confusion 78*62, G.P.I. 78*34, pellagra 
69*60, dementia prsecox 69, epilepsy 65, imbecility 65, mental 
debility 61, and senile dementia 55*43 gr. The importance of 
toxic and digestive disturbances in several of these groups is 
insisted on. Thus, the pancreas is heaviest in those psychoses in 
which gastro-intestinal intoxication plays an important part. It 
is uncertain whether these toxic substances act primarily on the 
pancreas or whether its hypertrophy is due to hepatic troubles (the 
liver being regarded as antagonistic to the pancreas). The low 
average weight in the senile dements is probably due partly to 
atrophic changes and partly to the fact that most of these patients 
were females. Out of the 240 cases the commonest weight was 
70 gr. (41 cases), then come 28 cases of 60 gr., 24 of 50 gr., 22 of 
80 gr., 19 of 100 gr., 18 of 90 gr., and 14 of 75 gr. The greatest 



REVIEW 


173 


weight was 150 gr. in a male 6.P.I. (compare this paper with 
the author's one on the adrenals, v. Review, 1913, xi., p. 619). 

Leonard J. Kidd. 


TREATMENT. 

PINEAL GLAND IN TREATMENT OF CERTAIN GLASSES OF 
(235) DEFECTIVE CHILDREN. W. N. Berkeley, Med. Record, 1914 
March 21, p. 512. 

Mainly a shortened account of Dana and Berkeley’s paper (v. 
Review, 1913, xi., p. 274). Berkeley adds that in about a dozen cases 
of premature mental failure in middle-aged or elderly persons, 
showing no distinct organic lesion, a fair trial of bullocks’ pineals 
in capsules has given good results; some of these patients show 
cheerfulness and increased mental activity while taking pineal, so 
that it seems as if it “ stimulates the ageing brain to the faster 
chemistry of younger days.” Berkeley insists on the importance 
of keeping up pineal medication regularly for at least four to six 
months in the case of backward children or Mongols on whom it is 
being tried. Leonard J. Kidd. 


"Review. 

THE INTERNAL SECRETORY ORGANS: THEIR PHYSIOLOGY 
(236) AND PATHOLOGY. Prof. Artub Biedl. With an intro¬ 
ductory preface by Leonard Williams. Translated by Linda 
Forster. Pp. 606. John Bale, Sons A Danielsson, Ltd., London, 
1913. Pr. 21s. net 

Every day fresh advances in our knowledge of the function 
of the internal secreting glands is being made, especially in their 
relation to disease, and it becomes very necessary from time to 
time that the literature on the subject should be collected together 
in a compact and concise form. How extensive this literature 
actually has become may be gathered from the fact that in this 
book 158 pages are devoted to the mere enumeration of the papers 
which are arranged in alphabetical order under their authors. 

The book is divided into two parts, a general and a special. 
The former is very short, extending to only twenty-three pages; 
the latter is the most important part of the book. The thyroid, 
thymus, suprarenal (to which alone 178 pages are devoted), 
pituitary, pineal, and generative glands are described in turn, 
and short accounts are given of the internal secretion of the 
pancreas, of the gastric and intestinal mucosa and of the kidney. 



174 


BOOKS AND PAMPHLETS RECEIVED 


We can confidently recommend this volume to all those 
interested in this increasingly important branch of medicine. 
The amount of matter compressed within these pages is enormous, 
and is easy of assimilation on account of the large number 
of headings under which it is arranged. The translation has 
been well done and is remarkably free from errors; the type is 
large and easy to read. 


BOOKS AND PAMPHLETS RECEIVED. 

Abbot, E. Stanley. “Psychology and the Medical School” (Amer. 
Joum. Insanity, 1913. lxx., Oct.). 

Anton, Prof. Dr Q. “ Psychiatrische Vortrage fur Arzte, Erzieher und 
Eltern ” (Dritte Serie). Berlin, 1914, S. Karger. 

Buckley, A. C. “ The Relation of Hyperthyroidism to the Nervous 
System ” (N. Y. Med. Joum., 1913, Dec. 6). 

Flexner, Simon. “The local specific Therapy of Infections” (Joum. 
Amer. Med. Assoc., 1913, lxi., pp. 447 and 1872). 

Frugoni, Prof. Cesare. “Contributo alio studio delle ‘crisi emateme- 
tiche essenziali’ e dell’ ‘ osteoartropatia vertebrale’ nelle tabe” (Riv. Crit. 
di Clin. Med., 1914, xv., N. 1, 2. and 3). 

Frugoni, Prof. Cesare. “ Espir&zione cardiosistolicamente intercisa e 
polso toracico negativo” (Riv. Crit. di Clin. Med., 1914, xv.). 

Goodall, E., and Scholberg, H. A. “ On Complement-fixation, and on 
the Cell-and-Protein-Content of the Liquor Cerebro-spinalis; a second 
Series of Observations” (XVIIth Intemat. Congress of Med,., London, 
1913). 

Heiman, H, Feldstein, S., and Koplik, H. “ Meningococcus Meningitis.” 
J. B. Lippincott Co. Pr. 12a 8d. net. 

Jnstscnenko, A. “ Das Wesen der Qeisteskrankheiten und deren biolo- 
gisch-chemische Untersuchungen.” Theodor Steinkopff, Dresden, 1914. 
Pr. M. 4, geb. M. 5. 

Oppenheim. “ Zur Kenntnis der Schmerzen, besonders bei den 
Neurosen” (Deut. Ztschr.f. Nervenheilk., 1913,1.). 

Oppenheim, H.. and Borchardt, M. “ Erfahrungen bei Operationen von 
Kleinbirngeschwulsten ” (fieri, klin. Wchnschr., 1913, Nr. 44). 

Oppenheim, H., and Krause, F. “ Operative Erfolge bei Geschwiilsten 
der Senhugel- und Vierhugelgegend ” (Berl. klin. Wchnschr., 1913, Nr. B0) % 

Oppenheim, H. ; and Krause, F. “ Ueber erfolgreiche Operationen bei 
Meningitis spinalis chronica serofibrosa circumscripta” (Mitteil. a. d. 
Grtntgeb. d. Med. u. Chir ., 1914, xxviL). 

Prince, Morton. “The Unconscious.” Macmillan Co., New York, 
1914. Pr. 88. 6d. net 

Rixen, Peter. “ Zur Frage der Anrechnung des Irrenanstaltsaufenthaltes 
auf die Strafzeit” (Jurist, -psychiat. Gremgeb., 1914, ix.). Carl Marhold, 
Halle a S. Pr. M. 2,20. 

Scholz, Dr Ludwig. “Nervos.” S. Karger, Berlin, 1914. Pr. M. 4, 
geb. M. 6. 

“ Klinik fiir psychische und nervote Krankheiten," 1913, viii., H. 4. 
Pr. M. 3. 

“ The Training School Bulletin,” 1914, xL, March. 



IRmew 

of 

fleurolog^ anO ps^cbiatt*^ 


©dgfnal Reticles 


ON THE MECHANISM OF SOME CASES OF 
MANIC-DEPRESSIVE EXCITEMENT . 1 

By C. MACFIE CAMPBELL, B.Sc., M.R.C.P.E., 

Associate in Psychiatry, Johns Hopkins Hospital, Baltimore; formerly First 
Assistant Physician, Bloomingdale Hospital, White Plains, N.Y. 

Cases of mental disorder may lie studied from more than one 
point of view, and in a previous communication 2 emphasis was 
laid on the importance of studying the individual case not only 
from the point of view of formal differentiation, but also witli 
the aim of understanding the content of the disorder, the meaning 
of the morbid utterances and actions, the fundamental significance 
of the distorted adaptation of the patient. Such an analysis leads 
down to factors of more than historical significance, dynamic 
factors at the roots of the individual’s activity. While the 
importance of this line of study is sufficiently demonstrated in the 
psychoneuroses, and is gradually becoming recognised in relation 
to dementia prsecox (schizophrenia, paraphrenia), the manic- 
depressive group has been chiefly studied from the point of view 
of formal characterisation. 

In the communication above referred to, brief summaries were 
given of cases in which “ the individual attack appeared to be the 
reaction more or less intelligible to a definite set of circumstances, 
and therefore was not adequately conceived when considered to 1 >e 

1 Read before the New York Psychiatrical Society, 7th January 1914. 
a “The Form and Content of the Psychosis: the Role of Psychoanalysis in 
Psychiatry,” Beview of Nevr . and Psych ., Sept. 1911, 

*5 



176 


C. MACFIE CAMPBELL 


a quite unexplained explosion of a somewhat unstable emotional 
constitution.” The occurrence of a manic excitement as a reaction 
to disturbing undercurrents or painful experiences was brought 
into relation with the phenomena of everyday life; “ the tension 
of painful feeling may lead to a paradoxical appearance of mirth, 
and flippant talkativeness of a superficial order may conceal a 
serious pain.” 

The continued study of cases from this point of view has 
thrown much light on the mechanism of the manic excitement, 
and it seems worth while to publish briefly a few cases in which 
the situation has been made clear. 

The first case 1 is that of a young woman, who presented tjie 
picture of a typical manic excitement when she came under 
observation; at that time the psychosis was of less than one 
month’s duration. The patient was overactive, talked continuously, 
was easily distracted by casual sounds or objects, showed some 
flight of ideas; the mood was one of elation with considerable 
irritability. There was no evidence of hallucinations, nor of fixed 
delusions, but the patient made a number of extravagant statements, 
the meaning of which was difficult to interpret at the time they 
were noted. Her orientation was not quite clear; her general 
condition made an accurate examination of the memory and of 
other intellectual functions impossible. The patient complained 
of dizziness and of buzzing in the ears; she had a burning pain 
in the back of the head, like an X-ray, “ as though someone were 
staring.” The neurological status was otherwise negative; apart 
from a valvular heart lesion there was nothing to note in her 
physical status. 

The patient was treated with wet packs and in the continuous 
bath; the excitement soon subsided, and in less than two months 
the patient had completely recovered. 

Here then was a typical manic excitement, said to have been 
brought on by overwork and sunstroke. The question was 
whether one had to be content with the general description, and 
had to regard the case as a well-known type of explosive reaction 
in a person of a certain constitution, the reaction having been 
precipitated by the banal etiological factors above mentioned. As 

1 I wish to express my thanks to Dr William L. Russell, Med. Sup., Bloom - 
ingdale Hospital, for permission to use the eases referred to in this communica¬ 
tion, 



CASES OF MANIC-DEPRESSIVE EXCITEMENT 177 

an alternative the attempt was made to understand the psychosis 
as the resultant of the actual forces in the individual’s life. No 
excuse waa necessary for making such an attempt; for on the 
assumption that the disorder was an explosive reaction elicited by 
somewhat banal causes, the patient on recovery would be hardly 
better able to meet difficulties in the future than in the past. 
If, on the other hand, the psychosis were the resultant of more 
definite factors which could be traced, these might to a certain 
extent be open to modification and be managed in a different way. 

The reconstruction of the whole situation was begun by follow¬ 
ing certain clues given by the utterances of the patient during the 
excitement In the psychosis she frequently referred to coloured 
men, coloured disease, coloured blood; she also said that she was 
“ a poor white coloured actress ”; she harped on being a spinster, 
talked of her married name, her unmarried name ; she asked what 
her name was. She talked of being “ an old tired cock,” said that 
she could not crow any more; “ I know what it means when the 
cock crows twice.” In close connection she referred frequently to 
the “ Scarlet Pimpernel ”; she talked of dying like a scarlet cock; 
“ I broke my word to Miss A. as a white woman. No one knows 
it but the scarlet doctor whom I told here.” 

She frequently opened her mouth widely, and talked of some¬ 
one spitting into the mouth; “ Let me spit in your mouth—I will 
spit straight in your face.” 

A few weeks after admission the trends, which were beneath 
these utterances, were gone into in the course of an association 
experiment. 

The references to coloured blood were at once admitted to be 
references to sexual passion; she said that she had taken a morbid 
view of herself; she had not been white through and through. 
She had referred to herself as “ a poor white coloured actress "; at 
the very beginning of the disorder she felt that she had to give Up 
her work, and take up acting or be a nun. These obviously 
represented two ways of escaping from the real world. In her 
associations to the word “ angel," the patient, a Presbyterian, 
expressed strong leanings towards the Roman Catholic Church, 
“ they look after their people ”; she laid weight on confession, on 
having someone to talk over things with, “ this might have pre¬ 
vented some things.” 

As to the reference to the “ tired cock ” crowing, she had 



178 


C. MACFIE CAMPBELL 


frequently lied to conceal the fact of her illegitimate child, she 
had lied to a woman (Miss A.) who had done much to protect her. 
Some of the utterances during the psychosis may be here quoted: 
“ When I lied, lied, lied—that’s the third time the cock crowed ”; 
“ that’s the fourth time the cock will have to crow to a Scotchman 
who is married ”; “ I shan’t apologise all my life, die like a scarlet 
cock ”; “ I’m only a poor old tired cock ”; “ I know what it means 
when the cock crows twice—can you tell me how a tired cock 
crows—I can’t crow any more.” 

Behind these utterances was more than a reference to Peter’s 
denial; she gave the following associations to cock, “ bird—tired 
cock, symbol of tiredness—a picture in Life of a cock with its 
head hanging down and the legend, * What’s the use anyway; one 
day a rooster, the next day a feather duster’; have seen it 
frequently in book stores.” She first saw it during the strenuous 
period when she was trying to reconstruct her life and struggling 
to support her illegitimate child. 

For her the “ tired cock ” symbolised the futility of the struggle 
which she felt was too much for her. In the utterance “ a good 
woman if I have to go through life apologising to married men— 
then you don’t know how a tired cock crows,” “ I shan’t apologise 
all my life, die like a scarlet cock,” the association l)ecomes clear in 
view of the reference to the illustrated periodical Life. 

The cock was therefore “over-determined,” and represented 
the meeting-point of two very important associative constellations. 
The word crow, too, was probably over-determined. 

The following were the associations to crow, “crow—bird 
(l sec.; unusually wide deviation of the galvanometer mirror), 
black disagreeable bird, can’t bear them, make so much noise, 
always go in groups, I always have to count them, one a wish, two a 
kiss, three a disappointment, not that I want a disappointment.” 
Beneath the cultured woman there was enough of the pagan to 
compel her to read the signs of nature to see if, after all, there 
were not to be granted to her some satisfaction of her deepest 
cravings which refused to be eliminated, even after her mistake 
had seemed to put such satisfaction out of reach. 

The “ scarlet cock ” was intimately associated in her utterances 
with the “ Scarlet Pimpernel.” Her association to scarlet was red 
(time 1*6 sec.; unusually wide deviation of the galvanometer 
mirror). After a few associations relating to an attack of scarlet 



CASES OF MANIC-DEPRESSIVE EXCITEMENT 170 


fever, she referred to the “ Scarlet Pimpernel.” “ I don’t know why 
I associated it so much, I talked of it in my sickness, it was used 
as a password, I felt I had a password with Miss A., it seemed 
to me there was a password to be exchanged—I had to hang on 
to some password to save my reason, just the same as I was 
discussing whether I should give up teaching to be an actor or a 
nun, yet I had to keep in touch with Miss A., save my work, 
perhaps my reputation, what could I do ?—that was uppermost, I 

had to save myself to work, save my mind to work for my child- 

the hero in the ‘ Scarlet Pimpernel ’ has two characters; in Denver 
(where she fell sick) I couldn’t sleep, I asked if they couldn’t put 
adhesive over one eye, give it a rest, then over the other, the hero 
could sleep with one eye open, in one character he was stupid, in 
his own life among his own people he appeared stupid, but he had 
a brilliant intellect-”; a password meant “ standing for some¬ 

thing else, perhaps I want to get away from myself, I have tried 
to stop thinking of my life in Washington" (period of careless 
living and seduction). 

The "Scarlet Pimpernel” was no trivial utterance, but ex¬ 
pressed her longing to gain recognition and admiration for 
brilliancy, to have her apparent stupidity recognised as a mere 
cover, to live an efficient life, to save her reputation, to save her 
personality and support her child. In that “password” was 
focussed the whole conflict of her life, and in the psychosis the 
consciousness of that conflict was not submerged. 

A few further associations may be mentioned in this connection; 
to wicked, stupid, she merely repeated the stimulus words after 
a long reaction time (9 - 4 sec., 4 0 sec.). “ Stupid—stupid, just as I 
did to wicked, I just seemed to see that, I suppose I was thinking 
about myself, but if I have self-confidence, I don’t think I am so 
stupid—I have always more or less depended on other people.” 
“Pride— myself, 1 have a good deal of pride, I wouldn’t acknow¬ 
ledge it, pride about my work, my looks, I like commendation, 
thrive under it-” 

“Pity—(she had given poor in the association test)—I don’t 
remember it at all, charity, I wonder whether I do pity myself 
(smiles), I think I have (hesitates), not because I’ve had a child, 
because I didn’t take advantage of my opportunities ”; but she 
regretted the lack of intellectual accomplishments because they 
would have been means to secure admiration and affection. 



180 


C. MACFIE CAMPBELL 


In this connection there was an interesting pseudo-reminis¬ 
cence. After giving her associations to stupid, she said—" And it 
was the same with awkward, I gave awkward, I’m not clumsy, 
perhaps the same as stupid—(give an example of awkward!)— 
such as not to know when asked a question.” As a matter of fact 
awkward had not been given as a stimulus word. 

The length of the association time was frequently acknowledged 
to be the result of a deliberate suppression, c.g., “child—I gave 
niece, I was going to say mine, I remembered the nurse was in the 
room”; “to paint—pink—pink carnations,” but she admitted that 
she had suppressed the personal association that she had rouged— 
“ I wouldn’t have got through my teacher’s course without it, they 
would have thought me sick, I did not want to be sick ” (danger 
of examination and disclosure of her secret). 

How closely the utteranoes in the psychosis were related to 
the dominating trends in the patient’s life was also seen in the 
frequent recurrence to the topic of spitting, of which several 
examples have been given above. In the same context we may 
also quote the following utterances: “Have you ever wiggled 
from a snake, and died to haemorrhage like a perfect woman ? ” 
“ I can wiggle my leg like a snake,” “ the only way I can get 
well is to wiggle and make someone laugh”; “I have Mrs S.’s 
disease.” 

The patient had once temporarily cared for Mrs S., who was 
delirious; Mrs S. spat a good deal, thought she was having a 
baby, thought a restraining strap was a snake. The patient had 
been much impressed with the possibility that if she herself 
became delirious she might give up her secret, and in her manic 
condition she felt that she was behaving like Mrs S. The utter¬ 
ances were probably further determined by the erotic content of 
the utterances of Mrs S. 

The result of the above analysis had been to show that 
beneath the smooth conventional surface of the routine life was 
the actual woman, striving rather wearily and with a feeling of 
futility to reconstruct her life (“tired cock”), supporting her 
illegitimate child by consistent work and the sacrifice of all the 
usual pleasures, ashamed at having lied more than once (the cock 
crowing) to an admired woman friend, regretting the want of an 
opportunity to unburden herself (leaning towards the Roman 
Catholic Church), but also longing for a more positive happiness, 



GASES OF MANIC-DEPRESSIVE EXCITEMENT 181 

eager for any omen to indicate the possibility of it (associations to 
crow), sensitive about her lack of attractiveness, but consoling 
herself by the feeling that beneath the self seen by the world was 
the real self of brilliant capabilities (“Scarlet Pimpernel”); in 
addition, giving way from time to time and with much conflict to 
an old-standing habit of masturbation. 

It is sufficiently plain that such a working adjustment involves 
considerable strain, and an equilibrium of this nature is not of the 
most stable. What explained the actual break in the adjustment, 
the date of the onset of the disorder ? Was it that the limit of 
resistance had been readied, or had certain internal factors 
received an augmentation of strength, or had Destiny created a 
situation beyond her power to cope with ? A careful review of 
the actual situation preceding the attack made the problem more 
clear. A very short time before the attack the patient and her 
mistress were interested in a sensational newspaper paragraph. 
This contained the statement of a girl, picked up on the streets of 
Chicago, who said that she had taken a berth on a train three days 
previously, but remembered nothing subsequently, as she had been 
probably drugged and assaulted on the train; she had come to 
herself two or three days later, and found a mark on her throat as 
if received during an assault. The railway company maintained 
that the bruise was self-inflicted, and the patient and her mistress 
discussed the improbabilities of the case, and agreed that the girl’s 
statement was a falsehood. Immediately before the onset of the 
psychosis the patient had to take a long railway journey ; she was 
in the position of the girl of the newspaper paragraph, whose story 
came back to her mind. She felt afraid the first evening that she 
might be drugged, she thought that someone might look through 
the curtain of her berth, she was suspicious of the coloured porter, 
she felt chilly and took a little whisky. The next day she was 
menstruating; she felt better, but on arrival at her destination 
her usual control was disappearing. She realised that she was 
talking too much, in conversation with a young man, who happened 
to be at the hotel, her usual reserve was gone, and in a few days 
the full-fledged manic picture had developed. The exposure to 
heat was subsequent to the first indication of loss of balance. 

When the patient was asked why the newspaper story should 
have so much importance for her, she did not see that it had any 
special significance; she did not realise that it had an intense per- 



182 


C. MACFIE CAMPBELL 


sonal significance until the physician had put the pointed question 
whether it was not in its essence her own story. Only then did 
it slowly dawn upon her; yet she had previously told the physician 
of the circumstances of her seduction, how after a champagne 
dinner she was unconscious, and must have been seduced, for her 
menstruation ceased, and after the third month the diagnosis of 
pregnancy was made. She herself denied any more precise 
memory of the actual seduction. How far this amnesia was 
complete, or how far it might have been possible to resuscitate 
memories repressed on account of their painful nature, is a matter 
of doubt. The question was not pushed. The precipitating factor 
was now apparently demonstrated ; the conscious and subconscious 
forces, reactivated by the newspaper paragraph and accentuated 
by the actual situation of the journey, were powerful enough to 
make the usual control no longer possible, and the patient at last 
gave expression to the forces so long controlled with difficulty. 

The case shows how a manic excitement may be the expression 
of a rather intense conflict in the patient's inner life, certain factors 
in which have happened to attain an intensity which breaks down 
the existing equilibrium, so that the repressed factors assert 
themselves in only slightly disguised form. The characteristic 
feature is that this conflict is not carried on at the deep level 
where the schizophrenic tragedy is acted, but takes place on the 
very threshold of clear consciousness; the patient has a fair 
inkling of the factors at work, may realise to a large extent the 
meaning of the reaction, and to appear on the stage of conduct the 
forces at work do not need to assume the subtle disguises which 
make the schizophrenic drama so hard to follow. When the patient 
in the midst of her excitement was asked about her child, and told 
that her reaction was an evasion of her difficulties, she said, “ I am 
not fooling with you, I’m hysterical—I don’t want to get well, and 
you’ve been posted like everybody else, and I haven’t had a baby, 
and I haven’t coloured blood.” 

In this statement the patient gave notice of the cessation of 
her struggle, and welcomed the relief, and the cheerful abandon of 
the manic no doubt largely depends on the cessation of the 
continual inhibition. The emphasis which the patient laid on her 
desire for confession encourages one in such a case to penetrate 
beneath the flippant surface of the psychosis, and to help the 
patient to talk frankly over the really serious factors in life; in 



CASES OF MANIC-DEPRESSIVE EXCITEMENT 183 


some cases a serious interview exerts a demonstrable influence un 
the clinical picture, at least temporarily. The onset of the 
psychosis in this case at the time of menstruation is also a fact not 
to be overlooked, for the break of adjustment was no doubt 
favoured by the periodic variation in the crude instinctive factors. 

It is not pretended that the above attempted reconstruction of 
the mechanism of the disorder is a complete answer to the question 
why this woman should have had a manic attack at the given 
date. Why did she not have a reaction of another type ? As in 
the psychoneuroses and in the schizophrenic group (dementia 
prscox) we have been forced to go down to the roots of the 
personality in order to understand the surface phenomena, so here 
too the type of reaction would have to be understood in the light 
of the forces that were at the bottom of the individual character. 
We would have to explain how it was that the patient had early 
drifted into a rather frothy social life, how she had been accustomed 
to take alcohol rather freely, and how her sexual instinct had been 
so poorlytaken up into her adult life that an illegitimate pregnancy 
was the result—such familiar facts of the anamnesis are in reality 
a series of further problems. In attempting to estimate the 
factors which had hampered or favoured the development and 
elaboration of her sexual life, one would be forced to take into 
account its earlier stages. That this factor had from an early 
age been a difficulty in the patient’s life was shown by the fact of 
masturbation since the age of 5 or 6; the habit had been self- 
taught, and involved much internal conflict. In the association 
test frequent references to her father cropped up, and the role * 
played by her affection for him had no doubt been an important 
factor in her life. She had a great deal of pride in her father’s 
unpretentious family; she had been much fonder of her hard-work¬ 
ing father than of her ambitious mother, whose chief pleasure was 
in society. The full bearing of these facts was not gone into. 

It is evident that the complete study of such a case is a task of 
considerable magnitude. 

The second case is that of a rather brilliant young woman who 
came under observation a few weeks after the development of 
mental symptoms. The patient presented a typical manic picture; 
she was overactive, elated, talkative, played on words, was easily 
distracted by casual stimuli; there was no evidence of hallucina¬ 
tions nor delusions; her flippant answers made it impossible to 



184 


C. MACFIE CAMPBELL 


examine accurately her intellectual functions, but she was 
apparently oriented and showed no defect in her memory. The 
following samples were typical of her utterances: (Name of this 
place ?) “ The House of Mirth, Marathon, marry you; ” “ I’m a 
club-ioot sandwich , a southern negro, that knee won’t grow” 
(tapping her knee). She was keenly observant, and made pertinent 
remarks on the details of the environment. Her physical health 
was excellent. 

The patient had been working very hard in a new and 
responsible position, and the psychosis was attributed to overwork. 

The spontaneous utterances of the patient consisted largely 
of flippant comments, rhymes, plays on words, but interspersed 
through these were open references to certain tragic circumstances 
in her life; she had married a man of perverted habits, whom she 
left on her wedding night, and subsequent divorce proceedings 
had subjected her to humiliation and yielded unsatisfactory results. 

While the patient was still definitely manic, although less 
active than on the first observation, an endeavour was made to re¬ 
construct the situation out of which the psychosis had developed; 
it was considered possible that a serious review of the important 
factors might tend to cut short this inferior type of adjustment. 

During the interview the patient frequently smiled, drifted a 
little along superficial lines of association in her talk, showed a 
tendency to resume her previous antics. She listened, however, 
seriously; and although her conversation was mixed up with 
drifting allusions, at times she talked in a very direct and sober 
way about her troubles. 

She talked of having been “murdered spiritually” and of 
having caused “murder”; she was not to blame for being so 
attractive; all her women colleagues had had trouble similar to 
hers; she was very sympathetic, but had been a source of danger 
to others. She regretted that she had been a danger to one 
woman, her ideal, on whose beauty she commented again and 
again. She had found this friend tired, had massaged her; this 
had aroused a dangerous attitude in the other, and she herself had 
become quite passionate. She suspected that similar improper 
proceedings were going on throughout the house (“ projection ”). 
She then felt that she had to go crazy. 

As to the fiasco of her marriage, this had made it impossible 
for her to love any man; she had felt that she could only find an 



CASES OF MANIC-DEPRESSIVE EXCITEMENT 185 


outlet for her affections in work for her own sex, but there, too, 
she had met difficulties; “ I had either to go crazy or to die—one 
can’t always be struggling.” 

In this connection reference may be made to other facts con¬ 
firming the importance of the homosexual trend in her nature. 
Among her intimates she was nicknamed David, “ as she had a talent 
for friendship ”; when asked about this during her convalescence 
she was a trifle embarrassed, said that the similarity was not 
meant to be an identity, referred to the main incidents in David’s 
life but made no reference to his friendship for Jonathan. When 
this was referred to, however, she went on to discuss such 
relationships and the fundamental trends underlying them, and 
referred to certain suspicions touching the friendship of two 
clergymen. One morning the patient, while still hypomanic, 
dressed herself up like a man, with pyjamas rolled up to the knee; 
on another occasion she said, “ I was meant to be a man, my father 
meant me to be a man, I had my father’s heart ” (many of her 
references showed the important role in her emotional life played 
by her affection for her father). At the very onset of the psychosis 
the patient had shown an exaggerated solicitude for the health of 
a woman friend, which led her into rather absurd extremes. 

The analysis had thus revealed dangerous elements in the 
patient’s equilibrium previous to the attack, and some factors 
which had probably made these elements unusually prominent. 
As the patient became better she made the situation still more 
clear; she told how the man she had married had recently got into 
trouble, and just before the onset of the psychosis she had been 
appealed to in order to save him from the threatened consequences 
of his own acts. She had thus been put in a position out of 
which she saw no outlet: “ I had either to go crazy or to die.” 

In this case, as in the previous one, the analysis did not go far 
back into the development of the patient’s character and of her 
mode of getting satisfaction out of life. The painful episode of 
her marriage did much to explain her later difficulties, but on the 
other hand itself required explanation. That her sexual instinct 
had early been a source of difficulty was obvious from references 
to experiences at an early age, while the later prominence of a 
homosexual trend was further evidence of the fundamental 
difficulties placed by this instinct in the way of a smooth adapta¬ 
tion to life. 



186 C. MACFIE CAMPBELL 

In this case, too, the important disturbing factors were to a 
large extent within the realm of clear consciousness, and the 
patient had remarkable insight into the nature of the mental 
reaction as indicating an inability to continue the struggle with 
her instincts: “I had either to go crazy or to die.’' Another 
possible solution of the struggle had suggested itself strongly to 
her, namely, that she should enter the Roman Catholic Church 
(rf. the previous case: “ I had either to become an actor or a 
nun”). During her menstrual period the patient became much 
more excited and irritable; she talked of the physician as her 
murderer (cf. her earlier statement that she had caused murder, 
referring to her sexual experiences). When quieter, her attitude 
to the physician was somewhat erotic, but she would apologise 
and say that if any woman, man, or child likes their doctor, they 
say “ any old thing ” without wanting to flirt. 

The third case is that of a middle-aged woman, a respectable 
dweller in the suburbs, the wife of a hard-working clerk, absorbed 
in his business and his own precarious health, which had precluded 
marital relations for a long time. The patient had had one previous 
attack of excitement, from which she made a complete recovery. 
The present attack came on immediately after nursing her boy 
most devotedly during an acute illness. The clinical picture was 
that of a typical manic excitement. She was overactive, talkative, 
exhilarated, but occasionally tearful; her stream of talk was 
directed by superficial associations. There was no evidence of 
hallucinations nor of delusions; she was clearly oriented, had an 
excellent memory, and some degree of insight into the nature of 
her disorder. The patient had mitral incompetence well com¬ 
pensated; she was slightly deaf, otherwise her physical health 
was good. 

The attack was attributed to the protracted strain of nursing 
her lx>y; but it was clear that the nursing had been itself a rather 
feverish and exaggerated activity, and it was interesting to know 
that previous to this devoted nursing she had been an intolerable 
nagging mother for more than a year, while in the psychosis she 
more than once stated that her children would never have been 
born if she had known how to avoid conception. 

During the prolonged manic attack it became i>ossible to form 
an approximate idea of the actual structure of the patient’s life, of 
the factors which had led to the former attack, and of those which 



CASES OF MANIC-DEPRESSIVE EXCITEMENT 187 


had precipitated the present attack. It is difficult to condense the 
results and at the same time to give a correct impression of the 
material from which these results were drawn; the material 
consisted of observations during a period of many months of her 
behaviour, her spoken utterances, her letters, her dreams. When 
the excitement simmered down and the patient was able to co¬ 
operate in a more consecutive review of her life, she gave still 
more definition to the interpretation which had been tentatively 
arrived at. 

At the first interview her drifting talk contained many references 
to her husband (“he is a fool—physically weak on account of 
masturbation ”), and she spoke of being divorced; she referred to 
“ an anniversary coming round—a broken engagement," an engage¬ 
ment when young to a bad man. On the third night after marriage 
she had unconsciously murmured “ forgive me,” as she thought she 
saw the figure of her former sweetheart (Mr B.) at her bedside; 
to her husband’s query she had answered that she wa3 repeating the 
service. She talked of her own age, said that she would allow any 
young man to do anything to her; on the other hand she empha¬ 
sised her correctness: “ I wouldn’t speak to a man unless I had to” 
(here she took the hand of the examiner); “ I was a flirt, but now 
I am an old hag.” Tire contrast between youth and age occupied 
her much, and in another interview, on seeing the stethoscope, she 
said, “ You’re young. I’m old—you old flirt—try my heart—I’m 
too old." Again and again she referred to the fact that beneath 
her conventional married life were persistent regrets with regard 
to an old love affair; she apparently felt it necessary to balance all 
her references to this past affair by emphasising her satisfaction 
with her married life. “ I have a lovely li/e, interested in charity 
and society in a small way. I got through with my life before I 
was 25 ’’; in the second half of the statement the truth breaks 
through the conventional crust of the first half. She referred to 
“awful things before marriage”; her husband would not let her 
talk to him about them: she still wanted to talk over these matters 
with him. As to divorce she said, “ No one thinks of a divorce 
unless they are ready to step into a second home” (vid . infra, 
Dream). 

At a later period of her attack the patient made her statements 
much more definite, and referred to her personal difficulties and 
the rdle they had played in her life. During interviews the 



188 C. MACFIE CAMPBELL 

patient would, as a rule, be cheerful and flippant, but would 
occasionally break down and cry, only to resume her cheerfulness 
and make light of her tears. She stated that when out automobile 
riding she would scan every passing car to see if it were that of 
Mr A., an old friend; she thought this attitude childish, probably 
the result of her protracted mental attack. She denied any 
affection for Mr A., “ I was fond of interchanging ideas.” She then 
admitted that she had not realised her true feelings towards this 
man until she heard of his marriage; it came as a shock to her. 
She did not wish to give the date of this shock, evidently so that 
it might not be brought into relation with her own mental 
symptoms. “ I don’t want to tell you when I felt badly—but 
that was over my son. I gave my thoughts to my family. I 
never had any foolish thoughts when I was caring for my son— 
(When did you get the shock ?) It was in January. That is as 
near as I will tell you—don’t ask me any more. I worried about 
my son in December ” (but the husband placed the onset of the 
boy’s symptoms in January), “ I don’t like to tell you dates.” She 
still wished to see the cause of her sickness in her care of the boy, 
and hesitated to have her convenient dates corrected. The 
sequence had been that she had learnt suddenly of the marriage 
of Mr A., with whom she had “interchanged ideas” for many 
years, and for whom she had evidently had a very deep affection; 
to ward off the realisation of the aotual situation she had devoted 
herself with unsparing assiduity to the nursing of her boy. Even 
this method had not been quite successful, and the situation was 
complicated further by certain resemblances between her boy and 
Mr A. Her complex mental state was probably also influenced 
by the fact that she had been for some time nagging the boy, that 
she had a latent desire that he had never been born, that she felt 
that her husband’s weakness was partly due to past masturbation, 
and that her son’s mental breakdown had also to be attributed to 
this fact. During the period of nursing, the patient’s resistance 
had given way, the conventional adjustment was no longer 
tenable. 

In a later interview, which was at first characterised by the 
usual mixture of flippancy and tearfulness, of admission and with¬ 
drawal, the patient became quite serious, and said that the trouble 
was outside her home; she had a liking, not an affection, for 
Mr A., she intended to get a divorce, and leave home. She said 



CASES OF MANIC-DEPRESSIVE EXCITEMENT 189 


that she would have no scruples in making plans that would 
involve the other man’s home. But after this assertion of her 
resolve to get satisfaction at whatever cost, she asked the physician 
seriously if he could influence her to prevent her from wishing to 
leave her home. The patient had evidently a remarkable insight 
into the nature of her trouble. She later wrote: “ I don’t think 
Mr A/s wife is half good enough, but if he is content that is all 
there is to be said, but I wish I didn’t every morning at my 
solitary breakfast think of those two together; I must be turning 
into a semi-idiot.” 

So much for the precipitating factors of the patient’s second 
attack. A further review of the case threw light on the onset of 
the first attack, which had occurred many years previously. 

The patient had frequently referred to an intrigue with Mr B. 
before marriage; after a time she became more explicit, and 
admitted how laige a part this affair played in her whole life. 
The intrigue had been carried on over a period of about one year; 
she gave a definite date for her seduction. She broke off relations 
with this man because he was dragging her down, and she could 
not raise him up. After two abortive engagements with other 
men she married her present husband. “It was a marriage 
without a shred of affection, a marriage of respect.” She thought 
it “more proper, more lasting.” Her old love had not died, 
“ absence makes the heart grow fonder ”; she still had “ a lonely 
feeling under the heart.” She admitted having fantasies about 
going away, having a lovely time for a month or so, and then 
paying up. She talked of “ the lovely life I expected in a sunny 
land, with flowers all the time, and music and pleasure-loving 
people in the land of the siesta ” (Mr B. was of Italian origin). 

Married to an invalid of narrow interests, her sexual instinct 
unsatisfied, she had just before her first attack visited the scene of 
the old intrigue and gone over all the hallowed spots; it was the 
anniversary of her seduction. She returned home with the desire 
to confess all to her husband ; she already presented symptoms of 
loss of balance, was exhilarated, talkative, referred to divorce, 
accused her husband of infidelity; the clinical picture was that of 
a manic excitement. This condition, after lasting for more than 
one year, was followed by a phase of depression, after which the 
patient regained her previous equilibrium, but the memory of the 
old love affair was only dormant, 



190 


C. MACFIE CAMPBELL 


BeneAth the surface the old longing persisted, and it manifested 
itself very clearly in the second attack; it furnished the material 
of her fantasies by day and of her dreams at night. The 
following is a good example of her dreams, and was written only 
after she had refused to communicate it orally. 

“Dr Campbell, now I will write you my dream—I really 
couldn’t tell it to you and look you in the eyes afterwards.—I will 
tell it exactly as it was, except I will omit some of the affectionate 
conversation, if you please. I seemed to be taking a long journey 
by railroad and hunting for some place—I was not comfortably 

dressed and had little money—at last the guard called out D- 

and I got out. (I never heard of that place, did you ?) Well, the 
road was rough, and I walked and walked and walked past many 
gangs of foreign workmen. I was dreadfully tired and all alone, and 
in fear for night was near. The street lights shone in the distance 
and I seemed to be in an impassable swamp—I think I was fleeing 
from my family and they were hostile to me (I am a little hazy 
on that point). Well, I saw a bright light, and in great fear I half 
awoke and the lantern was going by, then I dreamed on and this 
is not so clear. I was sick and faint with fright and I went up a 
path in the swamp and into a new house and up the stairs, and 
my shoes were full of water. I was helped to undress and put 
into l>ed, and then the door opened and in came my ghostly friend 
whom I imagine by my side when I am sleepless, as I told you, 
but whose name I am not willing to speak to you. He came in 
and shut the door. His brown hair had turned grey [identification 
with a rich man, who appears in another dream; Mr B. had 
postponed marrying patient on the ground of poverty] and he had 
on his mixed business suit. He is very quiet in his ways. He 
sat close by the bed and said, ‘ Now Mrs S. I want you to rest, no 
one shall harm you,’ and we talked for a long time and my clothes 
lay wet on the floor. He held my hand and my head too, and the 
talk was the affectionate part which I shall certainly omit, and 
suddenly there was a bright light and I woke up. So dreams do 
make a difference, for I am generally so unhappy when I wake 
up.” 

The dream is sufficiently clear to require no detailed explanation. 

The patient said that in the daytime she continually felt that 
she was accompanied by someone. She referred to him as “ my 
ghost ”; she would go to sleep by imagining that he was beside 



CASES OF MANIC-DEPRESSIVE EXCITEMENT 191 


her, “ good-night now, it is time for me to think of my ghost ”; 
she felt that she oould not eat her breakfast unless she imagined 
that someone was in the room. 

To make clear the level of consciousness at which the conflict 
in the patient’s mind took place, to show how little the actual 
difiiculties were submerged, how good was her own realisation of 
the difficulties, a few of the patient’s own statements may be 
quoted. They show that she herself considered her condition to 
be a mental disorder, a reaction to a situation which she felt to be 
too much for her, a situation in the face of which her usual 
working compromise could not be maintained, and for which no 
solution within the limits of health was available. In the midst 
of her flippancy she said, “ I’m not so sensible as I make myself 
out to be. I keep thinking of things I don’t want to think of.” 
She used the following expression, which is somewhat pathetic 
in its appeal, “ I am not begging to be happy, Fm trying to get rid 
of being artificially happy." In a letter she writes: “ I know I 

shall be punished for this (i.e., leaving her home) and I am afraid, 
but I have made my choice, and I go over it over and over agaiu 
and think why cannot I go on with my life always as it seems 
marked out for me, but I cannot. I realise I cannot, I must let 
myself go. I guess I lived in a fool’s paradise for a long time and 

didn’t know it.-1 think I write rather more honestly than I 

speak. When I talk to you I like to gloss things over, so they 
sound at least half way respectable.” She said that her life was 
over, “my instincts were crushed years ago, I don’t think I’ll 

have strong health again, you need something to back that up-.” 

As to her manic behaviour, “ I like to make a fuss all the time just 
to forget , that’s why I made this awful fuss.” 

In her attitude towards the physician the patient showed an 
alternation and mixture of like and dislike. In her irritable and 
impatient condition she would make accusations which relieved 
her of any personal responsibility for distressing thoughts, and 
into these accusations she carried an excess of feeling which was 
only intelligible when traced to its source. This method of 
relieving the personal tension by indignation and accusation 
against others is an important factor in determining the attitude 
of the manic patient to the environment. Thus, one day after 
a pleasant greeting, she came back to the physician, spoke to him 
white with rage, stamped her foot, called him a nasty liar and 
16 



192 C. MACFIE CAMPBELL 

other opprobrious names, and asked him if he would have dared 
to make the same remarks in the presence of her husband. An 
explanation was not forthcoming. A few days later, when more 
accessible, she said that the physician had suggested that she 
leave her home; she then corrected this to the statement that he 
had said she was not satisfied at home. After playing on this topic 
for a little, she vigorously asserted that she would leave her home, 
that she intended to get a divorce and live out her own life. The 
furious reaction against the physician was therefore a reaction 
towards her own strong desire, for the presence of which she 
would have made the physician responsible. On another occasion 
she said, “ I don’t get angry at you, I get angry at myself for not 
being able to keep it all to myself.” She asked the physician 
to “ swallow down your anger and disgust, which influence your 
actions more than you are aware.” 

The patient on several occasions reacted rather well to an 
interview with a frank review of her actual difficulties, and fully 
appreciated the bearing of the treatment. “You are right, my 
treasured friend, I am growing a little better, and I do see things 
I don’t like a little clearer, that is an awfully involved period; ” 
“ the past is over. You may help me arrange my present way of 
regarding things all you wish, and I will follow you to the best 

of my ability. I am far from being flippant-1 honestly enjoy 

talking with you, and I have slept so much better these last few 
nights, but don’t ask me any unnecessary questions, please. Vital 
matters I do not mind at all discussing, as you seem to think ” 
(extracts from her letters to the physician). 

In this case the nature of the conflict and the level in 
consciousness at which that conflict is staged, correspond with 
what has already been observed in the two previous cases. The 
conflicts which proved disastrous in later life had their founda¬ 
tions laid in earlier life; an intrigue of one year, two abortive 
engagements, and finally “ marriage without a shred of affection,” 
indicated a manner of dealing with her sexual instinct which 
could hardly pass with impunity. What earlier factors had 
determined this faulty adaptation of the young woman to her 
adult responsibilities was not investigated; a thorough review 
of her childhood was not taken up. It was known that her 
mother became insane during the patient’s girlhood, and the 
patient had lieen devoted to her father. 



CASES OF MANIC-DEPRESSIVE EXCITEMENT 193 


The fourth case is that of a young woman who presented 
the symptoms of a typical manic excitement She was overactive, 
talkative, easily distracted by casual impressions; there were no 
hallucinations nor delusions, her orientation and memory were 
excellent; she had good insight into the nature of her condition. 
Her general nutrition was good, there was no disorder of the 
internal organs; she had difficulty in control of her sphincters, 
and some anaesthesia in the distribution of the lower sacral roots, 
owing to an old spinal trauma sustained during a previous attack. 
After a period of several months, during which the excitement 
varied in degree from time to time, the patient was able to 
resume her usual social life. 

The patient attributed her attack partly to the strain of some 
routine nursing she had to do at home, but laid special emphasis 
on the rdle played by the sexual instinct. She at once plunged 
into this topic: “ First one (i.e., engagement) was broken off, then 
one was hopeless, terrible sexual pains, no satisfaction for it, if I 
only had some way of curing it, aren’t the baths good for it ? ” 
She was affable, bright, and eager, but said that she was sad and 
melancholy: “I broke off a first engagement without exactly 
knowing why, now he has married another woman”; she again 
spoke of “ terrible sexual pains with no satisfaction. It’s terrible 
to see my two sisters married with such lovely babies.” Just 
before her attack her sister with two babies had come to stay at 
her home, and this had made somewhat more acute the tension 
of the forces which she was already barely able to control. The 
leading interest in the patient’s life was a rather hopeless 
attachment for a distinguished professional man which she was 
carefully nursing; the hope of marrying him, although to an 
outsider extremely fragile, meant everything to her, and probably 
did much to sustain her in the cheerful conduct of her life. The 
patient had already had several attacks; between the attacks she 
was described as "an exceedingly agreeable personality.” A 
review of the earlier attacks elicited several facts of cardinal 
importance. 

The onset of menstruation had been a critical period in her 
life, and during the second menstruation, which came on after a 
horseback ride, the patient was said to have been hysterical. 
At each succeeding period she was a little upset. At the age of 
14, after a period of depression with ideas of unworthiness, she 



194 C. MACFIE CAMPBELL 

passed into a condition of overactivity, and did many curious 
things; at one period of this attack she persistently soiled 
herself. One of her favourite forms of activity during this period 
was to go through various military manoeuvres. During her 
college period she had an attack in which from a “ modest, sweet, 
innocent girl,” she changed into a boisterous, careless, and quarrel¬ 
some one; this condition persisted for several months; the patient 
was boastful, talked a great deal about religion, but after a period 
of several months returned again to her previous condition. At 
the age of 20 the patient had a prolonged period of excitement, 
in the early stage of which she jumped from a window and sustained 
a fracture-dislocation of the spine. Three years later she had an 
excited attack of five months’ duration; during this attack she 
was hostile to her family, thought her sister was dead, wrote to 
her father that God had told her that her mother hated her, she 
showed a strong religious trend; masturbation was noted during 
this attack. One more attack of a mild character, in which her 
religious trend again appeared, occurred four years later, and then 
the attack which is at present under consideration. The account 
of these attacks from the patient herself threw a great deal of 
light on many of the incidents. The role which her childhood 
affection had played in her life stood out in sharp relief. In an 
early attack she had gone through military manoeuvres; her 
father was a soldier; he, the patient, and her sister had visited 
the scene of his old exploits, and on the journey her sister had 
shared the father’s berth to the patient’s indignation. After one 
day’s riding together, menstruation came on, and she had to rest 
while her sister rode round with her father (in one attack her 
sister is dead); the patient had then shown “ hysterical ” 
symptoms, and these tended to reappear at each period. When 
the patient was older she became engaged, but the engagement w'as 
broken over some trifle, as she refused to accept some condition; 
another match which was possible did not result in anything, 
partly on financial grounds. The attack during the college period 
had come on immediately after the rupture of the engage¬ 
ment. 

Her account of the following attack, during which she jumped 
from the window, was striking. She had gone to join her father 
in a separate establishment of his own, as he was now estranged 
from the family; she was menstruating. She was ruminating 



CASES OF MANIC-DEPRESSIVE EXCITEMENT 195 


over her broken engagement, was evidently rather excited, and 
aroused the anxiety of her father; when he entered her room, she 
felt that it was in order to assault her, and she was panic-stricken 
and became wildly excited. When taken home she jumped from 
the window. 

In the next attack the hostility to the family, especially to the 
sister and mother, with the letter written to the father, again 
revealed the importance of the same component in her life. All 
these facts stood out in still greater relief in view of the complete 
estrangement of the psychopathic father from the rest of the 
family. 

On further examination of the situation out of which the 
present attack had developed the patient referred to a quite 
recent visit to her home of her father; he had come, had spent 
a few days, and again gone, but the emotional value of his 
visit to her would have to be estimated in the light of the facts 
related above rather than judged by her own clear feelings. 

In this case, as in the others, we find an intense conflict which, 
to a large extent, is clearly conscious, but here, much more than 
in the other cases, we receive an unmistakable indication that in 
estimating the whole conflict of forces the influence of the 
affective life in childhood must also be taken into consideration. 
In the three previous cases, too, the father had dominated the 
affective life of the child, and it is striking that in all cases the 
instinctive life had been so inadequately handled. The conflict of 
later years has been brought into relation with earlier mishaps in 
the sexual life; but these mishaps are not to be taken as incidents 
purely of accidental origin, into which the personality of the 
individual did not enter at all. One must try and understand 
these mishaps, just as we try to understand the psychosis; if the 
psychosis is to be looked upon as an inferior type of adaptation 
in face of a difficult test imposed by the circumstances of life, is 
the earlier mishap not also to be considered as an inadequate 
adjustment in face of the crucial test of the adequate external 
application of the sexual instinct ? If, then, one cannot so easily 
absolve the patients from their share of responsibility in these 
earlier mishaps, the problem is to determine what factors stood in 
the way of a more normal adjustment. We are thus carried back 
to an analysis of those intimate factors which lie down at the 
roots of the instinctive life of the adult, and which can only be 



196 


C. MACFIE CAMPBELL 


adequately understood when we have traced the development of 
the affective life from early childhood. 

In the cases above reported autoeroticism, childhood fixation 
of the affection on the father, and homosexuality were factors of 
importance, but in none of the cases was the analysis carried 
very far; that is a point yet to be done, and Abraham has 
already emphasised this aspect of the problem. The point 
of attack in the present investigation was somewhat different, 
the aim was to try to understand the attack in relation to the 
situation out of which it evolved; but while this examination 
has yielded fruit, it has also shown that one cannot rest there; 
the situation cannot be understood until the patient is completely 
understood in the light of the individual development. 

In discussing the different types of neurotic disorder Freud 1 
has separated one group where the most striking factor is the 
denial by the outer world of a suitable opportunity for satisfaction 
of the libido, while in a second group greater importance is to 
be laid on the internal difficulties which prevent the adjustment 
of the individual to a situation which offers fair opportunities of 
satisfaction. In the latter type the individual cannot adjust 
himself because he is unable to exchange certain forms of 
satisfaction for those other forms which would naturally supplant 
the former in the course of development. Freud emphasises the 
point of view gained from psychoanalytic treatment, that we must 
give up a fruitless contrast of external and internal factors, of 
fate and constitution, and try to find the cause of the disorder 
in a definite psychic situation winch may be determined in 
different ways. These remarks, deduced from the study of the 
psychoneuroses, apply equally well to the formulation of the 
etiology of such cases of manic-depressive excitement as have 
been reported above. 

The patient, whose manic excitement can be more or less 
understood in the light of the above considerations, may at 
another period present a typical depression. In my previous 
communication I have referred to the case of a young woman of 
25, who iu her adult life had twice reacted to a painful experience 
(marriage of adored brother, marriage of a man she admired) with 
an excitement, while in girlhood she had twice reacted to a painful 

1 8. Freud : “ Cher neurotische Erkrankungaten,” Zentralbl.f. PsychoawUytt, 
1912, p. 297. 



CASES OF MANIC-DEPRESSIVE EXCITEMENT 197 


experience (death of father, drowning of favourite brother) with 
an attack of depression. The analysis of attacks of simple 
depression made along the same lines yields results of no less 
interest than those obtained from a study of the excitements. It 
would go a little beyond the scope of the present communication 
to furnish an example of such an analysis, and this is perhaps not 
necessary in view of Abraham’s 1 recent paper. 

Abraham has stated his views in the rather dogmatic and 
involved terms of a certain libido theory. In this communication 
I have endeavoured to keep as closely aB possible to a clinical 
formulation of the problem in terms which involve as little theory 
as possible, a formulation which is easily open to the control of 
wider observations. 

The question may arise as to how far the above cases are 
typical of the manic excitement in general, and whether the 
formulation of the mechanism in these cases may not be applicable 
only to a comparatively small group of cases. One point which 
determined the detailed study of the above cases was their very 
typical clinical picture; it was felt that the principles which 
would explain these cases would be applicable to a very 
large proportion of cases. In many other cases it has been 
possible to see the same mechanisms at work, although they have 
not been traced out in the same detail. It is true that in many 
cases a satisfactory analysis is not possible; during the attack the 
symptoms may prevent an analysis, while on their return to their 
normal equilibrium the patients may not be willing to co-operate 
to the necessary extent. From the point of view of prophylaxis, 
a thorough analysis of the case is very advisable. 

The insight gained from these typical cases enables one to deal 
much more satisfactorily with many cases of acute excitement, 
where in a setting of overactivity, talkativeness, and exhilaration 
there occur many peculiar reactions, and where there is a florid 
development of peculiar ideas, which evidently represent the 
distorted symbolic expression of repressed trends. Here there 
are obviously conflicts in the patient’s life at different levels, and 
instead of trying to make a formal differentiation between manic- 
depressive insanity and dementia praecox, we are encouraged to 

1 K. Abraham, “ Ansitze zur paychoanalytischen firforsohung und Behandlung 
dea manuoh-depreaaiven Irreaeina und verwandter Zuatifcnde,” Zentralbl. /. 
Psychoanalyst, 1912, p. 302, 



198 


ABSTRACTS 


try and estimate at what level the most important conflict takes 
place, and to formulate our diagnosis and our prognosis in dynamic 
terms which take account of the individual psychology of 
the patient. 

Summary. 

In many cases of manic-depressive excitement the onset of the 
attack becomes intelligible in the light of a careful reconstruction 
of the whole situation out of which the attack has developed. 

The difficulty of adjustment which leads to the manic attack 
in these cases is much less deeply seated than in dementia praecox 
and allied conditions; the conflict is much more clearly realised 
by the patient, the flight into the psychosis coincides with the 
relaxation of efforts which are recognised as inadequate to deal 
with the actual situation, the cessation of the struggle permits the 
frank expression of repressed elements. The elated mood and 
exuberant activity of the manic patient are thus partly explained. 

It is important to study closely the content of the utterances 
of the manic patient in order to understand the meaning of the 
situation leading to the attack; this line of investigation includes 
an accurate estimate of the equilibrium of forces which make up 
the patient’s personality, and involves a thorough study of the 
individual’s development. 

A thorough review of the above factors may put the patient 
in a better position with regard to the possibility of avoiding 
further attacks. - 


abstracts. 

ANATOMY. 

THE TRACT OF LI88AUER AND THE SUBSTANTIA OELATlNOSA 
(237) ROLAND! S. Walter Ranson, Amer. Joum. Anat., 1914, xvi. 
March, p. 97. 

The tract of Lissauer is present in man and in the monkey, cat, 
rabbit, squirrel, rat, and guinea-pig, and possesses the same 
structure in alL It is composed of small, somewhat widely- 
separated medullated fibres and great numbers of fine non-medul- 
lated axons, and lies in the apex of the posterior horn between the 



ABSTRACTS 


199 


substantia gelatinosa Rolandi and the periphery of the cord. The 
number of medullated fibres entering the tract from the dorsal 
root is not sufficient to account for all the vertical medullated 
fibres found there, many of which are probably of endogenous 
origin. The major part of the non-medullated fibres of the tract 
can be traced in man from the dorsal roots. In all cases there is 
a tendency for the tract to spread out into the lateral column of 
the cord, and as no oblique fibres pass ventro-laterally from the 
dorsal paid into this lateral expansion, it seems certain that this 
lateral part of the tract is of endogenous origin. The tract of 
Lissauer and the substantia gelatinosa Rolandi are intimately 
related to each other, although in the rat and guinea-pig, where 
the substantia gelatinosa is excessively developed, the tract of 
Lissauer (exclusive of the lateral expansion) is least well developed. 

Two layers can be distinguished in the substantia gelatinosa, 
and a third at the border between it and the ventrally-lying grey 
substance. The most superficial layer of the substantia gelatinosa 
is the stratum zonale. It contains many non-medullated axons 
and fewer medullated fibres. It is most abundant just beneath 
the tract of Lissauer, and between the two there is a free inter¬ 
change of fibres. From these facts one may assume that this layer 
serves as a means by which the fibres of Lissauer’s tract reach the 
substantia gelatinosa. The second layer, the substantia gelatinosa 
proper, contains a plexus somewhat less dense than that in the 
preceding layer. The fibres are almost all non-medullated. The 
intermediate layer at the boundary between the substantia 
gelatinosa and the neutrally-lying grey matter is a dense plexus 
of fibres, mostly non-medullated. A majority of these fibres have 
a vertical course. 

The tract of Lissauer, the intermediate layer of vertical fibres, 
and the substantia gelatinosa Rolandi, are all intimately related 
to each other, and, taken together, form a complex system, the 
function of which is unknown. The author thinks it is an apparatus 
for pain and temperature sensations. The non-medullated fibres 
of the dorsal roots have been shown to arise from the small cells 
of the spinal ganglion, which are typical unipolar cells, i.e., they 
are afferent in function. They have nothing to do with afferent 
impulses from muscles and joints which pass up the posterior 
columns. The assumption that the tract of Lissauer and the 
substantia gelatinosa form an apparatus for the reception and 
conduction of pain and temperature sensations does not exclude 
the possibility that we are also dealing with a centre for vasomotor 
and pilomotor control. The apparatus may have a double function, 
serving as a central autonomic apparatus and for the reception and 
conduction of pain and temperature sensations. 

A. Ninian Bruce. 



200 


ABSTRACTS 


THE PHYLOGENETIC EVOLUTION OF THE CORPUS STRIATUM 

(238) De Lange, Lt Ntvraxe, 1913, xiv., p. 105. 

Among some of the author’s conclusions may be mentioned the 
following:—The palaeostriatum (globus pallidus) with the basal 
ganglion exists in fishes. Dorsal to it is formed, in the ganoids 
and bony fishes, a sort of epistriatum, in which are found the 
terminations of secondary olfactory neurones. (This nucleus 
does not, however, correspond to the epistriatum of reptiles.) 
The palaeostriatum can be traced through the whole vertebral 
series. 

The archistriatum (nucleus amygdalae, &c.) is most highly 
developed in the reptilia, and gradually diminishes through the 
mammalia. 

The neostriatum (putamen, nucleus caudatus) is found for the 
first time in the lower reptilia, increases in relative size in the 
lizards and progressively through birds and mammals: as a result 
the archistriatum forms in the higher mammals only a small pro¬ 
portion of the whole striatum. The earliest appearance of a 
separation by corticospinal fibres of the putamen and the caudate is 
in the higher reptilia (Ariens Kappers). S. A. K. Wilson. 

AN ANALYSIS OF THE JUZTA NBURAL EPITHELIAL PORTION 
(¥39) OF THE HYPOPHYSIS CEREBRI, WITH AN EMBRYO- 
LOOICAL AND HISTOLOGICAL ACCOUNT OF A HITHERTO 
UNDESORIBED PART OF THE ORGAN. F. Tilnky, Intemat. 
Monatichr. f Anat. u. Physiol ., 1913, xxx., H. 7/9, pp. 258-293 
(52 figs.). 

An embryological study in cat and fowl, and histological study of 
the adult hypophysis of fowl, cat, dog, sheep, rabbit, rat. An 
analysis of all the elements which enter into the formation of the 
hypophysis shows the following:— 

I. Pars Neuralis: 

1. Eminentia saccularis (of tuber cinereum). 

2. Infundibulum. 

3. Processus infundibuli. 

II. Pars Buccalis: 

1. Pars juxta-neuralis. 

(a) Pars tuberalis (this is the previously undescribed 

portion). 

( b ) Pars infundibularis. 

2. Pars dist&lis. 

“ The pars tuberalis differs histologically from the pare infundi- 
bularis. They are also morphologically distinct elements:—the 
pars infundibularis appears almost immediately after the anlage 



ABSTRACTS 


201 


of the buccal portion is formed; the pars tubcralis arises relatively 
late, and is formed from two secondary diverticula from the body of 
the pituitary sac, which later fuse together, displace the body of the 
pituitary sac ventrad, and thus secondarily assume their juxta- 
neural position: this latter portion is intimately connected with 
the neural portion by nerve fibres, blood vessels, and connective 
tissue processes, so that the attempted separation of these two 
portions cannot fail to lacerate or destroy the neural elements. 
Complete hypophysectomy is impossible without removal of the 
infundibular process, infundibulum, and saccular eminence of the 
tuber cinereum. In accounting for the syndrome which follows 
complete hypophysectomy, critical analysis cannot be too carefully 
made in differentiating between the symptoms due to removal of 
the glandular tissue on the one hand and the neural elements on the 
other. Such an analysis is obviously wanting in many of the 
reported accounts of experimental complete hypophysectomy, and 
the conclusions drawn are hence open to criticism.” 

Leonakd J. Kidd. 

THE TWBENBRAIN AND MIDBRAIN OF REPTILIA. (Das 
240 Zwirschenhirn und das Mittelhim der Reptilian.) De Lange, 
Folia Newro-biologica, 1913, vii., Nos. 1-2, p. 67. 

This is a long and valuable contribution to the study of the com¬ 
parative anatomy of the nuclei and tracts of the diencephalon and 
mesencephalon. The area covered extends from the optic thalamus 
to the nucleus ruber, fasciculus longitudinalis dorsalis, and nucleus 
oculomotorius. The article does not lend itself to the work of 
abstracting, however; but the student of the subject will here find 
adequate discussion on all the ganglia and paths of this important 
section of the brain. S. A. K. Wilson. 

THE NERVTJS TEBMINALIfl IN MAN AND MAMMALS. J. B. 

(241) Johnston, Anat. Record , 1914, viii., April, p. 185 (9 figs.). 

Thb telencephalic nervus terminalis, first described by Pinkus 
(1894) for Protopterus annectem, has been found in other fishes, 
amphibia, reptiles, and mammals up to Man. Johnston points 
out that it is larger in man than in many fishes and amphibians. 
Brookover suggested that it is vasomotor in function. Johnston 
finds that its central relations are different from those of the 
olfactory nerve. It is still uncertain whether all its fibres are 
afferent or whether some or all rise in cells within the brain: in 
the latter event they might be considered pre-ganglionic motor. 
Johnston thinks that probably it contains both afferent and motor 
components. He gives descriptions of it in pig, horse, sheep, 
porpoise, monkey, and man (foetus at term, four months’ baby, 



202 


ABSTRACTS 


and fourteen adult brains: it was present in all human adult brains 
examined). It contains some medullated fibres in the case of the 
sheep, horse, and monkey. Its independence of the olfactory 
nerve is well shown by its presence and large size in the anosmatic 
porpoise. Leonard J. Kidd. 

THE NBRVU8 TERMINALIS IN ADULT MAN. C. Bbookoveb, 

(242) Joum. Comp. Neurol., 1914, xxiv., April, p. 131. 

This short paper may be compared with Johnston’s ( v. supra). 
Most of the cells of the nerve are situated median to the olfactory 
bulbs on the surface of the dura, or embedded within it as far 
ventrally and peripherally as the cribriform plate. Its iutra- 
cranial course, posterior to the olfactory bulbs, lies over the middle 
of the gyrus rectus (figured). Leonard J. Kidd. 

CORRELATED ANATOMICAL AND PHYSIOLOGICAL STUDIES 

(243) OF THE NERVOUS SYSTEM OF AMPHIBIA (1. The 
afferent system of the trunk of Amblystoma.) Q. E. Coon ill, 
Joum. Comp. Neurol., 1914, xxiv., April, p. 161 (60 figs.). 

The greater part of this paper deals with Coghill’s anatomical and 
experimental studies of the dorsally situated, intraspinal ganglion 
cells (the giant ganglion cells of Rohon and Beard) in early 
embryos of Amblystoma before any perceptible dorsal roots from 
spinal ganglionic anlagm can be seen. These giant cells and their 
processes constitute the sensory column of the cord: their axons 
pass cephalad, their dendrites peripherally to end in skin and the 
myotomes. A single neurone of this system may innervate both 
skin and muscle. Coghill shows that these cells and their processes 
form an afferent conduction-path which, through the greater part 
of its extent, if not through it all, is physiologically distinct from 
the motor tract of the same side. It is an integral part of a reflex 
mechanism which has the essential characteristic of the typical 
reflex arc of higher vertebrates. He concludes that “the giant 
ganglion cells are muscle sensory as well as skin sensory in 
function.” Leonard J. Kidd. 

A NOTE ON THE CIRCULATION OF THE CORNU AMMONIS. 

(244) Samvel T. Obton, Anat. Record, 1914, viii., April, p. 199. 

The author injected six brains to determine how great a factor 
the blood from the carotid system of cerebral vessels plays in the 
supply of the cornu ammonis and its associated structures. The 
path of communication from the carotid system to the hippocampal 
region is by a branch of the anterior choroid artery, which lias 
been found to be of constant occurrence, though variable in size, 



ABSTRACTS 


203 


and which reaches the uncus hippocampi, to which it gives 
cortical branches, and then, as is apparent in the injected specimens, 
deeply penetrates the white matter of the cornu for a variable 
distance. Figures are given showing the distribution of an 
unopposed injection of the anterior choroid artery in a brain 
from a case of general paralysis, about three hours after death. 

A. Ninian Bruce. 

A COMMUNICATION AS TO THE CAUSATION OF LARGE 
(24ft) VASCULAR GROOVES FOUND ON THE INNER ASPECT 
OF THE OS PARIETALE. Bernard Coen, Joum. Anat. and 
Physiol ., 1914, xlviii., April, p. 293. 

Some of the large gutter-like grooves found in the inner aspect of 
the skull are due to diploic venous tissue, which has come to the 
surface by the erosion of the inner table of the skull. It is 
possible that when there is only one large gutter-like groove 
present the meningeal and diploic vessels may be contained in 
the same groove. 

The factors which produce these grooves are:—(1) large diploic 
vessels to commence with; (2) some degree of venous engorge¬ 
ment ; and (3) an atrophying skull consequent on advancing age. 

A. Ninian Bruce. 


PHYSIOLOGY. 

VITAL STAINING AND CHEMOTHERAPY. (Vitale F&rbung und 
(246) Chemother&pie.) Professor Goldmann, Perl. Klin. Wchnsckr ., 
1912, xlix., Sept 2, S. 1689. 

Goldmann describes the result of some researches as a sequel to 
his book on intra-vitam staining. Examining histologically the 
animals that had been injected during life through the vena jug., 
he found the central nervous system quite free from stain except in 
the plexus choreoideus of the lateral, the third, and fourth ventricles. 
This discovery led him to think that perhaps the choroid plexus 
plays an important part in the nutrition of the foetus. He finds 
that glycogen is stored up in the choroid plexus, and from there 
given out into the cerebro-spinal fluid from a very early period 
of foetal life onwards. 

With regard to the behaviour of the vital stains to the choroid 
plexus, they were fouud here in the form of minute granules. The 
cerebro-spinal fluid remains free except in the cases where toxic 
doses have been injected, and Professor Goldmann thinks the stain 
filters through in consequence of injury to the choroid epithelium. 
This view is confirmed by the observations of Evans, who found 



204 


ABSTRACTS 


the ganglion cells diffusely stained in a case of experimental 
poliomyelitis in a vitally stained animal. 

If the stain is injected directly into the cerebro-spinal fluid, it 
has a toxic effect, and the animal has severe spasms, and rapidly 
sinks into a comatose condition, and dies within three or four 
hours. A histological examination shows diffuse staining of the 
cord, and of the pedunculus cerebri The stain is found in the 
nerve roots as also in the cerebral nerves. Throughout the whole 
substance of the cord, including the ganglion cells of the anterior 
and posterior cornua, the stain is found, and the nuclei as well as 
the processes are affected. In Some parts the glia-cells are also 
stained. These results show that the choroid plexus acts as a 
protective membrane which prevents the entrance of substances 
injurious to the nervous system, in the same way that the placenta 
prevents the entrance of substances injurious to festal life. 

Laura Forster. 

THE CEREBRO SPINAL FLUID.-II. CEREBROSPINAL PRES- 

(247) SURE. W. E. Dixon and W. D. Halliburton. Jovrn. Physiol., 
1914, xlviii., p. 128. 

The authors here record a number of experiments in which the 
torcula pressure, the arterial blood-pressure, and the cerebro¬ 
spinal pressure were recorded simultaneously, and the effect of 
changes in one of these factors observed upon the others. They 
show that the cranial contents can no longer be regarded as a 
fixed quantity without the power of expanding or contracting in 
volume. The cerebro-spinal pressure is influenced passively to a 
small oxtent by changes in the arterial and venous pressures, 
but such alterations are insignificant compared with the 
independent changes in pressure which occur as the result of 
secretory activity. Of all the conditions which influence the 
cerebro-spinal secretion, the most important are deficiency of 
oxygen and excess of carbon dioxide in the blood. 

A. N ini an Bruce. 

POLYURIA FROM EXPERIMENTAL LESION OF THE OPTO 

(248) PEDUNCULAR REGION OF THE BASE OF THE BRAIN. 
THE REGULATING MECHANISM OF THE WATER CON¬ 
TENT OF THE ORGANISM. (Polyurie par ltfsion de la rdgion 
opto-pddonculaire de la base du cerveau. Mdcanisme rdgulateur 
de la teneur an eau de l’organisxne.) J. Camus and O. Roussy, 
Compt. Bend. >Soc. de Biol., 1914, lxxvi., May 15, p. 773. 

From their further experiments on this subject in dogs the authors 
give these conclusions: (1) In the opto-peduncular region of the 
base of the brain, in the neighbourhood of the tuber cinereum, 



ABSTRACTS 


205 


there is a nervous area, which remains to be accurately determined, 
a lesion of which gives polyuria; (2) this area appears to be a part 
of a mechanism which regulates the water-content of the organism. 
Lesions of this region may give—possibly according to their extent 
—either a polyuria with accompanying polydipsia, i.e., without 
disturbance of this regulating mechanism, or without consecutive 
polydipsia, it., with such disturbance; (3) in young animals this 
regulating mechanism appears to functionate less perfectly than 
in adults ; (4) of all the disturbances which we have attempted 
to produce in the absorption and elimination of water, viz., 
injection of urea or glucose or sodium chloride or caffeine, water 
diet, or puncture of the base of the brain, the last mentioned 
procedure acts with the greatest intensity and the longest duration. 

Leonard J. Kidd. 

VASOMOTOR NERVES IN THE LUNGS. Enid M. Tribe, Journ. 

(249) o/Phy$iol., 1914, xlviii., May 18, p. 154. 

Mrs Tribe here continues her previous researches (v. Review , 
1913, xL, p. 28). Her experiments were performed, by a slightly 
modified Brodie and Dixon’s method, mainly on cats, but also on 
dogs, rabbits, rats, guinea-pigs, and a ferret. She concludes: 
(1) All preparations of adrenalin, in amounts not less than 
‘01 mgm., under normal conditions of pressure and temperature, 
produce constriction of the pulmonary vessels. This constriction 
iB followed by a dilatation, especially marked in cats; (2) the 
minimum amount of adrenalin capable of producing constriction 
is ‘01 mgm., but dilatation is obtained with only *00002 mgm.; 

(3) the effects of adrenalin are due to action on the smaller 
arteries and arterioles, not merely on the pulmonary artery itself; 

(4) stimulation of the stellate ganglion produces slight vasomotor 
effects; (5) after ergotoxin, the constrictor effect of adrenalin is 
lost, only dilatation being produced; (6) the constriction is due 
to vasoconstrictor nerves of sympathetic origin. 

Leonard J. Kidd. 

OBSERVATIONS UPON DECEREBRATE RIGIDITY. Lewis H. 

(250) Weed, Journ. Phytiol., 1914, xlviii., p. 205. 

A number of experiments on cats are recorded here which were 
undertaken with the view that probably the cerebellum presents 
an essential link in the reflex which occasions decerebrate rigidity. 
Various portions of the cerebellum were removed after decerebrate 
rigidity had set in, and the effects recorded. The effect of section 
of the cerebellar peduncles and of different levels of the mid¬ 
brain were also examined. 

The main reflex centre and, in that sense, the source of decere- 



206 


ABSTRACTS 


brate rigidity, lies in the mid-brain, and is probably the nucleus 
ruber. The cerebellum forms a very important, if not absolutely 
essential, pathway for the afferent impulses from the limbs and 
trunk, concerned in decerebrate rigidity. The cerebellum forms 
an essential link in the inhibitory pathway from the cerebral 
cortex. The localisations of the cerebellum, as far as can be 
ascertained from study of the rigidities in the various extremities, 
are not sharply circumscribed or very minutely differentiated. 

A. Nin i an Bruce. 

THE HYPOTENSIVE ACTION OF PITUITARY POSTERIOR LOBE 

(251) EXTRACT ON THE PULMONARY CIRCULATION. (Sur 
1'action hypotensive de l’extrait dn lobe postdrieur cThypophyse 
sur la circulation pulmonaire.) L. Hallion, Com.pt. Rend. Soc. de 
Biol., 1914, lxxvi., April 10, p. 581. 

Hallion experimented on dogs, recording the carotid and jugular 
pressure, and that of the pulmonary artery and veins. He con¬ 
firms the findings of Wiggers (1911) that pituitary extract acts 
on the pulmonary circulation, and finds that intravenous injection 
of posterior lobe extract produces constantly in dogs a fall of the 
pulmonary arterial pressure. This fact, taken along with the 
known blood-coagulating power of posterior lobe extract (Weil 
and Boytf, 1909), justifies its therapeutic use in the haemoptysis of 
pulmonary tuberculosis recently adopted by Rist and others. 

Leonard J. Kidd. 

ADRENAL DEFICIENCY AND THE SYMPATHETIC NERVOUS 

(252) SYSTEM. R. O. Hoskins and Hombr Whselon, Amer. Joum. 
Physiol., 1914, xxxiv., May 1, p. 172. 

Authors’ conclusions: (1) Complete ligation of both adrenal 
glands of dogs at a single operation causes, within four to six 
hours, characteristic weakness of the skeletal muscles, including 
those of respiration; (2) the weakness is shared to a marked degree 
by the cardiac muscle; (3) at a time when cardiac weakness is 
strongly in evidence, blood-pressure remains at or near its initial 
height; (4) a compensatory activity of the vasomotor system 
therefore occurs; (5) vasomotor responses to Faradic stimulation 
of the crural nerve persist. The vasomotor reactions to adrenalin 
also persist undiminished. The reactions to nicotine are often 
somewhat exaggerated as compared with preliminary observations 
under the same dosages; (6) the vasomotor system, therefore, as 
well as the vascular musculature, are unimpaired at a time when 
marked asthenia of skeletal and cardiac muscle has developed; 
(7) this asthenia is sufficient alone to account for the final fatal 
results of adrenal extirpation; (8) we find no evidence, therefore, 



ABSTRACTS 


207 


that the sympathetic system suffers primarily in any degree from 
adrenal extirpation. Leonard J. Kidd. 

EFFECTS OF ADRENALECTOMY IN GUINEA PIGS. (Effets de la 

(253) capeolectomie chez le cobay e.) A. Marie and V. Morax, Comj>t. 
Rend. Soe. de Biol., 1914, lxxvi., May 8, p. 699. 

Marie showed in the same journal (1912, lxxii., p. 804) that 
adrenalin neutralises the toxines of tetanus and diphtheria in vitro. 
The most important point in the present experiments is that after 
complete bilateral adrenalectomy performed at two separate sittings 
with an interval of eight days—a method which gives a prolonged 
survival of guinea-pigs—inoculation with a dose of tetanus toxin, 
which is inactive for the controls and for incompletely adrenal- 
eetomised animals, provokes a perfectly definite local tetanus, a 
fact which seems to confirm Marie’s results obtained in vitro. 

Leonard J. Kidd. 

FURTHER OBSERVATIONS ON THE CONSTRICTING ACTION 

(254) OF ADRENALINE ON THE CEREBRAL VESSELS. Carl 
J. Wiqokrs, Joum. Physiol., 1914, xlviii., p. 109. 

Out of thirteen experiments upon the brain removed from the 
skull, adrenalin constricted the cerebral vessels in eight cases. 
In four no reaction occurred, and in one, which may have been 
due to an accidental rupture of vessels, an increased flow per¬ 
manently followed. A. Ninian Bruce. 


MECHANICAL STIMULATION OF THE COCCYGEAL GANGLION : 
(255) A CONTRIBUTION TO THE PHYSIOLOGY OF THE SYMPA 
THETIC NERVOUS SYSTEM. E. F. and R. V. Cyriax, Zeitschr. 
f. allg. Physiologie, 1913, xiv., Hft., S. 14, p. 297. 

The authors experimented on dogs, and exposed the coccygeal 
ganglion lying on the first coccygeal vertebra. Stimulation of the 
ganglion from the secondary of an induction coil produced con¬ 
traction of the circular fibres of the colon and rectum, the former 
only at the lower part of the descending colon. If the sympathetic 
nerves were cut immediately proximal to the ganglion, it was found 
that stimulation of the latter was without effect on the gut. 

The route by which the impulses reach the rectum from the 
coccygeal ganglion does not seem clear. The authors believe that 
in mechanical stimulation of the coccygeal ganglion in man they 
have discovered a useful therapeutic measure in the treatment of 
certain cases of chronic constipation. S. A. K. Wilson. 

i7 



208 


ABSTRACTS 


18 POLISHED BIOS PLUS VITAMINS A COMPLETE FOOD? 

(256) Casimib Funk, Jour *. Physiol 1914, zlviii, p. 228. 

The result of experiments upon pigeons shows conclusively that 
polished rice and vitamine constitute a complete food. There iB 
no justification at present to accept the necessity of two different 
vitamines, one for curing the nervous symptoms, and one for 
maintenance of body weight. A. Ninian Bruce. 


PSYCHOLOGY. 

THE PROBLEM OF THE THINKING DOG OF MANNHEIM. 

(257) William Mackenzie, Archiv. de Psychol., 1913, Dec., p. 312. 


THE MANNHEIM DOG. J. Labguieb des Bancels and En. Clapar^de. 
(268) Archiv. de Psychol., 1913, Dec., p. 377. 

We have here a detailed account of a three days’ visit paid to 
Rolf, the thinking dog of Mannheim, by W. Mackenzie. The dog 
answers questions, by means of rapping out with his paw numbers 
which stand for letters: he does simple sums, and he describes 
pictures: he sometimes makes remarks spontaneously. The writer 
was given ample opportunity to conduct experiments under condi¬ 
tions determined by himself, and he seems thoroughly satisfied 
of the genuine nature of the dog’s performances. Rolf’s work is 
distinctly more remarkable than that of the thinking horses 
of Elberfeld: and, as Mr Mackenzie does not fail to point out, any¬ 
one can become possessed of a dog, so that it may reasonably be 
hoped that the fame of Rolf’s achievements will lead to further 
experimentation in the same direction. 

MM. Larguier des Bancels and Clapar&de add a brief contribu¬ 
tion giving an account of their interview with the wonderful dog. 
They agree with Mackenzie in regarding the good faith of his 
mistress as beyond question; they unhesitatingly accept her state¬ 
ment that Rolf often gives facts in his answers of which she is 
unaware, yet they suggest that his answers may be derived from 
her in that he is the vehicle of her subconscious mind—that he is, 
in a word, an animated planchette. This hypothesis they en¬ 
deavoured to test. Any evidence they give tends to discredit it, 
but their investigations were stopped prematurely by the illness of 
\be dog. Margaret Drummond. 



ABSTRACTS 


209 


PATHOLOGY. 

PARTIAL AGENESIS OF THE CORPUS CALLOSUM. (Un cm 

(259) d’agta&ie paxtieUe da corps calleux.) Roubinovitch and Barb£, 
Nouv. Icon, de la SalpStriire, 1913, Sept-Oct. p. 407. 

A considerable number of cases of agenesis of the corpus 
callosum have already been recorded. As a rule they have occurred 
in association with idiocy. The authors describe the case of a boy, 
aged 5, an idiot, who could neither speak nor walk. His 
intelligence was nil, he was unable to feed himself, and took no 
apparent interest in his surroundings. He died of broncho¬ 
pneumonia, and at the autopsy it was found that there was no 
trace of a corpus callosum, properly speaking. Below the callosal 
gyrus on each side was a deep depression. On making a horizontal 
section of each hemisphere, however, immediately above the level 
of the optic thalamus, the authors found a band of white matter 
running along the mesial side of the lateral ventricles, and uniting 
the frontal to the occipital lobes. Thus although no corpus 
callosum was visible mesially, yet each hemisphere possessed a 
callosal association system. The view is taken that the case 
corroborates the opinion of Archambault, that in most cases of 
so-called agenesis of the corpus callosum, the agenesis is really 
partial, and concerns the actual commissure only. 

S. A. K. Wilson. 

IRON INFILTRATION IN THE FIXED AND WANDERING 

(260) CELLS OF THE CENTRAL NERVOUS SYSTEM. D. J. 

M'Oakthy, Amer. Joum. Med. Set., 1914, cxlvii., March. 

A case of extensive haemorrhagic encephalitis in the cortex is 
described. The iron reaction was not demonstrated in the cortical 
ganglion cells, but was obtained in a striking way in the plasma¬ 
like cells of the pia arachnoid and in the elastic coats of the 
smaller cortical arteries. D. K. Hrnderson. 


CLINICAL NEUROLOGY. 

THE SIGNIFICANCE FOR DIFFERENTIAL DIAGNOSIS OF 
(261) BArANY’S POINTING-TEST. (Zur differential-diagnoatischen 
Bedeutung des Bdrdny’schen Zeigeversuchs.) Rothmann, Neurol. 
Centralbl., 1914, Jan. 2, p. 3. 

It is now fairly well recognised that Bdrdny’s pointing-test, 
utilised after rotation of the patient on a revolving chair or after 
injection of water into the ear, is of very considerable value in 



210 


ABSTRACTS 


revealing what otherwise may be practically a latent defect of 
cerebellar function. It has been shown that the defect in pointing 
to the examiner’s finger may affect a whole limb, or a segment of 
the limb only, and that such local defects correspond strictly to 
local disturbances in specified portions of the cerebellar cortex. 
Bdr&ny has further stated that deviations in the pointing-test can 
only be detected when voluntary innervation is possible, and also 
that the cerebral cortex (and ? the rest of the cerebellar cortex) 
can compensate for the failure of cerebellar innervation in a 
particular direction: in such cases only the caloric test will bring 
out the mispoiuting, and so indicate the cerebellar impairment: 
there is no spontaneous mispointing. The question may therefore 
be asked whether there may not be normally in the cerebral cortex 
itself a mechanism for correct direction of limb movements, whose 
impairment may lead to similar mistakes in pointing by the 
B£r£ny tests. Rothmann describes the case of a patient of 28, 
with a traumatic subpial hsematoma over the left supramarginal 
gyrus, diagnosed and corroborated by operation. There was neither 
motor nor sensory defect of the right arm, yet in pointing tests it 
was found to be grossly defective. No cerebellar symptoms were 
present except a slight subjective feeling of giddiness. 

Rothmann discusses whether this impairment, confined to the 
right arm, was due to involvement of the cerebellum or to 
“ Fernwirkung ” on the opposite cerebellar hemisphere, or to the 
lesion of the supramarginal gyrus alone. He inclines to the last 
of these, and points out that it is the parietal region which is 
concerned with the correlation of visual and ocular and spatial 
sensations. He quotes a personal case in which, with a cerel>e!lar 
tumour invading the cortex of the gyrus quadrangularis posterior 
and semilunaris superior no pointing mistakes were discovered by 
B&rdny’s tests, and attributes this absence to complete cerebral 
compensation. S. A. K. Wilson. 


NERVOUS DISEASES OF ELEMENTARY SCHOOL CHILDREN— 
(262) BOVS AND GIRLS. J. Priestley, Brit. Joum. Child. Bis., 1914, 
xi., p. 113. 

In a table compiled from the records of 62,236 children aged from 
5 to 14 years, who were medically examined during the period 
1909-11, the writer shows that in functional disorders, boys and 
girls are approximately equal, but in every other nerve complaint 
including the more serious ones such as mental dulness and de¬ 
fect, stammering, paralysis, and epilepsy, there is a marked 
preponderance among boys. J. I). Rolleston. 



ABSTRACTS 


211 


HERPES AND ZOSTER OF DENTAL ORIGIN. (Herpes et son* 

(263) d’origine denture.) L. Lempkrt, Theset de Parity 1913-14, No. 138. 

Lempekt’s main conclusions are as follows:— 

1. A violent but transitory alveolo-dental irritation such as 
trauma or acute inflammation of the dental pulp may give rise 
to herpes. 

2. Prolonged irritation such as suppurative arthritis of the 
jaw, alveolo-dental cyst, or cutting of a tooth in association with 
other causes may give rise to zoster in a subject in a state of 
unstable nervous equilibrium. 

3. Zoster of this kind almost invariably occupies the domain of 
the fifth nerve or cervical plexus. Exceptionally it is situated at 
a distance. Ophthalmic zoster is due to lesions of the upper 
canines and premolars. Cervical zoster is related to lesions in the 
lower jaw. 

4. Zoster of dental origin is preceded by a long neuralgic 
phase which lasts for weeks or months. The eruption appears 
on the side on which the irritation exists. 

5. Zoster of dental origin belongs to the large class of non- 
infective zosters in the production of which reflex mechanism plays 
an important part (rf. Review, 1909, vii., p. 360; ibid., 1913, 
xi., pp. 211 and 485). 

The thesis contains the histories of twelve cases including an 
original one of a woman who developed herpes of the left half of 
the upper lip on the day following extraction of the second left 
upper molar. J. D. Rolleston. 

HERPES ZOSTER IN A PATIENT WITH SPINAL CORD SYPHILIS. 

(264) H. E. Alderson, Joum. Cut. Dis., 1914, xxxii., p. 230. 

In October 1912 a man who had contracted syphilis eight years 
previously had paralysis of the right lower extremity with crossed 
disturbance of sensibility. After treatment with salvarsan and 
mercurial inunctions he was so far improved that in January 1913 
he could walk without aid. In the following October he presented 
typical herpes zoster in the area corresponding to the sensory 
distribution of the right ninth and tenth dorsal roots. 

J. D. Rolleston. 

ON A CASE OF EARLY SPINAL SYPHILIS WITH BULBAR 
(266) PHENOMENA. (A propos dun cas de syphilis mddollaire 
prlcoce avec phfoomdnes bulbaires.) A. Legris and J. Benech, 
Pari* mdd., 1913, iv., p. 315. 

The writers describe a case somewhat similar to that reported by 
one of them some years previously (v. Review, 1910, viii., p. 564). 
A previously healthy man, aged 21, developed a chancre in 



212 


ABSTRACTS 


January 1913, and at the end of February secondary ulceration 
of the buccal and genital mucosae Three intravenous injections 
of 0 - 30 gr. salvarsan were given, followed by grey oil, and the 
symptoms disappeared. Towards the end of May he took to 
motorcycling, and shortly afterwards began to suffer from pains 
in the lumbar region and thighs. On admission to hospital a 
month later the knee and ankle jerks were abolished, there were 
definite ankle clonus, and constant jerkings of' the calf, thigh, and 
recti abdominis muscles, and a few, days later of the muscles of 
the upper limbs. Generalised secondo-tertiary skin lesions were 
present. The cerebro-spinal fluid showed hypertension and very 
marked lymphocytosis. On July 3 an intravenous injection of 
0 30 gm. salvarsan was given. On the 8th he began to suffer from 
dyspnoea without signs in the lungs, and on the 17th he developed 
strabismus, diplopia, and slight nystagmus, followed by loss of 
power in the upper limbs, difficulty of deglutition, and other signs 
of labio-glosso-pharyngeal palsy, and loss of sphincter control. He 
also had attacks of vomiting, and lastly delirium occurred. Larger 
doses of neo-salvarsan were given intravenously, as well as 
biniodide intramuscularly, and after the fifth dose of neo-salvarsan 
and the seventeenth of biniodide, improvement began, and by the 
middle of October the patient was able to carry out his military 
service without ill effects. 

The localisation of the infection in the spinal cord is attributed 
to the use of the motor cycle. J. D. Rolleston. 

BINASAL HEMIANOPSIA OCCURRING IN THE COURSE OF 
(266) TABETIC OPTIC ATROPHY. Charles K. Heed and George 
E. Price, Joum. Amer. Med. Astoc., 1914, Ixii., March 7, p. 771. 

A man, aged 48, unmarried, complained of failing vision, slowly 
progressing for the past three months, until now he cannot see to 
do his work. There was no history of diplopia. The pupils were 
unequal and did not react to light. Both optic papilla} presented 
a decided atrophic pallor, and on examination with the perimeter 
a clear-cut bi nasal defect was found. 

The gait was normal, Romberg’s sign was present, but not 
marked. No other cranial nerves were affected. The knee-jerks 
were normal, but both Achilles jerks were lost. A lymphocytosis 
was present in the cerebro-spinal fluid. The Wassermann reaction 
was negative, possibly the result of treatment by mercury and 
pot iod. 

The authors believe the binasal defect in the visual fields to be 
the result of a selective atrophy affecting the intracranial portion 
of the optic nerves, and refer to the rarity of the condition. 
Shoemaker collected 18 cases of binasal hemianopsia in 1905, 



ABSTRACTS 


213 


and added his own. Since then only one more case has been 
recorded, making, with this one, 21 in all. Of this series, in 3 
neuroretinitis was present, in 2 traumatic optic atrophy, 2 were 
optic neuritis from brain tumour, 2 were tabetic optic atrophy, 
2 chronic interstitial optic neuritis, 2 secondary optic atrophy, 4 
primary optic atrophy, and 1 traumatic optic neuritis. 

A. Ninian Bruce. 

A CLINICAL NOTE ON FIBROMA MOLLUSCUM GRAVIDARUM. 

(267) R. L. Sotton, A trier. Joum. Med. Set., 1914, cxlvii., p. 419. 

Sutton alludes to the recent papers by Hirst ( v . Review, 1911, ix., 
p. 570) and others, and records the following case of fibroma 
molluscum gravidarum or Brinckner’s disease. The patient was a 
woman, aged 38, above the average in intelligence, an unusual 
occurrence in well-marked cases of fibroma molluscum. During 
her first pregnancy about twenty pigmented pedunculated tumours 
appeared on her neck and chest but shrivelled up shortly after 
delivery, and three months later entirely disappeared. During her 
second pregnancy a second crop appeared but many persisted. 
Examination showed that the lesions were histologically identi ial 
with those of fibroma molluscum (the neurofibroma of von 
Recklinghausen). J. D. Rolleston 

FIBROMA M0LLU80UM GRAVIDARUM. S. M. Bkincknbr, Amer. 

(268) Joum. Derm., 1912, xvi., p. 240. 

This condition which was first described by the writer in 1906 is a 
lesion of the skin appearing in the latter half of pregnancy, bearing 
the histological characters of fibroma molluscum, but differing from 
it clinically in its almost total disappearance post partum. Its 
distribution is limited to the neck, breasts, and submammary area. 
The lesions are frequently but not always pigmented. 

J. D. Rolleston. 

ON PREROSEOLAR MENINGITIS. (Sur les mdningites prdroseoliques.) 

(269) C. Audry and Lavau, Anti, de Derm, et de Syph., 1914, v., p. 29. 

A man, aged 25, had noticed a chancre on the penis for about 
a month, but showed no eruption. Wassermann’s reaction was 
positive in the blood, but negative in the spinal fluid which was 
clear, under hypertension, and showed a well-marked lympho¬ 
cytosis. 0*60 areenobenzol and 10 cgm. of mercury were injected. 
The same evening he had headache and nuchal rigidity, and 
the following morning vomiting and Kernig’s sign. Within a 
fortnight the symptoms subsided. Two more injections of 606 
were well borne. A second lumbar puncture, three weeks after the 



214 


ABSTRACTS 


first, showed a clear fluid still under hypertension, and with 
increased lymphocytosis. Wassermann’s reaction was negative. 
No eruption had appeared. A similar case was recently reported 
by Achard and Desbouis ( v . Review, 1913, xi., p. 38). 

J. D. Rolleston. 

ON ASEPTIC REACTIONS OF THE MENINGES AND THEIR 
(270) DIAGNOSIS. (Sur les reactions aseptiques des mdninges et leur 
diagnostic.) J. Eoziebe, Paris mid., 1913*14, iv., p. 89. 

The symptoms may be very incomplete or indicate nervous dis¬ 
turbance without meningeal localisation. As a rule, however, 
there are signs of meningeal involvement which suggest tuberculous 
or cerebro-spinal meningitis. Acute symptoms are usually of short 
duration, and subside soon after lumbar puncture or spontaneously. 
Occasionally sequelm have been observed such as deafness, or more 
or less extensive paralysis. 

Lumbar puncture gives issue to a fluid which is sometimes clear, 
but often turbid and very frequently has the appearance of pus, 
from which it is distinguished by being aseptic, and by the absence 
of degeneration in the polymorphonuclear cells. The cerebro-spinal 
fluid shows no excess of albumin, but an increase of sugar. 

The syndrome is caused by meningeal congestion usually due 
to toxic irritation such as uraemia, alcoholism, the toxaemia of 
pregnancy or an acute lesion in the neighbourhood of the meninges 
such as otitis, cerebral haemorrhage, or abscess. Puriform cerebro¬ 
spinal fluid is also found in insolation, influenza, pneumonia, and 
syphilis, and in chronic diseases of the nervous system such as 
tabes and general paralysis. J. D. Rolleston. 


MENINGITIS IN MUMPS. (Les m&xingites ourliennes.) G C. Roux, 
(271) Gaz. des Hop., 1914, Ixxxvii., p. 549. 

Meningeal symptoms are very frequent in mumps, but typical 
meningitis is rare. Roux 6aw only three examples among 274 
cases of mumps admitted to the Claude Bernard Hospital in 1912. 
As a rule it occurs at the height of the disease, 3 to 8 days after 
the onset, but it may occur earlier, and even precede the parotid 
swelling. There is almost always intense spinal lymphocytosis. 
The symptoms usually subside rapidly and do not last more than 
5 to 6 days. 

An attenuated meningeal syndrome is much more frequent 
than typical meningitis. It may occur at the onset or precede 
the parotid swelling. The symptoms arq severe headache, vomit¬ 
ing, slight nuchal rigidity and rise of temperature. As a rule 
they do not last longer than from 24 to 48 hours. Sometimes 



ABSTRACTS 


215 


they are merely represented by bradycardia and spinal lympho¬ 
cytosis. The frequency of lymphocytosis in mumps is shown by 
Roux having found it in 31 out of 67 cases on whom he performed 
lumbar puncture. As a rule it is discrete, but it may be 
abundant, and vary from 50 to 300 lymphocytes in a field. 

Two theories have been put forward to explain the existence 
of meningitis in mumps. 1. Meningitis is a manifestation of 
the septicemia of the disease like the other complications of 
mumps, especially orchitis, with which it is frequently associated. 
2. Meningitis is an extension of the local inflammatory process 
which precedes the parotitis. Chautt'ard holds that there is a 
direct propagation of the infection of mumps to the basilar region 
of the pharynx and perivascular lymph sheaths. 

J. D. Rolleston. 

ON THE OEBBBRAL COMPLICATIONS OF WHOOPING COUGH. 
(272) WITH SPECIAL REFERENCE TO " PACHYMENINGITIS 
PRODUCTIVA INTERNA.’’ (Uber die Gehirnkomplikationen 
des Keuchhustens mit besonderer Berttckaichtigung der “ Pachy¬ 
meningitis productiva interna.”) B. Hada, Virchows Archiv , 
1914, ccxiv., p. 216. 

A MALE infant, aged 14 months, was taken ill with a cough and 
a fortnight later had four typical attacks of whooping with a 
severe convulsion and collapse on the same day. Four days later 
left otitis media developed, but both it and the cerebral symptoms 
soon subsided. On the 76th day left hemiplegia occurred, and on 
the 158th day erysipelas which was followed in a few days by 
signs of severe meningitis, and death took place on the 168th day. 

The necropsy showed purulent leptomeningitis with marked 
external hydrocephalus, old pachymeningitis productiva interna, 
extensive softening of the cerebral cortex especially on the right 
side, and right otitis media. No bacteria were found. 

The clinical symptoms showed that the acute leptomeningitis 
and associated encephalitis were in no way connected with whoop¬ 
ing cough, but were caused by intercurrent erysipelas or otitis 
media. 

On the other hand the pachymeningitis and pressure atrophy 
of the cerebral cortex which had given rise to hemiplegia probably 
dated from the convulsion observed on the 14th day. 

A review of the literature is appended in which it is stated 
that the only clear case of pachymeningitis productiva interna 
following whooping cough has been reported by Reimer. ( Jnhrb . 
/. Kinderhcilk., 1876, x.). 

Hada regards toxic or bacterial causes as responsible for the 
various cerebral complications of whooping cough, and as able to 



216 


ABSTRACTS 


produce various inflammations such as encephalitis, meningo¬ 
encephalitis, lepto-meningitis, and pachymeningitis, which frequently 
assume a haemorrhagic character. J. D. Rolleston. 

BRAIN ABSCESS CAUSED BY FUSIFORM BACILLI. G. F. Dick 

(273) and F. A. Emge, Joum . Amer. Med. Assoc ., 1914, hdi., p. 446. 

The writers allude to a previous paper by one of them (t>. Review, 
1913, xi., p. 626), and report a fatal case in a man, aged 40, with 
an abscess occupying the left frontal, temporal, and parietal lobes. 
A pure culture of fusiform bacilli was obtained, and injection of it 
into the brain of a rabbit was followed by convulsions in twelve 
hours, and in thirty-six hours by paralysis of all four extremities 
and death. J. D. Rolleston. 

A CASE OF BRAIN ABSCESS. Cecil E. Reynolds, Joum. Amer. 

(274) Med. Assoc., 1914, Ixii., Feb. 7, p. 449. 

A MAN was taken ill during the night with headache and nausea. 
These passed off, but his speech became indistinct, and mental 
excitement was noticed. Severe headache and sleeplessness 
developed, with slight weakness of his right arm. Pulse dropped 
to 50. Five days later the pain was localised to the left side of 
the head, and commencing optic neuritis on the nasal side of each 
disc was noticed. On trephining, the cortex was darker than 
nonnal, and the vessels swollen. Exploration deep into the 
lenticular nucleus disclosed a cavity the size of a walnut filled 
with thick, ill-smelling pus. This was drained, and a tube left 
in situ. He began to improve, but became later comatose, and 
died thirteen days after the operation. There were found at the 
autopsy two abscess cavities side by side in the white matter of 
the angular and intraparietal lobes, each about the size of half 
a walnut. No sign of ear or nose disease was present The 
organisms were the bacillus of influenza and Staphylococcus 
aureus (cf. Review , 1913). A. Ninian Bruce. 

PNEUMONIC HEMIPLEGIAS. C. F. Withington, Amer. Joum. 

(275) Med. Set., 1914, cxlvii., February. 

Cerebral accidents in pneumonia may be divided into two 
classes:— 

1. Those caused by gross anatomical lesions, such as meningitis 
of pneumococcus origin, thrombosis, embolism, abscess, &c. 

2. Those occurring in young, rather vigorous people, and having 
a better prognosis than those cases belonging to the first group. 

Four principal explanations have been advanced for the hemi- 



ABSTRACTS 217 

plegias belonging to this second group: (a) encephalitis, (b) 
hysteria, (c) circulating organisms, ( d ) circulating toxins. 

Pneumonic hemiplegia occurring without gross lesion is not 
common, but usually appears about the second or third day from 
the onset of the pneumonia. 

Four cases are reported. D. K. Henderson. 


A DEFECT IN INNERVATION OF THE FACIAL NERVE FROM 
(276) TUMOURS OF THE POSTERIOR FOSSA (Uber sine Sttfnmg 
der Innervation das N. facialis bei OeschwUlsten der hinteren 
SchEde lgm be.) Lasarew, Neurol. Cenlralbl., 1914, Jan. 2, p. 13. 

The author describes four cases of cerebellar tumour in which a 
dissociation of function in the homolateral facial nerve was 
observed. There was paresis of the lower face both for voluntary 
and involuntary movements, with overaction on voluntary innerva¬ 
tion of the upper face. By asking the patient to open his mouth 
and simultaneously to look up, the author was able to demonstrate 
readily this dissociation. He offers no definite explanation of the 
mechanism of this disturbance of innervation, but discusses several 
possibilities. S. A K. Wilson. 


TUMOUR OF THE MIDDLE CRANIAL FOSSA, INVOLVING THE 
(277) GASSERIAN GANGLION. W. A Plummer and O. B. New, 
Joum. Anver. Med. Assoc., 1914, lxil, April 4, p. 1062. 

The patient was a man, aged 21. No evidence of tubercle or 
syphilis. Three enlarged upper cervical glands had been discovered 
on the right side of the neck twenty-one months previous to 
examination. Three months later pain developed anterior to the 
right ear, and the glands were excised but not examined micro¬ 
scopically. The pain soon became constant, with intermittent 
tic-like paroxysms over the entire distribution of the fifth nerve. 
These paroxysms occurred once or twice a day, and lasted from a 
few minutes to an hour. Momentary attacks of diplopia and 
indefinite objective vertigo were complained of. Deep alcoholic 
injection of the branches of the fifth nerve gave some relief for 
a week. On careful examination no symptoms of general intra¬ 
cranial pressure such as headache, vomiting, choked disc, &c., 
could be found. He was somewhat dull and apathetic, and 
answered questions slowly. There were, however, definitely 
localising signs, viz., anaesthesia of the first and second divisions 
of the right fifth nerve and hypesthesia of the third division. 
The sense of taste was absent from the right anterior portion of 
the tongue, there was partial paralysis of all the right extrinsic 



218 


ABSTRACTS 


eye-muscles with a nearly complete ptosis, a large immobile right 
pupil and pallor of the right optic nerve-head. Possibly the 
alcohol injection was responsible for at least part of the anaesthesia. 

An operation by the Hartley-Krause method exposed a hard 
mass below the right temporal lobe. Its extent could not be 
determined, and removal was impossible. It proved to be a small 
round-cell sarcoma. The patient died a few months later. 

A. Ninian Bruce. 

ON THE COMBINATION OF CRANIAL HYPEROSTOSES AND 
(278) CEREBRAL TUMOURS. (Ober die Kombination yon Sch&del- 
hyperostosen und Hirngeschwtilsten.) Schlesinger and 
Schuller, Neurol. Centralbl. , 1914, Jan. 16, p. 82. 

The authors record a fresh case of the type where a bony cranial 
tumour corresponds exactly to an underlying meningeal or cerebral 
tumour. The patient presented the general symptoms of intra¬ 
cranial growth without a single localising sign. An X-ray 
photograph showed an osteoma the size of a hazel nut in the 
right frontal sinus. The patient died from an intercurrent 
affection, and a glioma, the size of a small apple, was found in the 
right frontal lobe, situated exactly opposite the frontal osteoma. 
The meninges were normal: the osteoma did not bulge into the 
general cranial cavity. S. A. K. Wilson. 


DIABETES INSIPIDUS AND INFANTILISM. (Di&bdte insipid® et 
(279) infantilism®: rfile probable de l’hypophyse.) Lereboullet, 
Faure-Beaulieu, and Vaucher, Nouv. Icon, de la SalpStribe, 1913, 
Sept-Oct., p. 410. 


The patient was a young man of 24, who developed normally up 
to the age of 14, when he sustained a shock from involuntary 
immersion in water. Shortly after he began to pass 7 or 8 litres 
of urine daily, and at the same time suffered from polydipsia. 
Neither sugar nor albumin was present in the urine. At the age of 
16 the patient’s teeth all dropped out in the course of a few months 
as the result of painful ulceration of the gums. A year or two 
later generalised eczema of severe type appeared and proved very 
intractable. On examination the youth was found to present well- 
marked signs of infantilism. There was no hair on face or pubes, 
and only one or two sparse hairs in the axillae. His voice had not 
“ broken.” There was atrophy of the testicles and penis. The 
sella turcica appeared to be of normal size and appearance in a 
radiogram. There were no visual or ocular symptoms. Under 
observation the patient often passed as much as 10 litres of limpid 
urine in the twenty-four hours. Hypophyseal, thyroid, testicular, 



ABSTRACTS 


219 


and pancreatic extracts were all given a trial without much result. 
For somewhat inadequate reasons the authors attribute the 
symptoms to defect of function of the pars intermedia of the 
hypophysis. S. A. K. Wilson. 

OXYCEPHALY AND THE OXYCEPHALIC SYNDROME. Charon 

( 280 ) and Courbon, Nouv. Icon, de la Salpetribre , 1913, Sept.-Oct, p. 422. 

The authors describe the cases of two male idiots presenting the 
characteristic cranial features of oxycephaly. One had also a 
degree of exophthalmos, but no other ocular symptoms. Both had 
suffered from rachitis, while neither showed any recognisable 
defect of function of the endocrinous glands. The authors discuss 
and dismiss as unsatisfactory both the rachitic and the glandular 
theories of oxycephaly. The idiocy suggests an early meningitis. 

S. A. K. Wilson. 

A CASE OF PROGRESSIVE FACIAL HEMIATROPHY. Grabs, 

(281) Neurol. Centralbl., 1914, Jan. 16, p. 85. 

This was a typical and advanced case of this rare affection, in 
a man of 32, who died from a pulmonary affection. A complete 
pathological examination was made, including the superior cervical 
sympathetic ganglion, the Gasserian ganglion, the branches of the 
trigeminal, the pons and medulla from the nucleus of the third 
to the nucleus of the twelfth. No difference between the two 
sides was found. This is the third recorded case where a patho¬ 
logical investigation was made, and it shows apparently that 
progressive facial hemiatrophy occurs without recognisable changes 
in the central, peripheral, or sympathetic nervous system. Un¬ 
fortunately the facial muscles were not examined. 

S. A. K. Wilson. 

THE DIAGNOSIS OF CEREBRAL HAEMORRHAGE BY MEANS 

( 282 ) OF LUMBAR PUNCTURE. Ouvrr ;P. Bigelow, Cleveland 
Med. Jovm., 1913, xii., April, p. 265. 

Cerebral haemorrhage can be detected by examination of the 
spinal fluid in about 90 per cent, of cases if the examination be 
made within three weeks after the “ stroke.” For the first four 
days or so there is a cloudiness or bloodiness of the fluid of 
varying degree, depending on the amount of blood which has 
escaped. Then a colour, due to haemoglobin, varying from light 
canary-yellow to reddish-brown, appears and persists in some 
degree for about three weeks. After that time our only guide 
in the spinal fluid is a probable persistence for some time of a 
slightly elevated cell count and proteid content. 

A. Niuian Bruce. 



220 


ABSTRACTS 


ON A CASE OF MUSCULAR ATROPHY FROM LEAD POISON 

(283) ING. (Su di un cmo di atrofla muscolare di intossicasione 
Batamina.) A. Scudkbi, Riv. ital. di Neurop., Psychic tr. ed 
Elettroter., 1913, vi., p. 560. 

The ner\ r ous complications of plumkism are extremely rare in 
Sicily, this being the first case that has occurred in Prof. 
d’Abundo’s clinique at Catania since its opening in 1894. The 
patient was a man, aged 54, employed in a colour factory where 
much lead was used and predisposed to nervous disease by having 
had an alcoholic father. 

For ten years he had suffered from lead colic, and for some years 
had had gradually increasing weakness in the hands. 

On admission the lesions were those of chronic poliomyelitis, 
the muscles of the scapula and pectoral regions, forearm, hands, and 
antero-external aspects of the legs being atrophied. The disease 
was arrested, and slight improvement occurred on the patient 
giving up his work and submitting to iodide and electrical treatment. 

J. D. Rolleston. 

THE SUPPOSED RELATION BETWEEN PARALYSIS AGITANS 

(284) AND INSUFFICIENCY OF THE PARATHYROID GLANDS. 

1. Geeen wald, Arner. Joum. Med. Set., 1914, cxlvii., February. 

In experiments with dogs the author has shown that after para¬ 
thyroidectomy there is a marked diminution in the excretion of 
phosphorus. This persists until tetany appears, and even longer. 
Analyses of the blood and serum of parathyroidectomised dogs show 
a decided increase in the content of phosphorus above the normal. 

It was argued that if parathyroid insufficiency is a factor in 
the etiology of paralysis agitans, then a similar increase in the 
amount of acid-soluble phosphorus would be found in the blood 
serum of patients with paralysis agitans. 

In comparing the blood serum of patients with paralysis 
agitans with the blood serum of other individuals, results were, 
however, obtained that do not support the view that parathyroid 
insufficiency plays a rdle in the etiology of paralysis agitans. 

D. K. Henderson. 

NUCLEINOTHERAPY IN PARALYSIS AGITANS. (La nucleino 

(285) thfeapie dans la maladie de Parkinson.) I. N. Buia, Compt. Rend. 
Soc. de Biol., 1914, lxxvi., March 27, p. 607. 

Hypodermic and intravenous injections of a freshly prepared solu¬ 
tion of nucleinate of soda were tried on five cases of paralysis 
agitans. The former improved symptoms, but failed to raise the 
temperature above 38° C. The latter gave much better results, 
and raised temperature to 39 8°: its fibrile reaction lasted about 



ABSTRACTS 


221 


four hours, and showed a short cold stage with violent shivering 
and marked trembling, a longer hot stage with calmness and 
lessened rigidity and tremor, and a stage of slight sweating. Two 
patients, bedridden for two years, walked up and down stairs 
after treatment. Intravenous injections give euphoria, greatly 
improved sleep, psychical benefit lasting for days, lessening of 
tremor, and increased power dynamometrically. Particulars of 
dosage and frequency of injections are given. 

Leonard J. Kidd. 

TWO DEATHS DDE TO SUPRARENAL INSUFFICIENCY. (Zwei 
(286) Todeadtlle infolge von Nebenniereninsufflciens.) J. Hobnowskj, 
Virchows Archiv, 1914, ccxv., p. 270. 

Case 1 . —Woman, aged 38. Sudden death during parturition. 
Post mortem, all the organs were found to be normal except the 
suprarenale. The cortex showed -no marked changes, but the 
medulla was very thin, the blood vessels were dilated, and more or 
less extensive haemorrhages were found. Death was attributed to 
insufficiency of the chromaffin system. 

Case 2.—Man, aged 52. Death twenty-four hours after an 
operation under chloroform for removal of cancerous glands in the 
groin. Both suprarenals consisted almost entirely of scar tissue 
and showed endarteritis obliterans, probably the result of syphilis. 
The thyroid presented marked increase of glandular epithelium 
similar to that found in Graves’ disease. J. D. Rolleston. 


THE SYNDROME OF XANTHOCHROMIA AND COAGULATION 
(287) BN MASSE OF THE CEREBRO SPINAL FLUID. (Snr le 
syndrome de la xanthochromie et de la coagulation massive du 
liquids cdphalorachidien .) Mabinesco and Radovici, Nouv. Icon, 
de la Salpetriere, 1913, Nov.-Dee., p. 484. 

In an interesting paper the authors report four new cases of 
disease of the spinal cord, in which the cerebro-spinal fluid was 
characterised by xanthochromia and massive coagulation. Most 
recorded cases have been cases of paraplegia, with a lesion towards 
the lower part of the cord. Some cases have been spastic, others 
flaccid: some acute, others chronic. Speaking generally, the 
clinical types in which this syndrome may occur are meningo- 
myelitis, compression of the cord, ascending paralysis, and a 
generalised meningitis. The fluid has a yellow coloration, and 
coagulates as a rule spontaneously, while its cytological content is 
quite insignificant. It is highly albuminous: fibrinogen and fibrin- 
ferment are present. The pathological anatomy of such cases is 
a morbid process invading the subarachnoid spaces, and thus to 



222 


ABSTRACTS 


some extent isolating a portion of the fluid. The xanthochromia 
is the result of the penetration of blood pigment into the sub¬ 
arachnoid spaces, pigment derived from haemoglobin, and probably 
of the nature of urobilin. In these cases Gmelin’s test is frequently 
positive. The pathogenesis is perhaps a series of minute and 
repeated meningeal haemorrhages. The derivation of the fibrinogen 
and fibrin-ferment (normally absent from the cerebro-spinal fluid) 
is from the blood, inflammation or other pathological process 
having impaired the integrity of the subarachnoid endothelium. 
It may Ire supposed that minute meningeal haemorrhages set free 
fibrinogen, and that it is passed by diosmosis via the colloids of the 
cellular membranes. In the case of tumours it has been supposed 
that toxins irritate the vascular surfaces, and that fibrinous 
exudation is favoured by the stasis of the fluid. 

S. A. K. Wilson. 


THE LUETIN CUTANEOUS REACTION FOR SYPHILIS. Alson 
(288) R. Kilgore, Joum. Amer. Med. Asnoc., 1914, lxii., April 18, p. 1237. 

Those who have reported results with the luetin reaction are 
practically agreed it is valueless in primary and secondary un¬ 
treated syphilis, and is of value only in the later stages. When 
positive it is highly specific for syphilis. 

The author, using Noguchi’s luetin, performed 150 tests in 120 
cases, of which 36 cases were syphilitic and 84 were controls. All 
the control cases gave negative reactions except two cases of 
tubercular joint disease, which left hospital before the result of a 
therapeutic test for syphilis could be observed. Of the 36 syphilitic 
cases, 22 were of the tertiary and latent type. Of these 14 were 
positive to the luetin test, i.e., 64 per cent., and 18 positive to the 
Wa88ermann reaction, i.e., 80 per cent.; 12 were cases of cerebro¬ 
spinal parasyphilis, and of these 5 were positive to the luetin test, 
i.e., 42 per cent., and 9 to the Wassermann reaction, i.e., 75 per 
cent. The remaining two were congenital syphilis, and neither 
reacted to the luetin test, while one gave a positive Wassermann 
reaction. 

Of 13 control cases none reacted positively on second inocula¬ 
tion. Of 15 luetic cases giving negative reactions, 5 gave positive 
reactions on second inoculation. In 2 cases the second injection 
gave a doubtful reaction. 

The Wassermann reaction is thus positive in a higher percentage 
of cases of late syphilis than is the luetin. The value of the luetin 
reaction appears in the small number of cases of syphilis in which 
it is positive, while the Wassermann is negative (4 out of 36 cases) 

A. Ninian Bruce 



ABSTRACTS 


223 


THE WAS8BRMANN REACTION IN THE BLOOD IN OASES OF 
(288) ALKAPTONURIA. Soderbergh, Neurol. Centralbl. , 1914, 

Jan. 2, p. 24. 

In a patient with ochronotic osteitis deformans the blood gave a 
positive Wassermann reaction. After a month’s mercurial treatment 
the reaction was negative. The author began to doubt the 
specificity of the reaction in this particular case, because of the 
alkaptonuria. Accordingly, as tyrosin is known to increase 
the quantity of homogentisinic acid in the urine, the patient 
received 5 gm. of tyrosin at intervals of two hours to a 
total of 15 gm. In less than twenty-three hours his completely 
negative Wassermann reaction had changed into a strongly 
positive one. S. A. K. Wilson. 


OBSERVATIONS ON A STRAIN OF SPIROCH/ETA PALLIDA 

(290) ISOLATED FROM THE NERVOUS SYSTEM. Henry J. 
Nichols, Joum. Exp. Med., 1914, xix., April, p. 363. 

Our knowledge of Spirocluda pallida is now entering on the stage 
of differentiation of strains, and the author records a strain which 
he isolated from the nervous system of a patient with definite 
primary and secondary symptoms. The nervous system was con¬ 
sidered to have been invaded during the early secondary period, 
and the patient would probably have suffered from nerve syphilis 
later. The strain was obtained from the spinal fluid and showed 
the following constant characters: (1) Thick form, (2) the pro¬ 
duction of hard, well-demarcated lesions with necrotic centres, 
(3) characteristic location of the lesion, (4) short incubation period, 
and (5) a tendency to generalise with lesions of the skin and eye, 
following local inoculation of the testicle and scrotum. 

It is suggested that these characters constitute a definite strain 
of highly invasive power, and that a classification of members of 
the pallida group may be made in accordance with this power. 

A. Ninian Bruce. 

THE TECHNIC OF THE INTRADURAL INJECTIONS OF NEO- 

(291) 8ALVAB8AN IN SYPHILIS OF THE NERVOUS SYSTEM. 

Uno J. Wile, Joum. Amer. Med. Assoc., 1914, lxii., April 11, p. 1165. 

Injections of cocain for spinal anaesthesia may be followed by 
vomiting, fever, headache, neuralgia, and troubles of micturition. 
This was at first attributed to the cocain itself, but it was later 
found that this resulted from an aseptic, sterile meningitis. A 
watery solution, which was not isotonic, could produce meningeal 
irritation, and by substituting cocain in isotonic solution, no 
18 



224 


ABSTRACTS 


harmful results followed. Later it was found that hypertonic 
concentrated solutions acted even better. 

The author, accordingly, uses a 6 per cent, solution of neo- 
salvarsan in freshly distilled water. This solution is hypertonic, 
and each drop contains 3 mg. of neosalvarsan. The dose injected 
is from 3 to 12 mg., i.e., from 1 to 4 drops of the solution. The 
patient is placed in the Trendelenburg position for at least an 
hour after the injection to allow diffusion to take place. By this 
method vomiting is eliminated. A little headache and neuralgia 
may result. A. Ninian Bruce. 

THE TREATMENT OF SYPHILITIC DISEASES OF THE CENTRAL 
(292) NERVOUS iSYSTEM RY INTRAVENOUS INJECTIONS OF 

SALVARSAN. Lesley H. Spooner, Boston Med. and Surg. 

Journ., 1914, clxx., March 26, p. 441. 

The author records a number of cases of syphilis of the central 
nervous system satisfactorily treated by intravenous salvarsan in 
an ambulatory clinic. As the patients had to go home after 
the injection it was thought wise to give only 0-3 gm. salvarsan. 
With the exception of six cases subsequently placed on serum 
treatment, symptomatic improvement resulted in many cases of 
tabes, and in all cases of cerebro-spinal syphilis. No distinct 
improvement took place in a few cases of general paralysis. The 
most striking improvements followed the first or second injection. 
Reactions were infrequent. The most pronounced successes are in 
those who show evidence in blood or spinal fluid of intense 
syphilitic infection. The failures occurred in those showing 
feeble reactions. Phthisis seems worthy of consideration as a 
contra-indication. A. Ninian Bruce. 


SALVARSANIZED SERUM (“SWIFT-ELLI8 TREATMENT”) IN 
(293) SYPHILITIC DISEASES OF THE CENTRAL NERVOUS 
SYSTEM. James B. Ayer, Boston Med. and Surg. Joum., 1914, 
clxx., March 26, p. 462. 

The author records the results of this method of treatment in 18 
cases. Eight were cases of tabes, 4 of which were active and of the 
lower spinal cord type. One of these showed no change after five 
injections, the other 3 improved, 2 of which had failed to respond 
to any other method of treatment. Of 2 cases of tabes of some 
twenty years’ duration, improvement was found in 1 case, and in 
2 cases where optic atrophy was marked, 1 was unaffected and the 
other seemed to become stationary. 

Four cases of early general paralysis, in 2 of which the diagnosis 



ABSTRACTS 


225 


was doubtful, showed little improvement. A fifth case, called 
"latent nerve syphilis," showed some improvement after four 
injections. 

The remaining 5 cases were of active cerebro-spinal syphilis, 
and all improved as regards symptoms, signs, and laboratory tests. 

The author considers this treatment reacts best in cerebro¬ 
spinal syphilis, in which a cure may be looked for in some cases 
with persistent treatment. The next best effect is found in tabes 
in which the disease may be arrested, and is least effective in well- 
developed general paralysis. The keynote to success is persistence 
in using this method of treatment. A. Ninian Bruce. 


THE INTBABPINAL INJECTION OF SALVARSANIZED SEBUM 
(294) IN PARESIS. J. A. Cutting and C. W. Mack, Jonm Amer. 

Med. Assoc., 1914, Ixii., March 21, p. 903. 

Seven cases are here recorded with two controls. The earliest 
case of the series was of five months’, and the most advanced of 
three years’ duration. They were all in the second stage of the 
disease, and none were paralytic. None had a remission before 
treatment. The injections were given at intervals of two weeks 
until each patient had received three injections. A cerebro-spinal 
fluid examination was made, and Wassermann reactions determined 
before the beginning of the treatment, and at the time of injection 
blood and fluid were taken for subsequent examination. In all 
cases salvarsan was taken in preference to neosalvarsan. Very 
few severe reactions followed the administration of the salvarsan. 
There was no reaction following the spinal injections. 

The cases are described at length. The neurological findings 
show no marked alteration following the treatment. The mental 
symptoms did not improve much except in one case. The Wasser¬ 
mann reaction was altered in two cases. The Noguchi butyric 
acid test remained positive. The most striking result was a 
reduction in the cell-count, the original counts, which were all 
very high, showing marked reduction following each injection of 
salvarsanized serum. A. Ninian Bruce. 


INTRASPINOU8 TREATMENT (SWIFT ELLIS) OF GENERAL 
(290) PARALYSIS: a preliminary note on four cases treated by this 
method. Edward MAPOTHERand Thomas Beaton, Lancet, 1914, 
clxxxvi., April 18, p. 1103. 

The technique used was briefly as follows: (1) The intravenous 
injection of 300 c.c. normal saline containing 0 - 4 gm. salvarsan 
neutralised with caustic soda. (2) One hour later 40 c.c. of blood 



226 


ABSTRACTS 


were removed and centrifugaiised, and 12 c.c. of the serum obtained 
was diluted with 18 c.c. of normal saline, the mixture being then 
heated for half an hour at 56° C. (3) The intraspinous injection, 
after removal of an equivalent quantity of cerebro-spinal fluid, of 
the 30 c.c. of this diluted serum prepared as above. The whole 
process was repeated four times at intervals of two weeks. 

The reaction immediately following the treatment was slight 
and diminished in severity with each repetition, the symptoms 
noted being vomiting, dizziness, slight pain in the head, neck, 
back, and legs. The occurrence of these, however, was not constant. 

The changes in the mental state have not been strikingly 
favourable. The changes iu the physical signs are not very 
marked, and not different from such as commonly accompanies 
states of remission in the ordinary course of the disease. The 
quantitative estimation of the Wassermann reaction in both blood 
and cerebro-spinal fluid showed no change whatever. The author 
concludes that there is little ground for the generally hopeful 
attitude adopted in regard to this treatment. 

A. Ninian Bruce. 

THE TREATMENT OF TABES DORSALIS AND GENERAL 
(296) PARESIS WITH S ALVARS AN. Gordon Bates, George S. 
Strathy, and C. S. M'Vioar, Canadian Med. Atsoc. Joum., 1914, 
iv., March, p. 197. 

Of six tabetics improvement took place in all. Two of the cases 
are reported, and in each the lightning pains were markedly 
increased after the injection, but, ultimately, they and other 
symptoms largely disappeared. The results in four paretics were 
encouraging. The best effects were obtained from intensive treat¬ 
ment, i.e., one or two full doses per week. A. Ninian Bruce. 


PSYCHIATRY. 

ON ATTEMPTS AT SPECIAL SEROTHERAPY IN GENERAL 
(297) PARALYSIS. (8ui tentativi di speciali sierotherapie nella 
par&lisi generals progressiva.) G. d’Abundo, Riv. ital. di Neuro¬ 
pat., Ptichiatr. ed Elettroter., 1914, vii., p. 1. 

After alluding to a recent communication by Levaditi, Marie and 
de Martel to the Society de Biologie on the treatment of general 
paralysis by injections of salvarsanized serum beneath the cerebral 
dura mater, d’Abundo refers to a paper read by him at the 
Psychiatric Congress of Naples in 1899, in which he related how 
the serum of general paralytics injected hypodermically into 



ABSTRACTS 227 

patients in a less advanced stage of the disease, exercised a 
sedative effect. 

The paper concludes with remarks on the prophylaxis of 
syphilis, in which the writer recommends that male visitors to 
houses of prostitution should be examined, and that only those 
should he admitted who were free from syphilis and other venereal 
diseases. J. D. Rolleston. 


CIVIL CAPACITY IN REMISSIONS FROM GENERAL PAR 

(298) ALYSIS. (La c&pacita civile nelle remissioni della paralisi 
generate progressiva.) A. Cbistu.ni, Riv. ital. di tfeun>pat. f 
Plichiatr. ed Elettroter., 1914, vii., p. 24 

The patient was a man aged 42, the head of a rich industrial 
concern, who had contracted syphilis at 21. General paralysis 
took on a severe course, and after it had lasted three years, bed¬ 
sores developed, the temperature became raised, and the patient 
appeared moribund. Improvement, however, took place, and 
finally only trivial somatic and psychical residues were left. At 
the time of writing, the remission had lasted 7 years, and the 
patient had resumed his work for 4 years. Other cases are on 
record in which the remissions have lasted 9, 12, 14, 19, 20, 21, 
and 25 years. J. D. Rolleston. 

CORRELATIONS OF CEREBRO SPINAL FLUID EXAMINATIONS 

(299) WITH PSYCHIATRIC DIAGNOSES. (A Study of 140 Oases.) 

Maby £. Mors*, Boston Med. and Surg. Jour w., 1914, clxx., March 
12, p.373. 

Systematic examination of the serum and cerebro-spinal fluid 
leads to a reduction in the number of cases diagnosed as general 
paralysis. Out of eighty cases in which the diagnosis had been 
made definitely or was suspected, examination of the serum and 
cerebro-spinal fluid only confirmed it in fifty-seven cases, i.e., 71 
per cent. On the other hand, three cases of paresis were discovered 
in patients diagnosed on admission as senile dementia, arterio¬ 
sclerotic depression, and alcoholic hallucinosis. The cases which 
have been found most difficult to differentiate from paresis without 
examination of the serum and cerebro-spinal fluid are cerebral 
syphilis, arterio-sclerosis, and Korsakow’s psychosis, and even the 
findings in the serum and cerebro-spinal fluid may leave one in 
doubt in the first case. 

It would appear that general paralysis is not actually so 
frequent as it appears to be from purely clinical observation. 

A. Ninian Bruce. 



228 


REVIEW 


TREATMENT. 

SOME OF THE BROADER ISSUES OF THE P8YCHO-ANALYTIC 
(300) MOVEMENT. James J. Putnam, Amer. Joum. Med. Set., 1914, 
cxlvii., March. 

The psycho-analytic method of treatment is not simply one more 
means of palliation. It is based on a recognition of the fact that 
the patients are suffering from emotional conflicts, the nature of 
which they cannot understand unaided, and is an attempt to make 
it possible for them to extricate themselves through self-study and 
self-education from the effects of these conflicts. 

The constant aim should be to encourage the patient to assume 
the responsibility for the success of the investigation, so that it 
may result in a sense of complete independence on his part. 

It is admitted that there are certain cases which do not react 
to this form of treatment, but if adequate care is taken in the 
choice of patients, if the physician is well trained, and the patient 
is in earnest, some good is almost certain to result. The phobias 
and anxiety neuroses are the most curable forms, while the 
compulsion neuroses are less amenable, and the well-marked 
hypochondriacal cases even less so. 

The article is a most clear and interesting one, and should be 
read in the original. D. K. Henderson. 


■Review. 

ARBEITEN AUS DEM PATHOLOGISGHBN INSTITUT DER UNI- 
(301) VERSITAT HELSINGFORS (FINLAND). Herausgegeben von 
Prof. Dr E. A. IIom(:n. Neue Folge, Erster Band: Erates und 
Zweites Heft, Mit 13 Tafeln and 34 Abbildungen im Text, pp. 190. 
Jena : Verlag von Qustav Fischer, 1913. 

The first volume of a new series of studies from the Pathological 
Institute of the University of Helsingfors, published under the 
iegis of the director, Professor Hom6n, contains a number of 
interesting communications dealing with neuropathology. 

1. Professor Hom&i contributes a long article on the develop¬ 
ment of abscesses of the brain, with especial reference to the types 
of cells found in connection therewith. It is excellently illus¬ 
trated. From experimental researches, Professor Hom^n con- 



REVIEW 


229 


eludes that the first result of the local invasion of the brain by 
bacteria and their toxic products is degeneration and necrosis of 
the tissue elements in the immediate vicinity. Exudative, in¬ 
filtrative, and proliferative processes follow at once. These 
depend on the degree of virulence, the type, the numbers of the 
invading bacteria, the resistive power of the individual and so 
on. The older the pathological process is the more extensive are 
the proliferative and reparative processes. At the margins of the 
lesion, in its early stages, the common cell-form is the polymor¬ 
phonuclear leucocyte: certain other cells occur in smaller quantity. 
In the infiltration zone, away from the actual bacteria, there 
are fewer leucocytes, but many small lymphocytes and plasma 
cells, and sometimes large lymphocytes: also large numbers of 
polyblast-like glial cells, as well as Gitterzellen and Komchen- 
zellen. At the margin of the infiltration zone are found proliferat¬ 
ing connective tissue elements from the adventitia, fibroblasts, 
proliferating glial fibres, &c. Various combinations of these 
differing processes are met with. 

2. Dr Axel Wallgren contributes an interesting study of the 
finer histological changes in acute poliomyelitis. It also is 
accompanied with excellent coloured plates. The writer enters 
into the fullest details as to the nature and origin of lymphocytes, 
lymphoid cells, plasma cells, polyblasts, transitional forms, Gitter- 
and Kornchen-zellen, &c. From this point of view, the paper will 
be found- of value in establishing clear distinctions between the 
various cell-forms. 

3. Dr Fabritius’ contribution is on the question of acute 
myelitis and so-called spontaneous hsematomyelia. He describes 
two cases of interest from both clinical and pathological stand¬ 
points, and inveighs once more against the terminology of the 
condition. He prefers the term paraplegia myelitiea or apoplectics, 
or preferably myeloplegia, as more non-committal. 

4. The same writer publishes a case of sclerotic atrophy of the 
cerebrum. The patient was a woman of 53 with a left infantile 
cerebral hemiplegia dating from the age of 14 months. Many 
epileptiform attacks had followed. The hemiplegia was charac¬ 
teristic, with contractures. It had become worse some ten years 
before the patient came under observation. The mental condition 
was poor. At the autopsy, it was found that the right hemisphere 
was much smaller than the left, the gyri on both sides were of 
normal configuration, but those on the right were smaller. The 
right froutal lobe was grossly atrophic. The cerebellar hemispheres 
were equal in size. Microscopically, the chief alteration in the 
atrophic region was loss of nerve cells, especially of the superficial 
cortical layers, with glia proliferation. There was no degeneration 
of the pyramidal path, and very little difference in the size of the 



230 


BOOKS AND PAMPHLETS RECEIVED 


two pyramids. The author goes fully and critically into the litera¬ 
ture of these difficult cases, and concludes that there is no mere 
“arrest of development,” but a pathological process the exact 
nature of which is not yet understood. The absence of pyramidal 
degeneration is attributed by the author to the conservation of 
the Betz cells of the motor cortex. 

Other papers combine to make this volume interesting and 
useful to the neurologist and neuropathologist. 

S. A. K. Wilson. 


BOOKS AND PAMPHLETS RECEIVED. 

Cyriax, Edgar. “ The mechano-therapeutics of chronic infantile 
paralysis (Poliomyelitis anterior acuta)” (Brit. Joum. Child. Du., 1914, 
xi., pp. 167-107). 

Freud, Sigm. “On Dreams.” Only authorised English translation by 
M. D. Eder from the second German edition. 1914. William Heinemann, 
Ltd., London. Pr. 3s. 6d. net. 

Fuller, Solomon C. “ Amyloid degeneration of the brain in two cases 
of general paralysis ” ( Atner . Juum. Insanity, 1914, lxx., p. 837). 

Mott, F. W. “ Archives of Neurology and Psychiatry ” 1914, vi. 

Salmon, Alberto. “ Le problfeme du sommeil ” (L’Enafphale, 1914). 

Tanzi, E., and Lugaro E “ Malattie mentali.” Vol. i. Societa 
Editrice Libraria, Milan, 1914. 

Internationale Zeitschrift fiir Arztliche Psychoanalyse. 1914, Jahrgang 
II., Heft 2, Marz. 

Klinik fiir psychische und nervose Krankheiten. 1914, ix., H. 1. Carl 
Marhold, Halle a. S. 

Kent County Lunatic Asylum. Annual Report for 1913. 

“ The Training School .” 1914, xi., April. 



IReview 

of 

IReurologs anfc pspcbiatn? 


Original articles 

THE NATURE AND THE TREATMENT OF THE 
SO-CALLED “GENUINE EPILEPSY." 

By Dr G. C. BOLTEN (The Hague, Holland). 

When we desire to arrive at a really efficient treatment for an 
illness, it is necessary first of all to have as complete a knowledge 
as possible of the causes, the kind, and the nature of the illness. 
If, therefore, we will discard the “ bromide ” treatment for epilepsy, 
and substitute for it a method which indeed takes into considera¬ 
tion the real causes of epilepsy, we have first of all to answer 
the questions: How, where, and in what manner does epilepsy 
arise ? 

These questions, asked for many centuries, have been answered 
times innumerable, but not one of the answers may be considered 
as validly consistent. In olden times Greek (Hippocrates, 
Herodotus, Aristotle, Avicennes) and Roman investigators (Plato, 
Celsus, Aurelianus, Paracelsus) occupied themselves in many 
researches of the “ falling sickness ”; most of them strongly be¬ 
lieved that the moon and the stars influenced the development of 
epilepsy. We find this idea, however foolish it may seem, existing 
even in recent years, but in a more modified form. Michalek 
(1910) observed that his patients had many more fits on a new 
moon than on a full moon; Halbey (1910) finds that the variations 
of the quantities of the atmospheric electricity have an influence on 
epilepsy, or at least on the appearance of fits. Lomer (1906) finds 
a connection between the number of the fits and the height of the 
barometer; Sokolow (1897), on the contrary, finds a certain relation- 
19 



232 


G. C. BOLTEN 


ship between the fits and the magnetism of the earth, while 
Lomer, still unconverted, even in the last year (1913) holds the 
same opinion about the constant relationship between the number 
of fits and the height of the barometer. 

Turner considers that epileptics have a distinct increased 
coagulation rate of the blood, and that the cause of the illness is 
situated there; Besta found quite the opposite, namely, a diminished 
coagulation rate of the blood, and therefore he declares the theory 
that epilepsy is a dyscrasy, characterised by the diminution of 
the quantity of the calcium salts of the blood. Hallager and 
Bussell ascribe the fits to brain-anaemia, caused by cessation of 
the pulse during the onset of the fit. In this way they resort in 
some manner to the already old opinion of Kussmaul and Tenner 
(1857), that epilepsy is caused by contractions of the blood¬ 
vessel muscles of the small arteries, especially in the medulla 
oblongata. But all these opinions have not a single reason for 
existence, and now they have only some historical value. 

As in almost every case of illness, in epilepsy also bacteria 
have been looked for, and, as a matter of course, found. Bra 
(1902 and 1905) found a “neurococcus”; Lion (1911) feels some¬ 
thing for a “ spirillosis.” It may be safely said of all those recent 
ideas, that no one at present accepts them except their inventors, 
so long as they are alive. 

In the last half century again and again they have endeavoured 
to declare all cases of epilepsy as an anatomic affection of certain 
parts of the brain, and thereby, as Redlich observes wittily, the 
localisation of epilepsy has gone a bul bo-cortical way: Kussmaul, 
Schroeder van der Kolk, and Tenner sought the cause in the 
medulla oblongata, Nothnagel in the pons Varoli, Ziehen, Fuchs, 
and Bothmann in the subcortical centres, and after this many 
other investigators considered the cortex cerebri as the seat of the 
alterations which might be the cause of epilepsy. Indeed, follow¬ 
ing the example of Chaslin (1890), a great number of neurologists 
have commenced to occupy themselves with the investigation of the 
microscopic alterations which might appear in the cortex cerebri 
of epileptics. 

Principally Alzheimer and Bratz have made statements to 
this effect, and many others have followed them (Marinesco, 
Marchand, Weber, Pohlmann, Lubimow, Heboid, Hajos, Orloff, 
Worcester, Clark, Prout, Jolly, and many others). They have 



TREATMENT OF SO-CALLED "GENUINE EPILEPSY" 233 


determined that one often finds in cases of epilepsy a diffuse pro¬ 
liferation (varying much in extensiveness) of the supporting 
tissues of the brain (indicated by Alzheimer as “ randgliose ”), and 
accompanied by a strong setting of the real cortex elements 
(ganglion cells, projection and association fibres), sometimes with 
forming of the so-called "corpora amylacea.” Besides these, we 
often find chronic alterations in the region of the ammon-horns, 
which are characterised by induration, and which are known as 
sclerosis of the cornu ammonia It is a pity, however, that the 
results of these investigations are not at all constant: in many 
cases they are wanting entirely; in fresh cases of epilepsy they 
never occur; on the contrary, they are only to be found in old 
and ehronic cases, which have already resulted in a secondary 
dementia (Binswanger, Bouchd, Marchand, Claude and Schmiergeld, 
Moore, Alexander, and others). Bratz, who is with many others a 
vigorous champion of the cerebral pathogenesis of epilepsy, could, 
in spite of that, determine the diffuse glia proliferation only in 
half of his cases. Indeed, it is certain that this proliferation of 
the glia tissue, which occurs constantly in every possible form 
of dementia (and also in some other chronic intoxications), is only 
the anatomical substate of the dementia; therefore it is not the 
cause of the illness, but the effect of the chronic epileptic 
intoxication. 

The sclerosis of the cornu ammonis is also very inconstant (we 
find it in about 50 per cent, of all cases), and consequently cannot 
be the cause of epilepsy. 

Opposite the great number of pathological anatomists who depart 
from the wrong point of view that one can determine on the section 
table or under the microscope the causes of a malady, and who 
assign genuine epilepsy to the pure primary-cerebral affections, 
and adjudge it a place amongst the cerebral diplegia of chil¬ 
dren (Little’s disease) and porencephaly, there are also a great 
number of other investigators who consider genuine epilepsy 
(“epilepsie essentielle” of the French; primary or idiopatic 
epilepsy) as a chronic auto-intoxication. Among the numerous 
followers of this theory are: Krainsky, Donath, Hall, Guidi, 
Marinesco, Collolian, Ballet, Hay, Voisin, Petit, Teeter, Jelgersma, 
Bouchd, and many others. 

Krainsky proposes the supposition that epilepsy might be an 
intoxication by carbamatic salts, but these, unless they are con- 



234 


G. C. BOLTEN 


ducted immediately in the blood-passages, are not poisonous, 
because they are changed by the liver into perfectly harmless 
urea; also Krainsky’s observations were not exact: he claimed 
that he could always determine immediately before the fit a rising 
of the quantity of the uric acid in the urine, but many other 
investigators did not find this, and, moreover, the uric acid and 
the carbamatic salts have not any relationship with each other, 
because uric acid is formed from the purin bases and not from 
the carbamatic salts. 

Donath thought that choline might be the cause of this chronic 
intoxication, but choline is far too non-poisonous, and also it 
is very doubtful if Donath is right; then many others failed to 
find an augmentation of choline in any part of the body of 
epileptics (Handelsmann, Ziveri, and others). 

There is also no question whatever about an intoxication by 
carbonate of ammonia (Guidi), because this substance is changed, 
like the carbamatic salts, into urea by the liver. 

A great number of investigators (Collolian, Ardin-Delteil, 
Mairet, Galdi, Tarughi, Albrecht, Meyer, and others) conducted 
experiments with the bodily fluids of epileptics, namely perspira¬ 
tion, blood-serum, cerebro-spinal fluid, and urine; they injected 
these liquids into different test-animals to show their eventual 
toxicity. It must be said in general that it seems by their results 
(although there are some exceptions) that the above-named liquids, 
unless gathered immediately before, during, or immediately after 
a fit, are very toxic and invariably excite convulsions in the test- 
animals (usually guinea-pigs); most of them died in consequence of 
the injections. 

There have also been very many investigations on the sphere 
of the metabolism, especially concerning phosphorus-, nitrogen-, 
and salt-metabolism (Bomstein, Lowe, Stromann, Goudberg, 
de Buck, Stadelmann, Frohner, and others). Principally the 
excretion of the phosphates, of urea, and of uric acid has 
been inquired into times innumerable in the case of epilepsy. 
Nevertheless it is not possible to come to definite conclusions in 
all those researches, however exact they may be, because the results 
of the one are quite opposite to the results of the other: on this 
moment we do not dispose of a single due settled fact on the 
sphere of the pathology of metabolism in cases of epilepsy. 

This ever-returning and inexplicable inconstancy of experiences 



TREATMENT OF SO-CALLED “GENUINE EPILEPSY” 235 


becomes clear to us when we understand that the experimenters 
did not take into consideration, on one occasion, that the word 
“ epilepsy ” conveys only a very indefinite idea, and that it contains 
quite a large number of pathogenetically divergent maladies, 
although these maladies are characterised by almost the same 
symptoms, especially the epileptic fit. 

Indeed, many influential neurologists (Pierre Marie, Oppenheim, 
Redlich, Binswanger, Heilbronner, Freud) draw attention to this 
fact that, as the technique of the microscopical anatomy of the brain 
and the methods of inquiry and research in general improve and 
increase, the sphere of the so-called genuine epilepsy diminishes, 
and continually there come fresh cases which, from a clinical point 
of view, give quite the impression of “genuine” epilepsy, and which 
were proved, after minute pathological-anatomical inquiry, to 
belong to the secondary epilepsies in consequence of primary organic 
cerebral affections. This had the result that they, little by little, 
have fallen into another extreme, and, following the example of 
Unverricht, declared that all epilepsies are of cerebral origin, and 
the more, while through the researches of Alzheimer, Bratz, and 
others the secondary alterations in the cortex cerebri of epileptics 
were better known. In 1897 Winkler drew attention that this 
conception was far too partial, and that it was not correct to regard 
the numerous forms and kinds of epilepsy in the same manner, 
and to ascribe them all to a primary cerebral alteration. Very 
divergent maladies thus show the same symptoms, and this, 
naturally, has led to a hopeless confusion; many investigators only 
speak of “epilepsy,” and so include all cerebral and genuine 
epilepsies; others always speak about “ genuine ” epilepsy, but in 
reality their cases seem to belong solely or in part to cerebral 
forms, and the one as well as the other leads to inconstant and 
completely useless results. 

I would propose the following classification of the different 
clinical forms of epilepsy:— 

1. Cerebral {secondary or symptomatic) epilepsy as a consequence 
of chronic meningitis or encephalitis (in most cases a combina¬ 
tion of the two, namely, meningo-encephalitis); traumatism of 
the cranium, the meninges, or the brain (so-called traumatic 
epilepsy); hydrocephalus internus; Alzheimer’s disease, sclerosis 
tuberosa; tumours of the cranium, of the meninges or of the brain 
(including acromegaly); cerebral abscess; lues cerebri (as wel 



236 


G. C. BOLTEN 


congenital as acquired), dementia paralytica, blood-clotting under 
the meninges, porencephaly, scars in the meninges, arterio-sclerotic 
foci, distrophia adiposo-genitalis, solitary tubercle, &c. 

When epilepsy is combined with cerebral diplegia of children, 
the epilepsy must be considered to be of cerebral origin, because 
the cerebral diplegia of children is nothing other than a more or 
less circumscriptive form of encephalitis. 

2. Epilepsy by endogenous intoxications, as diabetes, uHernia, and 
in case of children also with acetonsemia; in very close relationship 
to this group is also eclampsia. 

3. Epilepsy by exogenous intoxications, as chronic poisoning by 
alcohol, absinth, tobacco (Bychowski), camphora tribromidi, ergotine 
(von Jaksch and others), lead, santonine (Jeliffe), &c. 

To this group also belongs the intoxication we call pellagra, 
and which also causes sometimes epileptic or epileptiform fits (von 
Jaksch). 

4. The so-called “ affect-epilepsy ” (Bratz) of neuropaths and 
psychopaths. 

5. Cardiogenic epilepsy (Stokes-Adams’ disease). 

6. Epilepsia tarda (epilepsia senilis, “ Spatepilepsie ” of the 
German). 

7. Genuine epilepsy (“ dpilepsie essentielle” of the French, 
idiopathic epilepsy). 

To this group there also belong the rather peculiar cases of 
surgical — or wound — epilepsy, appearing after thyroidectomy 
when too great a part of the thyroid gland is removed. (All cases 
of surgical epilepsy are collected by Redlich.) 

We must observe, that the so-called epilepsia procursiva 
(poriomania or compulsory mechanical walking) in some cases 
has to be classified as genuine epilepsy, as I could prove ex¬ 
perimentally, while the same can be determined of the dipsomania. 
In other cases, on the contrary, dipsomania as well as poriomania 
are the effects of very divergent organic cerebral affections, or of 
various hereditary or acquired degenerative states. 

Thus we see, that the same illness (genuine epilepsy) can 
present itself in many very various forms: sometimes exclusively 
fits of " petit mal,” at other times only complete epileptic fits, in 
other cases only the so-called psychic epilepsy (dream-states, 
equivalents, &c.), or merely by symptoms of dipsomania or 
of poriomania. And opposite this stands the fact, that the 



TREATMENT OF SO-CALLED “GENUINE EPILEPSY” 237 

epileptic fits with all their peculiarities may occur in the seven 
above mentioned groups of maladies, which, however, are very 
divergent concerning their pathogenesis. 

Experimentally I have proved that epilepsia tarda has 
certainly not the same origin as genuine epilepsy; probably this 
affection is caused by chronic troubles of the circulation in the 
cortex cerebri (arterio-Bclerosis, See). 

Further, the epileptic form of paramyoclonus (Unverricht) and 
the so-called epilepsia corticalis continua or polyclonia epileptoides 
continua (Koschewnikow and Choroschko) have no reason to exist as 
separate maladies: they belong undoubtedly to the very large group 
of cerebral epilepsies, and depend on more or less circumscribed 
organic alterations of the cortex cerebri. (Choroschko accepts a 
subcortical localisation.) 

The series of minor fits (“ gehaufte, kleine Anfalle," Friedmann 
and Heilbronner) do not form pathogenetically a simple type of 
malady; they occur sometimes in organic cortex affections, and 
other times in genuine epilepsy, while in many cases the patho¬ 
genesis is still quite obscure and perhaps a great number of them 
must be incorporated with hysteria (Heilbronner). 

With my own investigations I always have tried as much as 
possible to separate the different groups of epilepsy, a necessity 
which is, in fact, quite neglected by the majority of workers: 
the groups 2, 3, and 5 are always easy to determine, because the 
primary affection (endogenous or exogenous intoxications, Stokes- 
Adams’ disease) presents itself in these cases very clearly, but for 
the moment we do not dispose of due differential diagnostic signs, 
which enable us to distinguish the cerebral from the genuine 
epilepsy or from the epilepsia tarda, apart from the comparatively 
rarer cases in which there exist undeniable focal symptoms 
or other signs of a primary cerebral affection, which cases then, 
of course, belong to cerebral epilepsy. Neither the nature and 
the great number of clinical peculiarities of the fit, nor the ulti¬ 
mate progress of the disease enable us to a right differential 
diagnosis. 

Perhaps Abderhalden’s dialysing method (the indication of the 
so-called defensive ferments), or may be the determination of the 
antitryptic force of the blood-serum, will give results which may 
be used for the differential diagnosis. (In cases of extensive 
organic cerebral alterations we find an augmentation of the anti- 



238 


G. C. BOLTEN 


trypsines of the blood; in due course the results of the researches, 
now begun by us in this subject, will be made known.) 

In my experiments I have limited myself, as far as possible, to 
the sufferers of genuine epilepsy and as this diagnosis until now is 
only to be made “ per exclusionera ” (thus one must exclude as 
well as possible the countless forms of cerebral epilepsy and also 
epilepsia tarda; consequently one had to manage previously with 
almost exclusive anamnestic information), it was not always 
possible to elude errors in the diagnosis of our cases. These errors, 
however, could always be experimentally proved, unless the 
sufferer had patience enough for a very prolonged and multifarious 
treatment. 

With a great number of sufferers of genuine epilepsy, I tried 
to discover if this disease might have originated by:— 

(a) Purification in the intestines (abnormal fermentations in 

the stomach or in the intestinal tract), intestinal 
parasites, chronic enteritis, or other intestinal affec¬ 
tions, such as ohronic constipation, &c. 

(b) Intoxication by decomposition products of albumin, first of 

all the purin bases (which play such an important 
part for many neurologists) or by the albumoses. Also 
the possibility of common salt-retention, and secondary 
salt-intoxication has been inquired into. 

(c) Troubles in the function of the so-called glands with internal 

secretion (hypophysis, thyroid, parathyroids, thymus, 
liver, pancreas, spleen, ovary, testicle and adrenals; 
only the epiphysis could not be experimented with. 

All these researches and experiments have taken nearly ten 
years, and have always been conducted upon several patients at one 
time, and nearly always on clinical sufferers, who thus were under 
our continual observation. 

The results of these experiments may be summarised as 
follows:— 

Purification in the intestines seems to occur in case of 
epilepsy only as a great exception, and when this symptom exists, 
there is then produced in the intestinal tract indol, phenol, and 
skatol, which appear in the urine as indican. Therefore, when 
there is purification in the intestinal canal one finds a heightened 
standard of indican of the urine. With a great number of epileptics 
the indican-standard was determined by us, but important increases 



TREATMENT OF SO-CALLED “GENUINE EPILEPSY" 239 


were never found; neither was acetone discovered in the urine 
of epileptics. 

For these reasons it must be an established fact that intestinal 
purification does not play a part with genuine epilepsy. And also 
one does not find chronic diarrhoea with epilepsy, unless due to 
faulty dieting; intestinal parasites and other intestinal troubles, 
as chronic constipation, have also no influence of any importance 
upon epileptic disease. 

Moreover, Moore Alexander controlled exactly the intestinal 
flora of epileptics and compared it with that of normal persons, 
without finding a difference of any importance. The great influence 
which many investigators (Rodiet, de Fleury, MacCaskey, Spratling, 
and others) ascribe to stomach and intestinal troubles does not 
exist at alL And the atonic and dilated stomach (Mangelsdorff, 
de Groot), whether accompanied or not by hyperchlorhydria, belongs 
to the secondary alterations, as there are found a great many in 
epileptics, and which, concerning the pathogenesis, do not count 
at all. 

The administration of an extraordinary easily digestible diet, 
the regular use of intestinal disinfectants, the continual cleansing 
of the intestinal canal, the careful prevention of chronic constipation, 
all that, in short, has not any influence worth mentioning upon 
the chronic intoxication which we call genuine epilepsy. 

Much attention was paid by me to the part played by the 
food-albumins and their decomposition products (purin bases, 
albumoses), but the results also were purely negative. 

It is really not quite clear why many workers have conceded 
and adjudged such an important position to the so-called purin 
bases, because all those substances (xanthine, paraxanthine, guanine, 
karnine, hypoxanthine, adenine, &c.; caffeine and theobromine 
also belong to them) are fairly harmless, and are changed by 
oxidation into uric acid. If the purin bases should be 
insufficiently oxidised and excreted, then there would be formed 
by epileptics less exogenous uric acid than by normal persons, 
who keep quite the same diet. Concerning this there was no 
evidence; epileptics (cerebral as well as genuine epileptic) show, 
as we could demonstrate by ample researches, quite the same 
standard of uric acid of the urine as normal persons, who 
have been kept to quite the same diet, and who live under 
quite the same conditions. And, moreover, the purin bases 



240 


G. C. BOLTEN 


are not, or but very little, poisonous; adenine is the most 
poisonous, and yet one can give adenine to epileptics with safety: 
they do not react to it in any way. The food, rich with purins, 
does not bring any change in the symptoms of epileptics, and 
even when one puts the patient for a considerable period on a quite 
“ purin-free ” diet (which is very well possible, and can be con¬ 
tinued for a long time), one does not get an obvious amelioration. 
Investigators, who meant to observe such an improvement, have 
not continued their experiments long enough, or else they have 
had experience with too few patients. Hoppe also did not observe 
the slightest difference between the phenomena, when rich purin 
or non-purin foods are distributed and carried as far as possible. 

And when one retains all albumins, animal as well as vegetable 
(as far as possible, which, however, cannot be carried through 
perfectly), one also does not notice any amelioration. And so it 
is impossible to ascribe any part to the albumoses, which are, as is 
well known, very poisonous (and which are transformed syntheti¬ 
cally to plasma-albumin during the passage through the intestinal 
wall); epilepsy thus is not an intoxication by albumoses, nor by 
purin bases. 

With the eventual common salt-retention and secondary 
intoxication we find the same. When one removes as far as 
possible all salt from the food (the salt-free diet) then this has 
not the slightest influence on the fits or on the other phenomena, 
unless one applies bromides at the same time, and by this, namely, 
the application of bromide salt in the diet poor of salt, the favour¬ 
able results proceed which many researchers (Roux, Gordon, Baluit, 
Lortat-Jacob, and others) obtained with the treatment of Tolouse 
and Richet; the diet poor of salt, however, is, without simultaneous 
bromide application, completely inactive, as Van der Kolk also found. 
The treatment, according to Toulouse and Richet, simply relies upon 
this, that by the abstinence of the common salt and the 
simultaneous application of bromide the lather accumulates much 
more rapidly in the organism than with a combination of usage 
of common salt; thereby a much larger bromide accumulation 
(“ bromide-depot ”) is formed (Hoppe, Laudenheimer), and the effect 
of the bromide salts is then much more intensive, but that is all. 

Also a pure milk diet, by which Bregmann should have 
obtained good results, has no more obvious influence on the fits 
and on the other epileptic phenomena. 



TREATMENT OF SO-CALLED “GENUINE EPILEPSY” 241 


In general one can declare, as seemed also by our experiments, 
that, firstly, all kinds of intestinal troubles carry on an unfavourable 
influence on the epileptic phenomena; and secondly, that in 
general there does not exist a single diet, that in the long run 
really carries on any noticeable influence on the kind, the intensity, 
and the quantity of the epileptic “ discharge ” (the fit). 

Very many and lasting experiments have been made by us in 
our endeavour to determine if one or more of the glands with 
internal secretion have any influence on the origin or on the 
symptoms of the epileptic disease. 

Moreover, there must, of course, be considered the possibility 
of an intoxication by a hyperfunction of one of those organs, the 
more so, because Volland, Ohlmacher, and others often found a 
persistent thymus and other congenital alterations at their 
pathological-anatomical researches. But neither by the applica¬ 
tion of extracts of fresh thymus, nor by that of fresh adrenals, may 
any lessening of the symptoms be caused, not even when great 
quantities were applied. (There must be observed that in these 
experiments there was always used freshly pressed extracts of the 
glands with internal secretion, and that these fluids were always 
given by the rectal way, in order to prevent their eventual 
destruction by the gastric juice. Dry organs, given in tablet form, 
are quite useless, because they contain, as appears by their odour, de¬ 
composition products, and therefore they cannot in any way imitate 
the physiological function of the organs; moreover, most of these 
glands contain ferments which are destroyed by the drying process.) 

Successive very durable experiments have been made with 
the pressed extracts of nearly all glands with internal secretion 
(hypophysis, thyroid, parathyroids, liver, pancreas, adrenals, ovary, 
testicle, spleen, and thymus). Their results can be recapitulated 
as follows:—Firstly, that by the application of no one of the pressed 
extracts of these glands there might be caused a deterioration of 
the epileptic symptoms, and that, consequently, genuine epilepsy 
surely does not depend upon a hypersecretion of one of the above- 
mentioned organs; and, secondly, that on the contrary we obtained 
a slight amelioration on the sufferers of genuine epilepsy (the 
diagnosis, for want of better, always taken “ per exclusionem ”) by 
application of pressed extracts of the parathyroids, and a very 
remarkable amelioration by the application of the combined pressed 
extracts of the thyroid and parathyroid glands. Cerebral epileptic 



242 


G. C. BOLTEN 


patients (diagnosis taken also chiefly from anamnestic information) 
almost failed to react in any way upon this treatment. 

It cannot be denied that the results were very positive; they 
were too constant and too durable, as any doubt should be justified. 
Amongst my patients there were two who formerly had numerous 
fits, and who now have been already more than three years free from 
all symptoms; ten already are quite free from symptoms for 
8 to 12 months, and ten others have not exhibited the slightest 
symptom during 3 to 4 months, although before this new treat¬ 
ment they had regularly four to ten fits per month. 

With this treatment all application of bromides was excluded, 
and so we can conclude from these experiments, with absolute 
certainty, that genuine epilepsy is a chronic auto-intoxication 
relying upon the hypofunction of the thyroid and parathyroid 
glands. 

In what manner must we consider now the pathogenesis of 
genuine epilepsy ? 

According to new researches of many physiologists (Biedl, 
Eppinger, Falta, Magnus, Levy, and others) the thyroid has a very 
divergent, complicated, and important function. Apart from the 
predominating part which it plays (in association with the hypo¬ 
physis and the thymus) on the development of the organism, it 
has an accelerating influence on metabolism in general; the salt 
as well as the nitrogen and the phosphorus metabolism are greatly 
under its influence, with the result that, when the thyroid’s 
function fails, a strong diminution of the excretion of phosphorus, 
calcium, and magnesium salts, as well in the urine as in the faeces, 
appears, while the gas change in the lungs is also importantly 
lessened. 

Moreover, the action of the chromaffine system and of 
adrenaline becomes less intensive by hypothyroidism ; the chromaf¬ 
fine system and the thyroid supply each other’s function, and 
both have to support a tonus in the sympathetic system, in opposi¬ 
tion to the pancreas, which has a retarding influence on it (Caro, 
Biedl). Thus the thyroid and the sympathetic nerve form more 
or less a closed system; the thyroid is innerved by the ganglion 
inferior of the sympathetic nerve (Steiner; according to Asher and 
Flak it would also receive branches of the n. laryngeus sup. and 
n. laryng. inf.), and reverse, the thyroid supports a tonus in the 
sympathetic system; consequently after thyroidectomy a diminished 



TREATMENT OF SO-CALLED “GENUINE EPILEPSY” 243 


sympathetic function appears (retarding intestinal peristalsis, 
lessenc i secretion of intestinal ferments, trophic and circulation 
troubles of the skin, &c.). 

Other investigators (Juschtschenko, Leopold Lfevi, Rothschild) 
have accomplished these experiments, and determined that the 
thyroid accelerates the formation of all kinds of ferments of the 
intestinal tract and of the intermediary metabolism. In con¬ 
sequence of hypothyroidism a quantitative decrease of all these 
ferments appears; Juschtschenko has determined this especially con¬ 
cerning nuclease, katalase, and phylokatalase. Further, according to 
Fassies, the thyroid accelerates the formation of alexines in the 
blood, and advances the antibactericidal action of the blood, whilst 
Walter has determined that with thyroidectomised animals the 
regeneration of injured nerves occurred much slower than with 
normal animals. It is still not certain if the thyroid has a directly 
depoisoning action on blood (Trendelenburg). 

Concerning the physiological function of the parathyroids, we 
know still less with sufficient certainty. Some workers believe 
that, after parathyroidectomy, the quantity of ammonia in the 
blood increases; however, the acidosis found by Morel, von Fiirth, 
and others, is probably not a direct consequence of the hypo¬ 
parathyroidism, but of the numerous and violent convulsions, 
symptoms of the parathyreoprivie tetany. 

Further, to declare the symptoms of genuine epilepsy we 
still need the important results of the researches of Guillain and 
Laroche, who were able to determine, experimentally, that the 
cerebral cortex has a great affinity to different poisons, as 
diphtheria and the tetanus toxin, and many others, as alcohol, 
ether, different alkaloids (morphine, cocaine, &c.), and other 
poisons, as absinthe, &c. 

In the case of genuine epilepsy there exists a hypofunction of 
the thyroid and parathyroid glands; the metabolism is retarded 
and less complete, because all kinds of ferments, indispensable for 
the metabolism, are insufficiently created, and all kinds of toxic 
products of our own metabolism, as well as decomposition products 
of feeding materials, come into the circulation, and gradually ac¬ 
cumulate and become lodged in the cerebral cortex, which, when 
this accumulation of toxins has reached its maximum, react upon 
that with a so-called “ discharge,” the epileptic fit, as a temporary 
remedy of the organism to deliver itself of the toxins for a short 



244 


D. MAXWELL ROSS 


period; we must thus regard the fit as a defence reaction of the 
organism. 

Summa summarum the following little recapitulation:— 

1. Of the numerous cases of epilepsy which make their 
appearance quite as genuine epilepsy, an important part, de¬ 
pending upon collective, divergent, primary cerebral affections, 
belongs to the cerebral (secondary, symptomatic) epilepsy, and but 
the smaller part ( ± 25 per cent, concerning our cases) to the so- 
called genuine (essential, idiopathic, or primary) epilepsy. 

2. Even now it is quite impossible to distinguish, less on pure 
clinical symptoms, most cases of cerebral from genuine epilepsy. 

The differential diagnosis between these divergent affections 
must move itself in the sphere of the pathology of metabolism. 

3. Genuine epilepsy is a chronic auto-intoxication, caused by 
a hypofermentation of the intestinal tract and of the intermediary 
metabolism, as a consequence of a hypofunction of the thyroid and 
parathyroid glands (or of troubles in their nervous elements, to 
know the sympathetic nerve). 

4. Genuine epilepsy is quite curable by the administration, 
rectally, of fresh pressed extracts of the insufficient glands, or better, 
it is possible, in this manner, to free the patient from all 
symptoms, as I have proved in a great series of cases. 


NOTES ON A CASE OF PELLAGRA. 

By D. MAXWELL ROSS, M.B., Ch.B., Assistant Medical Officer, 

Royal Edinburgh Mental Hospital. 

Since Dr Dods Brown and Dr Cranston Low 1 drew attention to 
this subject by reporting a case of pellagra discovered in this 
institution a few years ago, so many undoubted cases of the 
disease have been placed on record that it seems worth while 
recording cases in which the diagnosis has not proved quite so 
straightforward. For that reason the following case is reported. 

L. D., a mill girl from Leith, said to be of a quiet, retiring dis¬ 
position and good habits, was first admitted to this hospital in 
November 1909, suffering from delusions of persecution and 
auditory and visual hallucinations. Her family history was good, 

1 Dods Brown and Cranston Low, “Pellagra,” Edin. Mtd. Joum ., 1909, Sept. 




NOTES ON A CASE OF PELLAGRA 


245 


with the exception of a sister who died in thus hospital from 
insanity following organic brain disease. 

On admission her mental state was one of slight depression, 
with some confusion and slowing of all her facilities. Physically 
she was in poor condition, her skin was dirty, and she had an acne 
eruption on her face. She had fine tremors of the fingers, and her 
tendon reflexes were exaggerated. The Wassermann reaction was 
found to be negative in the blood serum. She made a gradual but 
good recovery from this attack, and was discharged in the spring 
of 1910. 

She is said to have remained fairly well until the summer 
of 1913, when she became so run down in health and melancholic 
that she had to be readmitted in July. She was found to be 
markedly depressed, slightly confused with somewhat ill-defined 
delusions and hallucinations. She was described as a flushed, 
excited little woman in poor physical condition. The acne 
eruption was again noted on her face but no rash elsewhere. She 
exhibited marked motor restlessness and her tendon reflexes were 
all exaggerated. She was looked upon at this time as probably 
a manic-depressive with toxic manifestations, the immediate 
diagnosis being mild delirious insanity. 

Within three weeks of her admission the delirious symptoms 
had disappeared, leaving her in a depressed and markedly neuras¬ 
thenic state. In the beginning of September she had a severe 
attack of diarrhoea, and it was then noticed that she had an eruption 
on the dorsum of both hands. The skin was red and slightly 
swollen, the epidermis dry and fissured, with large flakes separating 
off. It was noticed in addition that the facial acne was decidedly 
worse, there being a diffuse redness on the cheeks and forehead, 
and considerable complaint of a feeling of heat and burning. It is 
interesting to note that the condition was described by the charge 
nurse as a " very bad sunburn," a description not infrequently given 
of the milder skin manifestations of pellagra. 

The persistence of the diarrhoea, along with the presence of 
haemorrhoids from which she suffered severely, necessitated her 
confinement to bed. Mentally she was at this time slightly 
depressed and querulous, but gave no signs of either delusions or 
hallucinations. In spite of treatment the diarrhoea persisted, and 
she became extremely weak and emaciated. The stools were 
always liquid, latterly of a bright yellow colour, extremely offen- 



246 


D. MAXWELL ROSS 


8ive, and often streaked with blood, probably from the haemorrhoids. 
Her tongue was small, red, and dry, but she did not have any 
stomatitis. Her skin eruption gradually improved, and in 
November had disappeared from the hands, leaving, however, a 
slight hyperkeratosis over the knuckles, but no pigmentation. In 
November her weakness and emaciation became extreme, and her 
movements showed well-marked muscular inco-ordination. She 
now gave evidence of both visual and auditory hallucinations, and 
became somewhat confused and incoherent. A blood examination 
made at this time showed a mild degree of anaemia, a leucocytosis 
of 14,000, and a differential count of 70 per cent, polymorphs, 
298 per cent, lymphocytes, and *2 per cent, mononuclears. On 
24th November diffuse clonic muscular twitchings commenced, 
affecting at first the facial muscles, and later those of the limbs 
and trunk. She was unable to speak, and could only swallow with 
difficulty, but till a few hours before her death, on 26th November, 
she appeared to be conscious. The temperature shortly before 
death rose to 101°, but this was the only occasion during the 
illness on which it rose above 100''. 

A few hours after death some cerebro-spinal fluid was 
obtained. The Wassermann reaction in this fluid was negative, as 
was also the Fontana test; both the Noguchi and the Nissl Nonne 
tests were positive, and the cell count was 141 per c.mm. 

A post mortem examination was made sixteen hours after 
death with the following findings:— 

The skin on the dorsum of the hands showed brownish patches 
of rough, dry, and thickened epidermis, more especially over the 
knuckles. There was a small patch on each knee of a similar 
character, but elsewhere, except for the acne on the face, the skin 
presented no peculiarity. 

On removing the calvarium the meninges were found much 
injected, and in several places on the cortex there were minute 
pial htemorrhages. There was marked excess of cerebro-spinal 
fluid. The brain was soft, and weighed only 43£ ounces. Subse¬ 
quent microscopic examination of tissue removed from the cortex 
showed little pathological change. There were no definite degenera¬ 
tive changes, no arteritis, and no increase of neuroglia. Unfortu¬ 
nately, the cord was not removed. 

The heart and lungs were of normal appearance, the only 
change of note being a marked congestion at the pulmonary bases. 



NOTES ON A CASE OF PELLAGRA 247 

The large intestine was found distended with gas and markedly 
injected, as were also the small intestines and the mesentery, in 
which there were numerous enlarged glands. Twelve inches above 
the ilio-caecal valve was a recent intussusception easily reduced, 
and evidently of only a few hours’ duration. The intestinal 
mucosa was markedly injected, but at no point was there any 
ulceration. 

The liver weighed 35£ ounces, and was of fatty appearance. 

The kidneys and spleen appeared normal. 

Cultures were taken from the spleen and the intestinal mucosa. 
From the former a gram positive coccus was isolated, and from the 
latter a mixed culture was obtained, which was found to consist of 
a coccus similar to that obtained from the spleen, and a bacillus 
giving the characteristic reactions of the pyocyaneous group. 

The symptoms of pellagra have been divided into four groups, 
the mental, the alimentary, the nervous, and the dermatological. 
It will be seen that this patient presented fairly characteristic 
symptoms in each of these groups. Mentally, she was at times 
mildly delirious, and when not delirious was depressed and 
neurasthenic. According to Wood, Tanzi, and other authorities, 
the mental symptoms of pellagra may present a wide diversity 
of type, but the most characteristic is a neurasthenic depression, 
while symptoms of delirium are frequently present during the 
course of the illness, and especially towards its termination. 

In the alimentary group gastro-intestinal irritation, stomatitis, 
indigestion, and diarrhoea with frequently proctitis and. haemor¬ 
rhoids are the outstanding symptoms. The patient in this case 
suffered most markedly from diarrhoea with haemorrhoids, but 
there was no stomatitis, nor were the gastric symptoms at all 
prominent. In passing it is interesting to note that her stools 
were of a peculiarly offensive character, and Box in his article 
on pellagra in the Practitioner (June 1913), notes that the odour 
of the stool is said to be peculiar and offensive, suggesting 
putrefactive changes. 

With regard to the nervous symptoms much seems to depend 
on the duration of the disease. Changes in the nervous system 
in the cases of shorter duration are indefinite, consisting princi¬ 
pally of degenerative changes in the cortical cells. The symptoms 
referable to sclerotic changes in the cord are of insidious onset, 
and were not noted in this case, where indeed the most prominent 


20 



248 


I). MAXWELL ROSS 


nervous system was the exaggeration of the reflexes, which is 
said to be the commonest change in pellagra. Though I can find 
no reference to a terminal attack of clonic convulsions exactly 
similar to that in which this patient died, convulsions do occur, 
and one of Wood’s cases died from epileptiform convulsions after 
having had three yearly recurrences of the disease. 

The dermatological symptoms were very slight and transient 
in character, but were the first to attract attention. I was 
fortunate, while working in an American hospital, in seeing 
several cases of pellagra, and the site rather than the character 
of the lesions on the hands associated with a condition of neuras¬ 
thenia and depression at once raised tho suspicion of pellagra. I 
was very interested to find that my colleague, Dr Neill, who had 
charge of the case during October, and until a few days before 
her death in November, considered pellagra as a possible diagnosis, 
although the skin lesions were then much less than in September. 
The acne of the face made it difficult to draw any definite conclu¬ 
sion from the skin condition there, but there was undoubtedly an 
erythema, and the feeling of burning she complained of is a 
fairly constant symptom in pellagra, though usually referred to 
some other locality. Miller 1 describes a case in which in October 
the patient used to stand with bare feet in the sea to obtain relief 
from the sensation of heat. 

The blood in this patient presented nothing very characteristic, 
and in pellagra the only blood change that appears constant is a 
tendency to an increase in the lymphocytes. With regard to the 
examination of the cerebro-spinal fluid as it was obtained after 
death no great importance can be attached to the findings. An 
increase in the cell content has been noted, but not to the marked 
extent present here. 

The presence of the Bacilli pyocyaneus in the intestine was of 
interest, and it is unfortunate that no bacteriological examination 
of the 8tools was made during life. Whether the organism had 
any relation to the diarrhoea is difficult to say. Several cases of 
septicaemia in children with marked gastro-intestinal symptoms 
caused by Bacillus pyocyaneus have been recorded, and it is 
possible that the severe persistent diarrhoea may have had a 
definite cause in this organism. 

The pathological findings are quite in accordance so far as they 
1 Amtr . Journ. Insanity , 1913, Jan., p. 551. 



NOTES ON A CASE OF PELLAGRA 


249 


go with those of pellagra, although degenerative changes might have 
been expected in the cortical cells. The absence of perivascular 
infiltration and endarteritis is exactly in accordance with Mott’s 
findings as described in a fatal case of Box’s examined by him. 

The chief interest of the case lies in the mildness of the skin 
manifestations, and in the fact that it raises the question of the 
relations of sunburn and pellagra. 

Pellagra sine pellagra is not generally accepted as a definite 
clinical entity, but it is admitted that the erythema may be so 
slight that it is either mistaken for a sunburn, or escapes 
altogether the notice of the patient or his friends. A further 
difficulty in diagnosis lies in the fact that during the remission 
of the skin lesions there may be very little local evidence of their 
ever having been present. Tucker, in an article contributed to 
this year’s Medical Annual, states that during the intervals 
between the attacks the skin may look either normal or smooth 
and glistening. 

Now that pellagra is so much to the fore, every case of sunburn 
is looked upon with a suspicious eye, and yet in every asylum 
numerous cases of most severe sunburn are to be seen every year, 
so that a real pellagrous erythema may be very readily overlooked, 
or a severely sunburnt melancholic all too readily labelled a 
pellagrin. The modem open-air treatment so much used in 
asylums and other kindred institutions has many benefits, and it 
is not impossible that to it may be due the doubtful advantage of 
adding many to the number of pellagrins in this country. It is a 
point that seems worth remarking that in asylums the patients, 
especially the female patients, are far more exposed to sunlight 
and fresh air than they are when leading their normal life, and 
more especially does this apply to town dwellers; and further they 
usually have a diet consisting much more of rice and other cereals 
than the diet they are accustomed to at home. In view of the 
older theories as to the etiology of pellagra, these points seem of 
some interest. 

I have to thank Dr G. M. Robertson, Medical Superintendent 
of the Royal Edinburgh Mental Hospital, for his kind permission 
and encouragement in recording the case. 

To Dr W. Abel, Pathologist to the Hospital, I am indebted for 
the reports on the bacteriological and microscopical examinations. 


250 


ARTHUR F. HERTZ 


BABINSKI’S “SECOND SIGN” OF ORGANIC HEMI¬ 
PLEGIA IN HEMICHOREA, AND ITS BEARING 
ON THE ORGANIC NATURE OF CHOREA. 

By ARTHUR F. HERTZ, M.A., M.D., F.R.C.P., 

Assistant Physician and Physioian-in-Charge of the Neurological 
Department at Guy’s Hospital. 

Although it is universally agreed that chorea is an organic disease, 
the recognition of this fact depends less upon the symptoms of 
the disease itself than upon its association with rheumatic fever 
and its obvious organic complications, such as endocarditis and 
pericarditis. There is indeed no feature about the symptoms of 
chorea, which by itself would indicate the presence of organic 
changes in the brain or spinal cord, and the anatomical lesions 
which have been discovered in fatal cases are slight and inconstant. 
Thus the optic discs are never affected and the pupils are normal; 
the cutaneous and deep reflexes are neither increased nor diminished; 
and the plantar reflexes are always flexor. 

I have elsewhere 1 drawn attention to the great diagnostic 
value of the sign described by Babinski as “ combined movement 
of the trunk and pelvis”; for convenience I have called it 
Babinski’s second sign. When a normal individual, lying on his 
back with his arms folded and his legs widely separated, attempts 
to sit up, both legs rise equally into the air; on falling back to the 
ground, the legs again rise. In these circumstances in organic 
hemiplegia the affected leg always rises higher than the other, 
whereas in hysterical hemiplegia the paralysed leg remains flat on 
the ground, although several muscles are brought into powerful 
action when this occurs. I have recorded several cases in which 
this sign proved the organic nature of the hemiplegia, although 
the plantar reflex was flexor; in other cases, in which the plantar 
reflex was unobtainable, the presence of Babinski’s second sign 
has been very helpful in diagnosis. 

I have had the opportunity of testing Babinski’s second sign 
in seven cases of hemichorea. Without a single exception the 
leg on the affected side rose higher than the other, although the 
plantar reflex was flexor and the cutaneous reflexes and tendon- 
responses of the two sides were equal. As this sign has never been 

1 A, F. Hertz, Guy's Hospital Reports, 1911, lxv., p. 54. 



ABSTRACTS 


251 


observed in any case of hemiplegia which was not organic, its constant 
presence in hemichorea points strongly to the conclusion that the 
upper motor neurone is affected by some organic change in 
hemichorea, even if it is of a kind which escapes recognition by 
the ordinary methods of histological examination. There is at 
present no anatomical evidence to show what special significance the 
presence of Babinski’s second sign has when the plantar reflex is 
flexor, but it is highly probable that the two signs depend upon 
lesions to different parts of the upper motor tract. The two parts 
are generally affected together, so that both signs are present, but 
in rare instances of otherwise unremarkable hemiplegia, and in all 
cases of chorea, the part associated with Babinski’s second sign is 
affected when that associated with the extensor plantar reflex is 
spared. In much rarer cases of hemiplegia, but never in hemi¬ 
chorea, the opposite is the case. 

As Babinski’s second sign is constantly present in hemichorea, 
it may reasonably be concluded that the lesion with which it is 
associated is constantly present in ordinary cases of bilateral 
chorea. As this sign is the only evidence of the existence of an 
organic lesion in hemichorea, and as it depends on a comparison 
between the two sides, direct evidence of the organic nature of the 
nervous symptoms in ordinary chorea is still wanting. 


abstracts. 

ANATOMY. 

THE NERVE ARBORISATIONS OF THE BLOOD-VESSEL WALLS. 
(302) (tfrber die Nervenverzweigungen innerh&lb der GeiUsswand.) 
Glaser, Deut. Zeitschr. f. Nervenheilk., 1914, 1., Hft 5-6, p. 305. 

By special histological methods the author has determined that 
nerve plexuses are found in the middle and outer coats of the 
blood vessels. The capillaries are accompanied and surrounded 
by nerve twigs. It is possible to demonstrate nerve-end organs in 
the blood vessels: the very finest twigs reach the intima. 
Ganglion cells are found only in the outer layers of the adventitia 
of such vessels as the aorta, internal carotid, and renal arteries: 
they are awanting in peripheral arteries. 


S. A. K. Wilson. 



252 


ABSTRACTS 


PHYSIOLOGY. 

THE MECHANISM OF MUSCULAR TONUS, OF THE REFLEXES, 

(303) AND OF CONTRACTURE. Crocq, L’Enctphale , 1914, ix., 
Feb., March, April, pp. 147,197, and 293. 

The author’s main conclusions are somewhat as follows:— 

In the frog, tonus is a purely spinal phenomenon, and is 
dependent on the integrity of short reflex paths. In the dog, 
there are three “ centres ” for tonus: the spinal, the basal, and 
the cortical; of these, the basal appears to be the most important. 
Tonus depends on the integrity of long reflex paths, but if these 
are interrupted, it appears that short reflex paths may supplement 
them. In the ape, short reflex paths play only a subsidiary role: 
the tonus centres are basal and cortical; the latter is at least 
as important as the former. In man, the paths concerned with 
the maintenance of tonus in voluntary muscles are the long reflex 
paths, and the tonus centre is cortical. Destructive lesions of 
the cortico-spinal path diminish or abolish tone in man: “irri¬ 
tative ” lesions produce hypertonus. In the new-born child, tonus 
is spinal, and not cortico-spinaL As far as the reflexes are con¬ 
cerned, in the frog they are spinal. In the dog, tendon reflexes 
and reflexes of defence are spinal: cutaneous reflexes are effected 
normally by long paths, with a basal centre, and they are only 
secondarily spinal In the ape, defence reflexes are spinal, tendon 
reflexes are basal, cutaneous reflexes are both basal and cortical. 
In man, defence reflexes are spinal, tendon reflexes basal, and 
cutaneous reflexes cortical. 

According to Crocq, contracture is the same as, and results 
from the same causes as produce, hypertonus. He believes the 
condition is caused by pericellular or periaxonal irritation of the 
cortico-spinal path. Crocq depends to some extent for his position 
on the results of complete transverse section of the cord in man, 
which he says corroborate his views, and apparent contradictory 
cases have been those in which it has been impossible to 
demonstrate that the cord has been completely severed. 

S. A. K. Wilson. 


PATHOLOGY. 

FURTHER OBSERVATIONS ON THE INFLUENCE OF TOXINS 
(304) ON THE CENTRAL NERVOUS SYSTEM. D. Orb and R. G. 

Rows, Joum. of Ment. Sci. t 1914, April, p. 184. 

The previous researches of these authors have shown the 
possibility of conduction of bacterial toxins to the central nervous 



ABSTRACTS 


253 


system along the sheaths of peripheral nerves. The present 
experiments throw light upon the method by which the spinal cord 
and brain are affected by toxins in the abdomen. Celloidin 
capsules of staphylococci were placed in different parts of the 
abdomen of rabbits, and the animals were killed after six weeks. 
The chief changes found in the cord were hyaline degeneration of 
the blood vessels of both the grey and white matter, with hyaline 
thrombi occluding them in many cases, myelin degeneration of 
the peripheral areas of the cord, especially of the upper part, and 
glial proliferation around the affected vessels. The nerve cells 
were but slightly affected. The sympathetic ganglia in the 
abdomen were found to be inflamed in every case. 

The authors think that the cord changes are due to disturbance 
of the circulation in the vessels of the cord from infection and 
inflammation of the sympathetic nervous system, although direct 
action of the toxins upon the affected vessels may have had a 
secondary effect. They think that analogous changes may be 
responsible for the lesions of general paralysis. 

W. D Wilkins. 

CLINICAL NEUROLOGY. 

THE CEPHALOGRAPH, A NEW INSTRUMENT FOR RECORD- 

(305) INO AND CONTROLLING HEAD MOVEMENTS. A. Knaubr 
and W. J. Maloney, Joum. Nerv. and Afent. Dig., 1914, xli., No. 2, 
Feb. 

A clinical instrument has been constructed to record graphically 
oscillations about a vertical axis of the upright standing or sitting 
body, oscillations which, when exaggerated, are known as Romberg’s 
phenomenon. 

The instrument devised records the movements of the head in 
two dimensions, in the sagittal and in the frontal planes. The 
exact description of the apparatus with drawings is given. 

It is said that in organic disturbances of the nervous system, 
such as locomotor ataxia, and in many of the psychoneuroses, 
especially in all kinds of tics, the chart will soon be covered with 
lines of characteristic shape and direction. In the treatment of 
morbid conditions the patient is systematically exercised to control 
the excursions of the recording pen. D. K. Henderson. 

THE CENAjSTHOPATHIBS. (Lea Gdnesthopathies.) Adstbbgesilo 

(306) and Esposkl, L’Enctphale , 1914, ix., May 10, p. 425. 

By the term cenaesthopathy is meant an alteration of common 
sensibility (cenaesthesia), i.e., of those sensations from the different 



254 


ABSTRACTS 


parts and organs of the body which, normally, do not impress 
themselves on consciousness by any peculiarity either of intensity 
or of modality. The health of our organs is affirmed by their 
negation, so to speak. Censesthopathy is the constant subjective 
sensation^ of the body. Disturbances of censesthesia are very 
common in the general neuroses and psychoses, but the term 
censesthopathy should be restricted to those cases where the 
psychoneurosis take almost entirely the form of a disturbance of 
centesthesia. The syndrome may occur by itself, or it may occur 
with other psychoneuroses and be incorporated with them. 

One of the predominant features in centesthopathy is a strange, 
painful sensation which is usually distinguished by the patient 
from ordinary pain. The head and the abdomen are the most 
constant seats of these unpleasant sensations, which the patients 
often have difficulty in describing. The authors record excellent 
clinical instances of the syndrome, and discuss its etiology and its 
treatment. S. A K. Wilson. 


THE OCULO CARDIAC REFLEX IN GRAVES’ DISEASE. (Le 
(307) rdflexe oculo-cardiaque dans le syndrome de Basedow.) B. 

Qcillaumont, Theses de Paris , 1913-14, No. 229. 

The oculo-cardiac reflex was first described by Aschner in 1908 
(Wien. klin. Woch., 1908, xxi., p. 1529). In three-fifths of all 
persons examined a slowing of the radial pulse by 5 or 6 pulsations 
normally occurs when the eyeballs are pressed back into the orbits 
(positive reflex). In other cases tachycardia results (inverted 
reflex), or there is no change in the cardiac rhythm (negative reflex). 

The writer examined 33 cases of Graves’ disease and found the 
reflex was positive in 22, absent in 8, and inverted in 3. When 
improvement took place and tachycardia diminished, difference in 
the pulse rate caused by ocular compression was also less marked. 

The anatomical substratum is the fifth nerve, bulb and vagus 
or sympathetic, according as the reflex is positive or inverted. 

J. D. Rolleston. 


THE OCULO CARDIAC REFLEX. (Le rdllexe oculo-cardiaque.) 

(308) Gautbblet, Paris Mid., 1912-13, iii., p. 583. 

Gautrelbt never found cardiac acceleration after ocular com¬ 
pression in Graves’ disease, tuberculosis, or pulmonary disease in 
general rheumatism or alcoholism. In three cases of tabes he 
found slight diminution in the number of radial beats, but in two 
cases there was acceleration, and in five no change at all after 
ocular compression. Slight slowing of the pulse was found in 



ABSTRACTS 


255 


heart disease, sciatica, and facial neuralgia, and slight acceleration 
in radiculitis, polyneuritis, and hysteria. No reaction was noted in 
cases of hernia, haemorrhoids, ulcer of the leg, and fractures of the 
thigh. J. D. Rollbston. 

THE OCULO CARDIAC REFLEX IN NORMAL SUBJECTS WITH- 

(309) OUT BRADYCARDIA. (Le rlflexe ocnlo-cardiaque chez les 
sujeta nonnaux non bradycardiques.) Petzetakis, Bull, et mbn. 
Soc. mid. Hip. de Parity 1914, xxxviL, p. 662. 

The writer examined seventy-five persons whose pulses varied 
between 70,80, and 85, in the dorsal decubitus and found that the 
oculo-cardiac reflex was normally manifested by slowing of the 
cardiac rhythm. The slowing varied on the average from 5 to 12 
beats per minute. In only three cases, two of whom were females, 
was acceleration of the pulse noted. After injection of atropine 
the reflex was abolished. After injection of pilocarpine the reflex 
persisted, and in some cases was exaggerated. 

The greatest slowing was caused by compression of the right 
eye, which shows that the right vagus is the most excitable, as 
has already been observed by S. Arloing and Trippier in animals, 
and is the rule in normal subjects. J. D. Rolleston. 

CIRCULATORY AND RESPIRATORY PHENOMENA PRODUCED 

(310) BY OCULAR COMPRESSION. (Phlnomdnes drculatoires et 
respiratoires produites par la compression oculaire.) Pktzetakis, 
Compt. rend. Soc. dc Bud., 1914, lxxvi., p. 366. 

Slowing of the cardiac rhythm is not the only phenomenon pro¬ 
duced by ocular compression. In a few cases acceleration occurs, 
while in others both phenomena take place, a period of slowing 
being followed by a few hurried beats. 

These facts show that both cardio-moderator and cardio- 
accelerator elements are concerned in the reflex, and that the 
anatomical paths are the pneumogastric and the sympathetic. 

In most cases the blood pressure rises while the number of 
cardiac pulsations is diminished. This rise of pressure is to be 
attributed to stimulation of the vaso-motor centre. 

Ocular compression causes slight diminution in the number of 
respirations. The amplitude of the respiratory movements may 
be increased, the respiration often becomes spasmodic at first, and 
subsequently there are inspiratory pauses which are the most 
constant respiratory phenomena during ocular compression. As 
these symptoms persist after injection of atropine, the phrenic 
appears to be responsible for their occurrence. 

J. D. Rolleston. 



256 


ABSTRACTS 


OCULO CARDIAC REFLEX PRODUCING STOPPAGE OF THE 

(311) HEART. VENTRICULAR AUTOMATISM AND AURICULO- 
VENTRICULAR DISSOCIATION. OVARIAN INSUFFIENCY 
ASSOCIATED WITH THYROID OVERACTIVITY. EPI¬ 
LEPTIFORM ATTACKS. (Rdflexe oculo cardiaque provoqu&nt 
l’arrfet du coeur, l’automatisme ventriculaire et la dissociation 
auriculo - ventriculaire. Syndrome hypo-ovarien et hyper¬ 
thyroidism Crises dpileptiformes.) H. Dufoue and Legras, 
Bull, et mim. Soe. mid. H6p. de Paris, 1914, xxxvii., p. 686. 

A woman, aged 22, after a miscarriage, developed signs of ovarian 
insufficiency, characterised by amenorrhoea, complete loss of pubic 
and axillary hair, and partial loss of hair on the scalp. On the 
other hand, thyroid overactivity was shown by a slight goitre, 
tachycardia, exophthalmus, and renewed growth of the hair on 
the pubis. 

Cerebro-spinal hypertension was shown by epileptiform attacks. 

According to the degree of compression exerted, the oculo¬ 
cardiac reflex produced the following results:— 

1. Total stoppage of the heart. 2. Slowing of the heart. 
3. Auriculo-ventricular dissociation. 4. Ventricular automatism. 

J. D. Rolleston. 

CONSTANT SUPPRESSION OF THE OCULO CARDIAC REFLEX 

(312) BY ATROPINE. (Suppression constants par l’atropine dn 
rdflexe oculo cardiaque.) A. Monoeot, CompL Betid. Soc. de Biol., 
1914, lxxvi., p. 162. 

Mongeot found that subcutaneous injection of 1 mm. of atropine 
sulphate attenuated the oculo-cardiac reflex, and that a dose of 
1J mm. in women and 2 mm. in men completely abolished it, 
whether it was normal, exaggerated, or inverted before injection. 
This result occurred 25 to 45 minutes after injection, and was 
obtained both in normal persons and in cases of tachycardia 
without arrhythmia. J. D. Rolleston. 

CHANGES IN THE REFLEXES PRODUCED BY OCULAR OOM- 

(313) PRESSION IN EPILEPSY. (Considdrations but les modifications 
des rdflexes produites par la compression oculaire chez certains 
Fpileptiques.) C. Lesieur, M. Vbrnet, and Petzbtakis, Bull, et 
mfan. Soc. mid. H6p. de Paris , 1914, xxxvii., p. 510. 

The writers first investigated the condition of the reflexes in 
epilepsy apart from ocular compression, with the following 
results:—Except in fits, the tendon reflexes were normal in most 
cases. There was no knee nor ankle clonus. The abdominal 
reflex was almost invariably absent or diminished. As a rule 



ABSTRACTS 


257 


the cremasteric reflex was present. The corneal reflex was variable. 
After slight fits there was no change in the reflexes. If the fit 
was severe, a very limited period in which the reflexes were 
absent was followed by a period in which they were exaggerated. 

In some cases ocular compression produced a very marked 
exaggeration of both tendon and skin reflexes. Ankle clonus 
might occur. The writers attribute this exaggeration to a 
stimulation of the reflex centres in the bulbo-pontine region. 
In normal subjects this phenomenon does not occur on ocular 
compression, because their reflex centres are not so excitable 
as those of the epileptic. J. D. Rolleston. 

STOPPAGE OF THE HEART BY THE OCULO CARDIAC REFLEX 

(314) IN AN EPILEPTIC. (Considerations physio-p&thologiques but 
un cas d’arrSt du cceur par le rdflexe oculo-cardiaque chez un 
dpileptique.) C. Lesieur, M. Vernet, and Pbtzetakis, Bull, et 
mim. Soc. mid. HGp. de Paris, 1914, xxxvii., p. 394. 

In a man, aged 31, the subject of Jacksonian epilepsy and right 
hemianiesthesia, extremely moderate compression of the right 
eye produced complete stoppage of the heart. After eight or nine 
seconds’ compression syncope ensued and compression had to be 
interrupted, but later complete stoppage of the heart for fourteen 
seconds was obtained. 

The patient then showed considerable hyper-excitability of the 
vagus, as is the rule in most epileptics. Associated with the slow¬ 
ing and arrest of the heart were disturbances of respiration, 
mastication, deglutition, and vaso-motor troubles which undoubtedly 
corresponded to bulbar stimuli. After subcutaneous injection of 
2 mgm. of atropine the oculo-cardiac reflex was abolished, but 
the respiratory disturbance continued, being due to the persistence 
of an oculo-phrenic reflex, and was accompanied by disturbances 
of deglutition and mastication, ptosis, mydriasis, and vaso-motor 
troubles. The vagus, therefore, was exclusively paralysed. 

J. D. Rolleston. 

EXAGGERATION OF THE OCULOCARDIAC REFLEX IN 

(315) EPILEPSY. ITS VARIATIONS UNDER THE INFLUENCE 
OF MEDICINAL AND TOXIC CAUSES. (Contribution & 
l’dtude du rdflexe oculo-cardiaque: son exagdration dans 
l'dpilepsie. Ses variations sous l’influence d’actions mddicament- 
euses ou toxiques.) C. Lrsieor, M. Vernet, and M. Petzetakis, 
Bull, et mem. Soc. mid. H6p. de Paris, 1914, xxxvii., p. 440. 

The writers examined 33 cases of epilepsy, 23 of whom were men 
and 10 women, with the following results:— 



258 


ABSTRACTS 


1. The reflex was always considerably exaggerated: 9 showed 
slowing of from 30 to 50 beats per minute, and 20 slowing of more 
than 16 beats per minute; in the remainder the slowing was from 
12 to 16. The reflex was more exaggerated in female than in 
male epileptics. With two or three exceptions patients with 
fewest fits were those in whom the reflex was least exaggerated, 
and those with frequent fits were those in whom the reflex was 
most exaggerated. 

2. Action of Potassium Bromide. —Epileptics with few fits who 
were taking bromide had a less exaggerated reflex than those in 
whom the bromide had been stopped. Cessation of bromide was 
always followed by exaggeration of the reflex. The stronger the 
dose of bromide, the nearer did the reflex come to normal. The 
state of the reflex was thus a guide to the suitable dose. 

3. Effects of Tobacco on the Cardiac Nerves. —Two epileptics, who 
were heavy smokers, with a moderately increased reflex, were 
chosen, and prevented from smoking for three days. The reflex 
was noted before and after the deprivation of tobacco, and after 
their return to it. The most typical case showed a slowing of 
12 beats before cessation, during cessation a diminution of 8 
beats, and after resumption of tobacco a slowing of 28 beats. 

4. The State of the Reflex Before and After Fit. —The fit seemed 

to diminish the hyperexcitability of the vagus, as the diminution 
in the number of the beats, which before the fit had been 24, 
immediately after was only 8. J. D. Rolleston. 

PERSISTENCE OF OCULO CARDIAC REFLEX IN GENERAL 

(316) ANAESTHESIA. (Persistence du rdflexe oculo-cardiaque pendant 
l’anesthdsie gdndrale.) Fabbe and Pbtzetakis, Compt. Rend. Soc. 
de Biol., 1914, lxxvi., p. 343. 

The writers found that the oculo-cardiac reflex persisted longer 
than the corneal reflex under general anaesthesia. During ether 
anaesthesia the reflex persisted the whole time, while in chloroform 
anaesthesia it only disappeared in very deep anaesthesia. 

J. D. Rolleston. 

INHIBITORY ACTION OF OCULAR COMPRESSION ON THE 

(317) ABNORMAL MOVEMENTS IN A CASE OF DOUBLE 
ATHETOSIS. (Action inhibitrice de la compression oculaire 
sur les mouvements anormaux das un cas d’athdtose double.) 

G. Guillain, Bull, et mdm. Soc. mid. H6p. de Paris, 1914, xxxvii., 
p. 850. 

A record of a case of a girl, aged 20, in whom choreo-athetotic 
movements of the face and limbs were almost completely stopped 



ABSTRACTS 


259 


by ocular compression. Exaggeration of the oculo-cardiac reflex 
was shown by diminution in the pulse rate of twenty-nine beats 
per minute. The compression had to be discontinued, as it caused 
a tendency to syncope. J. D. Rolleston. 

THE OCULO CARDIAC REFLEX IN PATIENTS SUFFERING 

(318) FROM VARIOUS TREMORS. (Le rlflexe oculo-cardiaque chez 
des sujets attaints de divers tremblements.) C. Lksieur, 
M. Vernet, and Petzetakis, Bull, et mem. Soc. mid. Hop. de 
Parity 1914, xxxviL, p. 593. 

The writers found the reflex normal in alcoholic and senile tremor, 
lost in paralysis agitans, sometimes exaggerated in general 
paralysis, and variable in disseminated sclerosis. 

J. D. Rolleston. 

THE OCULO CARDIAC REFLEX AND PARALYSIS AGITANS. 

(319) (Rdflexe oculo-cardiaque et maladie de Parkinson.) C. Lesieur, 
M. Vernet, and Petzetakis, Bull, et mini. Soc. mid. Hop. de Paris, 
1914, xxxvii., p. 599. 

The writers found complete and constant absence of the oculo¬ 
cardiac reflex in fifteen out of sixteen cases of paralysis agitans. 
Their conclusions are as follows:— 

1. The loss of this reflex can only be explained by some change 
in the reflex centre. 

2. The constancy of this loss suggests the probability of a 
corresponding lesion in this centre in paralysis agitans, and so of a 
mesencephalic, or more precisely, a bulbo-ponto-cerebellar lesion. 

3. Morbid anatomy shows that this region is most frequently 
affected in paralysis agitans. 

4. The clinical study of paralysis agitans shows symptoms of 
disorder of equilibrium resembling an incomplete cerebellar 
syndrome. 

5. The intensity of the tremor appears proportioned to the 

intensity of the corresponding lesion. A unilateral tremor corre¬ 
sponds to a unilateral lesion, and causes a unilateral change in the 
oculo-cardiac reflex. J. D. Rolleston. 

FREQUENT ABOLITION OF THE OCULO-CARDIAC REFLEX IN 

(320) SYPHILIS. (Abolition frdquente du rdflexe oculo-cardiaque chez 
les syphilitiques.) Loepbr, Mongeot, and Vahram, Bull, et mim. 
Soc. mid. H6p. de Paris, 1914, xxxvii., p. 506, and Progres mid., 
1914, xli., p. 157. 

The writers examined 40 patients in various stages of syphilis, and 
found the reflex absent in 30. Its absence was more frequent in 
secondary than in primary syphilis, especially when the lesions of 



260 


ABSTRACTS 


the skin and muoosfe were well marked. It was invariably absent 
in nervous syphilis, and almost always so in tertiary syphilis, 
independently of any cutaneous osseous or arterial lesions. The 
loss of the reflex may be due to neuritis of the fifth or of the 
vagus, and perhaps to mediastinitis and periaortitis, but it is chiefly 
caused by a bulbar lesion. The frequency of the loss of the oculo¬ 
cardiac reflex in syphilis contrasts with the rarity of its abolition 
in other infectious diseases, such as tuberculosis, pneumonia, 
typhoid fever, or malaria. J. D. Rolleston. 

ON THE FREQUENT ABOLITION OF THE OCULOCARDIAC 

(321) REFLEX IN TABES. (Note but l’abolition frdquente du rdflexe 
oculo-cardiaque dans le tabes.) C. Lesieub, M. Vernet, and 
Petzetakis, Bull, et mem. Soc. mid. H6p. de Paris, 1914, xxxvii., 
p. 446. 

Like Loeper and Mongeot the writers found the oculo-cardiac 
reflex almost always abolished in tabes. In 9 out of 13 cases the 
abolition was complete, in 3 the reflex was almost imperceptible, 
and in 1 it was nearly normal. They also found that this reflex 
may be absent although there is no Argyll Robertson pupil. The 
writers think that the loss of the reflex indicates the condition of 
the bulbar or the bulbo-pontine sensory roots, and therefore the 
degree of upward extension of tabes. J. D. Rolleston. 

ABOLITION AND INVERSION OF THE OCULO-CABDIAC BEFLEX 

(322) IN PSEUDO-BULBAB PARALYSIS. (Abolition et inversion 
dn rdflexe oculo-cardiaque dans les paralysies pseudo-bulbaires.) 
G. Guillain and J. Dubois, Bull, et mem. Soc. mid. U6p. de Paris, 
1914, xxxvii., p. 584. 

Of six cases of pseudo-bulbar palsy examined, four showed loss of 
the reflex, and two inversion. J. D. Rolleston. 

FAVOURABLE ACTION OF OCULAR COMPRESSION ON 

(323) CERTAIN NERVOUS MANIFESTATIONS, ESPECIALLY 
HICCOUGH. (Action favorable de la compression oculaire sur 
certaines manifestations nerveuses et en particular sur le hoquet.) 
Loeper and Weil, Bull, et mim. Soc. mid. U6p. de Paris, 1914, 
xxxvii., p. 631. 

The writers found that bilateral compression of the eyeballs had a 
favourable effect on vertigo, tinnitus, pharyngeal and pharyngo- 
cesophageal spasm, but the most striking results were obtained in 
the treatment of yawning, sneezing, or obstinate hiccough. Most 
of these morbid symptoms are due to irritation of some of the 
bulbar centres, and ocular compression substitutes a new stimulus 
which has a regulating effect. J. D. Rolleston. 



ABSTRACTS 


261 


GLYCOSURIA, ALBUMINURIA, AND POLYURIA CAUSED BY 

(324) OCULAR COMPRESSION. (Glycosurie, albuminuria at 
polyuria provoqudes par la compression oculaire.) C. Lksikur, 
M. Vebnet, and Petzetakis, Bull, et mem. Soc. mid. Hop. de Paris » 
1914, xxxvii., p. 515. 

Three male and three female epileptics were examined. All 
showed marked polyuria after ocular compression. Three had 
albuminuria and four glycosuria. In two there was neither 
glycosuria nor albuminuria. The albuminuria appeared two hours 
after compression, and lasted about one and a half hours; the 
glycosuria appeared three hours after compression. Five hours 
after compression none of the urines showed either albumin or 
sugar. These results resemble those obtained by Claude Bernard 
after puncture of the fourth ventricle, and show that the centripetal 
path of the oculo-cardiac reflex may sometimes be the sympathetic. 

J. D. Rolleston. 

FIBROSARCOMA OF THE LEG IN A WOMAN SUFFERING 

(325) FROM RECKLINGHAUSEN’S DISEASE. (Fibrosarcome de la 
jambe chez une femme atteinte de la maladie de Recklinghausen.) 
H. Morestin, Bull. Soc. AnaL de Paris, 1914, xvi., p. 79. 

A woman, aged 30, had had a small swelling on her leg since 
childhood, but within the last few months it had grown rapidly. 
The typical phenomena of Recklinghausen’s disease were present. 
The tumour was successfully removed, and was found to be a 
spindle-celled sarcoma. J. D. Rolleston. 

TRANSITORY BROWN-S^QUARD’S SYNDROME AT THE ONSET 

(326) OF SPINAL SYPHILIS. (Syndrome de Brown-Sdquard au ddbut 
d’une syphilis m6dullaire.) Duhot and Boez, L'Echo mid. du 
Nord, 1914, xviii., p. 197. 

A man, aged 31, developed weakness of both legs, followed three 
days later by complete paralysis of the right leg and difficulty in 
micturition. There were thermal and tactile hyperesthesia in the 
right leg, and hypoesthesia in the left leg. Babinski's sign was 
present on both sides, syphilis was denied, but the tongue was 
fissured and showed patches of leucoplakia, and Wassermann’s 
reaction, though negative in the spinal fluid, was positive in the 
blood. There were cerebro-spinal hyperalbuminosis and moderate 
lymphocytosis. On the day following lumbar puncture the 
monoplegia diminished, and sensibility returned in the left leg. 
The patient was then treated with neosalvarsan, and the sensory 
troubles disappeared, and the gait improved. 

The transitory duration of Brown-S^quard’s syndrome and its 
spontaneous disappearance showed that it was due to ischaemia 



262 


ABSTRACTS 


and not to sclero-gummatous meningitis, which is the usual cause 
of the syndrome in syphilis. J. D. Rolleston. 

THE SEROTHERAPY OF OEBEBRO-SPINAL MENINGITIS. (La 

(327) slrothlrapie de la mlningite clrlbro-spinale.) A. Orticoni, Bull, 
et mim. Soc. mid. Hip. de Paris, 1914, xxxvii., p. 006. 

Thirty-eight cases of cerebro-spinal meningitis occurred in the 
20th Army Corps at Nancy between November 1913 and March 
1914. Of these 34 were due to the meningococcus, whereas in the 
previous year only 7 were observed during the same period. On 
subtracting 1 case in which the meningitis was due to an associa¬ 
tion of the pneumococcus with the meningococcus, and another 
who was injected in extremis, the mortality was only 8*8 per cent. 
—the lowest on record. This favourable result was due to the 
early use of anti-meningococcic serum. Each patient was given 
30 or 40 c.c. for three or four consecutive days according to the 
gravity of the case. Convalescence was early and rapid, and no 
sequelae occurred. J. D. Rolleston. 

RECURRENT FEVER AND MENINGEAL SYNDROME (EPL 

(328) DEMIC OF RECURRENT FEVER IN GREECE DURING AND 
AFTER THE TWO WARS OF 1912-13). (Filvre recurrent® et 
syndrome mining* (£pid6mie de filvre recurrent* en Grice 
pendant et aprls les deux guerres de 1912-13).) G. S. Coskin as, 
Bull, et mem. Soc. mid. Hip. de Paris , 1914, xxxvii., p. 772. 

Of 43 cases of recurrent fever treated at the Clinique Mldicale of 
Athens University from March 1913 to March 1914, 8 cases, or 
17 per cent., of whom brief histories are given, showed a meningeal 
syndrome consisting of Kernig’s sign, rigidity of the neck and 
other muscles, hyperesthesia, and mental disturbance. ThiB 
syndrome might occur at any stage of the disease, but was moBt 
frequent and intense in the first attack. Jt was not accompanied 
by any changes in the cerebro-spinal fluid except a very slight 
increase in the amount of albumin, and its occurrence did not 
aggravate the prognosis of recurrent fever. J. D. Rolleston. 

CEREBRAL RHEUMATISM EXPLAINED BY HEMORRHAGIC 
(329 MENINGITIS OCCURRING IN THE COURSE OF ACUTE 
ARTICULAR RHEUMATISM (Rhumatisme clrlbral expliqul 
par one mlningite hlmorragique survenant &u corns d’un 
rhumatisme articulaire aigu.) A. Robin and L- Lyon-Cabn, Bull 
et mim. Soc. mid. Hip. de Paris , 1914, xxxvii., p. 717. 

An alcoholic man, aged 37, had two attacks of acute articular 
rheumatism. The first was complicated by delirium and meningeal 



ABSTRACTS 


263 


phenomena, and the second by meningeal phenomena without 
delirium. 

The term “ cerebral rheumatism ” was justified by the following 
considerations:—(1) The appearance of violent delirium during 
the acute stage of acute articular rheumatism. (2) The pain and 
swelling in the joints disappeared when the delirium occurred, and 
returned when the mental state became normal. (3) The form of 
the delirium—mental confusion with hallucinations—was typical 
of toxi-infective delirium. 

Although many cases of so-called cerebral rheumatism are really 
examples of alcoholic delirium, the psychosis in the present case 
was differentiated by the absence of tremor and the intensity of 
auditory hallucinations. Alcoholism was, however, probably a 
predisposing cause of the cerebral phenomena. Salicylate delirium 
could be excluded because it is more sudden in onset and is 
accompanied by false bradycardia and extrasystoles. Uraemic 
delirium could also be excluded because there was no myosis, and 
only slight and transient albuminuria. Before attributing the 
meningitis to rheumatism, meningococcal, gonococcal, and syphilitic 
infection had also to be excluded by appropriate examination of 
the cerebro-spinal fluid. Recovery took place. 

J. D. Rolleston. 

TWO OASES OF SUPPURATIVE OTOGENIC MENINGITIS WITH 
(330) RECOVERY. (Deux cas de mtaingite otog&ne suppurde suivis 
de garrison.) G. Coulet, Rev. de Laryngol ., 1914, i., p. 621. 

These cases were reported to the Otological Section of the 
Seventeenth International Medical Congress. 

Case 1. A man, aged 20, who had suffered from left Suppurative 
otitis media from childhood was admitted to hospital with well- 
marked meningitis. Examination showed osteitis of the walls of 
the antrum and tympanum, with erosion of the labyrinth and 
infection of the perilymph. A radical mastoid operation was 
performed, followed by lumbar puncture, which showed a turbid 
fluid with abundant polymorphs, and a few cocci, isolated or in 
pairs. After a second lumbar puncture, by which a similar fluid 
was obtained, the temperature came down to normal, and the 
patient was discharged after a fortnight’s stay in hospital. When 
seen three months later he was in good health. 

Case 2.—A man, aged 36, developed acute right otitis media 
which was treated by irrigation, and soon subsided, but a fortnight 
later symptoms of meningitis ensued. Twenty c.c. of turbid 
cerebro-spinal fluid were removed under hypertension, and were 
replaced by 5 c.c. of electrargol. Microscopical examination showed 
abundant polymorphs but no meningococci. After a second 


21 



264 


ABSTRACTS 


puncture the symptoms subsided, and the temperature became 
normal five days after admission to hospital. A month later there 
was a return of the symptoms of meningitis. Fifteen c.c. of turbid 
spinal fluid were removed, and replaced by 5 c.c. of electrargol. 
The following day the temperature became normal, and the patient 
was discharged in good health six days after admission. 

J. D. Rolleston. 

HEREDO SYPHILITIC SPASTIC PARAPLEGIA. (Paraplegic spas- 

(331) modique h6r6do-syphilitique chez lea grands enfants.) A. B. 
Mabfan, Arch, de mdd. da enf., 1913, xvi., p. 561. 

In addition to the congenital variety of spastic paraplegia (Little’s 
disease), and the two postnatal forms, viz., the spastic paraplegia 
of Pott’s disease and Strumpell’s familial spastic paraplegia, there 
is a form which was first described by Marfan in 1909 under the 
title of heredo-syphilitic spastic paraplegia. It is characterised 
by spastic rigidity of the lower limbs which interferes with 
walking, but which almost disappears when at rest, and is accom¬ 
panied by only a slight diminution of muscular power. Sensory 
disturbance, sphincter troubles, muscular atrophy, and other trophic 
disturbances are completely absent. On the other hand, ocular 
troubles are always present. Argyll Robertson pupil or complete 
paralysis of the pupils, and disturbance of visual acuity are 
constant. Often there is some pallor of the optic discs, and 
interstitial keratitis is frequent. There may be some mental 
backwardness. The disease is progressive and shows no evidence 
to spontaneous recovery. Mercury and potassium iodide are 
ineffectual, but some improvement has followed intravenous 
injection of salvarsan. Marfan has seen six cases of the con¬ 
dition, but none has come to autopsy. J. D. Rolleston. 

SYRINGOMYELIA FOLLOWING A PERIPHERAL INFECTION. 

(332) (Syringomydlie consecutive k une infection pdriphdrique.) G. 

Guillain and J. Dubois, Bull, ct mim. Soc. mid. H6p. de Parity 
1914, xxxvii., p. 634. 

A plumber, aged 50, got a poisoned wound of the right middle 
finger necessitating amputation in 1893. In the following years 
multiple whitlows developed on both hands, and were followed by 
sensory disturbance. In 1898 his gait became affected, and in 
1909 he had arthropathy of the left shoulder. 

At the present time he presents trophic disturbances and 
enlargement of both hands, spastic paraplegia, with Babinski’s sign 
and ankle clonus, and the characteristic sensory changes of 
syringomyelia. 



ABSTRACTS 


265 


Lumbar puncture showed no excess of albumin nor cellular 
reaction in the spinal fluid. The tuberculin intra-dermo-reaction 
and luetin reactions are negative, and both the blood and the 
spinal fluid gave a negative Wassermann’s reaction. 

J. D. Rolleston. 

TWO OASES OF REMOVAL OF EXTRA DURAL TUMOUR OF 

(333) THE SPINAL CORD. Philip Coombs Knapp, Joum. Nerv. and 
Ment. Dig., 1914, xli., No. 1 , Jan. 

The report of two interesting cases in whom improvement took 
place after operation. The author believes that, owing to the 
hopeless outlook in most of these cases, operation is always justified, 
even where the growth cannot be wholly removed. 

D. K. Henderson. 

TRAUMATIC HJEMATOMTELIA WITHOUT VERTEBRAL 

(334) LESION. Claude and Loybz, L'Encephale, 1914, ix., May 10, p. 403. 

The number of cases of this sort, examined anatomically, appears 
to be but small. The patient, a young man of 26, fell some fifteen 
feet, and was diagnosed in hospital as a case of fracture of the 
spine about the level of the tenth dorsal segment. He presented 
the characteristic symptoms of a transverse lesion of the cord. 
Death supervened on the fifth day. No lesion whatever was 
found in the vertebral column, or in the spinal canal: the dura 
was intact and normal. Nevertheless a vast hsematomyelia was 
found to have taken place, extending from the fourth dorsal to 
the third lumbar segment. The authors lay importance on the 
occurrence of paralytic vasodilation as an explanation of late 
apoplexy: in their case something of this sort must have occurred. 

S. A. K. Wilson. 

A CASE OF LANDRY’S PARALYSIS. R. O. Douglas, Australian 

(335) Med. Joum., 1914, iii., April 25, p. 1530. 

A blacksmith, aged 30, complaining of headache and tendency to 
vomiting, followed by weakness of both legs, was admitted to 
hospital with a diagnosis of typhoid fever. The bladder was 
distended and required catheterisation. No reflexes could be 
obtained in either leg or foot. There were no movements of the 
toes or ankle, although the thighs could be moved well. Sensation 
was normal. An absolute flaccid paralysis of both legs developed, 
followed by weakness of both arms, and sudden cessation of 
diaphragmatic breathing. Artificial respiration was performed 
until death. Later, speech became inaudible, and diplopia developed, 
and death occurred from sudden heart failure. 

A. Ninian Bruce. 



266 


ABSTRACTS 


GLIOMA OF THE CORPUS CALLOSUM AND LEFT PARIETAL 

(336) LOBE: BILATERAL APRAXIA. Laignkl - Lav astute and 
L&vy-Valensi, L’Enctphale, 1914, ix., May 10, p. 411. 

Clinically. —A mental condition analogous to the dementia of 
dementia paralytica, without any of the somatic signs of that 
disease: spasmodic paresis of the limbs, bilateral extensor re¬ 
sponse: mixed bilateral apraxia (motor and ideational): death 
thirty-six hours after a lumbar puncture. 

Pathologically. —Glioma of the posterior two-thirds of the 
corpus callosum, invading the centrum ovale of the left parietal 
lobe: multiple small haemorrhages in both hemispheres. 

The significance of the case is fully discussed. The authors 
incline to the view that the parietal lesion was responsible for 
the bilateral apraxia, and that the involvement of the corpus 
callosum was a complication of little importance from the point of 
view of the determination of apraxia. They consider that where 
left-sided apraxia is produced by a lesion of the corpus callosum, 
it is always the anterior part of that commissure which is 
involved. S. A. K. Wilson. 

A CASE OF SUBCORTICAL OR PURE MOTOR APHASIA 

(337) (DEJERINE) OR ANARTHRIA (MARIE). F. X. Dercum 
Journ. Nerv. and Ment. Dis., 1914, xli., No. 3, March. 

A young man, 32 years, one day previous to his admission to the 
hospital, suddenly became unable to talk, and had a complete 
right-sided hemiplegia. There was no sensory involvement. The 
patient was unable to make the slightest articulate sound. He 
could grunt and make various discordant noises, but could not 
even say the words “ yes ” or “ no.” 

The patient’s understanding of spoken speech and com¬ 
prehension of what was said to him was perfect; he could read 
written or printed matter, and could carry out instructions 
perfectly. There was no agraphia. He could write from dictation. 
This condition persisted for three or four weeks, when he began 
to utter his own name and occasionally other words. It was 
thought that the patient had had a subcortical syphilitic lesion, 
involving the knee of the internal capsule, and probably the 
adjacent portion of the lenticular nucleus. D. K. Henderson. 

HEMIPLEGIA AND PROSTATECTOMY. (HemipMgie et prosta 

(338) tectomie.) Loumkau, Journ. de Mid. de Bordeaux, 1914, lxxxv., 
p. 252. 

A record of a successful operation in a man, aged 77, to show that 
hemiplegia, far from being a contra-indication to prostatectomy, 
may be an urgent reason for its performance. J. D. Rolleston. 



ABSTRACTS 


267 


DIABETIC FACIAL PARALYSES. (La paralysis facials diabdtique.) 

(339) Sarah Gaitz, Theses de Paris, 1913-14, No. 153. 

The thesis contains the histories of 28 cases, including the 
following original ones:— 

1. A woman, aged 62, diabetic for the last twenty years, 
developed right facial paralysis. About twelve months previously 
paralysis of the left upper limb had occurred. Under appropriate 
treatment the facial paralysis almost entirely disappeared in six 
weeks, but the neuritis of the upper limb persisted. 

2. A woman, aged 32, diabetic for the last two years, developed 
right facial paralysis. Recovery took place after three weeks’ 
treatment. 

3. A man, aged 40, diabetic for ten years, developed right 
facial paralysis which lasted for three years. After two months’ 
treatment recovery took place. 

The writer’s conclusions are as follows :— 

i. Diabetic facial paralysis is an undoubted form of peripheral 
facial paralysis. 

ii. Its onset is sudden. 

iii. It is often the first sign of diabetes. 

iv. An anti-diabetic regime and electrical treatment are 
sufficient in almost every case to effect a cure. 

J. D. Rolleston. 

A CASE OF FACIAL HEMIATROPHY. M. Neustabdteb, Med. 

(340) Record , 1914, lxxxv., p. 700. 

A case of right facial hemiatrophy in a woman aged 41, in whom 
the disease started at the age of 12 years after an injury to the 
forehead with a poker. The atrophy progressed till she was 21, 
when it became stationary. At 32 she was seized with epilepsy 
of the grand mod type, and had suffered at irregular intervals 
from it since. The atrophy involved the skin, muscles, and bone. 
There were no sensory changes beyond pain on deep pressure 
along the course of V 2 and V s . Wassermann negative. 

J. D. Rolleston. 

THE PROBLEM OF SLEEP. Salmon, L’Encephale, 1914, ix., Feb., 

(341) March, and April, pp. 168, 250, and 364. 

This is a long contribution to the study of the physiology of sleep, 
based on papers and other communications already made by the 
author. 

Briefly, his view is that sleep is neither toxic nor psychical 
in origin, but that it is a function of secretion. It is intimately 
related to the functional activity of certain special glands of 



268 


ABSTRACTS 


internal secretion. The particular secretory function associated 
with sleep has its seat in the nerve-cells of the cortex, and consists 
in chromatogenesis, or the elaboration and accumulation of 
chromatophil elements in the cytoplasm. The chromatic substance 
accumulates in nerve-cells during repose, and disappears in activity, 
in the same way as glycogen accumulates in muscle-cells. The 
author believes that the nucleus of nerve-cells acts on the 
chromatin substance, and that the latter may be regarded as the 
actual product of the internal secretion of the cells. Can this 
active process of internal secretion which goes on during sleep 
explain the mechanism of sleep ? The author advances arguments 
to suggest that the elaboration of the chromatic elements by a 
synthetic process is accompanied by a process of dehydration of 
the nerve-cells; with this dehydration the neurofibrils rapidly lose 
their excitability and their conductivity. Similarly, with the 
diminution of osmotic pressure, the metabolism of the cell is 
reduced. The tigroid bodies, it is known, are really colloidal 
granulations in the living cells, and the greater their molecular 
concentration, the less capable are they of transmitting nerve 
vibrations. The chromatogenic function of the cell ceases when 
the latter can no longer absorb any more material for its nutrition 
from the pericellular lymph. Then the dehydration comes to an 
end, and the chromatophil granulations undergo a process of 
fluidification. With that the excitability of the cell returns. 
Spontaneous awakening depends on the exhaustion of the secretory 
function presiding over sleep. We awake because we are tired of 
sleeping, as we sleep because we are tired of being awake. 

The author’s views are elaborated with skill and force; and 
the papers are well worth reading in the original 

S. A. K. Wilson. 

RESTITUTION PHENOMENA IN CEREBRAL PALSIES IN 
(342) RELATION TO PHYLOGENESIS AND THEIR THERA¬ 
PEUTIC INFLUENCE. (Die Restitutionsvorg&nge bei den 
cerebralen L&hmungen in ihrer Beziehnng zur Phylogenese und 
ihre therapentische Beeinflnssnng.) Rothmann, Deut. Zeitschr. 
f. Nervenheilk ., 1914,1., Hft. 5-6, p. 406. 

In man a flaccid palsy follows section of the path between the 
senso-motorium and lower motor centres. This flaccid palsy does 
not persist, and eventually a degree of return of power takes place 
with the development of spastic contractures. The conditions are 
very different in this connection between man and the lower 
animals. It has been supposed that the return of movement, such 
as it is, and the development of contracture, are associated with the 
assumption of function on the part of “lower motor centres.” 



ABSTRACTS 


269 


Phylogenetically old centres assume a compensatory function when 
phylogenetically recent centres are thrown out of gear. The 
question arises whether and to what extent the intact hemisphere 
can function for the injured hemisphere. It is known that in apes 
a paresis produced by removal of one cerebral hemisphere is less 
than that produced in the opposite limbs when their cerebral 
centres are subsequently removed. Rothmann has shown that the 
removal of the centres on the same side does not prejudice the 
paretic movements that remain when the corresponding ( i.e ., 
contralateral) centres have previously been removed. It is 
supposed that commissural connections between “ midbrain motor 
centres,” which are normally very incomplete, after removal of 
cortical motor centres on one side, and the gradual increase of 
function of “subcortical motor centres” of the corresponding 
hemisphere, enable stimuli from the unimpaired cortical motor 
centres passing to the “midbrain centres” of the same side, to 
reach also the corresponding centres of the opposite side. In this 
way “secondary” movements may take place in the originally 
injured extremities. As phylogenetically old “subcortical motor 
centres” Rothmann specifies particularly the nucleus ruber and 
the tractus rubrospinalis. The size and importance of these are 
in inverse proportion to the development of the cortico spinal 
path. Hence there is greater difficulty in their assuming their 
old function the higher the animal is in the series. Rothmann 
also mentions extra pyramidal paths in the anterior columns of 
the cord as capable of assuming motor functions, without, however, 
specifying what these paths are. 

Rothmann, however, is careful to point out that it is insufficient 
to argue from the (possible) condition in apes to that in man, 
inasmuch as the assumption of the erect attitude in man has 
changed the functions of the motor cortex and “ subcortical motor 
centres.” Weeks or months may elapse, in the case of man, before 
the excitability of the “ ganglion cells of the midbrain centres ” is 
raised sufficiently to send impulses to the spinal cord centres 
capable of raising muscle tone and effecting “voluntary” move¬ 
ments. In the leg the flexors are apt to be most seriously 
affected after a pyramidal lesion, whereas in the arm it is the 
flexors that first show return of movement. There is an extension- 
contracture of the leg and a flexion-contracture of the arm. This 
is explained, according to Rothmann, by the assumption of the 
erect attitude. He declares, further, that the first returning motor 
impulses in paralysed limbs, after a pyramidal lesion, are solely of 
“ subcortical ” origin, and that these are of a certain type (“ phylo- 
geneticaUy old movement forms”). Later, the influence of the 
intact homolateral hemisphere comes into consideration. 

It is not the reviewer's duty to criticise the paper he abstracts; 



270 


ABSTRACTS 


nevertheless, attention may be drawn to the fact that the interesting 
hypotheses of this paper are not supported by any definition of 
the “subcortical motor centres” constantly assumed, with the 
exception, already mentioned, of the red nucleus. Rothmann 
may be referring to certain “ Haubenbahren,” to which a motor 
function was assigued by Probsfc, whose name Rothmann does not 
mention. But the function of some of these paths is known not 
to be that here presumably assigned to them. S. A. K. Wilson. 

A CONTRIBUTION TO THE STUDY OF SO CALLED PSEUDO- 
(343) SCLEROSIS, WITH CHANGES IN THE CORNEA AND IN 
THE LIVER. (Em Beitrag zur kenntnis der sog. Pseudosklerose 
mit gleichzeitiger Ver&nderung der Hornhaut und der Leber.) 
Stbumpbll and Handmann, Deut . Zeitschr . f . Nervenheilk ., 1914, 
L, Hft. 6-6, p. 465. 

The patient was a man of 37, who for about six years had suffered 
from tremor of the head and arms and fingers, and became 
incapable of work. The onset of the disease was gradual. With 
active movements the tremors increased. There was a certain 
stiffness in facial expression. There was no tremor of the tongue. 
Articulation was slow and somewhat syllabic. The tremors of 
the arms were rhythmical and quick, and quite symmetrical. The 
tonus of the musculature was not obviously altered. Cutaneous 
and deep reflexes were normal. On the outer section of the 
cornea was a brown-grey pigmented ring, about 2-3 mm. broad. 
On close examination it was found to consist of minute dark 
pigment particles. The liver dulness was unusually small, while 
the spleen seemed enlarged. 

There were no obvious psychical symptoms, and no apoplecti¬ 
form attacks, both of which are supposed to be common signs in 
so-called pseudosclerosis. In spite of their absence, the authors 
conclude that there can be no doubt that their case is one of 
pseudosclerosis. 

The argument is (1) that the tremor disappears entirely with 
complete resting of the muscles; (2) it is most marked in the 
muscles which are most in active contraction; (3) there is an 
expressionless facies; (4) the peculiar pigmented ring of the 
cornea is found only in pseudosclerosis; (5) there is evidence of 
disease of the liver. Only (4) and (5) are of diagnostic significance, 
however. Perhaps (4) may prove to be a point of distinction 
between pseudosclerosis and progressive lenticular degeneration. 
It must be clearly understood that various cases of pseudosclerosis 
have been recorded where no liver cirrhosis was noted. In the 
group, however, are several recent valuable cases where liver 
changes were present. To this sub-group the present case may 
belong. S. A. K. Wilson. 



ABSTRACTS 


271 


ASEPTIC LEUCOCYTOSIS OF THE CEBEBRO SPINAL FLUID 

(344) WITH SUBACUTE MENINGEAL SYNDROME IN THE 
COURSE OF CEREBRAL HAEMORRHAGE. XANTHO¬ 
CHROMIA AND POLYNUCLEOSIS. (Leucocytose aseptique 
du liquide cdphalo-rachidien avec syndrome m4ning4 snbaign 
an cours dea h&norragies c4r4brales. Xantocromie et poly- 
nndeose.) J. Amandrut (de Laval) and A Gendron (de Nantes), 
Bull, et mem. Soc. med. H6p. de Paris, 1914, xxxvii., p. 766. 

A record of two cases of cerebral luemorrhage, accompanied from 
the first with meningeal phenomena such as nuchal rigidity, 
Kernig, and Brudzinski. In both cases lumbar puncture showed 
an amber-coloured fluid, the coloration of which gradually 
diminished until it completely disappeared, with considerable 
leucocytic reaction. 

In the first case, that of a man aged 38, 5 days after the 
onset of cerebral luemorrhage, the spinal fluid showed 688 
leucocytes in each cubic millimetre, 18 days later 108, and at the 
end of 35 days 41. The leucocytic formula evolved as in ordinary 
meningitis, there being exclusive polynucleosis at the onset, then 
polynucleosis and lymphocytosis, and finally pure lymphocytosis. 
Recovery took place. 

In the second case, that of a man aged 30, examination of the 
spinal fluid at a date nearer the onset of the hemorrhage showed 
a pink fluid not coagulating spontaneously, and yielding a red 
clot on centrifugalisation. Subsequently the fluid became amber- 
coloured, and showed a less marked leucocytosis than in the first 
case (fifty leucocytes in each cubic millimetre). 

Post mortem an encysted hemorrhage was found which had 
destroyed the internal capsule and part of the grey nuclei. There 
was no blood on the convexity nor trace of meningitis. 
Wassormann’s reaction in the blood and cerebro-spinal fluid was 
negative. J. D. Rolleston. 

THE PROGNOSTIC AND DIAGNOSTIC VALUE OF THE SIGN OF 

(345) ISOLATED HYPERALBUMINOSIS IN THE CEREBRO¬ 
SPINAL FLUID. (De la valeur pronostique et diagnostique da 
signe de lbyperalbuminose isolde du liquide cdph&lo-rachidien.) 

A. Vernes, Compt. rend. Soc. de Biol., 1914, lxxvi., p. 280. 

A RETROSPECTIVE SIGN OF SYPHILIS — PURE HYPERAL 
(316) BUMINOSIS OF THE CEREBRO SPINAL FLUID WITHOUT 
LEUCOCYTOSIS AND WITHOUT WASSERMANN. (Un signe 
retrospectif de la syphilis; hyperalbuminose pure du liquide 
cdphalo-rachidien, sans leucocytose et sans Wassermann.) M. 
Bloch and A Vernes, ibid., p. 281 . 

Vernes has found isolated hyperalbuminosis not only in patients 
without any clinical sign of nervous syphilis, but also in former 



272 


ABSTRACTS 


syphilitic patients who no longer showed any signs of visceral or 
cutaneous disease, and in whom Wassermann’s reaction had been 
negative for many months. 

In forty cases of syphilis Bloch and Vemes found that the 
amount of albumen in the cerebro-spinal fluid ranged from 0 30 g. 
to more than 1 g. per 1,000, as compared with the normal 018 to 
0*20 g. per 1,000, while the number of leucocytes in the fluid was 
normal, and Wassermann’s reaction was negative. It is difficult 
to say whether this sign indicates an extinct lesion of the 
meninges, or if it is due to some other cause. It may be met 
with from one to thirty-five years after the onset of syphilis. 

J. D. Rolleston. 


XANTHOCHROMIA OF THE CEREBRO SPINAL FLUID IN 
(347) A8TST0LIC PATIENTS. (La xanthocromie du liquids cdphalo- 
rachidien chez les asystoliques.) A. Babes, Compt. rend. Soc. de 
Biol., 1914, lxxvi., p. 313. 

In examining the cerebro-spinal fluid of patients with failure of 
compensation, Babes was struck by its yellow colour. In eight 
cases it was intense, corresponding to 5 c.c. of 1 in 100,000 solution 
of bichromate of potash, and in two it was hardly perceptible. 
None of the cases showed any icterus, and none of the fluids gave 
the reaction for bile pigment. Babes attributes the xanthochromia 
to a transudation of the pigment of the blood serum into the 
cerebro-spinal fluid. J. D. Rolleston. 


SOME OBSERVATIONS ON THE OCCURRENCE OF THE WA8SER- 
(348) MANN REACTION IN THE SERUM OF THE CHILDREN 
OF THE POORER CLASSES. W. M. Elliott, QIclbqow Med. 
Joum., 1914, Ixxxi., May, p. 339. 

The method of carrying out the test was that recommended by 
Browning and Mackenzie, and it was found that about 8 per cent, 
of all classes of children from the poorer classes of Glasgow give 
a positive Wassermann reaction, and thus, if this reaction is to 
be taken as pathognomonic of syphilis, a considerable portion of 
the children of the poorer classes are infected with this disease. 
Congenital syphilis may exist without any apparent effect on the 
general health of the child. Poorly nourished children are not in 
that condition to any extent because of syphilitic infection, and 
treatment to improve their health need not run on these lines. 

A. Ninian Bruce. 



ABSTRACTS 


273 


BIOLOGICAL REACTIONS IN SYPHILITIC DISEASES OF THE 
(349) CENTRAL NERVOUS SYSTEM. (Biologische Reaktionen bei 
syphilogenen Erkrankungen des Zentralnervensystems.) Nkue, 
Devi. Zeittchr.f. Nervenheilk ., 1914,1., Hft. 5-6, p. 311. 

1. The author uses Hauptmann’s method for the Wassermann 
reaction, and finds it gives positive results in 100 per cent, of cases 
of general paralysis; in tabes and cerebro-spinal syphilis it gives 
positive results in “ a preponderating number ” of cases. 

2. In organic nervous diseases not of syphilitic origin the test 
is negative for the cerebro-spinal fluid even in individuals who have 
formerly had syphilis, and in whom a positive reaction may be 
present in the blood. 

3. Hauptmann’s method is of the greatest value in determining 
the etiology of an organic nervous disease. 

4. Only the finding in the cerebro-spinal fluid is of significance 
when it is positive, and the serum Wassermann reaction negative. 

5. The Weil-Kafka hfemolysin reaction of the cerebro-spinal 
fluid was positive in 90 per cent. (32 cases total) of general 
paralysis, in 22 per cent, of cerebral syphilis, and 20 per cent, of 
tabes cases. It was positive in 8 per cent, of 25 non-syphilitic 
nervous cases. In combination with the “ four reactions ” it may 
help to diagnose between general paralysis and cerebral syphilis. 

6. Abderhalden’s reaction is positive only with the cortex in 
cerebral syphilis, as a rule, whereas it is positive with the albumin 
of various other organs as well (notably the liver, kidneys, and 
pancreas) in general paralysis. 

7. The luetin cutaneous reaction is of value in distinguishing 
between cerebral syphilis and general paralysis. 

8. The goldsol reaction of Lange (colloidal gold chloride) in the 

cerebro-spinal fluid is of value in distinguishing syphilitic from 
non-syphilitic nervous diseases. S. A* K. Wilson. 


LATE SYPHILITIC FACIAL PARALYSIS ASSOCIATED WITH 
(350) CHRONIC PULMONARY SYPHILIS. (Paralisi sifllitica tardiva 
del 7° paio associata a sifllide pulmon&re cronica.) E. Verde, 
Giom. internal, di Sci. med., 1914, xxxvi., p. 199. 

The patient was a man, aged 31, who had contracted syphilis 
many years previously, and had since suffered from cough and 
night sweats. A few days before being seen by Verde he suddenly 
developed right facial paralysis. Signs of broncho-pneumonia 
were found at the left apex. He was treated with daily injections 
of biniodide of mercury, and after thirty-eight injections complete 
recovery took place. J. D. Rolleston. 



274 


ABSTRACTS 


PRESENT STATUS OF NEOSALVARSAN IN THE TREATMENT 

(351) OF PARASYPHILIS OF THE NERVOUS SYSTEM E. D. 

Fibber, Joum. Nrrv. and Ment . Dis., 1914, xli., No. 1, Jan. 

A short general statement, without value either from the laboratory 
or clinical point of view. D. K. Henderson. 

ON REFLEX EPILEPSY OF THERAPEUTIC ORIGIN. (De ftpilepue 

(352) rlflexe thtoapeutique.) H. Dufotjr, Pari » mid ., 1913-14, iv., p. 511. 

Dufour records several cases of typical epileptic convulsions 
occurring after various trivial operations, such as thoracentesis, 
phlebotomy, vaccination, lumbar puncture, injection of 606, or 
even rectal or vaginal examinations. A personal or family history 
of epilepsy can often be obtained in such cases, but undue appre¬ 
hension on the part of the patient is an important factor. 

J. D. Rolleston. 

ALCOHOL AND DELIRIUM TREMENS. Dbmole, L'Encephale, 1914, 

(353) ix., Jan. 10, p. 5. 

The author has employed the qualitative method of Lieben and 
the quantitative method of Nicloux for the determination of the 
presence of alcohol in the cerebro-epinal fluid, urine, blood, saliva, 
and respired air of twenty-three cases of alcoholism. His conclu¬ 
sions are that at the commencement of an attack of delirium tremens 
alcohol is found in the above-mentioned places only if the patient 
has taken alcohol during the preceding twenty-four hours. It is 
eliminated in twenty-four hours as in a normal individual, so that 
the attack continues though there is no alcohol in the system. In 
many cases of delirium tremens no alcohol is discoverable in the 
system. Treatment by alcoholic drinks in gradually diminishing 
quantity is quite unjustifiable. S. A. K. Wilson. 

EXPERIMENTAL STUDY OF INTRANEURAL INJECTIONS OF 

(354) ALCOHOL. Alfred Gordon, Joum. Nerv. and Ment. Pi*., 1914, 
xli. No. 2, Feb. 

In this paper the histological and corresponding functional results 
obtained from injections of alcohol into motor, sensory, and mixed 
nerves has been studied experimentally. 

The same strength of alcohol (80 per cent.) was used, the same 
number of drops (five), the same degree of penetration of the 
needle into the substance of the nerve, the same dissection and 
exposure of the nerve trunks, the same after care of the wounds, 
and finally the same species of animals, viz., dogs. 

The experiments were divided into two series: one series of 
three dogs were kept alive nine days, the other series of three 



ABSTRACTS 


275 


dogs lived twenty-nine days. The facial, infra-orbital, and sciatic 
nerves wore experimented upon. The first was traced in its intra¬ 
medullary course. The other two were removed with their re¬ 
spective ganglia (Gasserian and spinal). 

In the first series the infra-orbital nerve showed peri- and 
endoneuritis, with accumulation of small cells around and in the 
vicinity of the smallest nerve bundles. The latter were intact,, 
with the exception of an occasional nervus nervorum which was 
degenerated. The Gasserian ganglion showed chromatolysis in 
some of the cells; the majority of the cells were intact. The 
facial nerve at the periphery and in the medulla was found 
intact. 

The sciati: nerve presented about the same changes as the 
infra-orbital, viz., perineuritis, with occasional degeneration of a 
nervus nervorum. 

In the second series the infraorbital nerve presented peri¬ 
neuritis with a very marked proliferation of round cells around 
each individual nerve bundle; they were also seen in the 
adventitia of the arteries. The Gasserian ganglion presented 
marked chromatolysis and proliferation of cells of the capsule. 
The peripheral facial nerve presented slight neuritis and evidences 
of regenerating connective tissue fibres. The course of the nerve 
in the medulla appeared to be normal. The sciatic nerve showed 
very marked perineuritis, with extensive degenerative changes in 
the nerve bundles. From these findings it is evident that the 
changes are almost identical in sensory and mixed nerves, and that 
these changes are in striking contrast to those found in the motor 
(facial) nerve. 

In the therapeutic management of affections of nerves, the 
above differences in the susceptibility of motor and sensory nerves 
to the effect of alcohol must be borne in mind. 

D. K. Henderson. 

ANTERIOR CRURAL NEURITIS. C. M. Byrnes, Joum. Nero, and 
(355) Ment. Die., 1914, xlL No. 1, Jan. 

The first portion of this article has already been abstracted in this 
Review, The author, from a review of the literature and from 
personal observations, has collected 136 cases in which the femoral 
nerve of one or both sides has been the seat of an inflammatory 
process originating from some internal or medical disorder. 

The disease is chiefly met with in middle-aged and elderly 
people, but one case has been described in a child 7 years old. 
The onset of the disease may be acute or subacute. By far the 
commonest and earliest symptom is pain in the distribution of 
the crural nerve, or one of its neighbouring branches. In sub¬ 
acute cases, in the course of a week or month, the pain becomes 



276 


ABSTRACTS 


more persistent, of wider distribution, greater intensity, and of a 
continuous paroxysmal nature, with nocturnal exacerbations. 

In regard to locating the pain, the striking feature is the 
rather indefinite and vague effort to outline the exact area. 
Sensory changes of a destructive nature are rather uncommon, 
and the author has found only one case in which there was 
.definite loss of sensation. 

Vasomotor and trophic changes occur, and except in the 
mildest cases there is always some motor disturbance. 

The knee jerks are nearly always altered; in the mild cases 
there is merely a diminution of the tendon reflex upon the 
affected side, but in severe cases the knee jerk is invariably lost. 

One definite personal case of idiopathic femoral neuritis is 
"reported. D. K. Henderson. 

THE RELATIONS BETWEEN EXOPHTHALMIC GOITRE AND 

(356) THE PUERPERAL STATE. (Contribution k l’6tude des rapports 
rdciproques dn goitre exophtalmique et de l’dtat puerperal.) 

L. Boisboux, Theses de Paris , 1913-14, No. 127. 

Both experimental work and pathology prove that a close relation 
exists between the thyroid and the genital organs. The influence 
of pregnancy on exophthalmic goitre may be favourable or the 
reverse. Thus a goitre may develop during pregnancy, or a simple 
goitre may be converted into Graves’ disease, or pre-existing goitre 
may get worse. On the other hand, Graves’ disease may improve 
during pregnancy. 

Exophthalmic goitre may act on pregnancy in one of two ways. 
Sometimes it causes abortion, premature labour, or haemorrhage 
during and after delivery. More frequently it has no influence 
at all on pregnancy or the puerperium. 

In old standing goitre the effect on the puerperium is uncertain. 
In such cases marriage or fresh pregnancies should be forbidden. 
When pregnancy is normal, the ordinary medical treatment for 
goitre should be carried out. Surgical and obstetrical treatment 
should be reserved for the worst cases. The thesis contains the 
histories of twenty cases, including two original ones, in one of 
which the symptoms of Graves’ disease improved, and in the other 
became worse during pregnancy. J. D. Rolleston. 

EXOPHTHALMIC GOITRE AND GLTCOSURIA. FAILURE OF 

(357) PITUITARY OPOTHERAPY. (Goitre exophtalmique et 
glycosurie. Essais nlgatifs d’opothdrapie hypophysaire.) Duhot 
and Hallbz, Echo mid. du Nord , 1914, xviii., p. 128. 

The patient was a man, aged 38, who had suffered from 
exophthalmos for twelve years, and goitre for the last three 



ABSTRACTS 


277 


months. The urine did not exceed a total of from 1,500 to 
2,000 g. in the twenty-four hours, but showed a slight and inter¬ 
mittent glycosuria (5 to 38 g. per litre). Repeated subcutaneous 
injections of 1 c.c. of the posterior lobe of the hypophysis 
caused slight improvement of the subjective symptoms, but did 
not influence the glycosuria. A subcutaneous injection of 1 c.c. 
of adrenalin was followed by malaise, vertigo, arterial hypertension, 
and palpitation. J. D. Rolleston. 

DEFACED TYPE OF ADDISON’S DISEASE. A. O. Holmes, Joum. 

(358) Amer. Med. Assoc., 1914, lxii., p. 532. 

The patient was a man, aged 72. The diagnosis during life lay 
between pernicious anaemia and cancer of the stomach. The blood 
pressure was not remarkably low (110), probably because the other 
chromaffin cells of the chromaffin system supplied part of the 
necessary pressor substance. Post mortem the only tuberculous 
lesions besides those found in the suprarenals were slight puckering 
and calcareous infiltration of the left apex. J. D. Rolleston. 

TETANY IN THE ADULT AND ITS PARATHYROID ORIGIN. 

(359) (Contribution k l’ltude de la tdtanie chez l’adulte et de son origins 
parathyroldienne.) Mile. R. Lifschitz, Theses de Paris , 1913-14, 
No. 221. 

Tetany in the adult may be due to a variety of causes which 
include infections and intoxications, exogenous and endogenous, 
such as the puerperium (v. Review , 1911, ix., p. 515), gastric dilata¬ 
tion, and uraemia; it may follow partial removal of the para¬ 
thyroids; or, finally, it may occur without any obvious cause 
(essential tetany). 

In every case it seems to depend upon a disturbance of function 
in the parathyroids. This hypothesis is undoubtedly true in the 
case of surgical tetany, and appears probable in essential tetany, 
and in tetany due to toxic causes. 

One of the most important functions of the parathyroids is 
to regulate calcium metabolism. When there is a disturbance of 
function in these organs there is an excessive elimination of 
calcium, and the tissues are left in a state of hyperexcitability 
manifested by tetany. 

Parathyroid opotherapy is the best treatment for tetany. 
Calcium salts and bleeding have given good results in experimental 
cases. 

The thesis contains the histories of two original cases in 
patients aged 17 and 18, the first associated with late rickets 
and epilepsy, and the second being an example of essential tetany. 

J. D. Rolleston. 



278 


ABSTRACTS 


PSYCHIATRY. 

THE COMPLEMENT DEVIATION IN CASES OF MANIC- 

(360) DEPRESSIVE INSANITY. Lewis C. Bruce, Joum. of Merit. 
Sci., 1914, April, p. 178. 

An account of some further researches by this author to demon¬ 
strate the existence of specific toxins in cases of manic-depressive 
insanity. He employed the serum of one case as the complement 
and urine of another case as the antigen, or vice versa, and found 
that in both instances deviation of the complement was obtainable, 
whereas serum or urine from sane healthy persons did not give 
the reaction. The urine of depressed cases has much greater com¬ 
plement-deviating power than the urine of elevated cases, while, 
on the other hand, the serum from depressed cases has very much 
less power than that from elevated cases. This holds good also 
for urine or serum obtained during the depressed and elevated 
stages of the same case of manic-depressive insanity. The sug¬ 
gestion is made that the presence in sufficient quantity of immune 
body in the serum neutralises the toxin, and that whenever the 
amount of immune body falls, the toxins become able to affect the 
nerve tissues and produce depression. W. D. Wilkins. 

THE CLINICAL SIGNIFICANCE OF KATATONIC SYMPTOMS. 

(361) Henry Devine, Joum. of Ment. Sci., 1914, April, p. 278. 

Two cases are reported of young women who presented character¬ 
istic symptoms of dementia praecox, but who recovered and were 
discharged. They both relapsed and have again recovered, one case 
having had three attacks. Neither showed any evidence of 
permanent dementia. The author maintains that such cases 
should be separated from those that show steady deterioration, 
and are not to be looked upon as recoverable cases of dementia 
prsecox, but rather as cases of hysterical insanity or as manic- 
depressives with symptoms coloured by the youth of the patients. 
He gives as the essential difference between the two types the 
presence of confusion in dementia prsecox and its absence in the 
recoverable cases, and maintains that katatonic symptoms, without 
confusion, may occur in a variety of mental disorders, especially 
in youth. W. D. Wilkins. 

THE PUPIL AND ITS REFLEXES IN INSANITY. A. H. Frith, 

(362) Joum. of Ment. Sci., 1914, Jan., p. 82, and April, p. 224. 

A very full and exhaustive account of the condition of the pupil 
and its reflexes in the various forms of insanity. A large number 
of cases were carefully examined and tabulated, and the results are 
compared with those of previous observers. The author finds that 



REVIEW 


279 


minor changes are commoner than is generally supposed, 
especially in alcoholic and other toxic insanities, but that well- 
marked defects are uncommon except in general paralysis and 
syphilitic insanity. 

The view that diminution and loss of the sensory and psychical 
reflexes and of pupil unrest are of diagnostic importance in 
dementia praecox is not confirmed by these researches, as these 
symptoms were found to be not uncommon in other types of 
insanity. W. D. Wilkins. 

THE IMPORTANCE OF DISTURBANCES OF THE PERSONALITY 
(363) IN MENTAL DISORDERS. R. G. Rows, Joum. of Ment. Sci., 
1914, April, p. 192. 

A full analysis of two cases in which the basis of the disorder was 
a change in the personality of the patients. They first noticed a 
feeling of strangeness, a feeling that their thoughts were not their 
own, or as one of the patients expressed it: “ It was like two 
circles of thought in one person.” Engrafted upon this, and 
arising from an involuntary wish for explanation of the disturbing 
feelings,' came numerous delusions. The author fully discusses, 
but rejects, the theory that the consciousness of personality is 
formed by the sum of all the organ sensations, and that such 
disturbances of personality as are here considered, are due to 
disturbances of these organ sensations. He considers that the 
essential change is a failure of apperception, the patients being 
unable to obtain clear consciousness from an inability to comprehend 
external and internal impressions. Such failure of apperception 
has been found to follow disturbances of the feelings, and in the 
present cases these were of a sexual character. The patients were 
unmarried women of 33 and 36 respectively, and had both 
obviously suffered from their enforced and unwilling celibacy. 
However, the author thinks that such cases as these may be due in 
part to alterations of the organ sensations arising from lesions of 
the sympathetic system, the result of toxic infections in the 
abdomen and elsewhere. W. D. Wilkins. 


■Review. 

MALADIES DES MENINGES. By Professor Hutinel and Drs 
(364) Klippel, Claude, Voisin, and Levy-Valensi, M6decins des 
hdpitaux de Paris. With 49 illustrations. Paris: J. B. Baillifere et 
Fils, 1913. Pp. 383. Pr., paper, 8 fr.; bound, 9 fr. 60. 

The subject of meningitis is one of those which is claimed by 
experts in different branches of medicine, or rather, which appeals 


22 



280 


BOOKS AND PAMPHLETS RECEIVED 


to the exponents of several specialties. Epidemic cerebro-spinal 
meningitis seems to belong to the fever physician more than to 
the neurologist; syphilis in its meningeal manifestations is being 
taken in charge by the bacteriologist; while the neurologist may 
be left with various meningeal conditions, not a few of which he 
must hand over to the surgeon sooner or later. In the study of 
the diseases of the meninges, in short, there is common ground for 
the meeting of surgeon, physician, neurologist, bacteriologist, 
syphilologist, and others still, no doubt. In view of these facts, 
the compilation of a text-book on the diseases of the meninges is 
bound to be effected satisfactorily only by collaboration. We may 
claim justly that it is the province of the neurologist first of all, 
but he finds himself therefore in the position of having to widen 
his marches if he is to remain master of his subject. 

The volume under review deals with the varieties of acute 
meningitis of the brain and cord in a very elaborate fashion, but 
the chapters on the more chronic forms, if less full, are at the 
same time sound and well written. Sections are devoted to the 
anatomy and physiology of the spinal meninges, to the cerebro¬ 
spinal fluid, meningitis circumscripta serosa, so-called meningism, 
haemorrhagic meningitis, and so on. One of the sections is 
concerned with the varieties of meningitis from the etiological 
standpoint, and it is excellently done. The sections on treatment 
commend themselves to the reader’s consideration by the careful 
and practical nature of the suggestions they contain. 

We suspect that the apparent rarity of meningitis circumscripta 
serosa in France—there are no references to French cases in the 
volume—has perhaps somewhat handicapped the authors of the 
chapter concerned: it is no rarity in this country, and is met with 
in forms not apparently familiar to them. There is comparatively 
little reference to syphilitic meningitis in the book, as it is 
dealt with in another volume of the series. In view of the 
importance of the subject, the description of the cerebro-spinal 
fluid deserves rather more space than is devoted to it, especially 
since there is so much allusion to its pathology. 

The book contains a thoroughly up-to-date account of the 
diseases of the meninges, and may be cordially recommended to the 
attention of all interested in the subject. S. A. K. Wilson. 


BOOKS AND PAMPHLETS RECEIVED. 

Aronsohn, Oscar. “ Der psychologische Ursprung des Stotterns.” 
Sammlung Bumke , 1914, xi., H. 1 . Pr. M.l. 

DSjdrine, J. “ S4miologie des Affections du Systfeme Nerveux.” Avec 
560 figures en noir et en couleurs et 3 planches hors- texte en couleurs). 
1914, Masson et Cie. Paris. 

“ The Training School .” 1914, xi., May. 



■Review 

of 

IReuroloQp mb flb8£cbiatii> 


Original Hrticles 

A CASE OF AMAUROTIC FAMILY IDIOCY. 

By W. E. HUME, Newcastle-on-Tyne. 

(With Plates 5-8.) 

Cases of amaurotic family idiocy, or Tay-Sachs disease, are by 
no means frequent in any part of the country, and in the North of 
England are exceptional. And the reason for this local infrequency 
lies in the fact that the disease is confined to the Jewish race, and 
the latter do not collect in such large numbers in the northern 
cities as they do, for instance, in certain parts of London. 

Since Warren Tay first described the disease in 1881 many 
instances of this affection have been recorded, and the clinical 
manifestations of the disease are very definite and unmistakable. 
Permission for post-mortem examinations is not easy to obtain 
from Jews, and therefore the material available for complete 
investigation in this uncommon disease has not been abundant. 
A few cases, however, have been subjected to pathological investiga¬ 
tion, and Mott, amongst others, has described the histological 
changes in the nervous system in great detail. 

The present case was kindly transferred to me by Mr Wardale, 
Senior Ophthalmic Surgeon to the Royal Victoria Infirmary, 
Newcastle-upon-Tyne. 


Clinical History. 

Cissie A., aged 12 months, was brought on 4th April 1910 to 
Mr Wardale, as the mother thought that the child was blind, and 
she was afraid that “Cissie was going like the other two.” 

*3 



282 


W. E. HUME 


Attention will be drawn to the fact that it is probable that two 
other children suffered from, and died of, this complaint. 

The present patient, bom at full term, and breast fed, was the 
youngest of five children, and the mother thought that she had 
been blind since birth. The child had never tried to sit up nor 
crawl about. During the last six months the mother stated that 
there had been frequent fits. 

On admission she was well covered with subcutaneous fat, 
though pale and flabby, and gave no indication of taking notice of 
anything around her. There was some retraction of the head, and 
the child cried when attempts were made to flex the head on the 
chest. There seemed to be some general hyperesthesia, as the child 
usually cried when she was touched or moved. Food was abundantly 
taken, and she slept well. There was no strabismus and the pupils 
reacted slightly to light. On ophthalmoscopic examination, in the 
region of the macula the characteristic appearances were well 
marked. There was a large circular white patch with a bright red 
spot in the centre. The disc itself was pale and atrophied. It 
was evident that the child had some appreciation of light, as the 
eyes occasionally followed a lighted match. 

The arms and legs could be moved, though little voluntary 
effort was made to move them. The legs were flabby, and no knee 
jerks could be obtained. There was an extensor response of the 
big toe when the sole of the foot was scratched. When she was 
lifted out of bed the general atony of the musculature became 
very obvious. 

After being in the hospital for one month, the irritability 
and fretfulness gave place to perpetual apathy, and the child was 
content to lie in any position in which she was placed, and could 
not easily be made to cry. 

She was discharged in this condition on 21st May 1910, and 
was brought by the mother as an out-patient from time to time. 

In July 1910 the child was thinner than she was during her 
stay in the hospital, and it seemed that she was weaker. 

In October 1910 the flaccidity of the muscles had been replaced 
by rigidity. The thumbs of both hands were flexed into the 
palms, and were grasped by the closed fingers. The legs were 
extended at the knee joints, and the foot was likewise extended 
at the ankle. The knee jerks were very active. The mother 
stated that the child did not seem to notice anything, and that 



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Flo. 1. — Tay-Sachs Disease. 
Motor cortex, x TOO. 


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Fr;. 2. — Tay-Sachs Disease 
Phagocytic cells contain¬ 
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3. — Tay-Sachs Disease. Motor cells, 
with numerous fat granules in proto¬ 
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A CASE OF AMAUROTIC FAMILY IDIOCY 283 


at times she had difficulty in swallowing. The ophthalmoscopic 
appearance of the eyes remained the same. 

In January 1911 the mother was persuaded to le^ve the 
child in hospital. From the time of readmission until the child 
died on 3rd March 1911, she remained in a semi-conscious condi¬ 
tion. She was always able to swallow small quantities of liquid, 
and nasal feeding was unnecessary to the end. 

The wasting became very marked, and the rigidity of the 
muscles increased, the hands assuming the main-en-grifft posture. 

The child died on 3rd March 1911, at the age of 23 months. 


Family Table. 


Gt. -Gt. -Grandfather 
(died of eancer) 


Gt. -Grandfather 
(died at 30 years) 


Grand¬ 

father 

Male 


Father 


Gt. -Grandmother 
(living) 

I Grandfather Grandmother 


(died j 

foung) (died young) 

XU _ 

1 Grand- ! 

mother | | 

Female Female 

_iJ' Jv _\ 

Male Male Male 

looiftie tuimij Itiviug; 

V 

(living and healthy) 


Mother 

I_ 


Female Male Female Male Female 

(died at 14 months (living and (died at 11 (living and (present ease died 
10 days) healthy) months) healthy) at 23 months) 


Family History. 

The parents were Russian Jews, and had always enjoyed good 
health. The patient was the youngest child of a family of five. 
Of the other four children two had died, and from the accom¬ 
panying pedigree it will be seen that they were both females. 
The eldest child died at the age of 14 months and 10 days, and the 
third child of the family died at the age of 11 months. The 
mother was quite positive that both of these children suffered 
from the same complaint as the present case. They had both 
been blind from their earliest days, and had become paralysed 
and rigid before death. They never “ noticed things ” like other 
children. During the lifetime of these two children the parents 
were living in Leeds, and their medical attendant was communi¬ 
cated with, but he was unable to recall the cases. The remaining 



284 


W. E. HUME 


children, both males, are strong and healthy. The father’s father 
died at the age of 30; his son thought that he had brought about 
his own early demise by taking vinegar and oil, so that he might 
render himself unfit for military service. The father’s mother 
is living and well. He has one sister and one brother, who are 
both said to be strong and healthy. The father’s grandfather 
died from cancer. The mother’s parents both died when they 
weTe comparatively young, and when she herself was only a 
small child. The cause of their death is unknown. She has had 
two sisters and three brothers, four of whom are living and 
well: one sister died after confinement. No history could be 
obtained which gave rise to a suspicion of any other nervous 
disease being present in the family. 

Pathological Examination. 

Considerable difficulty was experienced in obtaining the 
necessary permission to make a post-mortem examination, but 
after much persuasion the parents gave consent for a limited 
examination. This was done on the day following death. 

The physiognomy did not suggest the characteristics of an idiot 
or an imbecile. The calvarium was thin. On exposing the brain 
there was no flattening or shrinking of the convolutions; in fact, 
the brain appeared to be particularly well formed, and the gyri 
were large and prominent. The brain was heavier and tougher 
than normal. There was no excess of fluid in the basal cisterns. 
The brain, a portion of the cervical cord, and one eye were removed 
and forwarded to Dr Mott, to whom I am indebted for the histo¬ 
logical preparations from which the following figures were made. 

Dr Mott has shown that the morphological changes in the 
brain are very characteristic in this disease. Briefly, it may be 
stated that there is a progressive failure of Nissl substance which 
commences in the peripheral part of the cell, and gradually extends 
inwards towards the nucleus, the latter becoming eccentric. A 
fatty substance, of the nature of a lipoid, accumulates in the cell. 
This accumulation and a process of hydrolysis cause the swelling 
of the cell. These characteristic changes are best seen in the 
cells of the motor cortex, the Purkinje cells of the cerebellum, the 
anterior cornual cells of the spinal cord, and the ganglionic layer 
of the retina. 




Microphotooraph II. (x300 diam.). 

Stained by Cajal’s method. Tlie large cells are distended 
pyramidal cells. 


Plat*: «> 


Mkrophotocraph I. ( x 300 diam.). 

Section of Motor Cortex. In centre of field is a large Betz 
cell surrounded by degenerated pyramidal cells. 









A CASE OF AMAUROTIC FAMILY IDIOCY 285 


The Cerebrum .—Microphotograph I. represents a section from 
the top of the ascending frontal and parietal regions of the motor 
cortex, stained with methylene blue. In the centre of the figure 
is a large Betz cell which has undergone considerable degeneration. 
The whole cell is swollen. In a large part of it the Nissl substance 
has completely disappeared, and this part of the cell has a bladder¬ 
like appearance. The nucleus is displaced towards the base of 
the apical dendron, and does not stain well. There is some 
incrustation of the nodal points in the intracellular network 
around the nucleus. Two other cells above and below the Betz 
cell are in a more advanced stage of degeneration, and are mere 
shadows. The small deeply stained cells scattered throughout 
the section are probably neuroglial cells, wandering and phagocytic, 
and named “ Kronchenzellen ” by Alzheimer. 

This is a section (Microphotograph II.) of the cortex stained 
by Cajal’s neurofibril method. Throughout the section there are 
numerous pyramidal cells which have the appearance of bladders, 
studded over with minute globules or particles. The cell substance 
is finely granular, and the cell is bounded by darkly stained fibrils. 
In some of the cells the basal neurofibril process is split. 

Coloured Drawing 1 ( x 700 diam.). 

Section stained by Cajal’s method. 

Coloured drawing 1 is a higher power drawing of Micro¬ 
photograph II., and shows very clearly the swollen and degenerated 
pyramidal cells. To the left of the figure are two darker stained 
neuroglial cells, which in other places are found to be freely 
proliferating. The pyramidal cells in the figure demonstrate 
different stages of degeneration. 

Coloured Drawing 2 ( x 800 diam.). 

Section stained with Sharlach R. Pyramidal cells are distended 
and full of fine droplets of fat. 

Coloured - drawing 2 is a section of the motor cortex stained 
with Sharlach R., to show that the small granules and droplets 
in the degenerated pyramidal cells are of a fatty character. In 
this figure there are four distorted pyramidal cells, in one of 
which no nucleus is visible. The whole cytoplasm of the cells 
is infiltrated with fine droplets of fat. 



286 


W. E. HUME 


The Spinal Cord .—Microphotograph III. represents a section 
of the anterior horn of the cervical cord. In it the anterior 
cornual cells are swollen (hydrolysis) and shadowy. The cell 
outline is indistinct, and the nucleus has taken up an eccentric 
position. As in Microphotograph I., there is some incrustation of 
the nodal points in the intracellular network around the nucleus. 
One or two anterior cornual cells in this figure have almost 
completely disappeared. 

The Cerebellum .—When sections of the cerebellum are stained 
by Ranke’s Victoria blue method (Microphotograph IV.), it is seen 
that there is considerable thickening (felting) of the surface, and 
that below this there is a large increase in number of Bergmann’s 
neuroglial fibrils. In the deepest part of the section near the 
middle line, a Purkinje cell can be seen which has undergone 
exactly the same type of degeneration as has been described in 
the pyramidal cells of the motor cortex, and the anterior cornual 
cells of the spinal cord. The more deeply stained cells are 
“ Kronchenzellen.” 

The Retina .—In the lower part of Microphotograph V. is 
the ganglionic layer of the retina. The ganglionic cells are 
abnormal in shape, and their processes in places cannot be seen. 
The nuclei are fairly well stained, but the cytoplasm is poorly 
stained, and the cell has a swollen appearance. With a higher 
power no Nissl substance can be seen. Nothing abnormal can be 
detected in the other layers of the retina. 

Coloured Drawing 3. 

The Removal of Fat .—The appearances represented by coloured 
drawing 3 (x800 diam.) can usually be made out in sections 
of the cortex stained by Sharlach R. It represents a perivascular 
lymphatic in which numerous phagocytic cells are bearing away 
the fat of the degenerated cortical cells. The most obvious 
pathological characteristic is the degeneration of the cytoplasm 
of the essential cells of the central nervous system into some 
fatty substance which stains readily with Sharlach R. In order 
to account for this fatty degeneration, Mott has suggested that 
the nucleus provides a ferment which breaks down the cell 
protoplasm into some substance or substances which he regards 
as the first half of a vital process. The second half, which 




Plate 7 


Microphotchiraph III. ( x 300 diam.). 

Cervical cord. Anterior cornual cells are swollen 
and shadowy. 


MiCROPHOTooRAPH IV. ( x 3(H) diam.). 

Cerebellum stained by Ranke’s Victoria Blue method. Felt¬ 
ing of surface, below which there is an increase of 
neuroglial fibres. In the deepest parts of the section 
Purkinje cells are seen to be swollen and shadowy. 







ACTION OF ADRENALIN ON THE PUPIL 287 


normally consists in the synthetic building up of tissue (Nisei 
substance), does not occur in this disease, because the nucleus 
activity fails. “There may be a chemical decomposition on the 
way to a fatty acid, e.g., choline glycerophosphoric acid and 
stearic acid, and no recomposition” (Mott). In this way he 
would account for the inherent failure of normal development 
in these cases, and the occurrence of a fatty substance in the 
nerve cells. 

Summary .—A case of Tay-Sachs disease is described which 
bears all the characteristic clinical and pathological features 
of this disease. 

The microphotographs and the coloured drawings were made 
by Mr Richard Muir. 


Reference. 

Mott and Carlyle.— Proc . Roy . Soc . Med. y 1911. Path., pp. 147-198. 


THE ACTION OF ADRENALIN AND EPININE 
ON THE PUPIL IN EPILEPSY. 

By R. M. STEWART, 

Pathologist and Assist. Med. Officer, County Asylum, Prestwich. 


Although epilepsy is a disease which has been known and studied 
since the time of Hippocrates, we are still without any exact 
knowledge of its pathology. Indeed, in no other department of 
medicine has knowledge been more slowly gained, for at the 
present day, after years of arduous research, we are in possession 
of little more than a mass of conflicting hypotheses, and in treat¬ 
ment are guided solely by empirical rules. 

In epilepsy, we cannot even claim the guidance of pathological 
anatomy and are compelled to seek a solution of its problems in 
the objective study of clinical cases. Accordingly, the convulsive 
seizure has been so minutely investigated by both neurologist and 
chemist that one might imagine that every mode of approach had 
been thoroughly explored. But the discovery of new clinical 
tests, rendered possible by the recent advances on our knowledge 



288 


R. M. STEWART 


of the internal secretions of ductless glands, has brought to light 
many new facts in relation to the central nervous system of great 
importance, and will probably be of value in the elucidation of 
many obscure diseases. 

One of the most interesting of these is the employment of 
extracts from the suprarenal body for purposes of diagnosis, and 
by its use in epilepsy the writer has been able to observe certain 
interesting phenomena not hitherto described, which suggest the 
possibility of disturbance of the sympathetic as a factor in the 
production of epileptic fits. 

The occurrence in epileptics of derangement of the sympathetic 
nervous system, and more especially of that part concerned with 
vasomotor control, is not disputed, but the question of the part it 
plays as a causal agent in the genesis of fits has long been a 
subject of debate. 

Of the many theories which have been promulgated, that which 
assumes a sudden failure of the cerebral circulation seems worthy 
of consideration, and is supported by a certain amount of collateral 
evidence. It is well known, for example, that amemia of the 
brain may be associated with involuntary muscular spasms, and it 
is obvious that such a condition may be determined in one of 
several ways. Temporary cardiac arrest, such as occurs in heart 
block, may give rise to typical epileptiform convulsions, and it 
can easily be demonstrated with the sphygmograph that arrest of 
the pulse precedes the epileptic attack. 

A considerable amount of evidence is forthcoming to show that 
in idiopathic epilepsy a sudden cardiac inhibition may occur. 
The pulse may be observed to disappear during the onset of an 
attack, and to remain in abeyance until the commencement of the 
clonic stage. But such an event is by no means constant, or even 
frequent, and too much importance, therefore, cannot be attached 
to it. 

A comparable failure of the cerebral circulation might be 
explained on the assumption of an abnormal vasomotor activity, 
acting in such a way as to produce sudden vasomotor spasm of 
the cerebral vessels. Direct evidence of such an event is of course 
lacking, but its possibility cannot be entirely disregarded, since it 
is known that in other diseases allied to epilepsy, such as 
Raynaud’s disease and migraine, vasomotor constriction or dilata¬ 
tion occurs, and is the most probable factor in the production of 



ACTION OF ADRENALIN ON THE PUPIL 289 


the characteristic clinical signs. Moreover, a condition of spasm 
of the retinal arteries during epileptic fits was described by 
Hughlings Jackson, and termed by him retinal epilepsy. 

But while it has been established beyond contention that 
nerve fibres are supplied to the cerebral vessels, the evidence of 
vasomotor activity is less positive. 

It has been shown also that the regulation of the amount of 
arterial blood in the brain is probably effected in an indirect 
manner, the condition of the cerebral circulation varying passively 
according to that of the skin and splanchnic area. 

When, for example, vaso-constriction occurs in the splanchnic 
area, the result is a rise of pressure in the circle of Willis, which 
then forces more blood through the brain. It therefore follows 
that a sudden splanchno-paresis would, if sufficiently profound, 
bring about a cerebral anaemia as complete as that produced by 
cardiac inhibition or other morbid agencies. 

It was a consideration of the above facts which led the writer 
to search for some test whereby a disturbance of the sympathetic 
nervous system might be demonstrated, and the very intimate 
physiological and embryological relationship between the supra¬ 
renal glands and the sympathetic suggested that in adrenalin one 
might find the agent required. 

Some success has been attained in the study of nervous and 
mental disorders by the employment of intravenous or sub¬ 
cutaneous injections of adrenalin, but there is a simpler and safer 
ocular test which may be termed “ adrenalin mydriasis.” 

Lewandowsky was the first to make the observation that, under 
normal conditions in man and in mammals, mydriasis is not 
produced by the instillation of suprarenal extract into the con¬ 
junctival sac. After excision of the superior cervical ganglion 
adrenalin produces a considerable enlaigement of the pupil, and 
this effect has been explained on the supposition that there are 
inhibitory fibres supplying the dilator pupillse, taking origin from 
the superior cervical ganglion, and which are therefore destroyed 
after excision of the latter. But the existence of such inhibitory 
fibres has not been satisfactorily proved. 

We can, however, with some confidence assume that adrenalin 
mydriasis may be an expression of derangement of the normal 
sympathetic mechanism. O. Loewi goes further and assumes that 
the occurrence or non-occurrence of mydriasis after adrenalin 



290 


R. M. STEWART 


instillation is an indication of the functional activity of the 
sympathetic inhibitory nerves. 

He considers that the pancreas normally exercises an inhibitory 
influence on certain organs innervated by the sympathetic, since 
enlargement of the pupil could always be produced in dogs and 
cats by removal of the pancreas. 

In artificial pancreatic insufficiency, and in many cases of 
diabetes, adrenalin mydriasis occurs, and by continuous feeding 
with thyroid extract Eppinger and others succeeded in producing 
mydriasis in dogs. 

The employment of adrenalin in epileptics demonstrated that 
mydriasis may frequently be produced after epileptic fits, and that 
such a phenomenon is subject to wide variations, manifested not 
only in different subjects, but after successive instillations in the 
same epileptic. 

These will now be considered in some detail. 

Solutions Employed. 

There are several synthetic products possessing chemical and 
physiological properties similar to those of the natural suprarenal 
active principle, adrenine; of these the following were em¬ 
ployed :— 

1. Adrenalin (C 9 H 13 0 3 N).—This well-known synthetic product 
of the suprarenal gland can be obtained in solutions of varying 
concentration. The writer has employed the 1 in 1,000 solution 
of adrenalin chloride. It contains chloretone as a preservative, 
and remains stable unless unduly exposed to air or light 

2. Epinine .—This preparation is closely allied to the active 
principle, adrenine, in both its chemical composition and physiological 
action. A solution of 1 in 100 produced effects similar to those of 
a 1 in 1,000 solution of adrenalin. It was the agent chiefly 
employed in the present investigation, in dilutions varying from 
1 in 100 to 1 in 100,000, and apparently remained perfectly 
stable. In a considerable number of cases it produced mydriasis 
where other synthetic preparations failed to have any effect. 

3. Suprarenal Extract .—A solution was prepared by scraping 
out the medulla of fresh suprarenal glands into normal saline. 
After filtration and precipitation of the albumens, a rough attempt 
was made to estimate the dilution by comparing the coloration 



ACTION OF ADRENALIN ON THE PUPIL 291 


produced by adding a few drops of 1 in 1,000 sublimate with that 
of a similarly treated solution of adrenalin 1 in 1,000. 

This solution, when fresh, gave results apparently not inferior 
to those obtained when synthetic preparations were employed, but 
extracts made from glands taken from patients succumbing to 
chronic diseases were not found satisfactory. 

The Effect of Adrenalin on the Normal Pupil. 

Although adrenalin produces no effect on the pupil when a 
single application is made, a moderate degree of dilatation may be 
brought about by repeated instillations. 

In an epileptic subject to long periods of freedom from attacks, 
one drop of 1 in 100 epinine was instilled into both conjunctival 
sacs every half hour, and a moderate degree of dilatation ensued. 
The time taken to produce this effect varied on different occasions, 
the shortest period being one and a quarter hours, and the longest 
seven hours. 

It was noticed that the pupil of one eye dilated several hours 
before the other, the mydriasis appearing very gradually, and 
remaining several hours after the application of drops had 
been discontinued. Similar results were obtained from two other 
patients. 

These observations the writer repeated on himself; a moderate 
degree of dilatation was produced in six and a half hours; that 
is to say after some 15 m. of epinine had been instilled in each eye. 

This amount was evidently sufficient to influence the general 
circulation as an intense frontal headache was experienced, with 
accompanying acceleration of the pulse rate. 

It is evident, therefore, that the continuous action of adrenalin 
on the sympathetic nerve endings is capable of producing a 
mydriatic effect, but this is never as pronounced as that which 
obtains in abnormal states. 

Before passing on to study the effects of adrenalin on the 
pupil of epileptics, it will be useful to briefly refer to certaiu 
phenomena which may be observed during the course of an 
epileptic convulsion, and to the various motor and sensory sequela;. 

The Pupil .—Rapid and wide dilatation of the pupil is an 
almost constant accompaniment of the tonic stage, and is of some 
value in differentiating epileptic fits from those of hysterical origin. 



292 


R. M. STEWART 


That it cannot be entirely ascribed to the effects of asphyxia¬ 
tion is indicated by the fact that it occurs at the commencement 
of the seizure, and is invariable in petit mal attacks where there 
are no tonic spasms. 

At the completion of the tonic stage or even before it the 
mydriasis ceases, and the pupils become contracted, remaining so 
until the stage of coma has passed off. 

In exceptional cases, however, a curious irregular fluctuation of 
the pupil may be observed during the third stage. 

Instead of remaining persistently contracted, the pupils may 
be seen to momentarily dilate, and to again slowly diminish in 
size, to subsequently dilate and contract a few seconds later, and 
so on, until eventually they come to rest in the normal state. 

This pupillary unrest differs from liippus in that the con¬ 
tractions are arhythmic, slower and irregular in their range. 

In one case this condition was observed in the interparoxysmal 
period. 

The cilio-spinal reflex is often abolished for, it may be, some 
hours after the seizure. 

Reflexes .—Temporary abolition of the knee jerks and abdominal 
reflexes during the comatose stage may be frequently noted, and is 
usually followed by exaggeration. Ankle clonus can often be 
elicited. 

The 'state of the plantar reflex varies considerably, and has 
been the subject of investigation by various writers. 

Immediately after the cessation of a fit it may be normal, 
abnormal, or more commonly, absent. 

Babinski was the first to call attention to the occurrence of an 
extensor response, and Keniston in a series of 1,088 observations 
noted that it occurs with greater frequency some little time after 
the seizure. When unilateral, it is more common on the left side. 
A crossed extensor reflex has been noted, and in one case in the 
present series Gordon’s paradoxical flexor response was found. 

Temperature .—A transient rise of temperature often follows 
the epileptic seizure, and cannot be entirely the result of muscular 
contractions, Bince it is equally common after petit mal seizures, 
(Spratling). 

Motor Paralysis .—A temporary loss of motor power, most 
marked upon the side which has shown the severer muscular 
contractions, is commonly observed, and in rare cases may be 



ACTION OF ADRENALIN ON THE PUPIL 293 


entirely unilateral, giving rise to a condition of post-paroxysmal 
hemiplegia. 

The state of the plantar reflex is an index of the degree of 
exhaustion of the nervous system, a unilateral extensor response 
indicating the side on which the tonic spasm was more pronounced. 

The Effects of Adrenalin on the Epileptic Pupil. 

Instillation of suprarenal extract into the eyes of an epileptic 
immediately after the cessation of a fit, may give rise to:— 

1. Dilatation of both pupils. 

2. Dilatation of one pupil only. 

3. No change. 

4. Contraction of one or both pupils. 

These conclusions were derived from the study of the pupillary 
phenomenon in fifty insane epileptics subject to major epileptic 
attacks, and some 500 observations were made. In none of the 
cases was any effect produced by the instillation of adrenalin 
during an interparoxysmal period. 

In every instance the period taken to produce any effect was 
carefully noted, and an attempt made to estimate the length of 
time during which such a change remained manifest. 

In addition the plantar reflex, and in some cases the body 
temperature, were noted. 

Many of these observations were made by nurses. The pro¬ 
cedure was carefully explained to them, and no test accepted 
until it was evident that they were competent to observe and 
record exactly what happened. 

The interest they displayed and their proficiency are here 
gratefully acknowledged. 

In order to eliminate error as much as possible, the first 
hundred results were discarded and controls established by the 
use of distilled water. 

The method of application was simple. The solution was 
distributed in phials of 30 m. capacity, and immediately after 
the cessation of a fit, one drop was conveyed to the conjunctival 
sac by means of an ordinary eye dropper, the time at which the 
instillation was made being carefully noted. 

The method of procedure will readily be grasped by reference 
to the following table. 



294 R. M. STEWART 


1 . 

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fc D 

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Absent. N = Normal flexor response. B = Babinaki’s extensor type. 






ACTION OF ADRENALIN ON THE PUPIL 295 


Dilatation of Both Pupils .—In 400 observations dilatation of 
both pupils was recorded 141 times. The degree of dilatation was 
subject to considerable variation, and was recorded as “slight/' 
“ moderate,” or “ wide.” Wide dilatation, that is to say, a my¬ 
driasis equal to that which could be produced by atropine, was 
noted in 120 instances. The time taken to bring about mydriasis 
varied within very considerable limits, the average being fifteen 
minutes. 

Each patient, as a rule, showed a fairly constant period before 
any change could be noted, which may be regarded as the time 
necessary for local absorption of the agent, as in several instances, 
where adrenalin had been instilled before a fit, the initial dilata¬ 
tion (which occurs under ordinary conditions) continued after the 
stage of coma had terminated. 

Absorption can, however, be very rapid, as in a number of 
cases wide dilatation occurred two minutes after the solution was 
employed. On the other hand, an interval as long as sixty minutes 
may elapse before mydriasis is produced. 

As a rule both pupils showed an equal dilatation, but this was 
not invariable; sometimes one pupil was more dilated than the 
other, the larger pupil dilating more quickly than its fellow. 

The duration of the mydriasis was also subject to a wide 
variation. Frequently the pupil remained dilated for fifteen to 
thirty minutes, and then gradually returned to normal, but in 
some instances it remained dilated for some hours, and not in¬ 
frequently a patient would have another fit before the mydriasis 
had passed off 

Of some interest was the discovery that in a few cases a second 
instillation of adrenalin when the pupil had returned to normal 
again produced a mydriatic effect, and even on a pupil which had 
previously failed to dilate. 

The above results obtained in epileptics differ very markedly 
from those which may be present in patients the subject of visceral 
disease, such as cancer of the pancreas, in that they are much 
more rapidly produced, and persist for a smaller length of time. 
Another important point of difference is the readiness with which 
dilatation may be produced when a very dilute solution is employed. 

A dilution of 1 in 100,000 of epinine (equivalent to 1 in 10,000 
adrenalin) produced pupillary dilatation thirty-nine times in a series 
of seventy observations, and in twenty-eight of these the dilatation 



296 


R. M. STEWART 


was wide. The time taken to effect it was no longer than that 
recorded when the stronger solution was employed. 

No Change .—In a series of 400 observations negative results 
were recorded 173 times, giving a percentage of 43-25. The most 
frequently employed agent was epinine 1 in 100, as is indicated in 
the following table:— 


Solution Employed. 

No. of 

Observations. 

Negative 

Results. 

Percentage. 

Epinine, 1 in 100 - 

282 

110 

41-9 

,, in 100,000 

70 

31 

44-2 

Adrenalin, 1 in 1,000 

Sup. ext., human - 

33 

20 

60-6 

35 

12 

34-2 


Failure of suprarenal extract to produce mydriasis of either 
pupil is a not infrequent event, but a constant negative result is 
rare. Three patients only showed a constant failure with 
adrenalin. Their fits were of the severe nocturnal variety, and 
there was nothing to suggest any variation from the ordinary type. 
The constant absence of the plantar reflex was noted in one, and 
in another, an old woman of 75, the number of observations was 
not sufficient to allow of any conclusion being made. 

It is equally noteworthy that in no case were positive results 
constantly obtained. The number of failures varied greatly in 
different patients, and bore no relation to the severity of the fit 
(leaving out of account petit mal attacks). Nor was it possible to 
correlate the state of the plantar reflexes with the pupil phenomenon. 
In 134 negative observations where the state of the plantar reflex 
was ascertained, an extensor response was present on thirty-four 
occasions; in seventy-nine the reflex was absent, and in the remain¬ 
ing twenty-one instances it was either normal or an extensor 
response was present on one side only. 

It was also noted that where a patient had a serial attack the 
later fits were as likely to give negative results as the initial one. 
Further, there was no similarity whatever in the successive 
pupillary changes in cases where fits occurred in groups. One 
patient, for example, had her convulsions always in groups of five, 
which were separated by a considerable period of freedom from 
attacks. 

A comparison of these series showed a complete lack of uni- 






ACTION OF ADRENALIN ON THE PUPIL 297 


formity in the behaviour of the pupils; on one occasion the first 
fit would be accompanied by wide dilatation, and on a subsequent 
one there would be no result, and so on. 

Unilateral Dilatation .—The occurrence of unilateral mydriasis 
was a striking event, and was capable of production with all four 
solutions. In the series of 400 observations it was noted 37 times 
in the right eye, and 30 times in the left In the majority of 
instances the dilatation was “ wide,” and the time occupied in its 
production very similar to that required to produce bilateral 
dilatation. 

The mode of production of this one-sided dilatation is a problem 
of great difficulty, and can hardly be conjectured, unless one invoke 
the aid of the sympathetic. 

In the same way that localised Jacksonian convulsions are 
succeeded by paralysis of movement, so also, in the epileptic, ex¬ 
haustion paralysis follows a seizure, and is more predominant on 
one side—the side on which the tonic spasm was most intense. 

This suggests a possible relationship between the motor 
paralysis and the unilateral pupil dilatation. The existence, of 
mydriasis might conceivably be found to occur on the side on 
which this exhaustion paralysis was most marked, in harmony 
with the unilateral extensor planter reflex, but careful inquiry 
showed that such a relationship did not exist. 

Attention has already been called to the fact that when the 
normal integration of the sympathetic is disturbed by experimental 
means, the phenomenon of adrenalin mydriasis is readily produced, 
and in certain clinical cases to be presently described, where 
evidence of sympathetic irritation or disturbance was forthcoming, 
a similar dilatation of the pupil could be brought about. 

From the above considerations we are therefore drawn to 
conclude that unilateral mydriasis, following the instillation of 
adrenalin after a fit, is an expression of some functional disorder 
of the sympathetic, in which there is perhaps an exhaustion of the 
inhibitory nervous function. 

Contraction of the Pupil .—This paradoxical behaviour was noted 
on seven occasions, twice in the same patient. 

In the first case both pupils, which were moderately contracted 
in the comatose stage, became “ pin point ” five minutes after a 
solution of epinine 1 in 100,000 had been instilled, and remained 
in this condition for fifteen minutes, when they became moderately 


*4 



298 


R M. STEWART 


dilated. At a subsequent date the same patient had another fit, 
and adrenalin 1 in 1,000 brought about wide dilatation, which 
lasted ten minutes. A second instillation when the mydriasis 
had passed off was again successful, and on its repetition both 
pupils, instead of dilating, became extremely contracted in fifteen 
minutes, and remained half an hour in that condition. A fourth 
instillation was then made, and the pupils now dilated widely. 

The patient was awake the whole time during which these 
phenomena were observed, so that the possible production of this 
myosiB by the sleep state did not require consideration. 

In another case, after the instillation of epinine 1 in 100, both 
pupils rapidly contracted, and in ten minutes were “pin point.” 
After remaining in this state half an hour they returned to normal, 
and the use of epinine a second time resulted in moderate 
dilatation. 

One patient exhibited contraction of the pupil in the left eye 
only, the other remaining unaffected. This condition was observed 
ten minutes after the instillation of epinine 1 in 100, and persisted 
for twenty minutes. Unilateral myosis was observed in two 
other instances. 

Since adrenalin affects only those tissues which have an 
innervation from the true (vertebral) sympathetic, the myosis 
produced in certain instances cannot be attributed to an effect on 
the sympathetic nerve endings in the sphincter pupillae. 

If, however, we accept the supposition that the sympathetic 
carries both motor and inhibitory fibres to the dilator pupillae, 
then it is possible that under certain conditions a disturbance of 
the normal antagonism between these two sets of fibres occurs, and 
operates in such a manner as to allow adrenalin to exercise an 
action on the inhibitory fibres only. 

Moreover, it has been conclusively shown that adrenalin is able 
to act on inhibitory fibres, producing vaso-dilator effects on vessels 
(such as the coronary arteries) where constrictor fibres are 
apparently absent, and some observers (Sollmann and Pari) have 
recorded vaso-dilator effects in certain vessels (the renal arteries, 
for example), where both constrictor and inhibitory fibres are 
present. These facts lend some support to the above hypothesis. 



ACTION OF ADRENALIN ON THE PUPIL 299 


Mydriasis in other Convulsive States. 

A number of observations were carried out with a view to 
determining whether adrenalin mydriasis occurred solely in idio¬ 
pathic epilepsy or in various other convulsive states as well. The 
following convulsive types were investigated:— 

1. Jacksonian epilepsy. 

2. Congestive attacks in G.P.I. 

3. Organic hemiplegia. 

1. Jacksonian Convulsions in an Adult Male. —This patient 
developed typical Jacksonian fits which involved at first the 
right side of the face, and later the whole of the right side of the 
body. He had in all ninety-eight fits, and developed aphasia of a 
mixed type. There was a history of syphilis, and the case was 
regarded as one of gumma cerebri in the neighbourhood of the left 
precentral gyrus. Under KI. and H.G. a complete recovery ensued. 
A solution of epinine 1 in 100 was employed on a number of 
occasions. Wide dilatation of the left pupil only, resulted in 
fifteen minutes. The eye returned to normal after three-quarters 
of an hour. Two trials with epinine after fits gave negative results. 

Thus epinine provoked dilatation of the left pupil in a patient 
whose fits were limited to the right side. 

2. Cerebral Thrombosis in a Female, aged 67.—This patient had 
two transient “seizures,” followed by a left-sided hemiplegia 
which developed in the course of a few minutes. Consciousness 
was retained, and after a few days partial recovery of power in 
the leg took place. Paresis of the lower part of the face was 
marked, but emotional movement was not lost. The behaviour of 
the pupils with epinine varied. 

During the first few days following the convulsive seizure 
both pupils dilated after epinine, the left more readily than the 
right. The latter never dilated as widely as the left, and a week 
after the onset of the illness it failed altogether to respond. 
There then ensued an interval of about a week, during which no 
mydriasis could be produced. This in its turn gave place to a 
period during which both pupils dilated, the right usually to a 
greater degree than the left. On several occasions epinine pro¬ 
duced mydriasis when adrenalin was without any effect. 

Congestive Attacks in General Paralytics. —The effect of adrenalin 



300 


R. M. STEWART 


and epinine on the pupils of G.P.’s was studied both after con¬ 
gestive attacks and during the ordinary course of the disease. 

In two patients wide dilatation of the pupil was produced 
after a seizure by the instillation of epinine. In one patient, who 
had a right-sided seizure with aphasia, mydriasis was provoked 
on the left side only, and in another no result followed the 
instillation of adrenalin. 

These facts seem to justify the conclusion that adrenalin 
mydriasis may occur in general paralytics, and is subject to a 
puzzling variation similar to that which prevails in the epileptic. 

The following additional cases may be referred to here:— 

A Patient subject to Convulsive Seizures associated with Brady¬ 
cardia. —This patient suffered from attacks of the nature of petit 
mal, associated with temporary slowing of the pulse. They were 
followed by marked mental confusion and automatism. 

In two observations epinine 1 in 100 produced dilatation of 
the right pupil only. 

A Case of Migraine. —This patient, a middle-aged woman, is 
subject to recurrent attacks of hemicrania, usually, but not always, 
right-sided. With the intense headache there are associated 
vomiting and nausea. On one occasion, in which the headache 
was limited to the right side, epinine 1 in 100 produced moderate 
dilatation of the left pupil, the right eye remaining unchanged. 

This result is of considerable interest in view of the supposed 
dependence of the clinical phenomena on abnormal vaso-motor 
activity of the cerebral vessels. 

Investigations on some twenty patients, the subject of 
pulmonary tuberculosis, showed no uniformity in results. 

In a considerable number negative results were obtained up to 
the fatal termination. In others bilateral mydriasis was pro¬ 
duced, but with no constancy. 

It was found, however, in some instances, that the production 
of unilateral mydriasis could be correlated with the morbid 
changes in the lung. 

Thus, in one subject, only the left pupil dilated, the right 
remaining unchanged although epinine or adrenalin were instilled 
into both conjunctival sacs on numerous occasions. At the autopsy 
a tubercular broncho-pneumonia was found affecting practically 
the whole left lung. The right lung was free from disease, with 
the exception of a small area near the hilum. 



ACTION OF ADRENALIN ON THE PUPIL 301 


In another patient Buffering from phthisis, epinine produced 
dilatation of the right eye only. P.M. advanced bilateral tuber¬ 
culosis was found, but microscopic examination of the cervical 
sympathetic chain showed that that of the right side was ex¬ 
tensively implicated by the disease at the apex of the right lung. 
These cases suggest that morbid changes in the sympathetic are 
to be suspected when adrenalin brings about a unilateral mydriasis 
in a patient the subject of pulmonary tuberculosis. 

As already stated, pancreatic “ insufficiency ” is associated with 
adrenalin mydriasis. The writer has had the opportunity of 
observing four cases in which the normal functions of the pancreas 
were presumably deranged. In all adrenalin produced mydriasis. 
Two were cases of carcinoma of the stomach with secondary 
deposits in the liver, and implication of the pancreas by the tumour. 
The fourth was a case of suppurative cholecystitis, with inflam¬ 
matory changes in the body of the pancreas. 

In contrast with the dilatation occurring in epileptics, the effect 
in these cases invariably remained marked for some hours. 

It would be easy to extend this list, but probably enough 
examples have been given to show that adrenalin mydriasis may 
occur in a large number of very dissimilar diseases. 

Careful scrutiny brings out a point of some importance, namely, 
that in all there is evidence either of sympathetic derangement or 
abnormal function of the ductless glands. 

With regard to epilepsy, we may shortly infer from the above 
considerations that not infrequently a disturbance of the normal 
sympathetic mechanism takes place, which may be readily shown 
by the employment of suprarenal extract as a clinical test; that 
further, this disturbance may be unilateral or bilateral, and is 
subject to variations which cannot at present be explained. 

Lastly, it is necessary to consider whether this sympathetic 
derangement plays any part in the production of epileptic fits. 

The inconstancy of adrenalin mydriasis in epileptics, the wide 
variations to which it is subject, and its occurrence in other con¬ 
vulsive types, make it probable that the convulsive seizure and the 
sympathetic disturbance are related, not as cause and effect, but as 
concomitant effects of a single pathological process, which has yet 
to be determined. 

References. 

1. Bikdis— “The Internal Secretory Organs,” 1913. 

2 . Spratling— “Epilepsy,” 1904. 



302 


ABSTRACTS 


Hbstracts. 

ANATOMY. 

A STUDY OF GANGLION CELLS IN THE SYMPATHETIC 
(365) NERVOUS SYSTEM, WITH SPECIAL REFERENCE TO 
INTRINSIC SENSORY NEURONES. F. W. Carpenter and 
J. L. Con el, Joum. Comp. Neurol ., 1914, xxiv., June, p. 269. 

Sympathetic ganglion cells of the cat prepared by the Cajal 
method show both Dogiel’s “ motor type ” of cell with heavy 
dendrites and his “ sensory type ” with slender dendrites. They 
also show cells with intermediate structural characters connecting 
the two “ types.” On the basis of external cell morphology we 
cannot say, therefore, that two distinct kinds of elements exist in 
the sympathetic ganglia. The “types” of Dogiel are, in the 
authors’ opinion, to be regarded as extremes of the variation which 
occurs among the multipolar sympathetic cells. 

Sympathetic ganglion cells of the rabbit prepared by the Nissl 
method present a quite constant picture of chromatophile bodies, 
which tend to be arranged near the periphery of the cell-body. 
The cells cannot be divided by this feature of their internal 
morphology into two well-defined groups. 

The authors could find no anatomical evidence that ganglion 
cells of opposite function ( i.e ., motor and sensory) exist in the 
sympathetic system. If their structural similarity is an indication 
of similarity in function, then all must be motor, since it is the 
presence of intrinsic sensory neurones only that is open to question. 

In the rabbit binucleate cells were found in the vertebral and 
prevertebral ganglia of the trunk system (sympathetic division 
proper of the autonomic system). Such cells were not seen in the 
cranial autonomic ganglia, nor in the plexuses of the intestinal 
wall (peripheral ganglia). A. Ninian Bruce. 


THE STRUCTURE OF THE VAGUS NERVE OF MAN AS DEMON- 
(366) STRATED BY A DIFFERENTIAL AXON STAIN. S. Walter 
R anson, Anal. Anzeig., 1914, xlvi., Juni 12, S. 522-525 (with 
one fig.). 

The author points out that while we possess a large number of 
excellent differential stains for distinguishing between medullated 
and non-medullated nerve fibres, it is only recently that we have 
possessed a similar differential stain for axons. 



ABSTRACTS 


303 


The method he describes is the “ pyridine-silver technique,” and 
is a modification of the Cajal stain, which itself does not differ¬ 
entiate clearly non-medullated fibres from connective tissue and 
neuroglia. The animal is exsanguinated, and the tissue placed at 
once in absolute alcohol containing 1 per cent, of strong ammonia 
for forty-eight hours, rinsed in distilled water, placed in pyridine 
for twenty-four hours, washed in many changes of distilled water 
for twenty-four hours, put into 2 per cent, silver nitrate at 35° C. 
in the dark for three days, rinsed in water, and then placed for 
one day in a 4 per cent, solution of pyrogallic acid in 5 per cent, 
formalin. The sections are cut in paraffin. By this method the 
medullated axons are stained yellow, and are surrounded by a 
colourless ring of myelin. Non-medullated fibres are stained 
black, and are sharply differentiated from the light yellow endo- 
neurium. 

Large numbers of non-medullated fibres were found by this 
method in the roots, trunk, and branches of the vagus. Most of 
the large medullated fibres leave the vagus through the pharyngeal, 
sup. laryngeal, and recurrent nerves, while practically all the non- 
medullated fibres are carried down into the thoracic vagus. Most 
of the medullated fibres in tbe thoracic vagus leave it through the 
bronchial and cesophageal branches, so that the vagus as it passes 
through the diaphragm is practically a non-medullated nerve. 

A. Ninian Bruce. 


THE ANATOMY AND FUNCTION OF BECHTEBEW’S NUCLEUS. 
(367) (Uber die Anatomic und Funktion des Nucleus Bechterew.) 

R. Leidler, Afonatsschr. /. Ohrenheilk., 1914, xlviii., H. 3, 8. 321. 

There has always been some confusion about the anatomy of 
Bechterew’s nucleus. Various writers have described different 
groups of cells as Bechterew’s nucleus, and Bechterew himself did 
not exactly describe its position. Leidler found Marchi’s method of 
great assistance in his investigations. After section of tbe eighth 
nerve in a rabbit, the degenerated fibres were seen to go to the 
nuclei of Deiters and Bechterew, to the nucleus triangularis, and 
also to a much broader area, where the ganglion cells were 
scattered into irregular groups. 

The writer quotes freely from a paper by Kaplan, who includes 
in the nucleus of Bechterew not only the small celled ventricle- 
angle group, but also a sharply defined mass of cells, which is seen 
well in frontal and sagittal sections. It is placed between the 
brachium conjunctivum and the motor and sensory nuclei of the 
trigeminal. The cells of Bechterew's nucleus are easily dis- 



304 


ABSTRACTS 


tinguished by their size from the nuclei of the trigeminal and 
Deiters. The cells of Bechterew are arranged in four groups— 
(1) Dorsoangular, (2) dorsolateral, (3) central or ventromedial, (4) 
ventrolateral. 

At present very little is known of the function of the nucleus. 
Leidler, working on rabbits, partially or completely destroyed the 
nucleus by puncture. 

In the first case, the puncture passed through the nucleus 
triangularis and destroyed the ventral part of Bechterew’s nucleus. 
This caused no reaction in the eyes nor head; no nystagmus nor 
head deviation. In the second case, the vestibular nerve, the 
whole of Bechterew’s nucleus, flosculus, corpus restiforme, and 
part of the lateral nucleus of the cerebellum of the left side were 
destroyed; Deiters’ nucleus escaped. This caused degeneration of 
the vestibular root, and its ascending and descending branches; 
the nucleo-cerebellar tracts caudalwards, the whole motor and 
part of the sensory and cerebral parts of the trigeminal, with 
their concomitant fibres. The posterior longitudinal bundle re¬ 
mained intact. On microscopic section, fine fibres were seen 
running towards the middle line and bending forwards just 
lateral to the posterior longitudinal bundle. They appeared to be 
fibres from Bechterew’s nucleus to the ocular nuclei. Soon after 
the operation, the rabbit showed deviation of the eyes to the 
right and nystagmus to the left (side of lesion). Next day 
deviation of eyes and head to the left and nystagmus to the right. 
Rolling of animal to the left. Vestibular reactions still present. 
A third case gave somewhat similar results. 

In all the animals in which the nucleus of Bechterew was 
destroyed, a small track of degeneration was found arching 
medially and then forwards lateral to the posterior longitudinal 
bundle. A few fibres enter it, but most of them remain lateral to 
it. It is not possible to be certain that all these fibres come 
from Bechterew’s nucleus, some of them may come from Deiters’ 
nucleus. The nucleus of Bechterew has very little, if any, 
connection with the posterior longitudinal bundle. From other 
evidence, also, Leidler concludes that the fibres from Bechterew’s 
nucleus are all ascending. He also concludes that damage or 
destruction of Bechterew has no influence on the excitability of 
the vestibularis, and produces no vestibular nystagmus. He also 
adds that Bechterew’s nucleus may perhaps produce some eye 
movement, e.g., simple rolling of the eyes. The chief function of 
Bechterew’s nucleus is not yet known, but is probably intimately 
connected with the cerebellar nuclei. 


J. K. Milne Dickie. 



ABSTRACTS 


305 


PHYSIOLOGY. 

THE ANATOMICAL LOCALISATION IN THE BASE OF THE 

(368) BRAIN OF THE LESIONS WHICH PROVOKE POLYURIA 
IN DOCKS. (Localisation anatomique a la base du cervean des 
ldsions qoi provoquent la polynrie chez le chien.) J. Camus and 
Q. Roussy, Compt. Bend. Soc. de Biol., 1914, Ixxvi., June &, p. 877. 

Four groups of operations are summarised: (1) Total hypo¬ 
physectomy by buccal route; (2) hypophysectomy followed by a 
subsequent experimental lesion of the base; (3) a deep basal lesion 
by red-hot needle after perforation of sphenoid by gimlet; (4) deep 
lesions purposely made (a) in front of, and (5) behind the pituitary 
region. Conclusions: (1) The lesion which causes polyuria in no 
way involves the pituitary: five times puncture failed to touch it, 
yet intense polyuria followed: this polyuria is neither greater nor 
less when the pituitary is involved; (2) total hypophysectomy 
without lesion of the infundibulum does not give polyuria; (3) a 
preliminary hypophysectomy does not prevent the production of 
polyuria by means of a subsequent experimental opto-peduncular 
lesion; (4) the depth of the puncture, or a lesion of thalamus or 
peduncle, seems to have no influence on the production or intensity 
of the polyuria; (5) the really important thing is the superficial 
basal lesion often unintentionally produced in hypophysectomies 
which are followed by polyuria; (6) in dogs the polyuria-producing 
zone is limited to the opto-peduncular region: its seat is the grey 
matter of the tuber cinereum in the neighbourhood of the infundi¬ 
bulum ; (7) a lesion made either in front of, or behind this zone 
does not give polyuria. Leonard J. Kidd. 

THE HYPOTENSIVE CCELIAO REFLEX. (Sur les modifications 

(369) dn pools radial conadcutives aux excitations du Sympathique 
abdominal (plexus solaire et ramifications terminates). Rdflexe 
coeliaque hypotenseur.) Andb£-Thomas and J. C. Roux, Compt . 
Rend. Soc. de Biol., 1914, Ixxvi., May 29, p. 867. 

It is sometimes possible to produce in man by a moderate, even 
painless, manual compression of the abdomen halfway between the 
navel and xiphoid cartilage a very marked feebleness of the radial 
pulse, occasionally even abolition. As a rule, the greater the pain 
the greater is the degree of the phenomenon. It is specially 
marked in anxious melancholic neuropaths, and is usually less 
marked in organic abdominal affections, partly because firm 
pressure cannot be always safely applied. The writers compare 
this abdomino-cardiac phenomenon with the similar condition 
obtained experimentally by Brown-Sdquard, Goltz, and Laignel- 
Lavastine. Leonard J. Kidd. 



30G 


ABSTRACTS 


▲ NEW VASO DILATOR REFLEX IN THE DOG’S HIND LIMB. 
(370) (Sur un nouveau r<flexe vaso-dilateur du membra postdrieur 
chez le chien.) H. Busquet, Reunion, Biol, de Nancy , 19 Mai, 
1914 ; Com.pt. Rend. Soc. de Biol., 1914, lxxvi., June 5, p. 891. 

Experimental summary and conclusions:—In chloralosed dogs 
cutaneous stimulation by prick of the hind limb, especially the 
pad, or succession (striking table with wrist or hammer) gives a 
rise of the femoral venous pressure simultaneously with a fall of 
the carotid or femoral arterial pressure. Appropriate experimenta¬ 
tion shows that the discordant manometric variations of the vein 
and artery can be explained only by an expansion of the system 
between them. This new rettex is differentiated from the other 
known vascular ones by the nature of the stimuli which evoke it, 
by the objective criteria which testify to its reality, and by its 
purity, i.e., absence of all appreciable concomitant vaso-constriction. 
The phenomenon is still obtained after atropinisation or curarisa- 
tion, but is abolished by infra-bulbar section of the spinal cord; its 
centre is therefore encephalic. (The technique is described.) 

Leonard J. Kidd. 


ADRENALIN AND THE PUPILS. Antoni, Neurol. Centralbl., 1914, 
(371) June 1, p. 674. 

Intravenous injection of adrenalin dilates the pupil, but its 
instillation into the conjunctival sac does not produce the same 
effect, in normal conditions. In certain pathological conditions, 
however, it does so: (1) in lesions of the conjunctival epithelium; 
(2) when the sympathetic system is hyperexcitable, e.t/., in cases 
of exophthalmic goitre, dial>etes, after lesions of the peritoneum 
(laparotomies, &c.). Compare transient glycosuria after lesions of 
the peritoneum; (3) after lesions of the sympathetic path to the 
pupil, anywhere on its course. The author has reinvestigated the 
phenomenon in other conditions. In 20 cases of dementia paralytica, 
9 gave dilatation of the pupil with conjunctival instillation: it 
begins within half an hour, and may continue for hours. Whether 
these cases belong to group (2) or (3), mentioned above, is not 
clear. In a large number of control cases (healthy and diseased) 
a few cases were found where the pupils dilated by this method, 
but only after some three to five hours; it is supposed they are 
cases of physiological sympatheticotonus. In certain cases of 
tuberculous meningitis, encephalitis, diffuse cerebral sclerosis, 
hydrocephalus, &c., where the reaction is positive, it is supposed 
that the frontal sympathetic centre is affected. 

S. A. K. Wilson. 



ABSTRACTS 


307 


PARATHYROID DEFICIENCY AND SYMPATHETIC IRRITA 
(372) BILITY. R. Q. Hoskins and Homer Wheelon, Amer. Joum. 

Physiol., 1914, xxxiv., June 1 , p. 263. 

Conclusions: —(1) Parathyroid destruction in dogs results in a 
marked increase of vasomotor irritability as shown by the reactions 
to nicotin, epinephrin, and pituitrin; (2) all components of the 
vasomotor mechanism, sympathetic cells, myoneural junctions, and 
musculature, seem to be affected. The effects are of varying 
degree in different cases; (3) there was observed no strict parallel¬ 
ism l)etween the external symptoms of parathyroid deficiency and 
the degree of vasomotor irritability; (4) inconclusive evidence 
indicates that calcium injections in some measure restore vasomotor 
irritability toward normal; (5) the sympathetic system offers no 
exception to the general increase of irritability that results from 
parathyroid extirpation. (The authors confirm Carlson’s observa¬ 
tion that salivation is a common result of parathyroid deficiency.) 

Leonard J. Kidd. 


PSYCHOLOGY. 

PSYCHOLOGY OP RELIGION. Georges Berguer, Archiv. dt Psychol., 
(373) 1914, Feb., p. 1. 

This paper is divided into three parts, of which the first deals 
with the normal, the second with the abnormal, psychology of 
religion, and the third with theories of the origin and nature of 
religious phenomena. In the course of fifty pages the author 
gives an excellent survey of the field thus marked out. The fact 
that the article is followed by a bibliography of forty pages gives 
some idea of the amount of work — most of it comparatively 
recent—which has been done on this subject. 

Margaret Drummond. 


ARTICULATE LANGUAGE IN THE NORMAL MAN AND IN THE 
(374) APHASIC. J. Fboment and O. Monod, Archiv. dt Psychol., 
1913, April, p. 1. 

This is a study of the psychology of aphasia. The authors 
maintain that in the psychology of language in general the 
hypothesis of motor images, whether articulatory or graphic, is 
entirely gratuitous and unsubstantiated. The only images which 
are called into play in speech or writing are sensory, i.e., auditory 
or visual. These, then, are the images which are affected in motor 
aphasia and agraphia, if like every other aphasia these disturbances 
are due to a veritable amnesia. Margaret Drummond. 



308 


ABSTRACTS 


ABE DEFECTIVE CHILDREN LACKING IN MORAL QUALITIES? 

(376) Alick Dbmxeudres, Archiv. de Psychol, 1913, April, p. 21. 

The author of this paper is instructress of a special class in Geneva, 
in which there are thirty backward and twenty defective children, 
the distinction being determined by the use of Binet’s scale, and 
in accordance with his use of the terms. She writes to oppose 
the very common opinion that moral qualities are at a low ebb in 
such children. She gives many illustrations to show that qualities 
of the heart, such as kindness and affection, are well developed 
among her pupils. Margaret Drummond. 

DOES THE MOTOR VERBAL IMAGE EXIST? E. Clapar^dk, 

(376) Archiv. de Psychol., 1913, April p. 93. 

The author takes the opportunity afforded him by the paper 
referred to above to distinguish the various questions which arise 
in connection with the function of articulate speech. With 
respect to the special question of motor images of words, he differs 
from Froment and Monod, and maintains that these images not 
only exist, at least in certain subjects, but play an important part 
in the mental processes leading on to speech. 

Margaret Drummond. 

ANALYSIS OF 80 0ALLED NEURASTHENIC AND ALLIED 

(377) STATES. Trigant Burrow, Jowm. Abnorm. Psychol., Oct. -Nov. 
1913. 

The author suggests that the aetiology of neurasthenia should be 
more carefully studied from the standpoint of its psychological 
mechanism, so that through the establishment of the psychogenic 
factors involved in these conditions a more systematised knowledge 
may at last be resolved out of the present chaos of inco-ordinated 
anatomical assumptions. H. de M. Alexander. 

THE PSYCHOPATHOLOGY OF A CASE OF PHOBIA-A CLINICAL 

(378) STUDY. Morton Prince, Joum. Abnorm. Psychol., Oct.-Nov. 
1913. 

A clinical detailed analysis of a case of phobia towards church 
steeples and towers of any kind. H. de M. Alexander. 

THREE EXAMPLES OF NAME - FORGETTING. H. W. Frink, 

(379) Jowm. Abnorm. Psychol., Feb. -March 1914. 

The writer formulates the following rule to account for many cases 
of difficulty in recalling familiar names (or phrases) : The name 



ABSTRACTS 


309 


forgotten is connected (accidentally or otherwise) with a repressed 
complex, and is prevented from coming into consciousness by the 
protective resistance against the painful ideas contained in the 
complex. H. de M. Alexander. 


SLIPS OP THE TONGUE AND PEN. C. P. Obebndorf, Joum. 

(380) Abnorm. Psychol., Feb.-March 1914. 

The author gives examples of lapses of the tongue and pen which 
have given expression to the suppressed tendencies and thoughts, 
instead of the more circumspect or correct utterance which was 
intended. H. de M. Alexander. 

INVENTOBIAL RECORD POEMS OF USE IN THE ANALYSIS OF 

(381) DREAMS. Lydiaed H. Horton, Joum. Abnorm. Psychol Feb.- 
March 1914. 

Illustrations are given of record forms for the purpose of 
analysing dreams. H. de M. Alexander. 

RECENT LITERATURE ON JUVENILE SUICIDES. Lewis M. 

(382) Terman, Joum. Abnorm. Psychol., April-May 1914. 

At present the children of France (16 years of age and under) are 
committing suicide at the rate of about 150 per year, though the 
numbei* is now slightly decreasing. In Germany the situation 
is little better. In Russia it is very common. The problem 
exists with but slight variations in every country of the civilised 
world. A table of causes of juvenile suicide is given by the author 
as analysed by Eulenberg, Proal, and Oholpine. In this table 
“fear of punishment” easily heads the list. The causes which 
relate to the school exceed one-third of the total. Contrary to 
common opinion, love affairs and insanity account together for not 
more than 2 per cent. 

Suicides of children are characterised by less deliberation than 
those of adults, and are more likely to result from a momentary 
passion, such as rage or the shock of sudden humiliation; and 
cases of juvenile suicide are much less common in the country 
districts. 

The school cannot absolve itself of all responsibility merely by 
guarding against becoming the immediate occasion of the tragedy. 
It needs to train children in habits of healthful activity instead of 
cramming the mental storehouses with knowledge which does not 
function. H. de M. Alexander. 



310 


ABSTRACTS 


PATHOLOGY. 

REMARKS ON THE HI8TOPATHOLOOIOAL CHANGES IN THE 
(383) SPINAL CORD DUB TO IMPACT. AN EXPERIMENTAL 
STUDY. A R. Allen, Joum. New. and Mmt. Du ., 1914, 
zll, March. 

The present report is a continuation of previous experimental 
work. After laminectomy had been performed on the dog and 
without opening the dura, there was determined the maximum 
amount of impact in gram-centimetres to the spinal cord, delivered 
by a special mechanism, from which the animal would recover 
with normal motor function without further operative procedure. 
Then the amount of impact from which the dog would not recover 
without operative procedure was determined. 

Any impact up to 340 gm.-cm. was found to be hypo-impact; 
and anything above this was termed hyper-impact. When an 
impact of 450 gm.-cm. was used, the animal would invariably die 
unless a median longitudinal incision was made through the 
injured area of the cord. The beneficial change resulting is 
ascribed to drainage of blood and serum. 

In this communication the following points are discussed: 
(a) the histopathological changes in the spinal cord of the dog 
from fifteen minutes to six hours after hyper-impact injury; ( b ) 
the effect on the histopathological picture of the median longi¬ 
tudinal incision performed two hours after impact, the dogs being 
killed six hours after impact; (c) consideration of hemolytic 
change in the extravasated blood, in the substance of the cord due 
to the action of crushed myelin; (d) three cases of median 
longitudinal incision after fracture dislocation of the spinal 
column in the human subject. D. K. Henderson. 


AN ADRENAL TUMOUR IN A OOW. (Tumeur del a surrfoale chez 

(384) un bovidd) C. Farise, Rivnion , Biol, dt Nancy , 19 Mai 1914; 
Compt. Rend. Soc. de Biol., 1914, lxxvi., June 5, p. 902. 

An account of an adrenal tumour in a cow: it measured 15 cm. 
in diameter, and weighed 2 kilos. 500. Farise gives a histological 
description and discusses its nature. He says that these adrenal 
tumours are in the Hcrbivom compatible with perfect health, and 
that they show a greater tendency to necrosis and calcification 
than to generalisation. Leonard J. Kidd. 



ABSTRACTS 


311 


CLINICAL NEUROLOGY. 

CONTRALATERAL OPPENHEIM AND GORDON REFLEXES. 

(386) Alfred Gordon, Joum. Nerv. and Ment. Dig., 1914, xll, March. 

A short note mentioning the various conditions in which the 
sign occurs. D. K. Henderson. 


CONTRALATERAL PERIOSTEAL REFLEXES OF THE ARM. 

(386) A Myerson, Joum. Nerv. and Ment. Dig., 1914, xli., March. 

With the patient lying flat on his back, and his arms at his sides 
in an easy, relaxed attitude, usually with slight flexion at elbow 
and moderate internal rotation, the examiner taps the middle of 
the clavicle with a reflex hammer. When present, the response 
elicited is a contraction of the biceps and pectoralis major of the 
other arm. Usually there is also a homolateral response. 

This reflex has been noted in general paralysis, hemiplegia, 
multiple sclerosis, brain tumour, and meningitis. It is present 
occasionally in dementia pnecox, manic depressive insanity, and 
hysteria. Its presence, therefore, indicates an abnormal condition 
not necessarily associated with organic disease. 

D. K. Henderson. 


THE OCULOCARDIAC REFLEX IN DIPHTHERITIC INTOXICA- 
(387) TION. (Le rtfflexe oculo-cardiaque au cours de l’intoxication 
diphttfrique.) E. C. Aviragnet, H. Dorlencourt, and H. 
Bottttier, Compt Bend. Soc. de Biol., 1914, lxxvi., p. 771. 

The writers examined the oculo-cardiac reflex in 26 children 
suffering from diphtheria either by simple digital compression of 
the radial or by the spliygmograph. 

In 15 it was abolished and in 11 it was normal. In 3 of the 
latter the clinical diagnosis of diphtheria was not confirmed 
bacteriologically. 

The later the case came under treatment the more frequently 
was the reflex lost, and in cases that required larger or repeated 
doses of serum the reflex was more frequently lost than in those 
in whom a small or a single dose was sufficient. 

These observations show the frequency of the affection of the 
pneumogastric in diphtheria and the influence of early treatment 
in the behaviour of the reflex. J. D. Rolleston. 



312 


ABSTRACTS 


THE OCULO CARDIAC REFLEX IN HEMIPLEGIA AND OBRB- 

(388) BRAL DIPLEGIA. (Le rdflexe oculo-cardiaque dans las hdmi- 
pldgies et les dipldgies cdrdbrales.) J. Roubinovitch and 
R£gnauld de la Soudiere, Bull, et mem. Soc. med. H6p. de Parity 
1914, xxxvii., p. 909. 

In 6 out of 7 cases of cerebral diplegia, the reflex was abolished. 
In one it was exaggerated. In 24 hemiplegics ocular compression 
was carried out first on the paralysed, and then on the sound side. 
The reflex was completely lost in 13, and inverted in 3, both on 
the right and the left side. In 2 it was normal. In only 6 cases 
was there obvious dissociation of the reflex ; on the sound side it 
was normal, while on the paralysed side in 3 it was inverted, in 
2 abolished, and in 1 weak. J. D. Rolleston. 


HERPETIC FACIAL PARALYSIS IN A PATIENT WITH 8YM 

(389) METRICAL LIPOMATOSIS. (Paralysis facials zostdrienne 
chez un malade attsint ds lipomatoss symdtrique.) Laignel- 
Lavastine and Romm*, Bull, et mem. Soc. mid. H6p. de Paris , 
1914, xxxvii., p. 875. 

An alcoholic cooper, aged 51, suffering from generalised sym¬ 
metrical lipomatosis developed right occipito-cervico-facial and 
otic zoster. There was an intense meningeal reaction shown by 
hypertension and excess of albumen and lymphocytes in the 
cerebro-spinal fluid. Eighteen days after the appearance of the 
eruption, right facial paralysis occurred, and was accompanied by 
marked tactile, painful and thermal hyposesthesia. 

The zoster affected the second, third, and possibly fourth spinal 
ganglia, and also the geniculate ganglion. J. D. Rolleston. 


ZOSTER WITH FACIAL PARALYSIS; TROPHIC AND SENSORY 

(390) TROUBLES OF THE LINGUAL MUCOSA. (Zona avsc paralysis 
faciale; troubles trophiques et sensitifs de la muqueuse linguale.) 
F. Ramon D and H. Poirault, Bull, et tnim. Soc. mid H6p. de 
Parity 1914, xxxvii., p. 847. 

A boy, aged 15 years, developed left facial zoster which was strictly 
limited to the region of V 3 . The buccal mucosa and tongue were 
affected as well as the cheek. In addition to the neuralgia 
characteristic of zoster there were contracture of the masticatory 
muscles and paresis of the muscles innervated by the lower 
division of VII. The skin of the face corresponding to the eruption 
showed a marked syringomyelic dissociation of sensibility such as 
the writer had previously noted in zoster ( v. Review, 1911, ix., p. 



ABSTRACTS 


313 


127). This dissociation was also present, though in a less degree, 
on the left buccal mucosa and left half of the tongue. The latter 
had lost the sensation of taste in its anterior two-thirds. Smell 
and hearing were normal. 

Trophic disturbances were shown by the smooth and shiny 
surface of the left side of the tongue, which offered a striking 
contrast to the thickly coated right half of the organ. All the 
symptoms—motor, sensory and trophic—disappeared within a 
fortnight. 

Ramond suggests that in addition to the otic ganglion the trunk 
and nucleus of V s were affected. J. D. Rolleston. 


ON A CASE OF FULMINATING PARAMENINGOCOCCUS 
(391) CEBEBBO-SPINAL MENINGITIS. (A propos d’un cm de 
mdningite cdrdbro-spinale suraigu k paramdningocoques.) 

M. Riser, Bull, et mim. Soc. mid. Hop. de Paris , 1914, xxxvii., 
p. 941. 

A record of a case in a female child of 11 months, which proved 
fatal in three days. The symptoms were those of meningococcal 
meningitis, but injections of antimeningococcal serum were useless, 
and bacteriological examination of the purulent cerebro-spinal fluid 
showed the true nature of the case. J. D. Rolleston. 


THE MENINGEAL SYNDROME IN RECURRENT FEVER. (Le 
(392) syndrome mdningd dans la fi&vre recurrent®.) Lafforoue, Bull, 
et mim. Soc. mid. H6p. de Paris , 1914, xxxvii., p. 883. 

Like Coskinas (v. Review, 1914, xii., p. 262), Lafforgue, during 
two years’ stay in Tunis, frequently observed meningeal syndromes 
in recurrent fever. There was never any cellular reaction in the 
cerebro-spinal fluid. «T. D. Rolleston. 


THE ORBITAL BRAIN -ABSCESS AND ITS OPERATION. (Die 
(393) orbitogene Himabsxess nnd seine Operation.) Elschino, Klin. 
Monatsbl.f. Angenheilk., 1914, Miirz-April, S. 359. 

The author describes fully the cases of abscess of the frontal lobe 
arising from orbital or nasal sinus infection, one of which re¬ 
covered. Such abscesses occur always in the frontal lobes and are 
easily attacked through the orbit, falling thus into the realm of 
the ophthalmic surgeon. H. M. Traquair. 

2 5 



314 


ABSTRACTS 


ON RECKLINGHAUSEN’S DISEASE. (Contribute*) para o estudo da 
(394) doenga de Recklinghausen.) L. Viegas, Anais Scient. da Faeult. 
de Med. do Porto , 1913, i., p. 76. 

A gikl, aged 12 years, presented all the features of Reckling¬ 
hausen’s disease except tumours in the nerves. There was no 
family history of a similar complaint, but her maternal grandfather 
and maternal uncle suffered from epilepsy. The most striking 
characteristic of her case was that the left side was the most 
affected. Thus the left side of her scalp showed atrophic mevi and 
pigmentation and pigmentary mevi were most marked on the left 
side of the forehead. The left side of her lips and tongue showed 
papillomatous growths; the left deltoid was atrophied; the left 
thumb, index, and ring fingers were shorter than the right; the 
left thigh showed larger molluscoid tumours than the right; the 
left foot showed skeletal deformities; and the left ear was 
misshapen and deaf. 

The patient also had complete anosmia, and tachycardia, attacks 
of suffocation, and enuresis. She was able to read and write and 
to do manual work, but suffered much from forgetfulness. 

J. D. Rolleston. 


A CASE OF HEMIPLEGIA IN DIPHTHERIA. (Un cas d’MmipWgie 
(395) dans la diphtdrie.) J. Hall£, M. Bloch, and Foix, Bull, et mbn. 

Soc. mid. H6p. de Parts, 1914, xxxvii., p. 896. 

A girl, aged 3| years, had a severe attack of diphtheria complicated 
by early palatal paralysis and myocarditis. Right hemiplegia and 
aphasia occurred on the thirteenth day. Slight improvement 
took place, but the child died from late diphtheritic paralysis 
li months after the onset of diphtheria. The necropsy showed an 
area of softening, probably of embolic origin, in the posterior two- 
fifths of the putamen. J. D. Rolleston. 


A OASE OF DYSTONIA MUSCULORUM DEFORMANS. C. C. 

(396) Beling, Journ. Nerv. and Ment. Dis., 1914, xli., March. 

A Russian Hebrew girl, at the age of 7 years, developed a progressive 
generalised muscular spasm of a tractile and torsion-like character. 
The disease began in the right foot, and exhibited itself as a dis¬ 
turbance of gait in which hypertonia and spasmodic components 
were evident. These spasms produced peculiar deformities in the 
trunk and extremities. The movements were almost always slow, 
rather stereotyped, and not so graceful and rhythmic as those of 
bilateral athetosis. The muscular spasms were not under the 



ABSTRACTS 


315 


influence of the will. Complicated motor acts, such as rising, 
walking, eating, &c., have been profoundly affected. The move¬ 
ments cease during sleep. The intellect has been entirely un¬ 
affected ; the emotional state has been normal. There have been 
no hysterical stigmata, and neither suggestion nor hypnosis has 
had any influence. 

The disease is very similar to double athetosis, chronic chorea, 
and degenerative tic. D. K. Henderson. 


THE INTRAMENINGEAL TREATMENT OF TABES AND 

(397) GERBBRO-8PINAL SYPHILIS. Thomas R Boons and R R. 
Snowden, Arch. Int. Med., 1914, xiii., June, p. 970. 

Brief accounts are given here of the results of the treatment of 
eight unselected cases by means of intraspinal injection of sal- 
varsanised serum. The method used was that described by Ellis 
and Swift, except that the serum was injected undiluted and in 
large quantities (25-35 c.c.). They found that the patients were 
uniformly relieved from pain, and, as far as locomotion was con¬ 
cerned, there was a slow but definite improvement. The psychic 
effect was also marked, the patients being encouraged by the quick 
relief of pain, and their nutrition improved rapidly. The effect on 
the cerebro-spinal fluid was very striking, the cell count first 
falling to normal and the Wassermann reaction becoming negative 
some time after the cells were reduced. They think that the fact 
that the serum was injected undiluted may have been the cause of 
their results being so favourable, and they point out that although 
the reactions were sometimes rather severe, they do not contra¬ 
indicate the larger doses. The reactions produced by the injection 
of the salvarsanised serum from another patient were very severe, 
and should not be attempted. A. Ninian Bruce. 

A CASE OF PROGRESSIVE THROMBOPHLEBITIS OF THE 

(398) BRAIN SINUSES FOLLOWING ACUTE OTITIS MEDIA. 
(Ein Fall von progredienter Thrombophlebitis der Himsinus 
nach Otit. med. acuta. Septische Verl&ufsform. Operation nach 
Jansen. Tod nach 36 Tagen.) C. J. M. Schmidt, Monataackr. /. 
Ohrenheilk ., 1914, xlviii., H. 2 , S. 270. 

A peasant woman, aged 40, in the beginning of June 1912, 
developed a right-sided acute otitis media. Great pain in ear 
and neck. Pain continued after ear discharged. Temperature 
39* C. One week from commencement of illness developed right 
facial paralysis. Two rigors. Vomited several times. Had great 
vertigo. Could not get out of bed. In August improved some- 



316 


ABSTRACTS 


what and came to see the writer. At this time had still complete 
facial paralysis. Swaying, on standing with eyes shut. Mucosa of 
right tympanum swollen and with granulations. Pus scanty but 
very foetid. Tuning fork on right mastoid heard only in left ear. 
Normal caloric reaction. 

Radical mastoid operation performed. Facial canal found 
exposed. No. fistula seen. After operation temperature rose at 
once to 38'5. Pain in neck. 

On 5th day after operation temperature still raised. Rigor. 
Vomited twice. 

On 6th day another rigor. Temperature, 39*6. 

On 9th day another rigor. Temperature, 39*8. 

On 10th day.—Delirious. Great headache and pain in neck. 

On 11th day.—Second operation. Sinus exposed as far as the 
jugular bulb. Opened. Clot removed. Labyrinth also opened. 
No pus. Seven days later suddenly became unconscious. Three 
weeks after second operation temperature had been steadily rising 
to 41° C. Delirium. Pyaemic abscesses. Sudden protrusion of 
right eye and oedema of eyelid. Two days later same appearance 
of left eye. Died a few days later. Post mortem showed 
cavernous sinus, right lateral sinus, and petrosal sinuses thrombosed, 
with here and there pus. Purulent meningitis of base of brain. 

The writer Bays that it is not common to get progressive 
involvement of the venous sinuses, and gives references of a few 
that had been described. He also discusses the anatomy and 
physiology of the venous sinuses. J. K. Milne Dickie. 


TWO BABE COMPLICATIONS OF FOBEION BODIES IN THE 
(399) (ESOPHAGUS. (Zwei seltene komplikationen von Fremdktirpern 
im (Esophagus.) Mieczyslaw Qantz, Monatuchr. /. Ohrenheilk., 
1914, xlviii., H. 2, S. 183. 

The writer reports two cases as examples of how cases of foreign 
bodies in the oesophagus should not be treated. 

The first case was a man, aged 35. Four weeks previously a 
fish bone had stuck somewhere in his throat. He went to his 
doctor about it, but the latter could not find it. Five or six 
days later the pain had become much worse, and there was now 
some fever. Another doctor was called in who diagnosed angina, 
as the fever was now over 40° C. A few days later he was advised 
to go to Berlin to see if the fishbone could be discovered. On the 
way to Berlin the patient felt very ill, and suddenly felt as if 
something had burst in his throat. He spat out some purulent 
fluid and immediately felt some relief. In Berlin he saw a 



ABSTRACTS 


317 


laryngologist, who examined him with an oesophagoscope, and told 
him that he would soon be well. The patient returned home and 
was quite well for two weeks, when he suddenly had a rigor, his 
temperature rose to 40°, and he had severe pain in the left side 
of his neck. Swallowing and speech were not interfered with. 
He resolved to go at once to Berlin, but stopped for the night at 
Warsaw. While there he consulted a doctor, who diagnosed a 
retropharyngeal abscess, and advised him to see Gantz in the 
morning. During the night the patient noticed that he could not 
move his left leg, and had to move it with his hand. He was 
fully conscious, and his speech was unaffected. On his way to 
the klinik next day he became unconscious. When seen by 
Gantz his breathing was stertorous, eyes shut, profuse perspiration. 
Meningitis diagnosed. Lumbar puncture gave stinking pus. 
Death in two hours. Probable cause of death, the bursting of a 
retropharyngeal abscess through the intervertebral canals into the 
spinal canal. 

The second case was a woman, aged 40. She had swallowed 
a little piece of bone which had stuck in the left side of the 
throat. She tried to push it down with bread, but only increased 
the pain. A doctor was called in who tried, unsuccessfully, to 
push it down with a wire covered with wool. Four or five people 
made attempts to dislodge the bone with various instruments, but 
without success. That night the patient could not sleep on 
account of the pain in her throat. She visited Gantz seventeen 
hours after swallowing the bone. There was great hyperaemia of 
pharynx and larynx. The piece of bone was seen in the left 
piriform sinus, surrounded by an area of great swelling. With the 
oesophagoscope the bone, measuring 2 cm. by £ cm., was removed. 
In spite of antiseptic painting, ice compresses, &c., the temperature 
rose in the evening, accompanied by great pain. Two days later 
the right wall of the pharynx became swollen. Symptoms of 
asphyxia. Neck incised on left side, and stinking pus welled out 
from region of oesophagus. Later an oesophageal fistula developed 
through the wound, but gradually closed up again. The patient 
eventually recovered, and in four weeks was quite well. 

The writer attributes the rapid onset of septic complications 
in the second case to the repeated and misdirected efforts at 
removal. He recommends that in all cases of suspected foreign 
bodies examination with the oesophagoscope should be carried out. 
He quotes numerous cases in which wounds of the oesophagus 
were observed after blind passage of instruments. 

He concludes that all blind methods of removal of foreign 
bodies should be carefully avoided, and that removal through the 
oesophagoscope under the guidance of the eye is the only allowable 



318 


ABSTRACTS 


procedure. If this is unsuccessful, oesophagotomy should at once 
be performed. J. K. Milne Dickie. 

SUDDEN DEATH FOLLOWING LUMBAR PUNCTURE. (La mort 
(400) subite suite de ponction lombaire.) J. Minet, Joum. de mM. 
de Paris , 1914, zzziv., p. 312. 

Minet and Lavoix in 1909 collected thirty-four cases ( v. Review, 
1909, vii., p. 479). The pathogeny of sudden death following 
lumbar puncture is probably multiple. Sometimes vaso-motor 
phenomena occur which may end in haemorrhage. In other cases 
the fall of the cerebellum on the bulb may be the cause of death. 
As a rule there is probably a bulbar shock. J. D. Rolleston. 


THE ALBUMEN CONTENT OF THE SPINAL FLUID IN ITS RBLA- 
(401) TION TO DISEASE SYNDROMES. A. Myrkson, Joum. Nerv. 
and Merit. Dis. y 1914, zli., March. 

A clinically quantitative estimation of albumen has been made 
as a part of the routine examination of the cerebro-spinal fluid. 
Into a narrow test tube, one with a bore of about 6 mm., 2 c.c. of 
spinal fluid is dropped. The fluid is heated short of the boiling 
point, and then six drops of a 33 J per cent, aqueous solution of 
trichloracetic acid is added. In the normal fluid there is at once 
a diffuse but not marked cloudiness, which gradually settles in 
thirty minutes into a flocculent precipitate just covering the 
bottom of the tube. Where there is a distinct increase, there is a 
dense cloud which almost immediately becomes flocculent and 
settles to a height of perhaps 5 cm. from the bottom of the tube. 
The following general conclusions are drawn:— 

1. In general paralysis the relationship of albumen, globulin, 
cells, and Wassermann reaction is quite constantly one of paral¬ 
lelism, but in the remissions the Wassermann reaction disappears 
first, the cell count and globulin diminish next, and the albumen 
most constantly remains at a high level of increase; in the pre¬ 
paretic stage, therefore, the albumen increase is probably the first 
sign of disease. 

(a) In Korsakoff’s disease, in certain cases of tumour and in 
other organic diseases, there is a dissociation of albumen and 
globulin in this sense, that there is either marked increase of 
albumen without globulin, or that a marked increase of albumen, 
say 3 + , is accompanied by a globulin increase of 1+. 

(b) The increase of albumen is a primitive reaction of the 

nervous system, and is the first as well as the most constant of 
the present known chemical and biological changes to appear in 
the spinal fluid. D. K. Henderson. 



ABSTRACTS 


319 


THE COLLOIDAL GOLD REACTION IN THE CEREBRO SPINAL 
(402) FLUID. Sydney R. Miller and Robert L. Levy, Bull. Johns 
Hopkins Hospital, 1914, xxv., No. 279. 

The paper deals with one of the newer tests applied to the cerebro¬ 
spinal fluid; one in which the colloidal chemistry of the fluid 
seems to be the determining factor. 

It was known to Lange, who first described the reaction in 
1912, that colloidal solutions of gold are precipitated by electrolytes, 
and that solutions of proteins protect colloidal solutions of gold 
from precipitation; also that the quantity and nature of proteins 
present in a solution could be determined with great accuracy by 
estimating the amount of the solution necessary to protect a 
constant amount of colloidal gold in the presence of a fluid of 
constant electrolytic power. 

In attempting to apply this knowledge to the study of the 
proteins of the cerebro-spinal fluid, he discovered that in 
conditions in which the spinal fluid contained an abnormal 
amount of protein substances, notably in syphilitic diseases of 
the nervous system, he was unable to secure protection, but that 
more or less complete precipitation of the gold occurred within 
certain dilution limits of the cerebro-spinal fluid. 

The dilution limits seemed to be definite and specific, and 
seemed to vary in different diseases, thus making their differentia¬ 
tion possible by this method. The exact nature of the reaction is 
unknown. 

Lange is inclined to interpret the reaction as an indication of 
the occurrence of different qualitative mixtures of protein sub¬ 
stances, rather than a true quantitative increase in one or other of 
the protein constituents; for the strength of the reaction ap¬ 
parently bears no relation to the amount of protein present as 
revealed by ordinary tests. Several other explanations have been 
given. 

The technique of the test is as follows:— 

Eleven test tubes are placed in a row. 

1*8 c.c. of a 0 4 per cent, salt solution are pipetted into the 
first tube, 1 c.c. into each of the remaining tubes. 

0 2 c.c. of cerebro-spinal fluid are then added to the first 
tube and mixed. 

1 c.c. of this 1-10 dilution of spinal fluid is transferred to the 
second tube, where the mixing process is repeated, a 
120 dilution resulting. 

In a similar manner, dilutions are made in the remaining eight 
tubes, giving ten dilutions from 1 in 10 to 1 5120. The eleventh 
tube serves as a control to which no spinal fluid js added. 



320 


ABSTRACTS 


To each tube 5 c.c. of colloidal gold solution are added, and 
the result may be read off in a few minutes. 

The result is deduced from the change in colour of the red 
gold solution through red-blue, lilac, violet, purple, and pale blue 
to the colourless solution which results from complete precipitation 
of the gold. 

In a negative reaction no change takes place; in different 
diseases the maximum precipitation takes place fairly constantly 
at certain dilutions. 

The authors examined 210 cerebro-spinal fluids from 171 cases, 
and give detailed particulars of their results. 

They conclude that normal fluids give negative reactions, and 
that the reaction peculiar to general paralysis is sufficiently con¬ 
stant to warrant its use as an aid in the differentiation of this 
condition from others with which it might be confused. But they 
are unable to agree with earlier workers, that the reactions in 
other diseases of the nervous system—syphilitic, and otherwise—are 
characteristic; or that the reactions seen in secondary and tertiary 
syphilis can be said with certainty to be the earliest sign of 
involvement of the nervous system. 

They consider, however, that the test may prove to be more 
sensitive as an indicator of the results of specific therapy than are 
those at present employed. The authors describe their technique 
and the method of preparing the gold solution in detail. A full 
bibliography is appended. W. J. Adie. 


PINEAL TUMOURS. (Lea tumours do la glande pintale.) A S£zary, 
(403) Gaz. des H6p., 1914, Ann. 87, June 20 and 27, pp. 1141, 1205. 

A good systematic account of pineal tumours. The macro- 
genitosomatic precocious syndrome is well described, also the 
differential diagnosis between pineal tumours and those of the 
pituitary and adrenals. As the palliative operation of choice 
Sdzary suggests ventricular puncture: he thinks that possibly 
trephining followed by ventricular drainage will give more 
persistent effects. A useful bibliography is given. 

Leonard J. Kidd. 


RESEARCHES ON TETANY AND SENILE CATARACT. (Fischer 
(404) Triebenstein und Untersuchungen fiber Tetanie und Alterstar.) 

Klin. Monattbl. f. Augenheilk ., 1914, 1 , S. 441. 

The authors investigated sixty-eight cataractous subjects of ages 
varying from 50 to over 70 years and found signs of latent tetany 
(Latenzzeichen der Tetanie) in the great majority. The cases, 



ABSTRACTS 


321 


with the signs found, are tabulated, as well as twelve cases of 
similar ages who had no cataract and no latent tetany. They 
suggest that the two conditions are connected and that all cases 
both of lamellar and other forms of cataract in early life and 
senile cataract should be examined by a neurologist. 

H. M. Traquair. 


ADRENAL VIRILISM. (Le virilisme surrlnal.) Tuffier, Bull, de 
(405) PAcacL de Med., 1914, lxxi., May 26, p. 726. 

A woman of 62 came for metrorrhagia, which examination showed 
was apparently due to a large fibroid. Owing to a considerable 
glycosuria operation had to be postponed. She was high-coloured, 
vigorous, had a thick black beard and moustache, red swollen face 
of masculine type, slight exophthalmos, masculine voice, great 
muscular development and strength; had become fond of hard 
manual work, digging, &c., which did not tire her at all; some 
almost confluent yellow spots on forearms and hands; clitoris 
hypertrophied, 4 cm. long, covered by a very large preface. 
(Tuffier does not state whether her pubic hair extended vertically or 
not.) All these abnormalities came on after the menopause. No 
organic signs outside abdomen. Glycosuria quickly lessened under 
treatment. Operation revealed a greatly hypertrophied uterus, 
which was removed: glycosuria soon disappeared During 
laparotomy examination of adrenal region revealed a bilateral 
mass, half the size of a kidney, over the kidneys, of fibrolipomatous 
consistence. Left ovary atrophied: right showed a tumour the 
size of a large nut. One of the two photographs of the patient 
shows a bearded face that every one would take for a man’s 
(v. Review, 1912, x, p. 345). Leonard J. Kidd. 


EPILEPSY IN CHILDHOOD. James H. Lloyd, Archives of Pediatrics, 
(406) June 1913. 

The author begins by quoting Gowers’ and Spratling’s statistics 
showing the frequency of the disease in childhood : he then draws 
attention to the relationship of infantile convulsions to epilepsy. 
In discussing the heredity of the disease he throws considerable 
doubt on the value of any investigations along this line. He 
characterises heredity as largely a “ Terra incognita.” The 
possibility of abnormal internal secretions, syphilis, and otitis 
media are mentioned as possible causative factors. He points out 
the value of surgery in certain traumatic cases, but warns his 
hearers against trephining in essential epilepsy which has a 
focal character. 



322 


ABSTRACTS 


The difficulty of diagnosing nocturnal epilepsy in relation to 
nocturnal enuresis is considered. Treatment is dealt with briefly, 
because, as the author points out, there is nothing new to add. 
He reiterates the importance of a strict hygienic, mental and 
moral regime. A. Fergus Hew at. 

THE RECOGNITION AND TREATMENT OF TRUE IDIOPATHIC 
(407) BPILEP8T IN CHILDREN. J. N. G. Nolan, Dublin Jour, of Med. 

Science , Aug. 1913. 

In this article a review is given of the treatment employed, at 
Hellingly Mental Hospital, for children suffering from idiopathic 
epilepsy. The author also deals briefly with cases which he terms 
“ secondary epilepsy ” arising from some cerebral lesion or defect. 
The causes operative in both types of case are detailed and the 
writer urges the more frequent use of the Wasserinann reaction as 
an aid to diagnosis, because such cases which give a positive 
reaction may be vastly improved by an antisyphilitic treatment. 

An outline of treatment for the cases of secondary epilepsy is 
mentioned, but the prognosis is acknowledged to be gloomy. Iu 
dealing with the treatment of the idiopathic type considerable 
stress is laid on the value of recognising early symptoms of the 
disease in neurotic children. General lines of treatment are briefly 
discussed under the following headings:— 

(1) Prophylaxis, (2) Medicinal, (3) Dietetic, (4) Surgical, and 
(5) Educational. 

No new doctrines are brought forward, but the author insists 
that manual and industrial work should figure largely in the 
curriculum. More detail about the educational treatment would 
have added largely to the value of this interesting paper. In 
spite of the fact that only the worst types of epileptics go to an 
asylum the author states that “80 per cent, of our defective 
epileptics are usefully employed in the various industrial shops; 
and the younger children all benefit by their school training.” 
Finally, the author urges the importance of a very careful regime, 
which must be started early and carried out with the utmost care 
and perseverance in idiopathic epilepsy. A. Fergus Hew at. 


SCORBUTIC POLYNEURITIS. (Polynlvrites scorbutiques.) A. 

(408) Austreoesilo, Rev. Neurol ., 1914, xxii., Janvier 30, p. 76. 

Scurvy may be difficult to diagnose from beri-beri, the difficulty 
being greatly increased if it be accompanied by polyneuritis. Two 
forms of scorbutic polyneuritis may be distinguished: (1) acute, 
subacute or dropsical, resembling beri-beri, but presenting the 



ABSTRACTS 


323 


general characters of scurvy, and (2) a post-scorbutic form, 
appearing during convalescence, atrophic, of a chronic type and 
difficult to treat. A. Ninian Bruce. 

ON NYSTAGMUS. J. Igeshkimkr, Klin. Monatsbl.f. Augenheilk ., 1914, 

(409) li., S. 337 and 66R 

The paper discusses nystagmus specially from the point of view 
of the oculist. After a short r&um6 of the relations of nystagmus 
to affections of the cerebrum and cerebellum and of the auditory 
apparatus, the author discusses the possibility of a connection 
between nystagmus and convergent strabismus and retinitis 
pigmentosa on the basis of inner ear disease as a common factor in 
such cases, and decides against such a suggestion. 

As differentiating points the nystagmus at the extremes of 
movement is mentioned as characteristic of multiple sclerosis, and 
the jerky nature of otogenous nystagmus oscillating nystagmus is 
never aural in origin. Excluding miners’ nystagmus the author 
recognises two groups of cases, those in which some local ocular 
condition appears to be the cause and those for which such an 
explanation is unavailable. 

In the first group is contained a large number of cases 
commonly termed Nystagmus Amblyopicus and frequently found in 
blind asylums. In albinos who have no macula lutea, nystagmus 
is frequent. 

In other cases the nystagmus is associated with partial or total 
colour blindness. In this group, while various cerebral processes 
may be assumed to be disordered it is the amblyopia which 
produces the nystagmus. On the other hand it is not easy to 
explain why some children who become amblyopic in early life fail 
to develop nystagmus. 

In another group there is no noteworthy amblyopia. Here the 
author has found that hereditary syphilis is very frequently the 
cause, a relationship for which increased pressure in the fourth 
ventricle is suggested as an explanation. 

The paper closes with short notes on hereditary and familial 
nystagmus. H. M. Traquair. 

BOMB OASES OF HYSTERICAL DEFECT OF THE FIELD OF 

(410) VIBION. (Binige F&lle von Hysterischem Gesichtsfelddefek.) 

Hbnning Rouwe, Klin. Monattbl. f. Augenheilk. ., Marz-April 1914, 
8.372. 

While, in general, hysterical fields belong to a characteristic type, 
there are many exceptions, and the author has shown in this 
paper that the field changes in hysteria may be very various. 



324 


ABSTRACTS 


The cases described include one in which the field was smaller 
for a large than for a small object, and cases of scotoma, really 
only subjective, some of which simulated toxic amblyopia or re¬ 
trobulbar neuritis. Great care is necessary to control the observa¬ 
tions so as to make certain as to the nature of the condition, as 
the observer is apt to obtain the kind of field he expects, and he 
should always bear in mind the possibility of a purely functional 
defect. H. M. Traquair. 

UNUSUALLY EXTENSIVE MBDULLATED NERVE FIBRES IN 

(411) HIGH MYOPIA WITH AMBLYOPIA. (Ungewohnlich 
ausgedehnte markhaltige Nervenfasem bei hochgradiger 
Myopie und Amblyopic.) Berg, Klin. Monattbl. /. Augenheilk., 
1914,1., S. 495. 

The present case occurred in a boy of 8 years who had a practically 
normal eye on the left side with full vision, while on the right 
there was high myopia with astigmatism and very poor vision. 
The fundus showed extensive opaque nerve fibres spreading out 
from the disc and arching over towards the macula illustrating 
the anatomical arrangement of the fibres in a very well marked 
manner. The condition is shown in an excellent illustration. 

A list, with short descriptions, of twenty-five somewhat similar 
cases is given. 

The author suggests that faulty development may explain both 
the opaque nerve fibres and the myopia. H. M. Traquair. 

CHRONIC PALSY OF LIMBS DUE TO PROLONGED USE OF 

(412) COLCHICINE. (Paralysie durable des membrcs par ingestion 
prolongs de colchicine.) A. Souques, Bull, de VAcad. de Med., 1914, 
lxxi., June 2, p. 750. 

A vigorous man of 50, subject to annual attacks of acute gout, 
took on his own responsibility repeated small doses of a colchicine- 
containing preparation for a period of three weeks, and per¬ 
sisted in this in spite of diarrhoea and abdominal pains: he did 
this to ward off what he regarded as an impending attack. He 
was then seized with paralysis of all four limbs and trunk; 
anaesthesia of feet at onset with severe deep muscular pains; 
muscle tenderness persisted; no psychical changes, no involvement 
of head, heart, or sphincters; no albuminuria or fever. (At one 
period, it is said that there was abolition of deep reflexes and 
respiratory disturbances, but Souques cannot vouch for this, as he 
did not see the case then.) Even now, six months after the onset, 
the motor and sensory troubles are not entirely cured. Souques 
shows that acute colchicine poisoning gives the same effects on the 
nervous system as the repeated continued small doses taken by 



ABSTRACTS 


325 


his patient. He insists on the importance of strict medical super¬ 
vision in colchicine therapy, and its suspension if diarrhoea occurs. 

Leonard J. Kidd. 

the medical aspects of the obbek anthology, j. d. 

(413) Rollkston, Proc. Roy . Soc. Med,., 1914, vii., Section of History of 
Med. , pp. 3-13 and 30-56; and Janus, 1914, xix., pp. 35-46 and 
105-131. 

In the first part of this paper the writer deals with the medical 
men connected with the Anthology, either as contributors or as 
the subjects of the poems, and in the second part discusses the 
numerous other medical allusions to be found in the work. Among 
these may be mentioned the epigrams illustrating the relation of 
medicine and religion; the prevalence of alcoholism in antiquity, 
and its association with prostitution, the absence of any reference 
to syphilis or any venereal disease, the homosexual, or rather 
bisexual, life of the ancients, as well as allusions to dwarfism, 
gigantism, hysterical paraplegia, hemiplegia or hemiatrophy, 
epilepsy, paracusia, and other disorders of special sense. In 
conclusion, the writer states that the Greek Anthology merits 
more attention than it has hitherto received from the medical 
historian for the following reasons:— 

1. It offers numerous illustrations of the relations between 
Greek medicine and Greek religion, especially as regards Asklepius. 

2. It contains definite references to certain diseases such as 
gout, alcoholism, and malaria, as well as numerous allusions to 
epidemic diseases, the nature of which cannot be determined. 

3. It supplies valuable negative evidence of the existence of 
syphilis in antiquity, in spite of the numerous facilities for the 
spread of the disease. 

4. It illustrates many subjects in the life of the ancients, more 
or less closely concerned with medicine, such as baths, latrines, 
cosmetics, prostitution, popular remedies, and superstitions. 

5. As a source of medical satire and caricature, it deserves to 
rank with the works of the Latin poets. 

Author’s Abstract. 


PSYCHIATRY. 

ON A PEDIGREE SHOWING BOTH INSANITY AND OOMPLI 
(414) GATED EYE DISEASE: ANTICIPATION OF THE MENTAL 
DI8EASE IN SUCCESSIVE GENERATIONS. £. I. Lidbktter 
and £. Nettleship, Brain, 1913, xxxv., p. 195. 

In Part I. a pedigree is described which formed the basis of an 
article by Mott, the data of which was supplied by the present 



326 


ABSTRACTS 


authors, but which they have more fully investigated from both 
the mental and ocular sides. The result shows an association 
between mental deficiency and ocular defects; the latter are fully 
gone into, and consist chiefly of detachment of the retina; disease 
of the choroid, with iritis, and in some cases secondary cataract; 
little is said about the forms of insanity, with the exception that a 
few are classed as imbecile. It is found on taking the third, 
fourth, and fifth generations, that out of sixty-five persons, forty 
are defective either mentally or physically. In the successive 
generations there does not appear to be any evidence of an earlier 
incidence in the eye disease, but there is an anticipation of mental 
disease. 

In Part II. there is given an anticipation in diabetes showing 
occurrence of the disease at age of 50, 37, and 22, in successive 
generations, and in a further pedigree at 58, 35, and 6|. 

Part III. consists of a series of cases showing extensive coarse 
disorganisation of the choroid in infants frequently associated 
with mental defect. 

The conclusions formed are that: (1) There is an association 
between mental deficiency and ocular defects which is partly 
developmental, partly morbid. (2) That amongst the members 
who have not shown any definite mental or ocular disease a large 
proportion have not been endowed sufficiently to compete success¬ 
fully in life, and have been in receipt of poor law relief. (3) 
Mental deficiency tends to appear at an earlier age in succeeding 
generations, but there is no anticipation in ocular defects. (4) 
Anticipation is well seen in the case of diabetes. 

A. W. Nkill. 

ARACHNOID INJECTION WITH THE SERUM OF SYPHILITICS 
(416) IN TABES AND GENERAL PARALYSIS. (Ein serothera 
peutischer Versuch bei Tabes und Paralysis progressiva: Arach- 
noideale Injektion mit Serum von Syphilitikem.) B£rikl and 
Duband, Neurol. Centralbl., 1914, May 16, p. 612. 

A number of intravenous injections of salvarsan are given to a 
syphilitic patient; not less than twenty-four hours after the last 
of these, serum is withdrawn by venipuncture. This serum is 
not a mere chemical solution of salvarsan, but contains syphilitic 
antibodes. The serum, be it noted, is not that of the patient to 
be treated, but is obtained from a syphilitic patient who shows 
recent evidence of the disease. The serum is injected by the 
lumbar route in cases of tabes, and by the cranial route in cases of 
general paralysis: twenty-four hours elapse after its withdrawal 
from the syphilitic patient before it is thus employed: it is also 
heated to 56° C. for half an hour. Some 10 to 20 c.c. are injected. 



ABSTRACTS 


327 


The authors have given four lumbar injections and seven cranial 
injections by this method. They consider it free of all danger, 
and the results are promising. S. A. K. Wilson. 

TREATMENT OF GENERAL PARALYSIS. H. Damayk, Progret 

(416) Midical, 1914, June 6, p. 270. 

A report of three cases of G.P.I., treated beneficially by essentially 
the same treatment as that used by the author in cases of 
syphilitic psychoses (v. Review, 1914, xii., April, p. 170), viz., first, 
over-alimentation and tonics, secondly, after establishment of an 
improved physical state, the addition to over-alimentation of 
antisyphilitic remedies. Leonard J. Kidd. 


METABOLISM IN DEMENTIA PRiEOOX. Ellison L. Ross, Arch. 

(417) Int. Med., 1914, xiii., June, p. 889. 

Five cases of dementia praecox, three in a chronic and two in a 
subsiding acute phase of the disease, were used in these metabolism 
tests. The metabolism of nitrogen, phosphorus, calcium, and 
magnesium was normal in both classes of patients. The metabolism 
of sulphur, except in the excessive total sulphate output and 
possibly the inorganic sulphate output, was normal for the 
chronic cases; but in the acute cases the excretion of total sulphur 
was maximum normal, the total sulphate and inorganic sulphate 
output was abnormal, and the neutral sulphur was above normal. 
The abnormalities in the sulphur metabolism of the acute forms 
indicate a reduced power of metabolic oxidation, a fact which is 
not surprising since seemingly every bodily activity is decreased 
in acute dementia prtecox. The fewer and less pronounced 
abnormalities of sulphur metabolism in the chronic group suggest 
a similar, though less extensive, deficiency than in the acute 
group. A. Ninian Bruce. 

ALZHEIMER’S DISEASE AND ITS RELATION TO SENILE 

(418) DEMENTIA. Simchowicz, L'Encephale, 1914, ix., March 10, 

p. 218. 

The clinical aspect of the case here recorded resembled that of 
Alzheimer’s disease, whereas the pathological picture was that 
of senile dementia: the pathological condition, however, was more 
localised than in the latter disease. The author thinks that the 
curious distribution of the lesions is the explanation of the 
differentiation of the clinical symptoms in his case, focal symptoms 
which are not found commonly in senile dementia. There were 



328 


ABSTRACTS 


marked changes in the cells of the cornu ammoniB, including a 
granulo-vacuolated degeneration of the pyramidal cells—changes 
which are found both in senile dementia and in Alzheimer’s 
disease. 

The case is worked out carefully on both the clinical and the 
pathological sides, and is well illustrated. S. A. K. Wilson. 


CLINICAL EXAMINATION OF THE MENTAL STATE OF DE 
(419) MENT8. (L’examen clinique du fond mental chez les dements.) 

Ballet and Genil-Pkrbin, L’Encephale , 1914, ix., Feb. 10, p. 101 

The authors have worked out a very practical scheme for the 
examination of the mental state in cases of dementia. It is 
essential for comparison of cases that some scheme should be 
adopted and regularly utilised, and the scheme here elaborated in 
detail appears very applicable to the task in hand. The authors 
analyse five different mental functions in their patients, viz., 
affectivity, attention, memory, association of ideas, general activity. 
Each of these is in turn subdivided, and suitable tests are 
devised for the examination of each. The results are expressed 
in figures, and thereby a graphic representation of the patient’s 
mental condition at any given period is obtained. The reader 
must consult the original for the details of this interesting 
investigation. S. A. K. Wilson. 


TREATMENT. 

THE TREATMENT OF NEURITIS BT ELECTRICAL METHODS. 

(420) W. F. Somerville, Brit. Med. Jovm., 1914, May 9, p. 1014. 

Nine cases of neuritis affecting various nerves are here recorded, 
all of which were either cured or greatly benefited by high- 
frequency electricity or ionic medication. 

For the relief of neuralgic pain, high-frequency currents of from 
500 to 800 milliamperes should be passed through the patient as 
he lies on the condenser couch, while the affected area may be 
stroked gently by the hand of the operator as he holds one 
electrode while the patient grasps the other. 

The best results in ionic medication were obtained by using a 
2 per cent, solution of quinine hydrochloride. The electrode 
lying on the pad soaked in quinine hydrochloride is connected 
with the positive pole, and bound in place by bandages. The 
current is slowly turned on, and may be increased from 50 to 100 
milliamperes, and applied for thirty minutes. It should be 
repeated daily unless the skin is tender. A. Ninian Bruce. 



ABSTRACTS 


329 


OXYGEN HYPODERMICALLY IN NERVOUS AND MENTAL 
(421) DI8EASBS. M. Dardxl, Rev. Med. de la Suinu Romande , 1914, 
March 20, p. 192. 

Oxygen increases the differential pressure, diminishes the viscosity 
of the blood, increases haemoglobinaemia, slows the pulse, increases 
the amplitude of respiratory movements, and usually gives some 
degree of euphoria. Toulouse used it hypodermically in mental 
affections with encouraging results: four acute psychoses yielded 
rapidly; it calmed agitation, promoted sleep, lessened frequency 
of epileptiform attacks, and always did some good. Dardel records 
twelve cases thus treated: he injected the gas from a Martinet’s 
oxygenator, connected by a rubber tube to a Pravaz syringe, into 
the outer side of the thigh (description of mode of charging, &c., 
given). He advises very slow injection, even up to ten or fifteen 
minutes: the skin bulges and there is pricking, tenderness, or 
even transient pain; at the end of a few hours the gas is absorbed, 
but usually next day some subcutaneous crepitation can be felt: 
the site of injection is changed daily, and recumbency for at least 
half an hour after injection is desirable. No accident or bad 
result was ever seen. The most constant favourable sequela was 
improved sleep, both during treatment and subsequently: it is 
natural, deep, and free from subsequent narcotic-like malaise; 
euphoria also occurred. Even in chronic incurable organic 
cerebral diseases, oxygen gave improved sleep and general quiet¬ 
ing. The difficulty of eliminating the possible influence of sug¬ 
gestion is admitted. The doses used were usually either 200 or 
300 c.c., at first given daily or on alternate days, gradually increased 
to 400 or 500 c.c. One patient, a pale, thin, badly developed, 
delicate boy of 11, bore 300 to 400 c.c. every other day extremely 
well: the rest were adults from 26 to 59 years of age. The 
patients comprised cases of neurasthenia, epilepsy, constitutional 
psychopathy with chronic depression, ideas of persecution with 
violent attacks of anger, circular insanity, chronic gastritis with 
obstinate insomnia, catatonic dementia with remissions, and a 
catatonic young woman who showed difficulty in collecting her 
thoughts, and in speaking, and in doing what she wanted to do. 

Leonard J. Kidd. 


26 



330 


REVIEWS 


■Reviews. 

MENTAL DEFICIENCY. (Amentia.) By A. F. Trkdgold, L.R.C.P., 
(422) M.R.C.S., Consulting Physician to the National Association for the 
Feeble-minded, and to the Littleton Home for Defective Children, 
«fec. Second edition, revised and enlarged. London: Bailli&re, 
Tindall, A Cox, 1914. Pp. 492 ; 67 illustrations. Pr. 12s. 6d. net 

The second edition of Dr Tredgold’s book on mental deficiency 
has been thoroughly revised, and many chapters have been entirely 
rewritten. A fresh chapter has been added dealing with the 
important practical points of case taking, and of tests of mental 
ability. There is also an addendum on the Mental Deficiency Bill, 
and its bearings on the relationship of the medical profession 
to mental defectives, considered from various viewpoints. Re¬ 
reading of the volume under review confirms the high opinion 
we have formed of its theoretical and practical value. The 
neuropathologist will find accurate descriptions of the pathology 
of mongolianism, microcephaly, and amentia in general, with its 
different varieties : the clinician will find excellent studies of the 
symptomatology of these conditions: the teacher and instructor 
will find numerous practical hints for the training and education 
of these types of mental deficiency. The legal and sociological 
bearings of the problem of mental defect are fully considered. No 
one who is called on to deal with this class of case, in any capacity, 
should fail to make himself acquainted with this volume of 
Dr Tredgold’s, which is written from the point of view of the 
scientific physician, and is brought completely up to date. 


FREUD’S THEORIES OF THE NEUROSES. By Dr Eduard Hitsch- 
(423) mahn, Vienna. Translated by Dr C. R. Payne, New York. New 
York: The Journal of Nervous and Mental Disease Publishing 
Company. 1913. Pp, 154. Pr. $2.00. 

Dr Hitschmann’s purpose in writing this book is to furnish the 
reader with a synthetic account of Freudian theories on the nature 
and etiology of the various neuroses. It is intended to serve as an 
introduction to the study of Professor Freud’s works, and as a 
stimulus to the application of the methods of psychoanalysis to 
the problems of psychiatry: as the writer says, “it aims at 
separating from the ranks of the indifferent and antagonistic those 
whose position is due to insufficient or erroneous information.” 
The book provides a lucid and coifcise summary of the chief 
principles enunciated by Professor Freud, illustrated by clinical 



REVIEWS 


331 


examples and supported by evidence from the works of other 
investigators. It is in the main expository, and for that reason 
may be recommended to those who wish to possess a logical 
working acquaintance with Freudian theory. The translation is 
well done: footnotes and a good bibliography increase the value of 
the book from the point of view of the English reader. 


THE PSYCHOPATHOLOGY OF HYSTEBIA. Chablks D. Fox, M.D. 
(424) Richard G. Badger, The Gorham Press, Boston. 

In this book Dr Fox sets forth the modern psychological theory 
of hysteria as developed by Janet, Sidis, Morton Prince, and 
Freud. He is well acquainted with the literature of the subject, 
and he gives numerous cases illustrating the phenomena of the 
disease—some well known, others drawn from his own clinical 
experience. He adopts the view that all the functional neuroses 
are dependent upon disintegration of personality, that is, upon the 
activity of dissociated complexes; the terms neurasthenia, 
psychasthenia, hysteria, hypochondria, &c., indicate differences 
of degree in the dissociation; they do not correspond to any 
distinction of kind, but only to clinical syndromes, thus being 
useful merely as indicating what symptoms the physician may 
expect. 

Among those who accept this theory in a general way there 
are, it is well known, many minor differences of opinion. Freud’s 
views, for example, are not received in their entirety by men like 
Morton Prince. Dr Fox gives a brief but clear and accurate 
outline of Freud’s main theory : he does not criticise, nor does he 
go deeply into the most controverted doctrines, but it is probable 
that he himself agrees more closely with Prince than with Freud. 

With regard to treatment he says, “the most logical and 
effective form of therapeusis includes the discovery, by means of 
some psycho-analytic method, of the causal submerged complexes ; 
synthesis of these with consciousness; and, through the agency of 
psychic re-education, the removal of psychopathic tendencies.” 

In opposition to Freud he recommends hypnotism as a method 
of reaching the submerged complexes. He also gives brief 
accounts of Freud’s method of psycho-analysis and Jung’s word 
association method. 

Dr Fox seems to view with favour the opinion held by some 
modem authorities that hysteria is potential in all of us, though it 
does not seem easy wholly to reconcile this with his view that the 
disease is rarely cured. The manifestations, he says, “ can be 
removed easily in most cases, and the morbid temperament of the 
patient somewhat modified, but all the accidents continue to exist 



332 


BOOKS AND PAMPHLETS RECEIVED 


as potentialities which may become actual at any time, providing 
that sufficient provocation occurs.” 

The author’s style leaves a good deal to be desired. Many of 
his sentences are loosely constructed, and unattached participles 
abound; while a few gross grammatical errors have escaped 
correction. But, as a whole, the book may be cordially re¬ 
commended as giving a sane and well-balanced account of the 
nature and symptoms of hysteria in the light of modern research, 
together with indications of the best methods of treatment. 

Margaret Drummond. 


BOOKS AND PAMPHLETS RECEIVED. 

Auer, John. “The Effects of Intraapinal Injections of Serums with 
and without Preservatives” {Journ. Amer. Med. Assoc., 1914, Ixii., p. 1799). 

Fearntudes, E. Q. “Acute Poliomyelitis” ( London Hosp. Gaz ., 1914, 
xx., March). 

Fearnsides, E. Q. “Diseases of the Pituitary Gland and their Effect 
on the Shape of the Sella Turcica” ( Proc. Roy. Soc. Med., 1914, vii., 
Electro-therap. Sect., p. 46). 

Gregor, Adalbert. “Lehrbuch der Psychiatrischen Diagnostik,” mit 
7 Abbildungen. Berlin, 1914, S. Karger. Pr. M. 4.80; geb. M. 5.80. 

Klemm, Paul. “Die akute und chrouische Infektiose Osteomyelitis 
des Kindesalters.” Berlin, 1914, S. Karger. Pr. M. 9; geb. M. 10.20. 

Klinke, Otto. “ Die Operativen Erfolge bei der Behandlung des Morbus 
Basedowii.” Berlin, 1914, S. Karger. Pr. M. 4. 

Oppenheim, H. “ Gibt es eine zystische Form der multiplen Skleroset” 
{Neurol. Centralbl., 1914). 

Oppenheim, H. “ Uber Vortauschung von Tabes und Paralyse durch 
Hypophysistumor. (Pseudotabes pituitaria, &c ) ” ( Ztschr. f. d. get. 
Neurol, u. Psychiat., 1914, xxv. (Orig.)). 

Oppenheim, H. “ Zur Therapie der syphilitischen Nervenkrankheiten ” 
{Berl. klin. Wchnschr., 1914). 

Taylor, Alfred S. “Conclusions derived from further experience in the 
surgical treatment of brachial birth palsy” {Amer. Joum. Med. Sci., 1913 
cxlvi., p. 836). 

“ The Training School Bulletin.” 1914, xi., June. 



“Review 

of 

TReurologv ant> psvcbiatrv 

©dginal Hrticles 

DROP METHODS OF COUNTING THE CELLS OF 
THE CEREBROSPINAL FLUID —THE RELA¬ 
TION OF THE CELL-COUNT TO THE WASSER 
MANN REACTION. 

By R. DONALD, B.Sc. (N.Z.), D.P.H. (Oxf.). 

(Bacteriological Laboratory, London Hospital—Prof. W. Bulloch, 

M.D., F.R.S.) 

Plan of the Article. 

PAQB 


Introduction --------- 334 

Outline of other cell-counting methods ----- 335 

A drop-chamber method (suggested) ------ 336 

The drop-film method -------- 337 

Brief outline --------- 337 

Precautions taken in the investigation ..... 338 

Counting “kept” specimens is still useful ----- 338 

Swollen (degenerated) cells ------- 338 

Centrifuging to be avoided ------- 339 

Red cells to be allowed for ------ 339 

Technique of the drop-film method ------ 339 

Measuring the fluid by drops ------- 340 

Drying and fixing the drop-films, collodioning, staining, mounting - - 341 

Examining --------- 342 

A useful lamp device -------- 342 


Results Obtained. 

Clinical indications for the punctions ------ 343 

Classification of the cases—“crucial” division by the W.R. in one 
direction and by the cell-count in the otherdirection - 

27 


343 









334 


R. DONALD 


Notes on the Tables. 

PAGH 


Group I.—Serum-W.R. negative, without pleocytosis . - 344 

Group II.—Serum-W. R. negative, with pleocytosis - - - - 344 

Group III.—Serum-W.R. positive, without pleocytosis - - - 344 

Group IV.—Serum-W.R. .positive, with pleocytosis (only Group IV. has 

the c.s.f.-W.R. positive) - 345 

Sub-group IVa.—Untreated nervous syphilis .... 345 

Sub-group IV b, —Nervous syphilis much improved under treatment - 345 

Sub-group IVc.— Nervous syphilis less improved under treatment - - 345 

Parallelisms and divergences of the W.R. “curve” and the cell-count 

“curve ( 1 ) to (7) 346 

The meiostagmin test and Phase I. test ..... 349 

Notes on kinds of cells found 350 

Abbreviations and notation in tables and in text .... 351 


The Tables. 

Group I. tables are omitted. 

Group II. ... 

Group III. .... 

Group IV. ..... 

Group IVa. ..... 

Group IV6. ..... 

Group IVc. - - . . . 

Summary - 

Acknowledgments .... 


353 

354 

355 
355 
359 
363 

367 

369 


In connection with the research on “ parasyphilis 99 now being 
made by Drs M'Intosh, Fildes, Head, and Fearnsides 1 more than 
260 cell-counts have been done by the writer, during the past year 
or so, on the cerebro-spinal fluids submitted simultaneously with 
the sera to the Wassermann test by Dr Fildes. 

An interim 2 report on the first hundred cell-counts and 
Wassermann findings was published in September last. A 
considerable number of cell-counts have since then been similarly 
done, some on patients that had been repeatedly so tested before 
September. The results of the 260 cell-counts (collated, through 
the courtesy of the authors named, 1 with their Wassermann 
findings, &c.) are of sufficient interest to justify a further report. 

1 M'Intosh, Fildes, Head, and Fearnsides, Preliminary Report, Proceedings 
of the Neuropathologieal Section of the XVIIth International Congress of 
Medicine, London, 1913. Extended Report, Brain, Vol. xxxvi., Part i., July 
1913, and following numbers. ’ ’’ 

* Donald, Folia Htrmatoloyica, xvii. (1913), 139-166. 







DKOP-METHODS OF COUNTING CELLS 


335 


The drop-film method of cell-counting, used throughout this 
research, was worked out in counting the earlier specimens of 
cerebro-8pinal fluids. 

Other cell-counting methods may first be outlined. They are 
practically of three types. 

Methods of the first type, comprising the French method and 
Alzheimer’s method, use centrifuging to collect the cells into a 
thick deposit. 

By the French method a small, rather uncertain, quantity of 
the deposit is dried on a slide, stained, and examined. 

By Alzheimer’s method the c.s.f. is dropped into alcohol 
before centrifuging. The resulting small mass of coagulum 
is then embedded in celloidin, and sections from this are stained. 

These methods show the kinds of cells present in the centri¬ 
fuged deposit, and not the absolute cell-counts, but merely an 
empirical indication of the relative cell-counts of such c.s.fs. 
as have been examined by exactly the same technique. Even 
as regards the kinds of cells present, some cells, as will be 
shown below, 1 may be lost through centrifuging, which also 
probably more or less upsets the uniform distribution of the cells. 
Moreover in Alzheimer’s process the red cells will be destroyed by 
the alcohol, whereas, whether due to the puncture or due to 
previous haemorrhages, they ought to be estimated. Indeed most 
workers supplement the French result or the Alzheimer result by 
a chamber count. 

Methods of the second type give by means of counting chambers 
an estimate of the total cell-count of the c.s.f. The principal 
difficulty lies in distinguishing with ewe and certainty the 
various kinds of cells in the chamber. 

For c.s.f. one or even two fills of the Fuchs-Bosenthal 
counting chamber, the capacity of which is about 3 c.mm., is 
none too great a quantity to count through. The heavy cover- 
glass, 0*4 mm. thick, and the deep counting chamber, 0‘2 mm., 
necessitate a low power objective, while the thickness of the 
counting chamber floor hinders critical illumination. Now if 
the c.s.f. be examined unstained, as recommended by one 
worker, 8 narrow angle illumination must be employed, so these 
just mentioned three circumstances combine to call for such 
special skill and such patient effort as few can command. 

1 See p. 339. 8 Frenkel, Neurol. Centralbl., 1912, Nr. 31, 8. 1085. 



336 


fi. DONALD 


If, however, the c.s.f. can be satisfactorily stained in 
the counting apparatus, the process of observation will be 
considerably facilitated. A process that while staining the 
white cells destroys the red cells may at once be dismissed as 
misleading, unless when used by an experienced worker. The 
only staining process that promises facility in distinguishing 
clearly among the various types of cells, white and red, in the 
counting chamber is that recently described by Dunzelt. 1 This 
process, however, is described as requiring some considerable 
time for the staining of c.s.f. cells—indeed more than half an hour 
for the staining of the red cells in ordinary diluted blood. So, 
probably, several chambers would have to be provided if half a 
dozen c.s.fs. had to be dealt with in a sitting. 

Suggested Drop-Chamber Method. —For the simultaneous 
mounting in chambers of any number of c.s.fs., to be examined 
alternately or repeatedly, eg., for comparison of the cells, there 
may here be suggested a simple and efficient device, suitable also 
for dark-ground illumination. 

For each chamber there is taken an ordinary clean slide of the 
thickness suitable for the dark-ground condenser, and to its under 
side is applied a drop of immersion oil. Then on the upper side 
are placed a pair of slips of ordinary cover glass about three- 
quarter inch apart. Midway between these slips is deposited one 
Morse 80 drop 2 of c.s.f. Then without delay there is lowered on to 
the drop a clean ordinary cover glass, say 1 by £ in., to rest on the 
placed slips. Vaseline may be used to steady the parts of this 
simple chamber, as also to prevent drying, especially if the drop 
(deposited on a spot previously wetted with HgCl, and then dried) 
is to be kept some little time. It is well that the two slips be not 
grossly unequal in thickness or the liquid will be drawn into the 
thinnest part of the chamber. 

Of course, the thinner the equal supporting slips are chosen 
(from cover glasses 0*10 to 0'20 mm. thick), the larger proportion¬ 
ately is the area of the spread-out drop. The volume of a Morse 80 
drop of average c.s.f. is 7| c.mm. Accordingly, the area of the drop 
with supporting slips 015 mm. thick is 7*5/0*15, i.e., 50 sq. mm. 

Such a chamber is well adapted for dark-ground illumination, 2 

1 Dunzelt, Miinchener med. Wochenschrift, 1913, 8. 2616. 9 See p. 340. 

* Ruled counting chambers have too thick a floor for use with ordinary 
dark-ground condensers. 



DROP-METHODS OF COUNTING CELLS 337 

and the whole area may easily be scanned with a medium-power 
objective and a moderately high eyepiece. But the chamber is 
easily within the working range of a 4 mm. objective, and 
practically within the ordinary collar-correction range, if thin 
cover glasses and thin supporting slips are used. 

Of current methods of cell-counting, there remains to be 
described a third type, represented by Geissler’s ruled slide method, 
devised to^ive in a stained film both a numerical and a qualitative 
count. On a space 20 by 20 mm. ruled with parallel lines on an 
optically finished slide, 40 c.mm. of the cerebro-spinal fluid is 
deposited by means of an accurately graduated capillary pipette. 
After drying and heating in an incubator, the film is fixed by 
alcohol-ether mixture (one to two minutes), and is stained with 
Pappenheim-Unna stain or with Leishman stain, then soaked 
carefully in water and gently “ blotted.” Various other workers 
had estimated the cell-count, by counting through some subjectively 
chosen fields in dried films from a known volume of c.s.f. But 
Gewsler makes an “ objective" estimate by counting through the 
whole 40 c.mm. film. 

Unfortunately, this method demands very special skill. 
Ordinary skill can hardly stain and wash such films without con¬ 
siderable loss of cells. Moreover, in examining, as recommended, 
uncovered films with a dry lens, the details of the cells will be 
imperfectly made out unless the lens is specially constructed. 
Thirdly, the slide is expensive, and the preparation cannot be 
kept for reference, but the slide has to be cleaned off, with 
special care, till under the microscope it is Been to be quite free 
from cells. 

The drop-film method of cell-counting described in this article 
avoids some of the disadvantages of the above-mentioned methods, 
and combines most of their advantages in a simply-prepared 
permanent preparation. 

On each of any number of ordinary slides, a couple of separate 
drops of the c.s.f. are easily and accurately deposited, and 
then dried and fixed. Next the slides are Boaked for a few 
seconds in dilute collodion, and dried. Thus are obtained drop- 
films that are practically thin collodion sections at most only one 
dried cell in thickness. These films can now at leisure be stained, 
e.g. y Giemsa, or Leishman, and Pappenheim-Unna, washed, and 
dried, without the loss of even a bacterium from the film, A 



338 


R. DONALD 


cover glass attached with clear soft paraffin completes a permanent 
preparation that gives easily an accurate cell-count, and at the 
same time a good cell-picture. The variously stained preparations 
are permanent for reference and for comparison. The method 
uses no special apparatus and avoids centrifuging. 

Some details of the drop-film method may now be given. 
Other details are given in a preliminary article in Folia Hoemato- 
logica. 1 ' « 

First may be mentioned some precautions taken. 

The c.8.fs. were counted as soon as possible after puncture. 
But a good many were not available until a day or so old. 
However, by counting early in the research a number of c.s.fs. of 
various types when fresh, and then again when twenty-four hours 
old, it was found that at ordinary laboratory temperatures the loss 
of cells in the twenty-four hours was negligible, 2 if the cells now 
swollen in degeneration were stained and counted in. 

Even after being kept nearly a week at laboratory temperature, 
averaging 15* C., aseptic specimens of c.s.f. were found to yield a 
useful indication of pleocytosis, especially when the preparation 
was stained strongly and clearly with Giemsa or with Leishman stain. 
For instance, the c.s.f. of F. S., case 134, taken on the evening of 
May 11,1914, showed next day thirty-one cells per c.mm. Another 
tube of the same specimen, kept at laboratory temperature 
averaging 15° C. till May 16, 1914, showed fourteen cells per 
c.mm., 75 per cent, of these being, indeed, considerably swollen. 
Similarly a c.s.f. left by mistake undelivered for fully six days at 
about 15° C., was on April 15, 1914, found to have forty-two 
cells per c.mm., about 50 per cent, of them being swollen. (J. W., 
case 80. The fresh c.s.f. had probably over a hundred cells.) 

So the c.8.fs. not available for a day or so could thus be 
reliably counted, especially as for most of the time they were kept 
in an ice-safe. 

These swollen cells were, by strong clear Giemsa or Leishman 
staining, found to arise in large numbers in many c.s.fs. a day or 
so old, from the degeneration of cells, mononuclear and polynuclear, 
that were unswollen in the fresh fluid. Also similar swollen cells 
were seen to occur in considerable numbers in some freshly drawn 

1 Donald, Fol. Ham., xvii. (1913), 139-166. 

9 Donald, Fol. Ham., xvii. (1913), 144. Contrast Bigelow, Amir. Joum. of 
Inanity, lxvii. (1911), 746. 



DROP-METHODS OF COUNTING CELLS 339 

c-s-fs., 1 indicating the activity of cell passage into the c.s.f. The 
swollen cells have, accordingly, in this research been included in 
the total cell-count. 

Centrifuging was avoided. It was found to be a disturbing 
factor difficult to deal with. Various c.s.fs. 2 were counted just 
before centrifuging, and again after centrifuging and agitating. 
The loss of cells after this treatment proved in the seven experi¬ 
ments to vary from a negligible quantity to 50 per cent, of the total 
count, the greatest loss being of the swollen degenerating cells. 

Any red cells present were demonstrated, counted, and allowed 
for 8 according to a leucocyte count done, by a drop-film, on the 
patient’s blood. 

If the ordinary Fuchs-Rosenthal counting method be used, 
then, as Dreyfus recommends, 4 any considerable blood admixture 
must be avoided in performing the punction, or else not much 
reliance must be placed on the result. But an important c.s.f 
may at two consecutive punctions 6 happen to be the only blood- 
mixed specimen in half a dozen; and, if a suitable method is used, 
then, in spite of the red cells—nay, by their assistance—a 
practically reliable count is usually possible. 

Clotted blood in the specimen, of course, prevents a count. 

The technique of the drop-film method is as follows:— 
The slides are polished with a tuft of long-fibre grease-free cotton 
wool. Before receiving the drops of c.s.f. they are conveniently 
marked with a quill pen and, e.g., a waterproof Iudian ink. 
This writing, when later collodioned, stands either wetting or 
reasonable rubbing, though hardly both at once. 

The specimen was shaken thoroughly just before measuring. 
Even fine gauzy blood-free clots could then be well distributed. 
A small square of washed smooth sheet rubber and the thumb are 
convenient for closing the tube in shaking. 

1 These findings are in line with those of Rous, of Rubinato, and of others; 
Rous, Amer. Joum. Med. Science, 1907, p. 667; Cornell, Amer. Joum. of 
Insanity, 1907-8, Vol. 64, p. 73; Villaret et Texier, Joum. de Physiologie et de 
Pathologie gintrale , 1905, VoL 7, p. 841 (quoted by Rous); Rubinato, Fol. 
Hamatologica, 1905, Bd. ii., 8. 781; Turner, Joum. of Mental Science, July 
1910, p. 485. 

2 Donald, Fol. Ham., xvii. (1913), 146, 147. 

* Rous, Amer. Joum. of Med. Science , 1907, April, 567 ; Bigelow, Amer. 
Joum. of Insanity, lxvii. (1911), 745. 

4 Dreyfus, Miinchener medizinische Wochenechryft, 1912, 2567. 

• E.g., A. C., case 84; cf. A. P., case 97, pp. 359, 361. 



340 


R. DONALD 


Measuring' the c.s.f. was carried out by the easily calibrated 
dropping-pipettes, described in a recent brief communication 1 to 
the Royal Society. 

Pipettes, with body about 4 cm. long, are drawn from glass 
tubing about 3 mm. external diameter heated in a large by-pass of 
a Bunsen burner. They are then pushed gently down into the 
suitable hole of a wire gauge until just arrested, and are cut off 
close to the upper surface of the plate. A convenient size. No. 80 
of the Morse drill and wire gauge, is 0‘34 mm. in diameter. A 
clean pipette of this size will, when held vertical, yield, at a 
drop-rate not faster than one per second, at ordinary laboratory 
temperature, a drop of average c.s.f. 1/135 c.c. in volume. The 
pipette-capillary must be quite clean, and must be carefully kept 
from contact with any trace of greasy matter. A fresh pipette is 
used for each specimen measured out 

The required slow steady rate of dropping can be conveniently 
attained by means of a small mercury-plunger tube. 8 In use, this 
is held at such an angle that the drop-rate is not faster than 
one per second. At all rates slower than one per second a 
dropping-point as small as 0*3 mm. in external diameter yields, of 
a given liquid at a given temperature, drops that are practically 
constant in weight 3 

To prevent settling down of the cells in the pipette, during 
the depositing of a number of equal drops on slides, the pipette 
may be furnished with a bulb blown just above the capillary part 
before gauging. During the blowing, the pipette may be held at 
visual distance in a short rubber tube attached to a glass blowpipe. 
An almost closed U of clean copper wire dropped into the bulb 
will serve as a shaker without any ball-valve action. 

1 Donald, Proc. Royal Society, B., Ixxxvi. (1913), 199. 

3 Made thus: A piece of clean dry tubing 12 to 13 mm. long and 1} or 2 mm. 
bore, is opened out slightly funnel-shaped at each end, one end is tightly plugged 
with grease-free cotton wool, the tube is filled two-thirds with clean meroury, the 
other end is tightly plugged with cotton wool, and a short pieoe (about 3 cm.) of 
rubber tubing is fitted for attachment to the small pipettes.—Donald, Lancet, 
1913, i., 1447. 

To secure elastic air-tight fitting, the rubber tubing may have an external 
“ sphincter ” formed of several turns of a very small rubber ring. This 
“ sphincter ” is rolled back, the small pipette is inserted, and the sphincter rolled 
down over it. 

* OUivier, Annales de chimie el de physique, S4r. 8, Tom. x. (1907), p. 229; 
Donald, Proc. Royal Society, Series B, 1913, Vol. Ixxxvi., p. 198. 



DROP-METHODS OF COUNTING CELLS 


341 


The drops are conveniently dried at a temperature of about 
37° C. on, e.g., a copper fixing-plate covered with several folds of 
blotting paper. 

The drop-films must be fixed by a water-free process, for any 
water treatment of such a crust (of much soluble salt with, often, 
few cells and a mere trace of albuminous matter) is, even after 
fixation, altogether too precarious. 

Heat-fixation, if thorough, is simple and satisfactory. 

Heat-fixation under observation served, in the case of one 
c.s.f., to suggest by the smell of ammoniacal fumes the pres¬ 
ence of urea in the specimen. Further tests confirmed the 
suggestion. 

Fixation by alcohol may be used for Pappenheim stain, but 
the alcohol must be absolute. 

Next comes the collodioning of the drop-films. While they 
are still warm and dry, the slides are stood upright back to back 
for a few seconds in a jar of dilute collodion (1 part collodion B.P. 
with 9 parts alcohol and ether mixture). Then they are kept 
upright to drain and to dry, with the least possible injury to the 
collodion coating. Finally they are heated gently on the fixing 
plate to dispel the last trace of alcohol, and so to render the 
delicate film unlikely to be detached even by staining for 
tubercle bacilli 

Staining may be done as required. 1. For showing up all the 
cells, including the swollen cells, and the ordinary stainable micro¬ 
organisms, dilute Giemsa or Leishman stain may be left in a 
plump pool on the surface of the drop-film for about twenty minutes. 
A large pool of dilute, e.g., Leishman, stain rocked from time to 
time will dissolve out the salts, and so prevent some of the stain 
pattern otherwise left. The use of warm stain in the incubator 
dissolves out the salts and stains the film in half the time. The 
stain is washed off with distilled water, containing about one part 
of acetic acid in 20,000. This is left on for two to five minutes, 
to remove the excess of stain adsorbed by the alkaline salts, and 
to bring up a distinct red in the erythrocytes. Then a rinse with 
the same, and gentle drying with blotting paper, pressed down by 
a soft pad of gauze and cotton wool. On the warm drop-film is 
melted the minimum quantity of clear soft paraffin, and the 
cover-glass is well pressed down. If the procurable soft clear 
paraffin is not optically fairly free from crystallising-out scales of 



342 


R. DONALD 


higher homologues, then the minimum quantity of thick paroline 
may be used. Such preparations are apparently permanent. 

If any paraffin gets on to the upper surface of the cover glass it 
is not so easily cleaned off as cedar oil would be, to leave the 
cover glass bright and clear. The simplest plan is to put on a 
clean cover glass. 

If the paraffin has for any reason to be washed off a Giemsa 
drop-film or other Romanowsky preparation, ligroin or other 
paraffin spirit of similar boiling point ought to be used, not an 
aromatic hydrocarbon such aB xylol, which dissolves out some of 
the stain. 

2. For showing up the finer structure of the cells, a drop-film 
similarly stained for about ten minutes may be mounted. 

3. Any plasma cells present may be demonstrated by Unna- 
Pappenheim stain (pyronin-methyl green). About ten minutes at 
37° C. will suffice. The stain is rinsed off with tap water and 
finished as described. This stain, of course, shows up in pyronin 
red any yeast cells, which, occurring singly in a Giemsa preparation, 
might by cursory low power observation be mistaken for 
micro-lymphocytes. 

If Unna-Pappenheim staining is at all prolonged at 37°, the 
preparations ought to be kept under an air-tight Petri cover on 
a glass plate with a piece of cotton wool wet with alcohol and 
phenol to prevent loss of those substances. 

4. To show up either gram-positive or tubercle bacilli the 
corresponding stains are used in the ordinary way on the film. 
After decolorising by 90 to 95 per cent, alcohol, the gram film is 
gently blotted and then dried before the watery neutral-red 
solution is used. 

Before examination of the slide the collodion may be rubbed 
off the under side with a damp duster. 

Examination of the stained drop-film may be done by powers 
of 120 diameters upwards. A good system of 240 diameters, if 
skilfully used, is sufficient for most differential counts. 

Illumination is, of course, of great importance for rapid certain 
work. A good simple lamp device may be suggested. Vertical 
and on a level with the microscope mirror a small square, say 
6 by 6 cm., of light opal glass in a simple lantern is strongly 
lighted by a 32 c.p. metal-filament lamp at the focus of a 
hemispherical mirror. Not the reflected light from the mirror, 



DROP-METHODS OF COUNTING CELLS 


343 


but only diffused light from the front of the opal glass is used; so 
the mirror may be merely the silvered back-hemisphere of a 
spherical lamp, or even the bright tinned hemispherical bowl from 
a kitchen ladle cut to accommodate a pear-shaped lamp. 

Veiy useful for counting a cell-rich film is a square eyepiece 
diaphragm with cross-lines. If the professionally-made appliance 
is not available, a substitute may be made of black paper with 
three or four parallel lines of a fine black hair laced, across the 
square opening, through needle holes, and fastened at its two ends 
by a touch of sealing-wax soldered down with a hot wire. Ruled 
glass eyepiece “ diaphragms ” do not improve definition. 

But, at any rate for cell-poor films, the ordinary circular 
eyepiece diaphragm can be made to suffice. And even a very rich 
film may be reckoned up by measuring the number of times that 
the diameter of the circular field is contained in the mean diameter 
of the nearly circular drop-film, squaring this number, and then 
multiplying by the average number of cells per field. 

A mechanical stage is practically essential. 

Results Obtained by the Method. 

In the patients on whom the 250 cell-counts were done 
lumbar punction was found advisable, either on account of 
probable meningitis without syphilis, or on account of possible 
meningitis with syphilis that was, in many cases, syphilis with 
evident nervous disease. 

By the courtesy of the above-named authors, hitherto un¬ 
published tables of Wassermann results have been lent as a setting 
for the cell-counts. 

As the most important conclusions drawn from the considera¬ 
tion of the cell-counts are connected with cases of pleocytosis in 
syphilitic nervous disease, we classify our matter so as to dispose of 
the other, less important, cases first. 

Classification of the Cases. 

The serum-WR and the cell-count may be used as “ crucial ” 
dividing tests, marking off the cases into four groups, as follows:— 

Group L—Serum-W.R negative, without pleocytosis. 

„ II.—Serum-W.R negative, with pleocytosis. 

„ III.—Serum-W.R. positive, without pleocytosis. 

„ IV.—Serum-W.R. positive, with pleocytosis. 



344 


R. DONALD 


The c.s.f.-W.R does not disturb the distribution that we have 
just made. For it comes out positive practically only in cases 
with both (1) positive serum-W.R, and (2) pleocytosis—that is, 
only in the most important group, IV., which we shall consider 
in detail after disposing of the other groups, I. to III. 

As the tables of Group I. possess interest in general rather 
than in detail, they are not printed in this article. 

They concern the cases with the W.R. negative in serum 
and in c.s.f. and without pleocytosis. 

These cases number 62, and include:— 


Peripheral neuritis 4 

Subacute combined de¬ 
generation 2 

Amyotrophic lateral sclerosis 1 

Non - syphilitic progressive 

muscular atrophy - 2 

Poliomyelitis (old) - - 1 

Spastic paraplegia - - 2 

Cerebro spinal tract lesion - 1 

Friedreich’s ataxy 1 

Neoplasm of cord 1 

Neoplasm of the vertebrte - 1 

Hsematomyelia 1 

Cerebral neoplasm - - 5 


Non-syphilitic cerebral and 

bulbar thrombosis - 2 

Labyrinthine disease 

(Meniere) - - - 2 

Neoplasm of ilium • - 1 

Gallstones 1 

Gallstones c. congenitally 
abnormal pupillary re¬ 
action- 1 

Non-syphilitic myocardial 
failure 1 

Epileptiform seizures - - 1 

Paranoia - - - 2 

Simple amentia 1 


In these 62 cases the cell-count rarely reached 4 per c.mm. 
In one case of neoplasm of the left crus cerebri, the cerebro-spinal 
fluid showed 10 cells in 7£ c.mm., while the ventricular fluid 
taken at operation showed no cells in the same volume. 

The cases in Group II. (serum-W.R. negative, and c.s.f.-W.R 
negative, but with pleocytosis), number 14. Taken along with 
the cases of syphilitic meningitis (of Group IV., to be dealt with 
presently) they illustrate the recognised fact that the cell-count 
indicates the activity of the meningeal reaction rather than the 
nature of the infective virus. One non-fatal case of meningitis 
showed 1500 cells (80 per cent, polymorphonuclear, and 1 per 
cent, plasma cells, the rest being lymphocytes). Other cases of 
non-syphilitic meningitis had cell-counts equalled by those of 
syphilitic meningitis. 

Group III., p. 354, consists of some thirty-five cases with 
serum-W.R. positive, but, at the time of observation, c.s.f.-W.R 
negative. 



DROP-METHODS OF COUNTING CELLS 


345 


Some of these cases have become c.s.f.-W.R. negative through 
treatment. 

Others again, e.g., M. C., case 19; W. C., case 21; G. C., 
case 22; E. H., case 24; C. K., case 25, are of special interest, as 
illustrating a fact pointed out by the authors 1 already mentioned, 
namely, that in the cerebral type of cerebro-spinal syphilis, 
the c.s.f.-W.R. either is only weakly positive or is negative. 

Group IV. consists of all the cases with the serum-W.R. 
positive and with pleocytosis. Practically speaking, all these 
cases, and only these cases, have, or had, or would have had, the 
c.s.f.-W.R. positive. If at first observation of these cases the 
c.s.f.-W.R. is negative, it is so because treatment either has made 
it negative or has prevented it from becoming positive. 

By their relation to treatment the cases are divided into 
three sub-groups:— 

First, untreated cases forming sub-group IVa. 

Second, cases much improved under treatment, sub-group IVi. 

Third, cases less improved under treatment, sub-group IVc. 

Sub-group IVa., p. 355, is made up of untreated cases, diagnosed 
with certainty through the indisputable aid that recent laboratory 
methods have brought to clinical observation. In many of the 
patients at the time of first observation it is impossible to say 
whether the condition is to be called “ cerebro-spinal syphilis,” and 
a hopeful prognosis given, or whether it belongs, or may presently, 
especially if no treatment now be applied, belong to the clinical 
group “ parasyphilis," with its relatively hopeless prognosis. 

But here come in alike the value of treatment and the value 
of modern methods in controlling treatment. The tables, of 
consecutive cases, merely re-grouped in this article, indicate, in 
sub-group IV£>. and sub-group IVc., p. 359, just how much the 
W.R. and the pleocytosis can be modified by intravenous injections 
of neo-sal varsan. In subsequent articles the authors mentioned 
will show that in the cases of sub-group IV6. (“ cerebro-spinal 
syphilis ”), the fall in the W.R. and in the cell-count is followed 
by actual improvement in function, which improvement in some 
cases proceeds to the recovery of good bodily health with some 
mental improvement, and in other cases amounts to practically 
complete recovery, e.g., F. J., case 92. 

Moreover, they will show that, even in the cases of sub-group 

1 M'Intoeh, Fildes, Head, and Feanuides, Brain, xxxvi., July (1913), p. 17. 



346 


R DONALD 


IVc. (“ parasyphilitic ” cases), considerable clinical improvement 
takes place in some cases, corresponding, no doubt, to some arrest 
of the inflammatory processes, though not to resolution of any 
secondary degenerations. 

Parallelisms and Divergences of the W.R. Curve 
and the Cell-Count Curve. 

Examination of the figures in Group IV. will show interesting 
parallelisms and divergences of, as it were, the W.R. curve and the 
cell-count curve. 

1. The c.s.f.-W.R. and the cell-count may fall together, either 
(a) under treatment, or ( b ) without treatment. 

(a) In seven cases the fall in the c.s.f.-W.R. and in the cell- 
count took place under treatment, and was followed by clinical 
improvement:—A. A., case 81; probably C. B., case 82, and D. B., 
case 83, although the specimen for the high cell-count in these 
two cases was not secured; J. G., case 89; F. J., case 92; E. W., 
case 105; W. Hr., case 122. 

(b) In two other cases the fall occurred without treatment, 
but the fall was slight, and merely no fresh manifestations of the 
disease appeared:—W. H., case 120; D. S., case 130. 

Similarly, a cell-count already near normal may, under treat¬ 
ment, fall still further along with some fall in the W.R.:—F. P., 
case 99. In this patient there has been continued fall in the 
W.R for the nine months since the cell-count reached 1 per c.mm. 

2. The c.s.f.-W.R. and the cell-count may rise together some 
time after treatment, probably through a recrudescence of the 
disease after insufficient injection of the drugs:—W. G., case 
90; G. P., case 98; A. B., case 106; A. G., case 117; Wm. G., 
case 118. 

These are our only instances of pleocytosis increasing after 
treatment with neo-salvarsan had been applied. They are 
probably all instances of relapse, and not of a pleocytotic rise 
provoked by salvarsan. 

In A. B., case 106, the c.s.f.-W.R. and the cell-count did 
improve after treatment, and then relapsed. G. P., case 98, showed 
recrudescence to W.R. 4444 2/44443 six months after treatment, 
then, after further vigorous treatment, the W.R. fell to 0/42000. 

3. In two classes of cases the very coincidence of negative 



DROP-METHODS OF COUNTING CELLS 347 

W.R. with negative cell-count is of interest, (a) cerebral syphilis 
and gumma cerebri (Group III., p. 354), probably examples of 
purely cerebral lesions, whether meningeal or not, “ when the 
cerebro-spinal fluid usually yields a negative reaction,” 1 (6) E. I., 
case 124, a naturally arrested case of tabes dorsalis. 

4. The cell-count may begin to fall sooner than the c.s.f.- 
W.R.:—S. 0., case 62; C. C., case 112; V. W., case 138. The 
cases mentioned in (6) are more advanced instances of this. 

5. The cell-count may remain high after the W.R. has fallen 
to 0:—F. R., ease 100; G. W., case 136. “ In both these patients 
the strength of the W.R. at the time of first observation was small, 
and the affection was in the region of the exit of the third cranial 
nerve. In case 100, the lesion was apparently basal; in case 136 
it was a thrombotic lesion giving rise to Weber’s syndrome.” 

6. The c.s.f.-W.R. usually falls more slowly than the cell-count, 
and may even for some time after the cell-count has reached 
normal (A. C., case 84; R. G., case 91; F. P., case 99; M. S., case 
102; F. G., case 119; T. M., case 127; F. S., case 134), still remain 
of appreciable strength, indicating that, even so far as concerns the 
c.s.f. and the tissues represented by the c.s.f., there is still an 
indication of unresolved mischief. Moreover, the serum-W.R. 
usually falls still more slowly, thus prolonging the warning:— 
F. P., case 99; M. S., case 102; E. W., case 105, and e.g., the other 
cases quoted under (1), p. 346. 

We may here remind ourselves that the c.s.f., and the tissues 
represented by it, constitute by no means the whole patient, and 
that, valuable as are these three signs (serum-W.R., c.s.f.-W.R., 
and cell-count), they have their limitations. 

But they have also their great significance, namely, that in the 
case of disappearance of even only two of them, c.s.f.-W.R. and 
pleocytosis, the neo-salvarsan injected into the blood-stream has 
reached the diseased meninges, and has profoundly affected the 
lesion to the patient’s benefit. 

It might suggest itself that the W.R. and syphilitic pleocytosis 
are caused by the presence of the same substance in the c.s.f., 
inasmuch as these two signs practically always occur together 
in the c.s.f. in nervous syphilis—as was pointed out in the remark 
on Group IV., p. 344. However, the tables of Group IV. indicate 
pretty consistently that in nervous syphilis pleocytosis (1) often, 

* Brain , xxxvi., July (1913), pp. 20, 28, note 5. 



348 


R. DONALD 


or perhaps always, appears before the W.R. in the c.s.f., and (2) 
often, or generally, disappears before the W.R. has disappeared. 

Now the earlier appearance of pleocytosis might suggest that a 
small amount of the just-appearing Wassermann substance suffices 
to stimulate pleocytosis. But the disappearance of pleocytosis 
while the W.R. is still strong indicates that the substance exciting 
pleocytosis is distinct from the Wassermann substance. 

The fact that these two tests are, as it were, independent 
witnesses, renders their concurrent testimony of much greater 
value. 

7. Pleocytosis may appear and even rise high before the 
W.R. appears in the c.s.f.:—A. M., case 59; W. G., case 90; E. W., 
case 104. 

This very important sign is, especially in these days of neo- 
salvarsan, at once acted on; and prompt treatment prevents the 
appearance of the confirmatory W.R. in the c.s.f. 

The following note on W. G., courteously supplied for this 
article, will be read with interest. 

“Clinically W. G. showed on his first admission to hospital 
merely subjective manifestations—malaise and pains in various 
regions—together with pyrexial attacks.” 

The brisk mercurial treatment applied resulted in apparent 
recovery, followed, however, two years afterwards by a recurrence 
with more severe pyrexial attacks. 

“ On his second admission, however, evidence of irritation of 
certain spinal nerve roots was forthcoming. This irritation 
disappeared within 36 hours after the first injection of neo- 
salvarsan. The presence of the root irritation gave a reasonable 
explanation for the cytological findings.” 

Of further interest is the case of C. G., case 44. This patient, 
with the secondary rash at its height, had W.R. 44444/44000 and 
a pleocytosis so high, 153, as to suggest that it might have appeared 
before the W.R. in the c.s.f. The methods of investigation used by 
Dr Head and Dr Fearnsides demonstrated irritation of some spinal 
nerve roots within four months of infection. J. W., case 80, is 
also a case of nervous disease in secondary syphilis. 

Instances (4), p. 347, and (7), p. 348, of divergences of the 
cell-count “curve” from the W.R "curve,” show that, both in 
the diagnosis of early cerebro-spinal meningitic disease, and in 
indicating progress under treatment, the cell-count is, on the whole, 



DROP-METHODS OF COUNTING CELLS 


349 


a more sensitive but not less reliable indicator than the W.R., and 
is certainly a diagnostic means that ought not to be neglected, 
especially when, in any case, the c.s.f. has been procured for the 
Wassermann test. Indeed, the W.R. and the cell-count are, of 
course, not rival diagnostic tests, but are mutually supplementing, 
mutually correcting, mutually supporting—just as the combined 
arguments of such laboratory findings, on the one hand, and the 
combined arguments of clinical findings on the other hand, are not 
rivals, but are co-operating combined arguments to show up clearly 
the condition from time to time of the patient. 


The Meiostagmin Test and Phase I. Test. 

Some work was done on two other tests. 

The meiostagmin test, performed by means of the author’s 
constant-pressure dropping apparatus, 1 was tried on a number of 
the earlier specimens after the Wassermann test. But the greatest 
fall in surface tension took place by no means always in the 
W.R.-positive c.s.fs. 

Phase I. test was done on most of the specimens. Usually the 
degree of opalescence, measured merely by the eye, was roughly 
proportional to the number of cells present, or to the W.R., 
whether meningeal affection was aljsent or was caused by any 
form of syphilis or by tubercle. But in other cases the opalescence 
was far from proportional either to the W.R. or to the cell-count. 
For instance, sometimes a case with W.R. negative in serum and 
in c.s.f. and with one cell per c.mm., showed more of opalescence 
than a case with W.R. positive in serum and in c.s.f. and with 
thirty-five cells. These apparent anomalies indicate the need for 
considerable experience in using this test and for considerable 
judiciousness in interpreting its findings. 

One source of possible error is serum globulin remaining in the 
c.s.f. after the corresponding few red cells have broken up and 
are represented by only a faint straw colour, easily missed by 
artificial light. 

In S. O., case 62, tabes dorsalis, the test gave a nearly opaque 
white, although two years before, with a very similar Wassermann 
result. Phase I. test had given “ only a slight opalescence.” 

1 Donald, Proc . Royal Society , 1913, Vol. Ixxxvi., pp. 198-202. 

28 



350 


R. DONALD 


Notes on Kinds of Cells Found. 

The cells of c.8.f. have been described by Cornell, 1 by Szecsi, 2 * * * * 
by Plaut, Rehm, and Schottmiiller, 8 and by others. 

Of the various cells demonstrated in this investigation, some 
kinds call for special mention. 

Plasma cells were found, forming 0 2 to 3 per cent, of the 
cell-count in syphilis meningo-vascularis, syphilitic encephalitis, 
tabes dorsalis, general paralysis, juvenile general paralysis, also 
in the meningitis of secondary syphilis, and in the following 
non-syphilitic conditions:—Disseminated sclerosis, hydrocephalus, 
cerebral haemorrhage, and in two non-fatal cases of meningitis of 
which the causative organism did not grow in culture. 

In the case of juvenile general paralysis (A. B., case 106), 
plasma cells were found in nearly the same percentage in the 
three specimens taken during the nine months after injection of 
1-8 g. of 914. 

One case of the meningitis of secondary syphilis (C. G., 
case 44) had 3 per cent, plasma cells, with 75 per cent, of 
polymorphonuclears in a total cell-count of 154. 

Polymorphonuclear leucocytes were found in the meningitis 
of secondary syphilis, as just mentioned, and in smaller proportions 
in some other cases as shown in the tables. 

Where not otherwise specified, the total cell-count or the 
balance consisted of lymphocytes. 

Swollen (degenerated) cells, whether present in the fluid when 
drawn, or developed later from sound cells, were included in the 
cell-counts as given. 

The total cell-count is, as shown in the tables and in the notes 
on them, of special value. 

The fairly large number of cell-counts considered above shows 
a remarkable concordance. For the periods, up to eighteen months, 
the successive counts, as many as five, of each case, are consistent 
with one another, and are, in nearly all the cases, roughly “ pro¬ 
portional” to the simultaneous Wassermann figures. The few 

1 Cornell, Amtr. Journ. of Insanity , 1907-8, Vol. lxiv., p. 73. 

2 Szecsi, Monatsechr. /. PsychicU. u. Neurol ., Bd. xxix., S. 76-82 ; Ztitschr .. /. 

d. ges . Neurol, u. Psychiat. Or., 1911, Bd. vi., 8. 637; Fol. Homed., 1910-11, 

Bd. x., Archiv ., 8. 534. 

* Plaut, Rehm, und Schottmiiller, Leitfadm zur Untermchung dtr Zertbro- 

spinalfliissigktit , Jena, 1913. 



DROP-METHODS OF COUNTING CELLS 351 


divergences of the cell-count from this rough “proportionality” 
are highly significant, and are consistent with the patient’s clinical 
condition. 


Case 90, F. P. 

44443/44443 

5 

44441/44400 

3 

44440/44200 

1 

4444-/44400 

1 

44440/30000 

1 

Case 98, 6. P. - 

0/44100 

85 

44442/44443 

90 

44200/44400 

3 


0/42000 

4 

Case 124, E. I. - 

20000/0 

1 

22000/0 
about 1 

20000/0 

1 

... 

... 

Case 107, A. B. - 

44444/44420 

46 

2 per cent, 
plasma cells 
5 per cent, 
polymorph. 

44440/44000 

21 

1 per cent, 
plasma oells 
3 per cent, 
polymorph. 

44440/44440 

38 

1 per cent, 
plasma cells 
1 per cent, 
polymorph. 



Case 89, J. G. - 

44444/44443 

44443/44300 

16 

44100/0 

4 

0/0 

2 

... 

Case 92, F. J. - 

44430/44440 

63 

44444/44000 

19 

44440/0 

2 

... 

... 

Case 120, W. H. 

43200/44300 

12 

43100/42000 

... 

... 


Case 122, W. Hr. 

44444/44400 

44 

44430/40000 

34 



... 

Case 125, F. K. - 

44442/44440 

44 

44444/44300 

6 

... 


... 


The many other cell-counts obtained in this research are all 
similarly consistent with the just-quoted counts. 

In face of this concordance in the cell-counts, we may assume 
that in the subarachnoid space, or at any rate in the part of it 
reached by lumbar punction, the cells are to a considerable extent 
maintained in suspension—by alterations in body-posture and in 
the amounts of blood within the bony spinal canal. 1 

Explanation of Abbreviations and Notation. 

The case numbers as assigned are merely for convenience in 
referring to the cases in this paper. 

1 0. Fischer found in P.M. subjects different cell-counts at different levels of 
tapping (Monatsschrifl fur Psychiatric und Ntwrologity June, 1910). Summarised 
in Folia Hcematologica. 






352 


R. DONALD 


The few necessary abbreviations will be readily understood— 
“606” for “salvarean,” “914” for “neosalvarsan,” “914-serum” 
for "neo-salvarsanised serum,” “S.” for “syphilis,” “Sc.” for 
“ syphilitic,” “ c.s.f.” for “ cerebro-spinal fluid.” 1 

The notation of the W.R. results is explained in the words of 
the authors above referred to. 2 

“Throughout this investigation we record the results of the 
W.R. in this form. The test is quantitative, and falling doses of 
serum and cerebro-spinal fluid are used. Formerly we followed 
the usual method of recording the reaction and represented 
complete inhibition by + + + + and incomplete inhibition by 
+ + +,++, or +. To economise space these would now be 
written 4, 3, 2, or 1. The figures 4, 4, 4, 4, 4 imply that the 
reaction was complete in each of the five dilutions, whilst 
4, 4, 4, 0, 0 shows that the reaction was complete in the first three, 
but negative in the last two dilutions. Such results as 2, 0,0, 0, 0 
or 1, 0, 0, 0, 0 have no diagnostic value. The figures above the 
line always refer to the serum, those below the line to the 
cerebro-spinal fluid." 2 

In this article, for further saving of space in the extensive 
tables, the horizontal line is represented by an oblique stroke, 
the figures to the left of the Btroke referring, of course, to the 
serum. Similarly, the negative result of the tests—here always 
quantitative—is represented by a single 0 instead of 00000. 

1 Apology is hardly needed for printing “c.s.f.-W.R.” for M Wassermann 
reaction in the oerebro-spinal fluid,” especially just before the terse notation 
of the quantitative reaction. The German * 1 Cerebrospinalfliissigkeit ” and the 
French expression are no shorter than the English name. Serious writers express 
their intolerance of the long term by often printing “fluid” in English or 
“ Liquor ” in German, and by probably never writing the long clear expression. 

9 MTntosh, Fildes, Head, and Fearnsides, Brain , Part I., 1913, VoL xxxvi., 



DROP-METHODS OF COUNTING CELLS 


353 


Group II. 


Serum- W.R. negative with pleocytosis ( c.sf.-W.R. negative). 


Case 

No. 

Initials 

Age. 

Diagnosis. 

Treatment 

W.R. 

Cells per c.mm. 

1. 

W. B. 

... 

Tuberculous menin¬ 
gitis. (P.M.) 

... 

Dee. 13,1913. 

84; 

4 per cent, 
polymorph. 

2. 

I. c. 

42 

Basal tumour. 

... 

Mar. 25, 1914, 
0/0. 

8. 

3. 

i 

j 

I. Dp. 

5 

Hydrocephalus. 


Dec. 3, 1913, 
0/0. 

200; 

20 per cent, 
polymorph., 
0*3 per cent, 
plasma cells. 
Many r.b.c. 
allowed for. 

4. 

L. E. 


Disseminated 

sclerosis. 


Oct. 29, 1913, 
0/0. 

63; 

1 per cent 
plasma cells 
(atypical), 2 
per cent 
polymorph. 

5. 

Em. H. 

... 

Cerebral tumour. 
(Proved by P.M.) 

... 

Deo. 20, 1913. 

15. 

6. 

J. H. 

9 

Tuberculous menin¬ 
gitis. (P.M.) 


Apr. 9, 1913. 

400; 

2*2 per cent 
polymorph., 
2*5 per cent 
swollen. 

7. 

D. J. 

... 

Cerebral tumour. 

... 

May 6, 1914, 
0/0. 

8. 

8. 

R. K. 

49 

Cerebral haemorrhage 
and fits. 


Nov. 12,1913, 
0/0. 

200; 

1 per cent, 
plasma cells, 
0*3 per cent 
mast oells, 
but blood 
present. 

9. 

H. L. 


Tuberculous menin¬ 
gitis. (P.M.) 


May 22,1914. 

100; 

40 per cent 
swollen, 0*1 
per oent. 
plasma oells 
(one day old). 

10. 

1 

1 

N. L. 

• • • 

Acute anterior polio¬ 
myelitis. 

... 

Nov. 4, 1913. 

52; 

70 per cent 
swollen. 

11. 

V. P. 

4 

Meningitis. Cause ? 


Apr. 3, 1913, 

280; 

3 per oent 
polymorph., 

4 per cent 
swollen. 

12. 

"Y.R.” 

... 

Cerebral tumour. 

... 

May 20, 1914, 
0/0. 

18. 

13. 

“T V ” 

... 

Mngtic. symptoms. 

... 

Oct. 22, 1913. 

7. 

14. 

Wm.Y. 

3 

Acute mngtis., non- 
fatal. 

Organism failed 
to grow in culture. 


1500; 

80 per cent, 
polymorph., 

1 per oent 
plasma cells. 





354 


R. DONALD 


Group III. 

Serum - W.R. positive without pleocytosis 
(c.s.f.-W.R. negative). 


Case 

No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c. mm. 

15. 

C. B. 

53 

Depression in a 

None. 

Deo. 3, 1913, 





syphilitic. S.I. at 23. 


4-/- 

Deo. 17,1913, 

1. 


M. B. 




44444/0. 


16. 

36 

Nephritis in a 

4 years’ Hg. 

June 4,1913, 

i- 




syphilitic. 

Myasthenia grav. in 

and Kl. 

4- JO. 

J 

t 

17. 

E. B. 

42 

None. 

April 23,1913, 

i. 

18. 

P. B. 

26 

a syphilitic. 
Transverse myelitis 

Has had much 

44444/0. 
May 14,1913, 

4. 




(stationary). 

Hg. and also 
salvarsan. 

0/0. 


19. 

M. C. 

57 

Cerebro spinal 8. 

|M 

April 1,1914, 

1. 


S. C. 


(Cerebral type.) 


44300/0. 


20. 

37 

Jacksonian seizures 

Bromides, 

April 29,1914, 

3. 


W. C. 


in a syphilitic. 
Gumma of post- 
central region 

(operation 1911). 

Iodides and Hg. 

3 years. 

43000/0. 

April 22,1914, 

i 

i 


21. 

38 

Old cerebral S. heroi- 

Inunctions of 

2. 




plegia. 

Hg. and much 

44400/0. 





KL in 1911. 



22. 

G. C. 

... 

Old cerebral 

3 “ doses ” 606 

Aug. 20,1913, 

i. 




thrombosis. 

in Canada. 

44441/0. 





Left hemiplegia. 


Dec. 17,1913, 

3. 




Jan. 1913. 


44441/0. 


23. 

W. G. 

53 

Progressive muscu¬ 

Hg. 

Jan. 29,1914, 

... 


: 


lar atrophy in a 
syphilitio. 

4-/0. 

Mar. 4, 1914, 

1. 



E. H. 



44444/0. 


24. 

39 

Gumma cerebri. 

June 28, 1913, 

June25,1913, 

3. 




Increased intra¬ 

0'6 (914). 

41000/0 




| 

cranial pressure. 

July 10, 1913, 
0-9 (914). 

July 25,1913, 





Secondary optio 

40000/—. 





atrophy. 

July 17, 1913, 
0-9 (914). 

Nov. 5, 1913, 
42100/—. 







Nov. 12,1913, 

2/7. 






30000/0. 

25. 

C. K. 

58 

Cerebral S. 

Hg. and KL in 

July 30,1913, 

2. 



i 

Aortic disease. 

1911. 

44444/10000. 

i 

26. 

B. L. 

43 

Psychasthehia in a 

Hg. 4 months. 

Oct. 23, 1912, 





syphilitic. 

April 1913, 0-9 

44444/0. 


1 

1 



(914) 3 doses. 

April 16,1913, 
44444/0. 
July 2, 1913, 

i. 







44444/—. 
April 1,1914, 

2/7. 






44440/0. 


27. 

A. M. 

41 

Cerebral S. 

Hg. and Kl. 

2 years. 

Jan. 1, 1913, 

i 




! 

44443/0. 




r 


DROP-METHODS OF COUNTING CELLS 


355 


Group III. ( continued ). 


Case 

No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c.mm. 

28. 

E. P. 

27 

Multiple gummata. 
Congenital S. 

None recently. 

May 21, 1913, 
44444/0. 

1. 

29. 

M. R. 

18 

Interstitial keratitis. 
Congenital S. 

TBs. hip. 

None. 

June 25, 1913, 
0/0. 

1. 

30. 

A. S. 

35 

Epilepsy in a 
syphilitic. 

Bromides only. 

Jan. 14, 1914, 

4-/-. 

Mar. 18, 1914, 
44420/0. 

2 - 

31. 

L. Sp. 

31 

Sc. thrombosis of 
cord. 

Kl. 

Oct. 3, 1913, 

0-9 (914). 

Oct. 8, 1913, 
44442/0. 

2 - 

32. 

E. W. 

31 

Vestibular disease in 
a syphilitic. 
Epilepsy in a 
syphilitic. 

Injections of Hg. 
and Kl. 

Jan. 8, 1913, 
42100/0. 

2. 

33. 

: j 

F. W. 

42 


June 11, 1913, 
44430/0. 

3. 


Group IV. 

W.R. pos. po8., with pleocytosis. 

(Only Group IV. has W.R. positwe in c.s.f.) 

Group IV. consists of:— 

• Group IVa.—Untreated nervous syphilis. 

„ IVA.—Nervous syphilis much improved under treatment. 

„ IVc.—Nervous syphilis less improved under treatment. 


Group IVa.—Untreated Nervous Syphilis. 


Case 

No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c.mm. 

34. 

J. A. 

60 

Tabes optica. 
Primary optic 
atrophy. 

No other manifesta¬ 
tion. (P.M.) 

... 

May 7, 1913, 
44300/44300. 

33. 

35. 

F. B. 

35 

i 

1 

Probably spinal 
thrombosis. 


Jan. 21, 1914, 
—/44400. 

Feb. 4, 1914, 

4-/-. 

Feb. 11, 1914, 
44430/—. 

80; 

41 per cent. \ 
polymorph. 

36. 

S. B. 

32 

1 

Acute Sc. enceph. 
P.M. verification. 

i 


May 27, 1913, 
44444/44444. 

35. 







356 


R. DONALD 


Group I Vo. (continued). 


Case 

No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c.mm. 

37. 

C. B. 

46 

Tabes dorsalis. 


June 10, 1914, 

9; 




Cerebro- spi nal sy ph - 


44310/44000. 

40 per cent. 


J. C. 


ilis, root lesion, 
primary atrophy, 
A. R. pupils. 


swollen (3 
days old). 



38. 

51 

Tabes dorsalis. 

... 

Mar. 29. 1912. 
44430/31000. 

36. 


39. 

A. C. 

40 

Tabes dorsalis with 


Aug. 20, 1912, 

... 




some amyotrophy 
of upper limb. 


41000/44441. 
Fob. 25,1914, 

100; 





40000/44440. 

0*5 per cent, 
plasma cells. 


40. 

R. C. 

36 

Amyotrophy with 
cerebral affection 


Dec. 4, 1912, 
44442/44100. 

39. 




and spasticity of 
lower limbs. 




41. 

VV. C. 

51 

Sc. mngtis, root 

None recently. 

Oct. 29,1913, 


43. 



lesions. 


4-/-• 

Dec. 3, 1913, 
44440/44440. 

30. 

S. 0. 

41 

Cerebro-spi nal 

. •, 

Mar. 4, 1914, 

35. 

44. 

C. G. 


syphilis. 

S. II. c., root 


44410/44400. 
June 10, 1914, 

154; 

| 



lesions. 


44444/44000. 

75 per cent, 
polymorph., 

3 per cent. 

; 45 . 

1 





plasma cells. 

! H. G. 

39 

Sc. spinal meningitis 

i .,, 

Feb. 11, 1914, 

74; 




with A. R. pupils. 


44440/44000. 

1 per cent. 







plasma cells. 
Red oells 

46. 

T. G. 

32 

Tabes dorsalis. 


Dec. 4, 1912, 

present. 

50. 




Perforating ulcer of 


43200/44400. 





foot. 


Jan. 29, 1913. 

... 






44310/—. 


! 47. 

48. 

W. H. 

H. H. 

39 

Tabes dorsalis. 

Tabes dorsalis, c. 


Feb. 25, 1914, 
44440/44400. 

18. 

37 


Apr. 1, 1914, 

10. 

49. 


1 

gastric crises. 


44440/44440. 


A. H. 

46 

Cerebral S. Mani¬ 


Feb. 18,1914, 





festations chiefly 


2-/-. 





mental. 

i 

1 

Feb. 25,1914. 

25. 

1 

50. 

K. H. 



i 

| —/44000. 

i 


Acute meningo 

1 

iNov. 6, 1913. 

426; | 




myelitis. 

i 

i 

! 


5 per oent. 
polymorph., 1 
3 per cent. | 







plasma oells; 

i 

I 

1 

1 


i 


3 per cent, 
endothelial 

1 

I 

1 


i 


oells. 



DROP-METHODS OF COUNTING CELLS 


357 


Group IVa . ( continued ). 


Case 

No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c.mm. 

51. 

W. J. 

47 

Spastic paraplegia. 


April 22,1914, 

35; 




’ 


444—/44200. 

5 per cent, 
plasma cells. 

52. 

G. J. 

35 

Sc. hemiplegia with 
amyotrophy of 
right upper limb. 


Nov. 12, 1913, 





4-/-. 

Nov. 19, 1913, 

1 . 

53. 

S. K. 


S. roeningo vascu- 


44441/44300. 


30 


Mar. 25,1914, 

64; 




laris, mental de- 
terioration. 


44430/41000. 

1 per cent, 
polymorph., 







I per cent, 
plasma cells. 

54. 

H. K. 

21 

Gummatous mngtis. 


Mar. 5,1913, 

23; 




So. lesions of nu- 


44440/0. 

(many red 




cleus of 9th, 10th 
and 11th cranial 


cells present. 
Blood leuoo- 





nerves. 



oyte count 




S.I. 12 months ago. 



not secured.) 

55. 

L. 


Dementia paralytica. 

• • • 

Feb. 3, 1914, 

60; 






Red cells 
allowed for. 


56. 

R. M. 

29 

Sc. enceph. 


Feb. 25,1914, 
44444/44440. 

65. 

58. 

E. M. 

49 

Cerebrospinal 

•.. 

July 9, 1913, 

6; 



1 

meningitis. 


444-/43000. 

specimen 

3 days old. 

59. 

A. M. 

42 

So. encephalitis with 


Mar. 4,1914, 

... 




leukoplakia. 


4-/-. 

Mar. 11,1914, 

250; 






-10. 

30 per cent, 
polymorph., 




i 



0‘3 per cent, 
plasma. 




1 


Mar. 18,1914, 

• • • 

! 





44442/—. 


60. 

J. M. 

42 

i 

Tabes dorsalis. 


Feb. 28,1912, 

4-/-. 

May 22,1912, 

AAAAA IAAAAA 

1 ■ XX f/ 1111 A* 

n. 

61. 

E. M. 

47 | 

Tabes dorsalis. 


Mar. 25,1914, 

12 . 






—/44440. 







April 1,1914, 
44444/—. 

... 

62. 

S. 0. 

36 

Tabes dorsalis. 

... 

May 15,1912, 







10000 /—. 
May 22,1912, 

16; 






10000/44441. 

Phase I., slight 






Apr. 1,1914, 
20000/44444. 

opalescence. 

3 | 

c. 8. f. markedly 







alkaline. 

i 

t 






Phase I., nearly 
opaque white. 




an 8 


K. DONALD 

Group IV«. (continual). 


Case 

No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

63. 

H. O. 

30 

Cerebrospinal 8. 





affection of many 
cranial nerves and 





spinal roots. 


64. 

A. O. 

55 

Cerebrospinal S. 





affecting many 

cranial nerves 





and several spinal 





nerve roots. 


65. 

C. P. 

35 

Sc. meningitis. 


66. 

(i. Pb. 

51 

Pseudo-tal>es 

... 




syphilitica. 


67. 

T. P. 

41 

Cerebro spinal S. 
A.R. pupils, root 
lesions, spastic 

paraplegia. 

Tabes dorsalis. 


68. 

G, R. 

50 





Primary optic 





atrophy. 


69. 

T. S. 

43 

Talies dorsalis. 


70. 

E. S. 

i 

30 

“ Gastric crises.” 


71. 

* t t $ )f 


! Meningo-myelitis. 


72. 

F. S., 
of B. 
1). T. 

42 

j Dementia paralytica. 

1 

j 

73. 

43 

i 

Spastic paraplegia, 
j c. A.R. pupils. 


74. 

W. T. 

39 

Cerebro-spinal S. 





(S. 20 years ago.) 
Gumma of testicle. 


75. 

C. W. 

41 

i 

Tabes dorsalis, 
i Ophthalmoplegia 



1 

! 

externa. 


76. 

s. w. 

52 

Basal mngtis. affect¬ 




: 

ing many cranial 

i 


1 


nerves. 


77. 

G.R.W.I 

60 

Sc. bulbar throm¬ 

... 


i 


bosis. (P. M.) 



W. R. Cells per e.mm. 


Feb. 18, 1914,, 
44444/44440. 

|june 19, 1914, 
44440/0. 
June 25, 1913, 
44000/44400. 


Dec. 17,1913, 

0 / 0 . 

Oct. 8, 1913, 
44444/44310. 
June 10, 1914, 
4-/44000. 


Nov. 19,1913, 
44444/44000. 

Apr. 17, 1913, 
44440/44100. 
Apr. 30, 1913, 
0/44100. 
Nov. 29, 1913, 
0 / 0 . 

July 16,1913, 
4-/4-. 


May 13,1914, 
44444/44440. 
Apr. 23, 1914, 
44444/44431. 
Dec. 15,1913, 
44444/44444. 

Apr. 23,1913, 

Mar. 4, 19U, 
44400/44440. 

May 12, 1914, 
44440/44400. 

uMar. 18, 1914, 

4-/-. 

Mar. 25, 1914, 
—/40000. 
Apr. 1, 1914, 
44444/—. 


55; 

0 3 per cent, 
plasma. 


90; 

1 per cent, 
mast cells, 
0'5 per cent, 
plasma cells. 
15. 

14. 

53; 

1 per cent, 
polyniorpli- 

6 . 


36. 

12 . 


200 ; 

nearly all 

expanded. 
Sample some 
days old. 

31. 

12 . 

36. 


104; 

02 per cent, 
plasma cells. 
40. 


27. 


i 

* 




DROP-METHODS OF COUNTING CELLS 


359 


Group IVa. ( continued ). 


Case 

No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c. mm. 

78. 

E. W. 

23 

i 

Acute encephalitis 
(mental manifesta¬ 
tions). 

Hg. 4 years ago. 

Feb. 11, 1914, 

4-/-. 

Feb. 18, 1914, 
—/44444. 

13. 

79. 

E. W. 

30 

1 

Depression. 


May 13, 1914, 
44444/44444. 

29; 

1 per cent, 
mast cells. 

80. 

J. W. 


Acute 8. II. 
c. affection of many 
spinal and cranial 
nerves. 

i 

i 

i 

Apr. 15, 1914, 
4 /44400. 

43; 

8 days old. 


Group IY6. 


Nervous Syphilis Much Improved under Treatment. 


Case 

No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c.mm. 

81. 

A. A. 

49 

Basal mngtis. affee- 

May 6, 1913, 

April 30,1913, 

33. 




tion of many cranial 

0-9 (914). 

44444/44432. 





nerves and several 

May 9, 1913, 

Oct. 29, 1913, 

4. 




spinal nerve roots. 

0-9 (914). 
June 26, 1913, 

44441/0. 






0'9 (914). 



82. 

C. B. 

41 

Brown-S&juard 

1911, Hg., 36 

June 19, 1912, 

... 




paralysis. 

inunctions. 

44410/41000. 





July 22, 1912, 

July 2, 1913, 

1 . 





0-6 (606). 

44410/0. 






July 27, 1912, 

Oct. 15, 1913, 

... 





0-9 (914). 

44410/—. 






June 28, 1913, 

Deo. 2, 1913, 

2 . 





0'9 (914). 

44000/0. 


83. 

D. B. 

42 

Sc. transv. myelitis 

Aug. 1912, 

Aug. 2, 1912, 

... 




(stationary). 

0-9 (914). 

44443/44432. 





Aug. 1912, 

April 30,1913, 

... 





0-9 (914). 

44443/—. 






May 1913, 

May 21,1913, 

4. 





0*9 (914). 

44430/0. 






May 1913, 

Feb. 18,1914, 

2 . 





0-9 (914). 

44440/0. 


84. 

A. C. 

41 

Gastric crises. 

Aug. 1913, 

0'9 (914). 

Aug. 6, 1913, 
444-/44440. 

40; 

23 per cent, 
polymorph. 





Aug. 1913, 

Feb. 18,1914, 
44440/44440. 

4; 





0-9 (914). 

red cells 





Aug. 1913, 

0-9 (914). 

Feb. 1914, 


allowed for. 





0-9 (914). 








300 


R. DONALD 


Group I Vi. ( continued ). 


Case 
j No. 

1 - 

Initial 

J Age 

1 

! Diagnosis. 

i 

| 

Treatment. 

YV.R. 

Cells per c. mm. 

f*. 

I 

G. D. 

40 

Sc. hemiplegia in 

Hg. 2 years. 

Feb. 7, 1912, 

2. 




1900. 

Feb. 11, 1912, 

32000/0. 


X 




0-6 (606). 

Feb. 17, 1912, 

June 15, 1912 
21000 /—. 






0-6 (606). 

May 21,1913, 

I 






0 /-. 

1 






July 2, 1913, 

( 






o/-. 







Nov. 12,1913, 

1 . 






0 /0. 







May 27,1914, 

1 . 

87. 

W. F. 

45 

Pseudo-tabes syphil¬ 

Iodides. 

0 /0. 

Mar. 5, 1913, 

| 




itica, with amyo¬ 


4-/-. 

1 

88 . 

u. f. 

57 

trophy of legs. 


Mar. 4, 1914, 
44420/44000. 

2 . 

Sc. basal mngtis. 

Hg. 

July 9, 1913, 





affection of several 

July 5, 1913, 

4-/-. 


89. 

J. G. 

‘27 

cranial nerves. 

0-9 (914). 

Mar. 4, 1914, 
44444/44000. 

1 . 

Acute cerebro-spinal 

Hg. 6 months. 

Oct. 8, 1912, 

i 




syphilis. 

Oct. 14, 1912, 

44444/44443. 





S.I. end of 1911. 

0-9 (914). 

Oct 13, 1912, 






Oct. 21, 1912, 

44444/44410. 






0-9 (914). 

Dec. 10,1912, 

16. 





Nov. 4, 1912, 

44443/44300. 





j 

0-9 (914). 

Mar. 5, 1913, 

4. 




! 

Dec. 11, 1912, 

44100/0. 

! 





0-9 (914). 

April 23,1913, 

... 





Mar. 6, 1913, 

10000 /—. 






0-9 (914). 

Oct. 29,1913, 






April 23, 1913, 

20000 /—. 






0-9 (914). 

April 22,1914, 

2 . 

90. 

W. G. 


Sc. mngtis. 

12 inunctions 

0 /0. 

April 3,1912, 

112 . 




Nerve root irritation. 

Hg. 1908. 

44444/0. 

117; 





Hg. and Kl. 6 

Mar. 4, 1914, 





weeks in 1911. 

44444/0. 

3 per cent ! 





Mar. 4, 1912, 

polymorph., ' 





0-9 (914). 


10 per cent, j 





Mar. 7, 1912, 


swollen. 





0-9(914). 

Mar. 10, 1912, 



91. 

R. O. 

62 

Diffuse gummatous 

0-9 (914). 

May 16, 1913, 

May 21,1913, 

23; 

! 



mngtis. 

0-9 (914). 

AAAAA IAAAAA 

I 1 I 1 1/ M M. M. M 

1 per cent 

1 



S. 10 years ago. 

May 31, 1913, 

microlympho¬ 


j 

i 


0-9 (914). 

July 14, 1913, 

July 23,1913, 

cytes. 

! 


i 


0-9 (914). 

44442/—. 

1 . 

! 


i 


July 31, 1913, 

Aug. 6, 1913, 

1 




0-9 (914). 

—/44430. 

i 



DROP-METHODS OF COUNTING CELLS 


361 


Group IV6. (continued). 


j 

! Case 
No. 

i 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c.ram. 

92. 

F. J. 

35 

Sc. "peeudoparesia.” 
B.I. at 29. 

Iodides only, 
1912. 

Mar. 13,1913, 
44330/44440. 

63. 





April 17, 1913, 

April 16,1913, 

19. 





0-9 (914). 

44444/44000. 






April 22, 1913, 

July 9, 1913, 


1 




0-9 (014). 

4-/-. 






April 26, 1913, 

Nov. 5,1913, 

2 . 

9a 




0-9 (914). 

44440/0. 


D.G.K. 

35 

Sc. myelitis. 

Local Sc. menin- 

July 10, 1912, 
0-6 (606). 

July 10,1912, 
44300/44410. 

... 




gitis, Th. Vffl. 

July 17, 1912, 
0-6 (006). 

May 15,1913, 
32100/0. 

10 . 





Jan. 1, 1913, 


' 




0*9 (914). 



94. 

A. K. 

33 

Diffuse meningitis 

Oct. 21, 1912, 

Oct. 16,1912, 





and gumma of 

0'9 (914). 

0/4-. 





scalp. 

Oct. 31, 1912, 

Oct. 30, 1912, 





0*9 (914). 

20000 /—. 


f 




Jan. 17, 1913, 

Jan. 22,1913, 


1 




0-9 (914). 

43200/0. 


[ 




April 24, 1913, 

April 23,1913, 

4. 

I 95. 

N. M. 



0-9 (914). 

Jan. 8, 1913, 
0*9 (914). 

40000/0. 


41 

Cerebro spinal S. 

(Vigorous 

Aug. 27, 1913, 

3. 

! 

, 



S.I. 3 years ago. 
Right hemiplegia, 

inunctions.) 

44200/0. 


97. 

, A. P. 


2 years. 




42 

Sc. encephalitis, 

July 3, 1912, 

July 3, 1912, 


1 

j 


44 pseudo - paresis ” 

0-6 (606). 

42000/43200. 





syphilitica, hyper - 

March 7, 1913, 

May 5, 1913, 

0 ; 




piesis. 

0-9 (914). 

0 /0. 

the white cells 




May 5, 1913, 

June 25,1913, 

are practically 



1 


0-9 (914). 

o/-. 

accounted for 





Oct. 15,1913, 

by the red 




i 


o /-. 

cells. 




| 


April 29,1914, 

l; 






0 /0. 

confirming 




j 



previous 

count. 

98. 

G. P. 

27 

Sc. encephalitis. 

He. 2 years. 

April 3,1912, 

... 

i 




Feb. 1912, 0 -6 

4-/-. 






(606). 

Nov. 13, 1912, 

... 





Feb. 11, 1912, 

40000/—. 






0-6 (606). 

Nov. 28,1912, 

85. 



j 


Nov. 27, 1912, 

0/44100. 




i 


0-6 (914). 

June 4, 1913, 

90. 



i 

i 

i 


June 6, 1913, 

44442/44443. 




1 


0-6 (914). 

July 31,1913, 

... 





July 12 to 26, 

44430/—. 






0*9 (914), 
in 4 doses. 

Aug. 13,1913, 
44200/44400. 

3. 






362 


R. DONALD 


CtKOUP IV/>. ( continued ). 


Cast* 
i No. 


Initials 


99. F. P. 


I 


100. 1 F. R. 


101 . 


E. R. 


102. M. S. 


i 


103. I E. T. 


33 


48 


Diagnosis. 

Treatment. 

W.R. 

Cells per c.mm. 


Jan. 26, 1914, 
0*9(914). 

■Sept. 24,1913, 
44200/—. 
Nov. 19,1913, 
01— 

Jan. 28, 1914, 
0/42000. 

4. 

Pseudo-tabes 

Jan. 4, 1913, 

Jan. 1, 1913, 

5. | 

syphilitica. 

0-0 (914). 

44443/44443. 


Jan. 14, 1913, 
0-9 (914), 

Mar. 2, 1913, 
44441/—. 

3. ' 


Jan. 21, 1913, 
0-9 (914). 

Apr. 23, 1913, 
44444/44400. 


April 25, 1913, 
0-1 (914). 

May 21, 1913, 
44442/—. 



April 29, 1913, 
01 (914). 

June 4, 1913, 
44441/—. 



May 2, 1913, 
01 (914). 

June 16, 1913, 
44441/—. 



May 3 to 27, 
2-3 (914), 

July 16,1913, 
44442/—. 

i. 


in 7 doses. 

Jan. 28, 1914, 

Sept. 3, 1913, 
44440/44200. 


0-9 (914). 
June 12, 1914, 

Jan. 28, 1914, 
4444-/44400. 

1 . 


0-9 (914). 

! 

June 10, 1914, 
44440/30000. 

1 . 

Gummatous mngtis. 

Feb. 25, 1913, 

Mar. 5, 1913, 

11. 

around 3rd cranial 

0-9 (914). 

44444/41000. 

1 

! io. 

i 

nerve. 

Mar. 8, 1913, 
0-9 (914). 

Apr. 23, 1913, 
0-9 (914). 

Apr. 23, 1913, 
44444/0. 

Old Sc. muscular 
atrophy and lateral 
sclerosis. S. 19 j 
years ago. 

i 

May 19, 1911. 
20000/0. 



Feb. 26, 1913, 
0/0. 

Oct. 29, 1913, 
0/0. 

i 

Sc. amyotrophy. 

July 20, 1912, 
0-9 (914). 

Mar. 14, 1912, 
44444/—. 

• • • 


Aug. 1, 1912, 
0-9 (914). 

Apr. 22, 1912, 
44444/44442. 

20. 

i 


Nov. 30, 1912, 
0-9 (914). 

Nov. 21, 1912, 
—/41000. 


Dec. 3, 1913, 
0-9 (914). 

Dec. 4, 1912, 
—/44300. 
July 9, 1913, 
44410/—. 
Dec. 3, 1913, 
44410/40000. 

! 

• • • 

1- 1 

Gummatous mngtis., 

Hg. and “606 ” 

Jan. 22, 1913, 

7. : 

affection of several 

injected abroad 

32000/0. ! 


cranial nerves. 

18 months ago. 

i 

___— 





DROP-METHODS OF COUNTING CELLS 


363 


Group IVi. (continued). 


! Case 
No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c.mm. 

104. 

E. W. 

33 

Syphilitic hemiplegia. 

“ Salvarsan.” 

Oct. 22,1913, 

31. 




Oct. 18, 1913, 

44444/0. 






0 6 (914). 

Oct. 23, 1913, 

Nov. 12, 1913, 

20. 





0*9 (914). 

Oct. 30, 1913, 

44444/0. 






0*9 (914). 



105. 

E. W.! 

23 

Sc. hemiplegia. 

Mar. 7, 1913, 

Mar. 5, 1913, 

19. 




0-9 (914). 

44444/44000. 






Mar. 10, 1913, 

July 2, 1913, 

• •• 





0*9 (914). 

44442/—. 






Mar. 17, 1913, 

Dec. 3, 1913, 

• • • 





0*9 (914). 

44440/0. 



Group IVc. 


Nervous Syphilis Less Improved under Treatment. 


Case 

No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c.mm. 

106. 

A. B. 

16 

J u venile dementia 
paralytica. 

July 19, 1913, 
0-6 (914). 

July 25, 1913, 

0 6 (914). 

July 30, 1913, 

0 6 (914). 

Oct. 29, 1913, 

0 6 (914). 

July 16,1913, 
44444/44420. 

Oct. 29, 1913, 
44440/44000. 

Apr. 27, 1914, 
44440/44440. 

46; 

2 per cent, 
plasma, 5 per 
cent, poly¬ 
morph. 

21; 

3 per cent, 
polymorph., 

1 per cent, 
plasma cells. 

38; 

1 per cent, 
plasma cells, 

1 per cent, 
polymorph. 

107. 

i 

A. B. 

47 

I 

Epilepsy in a 
syphili tic (old 
meningitis). 

| 

Apr. 5, 1913, 

0 9 (914). 

Apr. 12, 1913, 
0-9 (914). | 

Apr. 19, 1913, 

0 9 (914). 

July 9, 1913, 
0-9 (914). 

Apr. 2, 1913, 
44440/0. 
Oct. 15, 1913, 
4444^/ 

Dec. 17, 1913, 
44442/0. 

2. 

3. 

108. 

J. B. 

37 

Pseudo- paresis 
syphilitica. 

Hg. 4 months. 
Sept. 24, 1912, 
0-9 (914). 

Sept. 28, 1912, | 
0 9 (914). 

Sept. 18, 1912, 
43000/42000. 

Juno 18, 1914, 
30000/44200. 

8. 

109. 

H. B. 

42 

Taboparesis. 

S. 1894. (P.M.) 

Hg. 12 months. 
Oct. 25, 1912, 

0 9 (914). 

Oct. 23, 1912, 
44431/44441. 





364 


R. DONALD 


Group IVr. (continued). 


Case 

No. 

j Initials Age. 

Diagnosis. 

Treatment. 

W.R. 

'Cell* per c.mm. 

f 


1 

| 


Oct. 29, 1912, 

Feb. 5, 1913, 

... i 

1 


1 


0-9 (914). 

44410/—. 

4; 

| 

i 

1 


Feb. 1 , 1913, 

Sept. 3. 1913, 

, specimen 3 


1 



0-9 (914). 

44432/44420. 

days old. 

110 . 

I J. c. 


Dementia paralytica 

June 6 , 1912, 

June 5, 19J2, 


i 

1 

progressive. 

0-6 (606). 

44421/44432. 


! 

i 

1 

June 12, 1912, 

Aug. 20,1913, 

25; 

I 

1 

! 

1 

0-6 (606). 

44440/44420. 

1 per cent, 
plasma cells. 

111 . 

E. C. 

43 

Taboparesis. 

. .. 

Sept. 24,1913, 

| 

J 

1 



4 -/-. 

Oct 2, 1913, 

! 4 -/44444. 

i 

1 

j 


f 

i 



1 May 13,1914, 
44441/44442. 

24. 

112 . 

C. C'. 

43 

Tabes dorsalis. 

Nov. 3, 1912, 

i Oct. 8 , 1912, 





Leukoplakia, epi- 

0 9 (914). 

44200/44310. 





thelioma of tongue. 

Nov. 8 , 1912, 

Dec. 4, 1912, 

1 




Death from second- 

0-9 (914). 

43200/—. 

1 




ary carcinomatosis. 
(NoP.M.) 

May 4, 1913, 

Mar. 19,1913, 

... 1 

I 


i 

0-9 (914). 

44200/—. 

i 

i 



May 7, 1913, 
44420/44200. 

30. 

i 



1 

i 



1 


Sept. 10 , 1913, 
44420/44200. 

10 . 

113. 

S. I). 

29 

Taboparesis pro¬ 

June 1 , 1913, 

June 1 , 1913, 

22 . ! 

| 



gressive. 

0-9(914). 

44443/44444. 




1 : 

Later 4 intrathecal 

June 21, 1913, 

Oct. 8 , 1913, 


1 


j 

injections, each 

0.9 (914). ! 

44444/—. 

28; j 




10 c.c. of “ 914- 

June 27, 1913, 

Jan. 14,1914, 



i 

serum.” 

0-9 (914). 

44444/44444. 

30 per cent | 

| 




Sept. 29 to 

polymorph. 1 

! 

1 

1 


Oct. 10, 1913. 

4 times 0*3 (914) 

July 8 , 1914, 
44444/44444. 

18; | 
blood account¬ 

1 

1 

1 

1 


in 30 c.c. 

Jan. 1914, 

0-9 (914). 

ed for 9 cells. 

i 



119. ^ 

F. G. 

24 ! 

“Parasyphili tic” 

June 6 , 1913, 

June 4, 1913, 

40. 

i 


. 

epilepsy, congeni¬ 

0-9 (914). 

44-/44440. 


i 1 



tal S. 

June 15, 1913, 

June 11, 1913, 

... 

1 1 




0-9 (914). 

44200/—. 

: 

i i 

i 




June 18, 1913, 

Dec. 3, 1913, 

1. 


i 


Muscular atrophy. 

0-9 (914). 

44100/44000. 


122 . 

W.Hr. 

36 

April 5, 1913, 
0-9 (914). 

April 12 , 1913, 

Feb. 26,1913, 

4 -/-. 

April 3,1913, 
44444/44400. 

44. 






0-9 (914). 






April 19, 1913, 
0-9 (914). 

Sept 24,1913, 
44443/43000. 

... 





8 ept. 23, 1913, 

May 13,1914, 

3|. 




8 c. hemiplegia. 

0-9 (914). 

44430/40000. 


118. 

W. G. 

35 

May 20 , 1913, 

... 

i 




0-9 (914). 





DROP-METHODS OF COUNTING CELLS 


365 


Group IVc. ( continued ). 


Case 

No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c.mm. 





May 30, 1913, 

Aug. 20,1913, 

50. 





0.9 (914). 

AAAAA ! A A A A A 

Tim/ XTTTTi 






Sept. 14, 1913, 

Nov. 5, 1913, 






0 9 (914). 

44441/—. 






Jan. 14, 1914, 

Jan. 14, 1914, 

163. 


F. G. 



0*9 (914). 

44440/44444. 


119. 

24 

Parasyphilitio epi- 

June 6, 1913, 

June 4, 1913, 
44—/44440. 

40. 




lepsy, congenital S. 

0*9 (914). 


1 




June 13, 1913, 

June 11,1913, 






0-9 (914). 

44200/—. 






June 18, 1913, 

Dec. 3. 1913, 

i. 





0-9 (914). 

44100/44000. 


120 . 

W. H. 

54 

Erb’s Sc. spinal 

No treatment 

Feb. 28, 1912, 

12 . 




paralysis (stationary). 

in 1912. 

43200/44300. 
May 7, 1913, 







43200/—. 







May 21, 1913, 
43100/43000. 

7. 

121 . 

0. H. 


Dementia paralysis. 

Just finished 20 

Nov. 28,1912, 

7. 




injections of Hg. 

20000/40000. 
April 9, 1913, 








4- /-• 

Dec. 17,1913, 

1 . 

122 . 

W. Hr. 




43100/30000. 


36 

Parasyphilitio muse. 

April 5, 1913, 

Feb. 26,1913, 


1 



atrophy. 

0 9 (914). 

4 - /-. 

i 





April 12, 1913, 

April 2, 1913, 

44. 





0 9 (914). 

44444/44400. 


1 




April 19, 1913, 

Sept. 24,1913, 

• • • 




• 

0*9 (914). 

44443/43000. 






Sept. 23, 1913, 

May 13,1914, 

Si- 


P. H. 



0-9 (914). 

44430/40000. 

123. 

34 

Gastric crises. 

Sept.-Oct. 1913, 

Sept. 17,1913, 


1 

1 



A.R. pupils. 

K. J. and A. J. good. 

3 doses 0*9 (914). 

44444/44400. 
June 25, 1913, 

13 ; 

| 124. 

E. I. 



44443/44410. 

1 per cent, 
polymorph. 



55 

Tabes dorsalis, 23 

April 10, 1913, 

Mar. 5, 1913, 




years. 

0-9 (914). 

0 /— 





Charcot knee 


April 9,1913, 

1. 




(stationary). 


20000 /0. 
April 18,1913, 
£2000/0. 
April 22,1913, 

0*3. 






22000 /0. 
April 29,1913, 

1. 

125. 

F. K. 


Taboparesis (P.M.). 


20000 /0. 


37 

May 17, 1913, 

April 16,1913, 

44; 





0-9 (914). 

May 20, 1913, 

44442/44440. 

1 per cent, 
polymorph. 





Oot. 8, 1913, 
44444/44300. 

6 . 

0-9 (914). 

May 26, 1913, 





0-9 (914). 




29 




\l DONALD 


;)6G 


Group IVc. (I'oiiliniliif). 


Case 

No. 

Initial! 

Age. 

Diagnosis. 

i 

m. 

i 

H. Kn. 

55 

Sc. encephalitis 
(treated). 

Now in asylum. 

127. 

T. M. 

38 

Dementia paralytica. 
Now in asylum. 

1*28. 

i 

M. M. 


Sc. hemiplegia, with 
relapse and de¬ 
velopment of psy¬ 
chosis. 

129. 

1 

W. M. 

58 

Secondary optic 
atrophy. 

Old Sc. meningitis. 

' 130. 

D. S. 

53 

Tabes dorsalis. 

131. 

1 

i 

A. S. 

28 

Tabes dorsalis and 
optic atrophy. 

S.I., 1905. 

132. 

A. Ss. 

30 

Cerebro-spinal S. 
S.I., 1890. 

134. 

F. S. 

39 

S. meningo vascu¬ 
laris. 

S.I., 14 years ago. 

135. 

W.G.T 

35 

Dementia paralytica. 
Onset with manifesta¬ 
tions of basal menin¬ 
gitis (progressive). 

i 


Treatment. 

W.K. 

Cells per c.irnn. 

Get. 7, 191-2, 

Oct. 2, 1912, 


0 0 (914). 

44440/44100. 



Nov. 5, 1913, 

h; 


4- /O. 

c. bacteria. 

Oet. 16, 1913, 

Oct. 15, 1913, 

• • • 

0 9 (914). 

4 / • 


Oct. 22, 1913, 

Oct. 22, 1914, 

80; 

0 9 (914). 

44444/44444. 

4 per cent. 

Nov. 1, 1913, 

Feb. 18,1914, 

polvmorph. 

* 3. 

09(914). 

44444/44444. 


Feb. 4, 1914, 

May 18, 1914, 

2. 

0 9 (914). 

44420/44444. 


Oet. 5, 1912, 

Oct. 2, 1912, 

,,, 

0-9 (914). 

443J0/42000. 


Oct. 9, 1912, 

Nov. 25, 1913, 

67. 

0 9 (914). 

44410/44300. 

1 per cent. 


May 21, 1913, 

polymorph., 

2 per cent, 
mast cells. 


4-/-. 

June 18, 1913, 

20. 1 


44410/10000. 

... 

Hg. 

Dec. 14, 1911, 

21; 

May 7, 1913, 

44410/44400. 

(heart antigen). 

0-9 (914). 

May 7, 1913, 

6. 

Hg. 2 years. 

44442/44100. 
Nov. 20,1912, 

1 

Nov. 15, 1912, 

44442/44300. 


0-9 (914). 


Nov. 17, 1912, 

Oct. 15, 1913, 

6. 

0-9 (914). 

44444/44100. 

! 

Nov. 19, 1912, 
0-9 (914). 


i 

Feb. 1914, 

Nov. 5, 1913, 


0 9 (914). 

4-/-. 

! 

Mar. 1914, 

Feb. 25, 1914, 


0-9 (914). 

44443/44444. 

i 

7. 

Mar. 1914, 

May 15, 1914, 

0-9 (914). 

44440/44410. 


Apr. 1914, 

0-9 (914). 


30. 

Has had Hg. 

Nov. 12,1913, 

44444/44444. 
Dec. 9, 1913, 

4. 

Hg. 

—/44444. 
Jan. 22, 1913, 

50. 

Jan. 25, 1913, 

44430/44441. 


0-9 (914). 


39; 

Jan. 31, 1913, 

Oct, 15, 1913, 

0-9 (914). 

44440/44444. 

5 per cent. 


swollen. 




DROP-METHODS OF COUNTING CELLS 


367 


Group IVc. ( continued ). 


1 Case 
j No. 

Initials 

Age. 

Diagnosis. 

Treatment. 

W.R. 

Cells per c.mm. 





Feb. 5, 1913, 

June 10, 1914, 

38; 





0-9 (914). 

—/44444. 

7 per cent. 





Oct. 13, 1913, 


swollen. 





0-9 (914). 

Nov. 14, 1913, 


I 





0 9 (914). 

Nov. 18, 1913, 







0-9 (914). 
June, 1914, 







0-9 (914). 
June, 1914, 







0'9 (914). 



136. 

0. W. 

36 

Paralysis of 3rd 

Hg. and 914. 

Mar. 18,1914, 

30. 




cranial nerve and 
crossed hemiplegia 
(Weber’s syn- 

0/41000. 
May 8, 1914, 







o/-. 





drome). Sc. rash, 


May 13,1914, 

13. 

1 



Mar. 1913. 


0/0. 

i 

| 137. 

F. W. 

45 

Post-syphilitic amy¬ 
otrophic lateral 

2 doses “ 606,” 

Jan. 1913, 

l 

! 



1913. 

4-/-. 

1 

j 



solerosis. 

! 

Aug. 2, 1913, 
0*9 (914). 

Aug. 6, 1913, 
44200/44000. 

... 





Dec. 3, 1913, 

Dec. 3, 1913, 






0'9 (914). 

43000/44000. 






Dec. 4, 1913, 

Mar. 4, 1914, 

... 

i 

l 




0-9 (914). 

44300/—. 






Dec. 8, 1913, 

May 6, 1914, 

3. 





0-9 (914). 

42000/42000. 






Mar. 4, 1914, 

0 9 (914). 

May 5, 1914, 

• • • 

! 

1 




0-9 (914). 



138. 

V. W. 

• • • 

Pseudo-paresis 

3 times 0*9 (914) 

Nov. 26, 1913, 

14; | 




syphilitica, im¬ 

in Nov. 1913. 

44444/44444. 

3 per cent. 




proved under 


plasma cells. 




treatment. 


June 10, 1914, 

9. 






44441/44443. 


139. 

J. Z. 

40 

Sc. disseminated 

Much Hg. and KI. 

Dec. 3, 1913, 

3. 




sclerosis. Onset 

Dec. 22, 1913, 

0 /0. 





1909. 

0*45 (914). 

Deo. 30,1913, 

... 

1 




o/— 

_ 


Summary. 

The drop-film method of counting the cells of cerebro-spinal 
fluid is described, and more than 260 cell-counts, from cases dealt 
with by Dre MTntosh, Fildes, Head, and Fearnsides 1 are discussed 
in connection with extensive tables lent by those authors to show 
the quantitative Wassermann test, done two to five times on the 

1 Brain, Vol. xxxvi.. Part i., July 1913, and following numbers. 




368 


R. DONALD 


e.s.f. simultaneously with the cell-count, and oftcner on the serum, 
in a munher of cases in various stages of treatment. 

The method avoids centrifuging, which is found to cause loss of 
some cells, especially of the swollen degenerated cells. (These 
exist in some freshly drawn c.s.fs., and they develop from 
unswollen cells in e.s.f. kept for a day or two.) Also it avoids 
the addition of alcohol or of acetic acid, substances that destroy 
the red cells. (Red cells, whether due to the puncture or due to 
previous luemorrhage are, as Rous insisted, to he demonstrated 
and allowed for.) No special apparatus is used. The preparations 
are permanent, and may l>e easily multiple, r.//., for class purposes. 

On each of any number of ordinary slides a couple of separate 
small drops of the e.s.f. are deposited by the simple dropping 
pipettes described 1 recently in a short communication to the 
Royal Society. The slides arc then dried, heat-fixed, dipped in 
dilute collodion, and dried again. Thus are obtained drop-films 
that are practically collodion sections at most only one dried cell 
in thickness. These films, stained, <y/., Gieinsa, or Leishman, and 
Unna-Pappenheim, and mounted in clear soft paraffin, give, with 
the aid of a mechanical stage, at once clear cell-pictures and 
convenient accurate cell-counts, without the loss of a single 
bacterium. Staining for Grain-positive bacteria or for tubercle 
bacilli may be done. 

At any stage after the drying of the drop the process may be 
interrupted, at the worker’s convenience. 

When filed (c.g., by a “slide-index” method, to be described 
later), the permanent preparations give a valuable record of the 
cytological course of the case. 

The cases dealt with are marked off into four groups by the 
serum-W.R. and the cell-count. The main interest centres in 
group IV., with serum-W.R. positive and with pleocytosis. Only 
this group has the e.s.f.-W.R. positive. 

In many of the patients at the time of first observation it is 
impossible to say whether the condition is to l>e called “cerebro¬ 
spinal syphilis,” and a hopeful prognosis given, or whether it 
belongs, or may presently, especially if no treatment now be 
applied, belong to the clinical group “ parasyphilis,” with its 
relatively hopeless prognosis. Not by the presence or by the 
degree of pleocytosis—any more than by the presence or by the 
strength of the W.R. in c.s.f. or in serum—but only by their 
1 Donald, Proc. Royal Society, B, 1913, Vol. lxxxvi., p. 198. 



DROP-METHODS OF COUNTING CELLS 


369 


behaviour under treatment do these cases show up as belonging 
to the one type or to the other. The potency, in many of the 
cases, of treatment by intravenous injections of neosalvarsan is 
indicated in the tables of successive cell-counts and Wassermann 
tests. 

In subsequent articles the authors mentioned will show that 
in the cases of sub-group IV&. (“cerebro-spinal syphilis”) the 
fall in the W.R. and in the cell-count is followed by actual 
improvement in function, which improvement in some cases 
proceeds to the recovery of good bodily health with some 
mental improvement, and in other cases to practically complete 
recovery. Moreover, they will show that, even in sub-group IVc. 
(“ parasyphilitic ” group) considerable clinical improvement takes 
place in some cases, corresponding, no doubt, to some arrest of the 
inflammatory processes, though not to resolution of any secondary 
degenerations. 

As the published tables show, the cell-count is a test that, for 
significance and reliability, is a worthy co-operator with the 
W.R. Indeed it often gives earlier than the W.R. (1) warning 
of meningeal affection, and (2) after treatment, indication of 
improvement. 

The pleocytosis-producing substance is shown to be distinct 
from the Wassermann substance. 

A description is given of a simple microscope lamp, which has 
shown itself of value in rapid qualitative cell-counts, with 
moderate powers. 

Besides the mainly-used drop-film method, there is described 
a simple drop-chamber method, using ordiuary slides and cover 
glasses, and suitable for dark-ground examination of unstained cells. 

Acknowledgments are gratefully tendered to Professor 
Bulloch, F.R.S., for encouragement and facilities towards the 
working out of the method; to Professor Leonard Hill, F.R.S., 
who early recognised some value in the drop-method and gave 
very practical help; to Dr H. M. Turnbull, Director of the 
Pathological Institute, for advice in cytology; also to Dr G. 
Bartlett, Assistant Director; and especially to the authors of the 
work to which this has the honour of being a tributary, namely, 
to Dr Head and Dr Feamsides, for courteously supplying the 
notes of diagnosis and of treatment; and to Dr Fildes and Dr 
McIntosh for the Wassermann notes; finally to the London 
Hospital Medical College Research Fund for a subsidy. 



370 


ABSTRACTS 


abstracts. 

ANATOMY. 

THE P YE AMID TRACT IN THE RED SQUIRREL ( SCIURUS 
(425) HUDSONIANUS, LOQUAX) AND CHIPMUNK (TAM!AS 
STRIA TUS, LYSTERL) Sutherland Simpson, Joum. Comp . 
Neurol., 1914, xxiv., April, p. 137. 

The cortical motor areas in the left cerebral hemispheres were 
extirpated in three red squirrels and three chipmunks, and the 
resulting degeneration followed by the Marchi method. 

The degenerated pyramidal fibres were found to occupy the 
usual position in the crusta, pons, and medulla oblongata. At the 
lower part of the bulb a complete decussation occurs, no fibres 
remaining on the same side. The fibres cross the middle line 
abruptly in bundles which interlace with those of the sound side, 
and pass through the grey matter into the funiculus cuneatus, 
where they turn caudalwards and pass down the apex of the 
posterior column of the spinal cord as far as the lower sacral 
segments. No fibres pass down the lateral column of the cord. 

A. Ninian Bruce. 


THE BRAIN OF A BLACK MONKEY ( MACACUS At A UR US) : THE 
(426) RELATIVE PROMINENCE OF DIFFERENT OYRI. Harris 

E. Santee, Anat. Record, 1914, viii., May, p. 267. 

In this brain, those parts which are motor or sensory in function 
were well developed, while those regions which are concerned with 
psychic functions were poorly developed, e.g., the frontal lobe 
anterior to the prsecentral sulcus, the posterior parietal, and the 
inferior temporal regions. These areas which were deficient in 
this brain correspond, therefore, with the association areas of 
Flechsig. A. Ninian Bruce. 


THE DISTRIBUTION OF NERVES TO THE ARTERIES OF THE 
(427) ARM. J. G. Kramer. WITH A DISCUSSION OF THE 
CLINICAL VALUE OF RESULTS. T. Wingate Todd, Anat. 
Record, 1914, viii., May, p. 243. 

The subclavian and axillary arteries differ from the other arteries 
of the arm in receiving a nerve supply direct from the sympathetic 
chain. All other arteries in the upper limb obtain their nerve 



ABSTRACTS 


371 


supply from sympathetic filaments which have travelled along the 
spinal nerves, and which are distributed to the various blood 
vessels at irregular intervals. The distal and peripheral vessels, 
more especially those of the hand, receive nerve filaments at more 
frequent intervals than do the proximal channels. The distribu¬ 
tion of nerves to vessels corresponds roughly with the distribution 
of nerves to muscles and skin. 

The fact that the subclavian trunk derives its nerve supply 
direct from the sympathetic chain accounts for its escape from 
involvement in the lesion associated with cervical rib. The 
process of blood-vessel affection in this condition appears to be 
(a) stimulation of vaso-constrictor fibres; ( b) paralysis of vaso¬ 
constrictors (with undisturbed action of vaso-dilators ?); (c) patho¬ 
logical changes in the vessel wall consequent on the lesion of the 
nerve. (Cf. Review, 1913, xi., p. 92.) A. Ninian Bruce. 


PHYSIOLOGY. 

CEREBRO SPINAL FLUID.—III. THE GENERAL EFFECTS OF 
(428) INCREASING THE CEREBRO SPINAL PRESSURE. W. E. 

Dixon and W. D. Halliburton, Joum. Physiol ., 1914, xlviii., July, 
p. 317. 

A relatively small increase of cerebro-spinal pressure, artificially 
produced by a pump connected to the cranio-vertebral space by a 
cannula inserted into the subccrebellar cisterna, causes stimula¬ 
tion of the respiratory, vaso-motor, and cardio-inhibitory centres. 
This stimulating effect is least marked on the respiratory centre. 
When the pressure is increased to a height (300-400 mm. Hg.) 
considerably above the normal arterial pressure respiration ceases 
in a few seconds, but the other two centres remain active, and 
the arterial pressure rises enormously in spite of the slow beat; 
a little later the cardio-inhibitory centre is paralysed, and the 
continued activity of the vaso-motor centre still further raises 
the arterial pressure. This is a protective mechanism which 
continues to force the blood along the compressed blood vessels. 
Ultimately, however, if the high c.s. pressure is kept up, paralysis 
of the vaso-motor centre ensues, and the arterial blood pressure 
falls. On removal of the compression, the centres recover in the 
reverse order, the vaso-motor first and the respiratory centre last. 
The spinal centres, as tested by the occurrence of convulsions 
after an injection of strychnine, recover their activity later still. 
{Cf Review, 1913, xi., p. 591; and 1914, xii., p. 204.) 

A. Ninian Bruce. 



372 


ABSTRACTS 


THE PINEAL GLAND IN RELATION TO SOMATIC, SEXUAL, AND 
(429) MENTAL DEVELOPMENT. Carey Pratt M‘Cord, Joum. 

Amer. Med. Assoc., 1914, lxiii., July 18, p. 232. 

M'Corp’s experiments on 110 guinea-pigs, 16 chicks, 18 puppies, 
and 14 dogs show that the precocious macro-genito-somatic 
syndrome can be obtained by feeding young animals with small 
amounts of calves’ pineal tissue. Pineal-fed guinea-pigs gave 
birth to young—normal in size and all other respects—about 
fourteen days earlier than controls of the same age (with two 
exceptions). M'C’ord concludes that administration of minute 
quantities of pineal tissue from young animals to young animals 
stimulates rapid growth of the body, but not beyond normal adult 
size; and that there are also less well established indications of 
precocity of mental and sexual development. The large size of a 
pineal-fed chick and guinea-pigs is figured. (There is no state¬ 
ment that hypertrophy of the testes was produced, nor that young 
females showed the same overgrowth of body as the males; but 
from M'Cord’s description it seems probable that they did.) 

Leonard J. Kidd. 


PATHOLOGY. 

ON THE CHANGES IN THE CENTRAL NERVOUS STSTEM IN 
(430) EXPERIMENTAL DIPHTHERITIC INTOXICATION AND 
HUMAN DIPHTHERITIC INFECTION. (Sopra le altenurioni 
del sistema nervoso centrale nella intossicazione difterica 
sperimentale e nella infezione difterica umana.) U. Sartkschi, 
Jtiv. ital. di Neuropat., Psichiatr. ed Elettroter., 1914, vii., p. 145. 

The changes found by the writer after subcutaneous injection of 
diphtheria toxin in the central nervous system of rabbits, guinea- 
pigs, and dogs were as follows:— 

1. Degenerative lesions of an acute type in the tigroid 
substance of the nerve cells of the cortex, cerebellum, and spinal 
cord. 

2. Progressive changes in the neuroglia. 

3. Absence of vascular infiltration. 

4. Presence of substances due to basophilo-metachromatic 
disintegration. 

5. Slight increase (more marked in rabbits and guinea-pigs 
than in dogs) of lipoid substances stained by the Daddi- 
Herxheimer method: Marchi method negative. 

Examination of the brains of five children, aged from 1 £ to 
4 years, who had died of diphtheria showed the following:— 

1. Severe lesions in the majority of the nerve cells of the 



ABSTRACTS 


373 


cortex and cerebellum, and less severe lesions in the cells of the 
cord. 

2. Changes, chiefly of a progressive type, in the neuroglia. 

3. Abundance of fatty substances round the blood vessels, 
either in the form of masses of free fat or as an accumulation of 
granulo-fatty cells: a scarcity and often complete absence of nerve 
substances in the protoplasm of the nerve cells and neuroglia. 

4. Complete absence of perivascular infiltration and paren¬ 
chymatous haemorrhages. 

5. Presence of substances due to basophilo-metachromatic 
changes. 

The histopathology of the lesions of the nervous system 
produced by diphtheritic intoxication in man was therefore sub¬ 
stantially the same as in experimental diphtheria. 

J. D. Rolleston. 

ON A COUNTERSTAIN FOR WEIGERT PAL PREPARATIONS. 

(431) (Uber eine Nachf&rbung bei Weigert-Pal Pr&paraten.) Paul 
Rothig, Neurol. Centralbl., 1914, xxxiii., Feb. 15, S. 219. 

After staining according to the received Weigert-Pal methods the 
author recommends putting the sections for twenty-four hours, at 
room temperature in a saturated watery (distilled water) solution 
of “ vital-scharlach viiL” (Griibler), of which solution 10-20 c.c. 
are taken and added to 90 c.c. distilled water. Thereafter the 
sections are placed in tap water for fifteen minutes, 70 per cent, 
alcohol for one hour, and in fresh 70 per cent, alcohol for half an 
hour; this will take the colour out of the celloidin of the sections. 
Then they go into 96 per cent, alcohol, and so through carbol xylol. 

The ganglion cells and their processes, and the axones, are 
stained a beautiful red. The stain seems to be permanent. 

S. A. K. Wilson. 

PECULIAR ALTERATIONS OF THE MYELIN SHEATHS IN DE 

(432) GENERATING NERVE FIBRES. (Eigenartige VerStaderungen 
der Markscheide an degenerierenden Nervenfasem.) Matlau- 
schek, Neurol. Centralbl ., 1914, xxxiii., April 1, p. 403. 

The author describes what is really a fairly frequent change in 
degenerating nerve fibres—a swollen honeycomb-like network in 
the myelin sheath which nevertheless stains deeply with Weigert- 
Pal. He has found it in the central nervous system as well as in 
the peripheral nerves, and considers it is not a mere artefact from 
such a hardening solution as formalin. Its exact significance is 
still unknown. Inasmuch as the affected sheath stains well, there 
can not be any gross change in its chemical constituents. 

S. A. K. Wilson. 



ABSTRACTS 


•>*- 
<> i 


4 


CLINICAL NEUROLOGY. 

THE NATURE OF CUTANEOUS SENSATION, WITH AN 

(433) INSTRUMENT FOB ITS MEASUREMENT. Walter Timme, 
Journ. New. and Ment. Dis., 1914, xli., April, No. 4. 

Ca.iai. has stated that the nervous end-organs in the skin are so 
arranged that a nervous “discharge” is produced by excitation 
due to mechanical irritation, and furthermore that each terminal 
organ, after receiving a certain quantity of stimulation, becomes 
fatigued and ceases to react. 

The author believes that the al>ovc view is incorrect. 

Details and diagrams are given of an instrument which the 
author has devised for the measurement of sensation. 

D. K. Henderson. 

THE OCULO-CARDIAC REFLEX. (Le rdflexe oculo-cardiaque.) M. 

(434) Vernet and Pktzetakis, Gaz. d. Hop., 1914, lxxxvii., p. 83. 

THE OCULO-CARDIAC REFLEX. (Le rlflexe oculocardiaque) F. 

(435) Sainton, Paris Med., 1913-14, iv., p. 12*2. 

Both papers contain a full account of the reflex, illustrated by 
tracings and with a summary of the literature. 

J. D. Rolleston. 

PAINLESS TUMOURS OF THE SPINAL OORD. Pearce Bailey, 

(436) Journ. Amer. Med. Assoc., 1914, lxiii., July 4, p. 6. 

Four cases are here recorded. The first was a schoolgirl, aged 14, 
who suffered from paraplegia so profound that she was unable to 
stand or walk. The condition had begun three years previously after 
measles. The paraplegia improved greatly after an operation for 
right otitis media. The absence of pain and presence of scoliosis 
suggested tuberculosis or syringomyelia, but the symptoms got worse, 
and operation showed a brownish-red encapsulated tumour which 
was intramedullary, and had burst through the posterior surface 
of the cord. It proved to be a sarcoma. 

The second case occurred in a blacksmith, aged 47, and was of 
eight years’ duration. The special feature of his case was that, 
although there was pain, it was intermittent, varied in location, 
and the intermissions were so long that the pain was not associated 
with the spastic paraplegia from which he suffered, and in conse¬ 
quence he was shown to the clinique for three years as a case of 
multiple sclerosis. The tumour was intramedullary, and found in 
the cervical region. 

The third case was that of a woman, aged 28, who was found 



ABSTRACTS 


375 


to have an extramedullary psammosarcoma of the upper dorsal 
cord of six years’ duration. It was successfully removed, but the 
symptomatic improvement was slight. The pain in her case was 
never more than a dull ache, and was treated as rheumatism. 

The fourth case was a woman, aged 34, who had an intra¬ 
medullary perithelioma of the raiddorsal cord of nine months’ 
duration. The pain was referred to a floating kidney, which 
undoubtedly existed. 

Presence or absence of pain is no proof that the condition is 
intramedullary or extramedullary. A. Ninian Bruce. 

GIANT TUMOURS OF THE CONUS AND CAUDA EQUINA. 

(437) Joseph Collins and Charles A. Elsbbro, Amer. Joum. Med. Set., 
1914, cxlvii., April, No. 4. 

Three cases are reported. The important features of the clinical 
examination were the following:— 

1. Rigidity of the lumbar vertebral column. 

2. Weakness and stiffness of the lower limbs. 

3. Paralysis of the peroneal groups of muscles and sometimes 
of the tibialis anticus group. 

4. Absence of knee and ankle-jerks. 

5. Tenderness of the lower lumbar spines. 

6. Irregular and unsymmetrical sensory disturbances. 

7. Lumbar puncture was negative. 

At operation a large reddish-brown, not vascular, tumour 
within the dura was found. The results of the operative inter¬ 
ference were not satisfactory, although there was considerable 
improvement in two patients. It was impossible to remove the 
growths entirely, although most of it could be removed if the 
operation was divided into two stages. D. K. Henderson. 

▲ EASE CASE OF SPINA BIFIDA, WITH SUBSEQUENT DE- 

(438) VELOPMENT OF SYMPTOMS REFERABLE TO INVOLVE¬ 
MENT OF THE CAUDA EQUINA, CONUS MEDULLARIS, 
AND EPICONUS. (Ein seltener Fall von Spina bifida mit 
sp&terem Einsetzen der Symptoms seitens Canda equina, Conns 
mednllaris, Epiconus, usw.) Tutyscbkin, Neurol. Centralbl., 
1914, Feb. 1, p. 153. 

The patient was born with a spina bifida, which gave rise to no 
neurological symptoms until he was 21 years of age. At that age 
a gradual onset of weakness in the legs occurred, with subsequent 
muscular atrophy and contractures, trophic changes in the joints, 
enuresis, pigmentation of the skin, and sensory changes, extending 
from the fourth lumbar to the fifth sacral segment. 

S. A. K. Wilson. 



ABSTRACTS 


37 


6 


TRAUMATIC LESION OF THE DISTAL SEGMENTS OF THE 
(439) SPINAL CORD FOLLOWED BT PROGRESSIVE SPINAL 
AM7OTROPH7. (Sn di an caso di lesione traumatica dei segmenti 
distali del midollo spinale seguita da amiotrofia spinale pro¬ 
gressiva. ) G. Biondi, Riv. ital. di Neuropat ., Psichiatr. ed 
Elettroter ., 1914, vii., p. 49. 

A previously healthy man, aged 34, without hereditary ante¬ 
cedents, foil off a tree six metres from the ground. After a brief 
period of retention he had incontinence of urine and faeces, 
absolute sexual impotence, and paralysis of the lower limbs. 
There was no immediate loss of motor power in the upper limbs, 
but the distal segments of lx>th upper and lower limits gradually 
developed hypotrophy. On examination a year after the accident 
the incontinence of urine and fteces and loss of erectile power 
persisted. There were also “ riding-breeches ” anaesthesia, paralytic 
gait, hypotrophy, and hypotonus of the muscles of the dorsum 
pedis and leg on each side of the thenar and hypothenar emin¬ 
ences, and dorsal interossei of the hand. The movements of the 
fingers and distal segments of the lower limbs were feeble and 
limited. 

The lesions were attributed to one or more haemorrhagic foci 
in the lumbo-sacral cord, especially in the conus medullaris. 

J. D. Rolleston. 


FEMININE TABES. A COMPARATIVE STUD7 OF TABES AT 
( 440 ) BIC&TRE AND THE SALPETRIErE. (Tabes ftminin. Etude 
comparde du tabes k BicStre et & la Salpdtridre.) R. Peknet, 
Theses des Paris , 1913-14, No. 313. 

Peknet studied 40 cases of tabes in men at Bicetre and 
43 in women at the Salpetriere, and found that most of the 
symptoms in both sexes occurred with equal frequency and 
severity. Thus the percentage of ocular palsy in men was 14 ') 
and in women 16*2. Arthropathies occurred in 22 5 per cent, of 
the men and in 25 per cent of the women. 

Gastric crises were more frequent in women. The most 
characteristic feature, however, of feminine tabes was its para¬ 
plegic tendency, shown by a disturbance of gait necessitating 
confinement in bed, considerable loss of muscular power, especially 
of the dorsal flexors of the foot, frequency of club foot(Joffroy), and 
severe sphincter troubles. 

The preponderance of paraplegia in the female patients is 
attributed to the congenital weakness of the lower limbs in women 
(Duprd). (Cf. Review, 1912, x., pp. 233 and 551.) 

J. D. Rolleston. 



ABSTRACTS 


377 


A CLINICAL AND PATHOLOGICAL CASE OF ISOLATED 

(441) ARGYLL ROBERTSON PUPILS IN THE ABSENCE OF 
GENERAL PARALYSIS, TABES, AND CEREBRO SPINAL 
SYPHILIS. Nonne and Wohlwill, Neurol. Centralbl ., May 16, 
1914, p. 611. 

The patient was an alcoholic woman of 38, who had syphilis 
thirteen years previously. The only clinical nervous symptom 
was fixed pupils with slight myosis. The blood and cerebro-spinal 
fluid were normal to the usual tests. After death (cause not 
stated) the central nervous system was found to be normal: it is 
noted, however, that the arachnoid was thickened and contained 
more cells than usual: this the authors think is due to the 
alcoholism. 

Unfortunately there was no examination made of the veiy part 
of the brain likely to have been affected, viz., the origin of the 
third nerve nuclei. The authors nevertheless conclude that fixed 
pupils may be the only residuum of previous syphilis, and that 
they are not necessarily the expression of an already existing or 
commencing tabes, or general paralysis, or cerebro-spinal syphilis. 
They consider their case of “primary importance” for reasons 
which are not convincing. S. A. K. Wilson. 

ON RECKLINGHAUSEN’S NEUROFIBROMATOSIS. (Zum Stadium 

(442) der Recklinghausen’schen Nenrofibromatose.) G. Hebxhbimer 
and W. Roth, Beitr. z. path. Anat. u. z. allg. Path., 1914, lviii., 
pp. 319-389. 

This article contains the record of the following four cases, and 
an exhaustive discussion of every aspect of Recklinghausen’s 
disease. 

Case 1.—Man, aged 38. Multiple skin fibromata present since 
birth, and multiple fibromata of the large peripheral nerves. 
The father had also been similarly affected. A tumour in the 
region of the thyroid rapidly increased in size and caused con¬ 
siderable dyspnoea, which necessitated tracheotomy. Death 
occurred shortly afterwards. The necropsy showed sarcomatous 
changes in the fibromata and metastases in the lungs. 

Case 2.—Man, aged 55, with multiple skin fibromata for twenty 
years. A few months before death severe pain in the right hip 
occurred, and a rapidly growing tumour appeared on the right side 
of the os sacrum. Lumbar puncture showed no lymphocytosis. 
Wassermann’s reaction was positive. Death occurred from 
cachexia. The necropsy showed isolated fibromata of the inter¬ 
costal and lumbar nerves, a small sarcoma of the left lumbar 
plexus connected with a large tumour situated in the pelvis, 
tumours of the sympathetic cord and the sympathetic lumbar 



378 


ABSTRACTS 


intervertebral ganglia, a tumour in the medulla of the right 
suprarenal, and multiple subserous nodules in the jejunum. 

Com 3.—Man, aged 03. Multiple skin tumours of thirty 
years’ duration without obvious nerve tumours. No pigmentation 
nor blue spots. 

Case 4. — Girl, aged 21, witli skin tumours and anomalies of 
pigmentation. J. 1). Rolleston. 

PNEUMOCOCCAL MYELITIS. (Lea myllites pneumococciques.) 

(443) Mlle. N. Bachmachnicoff, Theses de Paris, 1913-14, No. 300. 

Myelitis is a very rare complication of pneumonia. It usually 
occurs after defervescence, and only exceptionally before the 
temperature has become normal. It may run a mild course 
manifested by incomplete paraplegia, with rapid recovery, or 
assume the type of acute ascending paralysis with rapidly fatal 
termination. The thesis contains the histories of eleven cases, 
including the following original one:— 

A woman, aged 24, two days after the temperature had 
almost reached normal, suddenly developed incontinence of urine 
and fteces, and complained of severe pain in the loins and lower 
limbs. There was paresis of the lower limbs, especially of the 
extensor muscles, and both knee and ankle jerks were abolished. 
The cerebro-spinal fluid escaped under hypertension, but was 
otherwise normal. Recovery took place in about a month. 

J. D. Rolleston. 

A CASE OF TUBERCULOUS DISEASE OF THE VERTEBRA, 

(444) COMPLICATED BY AN EXTENSIVE ACUTE SUPPURATIVE 
MENINGITIS. James Miller and A. Fergus Bewat, Lancet, 
1914, July 25. 

This case was seen after symptoms of acute meningitis had 
developed. There was a previous history of tuberculous disease 
of the spine. The pathological findings confirmed the presence 
of tuberculous vertebra;, and the terminal infection was due to 
the Streptococcus mucosas. The purulent exudate around the 
spinal cord was very thick, and stretched from the foramen 
magnum to the lowest part of the cord. Authors’ Abstract. 

MENINGEAL SYNDROME IN NORTH AFRICAN RECURRENT 

( 445 ) FEVER. (Syndrome mlningd dans la fidvre recurrent® nord- 
afiricaine.) Abdin - Deltheil, M. Raynaud, Coudray, and 
Derrien, Bull et Mem. Soc. me'd. Hop. de Paris, 1914, xxxvii., 

p. 1126. 

Of 41 cases observed by the writers, 16, or 39 per cent., showed a 
definite meningeal syndrome. With a single exception, in which it 




ABSTRACTS 


379 


appeared first during the second attack, this syndrome occurred 
constantly during the first attack. In most of the cases it 
appeared in the subsequent attacks as well. In all the cases 
the cerebro-spinal fluid was perfectly clear, and in most contained 
an excess of albumin. Cerebro-spinal lymphocytosis was always 
found. Bacteriological examination was invariably negative. 
Soulie ( Compt. rend. Soc. de Biol., 1907, lxiii., p. 249) is the only 
observer who has found spirilla in his cerebro-spinal fluid in 
recurrent fever. In some patients a more or less intense icterus 
occurred simultaneously with the meningeal syndrome. 

J. D. Rolleston. 

A CASE OF TYPHOID SPINE. (Tin cas de spondylite typhique.) E. 

(446) Job, Bull, et Mem. Soc. mid. H6p. de Paris, 1914, xxxvii., p. 990. 

A soldier, aged 22, contracted typhoid fever at the end of August 
and became convalescent on October 21. On December 7 symptoms 
of typhoid spine developed, and complete recovery did not take 
place till March 6. The presence of meningeal reaction was 
shown by cerebro-spinal hypertension, excess of albumin, and 
lymphocytosis. J. D. Rolleston. 

ORGANIC HEMIPLEGIA OF DIPHTHERITIC ORIGIN. (Les 

(447) htfmiplegies organiques d’origine dipht&ique.) A. Mollet, 
Theses des Paris, 1913-14, No. 264. 

The thesis contains the histories of seventy-four cases, including 
those recently reported by Leede (v. Rcvieio, 1913, xi., p. 436) 
and the abstracter {ibid., p. 280), and four not hitherto published. 

1. Hallo’s case ( v. Bemeto, 1914, xii., p. 314). 

2. Girl, aged 11 years. Severe faucial diphtheria. Left hemi¬ 
plegia on twenty-first day. Some improvement. 

3. Boy, aged 6 years. Severe faucial and laryngeal diphtheria. 
Right hemiplegia and aphasia on fourteenth day. Improvement 
of aphasia and persistence of flaccid hemiplegia. 

4. Boy, aged 3£ years. Moderate faucial and laryngeal 

diphtheria. Left hemiplegia on thirty-third day. Death from 
nephritis and broncho-pneumonia on thirty-ninth day. Necropsy 
record lost. J. D. Rolleston. 

INTRAMUSCULAR INJECTIONS OF ANTITOXIN IN THE 

(448) TREATMENT OF DIPHTHERIA J. D. Rolleston and C. 
Macleod, Brit. Joum. Child. Bis., 1914, xi., p. 289. 

The writers think that the more rapid absorption of antitoxin by 
the intramuscular as compared with the subcutaneous route is 
shown not by the effect on the faucial or laryngeal process, but 



3S0 


ABSTRACTS 


By the lesser incidence of paralysis, especially of a severe 
kind. 

Of 201 cases of diphtheria treated by intramuscular injections, 
33 eases, or 12 6 per cent., showed some form of paralysis, but only 
2 of these were severe. Eighteen were examples of palatal palsy, 
usually shown by a nasal voice only without regurgitation of fluids, 
8 of ciliary palsy, 1 of squint only, 2 of palatal palsy and 
squint, 2 of palatal and ciliary palsy, 1 of cardiac palsy, which died, 
and 1 of palatal pharyngeal and diaphragmatic paralysis, which 
recovered. Probably life would have l teen saved in the one case, 
and the paralysis have been less extensive in the other, had Larger 
doses of antitoxin been given during the acute stage. Though the 
total number of cases is too small to be absolutely conclusive, the 
comparatively low rate of paralysis, especially of a severe kind, 
is noteworthy, and is in striking contrast to the higher incidence 
noted by one of the writers (v. Jxcriar, 1913, xi., p. 398). Among 
2,300 cases treated by subcutaneous injection, of whom 477 cases, 
or 20 7 per cent., had some form of paralysis, 184 were severe and 
85 fatal eases. Authors’ Abstract. 

IS THERE A CYSTIC VARIETY OF DISSEMINATED SCLEROSIS? 

(449) (Gibt os eine zystische Form der multiplen Sklerose ?) Oppen heim, 
Neurol. Centralbl., 1914, Feb. 15, p. 211. 

Optic neuritis occurs every now and then in disseminated sclerosis. 
Its presence may be explained as resulting from an accompanying 
internal hydrocephalus or meningitis serosa, if the sclerotic process 
is localised in the immediate neighbourhood of the ependyma. 
Or it may result from an encephalo-myelitis disseminata in 
acute varieties of the disease. Or conceivably there may be a 
generalised cerebral oedema in acute cases, leading to optic neuritis. 
Oppenheim publishes two cases to show that another possibility is 
the occurrence of a meningitis serosa cystica. In these two cases, 
the patient was operated on for intracranial tumour: in each so- 
called meningeal cysts were found: eventually, unmistakable 
signs of disseminated sclerosis made their appearance. A few 
similar cases have been recorded. S. A. K. Wilson. 

HEREDITARY CEREBELLAR ATAXIA. S. A. Blauner, N.Y. Med. 

(450) Joum., 1914, c., July 11, p. 83. 

In this family three children were affected, each presenting 
different symptoms. In the first child, the eldest, the disease 
from the beginning until his death showed the cerebellar tendency, 
and the diagnosis was simple. In the second child the diagnosis 
was more difficult, and the condition resembled disseminated 



ABSTRACTS 


381 


sclerosis at first, until the cerebellar gait and the peculiar carriage 
characteristic of cerebellar ataxia began to manifest itself. In the 
third child, the youngest, death intervened too soon for the 
symptoms to become classical, but sufficient were present to justify 
the assumption that with time typical symptoms would have 
presented themselves. No autopsy. The father and mother were 
English Jews. A. Ninian Bruce. 

CLINICAL AND ANATOMO-PATHOLOGICAL NOTES ON A CASE 

(451) OF BULBO-PONTINE GLIOMA (Note cliniche ed anatomo- 
pathologiche su di un caso di glioma bulbo-protuberanziale.) 
G. Bolzani, Riv. ital. di Neuropat ., Ptichiatr. ed Elettroter ., 1914, 
vii., p. 205. 

A girl, aged 7 years, developed left internal strabismus in 
August, followed by slight left facial palsy in October. In 
November and December she had attacks of giddiness. In 
February weakness of the right upper and lower limb was noted, 
and shortly afterwards deafness in the left ear. In April she 
had frequent vomiting, the paresis of the limbs became more 
marked, there was difficulty of deglutition, and the respiration 
assumed the Cheyne-Stokes type. In June paresis of the right 
sixth nerve and lower facial occurred. Subsequently the palate 
and larynx became affected, and lastly the limbs on the right side. 
Death took place in November. The necropsy showed a giiomatous 
tumour embedded in the thickness of the pons. 

The tumour originated in the middle third of the pons on its 
dorsal surface, and first affected the nuclei of origin of VI., and 
almost simultaneously of VII. and later of VIII. on the left side. 
Gradually the tumour extended to the ventral surface of the pons 
and involved the left pyramidal tract, and at the same time the 
nuclei of origin of VI. and VII. and the pyramidal tract on the 
right side. Lastly, its invasion of the bulb was shown by the 
successive lesions of IX., X, and XII. J. D. Rolleston. 

LEFT HEMIPLEGIA OF CENTRAL ORIGIN WITH PERIPHERAL 

(452) HOMOLATERAL PARALYSIS OF THE TONGUE FROM A 
CEREBRAL TUMOUR WITH DOUBLE LOCALISATION. 
(Emiplegia sinistra di origine centrale con paralisi periferici 
omolaterale della lingua a doplice localizzazione.) Bandettini 
di Poooio Francesco, Riv. ital. di Neuropat., Ptichiatr. ed 
Elettroter., 1914, vii., p. 97. 

The patient was a man, aged 41, who had had syphilis at 17. 
Wassermann’s reaction was slightly positive in the blood and 
negative in the spinal fluid. The hemiplegia was gradual in its 

3° 



382 


ABSTRACTS 


onset, and only well marked during the last weeks of life. There 
were no contractures, abnormal reflexes (Babinski and Oppenheim), 
nor sensory disturbance. Death took place after three months’ 
illness. The necropsy showed a tumour which was histologically 
a round-celled sarcoma in the right Rolandic area, and a metastatic 
nodule adherent to the meninges near the left anterior condyloid 
foramen. J. D. Rolleston. 

ANOEIOMA IN CEREBELLAR PEDUNCLE: FATAL INTRA- 

(453) CRANIAL HAEMORRHAGE. C. Wynn Wiboman, Lancet, 1914, 
cIxxxtL, June 20, p. 1746. 

A man, aged 19, who had suffered from “nagging pain” at the 
back of the head from time to time, was suddenly found dead. 
He had been quite cheerful half an hour previously. At the 
autopsy a cavity measuring 4 by 2 cm. was found in the white 
matter of the right cerebellar hemisphere. It contained a blood 
clod. Anterior to this the section of the right cerebellar peduncle 
was marked by an irregular grey patch, which microscopically 
proved to be an angeioma. The vessel walls were mostly in a 
condition of hyaline degeneration and calcified in places. 

A. Ninlan Bruce. 

TUMOUR OF FRONTAL REGION OF BRAIN. Theodore Diller and 

(454) R. T. Miller, Jun., Amer. Joum. Med. Set., 1914, cxlvii., April, No. 4. 

The report of a case in which the tumour was successfully 
removed. D. K. Henderson. 

OPERATIVE REMOVAL OF A PINEAL CYST. (Die operative 

(455) Entfemung einer Zyste der Glandula pinealis.) Pussbp, Neurol. 
Centralbl., May 1, 1914, p. 560. 

The patient was a boy of 10, with symptoms referable to the region 
of the corpora quadrigemina: a tumour either of that part, or of the 
superjacent pineal gland, was diagnosed. The author operated by a 
large bilateral occipital craniectomy, in two stages. By opening the 
dura to one side of the middle line, dealing with the sinuses, and 
splitting the tentorium right forward, he was able to reach a cystic 
tumour of the pineal which was evacuated. The patient died on 
the third day after operation. S. A. K. Wilson. 

ANEURISMS OF THE VESSELS OF THE BRAIN. John H. W. 

(456) Rhein, Joum. Nerv. and Ment. Die., 1914, xli., April, No. 4. 

The case of a man, 57 years, is described, showing that paralyses, 
which are met with in some cases, may be coincidental rather 
than related directly to the aneurism itself. 


D. K. Henderson. 



ABSTRACTS 


383 


▲ CASE OF PEOGBESSIVE LENTICULAR DEGENERATION. 

(457) E. M. Auer, Joum. Nerv. and Ment. Bit., 1914, xli, April, No. 4. 

A CASE without autopsy in a woman, 62 years, showing continuous 
tremor, constant rigidity, true contractures, dysphagia, dysarthria, 
possible familial hepatic disturbance, and evidence of disease of 
the liver. D. K. Henderson. 

ON RIGHT-BRAINEDNESS IN BIGHT-HANDED INDIVIDUALS. 

(458) (Uber Bechtahirnigkeit bei BechtshKndern.) Mendel, Neurol. 
Centralbl., 1914, March 1, p. 291. 

This case is extremely important and deserves careful 
attention. The patient, a woman of 42, right-handed, with no 
left-handedness in the family, developed a sudden left hemiplegia 
with complete motor aphasia, which continued to her death many 
months later. The lesion was an embolic (from heart disease) 
softening in the distribution of the right sylvian artery, involving 
and destroying the right inferior frontal gyrus, the insula and the 
superior temporal gyrus. It was proved microscopically that the 
left hemisphere was intact. 

It is certain, therefore, that in this right-handed patient the 
motor speech centres were in the right hemisphere. As there was 
no trace of sensory aphasia, in spite of the situation of the lesion, 
the author concludes that the sensory speech centres were in the 
left hemisphere, and regards the case as one of dissociated or 
crossed aphasia. S. A K. Wilson. 

CLINICALLY NEGATIVE OASES OF APHASIA (Zur Casuistik 

(459) der kliniscb negativen FElle von Aphasie.) Bickel, Neurol. 
Centralbl., 1914, March 1, p. 287. 

The patient was a right-handed man of 50, suffering from a cerebral 
tumour found subsequently in the left island of Reil: both the 
inferior frontal gyrus and the superior temporal gyrus were 
compressed and flattened. The patient spoke slowly and in¬ 
distinctly, and had occasional difficulty in finding words. The 
author calls this a negative case, and explains the absence of more 
definite aphasia on the ground that with a slow growing tumour 
the right hemisphere had time to function vicariously for the left. 
He does not mention, apparently, the possibility of its being a case 
of so-called crossed or dissociated aphasia. S. A. K. Wilson. 

ON THE BELATION OF THE FUNCTION OF SPEECH TO INTONA- 

(460) TION, TONE, AND BHYTHM. (Uber die Beziehung der Sprech- 
funktion zur Intonation, zum Ton und Bhythmus.) Agad- 
schanianz, Neurol. Centralbl., 1914, March 1, p. 274. 

The first case was that of a patient of 62, who had a slight stroke 
producing hemiparesis on the left side. He had formerly been a 



ABSTRACTS 


'584 

good violin player. On examination lie was found to have vocal 
and instrumental motor amusia, sensory and motor defect in 
rhythm, and incomplete word deafness and melody deafness. 

The second case was that of a doctor of medicine, aged 50, who 
had been an expert pianist. He had a stroke on the right side, 
which cleared up as far as the paralysis was concerned. It was 
found, however, that while there was no instrumental amusia, the 
patient could no longer sing, although he could speak. He under¬ 
stood spoken words imperfectly, but much better than familiar 
melodies played in his presence. He repeated spoken words much 
better than melodies played over for him; there was gross defect 
in the appreciation and reproduction of rhythm. 

S. A. K. Wilson. 


A CASE OP AMYOTONIA CONGENITA. C. E. Belwg, Journ. Nerv. 

(461) and Afent. Dis., 1914, xli., April, No. 4. 

The main feature in the case was a loss of muscular tone, which 
was thought to lie due to a defect in the sensory mechanisms in 
the muscles. 

Certain points in the case suggested the possibility of a 
poliomyelitis. D. K. Henderson. 

THE PATHOGENESIS OF MYASTHENIA. Stern, Neurol . Centralbl., 

(462) 1914, April 1, p. 409. 

The author describes the case of a female patient of 31, who 
suffered from exophthalmic goitre. The first sign of the myas¬ 
thenia that subsequently complicated the case, was an almost 
complete ophthalmoplegia externa: a few months later, typical 
defects in speaking and swallowing appeared, with myasthenic 
fatigability and the myasthenic reaction. Later, Chvostek’s sign 
was prominently present on both sides, and the skin became 
bronzed in patches. In the case, therefore, clinical evidence was 
forthcoming of alteration of function of the thyroid, parathyroids, 
and suprarenals. A considerable number of other cases have now 
been reported, when the evidence may be taken to suggest that 
myasthenia is a disease of the ductless glands. 

S. A. K. Wilson. 

ON SUPRARENAL AND PITUITARY OPOTHERAPY IN MYAS* 

( 463 ) THENIA GRAVIS. (De l’opothtoapie snrrdn&le et hypophysaire 
dans certains c&s de myasthdnie gravis.) Mllk. S. Blumenfeld, 
1'heses des Paris, 1913-14, No. 270. 

In some cases of myasthenia gravis suprarenal opotherapy, either 
alone or associated with pituitary extract, may produce definite 




ABSTRACTS 


385 


results which can fairly be attributed to the treatment itself and 
not to remissions of the disease. In some cases recovery seems 
to have taken place, while in others there was considerable 
improvement. 

The thesis contains the histories of nine cases, including one 
hitherto unpublished, in which the treatment was ineffective. 

J. D. Rolleston. 

CRITICAL EXAMINATION OF ONE HUNDRED PAINTERS FOR 

(464) EVIDENCE OF LEAD POISONING. Emeby R. Hayhubst, 
Amer. Joum. Med. Sci., 1914, cxlvii., June, No. 6. 

Of one hundred painters examined under favourable conditions, 
seventy showed evidence of chronic plumbism. 

The factors most frequently of value in diagnosing chronic 
plumbism are:— 

(a) Significant past history of certain complaints, e.g., loss 
of strength, nausea, foul taste, constipation, headache, insomnia, 
arthritic pains, &c. 

(b) Neuro-muscular abnormalities such as tremor, slight inco¬ 
ordination, abnormal reflexes, weakened hand-grip, and weakened 
wrists. 

(c) Circulatory disturbances affecting the blood pressure, the 
heart, and the urine. 

(d) Conditions of the gums—pyorrhoea, rarely lead-line. 

D. K. Henderson. 

OBSERVATIONS ON 120 CASES OF LEAD ABSORPTION FROM 

(465) DRINKING WATER. W. W. Stainthobpe, Lancet , 1914, 
clxxxvii., July 25, p. 213. 

The outbreak occurred in Guisborough and was due to the fact 
that the water passed through lead service pipes. All stages 
of the intoxication were seen from the commencing general languor 
and debility, attended by anaemia, to the paralytic stage ending in 
convulsions and death. Four cases ended fatally, and three infants 
below 6 weeks, who had been nourished solely on the breast, were 
affected. Lead was found in the mother’s milk in each instance. 
Premonitory symptoms were present in every case, often very 
vague. Abdominal symptoms occurred in 108, headache in 91, 
anaemia in 96 (basophilia was not specially marked), nervous 
and muscular disorders in 89, menstrual disorders in 55, constipa¬ 
tion in 40, albuminuria in 20, blue line on gums in 15, abortions in 
5, and convulsions in 2. In all of the above cases the diagnosis was 
based on the presence of lead in the urine, which, when evapor¬ 
ated to dryness and dissolved in HC1, became brown with H 2 S. 



386 


ABSTRACTS 

The following test is also worthy of note: if the hand be painted 
with ammonium sulphide the skin becomes black from the con¬ 
version of the lead excreted by the skin into lead sulphide, best 
seen on the thenar eminence. A. Ninian Bruce. 

SYPHILITIC TESTS IN LATENT AND TREATED SYPHILIS. 

(466) E. P. Corson-White and S. D. Ludlum, Joum. Nerv. and Ment. 
Di»., 1914, xli., April, No. 4. 

The most marked reduction in the Wassermann reaction appears 
in those cases treated with mercury and salvarsan or neosalvarsan, 
and next in those with salvarsan or neosalvarsan alone. Salvarsan 
apparently acts more rapidly than the neosalvarsan, although 
apparently the neosalvarsan remains longer in the blood than 
the salvarsan. Mercury gives a slow, steady diminution. 

Negative reactions do not necessarily mean absence of 
syphilitic infection or cure, even although the reaction has been 
negative for a considerable time. 

The luetin skin test, the specificity of which has up to date 
never been disproved, is less easily influenced by treatment, and 
is to-day the best criterion of genuine cure or absence of infection 
in our hands. D. K. Henderson. 

SYPHILIS AND THE ADRENALS. (Syphilis et glandes surrtnales.) 

(467) A. Sf.zary, Gaz. des H6p., 1914, Ann. Ixxxvii., July 16, p. 1317. 

Congenital syphilis, when mild or of recent date, provokes a 
hyper-spongiocytosis of the adrenal cortex, but scarcely affects the 
medullary cells; but, when virulent or of long duration, it leads 
to cortical hypo-spongiocytosis and also medullary lesions: these 
are permanent and are accompanied by sclerosis. If a congenital 
syphilitic with adrenal sclerosis survives, he shows throughout 
life a chronic latent hypoadrenalism or adrenal debility which 
may become manifest under stress of any acute infection or 
intoxication. Acquired syphilis is less harmful to the adrenals, 
but it also can lead to sclerosis and adrenal debility. Sezary does 
not believe that mercury is dangerous in syphilitic subjects whose 
adrenals are affected; for he found that injection of even fatal 
doses of corrosive sublimate into guinea-pigs gave no marked 
adrenal lesions. He urges search for evidence of syphilis in cases 
of adrenal insufficiency, and vice versa ; in positive cases one 
should combine adrenal opotherapy with mercurial treatment: 
iodide of potassium seems to be a useful adjuvant. He urges 
great caution in the use of salvarsan or any arsenical treatment in 
syphilitics who present any evidence of adrenal involvement. 

Leonard J. Kidd. 



ABSTRACTS 


387 


THE PRODUCTION AND HISTOPATHOLOGY OF EXPERIMENTAL 

(468) SYPHILIS OF THE CENTRAL NERVOUS SYSTEM IN 
RABBITS. (Zur Erzeugung and Histop&thologie der experi- 
mentellen Syphilis des Zentralnervensystems beim Kaninchen.) 

Stbinsb, Neurol. Centralbl ., 1914, May 1, p. 546. 

Tub interested reader should consult the original. The author 
has found that frequent intravenous injection of an emulsion of 
syphilitic rabbits’ testicles into albino rabbits produces typical 
central nervous system changes more rapidly and, probably, with 
greater certainty than in dark-haired rabbits. 

S. A. K. Wilson. 

THE TREATMENT OF PARENCHYMATOUS SYPHILIS BY 

(469) INTRACRANIAL MEDICATION. Habby Campbell, Lancet, 
1914, May 30. 

The experiments earned out by Golla have led Campbell to treat 
cases of parenchymatous syphilis by injecting salvarsanised serum 
into the subarachnoid space through the anterior horn of the lateral 
ventricle. Golla found that, by introducing colloidal carbon into 
the upper cranial subarachnoid space, it found its way to all parts 
of the cerebro-spinal axis more or less evenly, whereas only a 
small fraction reached the cerebral hemispheres when it was 
injected into the spinal sac. 

While spinal injections usually suffice for ordinary cases of 
tabes, Campbell thinks that in the form in which optic atrophy 
occurs intracranial injections should prove of decided advantage, 
because by this means the optic nerves can readily be reached, as 
has been proved by Golla’s experiments. R. Dods Brown. 

SAL VARS AN IN OPHTHALMIC ZOSTER. (Salvarsan bei Herpes 

(470) Zoster ophthalmicus.) H. Gebb, Med. Klinik, 1914, x., p. 1096. 

A record of two non-syphilitic cases with negative Wassermann 
reactions in which intravenous injections of salvarsan or neo- 
salvarsau were followed by rapid healing of the lesions. Gebb 
suggests that this result is due to the specific bactericidal or 
trypanocidal action of salvarsan on herpes zoster, which is now 
generally regarded as an infectious disease. 

J. D. Rolleston. 

A METHOD BY WHICH REMEDIAL AGENTS MAY BE 

(471) MINGLED WITH THE CEREBRO SPINAL FLUID. Chablbs 
A. Ballance, Lancet, 1914, May 30. 

A most instructive article, the first part of which is devoted to the 
physiology of the cerebro-spinal fluid. The method of and the 



388 


ABSTRACTS 


reasons for carrying out the operation, which consists in the 
introduction of salvarsanised serum into the lateral ventricle, is 
fully described in the second part of the paper. 

R. Dods Brown. 

THE CAUSE OF DEATH FROM SUBDURAL INJECTIONS OF 

(472) SERUM. Worth Hale, U .S. Hygienic Laboratory Bulletin, No. 
91, December 1913. 

Hale’s experiments on dogs and cats showed that death from the 
introduction of anti-meningitis serum may result from an increase 
in intracranial tension, or from the presence in the serum of the 
poisonous preservative, tricresol. Tlie danger from tricresol is 
much greater and more certain than from increase in intracranial 
pressure. He recommends that blood-pressure observations should 
always be made when cerebro-spinal fluid is withdrawn, or when 
serum is introduced into the meninges. Sophian had found that 
the blood pressure was always lowered during injection, and that 
the rate of fall was much accelerated by larger quantities of serum 
or by smaller amounts introduced too rapidly. 

J. D. Rolleston. 

ANALYSIS OF BLINDNESS AS A SYMPTOM OF HYSTERIA 

(473) T. H. Ames, Archives of Ophthalmol ., 1914, xliii, July, p. 357. 

Two cases are recorded here, the first being a girl, aged 26, who 
was hopelessly overworked at home, and developed blindness as a 
means of escape from the drudgery of the housework. The second 
was a man, aged 39, who became totally blind overnight, and came 
under observation ten weeks later. His married life had been 
unhappy, and his blindness appears to have been the expression of 
his desire not to see his wife. An analysis of this case is given, 
with some dream interpretations. Both cases recovered. 

A Ninlan Bruce. 

ON HEREDO-ALCOHOLIO DEGENERATION. (Sulla degeneration© 

(474) eredo-alcoolica.) P. Nurzla, Riv. ital. di Neuropat ., Psichiatr. ed 
Elettroter ., 1914, vil, p. 106. 

Physically heredo-alcoholics are distinguished from other de¬ 
generates by regular bodily development which does not allow 
one to suspect the gravity of their condition. Physiologically they 
show a great vaso-motor sensitiveness. As a rule, they are 
intelligent. In their affective side and their will the anomalies 
are strongly marked, and consist of a violent impulsiveness which 
may tend to crime, hardness and coldness, and a tenacious male- 



ABSTRACTS 


389 


volence. Three illustrative cases are reported in women admitted 
to asylum for recurrent mania, hysterical psychosis, and dementia 
prsecox respectively. J. D. Rolleston. 

▲ CASE OF SUPPOSED PROGERIA (PBEMATUBE SENILITY) 

(475) IN A GIRL OF EIGHT YEARS. WITH REMARKS. Carl 

W. Baud, Boston Med. and Surg. Joum., 1914, clxxi., July 16, p. 107 

Progeria is an exceedingly rare condition in which the body is 
arrested in its growth, and becomes prematurely the subject of 
senile changes, i.e., infantilism and senilism are both present in the 
same body at the same time. Progerians pass from delayed child¬ 
hood directly into a premature old age. The first case was 
recorded by Jonathan Hutchinson in 1886, two more were 
reported by Gilford in 1904, and a fourth by Variot and 
Pironneau in 1910. The present case is a girl aged 8 years, 
who has all the appearance of old age. Her parents were 
Russian Jews, and she was the eleventh of twelve children. Her 
home surroundings were very bad, and she could not be kept at 
school on account of the effect of her peculiar appearance on the 
other children. A good description is given, together with four 
illustrations. A. Ninian Bruce. 

CARBON MONOXIDE POISONING IN THE SENGHENYDD. Ivor 

(476) J. Davies, Proc. Roy. Soc. Med., 1914, viL, June, p. 219 ; Brit. Med. 

Joum., 1914, July 11, p. 57. 

The Senghcnydd explosion happened on October 14, 1913, and is 
the worst disaster in the history of British mining. The number 
of men killed was 440, most of whom were asphyxiated by carbon 
monoxide gas. The symptoms, which are duo solely to lack of 
oxygen caused by the temporary impairment in the oxygen-carrying 
power of the blood, consist of a marked feeling of languor and an 
irresistible desire to rest quite regardless of immediate danger. 
Headache, tinnitus, palpitation, breathlessness, and weakness of 
the lower limbs were also usually present. No mental distress is 
found. Apart from injuries, the most marked appearance on the 
bodies was the bright pink colour. Cutaneous lesions were found 
in some cases over pressure points, e.g., the buttocks, &c., and 
peripheral neuritis, possibly also due to pressure, occurred. The 
author considers, however, that the cutaneous lesions are true 
manifestations of CO poisoning of neurotrophic origin. The 
treatment consists of removal to fresh air, inhalation of oxygen, 
Schafer’s artificial respiration, and avoidance of the effect of sudden 
cold outer air which is liable to produce serious collapse. 

A. Ninian Bruce. 


3* 



390 


ABSTRACTS 


CHRONIC OCULAR TUBERCULOSIS. NECROPSY FINDINGS IN 

(477) A CASE IN WHICH DEATH WAS DUE TO TUBERCULOSIS 
OF THE HYPOPHYSIS CEREBRI. F. H. Verhoeff, Joum. 
Amer. Med. Assoc., 1914, lxiiL, July 4, p. 13. 

A married woman, aged 36, became affected with keratitis in the 
right eye three years before death. This subsided after a year, 
and the left became similarly affected, the right eye soon becoming 
again inflamed. Fundus changes could not be made out on account 
of the corneal opacities. Tuberculin reactions were negative. 
During her final stay in hospital she became dull and apathetic, 
and developed polyuria and polydipsia. There was no sugar or 
albumin in the urine. The pulse rate showed extreme variations. 
At the autopsy the right lung showed tubercular foci. The 
meninges were normal. The pituitary was enlarged to about ten 
times its usual volume, measuring 21 mm. by 18 mm. by 15 mm. It 
was firmly united with the chiasma, which it had carried backward. 
The brain was normal on section and showed no evidence of 
tubercle. On section the pituitary was found to have been 
converted into a large tubercle of the fibroid type, with a central 
caseous centre about 5 mm. in diameter. From the pituitary the 
tuberculous process had invaded the chiasma. A description of 
the microscopic changes in each eye is given. The author could 
only find eight cases of hypophyseal tuberculosis, none of which 
were associated with ocular involvement. It is hardly conceivable 
that the pituitary lesion could have given rise to the ocular 
tuberculosis by way of the optic nerve, because the chiasma was 
only slightly involved at death, and there were no foci in the optic 
nerve or in the choroid. Probably the ocular and pituitary lesions 
were independent of each other, the primary seat being in the 
lung. A. Ninian Bruce. 

TWO CASES OF ACUTE RETROBULBAR NEURITIS, ASSOCIATED 

(478) WITH MARKED ACETONURIA. Joum. Amer. Med. Assoc., 
1914, lxiii., July 4, p. 27. 

The first case was that of a girl, aged 84, an exceptionally healthy 
child until a few days before examination, when she complained 
of not being able to see the Hack board, and of dull frontal 
headaches. The fundus revealed no change in the appearance of 
the nerve-head or retinal vessels, but an absolute scotoma for red 
was present, the fields for white and blue being normal. Nothing 
abnormal could be discovered except a mild acetone reaction in 
the urine, but no diace tic acid. Under a regulated diet the acetone 
disappeared, and a test with a red disc showed no colour defects. 

The second case was a man aged 31, married, who suddenly 
noticed that the vision of his left eye was blurred, and the sight 



ABSTRACTS 


391 


noticeably impaired. On examination, the discs were found to 
be sharply outlined, of normal colour and appearance. The 
visual field of the right eye appeared normal for white, blue, and 
red; on the left eye an absolute scotoma for red and a relative 
for blue were present. A “ very heavy acetone reaction ” was 
found in the urine, but no other evidence of disease. 

Hysteria was absent in both cases, and it is suggested that 
possibly the acetone may be an etiologic factor in cases of retro¬ 
bulbar neuritis of otherwise obscure origin. At the discussion 
it was suggested that such scotomas may represent and interpret 
fatigue of the macular region, or an oedema of the optic nerve analo¬ 
gous to the acute swelling of the eyelids. A. Ninian Bruce. 

LABYRINTH ACTIVITY, (fiber die Art der Labyrintht&tigkeit.) 

(479) O. Gobbkl, Berl. klin. Wchntchr ., 1914, May 11, 8. 872 and 979. 

A paper in which small details are discussed at very great length. 
The writer does not hold with Helmholtz’s theory of sound 
perception nor with Ewald’s, though it is not quite clear what 
his own theory is. He says that there is no guarantee that a soft 
note and a loud one of the same pitch are perceived by the same 
hair cells. He agrees with Helmholtz in so far as he believes 
that low tones are perceived by the apical coil and high tones by 
the basal coil of the cochlea. The mammalian maculae show a 
great resemblance in structure to the cochlea of birds. From this 
he concludes that the macula? are also concerned with sound 
perception in mammals. If acoustic function is granted in the 
case of the otolith membrane of birds, it probably is the same in 
higher forms. The human maculse are probably concerned with 
perceptions of very high tones. Noises are probably perceived 
by the cristse of the vestibuli. J. K. Milne Dickie. 

A8YMB0LY. (Le asimbolie.) A. Mochi, Ratsegna di Studi Psichiat., 

(480) 1914, iv., Gennaio-Febbraio, p. 1. 

The author defines asymboly as a disturbance of secondary identi¬ 
fication. Disturbance of primary identification is known as agnosia. 
The latter process of identification includes all the psychical facts 
which lead to the complete monosensorial analysis of a perception, 
and which may be considered as the exponent of the physiological 
phenomena which unfold in the cortical area of a single sense, 
e.g., in the case of sight, perception of the colour, shape, size, and 
distance of an object and the comparison of such a synthesis with 
the optic mnemonic image. Secondary identification includes 
those phenomena which produce the image but derived from 
other sources, e.g., in the case of sight, auditory, tactile, olfactory, 
and verbal images. All physiological and psychical phenomena 



392 


BOOKS AND PAMPHLETS RECEIVED 


which do not belong to this field are excluded. In actual practice 
pure clinical cases of agnosia and asymboly are impossible. 

Asymboly is divided into two kinds, optic and tactile. These 
are discussed here at great length, the article occupying more than 
300 pages. A short anatomical account follows the clinical dis¬ 
cussion, and the difficulty of transferring the more delicate results 
of the psychological analysis of perception to the field of anatomy 
is pointed out. A. Ninian Bruce. 


PSYCHIATRY. 

TRAUMA AND GENERAL PARALYSIS. (Traumi e p&ralisi pro- 

(481) gressiva.) L. Gatti, Riv. itaL di Neuropat., Psichiatr. td Elet- 
troter., 1914, vil, p. 58. 

A record of three cases in which pre-existent general paralysis was 
aggravated by trauma. In one case it was very probable that the 
accident—a fall off a bicycle—was the result of a paralytic attack 
rather than the cause of the subsequent disturbances. In each case 
the existence of syphilis was established, in one clinically and in 
the other two by Wassermann’s reaction. J. D. Rolleston. 

SOMATIC DISTURBANCES IN DEMENTIA PRiEOOX. (Uber die 

(482) korperlichen Storungen bei der Dementia procox.) Goldstein 
and Reichmann, Neurol. Centralbl., 1914, March 16, p. 343. 

1. As probably characteristic of dementia pnecox is the combina¬ 
tion of diminution in the total leucocyte count with relative in¬ 
crease in lymphocytes, and a high erythrocyte count, and absolute 
leucocytosis with hypoglobulia during periods of excitement. 

2. In dementia pnecox, the blood picture is influenced by 
minimal doses of adrenalin and pilocarpin. 

3. The anodal excitability in dementia pnecox is definitely in¬ 
creased, and in this respect differentiates it from other psychoses. 

Increase of anodal excitability is characteristic of spasmophilia, 
which is an expression of disturbance of function of the para¬ 
thyroids : it is probable, therefore, that in dementia pnecox these 
glands, at least, are not normal. S. A. K. Wilson. 


BOOKS AND PAMPHLETS RECEIVED. 

Lohmann, W. “Disturbances of the Visual Functions.” Translated 
by Angus Macnab. With 39 illustrations in the text, some in colours. 
John Bale, Sons & Danielsson, Ltd., London, 1913. Pr. 15s. net 

Rank, Otto. “ The Myth of the Birth of the Hero.” (A psychological 
interpretation of mythology.) Authorised translation by Drs F. Robbins 
and Smith Ely Jelliffe. ( Nervous and Mental Disease Monograph , No. 18. 
New York, 1914.) 

“Fifty-sixth Annual Report of the General Board of Commissioners 
in Lunacy for Scotland.” 1914 



IReview 

of 

IReurolog^ anO ps^cbiati^ 


©rigtnal Hrttcles 


THE ALLEGED SENSORY CUTANEOUS ZONE 
OF THE FACIAL NERVE OF MAN. 

By LEONARD J. KIDD, M.D. 

1. Introduction; 2. Evidence of Comparative Anatomy; 3. Anatomical 
Considerations ; 4. Clinico-Pathological Considerations ; 5. 

Needed Experimental Inquiries ; 6. Conclusions. 

1. Introduction. 

The teaching that the geniculate ganglion of man sends sensory 
fibres to the skin of the external ear, and external auditory meatus, 
which was urged by J. Ramsay Hunt 1 in the year 1907, has been 
accepted with alacrity by most clinical writers. However, C. K. 
Mills 2 has strenuously opposed it; but, as he was specially con¬ 
cerned with the much larger question of all the sensory functions 
attributed to the facial nerve, he did not make out anything like 
so damaging a case against what we may call the cutaneous 
facialis hypothesis as he could easily have done. There was a 
certain amount of plausibility about Hunt’s presentation of the 
subject which caused almost all readers of his paper to accept his 
teaching at once. Hunt arrived at his conclusion largely from his 
studies of herpes auris. The underlying argumentation seems to 
have been somewhat as follows:—We have known for many years 
(1) that the geniculate ganglion is, in part at any rate, an afferent 
root-ganglion, homologous with all spinal dorsal-root ganglia; (2) 
that spinal root-ganglia give origin to cutaneous sensory fibres; 
therefore (3) it must follow that the geniculate ganglion gives 
origin to cutaneous sensory fibres. Of course this does not in the 
32 



LEONARD .T. KIDD 


least follow. Again, herpes is commonly believed to be due to an 
acute intlammatory lesion of a dorsal-root ganglion or ganglia; it 
seemed, then, reasonable to suppose that an isolated herpes of the 
geniculate ganglion might really occur and give rise to a true 
geniculate otalgia. Rut, even if we had conclusive proof of the 
existence of an isolated geniculate herpes, we should still not be 
justified in concluding at once that this otalgia was, even in part, 
a cutaneous otalgia. Hunt divided his cases of herpes auris into 
several groups, but the most important of these, from the point of 
view of the cutaneous facialis hypothesis, are (1) those cases of 
herpes auris that occur without facial paralysis, and (2) those that 
occur with facial paralysis. Now, if we recall the fact that the 
geniculate ganglion of man is a swelling on the course of the facial 
nerve, we must conclude at once that there could be no such thing 
as a true isolated geniculate herpes without at any rate marked 
paresis of the facial nerve. It is certain, then, that all those cases 
of herpes auris which are unaccompanied by facial palsy or paresis 
are of non-genieulato origin. There is no doubt, however, that 
there really are cases of herpes auris with complete homolateral 
facial palsy that correspond closely in the distribution of the 
herpetic vesicles with Ramsay Hunt’s so-called “ zoster zone of the 
geniculate.” I have seen four examples of this variety: in one 
there was also present a herpetic eruption on the cutaneous area 
of the homolatcral fourth cervical nerve-root. But we lack con¬ 
clusive proof that these cases are ever purely of geniculate 
ganglionic origin. It is interesting to note that in 1910 Mills was 
sceptical on this point; thus ho writes:—“The cases of herpetic 
inflammation, cervico-occipital, auricular, and facial, which have 
been observed in connection with facial paralysis, or with facial 
paralysis ami acoustic symptoms, are best explained on the 
supposition of an involvement of ganglia other than the geniculate.” 
It is greatly to he deplored that we still too often hear or read the 
unqualified statement that herpes depends on an acute inflam¬ 
matory lesion of a dorsal-root ganglion or ganglia. The real truth 
is that the lesion is a predominantly ganglionic one, hut there are 
often present also neural, radicular, meningeal, and vascular 
lesions; and sometimes the neural and the radicular lesions are as 
much primary as is the ganglionic affection. We are just as much 
in error in describing herpes as a posterior poliomyelitis, as we are 
(or were till a few years ago) in calling acute polio-encephalo- 



THE ALLEGED SENSORY CUTANEOUS ZONE 395 


myelitis simply an affection of ventral horns. In both diseases 
we have a brutal, knock-down blow by an acute gross lesion which 
irritates, compresses, or strangles every structure which it meets, 
whether it be nervous, vascular, lymphatic, or meningeal. In two 
out of Head and Campbell’s twenty-one necropsies of herpes there 
was present a primary affection of spinal nerves. Clearly, before 
we can admit the existence of an isolated geniculate herpes, we 
must have the following minimum requirements fulfilled:—We 
must have during life a typical case or cases of Hunt’s geniculate 
herpes with facial paralysis; necropsy must include a searching 
histological examination of (1) the cells of all the afferent ganglia 
from the Gasserian to the third cervical, including, of course, the 
geniculate, petrosal IX., and jugular X.; (2) of their roots; (3) 
of all their issuing auricular branches; and (4) of the membranes 
of the brain and spinal cord. And only if all but the geniculate 
ganglion and its root and branchee be found to be normal can we 
admit the existence of an isolated geniculate herpes. Need I add 
that there appears to be no recorded instance of such an obviously 
needed thorough pathological examination having been made ? 
But let us now begin at the beginning, and ask what comparative 
anatomy has to teach us as to the existence of a cutaneous facialis 
component in vertebrates. 

2. Evidence of Comparative Anatomy. 

Not only is there a total absence of any anatomical or experi¬ 
mental evidence in favour of the existence of a cutaneous facialis 
component in mammals, but there is not even any well established 
instance of this in any vertebrate class above the cyclostomcs. 

In pctromyzon Johnston found 3 that the hyomandibularis nerve 
innervates the skin of part of the hyoid segment, but that even so low 
in the vertebrate scale as this the dorsal and lateral portions of this 
area are being encroached upon by the branches of the trigeminus: 
the hyomandibularis certainly innervates the ventral cutaneous 
area of this segment. He attributes the facialis innervation of the 
skin of the hyoid segment of peiromyzon to the absence of an 
operculum. But this can hardly be the real reason, for other non- 
operculated forms, such as the selachians, ought to show a facialis 
cutaneous component, but yet they do not. In his book 4 Johnston 
attempts to explain the matter thus:—“ In forms provided with an 



396 


LEONA I'D J. KIDD 


operculum, tlie operculum is innervated by rami from the V. and X. 
nerves, and rami from the V. nerve supply the ventral surface in 
the gill region. In cgdoslomrs, where there is no operculum, a 
simpler and more primitive arrangement is found. There is a large 
cutaneous component in the VII. nerve which is distributed byway 
of the post-trematic ramus to the skin of the hyoid segment, just 
as in the more caudal branchial segments. The skin of the 
corresponding dorsal area, however, is innervated by rami from the 
V. nerve. From this it would appear that the hyoid segment had 
originally its own cutaneous innervation, and that when the 
operculum was formed the component in VII. disappeared, and the 
V. nerve supplied the parts of the hyoid segment remaining 
exposed.” Sheldon, in his excellent paper 5 on the phylogeny of 
the facial nerve and chorda tympani, writes thus, after a reference 
to Johnston’s finding in pctromipon : —“In most forms above the 
cyclostomes the evidence is strong that the only sensory component 
remaining (is., in the facialis) is the visceral, which innervates 
mucous surfaces, while the cutaneous sensation for the hyoid 
segment is served by fibres from the trigeminal or the vagus 
nerves.” He shows that in selachian-s there is a small cutaneous 
component derived probably, however, from the trigeminus by an 
anastomotic branch from the Gasserian ganglion. In Iclcosts also 
there is a cutaneous branch from the Gasserian ganglion. In 
amphibia cutaneous fibres may be present, but when they are they 
come from the vagus nerve by a communicating branch. Kingsbury, 
in his paper on “ The structure and morphology of the oblongata in 
fishes,” a writes thus of the spinal V. tract system—which he 
accepts as representing the dorsal column of the spinal cord:— 
“The exit in amia calm of a small portion of the fibres with the 
VII.-VIII. appears to be an exceptional condition,* though constant 
in the few brains examined for it.” And on page 23 he writes 
“ The spinal V. furnishes a small contingent of fibres possibly in 
ganoid's (amia) to the VII.” I have failed to find that anyone has 
ever demonstrated the existence of a cutaneous facialis component 
in any reptile, bird, or mammal. J. Gordon Wilson, in his paper 
on “ The nerves and nerve-endings in the membrana tympani of 
man,” refers 7 to “ the teaching of (J. Judson Herrick, that there is 


* Evidently he means “ exceptional for yanouls” Other ganoids studied by 
him included L( p\do*tcm ossens and aa'puttcr. 



THE ALLEGED SENSORY CUTANEOUS ZONE 397 


no proof that the geniculate ganglion ever sends general sensory * 
fibres to the skin; in all cases where general sensory fibres are 
distributed to the skin by branches of the facialis, they either have 
a separate root of their own, as in cyclostomes, or else enter the 
facialis distal to the geniculate ganglion by anastomosing branches 
from the Gasserian ganglion.” And here we may well ask the 
question:—If Herrick does not know of general cutaneous facialis 
components in any vertebrate above the cyclostomes, where shall we 
find a comparative neurologist who knows more about nerve com¬ 
ponents than he ? Clearly, then, as the comparative neurologist 
does not know of a cutaneous facialis component in any mammal, 
it behoves the mere clinician to walk softly and ask himself whether 
Ramsay Hunt’s teaching will bear close scrutiny. It might, of 
course, be urged that mammals, up to man, may after all resemble 
cyclostomes in this matter; but though this is just theoretically 
conceivable, it can be shown that man certainly does not possess 
a sensory cutaneous facialis innervation. 

3. Anatomical Considerations. 

There are in man at least four possible anatomical routes by 
which the skin of the auricle might receive sensory fibres from 
the geniculate ganglion, viz:—(1) By the small superficial petrosal 
nerve, the otic ganglion, and the auriculo-temporal branch of the 
trigeminus; (2) by the communicating branch which the facial 
trunk gives to the auriculo-temporal nerve from its temporo-facial 
trunk before the latter splits into its three terminal branches; (3) 
by the temporal branches of the temporo-facial division which 
communicate with the auriculo-temporal nerve; (4) by the com¬ 
municating branch which the facial nerve sends to the auricular 
branch of the vagus nerve. To these four routes Ramsay Hunt 
adds the posterior auricular branch of the facial nerve. This 
branch is described by almost all anatomists as a purely muscular 
branch to the auricular muscles and the occipitalis muscle; but 
Valentin describes it as sending cutaneous filaments to the auricle. 
It is also to be remembered that the posterior auricular branch of 

* Thia term is used by American comparative neurologists to denote true 
sensory cutaneous fibres which subserve tactile sensibility: they use the term 
“special cutaneous” for those fibres whioh innervate the neuromasts (the 
acoustico-lateralis system), i.e., the pit and canal skin-organs of the head, and 
the lateral line of the trunk of fishes and aquatic amphibians. 



398 


LEONARD J. KIDD 


the facial nerve communicates with the great auricular branch of 
the cervical plexus, so that fibres could pass from the geniculate 
ganglion thus to the auricle. On putting all these points to¬ 
gether we see that (1) a lesion which destroys the geniculate 
ganglion will of course interrupt all these five sets of hypothetical 
sensory cutaneous facialis fibres; and that (2) a complete lesion 
of the facial nerve which involves the chorda tympani, and gives 
clinically loss of taste on the anterior part of the tongue with 
facial palsy, will interrupt all five sets of cutaneous fibres, with the 
possible exception of those which might pass out from the geniculate 
ganglion by the small superficial petrosal nerve. In Hunt’s later 
paper, 8 published two years after his first one, he figures the sensory 
system of the facial nerve of man as he conceived it: the sensor)' 
fibres are shaded, and we find that they include the posterior 
auricular branch of the facial nerve, and also the proximal end of 
the temporo-facial division; clearly, therefore, he intended us to 
regard those branches at any rate as constituting the anatomical 
paths of his cutaneous facialis fibres. It is necessary here to give 
an account of the experiments of both Amabilino and van 
Gehuchten, for not only has Hunt mixed them up in a surprising 
fashion, but we can also see how he probably came to favour the 
temporo-facial division of the facial nerve as at any rate forming 
one of the routes for the passage of his sensory cutaneous facialis 
fibres. 

Amabilino 9 performed two distinct sets of experiments on 
adult dogs. In the first group he opened the middle ear and per¬ 
formed avulsion of the chorda tympani nerve. The animals were 
sacrificed after from twelve to forty-six days. Typical Nissl 
degeneration was found in about four-fifths of the cells of the 
homolateral geniculate ganglion. In the second group of dogs 
Amabilino removed 1 cm. of the facial nerve below the stylo¬ 
mastoid foramen; subsequently no cell changes were found in the 
geniculate ganglion. And yet Ramsay Hunt definitely wrote in 
1909 * that “ the presence of such sensory fibres (i.e., rising in 
cells of the geniculate ganglion) in the facial trunk has been 
demonstrated experimentally by Amabilino. These experiments 
consisted in cutting the nerve at its exit from the stylomastoid 
foramen, and studying the retrograde degeneration in the cells of 
the geniculate ganglion; another proof that these cells have a 

* Loc . cit., p. 332. 



THE ALLEGED SENSOKY CUTANEOUS ZONE 399 


common sensory function apart from those subserving the function 
of taste. These sensory fibres in the trunk are destined for the 
cutaneous distribution of the facial on the external ear (zoster 
zone of the geniculate).” But Amabilino failed to (jet the changes 
which Hunt says he obtained; and it was van Gehuchten 10 who 
did find retrograde chromolytic changes in a very small number of 
the cells of the rabbit’s geniculate ganglion subsequently to a 
section of the facial nerve at the level of the stylomastoid 
foramen. And, further, van Gehuchten concluded that these 
ehromolysed cells of the geniculate ganglion give origin to 
afferent fibres which pass peripherally by the peripheral muscular 
branches of the facial nerve to its mimetic muscles; and he asks 
the question: “ Where else could they go ? ” It is obvious that 
if Amabilino had really obtained retrograde chromolysis of any 
cells of the geniculate ganglion after cutting out a portion of the 
facial nerve below the stylomastoid foramen, van Gehuchten 
would naturally have quoted this as agreeing with his own 
experimental findings, whereas he expressly points out that 
Amabilino must have overlooked the presence of ehromolysed 
cells, for in the rabbit they are very few in number. Probably 
Hunt believed that the number of ehromolysed cells of the 
geniculate ganglion found by van Gehuchten in the rabbit corres¬ 
ponded to about the number of cells which we might expect to 
find in the geniculate ganglion of man as the ganglionic centre of 
the hypothetical cutaneous facialis fibres. But we know that in 
the monkey * about one-third of the medullated fibres of the facial 
nerve, distal to the point at which the branches to the posterior 
digastric and stylohyoid muscles are given off, are afferent fibres 
which are distributed to the mimetic facial muscles. The ex¬ 
ceedingly small number of these mimetic facial muscle afferent 
nerve fibres in the rabbit is perfectly explained by the fact, to 
which I referred f in 1909, that in mammals below the Carnivora 
and the Primates the mimetic facial muscles are quite in¬ 
significantly developed in degree. In the next section of this 
paper I will show that the temporo-facial division of the human 
facial nerve does not convey any sensory cutaneous fibres to the 
auriculo-temporal nerve, and thence to the auricle. 

* F. H. Edgeworth, Jour, of Anat. and Physiol., 1899, N.S. xiv., p. 124. 

t L J. Kidd, Rer. of Neurol, and Psychiatry, 1909, vii., p. 173. 



400 


LEONARD J. KIDD 


4. Clinico-Patholocical Considerations. 

In studying the clinieo-pathological aspect of this subject we 
have to consider the question of either pain or diminution or 
loss of cutaneous sensibility in the area of distribution of the 
alleged sensory cutaneous fibres of the facial nerve. It is clear 
that the presence of an otalgia confined to Hunt’s zoster zone of 
the geniculate ganglion would not of itself prove the existence of 
any cutaneous facialis fibres, because the facial nerve may, as 
Hunt and others teach, supply sensory fibres to the membrana 
tympani, mastoid cells, &c. And, as all the alleged cutaneous 
facialis fibres rise in cells of the geniculate ganglion, it would follow 
that after a complete extirpation of that ganglion, or a complete 
division of its afferent root, the pars intermedia of Wrisberg, we 
should have a complete cutaneous anaesthesia of Hunt’s zoster 
zone of the geniculate ganglion, to say nothing of other sensory 
areas of the facial nerve ; and, further, this post-operative cutaneous 
amesthesia would be permanent because functional regeneration 
of divided afferent roots does not, as far as we know, ever occur. 
Now there is one such operated ease on record, viz., the case of 
L. Pierce Clark, operated on by Alfred S. Taylor, reported 11 before 
the New York Neurological Society in 1909. The patient had 
been previously shown by Clark before the American Neurological 
Association in June 1909, five weeks after operation, as a cured 
case of Ramsay Hunt’s peculiar form of geniculate otalgia. The 
case is entitled : “ The report of a case of tic douloureux of the 
sensory filaments of the geniculate ganglion: operation, recovery.” 
The patient was a young woman “ whose neuralgic pain was 
rather sharply limited to the anterior wall of the external meatus 
and a small portion of the skin just in front of the ear, the 
essential supply zone of the geniculate to the ear and face, as 
described by Hunt.” At the operation Taylor exposed and 
identified the facial, eighth, ninth, tenth, and eleventh nerves, 
but only the facial, pars intermedia, and the upper fasciculus of 
the eighth nerve were divided. And yet, amidst all the well- 
deserved rejoicings that followed the recital of this case on this 
New York joy-day, in which Ramsay Hunt took part, actually no 
speaker asked the question as to what was the post-operative 
state of cutaneous sensibility on the auricle, and there is even no 
mention whether it was ever tested! Among the personal cases 



THE ALLEGED SENSORY CUTANEOUS ZONE 401 


recorded * by Hunt was one of herpes occipito-collaris, in which 
a complete facial palsy supervened on the fourth day of the 
disease. Evidences of facial paralysis and objective sensory 
disturbances in the occipito-cervical region were still present at 
the time of death, eighty-seven days after the onset of the disease. 
Necropsy revealed, among other things, well marked degeneration 
of a large number of the fibres of the pars intermedia of Wrisberg. 
But clearly this fact does not prove, or even suggest, that the 
human geniculate ganglion innervates skin; for the pars intermedia 
(the afferent facial root, though it is something more than that) 
contains the ascending facialis root-fibres coming from the palate, 
tongue, facial muscles, and probably also the membrana tympani 
and mastoid cells, &c. And nobody has yet advanced so far as to 
be able to pick out from a degenerated nerve-root a particular 
fibre, or group of fibres, and say: “This degenerated fibre is a 
cutaneous root-fibre, and I prove the truth of my statement by 
the following criteria, &c.” Again, we know that the characteristic 
sensory disturbance of herpes elsewhere is pain, and only occasion¬ 
ally do we find any cutaneous anfesthesia associated with it. At 
the present stage of our inquiry, then, we may safely conclude 
that from the point of view of otalgia, on which Ramsay Hunt 
laid great stress, the cutaneous facialis hypothesis breaks down 
completely; there is a total absence of proof that otalgia is ever 
due to irritation of cutaneous fibres rising in cells of the geniculate 
ganglion. And yet it is easy to see that there is really such a 
thing as a geniculate otalgia, but that it is always due either to 
involvement of deep structures innervated by the geniculate 
ganglion or of auricular branches of trigeminus, vagus, or cervical 
origin, and is never, even in part, a cutaneous otalgia, unless other 
ganglia or their sensory cutaneous branches are affected simul¬ 
taneously with the geniculate ganglion. 

Let us now examine the cutaneous facialis hypothesis from the 
side of cutaneous anaesthesia, and notice a few of the recently 
recorded cases in which an insignificant degree of hypaesthesia of a 
part of the auricle has been found, often only after very careful 
repeated clinical testings, in certain cases of unilateral complete 
infra-nuclear facial palsy. To begin with, Ramsay Hunt, in his 
second paper, discusses f the question of sensory disturbances in 

# Loc. cit. y 1907. 

t Loc . rtf., 1909, pp. 343, 344. 



402 


LEONARD J. KIDD 


the common form of Bell’s palsy, “ in which the nerve has been 
involved in the Fallopian canal between the geniculate ganglion 
and the stylomastoid foramen.” In 2 out of 30 such cases 
examined by him there was a hypaesthesia of the face on the same 
side which needed a most careful testing for its recognition. This 
he regarded as “ a functional or physiological derangement of the 
fifth nerve ganglion, induced by the motor insufficiency of the 
paralysed face." And in 9 out of the 30 cases hypaesthesia 
in the concha was demonstrated: there was never any anecsthesia : * 
“The tactile sense was merely diminished or obtunded in this 
area.” By repeated careful testings Hunt satisfied himself of its 
existence. He says he failed to demonstrate any definite changes 
of sensibility within the canal. It is to be noted that he offers no 
explanation (1) why in 21 out of the 30 cases of complete Bell’s 
palsy there was not even any cutaneous hypaesthesia, nor (2) why 
there was not in all the 30 cases a complete anaesthesia of the 
skin of the concha and interior of the external auditory meatus. 
His negative findings prove that the temporo-facial division does 
not send any cutaneous sensory fibres to the auricle by way of the 
auriculo-temporal nerve. As a matter of fact, if there were any 
facialis cutaneous fibres in man, we should find in every case of 
Bell’s palsy as complete a cutaneous anaesthesia of its alleged 
auricular zone as any clinician ever found on the trigeminus 
cutaneous area after a complete Gasserianectomy. 

Dejerine, Tinel, and Heuyer record 12 a case of auricular herpes 
with facial palsy. There was complete motor facial palsy with 
reaction of degeneration; the earliest symptom was right facial 
palsy with a perversion of taste-function, and “ with the herpetic 
cicatrices were united interesting sensory troubles.” At first 
there was almost complete anaesthesia of the meatus, external 
auditory canal, all the concha, and the neighbouring parts of the 
antihelix. On the lobule, helix, and upper part of the antihelix 
sensibility was much diminished. Afterwards there was a marked 
hypaesthesia on the hairy scalp behind the ear and in all “the 
zone of the posterior auricular branch.” Finally, on the face there 
was slight hypaesthesia which diminished on leaving the auricular 
region, but could be recognised as far as the neighbourhood of the 
median line. The three authors write:—“ Finally, in our case 
objective sensory changes show the rOle of the geniculate ganglion 

* The italics are mine. 



THE ALLEGED SENSORY CUTANEOUS ZONE 403 


in the innervation of the ear, skin of scalp, and face.” Then, in 
commenting on the teaching of most authors that the sensory 
branch of the external auditory meatus is an anastomotic filament 
coming from the vagus or glossopharyngeal, they write:—“ Now it 
appears, according to observations similar to ours, that it really 
comes from the geniculate ganglion.” It is interesting to note 
that they admit (contra Hunt and Valentin) that the posterior 
auricular branch of the facial nerve “terminates solely in the 
muscles (occipital, temporal, and muscles of ear).” They go on 
thus:—“ Now, according to our observation, it is incontestable that 
this hypaesthesia cannot be attributed to anything but the lesion 
of the geniculate ganglion. This idea agrees with the fact 
observed by the physiologists that the facial is sensory at its exit 
from the stylomastoid foramen (Weigner), and that its section 
causes achromatosis of a certain number of the cells of the 
geniculate ganglion (van Gehuchten). The posterior auricular 
zone therefore seems to receive a certain number of sensory fibres 
from the geniculate ganglion.” A reference to their figure shows 
that there was marked hypaesthesia over a large part of the second 
cervical cutaneous area, and a very slight hypaesthesia over almost 
the whole of the trigeminus cutaneous area. And yet they ask us 
to believe that these vast cutaneous areas belong solely to the 
geniculate ganglion! If their view were correct, we should find 
in every case of complete unilateral facial palsy, between its 
ganglion and the pes anserinus, a slight hypiesthesia of almost all 
the homolateral trigeminus cutaneous area. But, although very 
slight sensory changes have often been found in that area in Bell’s 
palsy, it is certain that in the overwhelming majority of cases they 
are absent. We cannot, then, reasonably accept the interpretation 
of Dejerine and his two co-workers that their very slight 
hypaesthesia in the trigeminus area was due to “ the hypotonia of 
the cutaneous muscles and the consecutive feebleness of the 
dermal papillae.” Such hypotonia is present in all complete facial 
palsies, no matter at what level of the facial root or nerve-trunk 
the maximum intensity of the lesion may happen to be situated. 
The three authors actually state that “ the facial hypaesthesia was 
not in the area of the trigeminus! ” And yet their figure gives 
the slightly hypaesthetic area as reaching almost up to the mid¬ 
line of the face, and even on the forehead it reaches not far short 
of that line; it affects the side of the nose, cheek, temple, and 



404 


LEONARD J. KIDD 


hinder half of the lower jaw, extending there on to the third 
cervical cutaneous area. It is clear that, if all this vast cutaneous 
area belongs to the geniculate ganglion, all our anatomists and 
surgical neurologists have misled us woefully on the question of 
the trigeminus cutaneous area. Although one cannot agree with 
Ramsay Hunt, that the human facial nerve has any cutaneous 
area whatever, yet he at any rate has always claimed but a very 
tiny cutaneous zone for the geniculate ganglion. 

Souques has recently recorded 13 a case of cervical herpes with 
facial paralysis. At the beginning of November 1913 a woman of 
53 had intense tinnitus, without vertigo, in her right ear, 
with very severe lancinating pains inside the auricle, with irradia¬ 
tion behind and above it in the parietal region. Three days later 
herpes auris and cervicalis (C 2 and C 3 ) on right side; the former 
affected the internal and external aspects of the pinna, helix, 
antihelix, lobule, and concha; the pinna was red, swollen, and 
painful, and the meatus was narrowed by the swelling. In 
addition, the herpes encroached upon the face both in front of 
and below the auricle: there were also two “aberrant” vesicles 
on the lower lip (figured). Twelve days after the onset of the 
herpes a complete and total right facial palsy appeared. On 
25th November the herpetic eruption was drying up, but very 
severe pains persisted in and around the auricle; no objective 
disturbances of sensibility could be found either in the auricle 
or around it. Souques concludes that the case was one of a 
simultaneous affection of the second and third cervical dorsal- 
root ganglia and of the geniculate ganglion. He goes on to 
describe the cutaneous area of the facial nerve on the auricle, 
and yet he makes no comment on the fact that he failed to 
demonstrate any cutaneous sensory diminution or loss on that 
area. 

At the same meeting of the Paris Neurological Society at 
which the paper of Souques was read, Laignel - Lavastine 
mentioned * that he had lately had the case of a “ man who, as a 
sequel of a right-sided cervical and auricular herpes, showed a 
right peripheral facial paralysis with a partial reaction of degenera¬ 
tion. There were herpetic and anaesthetic disturbances in the 
concha and external auditory meatus, which territories belong to 
the geniculate ganglion; from this he was able, before the appear- 
* Herne Xenrol., 1914, May 20, p. 721. 



THE ALLEGED SENSORY CUTANEOUS ZONE 405 


ance of the facial palsy, to diagnose a participation of the pars 
intermedia in the herpes amis.” Again, in discussing the case of 
Souques, he says * that in his own case the subjective disturbances 
were much slighter than in that of Souques, but that there was 
“ a very marked anaesthesia,” which was absent in Souques’ case. 
Yet he seems to see no difficulty in concluding that in both cases 
the herpes auris was of geniculate origin, in spite of the fact that 
cervical herpes was present in both cases, and that part of the 
cutaneous innervation of the auricle is of cervical ganglionic 
origin, and also in spite of a total absence of objective sensory 
changes in Souques’ case. 

It is well known that in cases of complete unilateral Bell’s 
facial palsy one does occasionally find on examination a very slight 
cutaneous hypaesthesia over the whole, or a large part of the 
homolateral trigeminus area. Such cases have been recorded by 
von Frankl-Hochwart and several other writers, including myself.f 
At the time when my paper was written (1909) I believed that 
the geniculate ganglion sends sensoi'y fibres to the mimetic facial 
muscles; but we know now, thanks to the careful clinical study 
by Maloney and Foster Kennedy J on the sense of pressure in the 
face, eye, and tongue, that these muscle-afferent nerve-fibres from 
the geniculate ganglion are really postural afferent ( non-scnsory ) in 
function, and that the algetic afferent nerve-fibres of the facial 
mimetic muscles come from or through the Gasserian ganglion. It 
is quite untrue that at its exit from the stylomastoid foramen 
the facial nerve contains sensoi'y fibres. Let us all grasp the 
elementary truth that while all sensory fibres are afferent, all 
afferent fibres are not sensory. I am convinced now that, in all 
the cases of slight hypaesthesia in the cutaneous area of the 
trigeminus nerve in Bell’s facial palsy, either there is present a 
coexistent neuritis of the peripheral muscle-sensory fibres which 
the trigeminus sends just underneath the skin of the face to the 
facial muscles, or else the cutaneous hypaesthesia is psychogenic and 
is induced by the action of the clinical examination on a suggestible 
patient. Although I had, prior to the early part of the year 1909, 
seen about seventy cases of hypaesthesia of the trigeminus 
cutaneous area in Bell’s palsy, yet I have not once seen it since 

* Loc. cit p. 737. 

t L. J. Kidd, Rtv. of XturoK and Psychiatry , 1909, vii., p. 175. 

X Maloney and Kennedy, Brain , 1911, xxxiv., September, p. 1. 



406 


LEONARD J. KIDD 


that date. I attribute this fact mainly to our improved and more 
intelligently conducted modern sensory testings. One may 
mention that Mills refers * to these cases of facial palsy in which 
the patients are apparently hypothetic, not only over the entire 
face, but sometimes over portions of the neck and throat. He 
concluded from his own work that in all these cases the hypothesis 
was of a suggested or so-called hysterical character: his cases 
comprised a Polish Jew, a Russian Jewess, and a coloured woman. 
All these were of a well marked hysterical or suggestible 
temperament: one of the cases was an alcoholic man. If we 
try to put ourselves in the place of a patient suffering from Bell’s 
palsy, who knows nothing of human anatomy beyond what he 
himself invents for the occasion, what thoughts pass through his 
mind as we cover his eyes, touch his face on the affected side, and 
perhaps ask the very suggestive question : “ Do you feel me touch 
you ? ” If he be a fairly quick-witted person, he reasons thus: 
“ I can’t move the right side of my face, and the doctor asks me if 
I can feel on it; clearly he expects me to say I cannot.” And who 
can doubt that it is in this way that he is led to say he either does 
not feel a touch or that it feels different from the feeling on the 
sound left side ? To him it seems only natural that motion and 
feeling should go together. Such a suggested response to clinical 
sensory tests is all the more likely to lie evoked the more frequently 
repeated and the more careful and painstaking be the inquiry. 

There can be little doubt that, in many of the published cases 
of herpes auris affecting Hunt’s zoster zone of the geniculate, 
there has been present a lesion of the cervical ganglia or their 
cutaneous auricular branches. The cervical area of the auricle is 
much larger than most clinicians realise, and covers a large part 
of Hunt’s so-called geniculate zone. We have the exact testimony 
of an experiment in favour of my statement. Thus Trotter and 
Morriston Davies found 14 that twenty-four hours after section of 
the great auricular nerve in a man there was anaesthesia to a 
camel’s-hair brush over more than half of the external ear; and they 
found that by the use of their “ stroking method ”—which Mills 
has found f of great value—there was abnormal sensibility over a 
considerable part of the cheek and lower jaw (figured). On the 
question of the exact extent of the cutaneous area of the auricular 

* Loc. cit ., 1910. 

t Loc . cit ., 1910. 



THE ALLEGED SENSORY CUTANEOUS ZONE 407 


branch of the human vagus nerve there appears to be no satis¬ 
factory evidence; but it seems probable that in some of the cases 
described by Hunt and others as geniculate herpes, in which 
vomiting was a prominent symptom, there may have been an 
involvement of the jugular ganglion or the vagus roots, with or 
without involvement of the auricular branch of that nerve. As to 
whether the petrosal ganglion of the ninth cranial nerve of 
mammals does or does not contribute cutaneous fibres to the 
auricular branch of the vagus, and so to the auricle, we have at 
present no exact information. We may now sum up this clinico- 
pathological section as follows:—(1) We lack conclusive proof of 
the existence of an isolated geniculate herpes; (2) geniculate 
otalgia is never, even in part, a cutaneous otalgia; (3) an isolated 
complete unilateral infra-nuclear facial palsy never gives amesthesia 
of any part of the auricle; such amesthesia would be present in 
every case if the geniculate ganglion sent any sensory cutaneous 
fibres to the auricle; (4) those cases of Bell’s facial palsy in 
which hypjesthesia is found, often only after repeated and highly 
suggestible clinical testings, on either the whole or a large part of 
the trigeminus and cervical root-areas or on part of the auricle, 
are always either due to a coincident sensory neuritis of trigeminus, 
cervical, or vagus auricular branches, or else are psychogenic 
(i.c., manufactured by the patient’s reasoning suggested by the 
clinician’s testing). It was to these, or some of these factors, that 
the sensory changes found in the cases by Dejerine, Tinel, and 
Heuyer, by Souques, by Laignel-Lavastine, and by Ramsay Hunt 
were due, and not to involvement of any hypothetical (and non¬ 
existent) sensory cutaneous facialis fibres; (5) the afferent fibres 
which are contained in the trunk of the facial nerve of man, 
rabbit, and monkey are non-sensory: they are purely postural- 
afferent in function, and their functioning never rises into con¬ 
sciousness. The algetic afferent nerve-fibres which are distributed 
to the facial muscles of man come from or through the Gasserian 
ganglion; it is solely on them that the muscle-pain-sensibility of 
the facial muscles depends. 


, 5. Needed Experimental Inquiries. 

The experimental investigation of the question whether the 
mammalian facial nerve has a cutaneous sensory zone may con- 



408 


LEONARD J. K1I)D 


eeivably prove to be difficult unless a fairly large animal be 
selected. The subject might be approached in several ways:— 
(1 ) An attempt might l>e made to divide all the cutaneous nerve- 
filaments that enter the skin of the auricle from its circumference; 
if this could he done, it should be followed up a few days later by 
histological examination of all the afferent ganglia from the 
Gasserian to the third cervical for evidence of retrograde chromo- 
lytic changes in some of their cells : the geniculate, petrosal IX., 
and jugular X. would of course be examined ; (2) as it is nearly 
certain that the mammalian facial nerve has no cutaneous in¬ 
nervation, a section of (a) all the auricular filaments of the 
auriculo-temporal nerve before it has received its communicating 
fibres from the small superficial petrosal nerve, and of (b) the 
auricular branch of the vagus before it has received the com¬ 
municating branch from the facial nerve, and of (c) all the 
auricular branches coming from the cervical plexus, would prob¬ 
ably be found at a later date to have caused degeneration of all 
the cutaneous filaments of the auricle; (3) the operation of com¬ 
plete extirpation of the geniculate ganglion might be attempted: 
if it were successful, it would divide all the hypothetical cutaneous 
facialis fibres, and we should find later some degenerated fibres on 
the cutaneous zone of the auricle described by Ramsay Hunt 
as the “ zoster zone of the geniculate ganglion ”; further, we 
should find normal nerve-fibres on the auricle both in front of and 
behind the area of degenerated fibres; if all the auricular 
cutaneous fibres were found to be sound, the cutaneous facialis 
hypothesis would be disproved; (4) after a complete division of 
the facial nerve just below the geniculate ganglion, i.r., well above 
the point of exit of its posterior auricular branch and the com¬ 
municating branch to the auricular branch of the vagus nerve, we 
ought to find degenerated nerve-fibres in part of the skin of the 
external ear if, as Hunt suggests, these two nerves contain sensory 
cutaneous facialis fibres for the auricle; (5) a section of the 
posterior auricular branch of the facial nerve close to its origin 
might be performed in order to settle the question whether it is a 
purely muscular branch, or whether, as Valentin asserts, it gives 
also cutaneous filaments to the auricle. It seems to me very im¬ 
portant that before any of these experiments are attempted it 
should be exactly ascertained what cutaneous or subcutaneous 
nerve-filaments are liable to be severed in the performance of the 



THE ALLEGED SENSORY CUTANEOUS ZONE 409 


various operations; for, unless this precaution be observed, we 
might, in some of them at any rate, attribute the subsequent 
presence of degenerated fibres on the auricle to the wrong cause. 
Of the various experiments here suggested, it seems probable that 
the third, fourth, and fifth groups are the most likely to prove 
successful in deciding whether there is any cutaneous facialis zone 
in mammals. If the geniculate ganglion can be completely 
extirpated, it should be possible to trace degenerated fibres to the 
membrana tympani, mastoid cells, all the facial muscles, and 
possibly also to the lachrymal gland (there is some clinical 
evidence that the great superficial petrosal nerve conveys secretory 
fibres to that gland). It may quite well happen that the pro¬ 
fessional experimentalist will think of even better methods of 
attacking the question of the cutaneous facialis hypothesis than 
those here offered; but in any case a careful experimental inquiry 
is greatly to be desired in order to overthrow error and establish 
the truth. 

6. Conclusions. 

1. There is no anatomical or experimental evidence of the 
existence of a cutaneous sensory zone of the facial nerve in any 
vertebrate group above the Cyclostomata. 

2. Clinical studies prove that the human facial nerve has no 
sensory cutaneous zone on the auricle. 

3. The clinico-pathological evidence brought forward by 
Ramsay Hunt and his numerous followers in favour of the 
cutaneous facialis hypothesis breaks down completely on a search¬ 
ing critical scrutiny, as is set forth exhaustively in section 4 of 
this paper. 

4. It is unknown whether the petrosal IX. ganglion contributes 
any sensory cutaneous fibres, by way of the auricular branch of 
the vagus nerve, to the auricle. 

5. Some of the experimental methods by which the question 
of the existence of a sensory cutaneous supply of the mammalian 
facial nerve can be tested are outlined. 

References. 

1 J. Ramsay Hunt, Joum. of Nerv. and Meat. Die., 1907, xxxiv., p. 73.— 
“ Herpetic inflammations of the geniculate ganglion.” Also Archives of 
Otology, 1907, xxxvi., No. 6. 

* C. K. Mills, Joum. Nerv. and Menl. Die., 1910, xxxvii., (a) p. 273, (h) p. 355.— 
‘'The sensory functions attributed to the seventh nerve.” 

33 



410 


ABSTRACTS 


3 J. B. Johnston, Morphol. Jahrb ., 1905, xxxi r., p. 185.—“The cranial nerve 

components of Petromyzon.” 

4 /lid ,—“The nervous system of vertebrates/ 1 1907. London, pp. 107, 108. 

6 R. E. Sheldon, Anatomical Record , 1909, iii., p. 593.—“Thephylogeny of the 
facial nerve and chorda tympani.” 

6 B. F. Kingsbury, Journal of Comparative Neurology , 1897, vii., p. 1. 

7 J. Gordon Wii^on, American Journal of Anatomy , 1911, xi., p. 101. 

8 J. Ramsay Hunt, Journ . Nerv. and Ment . Die., 1909, xxxvi., p. 321.—“The 

sensory sj-stem of the facial nerve and its symptomatology.” 

9 R. Amabilino, II Pieani, 1898, xix., 1, 2.—“Sui rapporti del gangiiogenioolato 

con la corda del timpano e col facials. Ricerche anatomiche sperimentale.” 

10 A. van Gehuchten, “ Anatomie du systems nerveux de Thomme,” VoL 2,1900. 

11 L. Pierce Clark and Alfred S. Taylor, Journ. of Nerv. and Ment. Die., 

1910, xxxvii., pp. 242, 243. 

12 Dejerine, Tinel, and Hbuyer, Soc. de Neurol, de Paris , 7 Mars 1912; 

Revue Neurol., 1912, xx., March 30, p. 466. 
ly A. Souques, Revue Neurologique , 1914, Ann. xxii., May 15, p. 625. 

14 Wilfred Trotter and H. Morriston Davies, Rev. Neurol . and Psychiatry, 
1907, v., p. 761.—“ The exact determination of areas of altered sensibility.” 
Also Journal of Physiology , 1909, xxxviii., p. 134. 


abstracts. 

PSYCHOLOGY. 

ON THE ANALYSIS AND INTERPRETATION OF DREAMS 
(483) BASED ON VARIOUS MOTIVES AND ON THE THEORY OF 
PSYCHO-ANALYSIS. Meyer Solomon, Journ. Abnorm. Psychol., 
1914, June-Sept. 

Infantile primitive tendencies are always detectable by dream 
analysis, and this applies not only to dreams but to all adult 
tendencies and activities; these tendencies are not a priori of a 
sexual nature; and it is not only the infantile tendencies, but 
still more fundamentally the instinctive tendencies, which we find 
as the driving force of all dreams and of all other mental states. 
The Freudians have entirely neglected all instincts other than the 
sexual instinct. Their broad generalisations with regard to the 
role of sexuality in dreams, the neuroses, psychoneuroses, psychoses, 
&c., do not ring true, and Freudism must undergo wholesale 
modification, especially with respect to the conceptions of psychical 
determinism, psychical repression, sexuality, and symbolism. 
Psychology and psychoanalysis should be developed not on 
sexuality alone, but on man as he really and truly is. 

H. de M. Alexander. 



ABSTRACTS 


411 


▲ CONTRAST IN PSYCHOANALYSIS £ THREE OASES. Tom A. 

(484) Williams, Jawm. Abnorm. Psychol 1914, June-Sept 

Three cases are reported illustrating the author’s belief that a 
complete Freudian analysis does not, in itself, lead to a cure; 
that a cure may be effected without a complete analysis, provided 
the analysis reaches the genetic difficulty; and that readjustment 
may be accomplished without any reference to the sexual. 

H. de M. Alexander. 

PATHOLOGY. 

MEDULLARY CAVITIES AND CERVICAL MENINGITIS. (Carttfs 

(485) mfedull&ires et mlningites cervicalea. Etnde explriment&le.) 
Jean Camus and Qustave Roussy, Rev. Neurol ., 1914, xxii., 
F6v. 28, p. 213. 

The authors record the result of a number of experiments upon 
eleven dogs. After dividing the occipito-atlantoid membrane, 
they injected into the subarachnoid space a mixture of formic acid, 
sodium nucleinate, and talc suspended in water. A gradual and 
progressive meningitis resulted, followed by small areas of soften¬ 
ing and ultimate cavity formation in the interior of the cord. 
These areas of softening are probably ischemic in origin, and 
result from interference with the spinal vessels by the meningitis. 
They are often roughly symmetrical, in many places show evidence 
of inflammation, and resemble those of true syringomyelia. The 
meningitis is of that type known as cervical hypertrophic 
pachymeningitis, and is of interest in connection with the 
observations of Philippe and Oberthur that there is a pachy- 
meningitic form of syringomyelia. A Ninian Bruce. 

A STUDY OF THE SATELLITE CELLS IN FIFTY SELECTED 

(486) CASES OF MENTAL DISEASE. Samuel T. Obton, Brain, 
1914, xxzvi., p. 525. 

The fifty cases were selected to form five groups of ten each and 
comprised (1) maniacal depressive insanity, (2) dementia praecox, 
(3) senile dementia, (4) general paralysis, and (5) alcoholic insanity. 
Sections were cut from the following cortical regions: precentral, 
postcentral, frontal, temporal and occipital. The number of 
satellites was then counted and their distribution by laminae, 
Brodmann’s division into six layers being adopted. 

The results are tabulated for each case and it is pointed out 
that satellitosis cannot be considered to be in any sense indicative 
of the type of psychosis, although it has in this series appeared 
with more consistent intensity in the maniacal depressive cases 
and of much less prominence in dementia praecox. The reaction 



412 


ABSTRACTS 


is much more marked in the deeper cell layers, both in regard to 
frequence of occurrence and degree of reaction. The cortices of 
the dome, precentral, postcentral, and frontal, seem to show the 
reaction with greater intensity than do the temporal and occipital 
regions. Age at the time of death seems to play some part in the 
occurrence of severe reactions, but cannot be considered the only 
factor. The duration of the psychosis bears no demonstrable 
relation to satellitosis. A. Ninian Bruce. 

A MIOROOEPHALIO IDIOT WITH MALFORMATION OF BRAIN. 

(487) Report of a Case. Arthur K. Petbry, Joum. Amer. Med. Assoc., 
1914, lziii., Aug. 15, p. 536. 

The patient was the third child of a family of eight, born at full 
term, when he weighed about 6 lbs. There was no history of 
any miscarriages, tuberculosis, malignancy, or mental disease in the 
family. It was noticed that his head was small at birth, but his 
condition did not attract special attention until the age of 5. Owing 
to family inability to take care of him, he was sent to hospital, being 
then 21 years of age. He was found to be an idiot, could neither 
walk nor talk, had to be fed, and was unclean. He weighed 
Go lbs., and measured 4 ft. 2 in. in height. He showed athetoid 
movements of the upper extremities. Mentally he was dull, and 
“ in appearance he resembled more closely a monkey than a human 
being.” He was very destructive. 

The brain was small, weighing 220 gm., and measured 9 cm. from 
frontal to occipital poles, and 4 cm. in width. The fissure of Sylvius 
was well defined, the posterior limb reaching the great longitudinal 
fissure just behind the middle of the superior edge of the cerebrum. 
Its course closely resembles that of the normal fissure of Rolando. 
A well-defined fissure lies anterior to the posterior limb of the 
Sylvian fissure on the left side, and probably corresponds to the 
Rolandic fissure. No distinct parieto-occipital, calcarine, or 
parallel fissures were found. No corpus callosum was present, 
and the anterior horn of the lateral ventricle was absent in the 
right hemisphere. The circle of Willis and vascular supply 
were normal. 

The above points would appear to indicate that this is not 
a case of true microcephaly. A. Ninian Bruce. 

CLINICAL NEUROLOGY. 

ASSOCIATED MOVEMENT OF THE JAW AND UPPER LID: 

(488) “THE JAW-WINKINO PHENOMENON.” E. A. Cockayne, 
Brit. Joum. Child. Die ., 1914, xi., p. 362. 

Cockayne reviews the literature including the case reported by 
Sym {v. Review, 1908, vi., p. 337), and reports a personal case in a 




ABSTRACTS 


413 


female infant. The movements were first noted when she was 
about a month old. As the baby sucked the right lid was raised 
synchronously with the movements of the jaw, and as the jaw 
was moved away from the side of the lesion as in grinding the 
teeth, the lid was raised. There was slight ptosis of the right 
upper lid. The left lid was not affected. There was no history 
of a similar condition or of ptosis in the family. 

J. D. Rolleston. 

PSEUDO - HYPERTROPHIC MUSCULAR DYSTROPHY: TWO 

(489) CASES WITH PLATES. A. F. Bernard Shaw, Dublin Joum. 
Med. Set ., 1914, No. 512, Aug., p. 116. 

Two quite typical cases are described. They were brothers, and 
there was no history of any other cases in the family either on 
the father’s or mother’s side. Their sister was unaffected. The 
knee jerks were absent in both cases, and the Achilles jerks absent 
in one and diminished in the other. A. Niki an Bruce. 

ACUTE ATAXIA IN CONVALESCENCE FROM MEASLES. (Un 

(490) cas d’at&xie aigue pendant la convalescence d’une rougeole.) 

R. Morichau-Beauchant, Frey, and Rameix, Bull, et mem. Soc . 
mid. H6p. de Parte, 1914, xxxviii., p. 60. 

A bov, aged 7 years, about a week after the appearance of the 
eruption of measles complicated by broncho-pneumonia, suddenly 
developed the following symptoms: paralysis of the tongue and 
lower jaw, intention tremors, contractures, exaggeration of 
reflexes, adiadococinesis, disturbance of equilibrium, nystagmus, 
and transitory retention and incontinence of urine. There were 
no psychical troubles, sensory disorders, nor general disturbance. 
A month later only a slight degree of nystagmus, slight tremor, 
and spastic gait remained, and in another two months there was 
only slight exaggeration of the knee jerks. When seen a year 
after the onset of the symptoms, the child was perfectly normal. 
This case closely resembles that recently reported by Bari£ and 
Colombe (v. Bemew , 1913, xi., p. 493). J. D. Rolleston. 

ON NEUROFIBROMATOSIS. (Ueber Neurofibromatose.) W. Lier> 

(491) Zeiteckr.f. klin. Med., 1914, lxxx., p. 261. 

A record of a case of a boy, aged 9£ years, in whom general 
neurofibromatosis was associated with dystrophia adiposo-genitalis. 
There was no family history. There was bilateral optic atrophy, 
and the X-rays showed evidence of a tumour close to the 
hypophysis. No previous case has been recorded of the com¬ 
bination of neurofibromatosis with Frohlich’s syndrome. 

J. D. Rolleston. 



414 


ABSTRACTS 


PULMONARY LOCALISATIONS OF THE MENINGOCOCCUS. (Lei 

(492) determinations pulmonaires du mlningococque) Q. Loygue, 
Paris tne'd., 1913-14, iv., p. 231. 

A woman, aged .‘35, in the course of an attack of cerebro-spinal 
meningitis, developed acute lobar pneumonia. Meningococci were 
found in the sputum as well as pneumococci. Recovery took 
place. J. D. Rolleston. 


A CASE OF PARAMENINGOCOCCUS OERBBRO SPINAL MENIN- 

(493) GITI8. SEROTHERAPY. RECOVERY. (Un cas de m&iingite 
c6r6bro spinale k parainlningocoques. Stfrothlrapife. Garrison.) 

Brodin and P. Vallery-Radot, Bull, et mem. Soc. mid. Hop. it 
Parity 1914, xxxvii., p. 1210. 

A girl, aged 18, was admitted to hospital for meningitis, and in 
three days received 120 c.c. of antimeningococcus serum. As the 
symptoms became worse, the possibility of parameningococcus 
meningitis suggested itself, and 40 c.c. of antiparameningococcus 
serum were given when the patient was already comatose. Rapid 
improvement took place, and after three more injections, or a total 
of 155 c.c of antiparameningococcus serum, recovery took place. 
The presence of the parameningococcus in the cerebro-spinal fluid 
was subsequently shown by Dopter. J. D. Rolleston. 

MENINGEAL STATES IN SCARLET FEVER AND SCARLATINAL 

(494) URjEMIA. (Les 4tats mlningls dans la scarlatina at l’nrfaiie 

scarlatinense.) P. Mauriac and P. Philip, Joum. de Med. de 
Bordeaux , 1914, lxxxv., p. 437. 

A record of two cases:— 

1. A boy, aged 8£ years, in whom scarlet fever had been 
mistaken for measles a month previously was suddenly seized 
with vomiting and an epileptiform attack involving the left side. 
The urine contained much albumin, and the diagnosis of the 
epileptic form of nervous unemia was made, which was confirmed 
by the presence of a large amount of urea in the blood and 
cerebro-spinal fluid. After transitory improvement following 
treatment, coma set in. A second lumbar puncture showed the 
presence of pneumococcal meningitis which proved fatal. The case 
closely resembles one reported by Hutinel (v. llcview, 1909, vii., 
p. 363). 

2. A girl, aged 15 years, after a mild attack of scarlet fever 
uncomplicated by albuminuria, caught a chill. Acute nephritis 
developed, and respiratory unemia rapidly supervened. 

J. D. Rolleston. 



ABSTRACTS 


415 


LUMBAR PUNCTURE AS A SPECIAL PROCEDURE FOR CON- 

(495) TROLLING HEADACHE IN THE COURSE OF INFECTIOUS 
DISEASES. A. Gordon, Therap. Gazette , 1914, xxxviii., p. 392. 

Gordon has used this method with excellent results in typhoid 
fever, pneumonia, and intluenza. After the ordinary means for 
relieving headache had failed, 15 to 20 c.c. of cerebro-spinal fluid 
were withdrawn, and if the tension was very high 30 or 40 c.c. 
In the typhoid and pneumonia cases several punctures were 
necessary, in influenza one or two were sufficient. The cerebro¬ 
spinal fluid was sterile in all, and the tension was high. Some 
showed leucocytosis and others an increase of albumin in the 
cerebro-spinal fluid. (Cf. Review , 1913, xi., p. 165.) 

J. D. Rolleston. 

TYPHOID SPINE AND THYROID OPOTHERAPY. (Espondilitis 

(496) tiflca y opoterapia tirdidea.) A. Vit6n, Rev. Soc. Mid. Argentina , 
1914, xxii., p. 282. 

The patient was a man, aged 40, convalescent from typhoid fever, 
in whom the diagnosis of post-typhoid thyroid insufficiency was 
suggested by the absence of any history of gonorrhoea or syphilis, 
the febrile, chronic ankylosing character of the process, the X-ray 
features of the bony deformity, and the degree of cardiac excitement. 

Thyroid opotherapy was adopted, and complete recovery rapidly 
took place. J. D. Rolleston. 

AN ATTEMPT TO TRANSMIT POLIOMYELITIS BY THE BITE 

(497) OF LYPEROSIA IRRITANS. Edward Francis, Joum. Infec¬ 
tion* Die., 1914, xv., July, p. 1. 

Since it has been found that poliomyelitis may be successfully 
transmitted from monkey to monkey through the bite of Stomoxys 
calcitrans (v. Review, 1913, xi.), the writer thought that possibly 
Lyperosia irritans, a blood-sucking fly found in great numbers 
in Texarkana during an epidemic in June and July 1913, might 
be similarly concerned. These flies were accordingly allowed 
to bite rhesus monkeys inoculated with poliomyelitis virus, and 
then bite fresh monkeys. But the latter in no case developed 
poliomyelitic symptoms. A. Ninian Bruce. 

FURTHER NOTE ON THE USE OF CELLULOID SPLINTS IN 

(498) THE TREATMENT OF ACUTE CASES OF POLIOMYELITIS. 

Frederick E. Batten, Lancet , 1914, clxxxvii., July 26, p. 216. 

In 1912 the author recommended the use of celluloid splints in 
poliomyelitis ( v. Review, 1912, x., p. 387). He now states that 



416 


ABSTRACTS 


the more he sees of this method, the more is he convinced it is 
a good one. Of thirty-two cases of poliomyelitis admitted to 
hospital within three months of the onset, twenty-four were 
splinted, and it is known that in twenty-one no malposition has 
arisen. The splints have proved of greatest service in really acute 
cases by keeping the muscles at rest in a position of relaxation, 
and have prevented deformity. The advantages of this form of 
splint are: (1) it fits the limb perfectly, (2) it is easily applied 
and removed, (2) it is light, (4) it is rigid, (5) it will not break 
easily, (6) any form of shoe or Wot may be worn over it, (7) it is 
cheap, and (8) can be very easily made. The process involved in 
making them necessitates: (1) the taking of the “ negative ” cast 
of the limb, (2) the making of the “ positive,” and (3) the moulding 
of the splint on to the positive. This is fully described. 

A. Ninian Bruce. 


A PECULIAR UNDESCRIBED DISEASE OF THE NERVES OF 
(199) THE CAUDA EQUINA. Foster Kennedy, Charles A Elsberg, 
and C. I. Lambert, Amer. Journ. Med. Sci., 1914, cxlvii., May. 

Out of eighty-four spinal operations five cases have been met so 
alike in their history, clinical findings, and morbid appearances 
that the authors have been led to class them together as a definite 
clinical and pathological entity. 

1. A man, 40 years, eighteen weeks before admission suddenly 
experienced severe pain in the small of the back. This pain was 
replaced by pain in the right lower extremity which would come 
in attacks, and would extend down the thigh and leg to the ankle. 
Later he had a burning sensation in the right hip, and the right 
leg became weak. Difficulty in urinating developed and the 
bowels were constipated. 

The right lower extremity was weaker and thinner than the 
left; the knee jerks were exaggerated on both sides; ankle jerks 
could not be obtained, no clonus, plantar, right extensor, left 
flexor. There was diminution of all sensations over the right 
side of penis and scrotum, also over parts of the oval region, 
buttocks, and lower limbs. 

A laminectomy was done and several of the nerves were 
observed to be swollen, and of a bluish-red colour. No neoplasm 
was found. The affected roots were thoroughly washed with 
warm saline solution, and the patient, twenty-seven days after the 
operation, stated that he felt perfectly well. 

The other four cases reported are essentially similar to the 
above one. 

In the third and fourth patients the symptoms were pro- 



ABSTRACTS 417 

gresaive in each for about two years, in the second for about one 
year, and in the first for about six months. 

A sharp, shooting, burning pain was present in all the cases 
from the beginning, and was felt almost entirely in the backs of 
the thighs, and in the calves. 

Atrophy of the anterior tibial muscles with loss of power of 
dorsifiexion at the ankle was a prominent feature in four of the 
series; in the exception there was a spasticity of the lower 
extremities, which was more marked on the right than on the left 
side. 

The objective sensory disturbances showed an astonishing 
uniformity; in all, the main incidence of the disease had fallen on 
the lowest roots of the cauda, the sacral roots were always affected, 
and with the utmost severity. 

None of the patients gave either a history or indication of 
luetic infection. The histo-pathological examination of two of 
the cases definitely excluded a tuberculous or syphilitic meningo- 
myelitis or neuritis. There was evidence of a chronic degenera¬ 
tive type of arterio-sclerosis and also intimal proliferation identical 
with the reaction encountered in some of the acute infections or 
toxic processes. 

The degeneration of the nerve fibres and cells in the posterior 
lumbosacral roots of the cauda equina appeared to be relatively 
recent in origin, and compared to the cord involvement minimal 
in severity and extent; the cord degeneration stood out distinctly 
as the most affected district. 

Such a condition as that described by the authors has been 
reported by Marek as occurring in the horse, and was called by 
him a neuritis of the cauda equina. The authors believe that 
their cases are examples of a true toxic neuritis of the caudal 
nerve roots, and is similar to that produced experimentally by 
Orr and Rows, who have shown how toxins may travel from the 
sciatic and other nerves to the posterior root ganglia, along the 
spinal roots, and upward in the cord. D. K. Henderson. 

ROENTGEN DIAGNOSIS IN FRACTURES OF THE CRANIUM IN 
(500) CHILDREN. Geobge Rosenbaum, New York Med. Joum ., 1914, 
c., Aug. 29, p. 414. 

Fractures of the skull in young children are very uncommon 
because of the elasticity of the cranial bones. They are.best 
classified as fractures of the vault and fractures of the base, the 
former being caused by direct violence upon the vault, the latter 
by extension from a fracture of the vault or by indirect violence. 

Two cases are very briefly recorded. The first was a girl, 
aged 9 years, who was run over by a waggon and fractured her 



418 


ABSTRACTS 


femur. An X-ray examination also revealed a simple fissure of 
the right frontal hone. Recovery after many weeks. The second 
case was a girl, aged 8 years, who fell a distance of about 50 feet, 
landing on her head. An X-ray examination after death revealed 
a fracture of the parietal region of the vault extending into the 
middle fossa as far as the sella turcica. A. Ninian Bruce. 

THE BOLE OF THE CABOTID ABTEBIES IN THE CAUSATION 

(501) OF VASCULAB LESIONS OF THE BBAIN, WITH BEMABES 
ON CEBTAIN SPECIAL FEATUBES OF THE SYMPTO¬ 
MATOLOGY. J. Ramsey Hunt, Amer. Joum. Med. Sci,, 1914, 
cxlvii., May. 

The importance of obstructive lesions of the main arteries of the 
neck (the innominate, common carotid, and internal carotids) 
in the causation of softening of the brain is emphasised, and the 
routine examination of these vessels is urged in all cases presenting 
cerebral symptoms of vascular origin. 

Two eases are reported as showing the development of 
immediate cerebral symptoms after puncture wounds of the 
carotid artery. In both cases there was an absence of pulsation 
in the temporal artery of the affected side, showing that the 
external carotid artery was occluded. Emphasis is also laid on 
the distinct vascular changes in the optic disc on the side of the 
injury. 

Reference is made to a series of cases of hemiplegia associated 
with diminished pulsation of the carotid artery in the neck on the 
side of the softening. D. K. Henderson. 

SPASMODIC CLOSING OF CEBEBBAL ABTEBIES IN ITS BELA 

(502) TION TO APOPLEXY. Alfred Gordon, Albany Med. Annals, 
1914, xxxv., p. 423. 

The author,from an analysis of fourteen cases, points out that besides 
embolism, thrombosis, and hiemorrhage (the classical causes of 
apoplectic strokes), there is also a condition which is of hemiplegic 
or hemiparetic character, and which is produced not by a material 
lesion of the blood vessel, but by such a functional disturbance of 
the vessel wall as to interfere with the circulation, and therefore 
with the function of the nerve tissue supplied by this blood vessel. 

Of these fourteen cases, eight died. Their clinical histories are in 
their essentials identical, the chief symptom being a sudden onset 
of hemiparcsis, never complete. The number of attacks varied 
from one every three or four months to one every two years. All 
the attacks were transient. The fewer the attacks the longer 
their duration. The briefest time was two minutes, the longest 



ABSTRACTS 


41$ 


several hours. All terminated in severe attacks of permanent 
hemiplegia. At the autopsy, softenings were found in the internal 
capsule and basal ganglia. The ages of the patients varied from 
56 to 70. 

Of the six patients living all presented intermittent attacks of 
apoplectic nature. Four had a great many attacks of a sensory 
nature. Two have already entered the period of permanent 
hemiplegia. The only explanation possible of these attacks is an 
intermittent closing and opening of the cerebral vessels resulting 
in local ischaemia. As the disease develops complete occlusion of 
the vessels occurs. A. Ninian Bruce. 

A FAMILIAL CASE OF SPLENOMEGALIC ANiEMIA WITH 

(503) INFANTILISM. F. Pabkes Weber, Brit. Joum. Child. Bit., 
1914, xi., p. 345. 

A record of a case of splenomegalic anaemia in a male, aged 17, 
who was small and infantile in development. His height was 
5 ft. 1 in., and his weight 6 stone 9 lbs. He had no pubic nor 
axillary hair, and his penis and testes were small. All the 
thirteen children in the family had had a yellow skin at birth, 
and haul remained yellow for three to six months after birth, and 
another child, a girl, had shown splenomegalic anaemia as well 
There was no note of infantilism in any other member of the 
family. 

The author does not regard the case as one of Gaucher’s 
splenomegaly, which is never associated with infantilism, but 
rather as one of congenital haemolytic jaundice, in which infantilism 
has been recorded. J. D. Rolleston. 

EOSINOPHILIA IN CHOREA: A Preliminary Study. Simon S. 

(504) Leopold, New York Med. Joum., 1914, c., Aug. 1 , p. 225. 

Twenty cases of Sydenham’s chorea were examined. Of these, 
ten showed a distinct eosinophilia of from 4 to 16 per cent. 
Nine patients showed recurring attacks of chorea, the attacks 
varying from 2 to 5; eosinophilia was found in six of the nine 
cases. Of these, four had had only one recurrence, and eosinophilia 
was only present in one; the remaining five had had from three 
to five recurrences, and eosinophilia, ranging from 6 to 16 per 
cent., was present in every case. 

Eosinophilia is thus present in most recurring cases, especially 
if there has been more than a single recurrence, and its absence 
may prove of value in cases where the diagnosis is doubtful. Its 
presence is in favour of the infective origin of chorea. 

A. Ninian Bruce. 



420 


ABSTRACTS 


LEAD POISONING WITH PANALYSIS OF THE EXTERNAL 

(505) OCULAR MUSCLES. E. M. Williams, Jo urn. Amer. Med. Assoc., 
1914, lxiii., Aug. 1, p. 403. 

A woman, single, aged 36, typesetter for six to eight years, began 
to suffer from severe pains in all her limbs, and her leg and arm 
muscles became weak. This increased rapidly, and in two weeks 
she became confined to bed. Almost all the muscles of the body 
seemed weak and wasted. Fibrillary tremors were present in the 
thigh and shoulder muscles. There was double toe-drop, no 
Rahinski’s sign, no sensory changes, no basophilia, and no blue 
line on the gums. There was, however, diplopia on the extreme 
lateral field, with a weak right abducens. The patient had often 
noticed double vision when working in a poor light. 

A. Ninian Bruce. 

SOME MODERN CONCEPTIONS OF APHABIA. Donald Cork, 

(506) Med. Ckron., 1914, fix., Aug., p. 309. 

A brief historical account and summary of aphasia, the views of 
Marie and Ddjerine being specially compared with the older 
conceptions. A. Ninian Bruce. 

SEROTHERAPY WITH MASSIVE DOSES IN TETANUS (Con- 

(507) tribution h l’ltude de la s6roth6rapie h dose massive da tlttnos 
confirm^.) F. E. Sarrazin, Theses de Parts , 1913-14, No. 280. 

Sarrazin recommends the injection of 50-100 c.c. of antitetanic 
serum as soon as the diagnosis is certain. The dose should be 
repeated next day and even the following days until the con¬ 
tractures are completely controlled. The intravenous route should 
be used by preference. 

The thesis contains the histories of twenty cases, three of 
which are original: sixteen recovered and four died. 

J. D. Rolleston. 

WASSERMANN S REACTION IN AORTIC DISEASE. (Contribution 

(508) h l’ltude de la reaction de Wassennann ches lea aortiqnea) 

I. Moricand, Theses de Paris , 1913-14, No. 404. 

Moricanp examined thirty-four cases of aortic disease and found 
that the frequency of a positive reaction was as follows: aneurysm, 
70 per cent.; incompetence, 50 per cent.; aortitis, 33*3 per cent.; 
and multiple lesions, 50 per cent. 

In eleven out of seventeen cases in which Wassermann’s reaction 
was positive, syphilis had not been suspected, while in four out of 
fourteen cases in which the reaction was negative, syphilis was 
extremely probable. {Of. Review, 1912, x., p. 192.) 

J. D. Rolleston. 



ABSTRACTS 


421 


PRACTICAL STUDY OF THE ALBUMIN IN THE OEREBRO- 

(609) SPINAL FLUID IN SYPHILIS. (£tude pratique de 1’albumine 
du liquide cdphalo-rachidien chez las syphilitiques.) A Foucque, 
Theses de Pam, 1913-14, No. 419. 

In the great majority of cases increase in the quantity of albumin 
in the cerebro-spinal fluid in syphilis is closely associated with 
hyperleucocytosis and a positive Wassermann’s reaction in the 
cerebro-spinal fluid. These three signs are certain evidence of 
syphilitic involvement of the meninges. Increase of albumin is 
the easiest to detect, and not only can its presence be ascertained, 
but the precise amount can be tested. 

Apart from cases of isolated hyperalbuminosis in old cases of 
syphilis, who no longer show any signs of disease {?. Review, 1914, 
xii., p. 271), treatment of a syphilitic patient should never be 
stopped as long as there is an excess of albumin in the cerebro¬ 
spinal fluid. The thesis is based on the study of twenty cases. 

J. D. Rolleston. 

SYPHILITIC REINFECTION AFTER TREATMENT WITH NEO- 

(610) SALVAR8AN. (Reinfection syphilitique aprds le traitement par 
le ndo-salvarsan.) Milian, Bull, et mim. Soc. mid. H6p. de Parts , 
1914, xxxvii., p. 1207. 

A man, aged 26, developed a chancre on the dorsal surface of the 
penis in April 1912. Numerous typical spirochaetes were found 
in the lesion, and Wassermann’s reaction was positive. He received 
five injections of neo-salvarsan in May, and in July, August, and 
September was treated with biniodide of mercury and potassium 
iodide. Wassermann’s reaction remained positive, so he was 
given four more injections of neo-salvarsan in November, and in 
December the reaction became negative. 

In May 1914 a typical chancre appeared on the left side of the 
penis after coitus with a woman who was found to have a 
syphilide on the right side of the fourchette,. Wassermann’s 
reaction was now positive again in the man and also in the 
woman. J. D. Rolleston. 

MALIGNANT GANGLIO NEUROMA OF LEFT SUPRARENAL. 

(611) T. E. Monro and J. S. Dunn, Glasgow Med. Jovm ., 1914, lxxxii., 
Aug., p. 81. 

The patient was a boy, aged 3£ years, who had not been well for 
six months. He was very anaemic, and a large, firm mass was 
palpable in the region which an enlarged spleen might occupy. 
It was considered to be related to the kidney, and an attempt was 
made to remove it by operation, during which he died. 



422 


ABSTRACTS 


The tumour was later found to occupy the site of the left 
suprarenal body, having apparently developed within the gland. 
It was the size of a large orange. The cells present were mainly 
ganglionic nerve-cells supported by fibrillar material, in which 
it was easy to demonstrate large numbers of naked axis-cylinders. 
No myelinated fibres were present. Foci of smaller cells corre¬ 
sponding to embryonic nerve-cells which form the sympathetic 
nervous system in normal development, were also present. 

Metastatic deposits were present in neighbouring glands and 
in the ribs and bones of the skull. These consisted mostly of 
small-celled malignant tissue. 

About thirty-six such cases have been recorded, of which six 
were malignant. A. Ninian Bruce. 

A CASE OF ADDISON’S DISEASE OBSERVED IN 1902, OON- 

(612) SIDERED AS CURED. DEATH FROM GASTRIC CANCER 
IN 1913. AUTOPS7. (Addisonien observe en 1902. Consider* 
comme gudri. Rdtrouvd en 1913. Mort d’un cancer gastrique. 
Antopsie.) R Hirtz and R. Debr£, Bull, et mim. Soc. mid. H6p. 
de Paris , 1914, xxxvii., p. 1192. Netter, ibid., p. 1203. 

A man, aged 39, the subject of chronic alcoholism, presented 
typical symptoms of Addison’s disease in 1902, and was treated by 
injections of suprarenal extract. Rapid improvement and ap¬ 
parent recovery took place. In 1904 he was admitted to an 
asylum for subacute alcoholism and was then lost sight of till 
1913, when he was re-admitted for the same cause, and died a 
month later. The necropsy showed carcinoma of the pylorus and 
a metastasis in the liver. There were no naked eye changes in 
the suprarenals, but microscopic examination showed a cicatricial 
lesion in the right suprarenal. 

In the subsequent discussion, Netter alluded to a case of 
Addison’s disease successfully treated by suprarenal opotherapy 
some years ago, and who for" the last three years had been 
engaged as a chauffeur. Beyond a pleural rib nothing abnormal 
was to be detected on examination. J. D. Rolleston. 

TRUE LARYNGEAL SAG FORMATION IN MAN AND ITS 

(613) OPERATIVE TREATMENT, (ttber echte kehls&ckbildung 
beim menschen und ihre operative Behandlung.) A. Erich, 
Beitrdge z. klin. Chir. t 1914, xc., H. 3, S. 619. 

There is a median laryngeal sac in certain of the lower apes which 
lies in front of the thyroid cartilage and communicates with the 
larynx below the epiglottis. The occurrence of such a congenital 
sac has never been conclusively shown in man. They are nearly 



ABSTRACTS 


423 


all pathological. Lateral sacs are extensions of the appendicular 
sac. They are lined with tubular ciliated epithelium. They may 
extend upwards as far as the hyoid or the mucosa of the base 
of the tongue. These are not pathological. A pathological 
dilatation of the appendix also occurs, due to some obstruction to 
expiration. True congenital sacs are easily recognised. They grow 
slowly and appear early; they may grow in two directions: 

(1) into the ventricular band, causing a swelling in the vestibule; 

(2) upwards through the thyro-hyoid membrane. 

The writer reports the following case: Woman, aged 30. 
Seen first, 6th May 1913. In autumn 1912 became gradually 
hoarse with intermissions. Dyspnoea on exertion. At the same 
time a swelling appeared in the right side of the neck. On 
laryngoscopic examination the right ventricular band was seen to 
be swollen to about the size of a cherry. The swelling on the 
outside of the neck lay between the thyroid cartilage and the 
lower jaw. It was tympanitic on percussion, and when punctured 
with a syringe air was drawn off and the swelling diminished 
greatly in size. The tumour reappeared in a quarter of an hour. 
23rd May 1913, operation on account of dyspnoea. Local 
anaesthesia. Incision over swelling in neck. Tumour connected 
with digastric by connective tissue. Depressor muscles of hyoid 
divided and sac exposed. Sac pierced the thyro-hyoid membrane 
by a stalk as thick as the little finger. Opening in membrane 
enlarged, and another sac seen inside connected with the larger 
one outside. Superior laryngeal nerve anaesthetised with novocain. 
Sac dissected out. Opening into ventricle not seen. The tumour 
was the size of a hen’s egg, with a constriction at the site of the 
thyro-hyoid membrane. The air could not be pressed out, and no 
opening could be found. Probably there had been a valvular 
opening, as the sac filled up again so rapidly after puncture. 

Unlike most other cases, there had been no increased air 
pressure to account for its formation. The author believes in 
puncture with a hypodermic syringe as a diagnostic method. 

J. K. Milne Dickie. 


PSYCHIATRY. 

PHYSICAL DEVELOPMENT IN THE MENTALLY DEFECTIVE. 
(614) (Lo sviluppo flsico nei frenastenici.) L. Ciampi and H. Valdizan, 
Riv. ital. di Neuropat ., Ptichiatr. ed Elettroter 1914, vii., p.' 193. 

A statistical study based on the examination of 600 cases, aged 
from 5 to 14 years, and illustrated by tables showing the 
relation of increase in size and in weight to sex, and to the form 
of mental defect. J. D. Rolleston. 



424 


ABSTRACTS 


GENERAL PARALYSIS AND PREGNANCY. (Paxalysie gtfninle 
(016) et grosses*®.) J. de B. de Lavebqne, Tkiset de Paris, 1913-14, 
No. 443. 

The thesis contains the histories of seventeen cases, three of which 
are original. 

The writer’s conclusions are as follows:— 

1. Pregnancy is rare in general paralysis. 

2. Pregnancy may ocour at any stage of general paralysis, and 
appears to accelerate the course of the disease, and sometimes 
to aggravate the symptoms. 

3. In rare cases there is improvement or disappearance of 
the symptoms. 

4. Delivery is followed sometimes by aggravation of the 
disease, but usually hy a transient remission. 

5. Pregnancy as a rule goes on to full term. 

6. Labour is very often painless, and is in most cases very 
rapid. 

7. The infant is usually normal. 

8. Abortions, premature births, or births of children with 
syphilitic symptoms or malformations are rare. 

J. D. Rolleston. 


FOCAL SYMPTOMS IN GENERAL PARALYSIS. C. Macpie 
(516) Campbell, PsychiaU Instit. of the New York State Nospitalt, 1914. 

Q. E. Stechert «fe Co. Price 9 1.26 net. 

Nineteen cases are here analysed, both from the clinical and from 
the pathological points of view. They are classified into the 
following four groups:— 

1. Cases of general paralysis with focal symptoms on the basis 
of vascular disorders (4 cases). 

2. Cases of general paralysis with focal symptoms on the basis 
of localised severity of the process of general paralysis; Lissauer’s 
atypical general paralysis (6 cases). 

3. Cases of general paralysis with focal symptoms of traumatic 
origin (2 cases). 

4. Cases of general paralysis with focal symptoms which are 
correlated neither with vascular disorders nor with localised 
severity of the process of general paralysis (6 cases). 

It is only within recent years that the introduction of cyto- 
logical and serological methods, together with a definite histo- 
pathological criterion (Nissl and Alzheimer), have made the 
diagnosis of general paralysis at all certain, and even yet it is often 
impossible, clinically at least, to differentiate between general 
paralysis and cerebral syphilis. Among the cases which specially 



ABSTRACTS 


425 


present diagnostic difficulties is the large group of cases of general 
paralysis with focal symptoms. Focal symptoms may be due to 
vascular changes, frequently of syphilitic origin, and occurring 
before the onset, within the prodromal period, or after the disease 
has become established. In regard to cases of localised severity 
of the process of general paralysis, the factors which determine 
this are quite obscure, and there seems to be no tendency towards 
a systemic distribution. Traumatic lesions may precede or follow 
symptoms of general paralysis, but the term “ traumatic general 
paralysis” is unjustifiable. In the fourth group no anatomical 
findings could be found to account for the focal symptoms, and 
afford fresh evidence of the difficulty in correlating lesions and 
symptoms. A. Ninian Brucb. 


DIFFERENTIAL DIAGNOSIS OF GENERAL PARESIS. Adolf 
(617) Miybb, Amer. Joum. Insanity, 1914, lxxi., July, p. 61. 

By the "diagnosis of dementia paralytica” is meant progressive 
parenchymatous syphilis of the brain. The diagnostic problem is 
most difficult where we deal with processes also on a luetic basis, 
but with a different type of lesion, e.g., the diffuse luetic meningitis 
and gummatous processes; the luetic vascular affection of the 
smaller vessels; the tabetic conditions with non - paralytic 
psychoses, as well as syphilis combined with neurasthenia, 
epilepsy, alcoholism, arteriosclerosis, and functional psychoses. 

The best evidences of a parenchymatous syphilis are:— 

1. The findings in the cerebro-spinal fluid. Historically the 
points of importance are—(a) the platinum chloride reaction of 
Mott and Halliburton, ( b ) the demonstration of a pleocytosis (with 
plasma cells), (e) the demonstration of globulin, (d) the complement 
fixation according to Wassermann, (e) the colloidal gold chloride or 
Goldsol reaction. In importance these rank as follows— (a) 
complement fixation with various antigens, ( b ) the gold chloride 
reaction, if it involves the total discoloration of the first five 
dilutions, and relative discoloration of the dilutions, 6 , 7, 8 , (c) the 
presence of globulin either in the form of the first phase of Nonne- 
Apelt or with Noguchi’s butyric acid test or the Ross-Jones test, (d) 
the presence of more than ten or twelve cells per c.mm., especially 
when there are plasma cells and no leucocytes. A slight pleo¬ 
cytosis and traces of globulin may also occur in brain tumour. 

2. The findings from brain-puncture, of most value in connec¬ 
tion with the cerebral introduction of curative fluids. 

3. The “ cerebral symptom-complex ”; inconclusive, but consists 
of speech and writing disorders, tremor, difficulty of co-ordination, 
innervation, cerebral attacks, and exaggeration of tendon reflexes, 

34 



426 


ABSTRACTS 


occasionally with ankle clonus. Most of these symptoms occur 
also in toxic states, especially bromide intoxications. 

4. The “ tabetic symptom-complex,” mostly eye symptoms. 

5. Change in mental functions, loss of memory, change of 
personality, &c. 

6. Combined mental and neurogenic attacks of an apoplectiform 
or epileptoid nature. 

Next one must try and determine (1) if all the symptoms are 
paretic, (2) the chances of remissions, and (3) the localisation of 
the process. Here the cerebro-spinal findings are of special value. 

A. Ninian Bruce. 


WHAT IS PARANOIA? R Stanley Abbot, Amer. Journ. Insanity , 
(518) 1914, lxxi., July, p. 29. 

Kraepelin’s conception, as defined in 1904, was that “there is 
undoubtedly a group of cases in which delusions are the most 
prominent, if not the only symptoms of the disease. In these 
cases a chronic, stable system of delusions gradually develops 
without any disorder of the train of thought, of will, or of action." 
Two years ago he wrote of paranoia as being not a disease process, 
but a mental twist, an abnormal development, occurring under 
the ordinary stress of life in a person psychopathically predisposed 
by internal conflicts and by a mixture of egotism and suspicious¬ 
ness—the “ paranoid ” constitution. 

Bleuler (1906) and Hans Maier (1913) believe paranoia to be 
a psychosis in which some complex or group of complexes has for 
the patient such strong associated feelings or emotions that the 
content of thinking in lines related to the complex is determined 
by these affects instead of by facts or logic (Bleuler’s autistic 
thinking). Errors thus arise which the patient cannot correct. 
Hence, with persistence of the tendency to this affective response 
to the complex, whenever anything in the individual or in the 
environment arouses associations leading to it, errors are per¬ 
petuated, new ones are made, and thus delusions are formed, 
persist, and develop (Maier’s katathymic delusions). Wishes, fears, 
or internal conflicts are what give rise to such complexes. Only 
the thoughts and feelings connected with the complexes are 
abnormal; all the rest is normal. 

A special predisposition, perhaps consisting in constitutional 
defect with bad heredity (Krafft-Ebing), a primary disposition to 
think with short associations (Friedmann), a special psychopathic 
constitution (Kleist, Bleuler, and others), an egotistic and suspicious 
personality with internal conflicts (Kraepelin), or an imaginative 
personality with lively emotional reactions (Maier), may be the 
necessary soil for the development of paranoia. Practically all 



ABSTRACTS 


427 


* 

writers, except Ziehen and his followers, agree on the chronicity 
and incurability of paranoia, though a very few recoveries have 
been reported. 

The author concludes that unless the word be used in a 
symptomatic or descriptive sense, paranoia is a psychosis, but not 
a disease process. It is neither a pure affect-psychosis nor a 
pure ideation-psychosis, but rather a combined associational affect- 
ideation-psychosis. It is a continuous self-perpetuating faulty 
association of ideas and affects without disturbance of the thinking 
or affective or conative processes as such. It is purely functional, 
but not related to the manic-depressive or dementia praecox 
psychosis, which are ordinarily, though wrongly, called functional. 
Hence it does not lead to dementia, and it does not necessarily 
have any of the symptoms of the other psychoses except delusions, 
which may occur in all of them. Its mechanism is that of 
prejudice, but the basal complexes are very intimate and personal 
ones, with correspondingly strong and durable effects. This con¬ 
ception gives us some therapeutic hope, realised in at least 
one case. A. Ninian Bruce. 

DEMENTIA PRJECOX IN THE EIGHTH EDITION OF 
(519) KRAEPELDTS TEXT-BOOK. H. Douglas Singer, Journ. New. 
and Afent. Die., 1914, xli., June, No. 6. 

In 1902 Kraepelin defined dementia praecox as “a series of 
diseased pictures, the common characteristic of which is the 
outcome in peculiar states of weak-mindedness.” 

In the latest edition the above definition is in the main 
adhered to, but Kraepelin now proposes to separate off some types 
in which the outcome shows certain differences. This whole 
group of disorders is now designated by the general title, "Die 
endogenen Verblodungen ” (endogenous deteriorations). The group 
is defined as “ a series of diseased pictures, the reciprocal clinical 
relations of which are still entirely unclear, but which show the 
common peculiarity that they arise from internal causes without 
recognisable external occasion, and that, at least in the great 
majority of instances, they result in a greater or less degree of 
psychic infirmity.” This broad group is then subdivided into 
Dementia Praecox and Paraphrenia. 

The deterioration in dementia praecox is emphasised as in¬ 
volving principally the interest and activity, and much stress is 
laid upon the character of the sense-falsification and the absence 
of coherent relation between them and the patient’s thoughts. 

The three types, the hebephrenic, katatonic, and paranoid, have 
now been split into eight main forms with a few subdivisions. 

1. Dementia Simplex is defined as "an extremely insidious 



428 


ABSTRACTS 


impoverishment and erosion of the entire mental life.” Patients 
belonging to this group are slovenly, inattentive, indifferent, shy 
and retiring, fretful and irritable, without any very clear or 
definite signs of insanity. This disorder is of slow development, 
and may lead to extreme deterioration. 

2. “Silly” (. Ldppische ) Deterioration. —This group includes a 
large number of those cases previously classed as hebephrenia. 
Besides the progressive mental deterioration there is marked 
desultoriness in thought, feeling, and act. The most striking 
disturbances concern the conduct; the acts are often strange, 
absurd, and unexplained, more or less impulsive. In 60 per cent, 
the onset is before the age of 25. 

3. Simple Depressive or Stuporous Deterioration includes “ those 
cases in which, after an introductory phase of depression with or 
without the manifestations of stupor, there develops finally a 
psychic infirmity.” About 20 per cent, of this group are stated 
to begin acutely, especially when stupor is present. The mood 
is at first anxious and depressed, but later irritable, impulsive 
conduct, grimacing, mannerisms, and negativistic tendencies may 
show themselves. Some of the cases belonging to this group 
closely resemble the depressed form of manic-depressive insanity. 

4. Depressive Deterioration with Delusion Formations. —The 
onset is similar to that in the previous type, but is more frequently 
acute or subacute. In this form the delusions are widely 
developed and have a bizarre form. 

5. (a) Circular Form. —The onset may be gradual or acute, and 
is characterised by subjective complaints and hypochondria, sense- 
falsifications, and delusions of a depressive type. Following this 
stage of depression there appears one of excitement. The chief 
symptoms are the restless, aimless excitement with numerous 
impulsive acts. The excitement is one of considerable monotony 
and repetition, and finally passes into deterioration. This course 
is interrupted by remissions, with marked improvement in 53 per 
cent, of cases, and in 14 per cent, such remissions occur several 
times. 

(b) Agitated type. 

(c) Periodic type. 

6. Katatonia. —This name is now restricted to a group “in 
which the peculiar excitement with katatonic stupor controls 
the picture.” 

The onset is acute in 41 per cent, and gradual in 31 per cent. 
In one-third of the cases remissions occur, and in some this may 
amount to apparently complete recovery. 

7. Paranoid. —In this group the chief symptoms are delusions 
and sense-falsifications, and definite deterioration of the dementia 
praecox type ensues. 



ABSTRACTS 


429 


There are two sub-types, (a) dementia paranoides gravis and 
(6) dementia paranoides mitis. 

8. Cases of Speech Confusion .—“The development and course 
correspond in general with those of dementia prsecox. They differ 
in that the outcome is a state characterised essentially by an 
unusually striking disturbance of speech expression, with propor¬ 
tionately little interference with other mental functions.” 

In regard to the etiology of the disease, Kraepelin’s final 
conclusion is that it is probably an auto-intoxication. He refuses 
to consider the modern views as expressed by Freud and Jung, 
in regard to the psychopathology of the disease. 

Paraphrenia is the name proposed for a group of cases similar 
to those of the paranoid form of dementia prsecox, but differing 
in that the affects and will are only very slightly disturbed. 

Four sub-types are described:— 

1. Paraphrenia systematica. 

2. The expansive type. 

3. Confabulating form. 

4. Paraphrenia phantistica. 

D. K. Henderson. 

SIMILAR AND DISSIMILAR PSYCHOSIS IN RELATIVES. Charles 
(520) Ricksher, Amer. Joum. Insanity , 1914, lxxi, July, p. 133. 

The following conclusions were based upon an examination of 
the histories of 314 individuals, 61 parents and 62 children, and 
191 brothers and sisters from 90 families, in all 151 families. 

Similar psychoses occur in about 50 per cent, of parents and 
children, and in brothers and sisters in about 66 per cent, of the 
eases. The age of onset of the psychosis is, as a rule, earlier in 
the child than in the parent. When the father and daughter, or 
mother and son, each suffer from dementia prsecox, the difference 
in the age of onset is most marked. Idiot children are not found 
as often as children with less severe mental disorders. Epilepsy 
in this series was transmitted through the fathers to the sons. 
The transmission from mother to child is only a very little more 
frequent than from father to child. Dementia prsecox is the 
most frequent psychosis found in brothers and sisters, and is the 
psychosis most frequently found in one child when the brother 
or sister suffers from some other mental disorder. Mental disease 
is more apt to appear earlier in sisters than in brothers, except 
that when dementia prsecox is found in one child and manic- 
depressive insanity in the other, the average age of onset is less 
in the brother than in the sister, whether the brother suffers from 
manic-depressive insanity or from dementia prsecox. 

A Ninian Bruce. 



430 


ABSTRACTS 


AN INTOXICA TION P SYCHOSIS ASSOCIATED WITH CIRRHOSIS 

<521) OF THE LIVER. Guy H. Williams, Amer. Joum Insanity, 1914, 
lxxi., July, p. 149. 

Three cases are described, all occurring in men aged 60, 59, and 
72 years respectively. They all showed disorientation as to time, 
place, and persons. In one case this grew much better under 
eliminative treatment, but again became marked when the patient 
became toxic. It is impossible to say what the toxic agent was, 
but, as cirrhosis of the liver was present in all the cases, it is 
suggested that it may have arisen from defective liver metabolism. 
There were no autopsies. A. Ninian Bruce. 

IS THERE AN INCREASE AMONG THE DEMENTING P8Y- 

(522) CHOSES7 Charles P. Bancroft, Amer. Joum. Insanity , 1914, 
lxxi., July, p. 59. 

The writer feels that while it is demonstrably certain that paresis 
has increased during the last twenty-five years, it is by no means 
equally certain that an actual increase in the other dementing 
psychoses has occurred. A decrease in the dementing psychoses 
may be attained by curtailment of the immigration of mental 
defectives at the source, restriction of alcoholic indulgence, 
prevention of syphilitic infection, stricter segregation of the 
feeble-minded, and greater intelligence in entering upon the 
marriage relation. A. Ninian Bruce. 

A STUDY OF BRAIN ATROPHY IN RELATION TO INSANITY. 

(523) A J. Rosanoff, Amer. Joum. Insanity , 1914, lxxi., July, p. 101. 

Brain atrophy cannot be precisely measured by brain weight 
alone; both the cranial capacity and the brain weight must be 
taken into account. The measure which most nearly approaches 
a normal constant is that of the average width of the space 
between the skull and the brain, the cranio-encephalic space. An 
index of this space, and consequently an index of atrophy, may be 
obtained by subtracting the cube root of the brain volume from 
the cube root of the cranial capacity. The brain volume is 
obtained by dividing the brain weight by 1'037, the average 
specific gravity of the brain. 

The index of atrophy was measured in 452 cases, and it was 
found that it slightly increased with age and with emaciation. In 
cases of insanity it varied with the clinical group; it is greatest in 
cerebral arteriosclerosis, and is greater in general paralysis and in 
senile dementia than in dementia prrecox. Mental deterioration, 
of whatever nature, goes hand in hand with brain atrophy. An 
analysis also showed that the atrophy of the brain in dementia 



REVIEWS 


431 


praecox is not due to age or emaciation, and that, in consequence, 
dementia praecox must be a disease associated in some way with 
changes in the brain which lead to atrophy. 

A. Ninian Bruce. 


"Reviews. 

THE TRAINING SCHOOL BULLETIN, 1913-14. Published at Vine- 
(524) land, New Jersey, U.S.A. 

The Training School Bulletin is a small periodical published by the 
Training School at Vineland, New Jersey. The Training School 
is devoted to the study, care, and training of mentally-defective 
children. Private, State, and free patients are admitted to the 
school, where they are classified according to their physical and 
mental abilities. 

The “ Association of the Training College ” is engaged in promot¬ 
ing the colony idea, and encouraging the foundation, in the various 
States, of colonies for the permanent care of the feeble-minded. 

The Bulletin contains articles dealing with the study and care 
of the feeble-minded at Vineland and elsewhere, many of which 
should be of interest to those concerned in the operation of our 
own Mental Deficiency Act. Thus in recent numbers there are 
several articles on the Binet tests, an article on the de Sanctis tests, 
articles on Eugenics, Crime and Mental Deficiency, Moral Defec¬ 
tives, Laboratory Equipment for an Institution for the Feeble- 
Minded, The Montessori System, and reviews of recent literature. 

The following extract from the Superintendent’s report with 
regard to the founding of colonies indicates the kind of work 
which is being done under the auspices of the Association:—“ See 
how fast it (the colony idea) has moved at Menantico. The land 
was purchased May 5, 1913. The first two boys went into the 
portable buildings July 15, 1913. The other buildings are made 
of cement blocks, made by the boys, under the direction of the 
masons. To-day (April 1914) we have two dormitories holding 
twenty-five each, a dining-room and kitchen building, bath house 
with hot and cold water, sewer lines and cesspool, rooms for 
employees and for mending, and a shop building with pump and 
five-thousand gallon water tank fifty feet high. . . . The colony 
unit is to be one hundred. With the additional buildings and 
equipment for the extra fifty, we shall have provided the com¬ 
plete unit for $200 per capita.” This includes $5,455 for the 
land. W. B. Drummond. 



432 


BOOKS AND PAMPHLETS RECEIVED 


DISTURBANCES OF THE VISUAL FUNCTIONS. Prof. W. Lohmann. 
(526) Translated by Angus Macnab. Pp. 185. John Bale, Sons, A Daniels- 
son Ltd., London, 1913. Price 15a 

Under this title the author has collected a large number of 
observations mainly referring to the physiological and psychical 
aspect of sight, and thus provides much information on subjects 
which are barely, if at all, mentioned in most text-books. The 
reader is invited to explore that interesting but very difficult 
area, in which vision and its correlated processes meet and give 
rise to perception with its widespread associations, and which has, 
therefore, attractions both for the oculist and the psychologist 

The book is divided into twelve chapters, of which the first 
three deal with vision and blindness, while in the fourth the 
differences between central and peripheral vision are discussed. 
The next three chapters consist of expositions of current views on 
disturbances of adaptation and the light sense, and on the colour 
sense. The eighth chapter deals with the chromatopsias, and the 
remainder with colour hearing, binocular vision, visual disturbances 
in disease of the tracts and centres, and memory pictures. 

All of the subjects discussed are of great interest, and the 
book contains much that will stimulate further investigation: 
at the same time it iB somewhat disappointing to find that the 
greater part of the book consists of a compendium of the observa¬ 
tions and opinions of others, with many quotations, Bet down with¬ 
out much comment either favourable or the reverse. The evidence 
is presented, but very little in the way of a judicial summing 
up, and the author’s personal opinions are not easy to discover. 

For this the inherent difficulties of the subject are no doubt 
responsible, and therefore the greater is the credit due to Professor 
Lohmann, whose book is the first attempt to present the facts 
connected with the most difficult and abstruse aspect of the visual 
function in a collected, concise, and easily readable form. 

On these grounds alone the present work supplies a long-felt 
want, and will be heartily welcomed by all who are interested in 
the subjects with which it deals. 

The translation and the illustrations are excellent, and the 
publisher’s work is of the best, with the exception perhaps of the 
very shiny paper. H. M. Traquair. 


BOOKS AND PAMPHLETS RECEIVED. 

Campbell, C. Macfie. “ Focal Symptoms in General Paralysis ” 
(Ptychiat. InstituL of the New York State Hotpitale, New York, 1914. 
Pr. 91.26 net). 

Lohmann, W. “Disturbances of the Visual Functions.” Translated 
by Angus Macnab. John Bale, Sons A Danielsson, Ltd., London, 1913. 
Pr. 16a 



■Review 

of 

IFleurologiP anb ps^cbtatr^ 


©dginal Erttcles 


THE MECHANISM OF PERIODIC MENTAL DE¬ 
PRESSIONS AS SHOWN IN TWO CASES, 
AND THE THERAPEUTIC ADVANTAGES OF 
SUCH STUDIES . 1 

By L. PIERCE CLARK, M.D., New York City. 

Notwithstanding the fact that periodic depressions of a so-called 
simple neurasthenic or hypochondriacal character have been 
known so long that many special sanitoria have been largely 
devoted to their treatment, little effort has been made to make 
careful mental analyses of such cases to determine the psychogenic 
factors at work in these depressions. So great has been the stress 
laid upon somatic causes of disturbed brain metabolism that one 
has usually been quite satisfied to search for digestive or circulatory 
disturbances in the periodic neurasthenias, and when such physical 
disorders were found, as is usually the case, we have been willing 
to rest content and forthwith base a treatment upon these facts. 

It is not that the line of investigation in neurasthenia has been 
necessarily wrong, but that such researches are incomplete, and 
do not place us in possession of all the facts. I venture to say 
that every case of periodic depression usually has some somatic 
disturbance, but I hold it is equally true that in every case there 
is just as certainly an abnormal psychic mechanism at work. It 
matters little in this or similar studies whether one speaks of this 

1 Read before the N. Y. Psychiatrical Soc., June 3, 1914, 


35 



L. PIERCE CLARK 


4.‘U 


particular mechanism as the cause, or merely as a psychogenic 
factor in the production of the sequential symptoms of neurasthenic 
depression. At present no one would be so bold as to say that 
such depressions are really produced by either a somatic disorder 
or by mental factors, inasmuch as we are not pardoned in even 
considering mind disturbances in terms of brain structure altera¬ 
tions, much less in terms of remote physical disease. Be that as it 
may, I shall undertake to set forth here some analyses of the 
psychic mechanisms present in periodic depressions, which facts 
seem to me of sufficient moment in our full understanding of such 
disorders to warrant our close attention and consideration. Even 
though it may ultimately be found that recurrent neurasthenic 
depressions of every sort are essentially biochemic, and therefore 
essentially somatic and not psychogenic, studies upon the mental 
mechanism as entered upon here will not be in vain, as the latter 
studies may make plain the more delicate and successive order in 
which the somatic causes assault the psyche, the relative order by 
which its natural defences are broken down, and finally will give 
us definite information concerning the breadth and depth of 
subjugation its innate powers have sustained. It will finally 
disclose how strong the native trends are, and what chance they 
have in making the proper adaptations to a healthy life in future. 
Not a few data have already been presented upon a field closely 
allied to the one studied here; they are the intramural studies of 
the frankest manifestations of the manic-depressive syndrome. 
These studies have not only greatly cleared the nature and 
pathology of such syndromes, hut they promise therapeutic aid in 
a field hitherto considered hopeless so far as obviating recurrent 
attacks in such individuals are concerned. It is hoped these 
studies upon a simpler type, at the lesser end of the scale of 
depressions, may serve similar diagnostic and therapeutic ends. 
The work here presented has been prompted not a little by the 
psychiatric studies already alluded to, both in this country and 
abroad. I venture to hope the inspiration in this study may be 
mutual, and the work in future will be fully co-operative. 

In presenting such a study of periodic mental depressions, I do 
so with the greatest diffidence, for the reason that the cases I 
shall present do not suffer that degree of mental dilapidation which 
permits one to penetrate the psyche to the depth reached in the 
more frankly disordered melancholies. My first case, analysed six 



MECHANISM OF PERIODIC MENTAL DEPRESSIONS 435 


years ago, when she was 44 years old, had had two depreseive 
attacks yearly since 24 years of age, but has been entirely well 
since the treatment now finished over five years ago. 

In order that this study may be considered in a fair light, I 
must say that I shall hold no brief for the somatic symptoms of 
neurasthenic depression, as they have been too long uppermost in 
the final court of treatment of nervous disorders, and are well 
known to all. On the contrary, I shall make argument for the 
innate right for neurasthenic depression to be considered on its 
own basis of mental pathology, the laws governing which for a 
long time have been too lightly held by most of us. The study 
will embrace two case-presentations, given as briefly as possible, to 
show the mental or dynamic processes operating in each. If it 
be shown some time in future that there exists a large and 
important physical disorder, such as uterine displacement and 
adhesions in the one patient, or a long-standing chronic appendi¬ 
citis should be proven to be present in the other, the psychogenesis 
of the depressions will, to my mind, be none the less true although 
the mental mechanisms under study, as being the sole etiologic 
factors for the mental state, may be robbed of some of their value. 

The first case is that of a woman of 50, who has suffered from 
long-standing and recurrent attacks of mental depression of the 
neurasthenic type. I first saw her in 1909 in one of her 
characteristic depressions, at which time, as a result of the usual 
routine treatment of baths, rest, massage, and diet therapy she, 
gradually regained a fair state of physical and mental health in 
the course of two or three months. At present she suffers from 
a similar attack; there is physical fatigue and a great depression 
of spirits. She has had fearful dreams and nightmares, after 
which she is sleepless and restless for the greater part of the 
night. There is a heavy, dull headache, pains in the back, stiffness 
of the neck, and a sense of an encircling, constricting band about 
the top of the head. Now and then she feels dizzy, nauseated, 
has pains about the heart, and a feeling of impending collapse. 
All the above symptoms are worse in the morning and gradually 
wear off, with the exception of the mental depression, the slowness 
of thought and action, the mental indecision, the feeling of 
unworthiness, and that she is to lose her mind or become an 
invalid, or dependent on charity. It will be shown in the 
analysis of the case that many of the above symptoms are more or 



4.36 


L. PIERCE CLARK 


less 8yml)olie representations of wish-fulfilments of death trans¬ 
lated from the dream state to the waking, conscious life. 

Our patient was the fifth child in a family of fourteen, of whom 
five are now living. All the brothers and sisters were of the 
neurotic temperament, and in fact both branches of the family 
stock were of a highly nervous temperament, although of a 
different make up than that of our patient. There were no manic- 
depressive cases in the family history. As a school pupil our 
patient had a good standing in her classes except in mathematics, 
which she never mastered. She was of a musical temperament, 
lively, and of a sympathetic nature. She lived a very sheltered 
life, was much petted and protected by her mother. In brief, she 
was of a frankly open type of personality, and gratified herself 
freely in a care-free social life. She was very dutiful and obedient, 
easily controlled as a child, and always did as her parents wished 
in all things. At the early age of 16 she became engaged, and 
under the cover of an apparently strong attachment she continued 
her social interests to such a thoughtless extent that her engage¬ 
ment was broken off by her fiance', owing to her own acta. The 
engagement was renewed in a year or so by her surrender of a 
too free conduct with other young men. She was finally married 
at 26 years of age, and her husband died six yearn after. 

On her marriage she lived with her mother-in-law for three 
years. Her mother-in-law was extremely jealous, calling for our 
patient’s best effort in cheerfulness and tact to avoid conflicts. 
The mother-in-law always had the patient’s husband call her 
“ sister ” rather than mother, and seemed to require his childish 
petting and caressing. The father-in-law was a cold, stern man, 
and gave his wife little affection. There was an active rivalry in 
the affections of our patient’s husband on the part of his mother. 
Coupled with this, financial troubles soon began, and all were 
required to economise to the utmost. The mother-in-law now 
spoke of the lost opportunities of her son’s chance to marry a 
much richer girl. Coupled with this stress was the active rivalry 
of the husband’s younger brother, who was also closely attached 
to him, and considered the patient as an interloper. Even to 
this day he has not become reconciled to her having taken his 
brother away from the home. This younger brother is still 
unmarried, and lives with his mother. 

The sexual act in our patient was always painful and extremely 



MECHANISM OF PERIODIC MENTAL DEPRESSIONS 437 


unpleasant. She seems to have known nothing of the details 
of sexual life until she was married. She never spoke to anyone 
of the painful or depressive character of the sexual act, not even 
to her husband, although she doesn’t doubt that he was fully 
aware of how the act affected her, and how she dreaded it. 
Although there was no physical difficulty in the act, it was never 
pleasurable, and she avoided it as far as possible. She never took 
any artificial means to avoid pregnancy. After the sexual act 
she felt nervous and very tired and sleepy, but felt no depression. 
At the first pregnancy she had a miscarriage before she was aware 
that she was really pregnant. After each of the first two abortions 
she felt no depression, but within a few days after the successful 
and uneventful delivery of the child from the third pregnancy she 
felt bad, became depressed without obvious cause, and wanted to 
be alone. The next day she had pains in the arms and wanted 
them rubbed. She felt sick all over, but there were no physical 
signs of illness. She began to weep, thought she was to lose her 
mind, and thought of committing suicide, and thinks she would 
have attempted it if someone had not stayed constantly in her 
room. She didn’t care to have her husband about, and never 
asked to have her child with her. This depressive attack, which 
she calls her great nervous prostration, disappeared in two months, 
but ever since that time she has had depressions every four or five 
months of more or less the same character. She usually feels 
a slowness of action, hates to make decisions, there is a shaking, 
tingling sensation in the arms, the heart beats rapidly, and she 
feels as though she cannot live and doesn’t desire to do so. There 
is a loss of sleep and appetite, and there is always an aimless, 
undefined fear. 

To summarise up to and including the depression after the 
childbirth: We find a woman of rather superficial mental type, 
of a highly sensitive temperament, who, after marriage of a not 
very marked love-fixation, had financial and family worries of an 
intensive sort, who never had other than painful intercourse 
with her husband, with nervousness but no depression after each 
attempt of the act, but who, through desire for children and her 
feelings of duty to the husband, actually bore a child after the 
third pregnancy, at which time she passed abruptly into a deep 
and painful depression. Although the husband has been dead 
fourteen years, she still has a feeling as though there were some- 



L. TIERCE (’IARK 


4:58 

thing unfulfilled in her life with him, and reproaches herself for 
much of her past life with him. The son is viewed lately as 
a relic or remnant of the father, and on him she centres her love 
and fears. She places on him an over-determined contrition of 
spirit, as though to say, “ I brought you into the world, and now 
I must see you through it.” 

In a more frank review of her depressions she began to search 
her childhood for the first faults in character. She reproached 
herself because in the physician’s eye and in her own, too, she had 
blamed her parents unduly for not rearing her properly, and 
because she had cast reflections on her husband for not leaving her 
provided for by any life insurance. 

In a still franker talk, it was shown that the patient had kept 
alive a ghost-fancy of her dead husband, whom she mentally 
consulted as regards all her acts and thoughts; that he played a 
larger part in her life now' than when living, and when this grew 
indefinite the depression was not far off. She now sees she was 
so much attached to her mother and older sister that she was 
sexually a cold wife, and on the death of the mother, sister, and 
husband, she had but a child left as a remnant connecting her with 
the past, and now he is engaged and soon to be married. Even 
his announced intentions of marriage caused a continued depression 
lasting a year. 

Still deeper analysis shows that the patient surmised her 
painful intercourse with her husband was unnatural, and 
that to talk frankly with other women about it would only 
make her feel a sense of unworthiness and bring out her defect. 
Besides, she thought she could make up for this by being more of 
a sweetheart to him, and thus make him foiget she was not all to 
him a good wife should be. After each pregnancy there resulted 
a conflict between the desire for children for her husband’s sake, 
and the feeling that the birth of a living child would disturb the 
lover relations, a not uncommon conflict in such cases (reproaches), 
the “ ever to court and never to wed ” principle, which was her 
ideal of a happy marriage. Whenever she hears that one of her 
friends is about to have a child she feels a great pity for her, and 
a sort of depression and sadness. 

After each abortion there was a sense of reproach to the 
patient; she thought it might be her fault the pregnancies did not 
go on to term, and she was therefore examined repeatedly by 



MECHANISM OF PERIODIC MENTAL DEPRESSIONS 439 


physicians to determine that she was blameless. After the third 
pregnancy and its successful termination, instead of elation, content¬ 
ment, &c., she went into a morbid mental depression, disliked her 
child and husband, &c., and had grave fears her son wouldn’t live to 
grow up, and ever since he was born her fears have been centred 
about him and his welfare. In the dream he always falls seriously 
ill, but not fatally, nor does he ever die in the dream; being a 
remnant of the father this still protects him from the unconscious 
annihilation he might otherwise suffer in a more ambitious dream. 
She had wished she might avoid all pregnancies in future after 
the second abortion. 

Apropos of suicide being one of the ways out of her periodic 
depressions, we find the following dream of pertinence and interest 
in our patient. She dreamed she was in a large building thronged 
with all sorts of people from all walks of life, all on different 
floors (stratified class society of real life); she finally goes down 
a long flight of stairs (sexuality, See.), and there comes upon an urn 
placed upon a pedestal near which stands a Japanese, silent and 
grave, dressed in black robes (death). After looking long at her, 
the Japanese asks her if she wants a picture of herself, and without 
waiting for her reply he solemnly takes one from the urn, which 
she felt contained her “destiny.” She finds the picture is of 
herself, but the upper half of the face is entirely like a beautiful 
Japanese, and a confused identity masque-effect is produced. 
Consciously, in the waking state, she finally identified this with 
“ Madam Butterfly,” which play and opera she has seen very 
frequently. It will be remembered when Madam Butterfly finds 
her lover has left her, never to return to the old relations, she 
commits suicide. Madam Butterfly is the play-opera which 
fascinates our patient most, and next comes Shakespeare’s “ Romeo 
and Juliet.” 

To summarise the case. We have a woman of 50 subject to 
periodic depressions for twenty-four years, dating from the birth 
of her only child. She led a rather gay, superficial, restricted 
child and girl life. She was greatly attached to her mother, but 
became engaged at the early age of 16, which engagement con¬ 
tinued off and on for ten years before marriage. At marriage she 
had pronounced family and financial worries. The marriage 
relations were avoided when possible, were painful and extremely 
wearing to her health; at the third pregnancy a boy was born, 



110 


L PIERCE CLARK 


ami a sharp and marked mental depression ensued. Her child 
was an object of dislike—she could not or would not nurse it; 
the menstrual period was absent for two years. After a firm 
injunction by the surgeon who repaired the laceration, an opinion, 
which was concurred in by the family physicians was that she 
should have no more children, and the marital relations ceased 
thereafter. As is well known, one identifies himself with those 
statements of the physician which suit him best or enable him to 
do what he wants to do, it being only too frequently a case of a 
bribed oracle. Six years after marriage her husband died, leaving 
her penniless, with a child to care for. From that time to the 
present day she has never been more than six months free from 
neurasthenic depression, and its usual host of bodily ills following 
in the wake of such a nervous disorder. The depressions are 
always brought on by some new life adaptations or adjustments. 
First there is the shock, then regression and depression, and 
finally reproaches for an unalterable past with the husband, and 
finally the reproach is cast back upon the parents for defects in 
her bringing up as a child, and in the deepest depression, as at 
the childbirth, it finally rested on her own fault, and then deeper 
depression and thoughts ensued, and the idea of suicide followed. 
The mental mechanism would seem to be a regressive depression 
following an incomplete discharge of the libido ; the primary fault 
would seem to suggest a homosexual maternal-sister attachment 
as shown in the dreams and free associations. 

I n every depression she has had since the first great one, there 
is always the same mechanism ending in the conflict, “ I would 
not l»o having such depressions if I had not had that one at 
childbirth, and I wouldn’t have had that if I had not had a child.” 
This brings up unbearable wishes and fears in regard to the dead 
husband and her living son; then follow the reproaches as to 
the unsatisfied and incomplete marital relations, then parental 
reproaches, and occasionally, in deepest despair, the reproach that 
she is herself, after all, the one great fault, and then suicide 
musings enter. As the final note to the case, I would Bay that the 
present depression was relieved entirely in three weeks with a far 
superior ability at the end to meet life issues than had been 
attained by any previous plan of treatment. 

To summarise, we have a woman of the open type of personality 
who is not able to adapt herself to the new state of maternity. 




MECHANISM OF PERIODIC MENTAL DEPRESSIONS 441 


While many would call the latter an added bond in the married 
state, it really is a new adaptation in life quite different from that 
which formerly obtained. If we take into account the difficulty 
met in ordinary sexuality, coupled with the mental breakdown 
shown here at maternity, we will see how the whole adaptations 
required make for a more or less complete severance of the older 
or platonic love relations. There was therefore a new adjustment 
required which broke the libido attachment that formerly obtained, 
hence the shock and regressive depression. All subsequent 
upsetting causes have been in the nature of more or less complete 
temporary withdrawal of the libido in its larger meaning. Certain 
additional facts during the treatment and at its termination 
which, unfortunately, cannot be brought out here, proved over 
and over again that while the patient is now in a more comfort¬ 
able and understandable frame of mind than she has ever been 
before, there still remain certain primary antagonistic trends to 
sexuality which have not been essentially changed, and which 
it would seem to be unwise to attempt to alter at this late day 
in one who is no longer young and not primarily endowed with 
great innate plasticity for adaptations in life. A further develop¬ 
ment of the hypothesis to cover both cases will be elaborated at 
the end of the second case, which I will now briefly set forth. 
It is that of an unmarried man of 34 years of age who has had 
periodic mental depressions for thirteen years; during this time 
seven attacks have occurred, in 1901,1904, 1905,1906,1909,1911, 
and the present attack which began in December of last year. 

The general characteristics of the different attacks are as 
follows: He gradually grows quiet in manner, is disinclined to 
meet social demands, sits about the house, and worries in a mildly 
anxious manner that he is to lose his job, and that others are 
to be promoted above him. In a few days the depression appears, 
he loses his appetite, sleeps little, grows more restless and vague 
of purpose, at times becomes a little fault-finding, and cannot make 
decisions of a simple personal character. His thoughts come 
slowly, and finally he thinks he is going to die of insanity or 
brain disease, and often expresses a wish that he might contract 
some fatal disease like pneumonia or typhoid to end it alL In 
the final depth of the depression he lays his hopeless condition 
upon the fact that he indulged in excessive masturbation in youth. 

The patient is the youngest in a family of four, three of whom 



442 


L. PIERCE CLARK 


are living. There was evidence that the two sisters of the patient 
are of relatively the same temperamental make-up as our patient. 
The mother, who died eight years ago, suffered for twenty-five 
years prior to her death from manic-depressive insanity, with 
occasional lucid intervals. The circumstances under which her 
mental depression was brought about were as follows: After 
marriage the father was unable to support his wife and children, 
and the mother took a position as matron in what was then the 
Ward’s Island Immigration Hospital. Things went on fairly 
satisfactorily until a protest was made to the administrative 
authorities of the hospital that her home duties and the rearing of 
children were conflicting with her official duties in the institution. 
She was then pregnant, and although she remonstrated in the 
controversy with her husband as to what was to be done, the 
husband suggested and later gave her abortive remedies. From 
the time of the abortion there was a sharp depression, an intense 
hate toward the husband, and a condition of manic excitement 
which lasted continuously, with slight lucid intervals, until her 
death. The excitement took the phase of destruction, dilapidation, 
and disregard of home conditions, and the mother was practically 
maintained as an insane patient in her own home until her death. 

One of the first outbursts was on the occasion of her entrance 
to her husband’s room when she found one of the children naked 
on the floor outside the father’s bed while the father was asleep. 
With terrific fury the mother awakened him by throwing a couple 
of pailfuls of water on him in bed. 

The father’s temperament is designated by his oldest daughter 
as being that of a Catholic Puritan, extremely seclusive, and rather 
miserly, efficient, one who had never met the obligation of a father 
to his family in its broader sense. 

The foregoing facts relating to the mother’s mental disorder 
are mentioned here as it makes plainer the home setting and 
the background of family relationship upon which our patient 
developed his depression. 

Our patient had a common school education and a two years’ 
training in the New York City College. He had an open type of 
personality, a rather depreciative opinion of himself, was sociable, 
generous, little concerned with doubts and scruples in everyday 
life, and is fairly capable as a city surveyor, his present employment. 

He was always rather fantastical in youth, and has built air 



MECHANISM OF PERIODIC MENTAL DEPRESSIONS 443 


castles all through life. His mood is very variable, and has been 
so since early childhood. He was always affectionate and 
demonstrative with his mother, and has always had a very 
intensive dislike toward his father. 

At 21 years of age he began work as an office boy in a 
wholesale coffee house. From earliest childhood he had a great 
curiosity with regard to sexuality, and made insistent inquiries 
about it. He masturbated from 12 to 14 years of age, and had 
normal intercourse at 17, but each time he indulged in this latter 
act he was morally shocked, and a slight depression followed. He 
returned to masturbation, which act was not fully satisfying, and 
he could not bring himself to indulge in normal intercourse. He 
then entered on the clerkship as before mentioned. Through an 
intense application to work he sought to break off or to diminish 
masturbation. He succeeded in stopping the habit for one year, 
but during the latter part of this time he also fell in love, was 
jilted, and to get square with the irritable depression engendered 
he devoted himself more intensely to his work. To repress sexual 
thoughts he engaged excessively in athletics, and fancifully thought 
he would like to kill himself with work. He finally worked to 
the exclusion of all pleasurable enjoyments. He thought being 
an office boy was beneath his dignity, and strove to compensate 
for this feeling by still more fanciful ambitions in his work. He 
thought he would like to die in harness, get control of the entire 
coffee trade, and corner the market. After existing for nearly 
a year in this exalted mental state, which contrasted so strongly 
with the actuality of not being advanced in his work, and in fact 
of seeing others promoted over him, a genuine conflict began in 
his mind as to how he was to get square with life. He became 
a little over-fatigued, dispirited, and anxiously restless, couldn’t 
sleep as before, and grew thin. He then gradually began to drink 
more and more. Alcohol made him feel more efficient and 
deadened the pain of business disappointment. The drinking 
produced mild states of desire for inactivity and of depression, 
which, when yielded to, were on the whole satisfying and pleasur¬ 
able. Still there was an undercurrent of irritability which the 
alcohol less and less deadened, and besides there was a certain 
“ want in the mind ” which the alcohol only the more inflamed. 
Drinking was then discontinued, but in a few weeks the stomach 
became disordered, there was loss of appetite, and a heavy pain 



444 


L. PIERCE CLARK 


came in the stomach. The whole was found to have nothing to 
do with indigestion. He then felt he must take up masturbation 
again. The resumption of the habit eased all the old aches and 
pains in the stomach, and the irritable depression vanished at 
once. In a few weeks, however, masturbation failed of relief. 
He felt languid and detached from life. There succeeded headache, 
sleeplessness, loss of appetite, and a despair that his occupation 
was not a proper field of work for him, and that there was no way 
out At the earnest suggestion of his family, who now saw how 
miserable he had become, he changed his work to that of 
surveying, and studied very hard at both day and night school. 
He was then specially coached for the civil service. After the 
change of work, and in the light of new ambitions, sexuality 
concerned him not at all. Life was worth while once more, and 
he passed his service examination very successfully; he then went 
into an exalted hypomanic state which lasted for two or three 
days of elation, during which he neither indulged in alcohol nor 
sexual acts. He then quickly sobered down and went to work; 
the work, however, again proved rather disappointing. He was 
set at rather menial tasks at first, carrying stakes and acting 
practically as a lackey to older men in the service. Then, too, 
he started surveying at a season of the year when there was little 
to do and the hours of work were short. He felt listless, irritable, 
fault-finding, and began masturbating once more, and at the same 
time thought of renewing his studies for a better position in the 
service. On the day he reluctantly picked up his old books again, 
he felt that life after all was hopeless and that there was no way 
out—life was a miserable failure. At once he felt a terrific shock 
throughout the whole body, something broke in his head, he 
became dizzy and fearfully depressed. He saw a doctor, went 
to bed, and in a few hours regressed to youthful reminiscences, 
and in ruminating upon the causes of his depression finally saw 
the cause of his troubles was due to masturbation. In his own 
words, "All the occupations were not sufficient outlet for my 
ambitions; I felt overactive and beyond their poor possibilities. 
I let off some of this excess of feelings in masturbation. I now 
see I demanded too much of life, and there was no way out but 
for me to break as I did.” 

The history of this first attack is a rather tedious but detailed 
account of the conscious life; the facts all lay rather near the 



MECHANISM OF PERIODIC MENTAL DEPRESSIONS 445 


surface, aud were rather easily pieced together in a coherent and 
understandable pattern. The real fixed idea that has lain at the 
heart of all his several depressions is the reproach for masturbating. 
It was found on dream analysis, and by intense research of the 
child life, that he had an intense sexual aggression at 7 years 
of age toward a little girl friend, for which his mother gave him 
punishment, and which, because of the very intense love for the 
mother, caused him many sleepless nights and fearful dreams, in 
which he awakened crying he “would never do it, no never!” 
These renunciatory dreams now and then recur. He now knows 
their origin and their significance; the whole childish episode of 
sexual aggression which has now been fully recovered to conscious¬ 
ness was lodged against the habit of masturbation. The idea of 
the act was also heavily conditioned from many collateral conscious 
sources, such as quack books, supposedly good advice from friends 
and relations, various newspaper happenings, certain acquaintances, 
whose set habits he knew very well, becoming insane, &c. 

Without going into the varied types of the same general 
mechanism of the depression, I propose to submit for discussion 
a hypothesis of the genesis of depression in terms of the libido 
as shown in this case, and which applies equally well to all my 
cases of periodic depressions. This second case will be taken as 
a paradigm upon which I will elucidate the theory. Our patient 
was of the frankly open type of personality, began to show great 
sexual curiosity at 6 and 7 years of age, and even made sexual 
aggressions at this age. The same were painfully and severely 
repressed by the mother punishing the boy. He began masturba¬ 
tion at puberty in the face of the exaggerated and false knowledge 
of its immediate harm and its remote consequences. He tried to 
make the next normal sexual adaptation by ordinary intercourse, 
but this was a distinct offence against the mother, whom since her 
death he has more than once confused with the Holy Virgin. This 
sexual adaptation having failed, he reverted to his former sexual 
habits, which now proved no longer an adequate outlet, and so he 
tried to sublimate the unrequited libido into athletics and his 
work. His emotional adaptations proved inadequate for normal 
love, and he could not requisition them in the inhibitory process 
in the sublimation, consequently the work failed as it could not 
be made large enough to fulfil the desires of the growing libido. 
Then, too, the clerkship resulted in failure. There was, however, 



446 


L. PIERCE CLARK 


enough strength in the power of adaptation, together with the aid 
of the sister, to carry the whole life process on to one more tryout 
in adjustment. But the next occupation, as the first, was doomed 
to failure, and for the same reasons. A third effort was not 
possible; even a reversion to a cruder and simpler outlet of the 
libido by masturbation was not even temporarily effected at the 
third tryout. The result was a break, a shock, regression, 
depression, the reactivation of the prohibition of the mother, and 
finally the consciousness of guilt, and then thoughts of suicide or 
desire for annihilation. One might ask: But why did he have a 
depression ? The inquiry would be equally pertinent about the 
shock or the regression, as I believe the whole chain of symptoms 
are all but parts of the one great process of failure in the effort at 
compensatory sublimation of the libido. One must remember that 
the law of the libido requires a continuous attachment or out- 
streaming activity, and its withdrawal or cessation is as much an 
actual loss to the satisfaction in life as would be the loss of 
conscious pleasure shown in the loss of property or other simple 
sense gratifications. The feelings of depression indirectly act as 
a protective mechanism. Given a faulty adaptation in a manic- 
depressive individual in whom a break in compensation occurs, 
and the whole reaction which follows a depressive episode is 
essentially a conserving process. The libido having been more or 
less forcibly or abruptly torn from its customary attachments, it 
is permitted to recharge itself in its enforced rest, or, if more 
severe, it actively seeks the infantile attachments to the father or 
mother, or, when still more severe and the regressions of libidinous 
attachment to the living are not sufficient satisfaction to the 
patient, he strives for a more perfect union in death with the 
parent. The very manner of suicidal attempts to win this wish 
fulfilment are most infantile; there is often a refusal of food, 
holding the breath, refusal of discharge of faeces and urine, &c. 
In many instances the unconscious striving towards death is not 
alone an effort to escape the psychic stress and pain of the 
depressive episode, nor even a desire of a spiritual union with a 
dead parent, but rather a diffuse, general desire to return to the 
primal unity of the infinite force of inorganic nature. I believe 
this latter phase transcends all sexual content, and approaches in 
its make-up the completeness of an organic demand for a return 
to the inorganic, or oblivion. 



MECHANISM OF PERIODIC MENTAL DEPRESSIONS 447 


I believe in many not essentially pathologic depressions the 
process may be a superficial regressive depression, but in the 
severest grades of sudden severance of the activities of the libido 
the whole process, from a shock down to the depths of regression, 
self-blame, and suicide, may be so sharp, severe, and sudden as to 
carry an individual to instant suicide, or at least to the deepest 
mute plane of the melancholic stupor. In some cases it would 
seem that the quicker and more rapidly the final stage was reached, 
the better the prognosis. 

We all know, however, that many of the classic manic- 
depressives have slight depressive episodes, not essentially different 
from the grand attacks, both before and after their great depression 
under upsetting circumstances. However unhealthy the gradual 
cessation and continued presence of depressive perturbations may 
be considered, I believe it lends an ideal opportunity for making 
an analytic reconstruction of the personality, and of the whole 
mechanism by which the individual fortifies himself against future 
attacks. Cases in which the mental healing is abrupt may be 
quite satisfactory and sound clinically, but when one finds such 
individuals are even to a casual observer quite unreconstructed, 
one cannot help having many misgivings regarding their future. 
I believe the early discharge of many such asylum cases of this 
type is of positive harm. 

I may say, while I am conscious that this report of what I am 
pleased to call the mechanism of depression is based on too small 
a material for generalisation, I believe it indicates in a manner 
the general trend of psychiatric considerations which such cases 
demand, and which shall be in terms of a withdrawal or rupture 
of the libido, as the modern and rational approach to an intelligent 
understanding of the nature of periodic mental depressions. 
From a therapeutic standpoint I may say that in all my cases the 
relief of the depression has been astonishingly rapid as the analysis 
progressed. The transference occurs rapidly and is extraordinarily 
strong, so much more marked than in the ordinary psychoneuroses, 
and especially the compulsion neuroses. It must be added that 
the depression is not solely relieved, but the whole temperamental 
adjustment of the depressive individual’s life is so much improved 
that many of the patient’s relatives are as much gratified at the 
change for the better as the patients themselves. 



448 


ABSTRACTS 


abstracts. 

ANATOMY. 

THE MORPHOLOGY AND HISTOLOGY OF A CERTAIN BTRTJO- 
(626) TORE CONNECTED WITH THE PARS INTERMEDIA OF 
THE PITUITARY BODY OF THE OX. Rosalind Wulzen, 
Anai. Record ,, 1914, viiL, Aug., p. 403. 

Ip the cleft of the pituitary body of the ox be opened, there will 
be found almost invariably a mass of tissue attached to the pars 
intermedia, but very different from it. This structure is cone- 
shaped, and is usually symmetrically placed in the mid-sagittal 
plane, one-third or less of the way from the dorsal to the ventral 
end of the cleft. Out of 760 cases, only 38 showed no such 
structure. The cone differs in colour and consistency from the 
pars intermedia. Microscopically its cellular elements resemble 
those of the pars glandularis, numerous neutrophile cells being 
its most striking feature. It differs from the pars glandularis, 
however, through having in a general way finer connective tissue 
and smaller acini When this cone, which is very clearly shown 
in the figures accompanying the paper, penetrates deeply into the 
pars glandularis, the walls of the cavity into which it is so closely 
fitted are solidly packed with blood sinuses, thus suggesting an 
arrangement for the absorption into the blood stream of secretions 
from the cone or pars intermedia. A. Ninian Bruce. 


PHYSIOLOGY. 

NEW RESEARCHES ON THE FUNCTION OF THE PINEAL 
(627) GLAND. (Nouvelles recherches sur la fonction de la glands 
pineals.) C. Foa, Arch. Ital. de Biol., 1914, lxl, June 30, p. 79 
(1 plate). 

FoA. confirms his previous experimental findings in very young 
pinealectomised cockerels (v. Review, 1912, x., p. 439, and 1913, 
xi., p. 60); no results of any kind occurred in pullets nor in young 
female rats. But in young male rats a more rapid somatic 
development occurred than in controls of the same age: it reached 
its maximum degree about twenty-six to thirty days after opera¬ 
tion, and then gradually diminished till it equalled that of the 
controls: at the period of maximum development the testes also 
showed a relative increase of size, which likewise later disappeared. 
The testes of operated cockerels and also those of male rats (at 



ABSTRACTS 


449 


this maximum period) show a uniformly more advanced develop¬ 
ment of all their tissues; the tubules show a larger diameter and 
lumen, and contain a larger mass of spermatozoa: the interstitial 
tissue is increased, but only proportionately with the overgrowth 
of the tubular. Therefore we cannot say to which tissue is due 
the greater development of the secondary sexual characters in the 
cockerels, and the increased somatic development of the young 
male rats. No skeletal changes were found after pinealectomy, 
and all the organs of internal secretion were free from any histo¬ 
logical changes (the pituitary, adrenals, thymus, and thyroid are 
specially named). Fok concludes that his experiments tend to 
confirm the teaching that the pineal body exercises an inhibitory 
action on sexual development. Leonard J. Kidd. 

THE PINEAL GLAND IN RELATION TO SOMATIC, SEXUAL, 

(528) AND MENTAL DEVELOPMENT. Caret Pratt M‘Cord, 
Joum. Anver. Med. Assoc., 1914, lxiii., July 18, p. 232. 

The general plan here adopted was to feed very young animals 
with minute quantities of pineal tissue, and to record the weight 
changes, sexual differences, and, in the case of dogs, increased 
mentality. There were used altogether 110 guinea-pigs, 18 
puppies, 14 adult dogs, and 16 chicks. 

The conclusions were that rapid growth of the body resulted, 
but not beyond normal size, and less well-established indications 
of precocity of mental and sexual development were found. 

A. Ninian Bruce. 

THE SUPRARENAL BODIES AND DIURESIS. Douglas Cow, 

(529) Joum. Physiol ., 1914, xlviiL, Sept 8, p. 443. 

As the result of a number of perfusion experiments on the kidney 
of cats, supported by the evidence of carmine-gelatine injection, 
the author describes a direct vascular connection between the 
suprarenal bodies (medullary portion) and the kidneys. Under 
certain conditions adrenalin is poured in appreciable amount 
directly into the kidneys from the suprarenal bodies, producing 
a diminution in the flow of urine. The suprarenal bodies may 
thus be regarded as direct regulators of urinary activity. 

A. Ninian Bruce. 

GASEOUS EXCHANGE IN THE DECEREBRATE ANIMAL. 

(530) Charles G. L. Wolf and T. S. Hele, Joum. Physiol., 1914, xlviii., 
Sept 8, p. 428. 

The decerebrate animal responds to carbohydrates and proteins 
as does the intact animal. The rise in the total metabolism 

36 



ABSTRACTS 


4f>0 


following the administration of protein is accompanied by a rise 
in the non-protein nitrogen in the blood. A. Ninian Bruce. 


PSYCHOLOGY. 

SOME CASES OF PSYCHOLOGICAL INTEREST FROM PRIVATE 

(531) PRACTICE. J. E. Middlemiss, Joum. of Merit. Set., 1914, 
July, p. 451. 

An account of five cases of psycho-neuroses of varied type, which 
were treated by psycho-therapeutic measures, carefully adapted 
to the particular case. The author contends that at present no 
particular procedure can be looked upon as of paramount importance, 
to be used exclusively—for instance, psycho-analysis. He himself 
leans towards the use of suggestion, and of an early hypnotic or 
hvpnoidal state, but he occasionally tries true hypnosis. 

W. D. Wilkins. 


PATHOLOGY. 

A NEW METHOD OF PRODUCING EXPERIMENTAL LESIONS 
( r >32) OF THE NERVE CENTRES. (Sur tine nouvelle mtthode pour 
produire des lesions expdrimen tales des centres nerveux.) A. 

Bertolani, Rev. Neurol., 1914, xxii., Avril 15, p. 509. 

The best way to reproduce experimentally the mechanical effects 
of a ruptured cerebral artery is to inject some suitable substance 
into the cerebral tissue. The author recommends paraffin with a 
melting point of about 38 o -40°. The syringe is heated to 50*, and 
the paraffin rapidly injected just above its point of solidification 
through a fine needle. The area involved is proportional to the 
quantity of paraffin injected. 

The advantages of this method are its simplicity, and the 
greater chance of the animal surviving the operation. The dis¬ 
advantage is the difficulty of making the injection in exactly the 
desired place. A. Ninian Bruce. 

PARAFFIN - WEIGERT METHODS FOR THE STAINING OF 
(533) NERVOUS TISSUE, WITH SOME NEW MODIFICATIONS. 

Ralph Edward Sheldon, Folia neuro-biologica, 1914, viil, Jan., 
p. l. 

A long and very full account of the Weigert method for the staining 
of nervous tissue, with a large bibliography. The paper is not 
suitable to abstract. A. Ninian Bruce. 



ABSTRACTS 


451 


CLINICAL NEUROLOGY. 

THE FOREARM SION. (Le phenomena de l'avant-bras (de L4ri).) 

(534) Teixeira-Mendks, Rev. Neurol , 1914, xxii., Mars 15, p. 348. 

This phenomenon was first described by Ldri (v. Review, 1913, 
xl, p. 432), and consists in flexing the patient’s fingers into the 
palm, and the palm on the forearm, using a little force when the 
patient’s forearm is observed to flex gradually on the arm. 

The author found this sign positive in all normal cases, and 
negative ( i.e ., absent or greatly diminished) in organic hemiplegia, 
in tabes with cervical cord lesion, and in Huntington’s chorea. It 
is thus useful in the diagnosis of organic hemiplegia, and in certain 
other cerebral lesions. The results were based on the examination 
of sixty-five cases of nervous disease. A. Ninlan Bruce. 

ABSENCE OF THE RADIAL REFLEX AND OF THE REFLEX 

(535) OF PRONATION OF THE FOREARM, AND CONSERVATION 
OF THE REFLEX OF THE BICEPS TENDON FROM LESION 
OF THE 6TH CERVICAL ROOT. (Assenza del riflesso radiale 
e del riflesso di pronazione dell avambraccio, conservazione del 
riflesso del tendine bicipiteo per lesione della 6a radici cervicale.) 
Q. Campoba, Riv. ital. di Neurop., Psichiatr. ed Elettroter., 1914, 
viL, p. 241. 

The above phenomena were observed in a man, aged 39, who 
had fallen from a height of about 8 metres. The lower limbs 
and left upper limb were not affected, but there were slight 
paresis of the right upper limb and severe pain in the right 
shoulder, upper arm, and forearm. The X-rays showed a probable 
fracture of the body of the 3rd cervical vertebra and a forward 
dislocation of the 5th cervical vertebra. Under treatment with 
an extension apparatus the pain disappeared in a few days, and 
in about three weeks the radial reflex returned. 

J. D. Rolleston. 

TALALGIA IN DIABETES. (La talalgie au corns de la diab&te.) 

(536) M. Blumzweio, Theses de Paris , 1913-14, No. 440. 

A record of a case in a man, aged 46, who developed talalgia of 
the right foot a year after the first symptoms of diabetes. Both 
ankle jerks and the left knee jerk were lost, the right was barely 
perceptible. There was a patch of complete anaesthesia corre¬ 
sponding to and extending beyond the site of talalgia. The skin 
of the anaesthetic area presented exaggerated sweating. The 
X-rays showed no exostosis or other bony abnormality. No 
other cases of talalgia in diabetes haw been recorded. 

J. D. Rolleston. 



452 


ABSTRACTS 


GRUBAL PARAPLEGIA FROM EXTRA DURAL SPINAL TUMOUR. 
(537) OPERATION. RECOVERY. (Parapllgie crurale par neoplasme 

extra-dure-mlrien. Operation. Gu&ison.) J. Babinski, P. 

Lec&ne, and J. Jarkowski, Rev. Neurol., 1914, zzii., Juni 30, 

p. 801. 

A woman, aged 53, midwife, began to notice that she became easily 
tired, and experienced abnormal sensations in both legs. This 
slowly progressed until both legs became paralysed. Sensation 
diminished gradually in both lower limbs, and bladder symptoms 
developed. Pain, principally at night and never very violent, was 
also present, radiating towards the upper part of the vertebral 
column and towards the inferior angle of the right scapula. Later, 
sensation liecame altogether abolished from below the line of the 
nipples, while the paralysis became complete. The patient was 
also much annoyed by involuntary movements of the lower limbs. 
The condition was considered to be due to a tumour which 
appeared to extend as far up the cord as the level of the fifth or 
sixth dorsal segment, and as far down as the ninth dorsal segment. 
A laminectomy was performed, and an angiolipoma 11 cm. long 
was found in the extradural vascular adipose tissue. The result 
was good, sensation returning, and the patient became able to 
walk about again. A. Ninian Bruce. 


CLINICAL OBSERVATIONS ON NINETY CASES OF ACUTE 
(538) EPIDEMIC POLIOMYELITIS. Francis R. Fraser, Amer . 

Journ. of Med. Set., 1914, cxlviii., No. 1, July. 

In this paper the clinical observations are reported on 90 cases 
admitted into the hospital of the Rockefeller Institute, New York. 
These cases were admitted during the acute stage only. The ages 
of the patients varied from nine months to fourteen years. In 
three instances two members of a family were admitted, and in 
a fourth instance two cousins living in the same house. In no 
case could a predisposing cause be ascertained, but the majority 
of the patients came from the same general locality in New York. 

No cases were admitted in the pre-paralytic stage, but 5 
abortive cases were admitted, and in 22 cases the paralysis increased 
after admission to the hospital. 

The most common general symptoms were feverishness, drowsi¬ 
ness or heaviness, irritability or restlessness, and involuntary 
twitchings or jerkings during sleep. A temperature that varied 
from 101° to 103°, and gradually settled in the course of a few 
days, was seen in the majority of cases. A history of localised, 
profuse sweating was occasionally obtained, involving the part 



ABSTRACTS 


453 


that subsequently became paralysed, but more common was 
profuse general perspiration in the very severe cases. Gastro¬ 
intestinal symptoms were rarely absent, and vomiting was reported 
in 41 cases, and loss of appetite in 22 others. Stiffness in the 
neck and back, and pain and tenderness on handling the patient, 
were also important symptoms. This tenderness during the acute 
stages seemed to be of three degrees, e.g .: (1) hyperesthesia, 
(2) pain on mild pressure of the muscles, and (3) such severe pain 
that, on passive movements of the limbs, the child would cry out. 

This tenderness, as a rule, passed off in a day or two, but 
might persist for three or four weeks. 

Pain also may be present in the muscles, and a spastic condi¬ 
tion may be caused due to irritation of the pyramidal tracts 
during the healing process of the lesion in the upper part of 
the cord. 

In regard to paralysis, 31 cases showed involvement of the 
muscles of respiration; of these there was paralysis or weakness 
of both diaphragm and intercostal muscles in 9, and of these 6 
ended fatally. In 3 cases the diaphragm alone was involved 
without complete paralysis, and in each instance there lias been 
complete recovery in the action of the diaphragm; 19 cases 
showed paralysis, complete or partial, of the intercostal muscles, 
and of these 3 ended fatally, and 7 recovered entirely. 

A very large number of the cases showed involvement of the 
facial muscles. 

Difficulty with micturition and defsecation occasionally occurs. 
Treatment may be divided into three stages: (a) the acute stage 
of fever and general symptoms, including the period of onset and 
spread of paralysis; (6) the stage of recovery of muscle power; 
(c) the stage where recovery in muscle power is as complete as 
it is going to be, and the treatment is applied to the residual 
conditions of deformities, flail-joints, &c. 

The essential thing in treatment, at the present time, is to 
prevent crippling and deformities. 

Several of the author’s more interesting cases are reported. 

D. K. Henderson. 

THE USE OF CELLULOID SPLINTS IN THE TREATMENT OF 
(539) DISEASES OF THE NERVOUS SYSTEM. G. Wilse Robinson, 
Joum . Amer. Med. Assoc , 1914, lxiii., Aug. 29, p. 773. 

The author emphasises the advantage of using celluloid splints in 
poliomyelitis ( cf.\ Review, 1914, xii., p. 415), describes the process 
involved in making them, and points out that they render the 
same support and comfort in patients with Charcot’s joints and 
in extreme cases of hypotonia in tabes. A. Ninian Bruce. 



454 


ABSTRACTS 


THE GLYCYLTRYPTOPHAN REACTION IN MENINGITIS. 

(5-IO) Ralph H. Major and Edmond Nobel, Archives Intern. Med., 
1914, xiv., Sept, p. 383. 

The reaction is carried out as follows:—One c.c. of the suspected 
cerebro-spinal fluid is placed in a test-tube with an equal quantity 
of glycyl-tryptophan, and then 1 c.c. of toluol is added as a pre¬ 
servative. The mixture is placed in an incubator for three hours. 
It is then withdrawn and a few drops of dilute acetic acid added, 
and then oversaturated calcium chloride drop by drop. A red 
colour is produced if free tryptophan is present. The calcium 
chloride solution used should be briskly shaken just before using 
to give off free chlorine, and must be added cautiously, as an excess 
masks the reaction. The test should be made with various 
dilutions with sterile normal salt solution up to 1 to 200. 

The reaction depends upon the presence of a proteolytic or 
peptid-splitting ferment in the cerebro-spinal fluid in meningitis 
which is not usually present in normal cerebro-spinal fluid. 

In 12 cases of suspected meningitis, later found not to be 
meningeal, the reaction was negative. In 17 cases of true 
meningitis, all tubercular except one, a positive reaction was 
present, although not always in high dilutions. 

The authors think that in this reaction we have another 
valuable addition to our diagnostic measures in meningitis. 

A Ninian Bruce. 


MENINGEAL SYNDROME IN THE COURSE OF CEREBRAL 
(041) H&SMORRHAGE. (Syndrome m£ning6 au cours d’une h^morragie 
c6r6brale.) L. Levy and Gonnet, Rev. Neurol ., 1914, xxii., Avril 
15, p. 505. 

In most cases cerebral hemorrhage is not difficult to diagnose. If 
the hemorrhage should, however, happen to involve a silent area 
of the brain, the diagnosis may become one of great difficulty. 

A man, aged 56, did not feel very well on rising one morning. 
There was marked occipital headache followed by vomiting, 
delirium, and, in the evening, coma. There was no evidence of 
hemiplegia, and both plantar reflexes were flexor. The pupils 
were contracted, but there was no conjugate deviation of the eyes, 
nor paralysis of any of the ocular muscles. Uraemic coma was 
suspected, and 500 c.c. of blood were removed. This caused 
slight improvement, but the coma soon reappeared, followed by 
twitellings of the face and right arm resembling Jacksonian 
epilepsy. Later the movements became general, and a right 
hemiparesis was found, Babinski’s sign became positive, and the 
reflexes on this side were exaggerated. Lumbar puncture gave 



ABSTRACTS 


455 


issue to a slightly yellowish fluid under great tension, and sterile. 
The convulsive attacks became more and more frequent, and the 
patient finally died in a status epilepticus. 

At the autopsy a haemorrhagic focus about the size of an 
orange was discovered behind the left interparietal fissure, in¬ 
volving the second and inferior parietal, and first and second 
temporal convolutions, and spreading inwards as far as the 
occipital horn of the lateral ventricle. The right hemisphere was 
normal. A Ninian Bruce. 

UNUSUAL TYPE OF HEREDITARY DISEASE OF THE NERVOUS 

(542) SYSTEM. Pelizaeus-Merzbacher, aplasia azialis extra-corticalis 
congenita. Frederick E. Batten and Douglas Wilkinson, 
Brainy 1914, xxxvi., p. 341. 

A familial and hereditary disease of the nervous system is here 
described, the symptoms of which resemble disseminated sclerosis, 
and in its later stages Friedreich’s disease. It affects chiefly 
males, and is transmitted by healthy females. Those affected are 
either congenitally diseased or exhibit symptoms in the first 
months of life, the progress of the disease being very slow. They 
are mentally defective and ataxic, show nystagmus, speech defect, 
and defective development, with weakness and spasticity of the 
lower limbs. Four cases are described at length. 

A. Ninian Bruce. 

DISSEMINATED SCLEROSIS WITH CROSSED HEMIPLEGIA. 

(543) (Scldrose en plaques (?) avec hlmipldgie alteme.) B. Conos, 
Rev. Neurol., 1914, xxii, Feb. 28, p. 226. 

A man, aged 39, doctor, in good health, developed suddenly a 
partial paralysis of his right third nerve, with left hemiplegia, 
together with hemiansesthesia of the left side of his face and 
right half of his body. The cerebro-spinal fluid was normal. 
There was no history of syphilis, the Wassermann reaction in the 
blood was negative, and anti-syphilitic treatment proved of no 
avail. Alcoholism and botulismus could also both be excluded. 
Nystagmus was present. The condition was considered to be most 
likely due to an unusual manifestation of disseminated sclerosis. 
The symptoms improved rapidly. A. Ninian Bruce. 

ELECTROLYTIC TREATMENT OF LEAD POISONING. W. H. F. 

(544) Oxlet, Lancet, 1914, clxxxvii., Oct. 3, p. 848. 

The author throws doubt upon the possibility of the removal of 
lead from the body in lead workers by means of electrolysis, as 
described by Sir Thomas Oliver. He points out that the large 



45G 


ABSTRACTS 


proportion of total current used up by the tissue ions, and the 
slow rate of penetration of the ions through the skin, would only 
allow of the removal from the superficial layers of the skin of an 
amount of lead not exceeding TxWth part of a grain. 

Experiments upon rabbits under conditions even more 
favourable than in man showed also a consistently negative result. 

A. Nlnian Bruce. 

MENTAL MANIFESTATIONS IN TUMOURS OF THE BRAIN. 

(545) Alford Gordon, Amur. Jour. Med. Set., 1914, cxlviii, No. 2, August 

One of the cases here reported presented a most striking 
resemblance with paretic dementia, both from the standpoint 
of physical and mental manifestations; yet no meningo¬ 
encephalitis was found, and a tumour was seen in an area not 
at all suspected during life. 

The second case reported is one of a tumour of the pituitary 
body. In this case the diagnosis of paresis was repeatedly 
made by competent men. 

The third case is one of a tumour situated between the frontal 
lobe and insula in the left hemisphere. During life the patient 
presented a very marked dullness, apathy, indolence, and extreme 
somnolence. 

The author feels that mental symptoms are not of any 
special assistance in the localisation of tumour growths. 

D. K. Henderson. 

A PATHOLOGICAL INVESTIGATION OF FOUR CASES OF 

(546) PITUITARY TUMOUR. W. Johnson, Lancet , 1914, clxxxvii., 
July 4, p. 24. 

The first two cases came to necropsy, the remaining two were 
from specimens dated 1883 and 1877 respectively. Three of the 
tumours were classified as malignant epithelial tumours without 
secondary deposits, the fourth was a malignant columnar-celled 
growth with secondary deposits in the lung. 

Eye symptoms had been present in the first two cases for 
over two years, and pathologically a degeneration was found in 
the optic tracts, extending as far back as the primary optic ganglia, 
but not into the optic radiations or calcarine cortex. Both cases 
also showed that the uncrossed visual fibres tend to occupy the 
outer and lower portion of the optic tracts. A. Ninian Bruce. 

INFANTILISM. August Strauch, Amer. Jour. Med. Sci. t 1914, cxlvii., 

(547) No. 2, August. 

An interesting paper, which cannot be adequately abstracted, 
describing various forms of infantilism. D. K. Henderson. 



ABSTRACTS 


457 


METABOLISM STUDIES IN A CASE OF MYASTHENIA GRAVIS. 

(548) Theodore Diller and Jacob Rosenbloom, Amer. Joum. of Med. 
Set. , 1914, cxlviii., No. 1, July. 

It was found that the true cellular or “ endogenous " metabolism 
was not normal, as both the uric acid and creatinin excretion were 
much lower than normal. Such a finding makes one consider 
myasthenia gravis as a disease of deranged muscular metabolism. 

In addition, the amount of neutral sulphur excreted in 
relation to the total sulphur was below normal. 

Finally, 6 3 grams calcium oxide was lost by the tissues in 
eight days. 

On account of the great importance that the calcium ion plays 
in normal muscular action, it is possibly owing to lack of its 
utilisation that myasthenia gravis owes its origin, and the changes 
observed in the “endogenous” or cellular metabolism may be 
secondary to this fact; and as the inorganic ions are necessary for 
normal muscular action, it may be that some disturbance in 
metabolism in these substances, especially calcium, is responsible 
for the muscular symptoms of myasthenia gravis. During muscle 
work lactic acid is produced, and it is one of the factors in the 
production of fatigue of muscle. “ May it not be that owing to 
the fact that the calcium not being utilised normally, the lactic 
acid is not neutralised by the calcium, and fatigue, one of the 
characteristic features of myasthenia gravis, comes on readily ? ” 

D. K. Henderson. 

ENGLISH PELLAGRA IN EARLY CHILDHOOD. Charles R. Box, 

(549) Brit. Med. Joum., 1914, Aug. 29, p. 397. 

The patient was a little girl, aged 1 year and 8 months when a 
butterfly rash appeared on her face and lasted from March to 
September. It reappeared next spring. She had never suffered 
from digestive disturbance, and had never eaten maize. When 
seen at 4£ years of age the rash was found on her face, hands, and 
knees. Pronounced tremor, with occasional small jerky movements 
of the limbs, was present. A. Ninian Bruce. 


ATTEMPTS TO TRANSMIT PELLAGRA TO MONKEYS. C. H. 

(550) Lavindkr, E. Francis, R. M. Grimm and W. F. Lorenz, Joum. 
Amer. Med. Asaoc., 1914, lxiii., Sept. 26, p. 1093. 

The authors used 77 rhesus monkeys, 2 Java monkeys, and 3 
female baboons. The methods employed were: (1) inoculation of 
pellagrous tissues; (2) inoculation of pellagrous fluids and excreta; 
and (3) feeding with pellagrous material and spoiled corn meal. 
The pellagrous tissues used consisted of filtered extracts of 



458 


ABSTRACTS 


(a) the brain, spinal cord, and membranes from 6 necropsies; 

(b) the buccal, thoracic, and abdominal contents, except intestines, 
from 1 necropsy; (c) the intestines and faecal contents of 7 
necropsies; and (d) the skin from 5 necropsies. Extracts of 
these were made with normal saline, and injected intracerebrally, 
intraspinally, intraperitoneally, intravenously, or subcutaneously. 
The pellagrous fluids used were: (a) blood from 7 pellagrins; 
(b) pericardial fluid from 1 necropsy; (c) urine from 4 cases; 
(d) faeces from 1 case; and (e) cerebro-spinal fluid from 3 
necropsies. The feeding material consisted of (a) sputum from 
4 cases: (b) faeces from 2 cases; (c) thoracic and abdominal 
organs and contents from 5 cases; and (d) brain, cord, membranes, 
buccal, thoracic, and abdominal organs, with contents complete, 
from 1 necropsy. The monkeys were exposed daily to the direct 
rays of the sun. One hundred and three experiments were 
made. 

The result was 8 monkeys died, 4 clearly from some other 
cause than pellagra; the cause of death in the remaining 4 was 
undetermined. With one exception all the remaining monkeys 
showed no symptoms of pellagra. A. Ninian Bruce. 


SYPHILIS OF THE VERTEBRAL COLUMN: ITS SYMPTOM- 
(551) ATOLOOY AND NEURAL COMPLICATIONS. J. Ramsey 

Hunt, Amer. Journ. of Med. Set., 1814, cxlviii., No. 2, August 


At the present time there are about one hundred well- 
authenticated cases recorded in the literature, and the pre¬ 
ponderance of the cervical localisation has been quite striking. 

The pathological lesions consist of exostoses, gummatous 
periostitis, and osteomyelitis, with occasional necrosis and 
sequestration of bone. The tendency to pus formation is 
slight, and “ cold abscesses,” as found in tubercular caries, 
apparently do not occur. The greater number of the cases originate 
in the tertiary period of syphilis. 

Of the 100 cases which the author has analysed neural 
symptoms were present in 26, distributed as follows:— 


Cervical region - 
Dorsal region 
Lumbar region - 
Sacral region 


15 cases. 
5 
4 
2 


99 

99 


Of the 26 cases with neural complications, 14 were associated 
with symptoms that would indicate a lesion of the spinal cord 
corresponding to the level of the bone disease. 

In 9 cases the limitation of symptoms to paralysis and 



ABSTRACTS 


459 


paresthesia of one upper or lower extremity indicated a radicular 
origin. 

In 2 cases of sacral origin the symptoms indicated an 
involvement of the strands of the cauda equina. 

Four interesting personal cases are reported. 

I). K. Henderson. 

A CRITICAL STUDY OF LANCE'S COLLOIDAL COLD REACTION 
(552) IN CEREBRO SPINAL FLUID. Rogbr I. Lee and W. A. 
Hinton, Amer. Joum. of Med. Sci., 1914, cxlviiL, No. 1 , July. 

The technique employed is described, and the following conclusions 
are come to. 

A gold reaction typical for syphilis is nearly constant in cases 
of syphilis of the central nervous system. 

This test is more delicate than the blood Wassermann reaction, 
spinal fluid Wassermann reaction, cell count, and globulin content. 

The test has the advantage that it gives a reaction with 
pathological spinal fluids due to other causes than syphilis that 
is characteristic and easily differentiated from the reaction typical 
for syphilis. D. K. Henderson. 


OBSERVATIONS ON THE WASSERMANN REACTION. B. A. 

(553) Thomas and Robert H. Ivv, Amer. Joum. of Med. Set., 1914, 
cxlviii., No. 1, July. 

The authors call attention to several factors in technique which 
they believe are of importance in securing accurate results. They 
plead for the standardisation and uniformity of methods. 

D. K. Henderson. 

ATROPHY OF THE PELVIS IN INFANTILE PARALYSIS AND 

(554) ITS OBSTETRICAL CONSEQUENCES. (Atrophie du bassin 
dans la p&ralysie infantile et ses consequences obstdtricales.) 
Mllb. G. Schmouchbb, Threes de Paris, 1913-14, No. 411. 

Atrophy of the pelvis in infantile paralysis is rare. It is caused 
by the same spinal lesions as those which give rise to the motor 
and trophic disturbances in the lower limbs. The pelvic deformity 
resulting may be bilateral or affect one side only. Dystocia 
caused by atrophy of the pelvis is often slight and easily remedied 
by application of the forceps; sometimes it is more serious and 
necessitates premature delivery; in the severest cases Caesarean 
operation is required. The thesis contains the histories of 15 
cases, 3 of which are original. J. D. Rolleston. 



460 


ABSTRACTS 


THE RELATION BETWEEN EPILEPSY AND TUBERCULOSIS. 

(556) B. Hknry Shaw, Jottm. of Merit. Set., 1914, July, p. 477. 

The percentage of epileptics in the Staffordshire asylums is very 
high, being 20 8 per cent., as compared with an average for 
England and Wales of 12 8 per cent. The tuberculosis death-rate 
is also high, being 25*2 per cent., the rate for England and Wales 
being 16*6 per cent. The author gives tables to prove that the 
connection between a high epileptic ratio and a high tubercle 
ratio is very general throughout the country, and he believes this 
to be due to an association of the two diseases. He has found 
that 83*3 per cent, of his epileptics reacted to tuberculin, whereas 
only 33*3 per cent, of non-epileptics did so. His view is that 
the great majority of cases of idiopathic epilepsy are due to the 
toxaemia of tuberculosis at an early age, kept in check, however, 
by the curative effects of the auto-inoculation with tuberculin 
occurring during the fits. W. D. Wilkins. 


EPILEPSY: A THEORY OF CAUSATION FOUNDED UPON THE 
(556) CLINICAL MANIFESTATIONS AND THE THERAPEUTIC 

AND PATHOLOGICAL DATA. J. J. M. Shaw, Journ. of Merit. 

Sei., 1914, July, p. 398. 

This paper is a careful study of the etiology of epilepsy, embodying 
much original work, and giving also a full account of other data 
bearing upon the theory advanced. The theory is that the 
inherent defect in epilepsy is an instability, which may be 
hereditary, of the nucleo-proteid elements of the brain and blood. 
These nucleo-proteins break down and produce uric acid and other 
acid products, and there is a consequent diminution in the 
alkalinity of the blood. If this falls below a certain point, 
agglutination of the coagulative elements of the blood will occur, 
with consequent stasis in the cortical capillaries, cerebral anaemia, 
and the production of convulsive seizures and other cerebral 
symptoms. Among exciting causes of the seizures are the ingestion 
of nucleo-proteins and purins, and the relative sluggishness of the 
circulation occurring in early sleep. 

The author has demonstrated a greatly increased rate of 
agglutination in epileptic as compared with non-epileptic blood. 
The action of the bromides is to combine with the nucleo-proteins 
and prevent their disintegration. Alkalies naturally increase the 
alkalinity of the blood and diminish its coagulability, and have 
therefore a beneficial effect. Oxalic acid and ammonium oxalate 
have been found by the author to have a marked effect, not only 
in diminishing the number of fits, especially the attacks of petit 
mal, but still more in curtailing the post-paroxysmal states, and 



ABSTRACTS 


461 


improving the mental condition. Glycerophosphates, including 
sanatogen, were found to increase the severity and frequency of 
the fits. W. D. Wilkins. 

TWO NEUROLOGICAL CASES IN PjEDIATRIO PRACTICE. 

(557) M. A. Rabinowitz, Med. Record, 1914, lxxxv., p. 1031. 

Case 1.—Syphilitic pseudo-paralysis of the new born. The 
right hand became affected at the age of 4 weeks, and a few 
weeks later the child did not move any of its limbs. Rapid 
recovery ensued under mercurial inunction. 

Case 2.—Recurrent multiple neuritis. A girl, aged 9 years, 
developed symmetrical paralysis of all four limbs without fever 
or much constitutional disturbance. Recovery took place within 
a year. A similar attack occurred at the age of 12 years, and 
within a year of its onset recovery was almost complete. There 
was no history of alcohol, arsenic, or diphtheria. 

J. D. Rolleston. 

A CASE OF IMPLANTATION OF SUPRARENALS IN ADDISON’S 

(558) DISEASE, WITH FATAL RESULT. W. H. Beown, Med. Joum. 
Australia, 1914, i., August 8, p. 129. 

A man, aged 21, presented the typical symptoms of Addison’s 
disease—great weakness, low blood pressure, and pigmentation of 
the skin. Very slight improvement followed complete rest and 
tuberculin treatment for five months, but such improvement proved 
only temporary. It was decided to try the effect of implanting 
the suprarenal glands, and this was done into the rectus sheath 
two hours after their removal from a girl of 6 years dying from 
heart disease following rheumatism. During the first thirty-eight 
hours his condition gave no cause for anxiety, but four hours 
later his pulse became weak, his pupils dilated, and he became 
semi-conscious, dying shortly after. The wound was healthy, but 
“it seems clearly the case that the man was poisoned by the 
contents of the two suprarenal glands implanted.” 

A. Ninian Bruce. 

A CASE OF SCIATICA ENTIRELY CURED IN THREE WEEKS’ 

(559) TREATMENT. Harry Marcus, N.Y. Med. Joum., 1914, c.,Sept 
12, p. 520. 

The sciatica followed rapid delivery by forceps during eclampsia. 
The pain was uninfluenced by iodides, salicylates, massage, and 
electricity, and was so severe that the patient would not even 
allow her bed to be touched. The treatment consisted in the 
injection of a solution of 2£ drams of antipyrine and grs. of 
cocaine hydrochloride in 1£ drams of water, first over the 



462 


ABSTRACTS 


external popliteal nerve, and second, into the dorsum of the foot, 
sixteen minims were injected each time, and the pain gradually 
disappeared. A. Ninian Bruce. 


PSYCHIATRY. 

THE BIOLOGICAL CONCEPTION OF INSANITY. John Turner, 
(660) Joum. of Mmt. Scu, 1914, July, p. 352. 

Though many cases of insanity present no obvious pathological 
lesions, yet careful examination of such cases will usually show 
slight deviations from the normal. The author has found that 
the kidneys, liver, heart, and especially the blood-vessels, are all 
very commonly affected to a slight degree, the changes being 
principally degenerative. It is interesting to note that, in a series 
of 235 cases, a patent foramen ovale was found in 16 per cent. 

Systematic observation was made of the Betz cells in a large 
number of cases, and it was found that in every type of insanity 
a varying percentage of the cells presented the features of the 
axonal type of degeneration, usually in an early stage. The 
percentage was lowest in the general paralytics, viz., 20 per cent., 
and highest in epileptic imbeciles, viz., 60 per cent. The average 
for the whole series was 35-40 per cent. The author considers 
that the presence of these cells is an index of the inherent 
instability of the brain and its consequent liability to insanity. 
A series of 50 brains from hospital cases, all presumably sane, 
showed 20 per cent, in which there were Betz cells of this type, 
but generally to a more limited extent. Gliosis in the subcortical 
white matter and subcortical nerve cells were also more frequent 
in the asylum series. The author believes that insanity has 
always a biological basis, and that if the disordered bodily 
functions could be corrected, the mental would also be adjusted. 

W. D. Wilkins. 

THE REACTION OF MORIZ WEISZ IN MENTAL DISEASES. 
(561) (La reaction de Moriz Weisz dans les maladies mentales.) V. 

Demole, Rev. Neurol., 1914, xxii., Jan. 30, p, 85. 

The technique of this reaction is very simple, and consists in 
placing a small quantity of urine in a test-tube and diluting 
it with twice its volume of water. Half of this is used as a 
control, while to the other half three drops of a one per cent, 
solution of potassium permanganate are added. A yellow 
coloration denotes a positive reaction, the colour depending upon 
the oxidation of urochromogen into urochrome, the normal 
urinary pigment. The reaction is, like the diazo-reaction of 



ABSTRACTS 


463 


Ehrlich, found in wasting diseases, in fevers, and in tuberculosis, 
and has also been recorded in cases of meningitis, leukaemia, 
cancer, and in cardiac and renal disease. 

The author examined it in 139 cases of different mental 
diseases, and found it transitory in 11, and constant in 10. Two 
and a half months later 3 (i.e., 27 per cent.) of the transitory 
cases had died, and 6 {i.e., 60 per cent.) of the cases in which the 
reaction was constant had died. The reaction bears no special 
relation to any particular mental disease, and is to be regarded 
as a disturbance of metabolism resulting from the disease. The 
appearance of this reaction iu the course of a psychosis is there¬ 
fore to be regarded as an alarming sign, and its persistence as 
grave. A. Ninian Bruce. 

SOME OBSERVATIONS ON EARLY NERVOUS AND MENTAL 
(562) OASES, WITH SUGGESTIONS AS TO POSSIBLE IMPROVE¬ 
MENTS IN OUR METHODS OF DEALING WITH THEM. 

A Helen Boyle, Joum. of Meat. Set., 1914, July, p. 381. 

At present the last person asked to treat an early case of mental 
disease is the alienist, and it is not uncommon for the case to have 
reached an advanced stage before he is appealed to. Moreover, 
there is a large group of cases in which both nervous and mental 
symptoms are present, the consequence being that the patient 
gets inefficient treatment in one direction or the other according 
as he consults an alienist or a neurologist. The authoress urges 
that the two specialities should be welded together, and that 
physicians should be competent to deal with cases in either group. 
Further, that institutions should be established which would treat 
both nervous and early mental cases that have not yet reached a 
certifiable stage. W. D. Wilkins. 


TREATMENT. 

THE ROLE OF HYPNOTICS IN MENTAL DISEASES, WITH 
(663) INDICATIONS FOR THEIR SELECTION AND EMPLOY¬ 
MENT. Richard Eager, Joum. of Merit. Sci., 1914, July, 
p. 461. 

A systematic account of the chief hypnotics used in asylum work, 
with their indications and contra-indications. The author lays 
stress on the fact that paraldehyde should be avoided in cases 
with a tendency to respiratory trouble, on account of its irritant 
action, and he recommends sulphonal for use in senile dementia, 
accompanied by intractable insomnia. He incidentally compares 
the price of the various drugs he mentions. W. D. Wilkins. 



464 


REVIEWS 


■Reviews. 

THE MYTH OF THE BIRTH OF THE HERO. A Psychological 

(564) Interpretation of Mythology. By Dr Otto Rank (Vienna). 
Translated by Robbins and Jelliffe. Pp. 100. (Nervous and. Mental 
Disease Monograph Series, No. 18. $1.00.) 

Tins book should be read in conjunction with Abraham's “ Dreams 
and Myths ” (reviewed in the Review of Neurology and Psychiati'y, 
May 1913, p. 291), for the two books complement each other. 
Rank makes here an attempt to establish the scaffolding of a 
theory of mythology based on individual psychology. For this 
purpose he selects one type of myth, that concerning the birth of 
heroes, studies in detail a series of well-known ones—from Sargon 
to Jesus and (Edipus to Lohengrin—and abstracts the features 
common to the series. These features he then compares with 
similar traits in the fancies of the individual child on the subject 
of birth, and explains them as a glorified expansion of these. 

The work is avowedly based on investigations by means of the 
psycho-analytic method, and the reader’s judgment is likely to 
depend on his attitude towards this method. In any case, 
however, it cannot be denied that Rank has furnished here a 
number of novel and stimulating hints of considerable value to 
those working in this field. The subject also has its importance 
for the medical psychologist and psychiatrist, for fancies relating 
to childbirth play a part second to none in the pathogenic content 
underlying delusions and other morbid mental manifestations. 

The translation, which could not have been easy, is quite 
adequately done, and we may hope that it will be followed by 
translations of Rank's later and more extensive works. The 
author has added a number of additional footnotes for the transla¬ 
tion, dealing with knowledge that has accumulated since the book 
was first published five years ago. Ernest Jones (London). 

PSYCHOPATHOLOGY OF EVERYDAY LIFE. Prof. Sigmund Freud. 

(565) Authorised English Edition, with an Introduction by A. A Brill. 
Pp. 342. T. Fisher Unwin, London. Price 12s. 6d. net 

This book will be found of interest to all who have studied 
psychoanalysis as expounded by Professor Freud. It is an attempt 
to apply this method of investigation to all the faulty actions of 
everyday life, such as the forgetting of names, mistakes in speech 
and in writing, forgetting of resolutions, erroneous carrying out 
of actions, and all the numerous little errors which are so apt to 
occur in daily life. If a name be forgotten, it is because it is 
connected with some unpleasant association which has been 
repressed; if one accidentally knocks over and breaks some object 



REVIEWS 


465 


on one’s table, it is to be regarded as evidence that one did not 
really care for it, and designed unconsciously this way of removing 
it; if one addresses a friend by the wrong name, it signifies that 
one would rather be speaking to the friend whose name is 
unintentionally used, and so on. In fact, all these actions which 
one regards as “ chance ” actions are really not so; they are rather 
purposive, although the author may happen to be unconscious of 
their true significance. And it is surprising how many little actions 
one can remember which may be explained along these lines. But 
that the reader will be able to follow Professor Freud to the extremes 
to which he carries his argument is quite another question. That 
the explanation of many apparently purposeless actions is to be 
found in the complex analyses here elaborated is very doubtful, 
and although the greatest ingenuity has been used to devise means 
of adequately explaining these, it is obvious that many much 
simpler explanations have been entirely overlooked. This book, 
in fact, accepts no explanation except that based on psychoanalysis. 
If it be regarded, however, merely as representing one of the lines 
of research along which such problems may be approached, it will 
undoubtedly be found of interest. 

THE BRAIN IN HEALTH AND DISEASE. Joseph Shaw Bolton. 
(566) Pp. 479, figs. 99. Edward Arnold, London. 1914. Price 18s. net. 

This volume has been written with the object of elaborating a 
scheme of cerebral function which is based on clinico-histo- 
pathological proof. Coming as it does after a period when so 
many of the attempts to elucidate the function of the brain have 
approached the subject from the point of view of abnormal 
psychology, it is particularly welcome to have our attention again 
directed to the actual structural changes which may be found in 
the brain in disease, and their interpretation by correlation with 
the clinical symptoms observed during life. The author, in his 
preface, points out how “quite recently the psycho-analytical 
method of Freud, which is in reality a ‘catch unawares’ 
application of the ‘ confession and absolution ’ idea to the 
ordinary sympathetic case-taking of the hysterical and the 
psychasthenic, has introduced a still newer psychological 
terminology, but no fundamentally new method. On the other 
hand, this method has the great fault of appealing to those 
unaware of its strictly limited scope, as a new system of universal 
applicability to cases of mental disease, whereas its field of 
utility is for practical purposes outside the walls of asylums.” 

This work is based upon the personal researches of the author 
during the past eighteen years, and he points out that the book is 
to be regarded not as a text-book on mental disease, but as a 

37 



466 


REVIEWS 


treatise on general cerebral physiology and pathology. The book 
is divided into two parts, the first dealing with cerebral function 
in the normal brain, the second with cerebral function in mental 
disease. 

In the first part a very good description is given of the 
geography, histology, and development of the cerebral cortex, 
followed by chapters on the localisation of function and on the 
human cerebral functions of language, thought, feeling, emotion, 
and sentiment. 

In the second part all cases of mental disease are divided into 
two categories— (a) those classed under the term Amentia, the 
subjects of whom “ suffer from a more or less marked grade of 
sub-evolution of the brain,” and includes idiocy and imbecility 
together with cranks, asylum curiosities, true paranoia, &c.; and 
(b) Dementia, the subjects of whom “ suffer from a more or less 
marked grade of involution or dissolution of the cerebrum,” and 
includes senile, presenile, mature and premature types, general 
paralysis, and such kindred conditions, &c. This generalisation 
is based upon the fact that “ cases of mental disease exhibit a lesion 
of the cortex of the prefrontal region of the cerebrum, which lesion, 
in the case of amentia, is of the nature of a true sub-evolution, and 
in the case of dementia, is of the nature of a true involution or 
dissolution.” 

During the last few years we have often felt the want of a 
good English text-book on the pathology of the nervous system. 
This book, which is limited to the pathology of the brain, fulfils 
part of this want. The early chapters on the physiology of the 
normal brain are excellent, while the second part, which presents 
the author’s own views, are written in a clear and concise manner 
which may be easily followed and will well repay perusal. The 
book presents much room for thought, and although no references 
to literature are given, is a good starting-point for fresh work. 
We would recommend it as one of the more recent books which 
all workers in mental disease ought to be acquainted with, as 
we know of no book in English in which the whole question of 
cerebral physiology and pathology is more clearly defined. 


BOOKS AND PAMPHLETS RECEIVED. 

Binet, A., and Simon, Th. “ Mentally Defective Children.” Authorised 
translation by W. B. Drummond. 1914 Edward Arnold, London. Pr. 
2s. 6d. net 

Henderson, D. K. “ Korsakow’s Psychosis occurring during Pregnancy ” 
(Johns Hopkins Hosp. Bull., 1914, xxv., Sept.). 

Mercier. “A Text-book of Insanity ard other Mental Diseases.'’ 
Second edition. Entirely rewritten, 1914. George Allen A Unwin, Ltd. 
1914. Pr. 7s. 6d. net 

“The Training School,” 1914, xi., Sept. 



■Review 

of 

TReurologp anfc IPs^cbtatr^ 


Original Hiticles 


THE PYRIDINE-SILVER METHOD. WITH A NOTE 
ON THE AFFERENT SPINAL NON-MEDUL- 
LATED NERVE FIBRES. 

By S. WALTER RANSON, Ph.D., M.D., 

Professor of Anatomy, North-Western University Medical School. 

The pyridine-silver method is a modification of the Cajal method 
which has recently come into general use in America, and which is 
easy and reliable. It was devised as a differential stain for non- 
medullated fibres, but has been found to be of use in the study of 
a variety of problems. It is being used in a number of laboratories 
in the preparation of sections for class use of the spinal ganglia, 
sympathetic ganglia, and spinal cord. 

An account of the method is given here in the hope that some 
of the clinical neurologists, who have more ready access than the 
anatomist to fresh pathological material, will use the method in 
studying some of the problems for which fresh human material is 
absolutely necessary, and for the solution of which the method 
is especially adapted. A brief account of the method, and an 
enumeration of the purposes for which it has shown itself to be 
adapted, will be followed by a brief statement of some of the 
results which have been obtained by its use, and an indication of 
some of the problems which await solution. 

The method was first used in connection with a study of the 
structure of the peripheral nerves and published in a paper on 
38 



468 


S. WALTER RAN SON 


the “ non-medullated nerve fibres in the spinal nerves ” (Ranson, 
1911). The technique as given on page 69 of that paper is as 
follows:— 

“ The nerve or ganglion is placed in 100 per cent, alcohol, with 
1 per cent, ammonia for forty-eight hours (95 per cent, alcohol 
with 5 per cent, ammonia will give much the same results, but 
seems more likely to bring out the neurilemma nuclei). The 
pieces are then washed for from one-half to three minutes (accord¬ 
ing to their size) in distilled water and transferred to pyridine for 
twenty-four hours, after which they are washed in many changes 
of distilled water for twenty-four hours. They are then placed in 
the dark for three days in a 2 per cent, aqueous solution of silver 
nitrate at 35° C., then rinsed in distilled water and placed for one 
to two days in a 4 per cent, solution of pyrogallic acid in 5 per 
cent, formalin. Sections are made in paraffin, and after mounting 
are ready for examination.” 

The pyridine-silver method is the only one of the silver 
methods which gives a satisfactory stain of the peripheral nerves 
and is more reliable than the other methods in almost all parts of 
the nervous system, except the peripheral nerve endings. It has 
given good results in the study of the cells and fibres of the 
spinal ganglia of adult dogs (Ranson, 1912), and of the spinal 
ganglia of foetal and new-born rabbits (Huber and Guild, 1913). 
It has given “ uniformly satisfactory results" in demonstrating 
the developing neurofibrils in Squalus embryos (Neal, 1914). 
Used on the spinal cord it not only shows the structure of the 
grey substance, including the neurofibrils in the nerve cells, but 
it brings out, as does no other method, differences in the structure 
of the fascicles of the white substance (Ranson, 1913, 1914). The 
method has been successfully used by Black (1914) on the 
medulla of the new-born baby, by Chase (1914) on the vagus 
nerve of several mammals, by Kuntz (1913) on the sympathetic 
plexuses of the intestine, and by Ranson (1912) on regenerating 
nerves. 

Huber and Guild (1913) have found it possible to use the 
method on decalcified material, and thus to stain and cut into 
serial sections the entire head of a small animal or embryo. The 
details of the method as used by them are as follows:— 

“ 1. Adult or young animals and embryos of sufficient size to 
admit of injection are injected with ammoniated alcohol solution, 



THE PYRIDINE-SILVER METHOD 


469 


as above described,” i.e., with a solution of 95 per cent, alcohol 
and 1 per cent, concentrated ammonia through the arteries; and 
the tissues are dissected out, “and placed in the ammoniated 
alcohol for from two to four days, depending on the size of the 
tissue mass to be fixed. 

“ 2. Transfer to distilled water, in which the pieces remain until 
they sink. 

“ 3. The pieces are then transferred to a 7 per cent, solution of 
nitric acid, made with distilled water, in which they remain until 
the decalcification is complete; which varies with the age and size 
of the tissue block. 

“ 4. Wash in distilled water for about one-half hour, the water 
being changed frequently. 

“ 5. The pieces are then transferred to alcohols of 80, 90, and 
95 per cent., to each of which is added 1 per cent, of concentrated 
ammonia. A thorough treatment with ammoniated alcohol at this 
step seems to us essential; three to eight days, depending on the 
size of the pieces. 

“ 6. Rinse in distilled water and place for twenty-four hours in ‘ 
pyridine. 

“ 7. Wash thoroughly in distilled water for twenty-four hours, 
the water being frequently changed. As the immediate transfer¬ 
ence of the tissues from the pyridine to the distilled water is 
liable to result in a swelling of the tissues, which may lead to a 
bursting of the hemispheres, a gradual transference from the 
pyridine to the distilled water is recommended. 

“ 8. Transfer to a 2 per cent, solution of silver nitrate in distilled 
water, in which the tissues remain for from three to five days, in 
the dark and at a temperature of about 35° C. 

“ 9. Rinse in distilled water, and place for from one to two days 
in a 4 per cent, solution of pyrogallic acid in 5 per cent, formalin. 

“ 10. Dehydrate thoroughly, beginning with 80 per cent, alcohol. 
Acetone may be used to hasten the dehydration, but should be 
preceded and followed by alcohol Clear in xylol and embed in 
paraffin. A necessary stay in the warm oven, even to forty-eight 
hours, to ensure thorough paraffin penetration, does not seem to 
affect the stain. 

“ The possibility of decalcification combined with preliminary 
ammoniated alcohol injection greatly extends the applicability of 
the pyridine-silver method. We have found it possible to stain 



470 


S. WALTER RANSON 


half of the head of a six-day rabbit, head and neck of a medium¬ 
sized frog, head of a small turtle, and so forth. After the injection 
with the ammoniated alcohol we have removed the skin and 
exposed the brain. Further cutting of the pieces was delayed until 
after the decalcification and second ammoniated alcohol treatment. 
The paraffin sections may be cut serially, and fixed to the slide by 
the water albumen method in the usual way. 

“We are aide to confirm Ranson’s statement, and find it 
applicable to the method as here modified, namely, ‘ With freeh 
pure chemicals, absolutely clean utensils, and a reasonably constant 
temperature, this method can be relied upon to give uniform 
results.’ ” 

The chief advantages of the pyridine-silver method are: (1) It 
can be used in a study of the peripheral nerves where the other 
silver stains fail to give good results. (2) It is more reliable than 
the other silver methods and gives more uniform results. (3) 
Larger pieces of tissue can be successfully stained, and the im¬ 
pregnation is more uniform throughout the block than when the 
old Cajal method is utilised. (4) It is a differential stain for non- 
medullated fibres having a selective action for these axons, and 
staining them much darker than the other elements in the section. 
(5) It can be applied to decalcified tissue allowing the staining in 
toto, and cutting into serial sections of the entire head of a small 
animal or embryo. 

With this method it has been possible to demonstrate the 
presence of axons devoid of myelin sheaths in many parts of the 
nervous system where it had been supposed only medullated fibres 
were to be found. It has been shown (Ranson, 1911-12) that 
there are even more non-medullated than medullated fibres in the 
spinal nerves, and that they are not sympathetic but afferent 
spinal fibres with their cells of origin in the spinal ganglia (Fig. 1). 
These are the small cells of the spinal ganglia, the single processes 
of which are non-medullated and divide dichotomously into fine 
non-medullated fibres which run into the peripheral nerve, and 
still finer non-medullated fibres which run centralward in the 
dorsal root. The number of small cells in the spinal ganglion is 
greater than that of the large cells, while the number of large 
cells is sufficient to account for all the medullated fibres 
(Hatai, 1902). In pyridine-silver preparations of the spinal ganglia 
it is very easy to demonstrate the origin of the non-medullated 



THE PYRIDINE-SILVER METHOD 


471 
\ 

fibres from the small cells and of the medullated fibres from the 
large cells. 

In addition to the afferent spinal non-medullated fibres there 
are also sympathetic non-medullated fibres which enter the nerve 
by way of the grey ramus communicans. In a series of longitudinal 
sections through a spinal nerve and ganglion in the plane indicated 
in the drawing, stained by the pyridine-silver method, it is easy to 
follow the sympathetic non-medullated fibres into the spinal nerve 
from the grey ramus. At first they run in bundles of considerable 
size, which are readily recognised as sympathetic. Most of these 



Fin. 1 . —Diagram of a spinal nerve and ganglion to show the 
origin of the non-medullated fibres. The small cells of 
the spinal ganglia give rise to non-medullated fibres which 
divide into peripheral branches extending into the nerve 
and central branches running in the dorsal root to the 
spinal cord. Sympathetic non-medullated fibres are also 
indicated entering through the ramus oommunicans. 


bundles turn peripheralward into the ventral or dorsal rami, a few 
turn centrally into the dorsal root and spinal ganglion. 

The central branches of the non-medullated axons of the small 
spinal ganglion cells can be followed through the dorsal root to the 
spinal cord (Fig. 2). Here they are seen to separate out from among 
the medullated fibres just before the root enters the cord. And, 
turning lateralward, they run through the lateral part of the 
entering root into the tract of Lissauer (Ranson, 1913-14). These 
non-medullated fibres from the dorsal root run in the tract of 








472 


S. WALTER RANSON 


Lissauer for a short distance before terminating in the substantia 
gelatinosa Rolandi, which is probably the nucleus of reception of 
these fibres. The tract of Lissauer is composed of closely packed 
non-raedullated and scattered fine medullated fibres. The fibres 
in the tract have for the most part a longitudinal direction, but 



4*4. 


Fro. 2.—Diagram of the posterior root and postero lateral part 
of the spinal cord.—f.c., fasciculus cuneatus; L.t., Lis- 
sauer’s tract. The non-medullated fibres of the root are 
seen separating out from among the medullated fibres and 
running into the tract of Lissauer. 


some are seen running horizontally or obliquely forward into the 
substantia gelatinosa. 

We have in the non-medullated fibres of the spinal nerves, 
dorsal roots, and Lissauer’s tract, a system, the function of which 
is as yet unknown. It is clear from the nature of the cells of 
origin of these fibres in the spinal ganglia that the system is an 




THE PYRIDINE-SILVER METHOD 473 

afferent system, and it seems probable that its nucleus of reception 
is the substantia gelatinosa Rolandi. There is some evidence that 
these fibres carry pain and temperature, since they do not enter 
the posterior funiculus, but separate at their entrance into the cord 
from the fibres that carry the muscle sensations upward in that 
funiculus. The fact that the upward course of these fibres in 
Lissauer’s tract is very short—not more than one or two segments 
at most—is also in favour of their carrying pain and temperature, 
since the impulses corresponding to these impressions are known to 
enter the grey substance near the level of their entrance into 
the cord. 

It is obvious that a study of tabetic material would help in the 
solution of the problems which are here presented. Do the non- 
medullated fibres in the spinal nerves degenerate in tabes, and if 
so, early or late? What effect does tabes have on the non- 
medullated fibres in the spinal ganglia and in the dorsal roots ? Do 
the non-medullated fibres in Lissauer’s tract degenerate in tabes ? 
What relation do the non-medullated fibres seen by Nageotte in tabes 
bear to these normal non-medullated fibres ? What is the relation of 
disturbances of pain and temperature in tabes to the degeneration 
of these fibres ? These are some of the problems which should be 
investigated, and for the solution of which the pyridine-silver 
method is especially adapted. If material from cases of tabes in 
different stages of the disease could be secured fresh, i.e., within an 
hour after death, there should be no difficulty in answering these 
questions. Such an investigation should add something to our 
knowledge of the pathology of tabes, and at the same time clear up 
the physiology of the varieties of cutaneous sensation. 

References. 

Black, D. D., 1914. “On the So-called ‘Bulbar’ Portion of the Accessory 
Nerve.” AnaL Rec., Vol. 8, p. 110. 

Chase, M. R., and Ranson, S. W., 1914. “ The Structure of the Roots, Trunk, 

and Branches of the Vagus Nerve.” Joum. Comp. Neur., Vol. 24, p. 31. 
Hatai, S., 1902. “ Number and Size of the Spinal Ganglion Cells and Dorsal Root 

Fibres in the White Rat at Different Ages.” Joum. Comp. Neur., Vol. 12, 
p. 107. 

Huber, G. C., and Guild, S. R., 1913. “ Observations on the Peripheral Distri¬ 

bution of the Nervus Terminalis in Mammalia.” Anal. Rec., Vol. 7, p. 253. 
Huber, G. 0., and Guild, S. R., 1913. “ Observations on the Histogenesis of 

Protoplasmic Processes and of Collaterals, terminating in End Bulbs, of the 
Neuropes of Peripheral Sensory Ganglia.” Anal. Rec., Vol. 7, p. 331. 



474 


ERNEST JONES 


Ktntz, A., 1913. “ On the Innervation of the Digestive Tube.” Joum. Comp. 

Xeu/\, Vol. 23, p. 173. 

Nkai., H. V., 1914. “The Morphology of the Eye Muscle Nerves.” Joum . 
Morph., Vol. 2.1, p. 1. 

Ranson, S. W,, 1911. “ Noti-Medullated Nerve Fibres in the Spinal Nerves. M 

Amrr. Joum. Anat ., Vol. 12, p. 67. 

Ban-son, S. \\\, 1912. “ The Structure of the Spinal Ganglia and of the Spinal 

Nerves. ” Joum . Comp. X*nr. y Vol. 22, p. 159. 

Ranson, S. W., 1912. “Degeneration and Regeneration of Nerve Fibres.” 
Joum. Comp. Xrur. y Vol. 22, p. 487. 

Ranson, S. \V., 191.*1. “The Course within the Spinal Cord of the Non* 

Medullateil Fibres of the Dorsal Roots.” Joum. Comp. Xettr., Vol. 23, 
p. 259. 

Ranson, S. W., 1914. “Tlie Tract of Lissauer and the Substantia Gelatjposa 
Rolandi.” Am^r. Joum. Aunt., Vol. 16, p. 97- 


THE SIGNIFICANCE OF THE UNCONSCIOUS 
IN PSYCHOPATHOLOGY . 1 

By ERNEST JONES, M.D., M.R.C.P. (Lond.). 

Before discussing the question of the importance of the un¬ 
conscious it is necessary to be clear in what sense one proposes to 
use this term, for it is one to which very different connotations 
have been attached. There are three principal current uses of the 
word “ unconscious,” and mention will be made of each of them in 
order. 

The first of these, and probably the commonest, is where 
“ unconscious ” is regarded as a synonym for “ non-mental.” This 
is the general sense in which it is employed in medicine, for 
instance, in reference to the “ unconsciousness ” following a brain 
injury or the administration of an anaesthetic. Many psychologists 
also, notably Miinsterbcrg and Morton Prince, would adhere to 
this use of the word. It is plain that this attitude begs the whole 
question, by assuming that no mental processes can exist that are 
not accompanied by consciousness or awareness. The view held 
by most psychopathologists, on the contrary, is that processes 
certainly occur, as is shewn by the findings of hypnosis and 
psycho-analysis, which present all the attributes of mental ones 
except that the subject is not aware of them, and they therefore 

1 Read before the Section of Neurology and Psychological Medicine, British 
Medical Association, 26th July 1914. 



THE SIGNIFICANCE OF THE UNCONSCIOUS 475 


call them mental for the simple reason that it is impossible to 
describe them except in mental terms; according to this view, 
which is here adhered to, consciousness becomes merely one 
attribute of mentality, and not an indispensable one. The equating 
of “unconscious" with “non-mental” would remove the whole 
subject from the field of psychopathology, or of any branch of 
psychology, for the other question then involved, that of the 
influencing of the mind by non-mental, physical processes, belongs 
rather to the field of psycho-physics. 

The second conception of the unconscious is difficult to describe 
in positive terms on account of its essential vagueness. It might 
well be called the “ limbo ” conception, for in it the unconscious is 
regarded as an obscure region of the mind, the content of which is 
characterised by neglect and oblivion. It is on the whole a 
philosophical conception, and has been developed chiefly by such 
writers as Hartmann, F. W. H. Meyers, and most recently by 
Jung; with some of these writers a mystical element has been 
decidedly prominent. According to this view the unconscious 
part of the mind is a sort of lumber room to which various mental 
processes get relegated when they are in a state of inactivity. 
These processes are then usually considered to be of only quite 
secondary importance in comparison with conscious ones, and they 
are accorded no initiative of their own, or any primary dynamic 
functions, being purely of a passive nature. 

The third conception of the unconscious is the psycho¬ 
analytical one, developed by Freud. He divides those mental 
processes that are not accompanied by awareness into two groups, 
the preconscious and what he calls the unconscious proper, the 
latter being the sense in which the term is used in this paper. 
Freud’s conception of the unconscious differs sharply from the 
preceding ones in that it is a purely inductive one, being built up 
step by step on the basis of actual experience without the intro¬ 
duction of any a priori speculative hypothesis; it may therefore 
be called the scientific conception, in contradistinction to the 
philosophical one. Instead of starting with any notions, whether 
precise or nebulous, of what the unconscious ought to be, he 
investigated the actual mental processes that were inaccessible to 
his patients’ direct introspection, and which were only to be 
reached by means of some technical procedure such as the psycho¬ 
analytic one. As a result of these investigations, he acquired a 



476 


ERNEST JONES 


gradually increasing knowledge of the nature of unconscious 
processes, of their content, meaning, origin, and significance, and 
was therefore placed in a position of being able to formulate some 
general statements on these matters. 

The statement of most fundamental importance, and the one 
on which I wish to lay the greatest stress here, concerns both the 
origin and the content of the unconscious. It is to the effect that 
the existence of the unconscious is the result of “ repression.” By 
this is meant that unconscious processes are of such a kind as to 
be incompatible with the conscious ones of the given personality, 
and are therefore prevented from entering consciousness by the 
operation of certain actively inhibiting, “ repressing ” forces. The 
incompatibility in question is of a moral order, the word moral 
being taken in its widest possible sense. The processes concerned 
flagrantly conflict with the moral, social, ethical, modest, or aesthetic 
standards that obtain in the person’s consciousness; their very 
existence would be intolerable to him, and he automatically 
refuses to acknowledge to himself their presence in his mind 
In this action of repression only a very small part is played by 
the occurrence that may be described as a deliberate conscious 
pushing of certain thoughts out of the mind, though this is the 
one with which we are most familiar; much more extensive is 
the subconscious and automatic keeping apart of the two Bets of 
incompatible mental processes. 

The unconscious, then, consists of repressed mental material 
A second characteristic of it is its dynamic nature. The unconscious 
is not a depository for passive material, but a region where the 
most active functioning goes on. Unconscious processes are typi¬ 
cally conative in kind, and may thus be conveniently, and not 
inaccurately, described as wishes. These wishes are constantly 
striving for gratification, imaginary or real, and it is to this active 
striving that the external manifestations of the unconscious are to 
be ascribed. 

Closely allied to the preceding features of the unconscious is 
the third one of its relation to primary instincts. The unconscious 
is the part of the mind that stands nearest to the crude instincts 
as they are inborn in us, and before they have been subjected to 
the refining influences of education. It is commonly not realised 
how extensive is the work performed by these influences, nor how 
violent is the internal conflict they provoke before they Anally 



• THE SIGNIFICANCE OF THE UNCONSCIOUS 477 


achieve their aim. Without them the individual would probably 
remain a selfish, impulsive, aggressive, dirty, immodest, cruel, 
egocentric, and conceited animal, inconsiderate of the needs of 
others, and unmindful of the complicated social and ethical 
standards that go to make a civilised society. Yet, according to 
the findings of psycho-analysis, the results of this refining process 
are rarely so perfect as is generally supposed; behind the veneer 
of civilisation there remains throughout life a buried mass of 
crude primitive tendencies, always struggling for expression, and 
towards which the person tends to relapse whenever suitable 
opportunity is offered. 

In accord, again, with the features just described is the 
infantile nature and origin of the unconscious. The splitting of 
the mind into conscious and unconscious regions takes place in 
the earliest part of childhood life, probably in the first year, and, 
as was mentioned above, this splitting is the result of the conflict 
between the uncivilised and non-moral endowments with which 
we are born, and the inhibiting forces that make for adjustment to 
the standards of society. The primordial tendencies are repressed, 
and much of their energy is diverted to other, social aims. The 
fact that they are not allowed to find direct external expression, 
however, does not mean that they are abolished, but that they 
are compelled to lead an underground existence, manifesting 
themselves only by indirect and tortuous courses. The infantile 
character of the unconscious thus persists throughout the whole 
of life, giving an added signification to the old saying that the 
child is father to the man. 

To be correlated with the infantile nature of the unconscious 
is the circumstance that it ignores not only moral standards, but 
also logical ones. It has, it is true, a logic of its own, but this is 
one of the emotions and not of the reason; from the usual point of 
view, therefore, it would be called illogical. Just as the fantasy 
can overstep the bounds of time and space, so does the unconscious 
ignore all reasonable and logical considerations. 

The sixth attribute of the unconscious is its predominantly 
sexual character. This is only what might have been expected 
from the fact that the unconscious is in a state of moral conflict 
with the standards of consciousness, for none of the other primary 
instincts is subjected to anything like the intensity of repression 
that the sexual one invariably is. This attribute stands iq 



478 


ERNEST JONES 


apparent contradiction with the one previously mentioned con¬ 
cerning the infantile nature of the unconscious, but this contradic¬ 
tion is easily resolved when we remember the fallaciousness of 
the popular belief that would date the sexual instinct from the 
time of puberty. Freud and his co-workers have produced 
abundant evidence to shew that this instinct is actively operative 
long before this time, and probably from early childhood, though 
what is called infantile sexuality widely differs from the adult 
form, being, like other childhood manifestations, much more 
diffuse, tentative, and preliminary in nature. Amongst other 
striking differences, two special ones may be briefly mentioned 
here: the close association between infantile sexuality and 
excretory functions, and the sexual colouring in the child's 
relation to its near relatives (the so-called “incest-complex”). 
None of Freud’s conclusions has met with more bitter opposition 
than the last-named, concerning the normal occurrence of incestuous 
fantasies. It was at first met by a blank denial of the facts 
themselves. Of late, however, when the facts could no longer be 
ignored, more ingenious forms of opposition have been devised. 
Jung, for instance, who is familiar with the facts, has formulated 
the view that, though these incestuous fantasies unquestionably 
occur, they do not mean what they purport to, but constitute merely 
a symbol for various ethical ideals, and have no “real,” primary 
existence in themselves; according to him, therefore, these uncon¬ 
scious fantasies possess no dynamic initiative of their own, but are 
to be regarded as purely secondary products. The psycho-analytical 
view, as against this, is that Jung’s different formulation of the facts 
constitutes a distortion and manipulation of them that is dictated 
by moral repugnance to a distasteful conclusion. 

The preceding description may be summarised in a single 
statement: according to psycho-analysis, the unconscious is a 
region of the mind, the content of which is characterised by the 
attributes of being repressed, conative, instinctive, infantile, 
unreasoning, and predominantly sexual. A typical example of 
an unconscious mental process, illustrating all of these, would be 
the wish of a little girl that her mother might die so that she 
could marry her father. The six attributes in question, together 
with others not here mentioned, make up a consistent and clearly- 
defined conception of the unconscious which is formulated on the 
basis of experience that may at any time be tested. 



THE SIGNIFICANCE OF THE UNCONSCIOUS 479 


The significance of the unconscious, as defined above, for the 
science of psychopathology may be discussed under four headings. 
In the first place, a knowledge of the content and mode of operation 
of the unconscious furnishes us with a key for the understanding 
of numerous morbid manifestations that were previously incom¬ 
prehensible ; it has given us a consistent interpretation of them, 
and has revealed the coherent and intelligible structure of them. 
Without this knowledge no solution can be found to such problems 
as why a given patient has developed this or that particular 
delusion, phobia, or other symptom; with this knowledge the 
bizarrery and meaninglessness with which we are so familiar in 
psychopathology disappear or are replaced by quite other problems. 
The reason for this is that all psychopathological symptoms arise 
in the unconscious, which is the true seat of the disorder, so that 
the investigation of it is of cardinal importance for both pathology 
and therapeutics. 

In the second place, a knowledge of the unconscious makes 
clear not only the meaning of these symptoms, but also the 
causation of them. They are, namely, compromise-formations 
produced through the conflict between unconscious and conscious 
tendencies, and are brought about in the following way. It was 
pointed out above that normally a great part of the energy 
pertaining to the repressed trends of the unconscious is diverted 
to permissible, social aims, a process known as “sublimation.” 
This denotes a partial renouncement of the crude pleasures 
obtained by indulging in the primitive tendencies that are kept 
from consciousness, and a replacement of them by other, more or 
less satisfactory, refined ones. Now a great number of people 
find it by no means an easy matter to achieve this renouncement, 
and are in constant danger of relapsing into the old indulgencies 
and gratifications under various circumstances, particularly when 
the attractions of the more refined aims flag, as they must do 
whenever the mental environment becomes more painful, difficult, 
or disagreeable. Then the mental interests and energies are apt 
to “ regress ” towards older and more primitive modes of function¬ 
ing. In this regression, however, they are checked by the 
repressing forces on which the original sublimation depended. 
In the resulting conflict neither set of forces is entirely successful: 
on the one hand the repressing ones manage to prevent a complete 
return to the primitive modes of gratification, while on the other 



480 


ERNEST JONES 


they fail in transforming the energies in question into sublimated 
activities. A compromise is reached whereby both sets of forces 
come to expression, though only in a partial and disguised way; 
these compromise-formations are clinically called symptoms, and 
constitute the various psychopathological maladies. 

As was hinted above, the actual symptoms do not carry their 
meaning on the surface, but have to be interpreted and translated 
into the language of the unconscious before this can be reached. 
To do this a knowledge is necessary of the different mechanisms 
by means of which the distortion is brought about that changes 
the underlying repressed trend into the manifest symptom; it is 
impossible, however, here to discuss the nature of these mechanisms, 
such as displacement of the effect, inversion, projection, intro- 
jection, transposition, and so on. 1 It can only be said that the 
distortion is brought about in perfectly definite ways, and through 
the operation of specific factors, which vary in their exact nature 
according to the past experiences and mental development of the 
individual concerned. 

In the third place, the knowledge gained by investigation of 
the unconscious bridges over the gap between the normal and the 
abnormal by demonstrating that the same processes go on in both, 
though the control of the unconscious ones by consciousness is 
greater in the caso of the former. Roughly speaking, insanity 
presents a picture of the normal unconscious. This matter, 
important as it is for normal psychology, does not, however, 
pertain to the theme of the present symposium. 

Last, but not least, is the remarkable aid that this knowledge 
has yielded for the treatment of psychopathological maladies. 
Up to the present this has, it is true, been far greater in the case 
of the psychoneuroses than in that of the psychoses, such as 
dementia praecox, but there it has already proved so valuable that 
one is justified in entertaining the hope that further researches 
may be profitable from this point of view in the case of the latter 
group also. The mode of action of the treatment, in a word, is 
that the overcoming, by means of psycho-analysis, of the resist¬ 
ances that are interposed against the making conscious of the 
repressed unconscious material, gives the patient a much greater 
control over this pathogenic material by establishing a free flow 

For further information on these and allied topics reference may be made 
to my 4 ‘ Papers on Psycho-Analysis,” 1913. 



ABSTRACTS 


481 


of feeling from the deeper to the more superficial layers of the 
mind, so that the energy investing the repressed tendencies can 
be diverted from the production of symptoms into useful, social 
channels. 

I would conclude these highly incomplete remarks with the 
statement that a knowledge of the unconscious furnishes an 
indispensable key to the understanding and treatment of psycho- 
pathological manifestations. 


Hbstracts 

ANATOMY. 

MAST CELLS IN THE MENINGES OF NEOTUBUS, EASILY 
(567) MISTAKEN FOB NERVE CELLS. Paul S. M'Kibbbn, Anal. 

Record , 1914, viil, Oct. 20, p. 475. 

M'Kibben figures and describes the mast cells which exist in great 
numbers in the dura mater of Nectui'us ; they are elongated, 
irregular cells, with several long cytoplasmic processes. Thoir 
similarity to certain sympathetic nerve cells in shape, size, and 
extent, might lead one into serious error. But they differ from 
nerve cells in several respects. “ In a study in Amphibia of certain 
tissues where sympathetic nerve cells and these mast cells may 
occur simultaneously, when methods are used by which it is 
impossible to differentiate between the two types of cells, the 
value of observations is open to question. In Mammalia a similar 
confusion of nerve cells and certain cells of connective tissue is 
not altogether impossible.” Leonard J. Kidd. 


GANGLION CELLS OF THE NEBVUS TEBMINALI8 IN THE 
(568) DOG-FISH (Maatelus Can Is). Paul S. M'Kibben, Joun. Comp. 

Neurol ., 1914, xxiv., Oct. 15, p. 437 (6 figs.). 

The ganglion of the nervus terminalis of Selachians was found by 
Locy (1905) to contain a preponderance of bipolar nerve cells, 
with sometimes a few cells having angular outlines and throe 
or more processes. M'Kibben, using the intra vitam methylene 
blue method, the technique of which he gives, finds that in adults 
of Mustelus canis the ganglia of the nerve, ten of which were 
once seen, contain multipolar nerve cells: few, if any, bipolar cells 



482 


ABSTRACTS 


were demonstrated. “That the selective action of the methylene 
blue has picked out only the multipolar cells and left unstained 
the bipolar cells is not impossible but not at all probable.” 

Leonard J. Kidd. 

SOME FEATURES IN THE DEVELOPMENT OF THE CENTRAL 
(569) NERVOUS SYSTEM OF DBSMOONA THUS FUSCA. P. K 

Smith, Joum. Morj>hol., 1914, xxv., Sept 20, p. 611 (58 figs.). 

This Eastern American Urodde was chosen for study partly because 
it was easily available, the eggs during earlier stages are not 
pigmented, and the persistence of embryological characters and 
the retention of teUodean characters have been noted. Con¬ 
clusions: “(1) The epiphysis of Desmog-nathus fusca is morpho¬ 
logically double. The posterior outgrowth forms first; it is 
followed by an anterior evagination which forms independently. 
As growth proceeds they come to have a common ostium into 
the third ventricle. The epiphysis is formed on the second 
diencephalic segment. (2) No evidence is found in the cephalic 
portion of the medullary plate of divisions to which a segmental 
value should be assigned. There are irregularities and folds in 
this portion of the medullary plate which are normal but not 
constant. The primary fore-brain vesicle becomes secondarily 
divided into three segments: the cephalic one is included in the 
telencephalon, the other two in the diencephalon. The mid¬ 
brain vesicle is composed of two segments. These appear at the 
same time as the primary vesicle.” Leonard J. Kidd. 


THE DEVELOPMENT OF THE ADRENAL GLANDS OF BIRDS 

(570) Victor J. Hays, Anat. Record , 1914, viii., Oct 20, p. 451 (8 figs.). 

From observations based on embryos and adults of Gallus domcsticus 
Hays concludes: “(1) The Anlagcn which give rise to the cortical 
substance of birds appear as groups of cells which migrate doreally 
from the peritoneal epithelium. (2) The chromaffin substance is 
derived from indifferent cells which wander in from the Anlagen 
of the prevertebral sympathetic plexuses. (3) The chromaffin sub¬ 
stance of the glands lies in contact with the venous blood vessels. 
The vessels of the arterial system are found almost entirely in the 
cortical substance. In general, this is the same condition as Flint 
found in the adrenals of mammals. (4) The entire venous system 
is derived from the subcardinal veins. Within the glands the 
vessels of this system are sinusoidal in character. (5) During the 
period in which there is the greatest influx of cells from the Anlagen 
of the prevertebral sympathetic plexuses there is also the greatest 



ABSTRACTS 


483 


activity in the development of the vascular systems. It is possible 
that the relationship of cause and effect exists between the 
simultaneous activity in the development of these distinct systems 
of the adrenal glands.” Leonard J. Kidd. 


PHYSIOLOGY. 

A NEW THEORY OF HEARING. F. P. Sturm, Joum. of Laryngol ., 

(571) Jthinol., and Otol., 1914, April, p. 193. 

This theory is based on the supposition that the hair-cells of the 
organ of Corti respond to sound in the same manner in which the 
rods and cons of the retina respond to light, that is, by an actual 
process of contraction. 

“(1) The hair-cells of the organ of Corti are the end-organs 
of the auditory nerve. They respond to the stimulus of sonorous 
vibrations in two ways—the body of the cell by contraction, the 
sensory hairs by sympathetic vibration. 

“(2) The contraction of the cell frees the hairs from the 
pressure of the tectorial membrane, which acts as a damper. The 
cells contract until they are beneath the level of the reticulate 
membrane, whose function it is to prevent this heavy damper from 
sinking down upon the contracted cell. 

“ (3) Sound vibrations reach any particular hair-cell or set of 
hair-cells by means of the fibre or fibres of the basilar membrane 
which support them. 

“ (4) The so-called ligamentum spirale is in reality a muscle, 
and acts as the tensor of the basilar membrane. It is thus able 
to not only induce and inhibit paracusis by locking and unlocking 
the rods of Corti, but also to produce any degree of tension in 
every fibre of the basilar membrane, thus providing what is practi¬ 
cally an infinite capacity for sympathetic response to sound-waves.” 

When a stimulus occurs, and a small part of the basilar 
membrane vibrates, the hair-cells at once contract and free the 
hairs from the membrana tectoria. The basilar membrane is thus 
freed, and the hair-cells can now respond freely to the stimulus. 

J. K. Milne Dickie. 

THE STATE OF THE VASOMOTOR APPARATUS IN PNEU- 

(572) MONIA. W. T. Foster and L. H. and I. Newburgh, Amer. 
Joum. Physiol., 1914, xxv., Aug., p. 1. 

The writers deny the old proposition that the toxins of 
pneumonia specifically injure the vasomotor cells. “Earlier 
investigators, using the methods of their day, failed to show in 

39 



484 


ABSTRACTS 


this disease a normal change of blood-pressure upon the stimula¬ 
tion of nerves afferent to the vasomotor centre. The present 
investigation with more perfect methods demonstrates a normal 
vasomotor reflex, with almost wholly consolidated lungs, in animals 
about to die.” The organisms used for infection were the Pneumo¬ 
coccus Frdnkel for rabbits, and the Streptococcus mucosus ( Pseudo- 
pneumococcus, Pneumococcus mucosus) for rabbits, cats, and dogs. 
Conclusion: “Experimental evidence proves that the vasomotor 
centre is not impaired in fatal pneumonia.” 

Leonard J. Kidd. 


OVARIAN EXTIRPATION AND VASOMOTOR IRRITABILITY. 

(573) R. G. Hoskins and Homer Wheelon, Amer. Joum. Physiol., 
1914, xxv., Aug., p. 119. 

Symptoms of vasomotor irritability, e.g., hot flushes, dizziness, 
sweating, and increased pulse rate, which often follow surgical 
ovarian extirpation in women of child-bearing age, appear about 
the fifth week after operation, occur intermittently many times 
a day, and gradually decrease in frequency till they finally cease 
in about eighteen months. The writers find that “ovarian 
extirpation in dogs results within six to eight weeks in a marked 
augmentation in the vasomotor reaction to a standard dose of 
nicotine. The reaction to epinephrin is not similarly increased. 
These results, in conformity with clinical evidence, indicate that 
the operation causes a heightened irritability in the sympathetic 
nervous system.” The writers have not yet determined whether 
the augmented irritability would ultimately disappear in dogs 
as it does in the human species. Leonard J. Kidd. 


EXPERIMENTAL OBSERVATIONS ON THE SUPRARENAL 
(674) GLANDS WITH ESPECIAL REFERENCE TO THEIR 
INTER RENAL PORTIONS. S. J. Crowe and G. B. Wislocki, 
Bull. Johns Hopkins Hosp., 1914, xxv., Oct, p. 287. 

From the authors’ summary of their experiments on twenty-six 
dogs, young and old, the following conclusions are here selected: 
(1) In dogs the adrenals are vital organs: it is probably the cortex 
which is essential to life; (2) after partial adrenal extirpation 
there is cortical hypertrophy, chiefly of the fascicular layer, but 
none of the medulla; (3) acute and chronic infections in an 
animal with an adrenal insufficiency sometimes cause changes in 
the fascicular layer of the cortex, but none in the medulla; (4) 
after an “ almost total ” removal of both adrenals, the animals often 
have general convulsive seizures, a subnormal temperature, and 



ABSTRACTS 


485 


other symptoms of an acute adrenal insufficiency: sometimes 
gradual recovery follows, with subsequent normal growth and 
sexual functioning: there is no change in disposition and no 
polyuria: weight increases, but not to abnormal extent; (5) no 
permanent raising or lowering of carbohydrate tolerance follows 
an adrenal insufficiency; (6) transient glycosuria follows operative 
adrenal manipulation; (7) there seems to be a definite relation¬ 
ship between the adrenals and the lymphatic system: the most 
striking feature at autopsy of dogs with long-standing adrenal 
insufficiency is enlargement of mesenteric and retro-peritoneal 
lymph nodes and of the solitary lymph follicles in the intestinal 
walls: not infrequently there is also hyperplasia of the thymus. 
(There are twelve figures, the coloured ones being specially 
beautiful.) Leonard J. Kidd. 


PSYCHOLOGY. 

MENTAL TENDENCY IN TESTIMONY. Helens Lelesz, Arehiv. 
(576) de Psychol ., 1914, May, p. 1. 

The writer takes up Binet’s work on intellectual types, and 
endeavours by means of a series of experiments devised for this 
purpose to find out the comparative frequency of the different 
types, and whether any constant effect upon evidence can be traced 
to the type. She experimented on 124 persons, of whom 69 were 
children. These subjects were shown a picture for one minute, 
after which they were required to write an account of it, and also 
to answer a series of questions about it. The papers thus obtained 
furnished the evidence studied. It was found possible to arrange 
them in five groups, corresponding very closely to the five groups 
distinguished by Binet. The papers of each group were then 
considered from the point of view of their value as evidence, and 
certain general statements are made with regard to each group. , 
The practical value of the results, if they are confirmed by 
subsequent workers, is that they offer a judge the means of 
estimating the value of the evidence of any witness by a study of 
the nature and form of the evidence itself. 

Margaret Drummond. 


A CASE OF HYSTERICAL CONTRACTURE. Charles Odier, 
(676) Arehiv de Psychol ., 1914, May, p. 158. 

An account of a case of hysterical mutism with subsequent develop¬ 
ment of talipes, equino-varus, and a stiff leg. The ability to speak 
returned after nine months. The stiffness of the leg disappeared 



486 


ABSTRACTS 


under narcotics, but the condition of the foot remained unaffected. 
Hence it was thought necessary to divide the tendo Achillis. 

The psychological interest of the case consists in the analysis 
which shows that both symptoms resulted from psychic traumas, 
the mutism being equivalent to a retreat from the world motived 
by the death of the patient’s father, to whom she was deeply 
attached; and the contracture being the symbolic expression of a 
wish rooted in her subconscious life. Margaret Drummond. 


PATHOLOGY. 

COLLODION OOVBBSLIP8 IN MICROSCOPICAL TECHNIQUE. 
(577) (Ooprtogetti di collodion nella technics microscopies.) 
G. D’Abundo, Riv. ital. di Neurop ., Prickiatr. ed EletProter ., 
1914, vil, p. 296. 

The glass coverslips in ordinary use are very fragile and not 
sufficiently thin. The writer therefore recommends the substitu¬ 
tion of collodion coverslips made from a solution composed of 
collodion 10 parts, absolute alcohol 5 parts, and sulphuric ether 
5 parts. 

The transparency of these coverslips is equal to that of glass 
ones, and their thickness is considerably less. 

J. D. Rolleston. 

80MB OF THE HISTOLOGICAL CHANGES FOUND IN TABES. 

(678) Frederic H. Thorne, Jou m. of Med. Soc. of New Jertey, 1914. 

The material for this paper was taken from nine typical cases of 
tabes in all stages of degeneration. The conclusions are that tabes 
dorsalis is a degeneration of the spinal cord due to an invasion and 
proliferation of the treponema of syphilis. The pia was thickened 
in all the cases, usually equally so all round the cord, and extend¬ 
ing as far up as the pons and optic tractB. There is always a 
plasma cell infiltration into the pia, and in the adventitial lymph 
spaces of the vessels in the cord substance; this plasma cell 
infiltration is intense in the active oases, but scanty in the long¬ 
standing cases. It is seldom found above the pons. The degenera¬ 
tion found in the posterior columns is secondary, and is only one 
manifestation of the degenerative process. Its cause is obscure. 
The glial element in the cord is usually increased both in the grey 
and in the white matter. Many focal lesions were found scattered 
throughout the grey substance. The ganglion cells of the anterior 
horns and of Clark’s column are markedly involved. 

The meningitis, pia infiltration, and glia proliferation are 
identical with those found in the brain in general paralysis. 

A. Ninian Bruce, 



ABSTRACTS 


487 


PARAMENINGOCOCCUS AND ITS ANTISERUM. Martha 

(679) WOLL8TMN, Joum. Exp. Med., 1914, xx., p. 201. 

The parameningococci of Dopter are culturally indistinguishable 
from true or normal meningococci. Serologically, they exhibit 
differences in regard to agglutination, opsonisation, and complement 
deviation. This, however, is not sufficient to justify their being 
placed in a separate class, because considerable variation and 
irregularity in tne serum reactions is also found amongst otherwise 
normal strains of meningococci. It is therefore best to consider 
the parameningococci as merely a special strain of the meningo¬ 
coccus, and not wholly consistent in itself. 

As the distinctions in the serum reactions between normal and 
parameningococci are supported by the differences in protective 
effects of the monovalent immune sera upon infection in guinea- 
pigs and monkeys, it is advisable that parameningococcal strains 
be employed in the preparation of the usual polyvalent anti- 
meningococcal serum. A. Niki an ‘Bruce. 

LOCALISATION OF THE VIRUS AND PATHOGENESIS OF 
(580) EPIDEMIC POLIOMYELITIS. Simon Flexnrb and Harold 
L. Am 088 , Journ. Exp. Med., 1914, xx., p. 249. 

The virus injected into the blood is deposited promptly in the 
spleen and bone marrow, but not in the kidneys, spinal cord, or 
brain. In spite of the affinity which the nervous tissues possess 
for the virus, it is not removed from the blood by the spinal cord 
and brain until the choroid plexus and blood vessels have been 
injured. An aseptic inflammation, such as may be produced by 
an intraspinous injection of horse serum, facilitates and ensures the 
passage of the virus to the central nervous organs, and the pro¬ 
duction of paralysis. When the virus within the blood fails to 
gain access to the central nervous organs and to set up paralysis, 
it is destroyed by the body, in course of which destruction it 
undergoes diminution of virulence. 

The histological lesions which follow the intravenous injections 
of the virus in some, but not in all, cases differ from those which 
result from intraneural modes of infection. In escaping from the 
blood into the spinal cord and brain, the virus causes a lymphatic 
invasion of the choroid plexus and widespread perivascular 
infiltration, and from the latter cellular invasions enter the 
nervous tissues. A similar lymphoid infiltration of the choroid 
plexus may arise also from an intracerebral injection of the virus. 
The histological lesions present in the central nervous organs in 
human cases of poliomyelitis correspond to those that arise from 
the intraneural method of infection in the monkey. The virus, in 



488 


ABSTRACTS 


transit from the blood through the cerebro-spinal fluid to the 
substance of the spinal cord and brain, is capable of being 
neutralised by intraspinous injection of immune serum, whereby 
the production of paralysis is averted. 

The authors consider that infection in epidemic poliomyelitis in 
man is local and neural, and by way of the lymphatics, and not 
general and by way of the blood. Hence they uphold the belief 
that the infect ion atrium is the upper respiratory mucous membrane. 

A Ninian Bruce. 


PENETRATION OF THE VIRUS OF POLIOMYELITIS FROM 
(581) THE BLOOD INTO THE CEREBRO SPINAL FLUID. Simon 
Flexner and Harold L. Amoss, Joum. Exp. Med. t 1914, xix., 
p. 411. 

It is now generally conceded that the poliomyelitic virus enters 
the human body by way of the upper respiratory passages, and in 
particular through the nasopharyngeal mucous membrane. Once 
within this membrane the virus may pass through the lymphatic 
channels of the olfactory nerve to the leptomeninges, where it 
reaches the cerebro-spinal fluid, or it may first enter the blood. 
It may then pass indirectly by way of the cerebro-spinal fluid to 
the interstices of the central nervous system. To reach the 
cerebro-spinal fluid the virus must first penetrate the barrier of the 
choroid plexus, which requires time. By the inoculation test no 
virus was detected in the fluid at the expiration of forty-eight 
hours, only small amounts at the expiration of seventy-two hours, 
while at the expiration of ninety-six hours the virus had passed 
more freely. The virus was still to be detected in the fluid at the 
onset of paralysis nineteen days after the intravenous injection. 
Pathological conditions of the leptomeninges and the cerebro-spinal 
lluid play an important part in the pathogenesis of epidemic 
poliomyelitis. A Ninian Bruce. 


CLINICAL NEUROLOGY. 

CHANGES IN THE OCULO CARDIAC REFLEX UNDER THE 
(582) INFLUENCE OF PREGNANCY. (Modifications dn rtfexe 
oculo-cardiaque sons l’infinence do la gestation.) M. Garniks 

and G. L£vi-Franckel, Bull , et mem . Hoc . m £ d . H 6 p . de Pant , 
1914, xxxviii., p. 252. 

As the result of their examination of seventy women in the 
seventh to ninth months of pregnancy, the writers came to the 
following conclusions. Iu normal pregnancy a sympathico-tonic 



ABSTRACTS 


489 


syndrome is fairly frequent and is formed by the union of three 
symptoms, tachycardia, inversion or abolition of the oculo-cardiac 
reflex and mydriasis. 

These three elements of the syndrome may be dissociated; 
thus one may find tachycardia alone, or tachycardia accompanied 
by disturbance of the oculo-cardiac reflex without mydriasis, 
or disturbance of the oculo-cardiac reflex without tachycardia. 

After delivery all these symptoms disappear, but the pupil 
is the last to resume its normal condition. 

J. D. Rolleston. 


HERPES ZOSTER AND MALARIA. W. H. Deadebick, Med. Record, 
(683) 1914, lxxxvi, p. 421. 

A record of eight cases of herpes zoster in patients aged from 13 
to 72 years. Five of the cases were associated with malarial 
infection of the sestivo-autumnal form. J. D. Rolleston. 


ON THE OCCURRENCE OF A BILATERAL EXTENSOR RESPONSE 
(684) IN STATES OF UNCONSCIOUSNESS. C. O. Hawthorne, 
Practitioner, 1914, xciii., Sept, p. 330. 

The author considers that the association of a bilateral extensor 
response with coma does not necessarily mean an organic lesion, 
and that coma, however produced, may be sufficient to establish in 
the central nervous system the conditions upon which the appear¬ 
ance of the extensor response depends. He describes four cases of 
coma with bilateral responses, the first from morphine poisoning, 
the second from delayed chloroform poisoning, the third of toxic 
origin, and the fourth from a bullet wound to the head. 

A. Ninian Bruce. 


CONJUGAL ZOSTER. (Zona conjugal.) C. Audry, Ann. de Derm, et 
(686) de Syph., 1914, 6 s4r., v., p. 299. 

In December 1913 the wife developed typical zoster involving the 
right shoulder, front of the chest in the region of the third 
intercostal space, and upper arm and forearm of the same side. 
In February 1914 the husband, aged 38, developed zoster of the 
right side of the neck, deltoid region, and second intercostal space. 

The interest of the case lies in the probability of contagion 
(cf. Review, 1912, x., p. 531, and 1913, xi., p. 434). 

J. D. Rolleston. 



400 


ABSTRACTS 


MULTIPLE NEUROFIBROMATOSIS OF THE SKIN. (Beitng rur 

(586) Kasuistik and Kenntnis der maltiplen Neuroflbromatose der 

Haut.) P. H. Schoonheid, Derrnat. Zeitschr., 1914, rxi., p. 610. 

A review of the literature and record of a case previously 
published in a Dutch journal (r. Review, 191.3, xi., p. 623). 

J. L). Rollesto.w 

PERSISTENT HEREDITARY (EDEMA OF THE LEGS (MHiROYS 

(587) DISEASE), WITH ACUTE EXACERBATIONS. REPORT OF 
TWO CASES. J. Phillips, Cleveland Med. Jovm., 1914, xiil, 
p. 316. 

Case 1. Man, aged 40, with well-marked painless swelling of the 
left leg from the knee downwards. It had been present since the 
first year of life and had never caused him much inconvenience, 
but since the age of 10 years the leg at times became red, swollen, 
hot, and tender. The attack would subside in three or four days. 

Case 2. His son, aged 6 years, showed a similar condition, 
except that the right leg was affected. The swelling had first been 
noted when he was four months old. He had had only one 
exacerbation which subsided in a few days (cf. Review, 1908, vl, 
p. 663). J. D. Rollestox. 

ARSENICAL MYELITIS. (Des mydlites ars^nicales.) O. Fon-agtbs, 

(588) Theses de Paris, 1913-14, No. 271. 

A record of ten cases in patients, aged from 7 to 50 years, in 
whom the administration of arsenic, whether in a therapeutical, 
suicidal, or accidental manner, was followed by paralysis of the 
lower limbs with or without sphincter troubles. In four cases, 
two of which were fatal, the symptoms followed injection of 
“ 606 ” or “ 914.” J. D. Rollkston. 


NOTE ON TWO CASES OF INTRADURAL SPINAL TUMOURS. 

(589) D. Dopglas-Crawford, Proc. Roy. Soc. Med., 1914, vii., July 
(Surg. Sect.), p. 265. 

The first case was a man, aged 37, a dock labourer, who complained 
of pain on right side, with weakness of the right leg. The skin 
area supplied by the right eighth and ninth dorsal nerves was 
hypenesfchetic. The legs were spastic, with double ankle clonus 
and double Babinski. As the paraplegia became absolute, and 
sphincter troubles set in, a laminectomy was performed, and an 
encapsulated fibro-sarcoma was easily removed from the level of 
the eighth dorsal nerve. Recovery was rapid and complete. 

The second case was a man, aged 55, who gave a long history 



ABSTRACTS 


491 


of recurrent attacks of pain in the left lumbar and inguinal regions. 
Occasionally twitching of left leg. His gait became spastic, and 
he lost control of his sphincters. There was double ankle clonus 
and double Babinski. A laminectomy was performed, and a 
myxo-sarcoma was removed. He remained well for two years, when 
his old symptoms reappeared, the paraplegia becoming absolute. 
As a recurrence was feared, the cord was again exposed, and it was 
found that the symptoms were caused by a spur of new bone which 
had pressed the cord over to the right side. It was removed, and 
he recovered. A. Ninian Bruce. 


THE TREATMENT OF TABETIC OPTIC ATROPHY WITH INTRA 
(590) SPINAL INJECTIONS OF SALVAR8ANISED SEBUM. (A 

Preliminary Report.) George T. Johnson, L. Z. Breaks, and 

August F. Knoefel, Journ. Amer. Med. Attoc., 1914, Ixiii., Sept. 5, 

p. 866. 

Two cases are described. The first was that of a man, aged 35. 
The Wassennann reaction was positive. Apart from the absence 
of the left knee jerk, there were no other signs of tabes except 
the ocular findings. The right vision was 20/70, and the 
left 20/200. Pupils showed marked myosis, and the reaction to 
light was slight. The fundus showed the nerve heads greyish 
white with sharp-cut margins. He was given neosalvarsan intra¬ 
venously, followed by intraspinal injections of the serum. After 
six injections the vision improved a little, the right vision being 
20/50, and the left 20/100. 

The second case was a man, aged 37. There was right 
amaurosis; the left vision was 20/100. Both knee jerks were 
absent, Romberg’s sign was present, and there was marked inco¬ 
ordination of both upper and lower extremities. After similar 
treatment to the above case, his vision improved to 20/30, and 
he regained his ability to distinguish colour. Severe reactions 
often followed the intraspinous injections. A. Ninian Bruce. 


EPIDEMIC POLIOMYELITIS. Arthur A. Pim, Brit. Med. Journ., 
(591) 1914, Nov. 14, p. 831. 

A very short account of a number of widely separated cases in a 
village in Dorsetshire. It is suggested that the infection might 
have been distributed by four parents who worked together in a 
butcher’s shop, and lived in entirely separate parts of the town. 

A. Ninian Bruce. 



492 


ABSTRACTS 


HIGH INCIDENCE OF POST-DIPHTHERITIC PARALY SIS: A 
(592) CONTRIBUTION TO THE QUESTION OF THE NEURO¬ 
TROPISM OF CERTAIN INFECTIVE AGENTS. (GehSufte 
post diphtheriache L&hmtmgen; ein Beitrag znr Fnge der Neuro- 
tropie gewisser Infektionstoffe.) P. Schuster, Neurol. Centralbl ., 
1914, xxxiii., p. 891. 

Three persons, the mother, father, and son aged 11 years, fell ill 
at about the same time with severe faucial diphtheria. The 
parents received 4,500 units each of antitoxin and the boy 1,500. 
Each developed well-marked nervous symptoms. The father, six 
weeks after the angina, developed panesthesia in the feet and 
fingers, followed by weakness of the extensors of the hand, fingers, 
and left extensor of the foot, feeble knee jerks, and absent ankle 
jerks. The mother, about a fortnight after recovery from the 
angina, had transitory difficulty in swallowing, and a few weeks 
later developed an unsteady gait, tingling in the feet, ataxia of 
the fingers, tenderness of the nerve trunks, absence of the forearm, 
periosteal, and triceps reflexes, and absence of tendo Achillis 
reflexes. The knee jerks were very feeble. In the son the 
symptoms merely consisted of tingling in the feet and absence of 
knee and ankle jerks. 

Schuster has found only two other examples of familial 
diphtheritic paralysis, recorded by Feilchenfeld (v. Review, 1908, 
vi., p. 664) and Kayser (ibid., 1910, viii., p. 613) respectively. 

He attributes the high percentage of paralysis in a single 
family to a special neurotoxic variety of the diphtheria toxin, 
and suggests that a similar condition may be present in syphilis. 

J. D. Rolleston. 


PNEUMOCOCCAL MENINGITIS IN THE SHARPSHOOTERS OF 
(593) SENEGAL. (La mtfningite k pneumocoques des tirailleurs 
s4n6galais.) W. Dufougbb£, Bull. Soc. de Path. Exot ., 1914, vii, 
p. 466. 

Pneumonia is a very fatal disease among the black troops of 
Morocco. The pneumococcus rapidly invades the system, and has 
a predilection for the heart and brain. Sometimes the meninges 
are alone affected, and the symptoms suggest epidemic cerebro¬ 
spinal meningitis or typhus. Intravenous injections of collargol 
or electrargol are recommended as treatment. An illustrative case 
is recorded in a man, aged 22. The cerebro-spinal fluid was 
clear, but contained pneumococci which were also present in 
the pus in the cerebral meninges post mortem. There was no 
pneumonia. J. D. Rolleston. 



ABSTRACTS 


493 


ASEPTIC ENCEPHALO-MENINGEAL REACTIONS. (Contribution 
(694) K l’6tndo dea reactions encdpbalo-m^ningdes aseptiques.) R. 

Bourgeois, Theses de Lyon, 1913-14, No. 70. 

The term “encephalo-meningeal reactions” is applied to a 
syndrome caused by irritation of the neuraxis and its membranes, 
but unaccompanied by gross lesions of the meninges or the nerve 
centres, and running an essentially mild course. The syndrome 
occurs at the onset, during the course, at the end of, and 
during convalescence from, infectious diseases and intoxications. 
The origin of some cases is unknown, but is probably infective. 
The syndrome is found in various other morbid states, such as 
trauma, cerebral haemorrhage, and insolation. It may also occur 
after intraspinai injection of various substances. The symptomat¬ 
ology is that of meningitis, but sometimes only one or two 
symptoms are present, or the condition may be entirely latent, 
and only revealed by lumbar puncture. The lesions found after 
death, which is due to the primary infection, are congestion of the 
meninges and lesions of the pyramidal cells. 

The symptoms are due to microbial toxins and other poisons. 

The syndrome may be mistaken for acute meningitis or 
tuberculous meningitis. The diagnosis is made by lumbar puncture, 
which is also the best treatment. The condition is essentially 
curable, and usually leaves no residues. 

The thesis contains the histories of fourteen cases, including 
three personal ones, in which the primary disease was influenza, 
paratyphoid B infection, and trauma respectively. 

J. D. Rolleston. 


ON METAGHANOBAL AND PREROSEOLAR MENINGITIS IN 
(595) SYPHILIS. (Sur la mlningite syphilitique mltachancreuse et 
pr6ros6olique.) Lavau, Ann. de Derm, et de Syph., 1914, 5 sir., 
v., p. 280. 

A record of nine cases, including one previously published by 
Audry (v. Review, 1914, xii., p. 213), in males aged from 15 to 25. 
Of these, six showed changes in the cerebro-spinal fluid, viz., 
hypertension, lymphocytosis, increase in albumin, or a positive 
Wassermann’s reaction. 

The writer’s conclusions are as follows:— 

1. Preroseolar meningitis occurred in two-thirds of his cases. 

2. It may be manifested only by slight headache. As a rule 
it is absolutely latent, and is only revealed by physical, histo- 
clinical, and biological changes in the cerebro-spinal fluid. 

3. Treatment by arseno-benzol often exaggerates the meningeal 



494 


ABSTRACTS 


reaction, thus giving rise to Herxheimer’s reaction in the meninges 
This exaggeration, however, is not constant, and bears no relation 
to the intensity of the pre-existing meningeal lesion, being some¬ 
times absent in severe syphilitic meningitis, and present in cases 
with an almost normal cerebro-spinal fluid. 

4. Arsenical treatment, especially neosalvarsan, after exaggerat¬ 
ing the meningeal reaction, constitutes the best treatment for the 
condition. Caution is necessary, and in the severe meningitis at the 
onset of the secondary period intramuscular injections of mercurial, 
salts only should l»e given during the first four or five days. 

5. The metachancral meningeal reaction appears clinically in 

a relatively high number of cases treated by intravenous injections 
of neosalvarsan. Possibly lumbar puncture may favour their 
occurrence. J. D. Rolleston. 


PROGRESSIVE LENTICULAR DEGENERATION. Williams 6. 

(596) Cadwalader, Joum. A mer. Med. Assoc., 1914, lxiii., Oct 17, p. 1380. 

Two cases are described. The first case was in a man, aged 18. 
The present condition began at 14, while he was at school, and 
developed quickly. The symptoms were sluggish movements, 
indifferent table manners, drivelling of saliva, dysarthria, and 
general lassitude. A diagnosis of myxcedema with multiple 
myoclonus was made and thyroid extract given, which caused 
great improvement for a time. At 18 he showed a vacant facial 
expression, with a more or less constant smile. The muscles 
appear good. The most striking features are marked tremors, 
rigidity, and a tendency to contractures, all of which are never 
absent, although they vary in intensity. There is no Babinski’s 
sign, and the liver dullness appears normal. The mental condition 
is fairly good. 

Case 2 was a man, aged 36. The present condition began at 
the age of 16. The tremor at first affected the right side, the 
muscular rigidity and plasticity gradually increasing and spreading 
to the muscles of the neck, causing tremor of the head, and later 
the entire body. About five or six years after its onset the 
disease became stationary. Babinski’s sign is negative, and the 
liver dullness appears normal (v. Review, 1913, xl, p. 167). 

A. Ninian Bruce. 

THE CIRCULATORY SYSTEM IN ACEOMEGALY. (L’appareU 

(597) circulatoire au conn do l’acromig&lie.) G. Gkelubr, Theses de 
Parts, 1913-14, No. 441. 

The thesis contains the histories of thirty-eight cases, of which 
two are original. 



ABSTRACTS 


495 


The conclusions are as follows:— 

1. Cardio-vaseular troubles are frequently noted in acromegaly, 
and consist of palpitation, angina pectoris, asystole, and syncope, 
vasomotor symptoms (local asphyxia and gangrene of the 
extremities, transitory swelling of the hands and feet, and 
sweating), and epistaxis. 

2. Clinical and radiographic examination shows considerable 
hypertrophy of the heart. The arteries are rigid and atheromatous. 
The pulse is affected in frequency, rhythm, and force. The blood- 
pressure is fairly often increased, and the veins are varicose. 

3. Examination of the blood shows a more or less marked 
anaemia and slight leucocytosis. 

4. Post mortem, the heart is found to be increased in size either 
as a whole or in its right side only. This hypertrophy may exist 
alone or be associated with sclerotic myocarditis. The pericardium 
is fairly often affected. 

5. The pathogeny of these cardio-vascular lesions varies. In 

some cases it is due to thoracic deformity or to nephritis. In other 
cases a pluriglandular theory explains a large number of the 
symptoms. J. D. Roi.leston. 


THE OOOUBRBNOB OF PELLAGRA IN ENGLAND. R. W. 

(598) Willoocks, Practitioner , 1914, xciii., July, p. 106* 

After a short account of this disease, the author describes a 
typical case in a girl, aged 14, who had practically never been out 
of London. She had been employed at a printing establishment, 
and had never eaten maize. She had always been well fed and 
clothed. A Ninian Bruce. 


SUBFASCIAL LIPOMA OF THE FOOT CAUSING SYMPTOMS OF 
(599) SCIATIC NEURALGIA. (Un caso di lipoma subfasciale del 
piede determinants la sindrome della nevralgia sciatica.) R. 
Casali, Gait. d. o*p., 1914, xxxv., p. 705. 

A case of obstinate sciatic neuralgia in a man, aged 57, successfully 
treated by extirpation of the tumour. J. D. Rolleston. 


A CASE OF EXOPHTHALMIC GOITRE SIMULATING ACUTE 
(600) OBSTRUCTION. G. M'Call Smith, Lancet, 1914, clxxxvii., Oct. 
10, p. 894. 

The case is that of a domestic servant, aged 23, who exhibited 
symptoms of acute obstruction as shown by fajcal vomiting, 



496 


ABSTRACTS 


abdominal pain, and visible peristalsis, uncountable pulse, and a 
temperature of 101°. She did not, however, appear to be so ill 
as would have been expected if the symptoms were due to acute 
obstruction, and a diagnosis of hyperthyroidism was made, and 
operation deferred. She recovered, and two months later presented 
typical signs of exophthalmic goitre, namely, exophthalmos, enlarged 
thyroid, pulse rate 105, tremor of hands, and general nervousness. 

The case is of interest, as severe vomiting, when it occurs, is 
usually a terminal symptom of exophthalmic goitre. 

A. Ninian Bruce. 


TUBERCULOSIS AND EXOPHTHALMIC GOITRE. (Tuberculosa et 
(601) goitre exopht&lmique.) P. Ledoux, Theses de Paris, 1913-14, 
No. 415. 

Although it is well recognised that Graves’ disease may follow 
infections such as scarlet fever, rheumatism, measles, and syphilis, 
Ledoux maintains that too little setiological importance has been 
assigned to tuberculosis. He records four personal cases in which 
Graves’ disease developed in the course of attenuated tuberculosis, 
and also two cases which developed tuberculosis in the course of 
Graves’ disease. J. D. Rolleston. 


THYROID OPOTHERAPY IN GYNECOLOGY. (L’opotMrapie 

(602) thyroidienn# on gynecologic.) B. Chakhine, Theses de Paris, 
1913-14, No. 433. 

A record of twenty-nine cases, including two original ones, in 
which thyroid opotherapy sometimes associated with ovarian 
extract was used in the treatment of the various disorders of 
menstruation, uterine displacements, and chlorosis. 

J. D. Rolleston. 

GUMMATA OP THE THYROID. (Lee gommes syphilitiquea du 

(603) corps thyrolde.) R. Beaufils, Theses de Paris, 1913-14, No. 416. 

The thesis contains the histories of five cases, one of which is 
original. 

The writer’s conclusions are as follows:— 

1. Gumniata of the thyroid, whether due to inherited or 
acquired syphilis, are rare. 

2. Clinically they are manifested by hard swelling, dysphagia, 
and dyspnoea. 

3. They must be distinguished from tuberculous thyroiditis by 
heir course and by Wassermann’s reaction. 



ABSTRACTS 


497 


4. In every case of thyroid swelling in which acquired or 
inherited syphilis is suspected, treatment should be instituted 
in the form of injections of benzoate of mercury with iodide 
internally. J. D. Rolleston. 

OBBBBBAL SYPHILIS IN THE SECONDARY STAGE. C. B. 

(604) Craig, Med. Record , 1914, lzxzvi., p. 422. 

A record of two cases of meningitis coincident with a secondary 
rash in men, aged 28 and 35, in whom injections of salvarsan and 
neosalvarsan respectively produced rapid disappearance of the 
headache, the only symptom complained of. The cerebro-spinal 
lymphocytosis was reduced, and globulin excess in the cerebro¬ 
spinal fluid disappeared after treatment. J. D. Rolleston. 


SYPHILOPHOBIA. D. W. Montgomery, Med. Record, 1914, lxxxvi., 
(606) p. 464. 

A record of a case in a man who, on four separate occasions, owing 
to an eruption of herpes labialis, was convinced that he had 
contracted syphilis. Finally he developed herpes zoster of the 
lumbar region, accompanied by swelling of the inguinal lymph 
glands. The true nature of the eruption was explained to him, 
and nothing more was heard of his imaginary syphilitic infections. 

J. D. Rolleston. 

ERRORS IN THE INTERPRETATION OF WASSERMANN’S RE- 
(606) ACTION. (Erreurs ^interpretation de la reaction de Wasser- 
mann.) P. Ravaut, Ann. de Derm, et de Syph., 1914, 6 s6r., v., 

p. 286. 

In undoubted syphilis a positive Wassermann’s reaction is a 
definite symptom of the disease. On the other hand, the reaction 
may be negative in spite of active cutaneous or visceral lesions. 
A negative reaction, therefore, does not exclude syphilis. 

The reaction should not play too large a part in the direction 
of treatment. One should try to make and keep it negative, but 
in old cases of syphilis it is sometimes impossible to change the 
reaction. A negative reaction does not by itself allow one to 
consider the patient as cured and to suspend the treatment. In 
a patient suspected of syphilis a positive reaction should be 
regarded as corroborative evidence. 

In a patient without a history or signs of syphilis a constantly 
positive reaction indicates that syphilis should be sought for. 
Apart from syphilis the reaction may be positive, and as it has no 
absolute value, does not by itself justify the diagnosis of syphilis. 



498 


ABSTRACTS 


Ravaut records illustrative cases, including examples of positive 
reactions in non-syphilitic cases such as lupus, tuberculides, lichen 
planus, and psoriasis. J. D. Rolleston. 

THE OUTLOOK IN EPILEPSY. William Aldren Turner, Brit. 

(607) Med. Joum., 1914, Oct. 17. 

In defining the cure of epilepsy some feature other than a time 
limit should be introduced, as cases may remit for several years 
and then relapse into an incurable state. The mental condition 
of the patient is an essential factor. The cured epileptic should 
be able to earn his own living, and complete withdrawal of all 
sedatives need not be regarded as necessary for this. If the 
sedative drug can be permanently withdrawn, without any relapse 
of the seizures and with retention of good mental faculties and 
memory, the case belongs to the group of cured epilepsy. 

The epilepsies of infancy and early childhood form one of the 
most unsatisfactory types, as in many cases these arise from 
organic focal lesions of the brain. Temporary arrest may take 
place about the age of four or five. 

The epilepsies of puberty and adolescence are not unfavourable 
if the fits be not too frequent, and the mental condition satisfactory. 

The late epilepsies are favourable if alcoholism can be excluded, 
and organic disease of the brain is absent. 

Once dementia sets in the outlook is unfavourable, although 
the fits may be kept in abeyance by sedatives. 

A. Ninian Bruce. 

TETANUS: ITS PREVENTION AND TREATMENT BY MEANS 

(608) OF ANTITETANIO SERUM. Alfred MacConkey, Brit. Med. 
Joum., 1914, Oct. 10, p. 609. 

A very good account along the above lines. The great importance 
of recognising tetanus early is emphasised, as by the time the 
characteristic symptoms have developed the disease is far advanced. 
Premonitory symptoms must therefore be looked for, and these 
may be sleeplessness with distressing dreams, temporary giddiness, 
violent headache, excessive yawning, anxious expression, tremor of 
tongue, profuse sweating, darting pains, and slight jerking may 
follow pressure on the flexor tendons. Symptoms such as these, 
after a history of possible infection, justify administration of anti- 
tetanic serum. 

The method of procedure should be: (1) injection beneath the 
arachnoid of 3,000 to 8,000 U.S.A. units; (2) injection into a vein 
of 9,000 to 16,000 U.S.A. units to flood the system with antitoxin; 
(3) injection intramuscularly; and (4) subcutaneously to keep up 
the concentration in the blood; and the injections of antitoxin 



ABSTRACTS 


499 


must be continued after improvement has set in. The amount of 
phenol in the antitetanic serum as a preservative is not likely to 
have any serious consequences. A. Ninian Bruce. 


OCULOMOTOR PARALYSIS OF OTITIC ORIGIN. F. H. Westma 
(609) cott, Joum. of Laryngol ., Rhinol., and Otol., 1914, Sept.; Lancet , 
1914, Nov. 14, p. 1143. 

Paralysis of all the muscles supplied by the oculomotor nerve, 
unaccompanied by lesions of the other orbital nerves, is caused by 
a lesion of that nerve before its entrance into the cavernous sinus. 
The nerve in this part of its course is 2-3 cm. long. It is usually 
in this situation that involvement by extension of disease of the 
ear occurs. This extension of pathological processes may be direct 
through the temporal bone, or through thrombosis of the inferior 
or superior petrosal sinus. An interesting case is recorded:— 

A woman, aged 29, was seen on 22nd November 1912. On 14th 
November she had had a sudden attack of vertigo, but did not fall. 
In the evening she had vomiting and diarrhoea. Later on she had 
another attack of vertigo, and fell bumping her head. She could not 
open her right eye afterwards. She became unconscious, and re¬ 
mained so for sixteen hours, and vomited during that time. On 21st 
November complete paralysis of the oculomotor nerve with ptosis 
were present. No proptosis, no pain. The right external rectus 
and superior oblique were unaffected. The facial nerve was also 
unaffected. The fundus and retinal vessels were normal. 
Diagnosis: pressure on the trunk of the oculomotor behind the 
orbit. As there was also an intermittent foul discharge from the 
right ear, it was examined. The patient was dazed, but would 
answer questions. She could hear ordinary voice with each ear. 
The right ear contained cholesteatoma. There was no pain in the 
ear nor mastoid tenderness. There was ptosis on the right side, 
and the right eye was turned downwards and outwards. There 
was no ecehymosis nor oedema of the lids. No nystagmus. The 
temperature for the next few days was a little raised, pulse normal. 
Reflexes normal, Kernig negative. Patient became very drowsy, 
therefore operation performed on 24th November. The sinus was 
exposed, and pulsated normally. Dura of the middle fossa exposed, 
and pulsated feebly. Antrum contained pus and granulations. 
An aperture was seen in its roof, from which pus exuded. The 
opening was enlarged inwards, and about one drachm of pus 
evacuated. The track of the pus was found to extend inwards for 
about half an inch. The patient did well till the fourth day, when 
she had headache and vomiting. At midnight she had severe 
general convulsions lasting half an hour. After this, recovery was 

40 



500 


ABSTRACTS 


alow, but uneventful. The eye condition gradually improved, till 
in May 1915 the ptosis had almost disappeared, though there was 
still some diplopia. The writer believes that the infection had 
worked along the superior petrosal sinus. An analysis of the 
literature is given. J. K. Milne Dickie. 


A CASE OF PARALYSIS OF THE EXTERNAL RECTUS MUSCLE 
( 010 ) DUE TO THE PRESENCE OF AN ABSCESS IN THE APEX 
OF THE PETROUS PYRAMID. DEATH FROM BASAL 
MENINGITIS. Geo roe Wilkinson, Joum. of Laryngoi, Rhinol., 
and Otol., 1914, xxix., No. 8. 

A Bov, aged 8, came complaining of earache on the right side, and 
inability to keep the right eye open. A month before the patient 
was seen he had been feverish for a few days, after which he began 
to have pain in his right ear. He sweated and was feverish. No 
sore throat, no ear discharge, no vomiting. Three weeks later he 
began to keep his right eye closed, and was deaf in both ears. On 
examination the right tympanic membrane was normal, there was 
slight mastoid tenderness, and a little swelling in the neck. The 
right eye showed a pure external rectus paralysis. Optic discs 
normal. No nystagmus. Temperature 994, pulse 96. Para¬ 
centesis of the right membrane yielded to pus. Lumbar puncture 
fluid clear and not under pressure. Mastoid operation performed. 
The cells contained gelatinous muco-pus, which yielded a pure 
culture of Streptococcus nwcosus. Lateral sinus normal. The 
antrum contained no pus. Four days later discharge appeared 
from the meatus, and lasted ten days. For several days there was 
nothing particular to note except that the boy was abnormally 
quiet. Three weeks later the patient developed acute meningitis. 
Lumbar puncture fluid turbid, and contained Streptococcus mucosas. 
The patient died five days later. Post mortem—purulent basal 
meningitis. Collection of pus in the left middle fossa. On strip¬ 
ping the dura from the petrous a small bit of bone came away from 
the tip and disclosed a small smooth abscess cavity which had no 
direct communication with the meninges. The carotid was exposed 
in its wall for half an inch. The track of infection was along the 
cells above and below the Eustachian tube, and along the carotid 
artery. The sinus and labyrinth were normal. 

J. K. Milnb Dickie. 



ABSTRACTS 


501 


OPTIC NEURITIS WITH SYMMETRICAL LOSS OF THE LOWER 
(611) PORTION OF THE FIELD ASSOCIATED WITH DIABETES. 

M. S. Mayou, Proc. Roy. Soc. Med., 1914, vii. (Sect Ophthalmol.), 
p. 148. 

A man, aged 47, complained of loss of vision in lower half of right 
eye. The pupils were equal and active, and the Wassermann 
reaction was negative. A sector-shaped scotoma occupied the 
lower half of the right field, and the right disc showed a well- 
marked optic neuritis with a swelling of 5 D. As the antrum was 
full of pus a radical operation was performed, but no improvement 
followed. 

Seven months later pain in the left eye and headache developed. 
A definite optic neuritis was found, and a sector-shaped scotoma 
below. The right disc showed signs of optic atrophy at this time. 

A large quantity of sugar was present in the urine. 

A. Ninian Bruce. 


PSYCHIATRY. 

THE FOLDS OF THE SKIN HAIR IN THE INSANE. (Le pieghe 

(612) del cuoio capelluto negli alienati.) Alberto Zilocchi, Ratsegna 
di Stvdi Ptichiat., 1914, iv., p. 669. 

The author describes a case, and considers that the folds of the 
hair of the skin in the insane have a definite pathological signifi¬ 
cation. This, however, is not to be regarded as an atavism, but 
merely as a functional nervous or vascular disturbance. 

A. Ninian Bruce. 


PRECOCIOUS GENERAL PARALYSIS THREE YEARS AFTER 
(613) A CHANCRE TREATED BY “606.” (Paralysis gdndrale 
prfcoce trois ans aprds un chancre traits par le “606.”) 
G. B. Nowicki, Thiiet de Paris , 1913-14, No. 288. 

A man, aged 36, contracted a chancre in 1910 for which he was 
treated with four intravenous injections of salvarsan. Within 
three years typical symptoms of general paralysis developed. The 
case, though rare, is not unique, as similar ones have been recorded 
by Ehlers (y. Review, 1908, vi., p. 267); Marchand and Petit {ibid., 
1910, viii., p. 447), and others. 

Nowicki holds Gaucher’s view that salvarsan was a pre¬ 
disposing cause of the general paralysis. 


J. D. ROLLE8TON. 



ABSTRACTS 


r>oj 

GENERAL PARALYSIS RAPIDLY AGGRAVATED BT 606. 

(614) (Paralysie gdndrale rapidement aggravde par le 606.) J. Bobeix 
Ann. desmal. v^ne'r., 1914, ix., p. 521. 

A man, aged 35, of nervous temperament contracted syphilis 
in 1907. He underwent a regular treatment for four years with 
mercury with which potassium iodide was associated during the last 
two years. Beyond a roseola and mucous tubercles which occurred 
during the first two years no symptoms developed till 1913, when 
he became impotent and began to suft'er from gastro-enteritis. 

Wassermann’s reaction was found to l)e positive, and he was 
given an intravenous injection of 015 neosalvarsan. Three days 
later symptoms of general paralysis developed, which were so 
much aggravated by a second injection five days after that of the 
first that he had to be sent to an asylum (cj. Eeriav, 1914, 
xii., p. 154). J. D. Roi.leston. 


THE RESULTS OF SPECIFIC TREATMENT IN TABES AND 

(615) GENERAL PARALYSIS AT THE SALP2TRI&RE, 1912-1914. 
(Etude critique.sur les rdsultats du traitement spdciflque dans les 
cas du tabes et de paralysie gdndrale observes b la cliniqne des 
maladies nerveuses (Salp6tri6re) en 1912-1913-1914). G. C. J. 
Lkoendre, Theses de Paris , 1913-14, No. 417. 

A record of thirty-eight cases, the majority of whom had been 
kept under treatment for several years. Intravenous injections 
of neosalvarsan or enesol (mercury salicylarsenate), and intra¬ 
muscular injections of hectine were employed. Of twenty-eight 
cases of tabes, fifteen showed considerable improvement,ten slight, 
and three none. Of five cases of general paralysis, in two the 
improvement was very striking, in one very slight, and in two 
none. In no case was there a definite arrest of the disease, and 
treatment had to be prolonged indefinitely, as return of the 
symptoms always followed cessation of treatment. 

J. D. Roixestox. 


PARESIS PATIENTS TREATED WITH* INTBASPINAL INJEC- 

(616) TIONS OF SALVARSANISED SERUM. (A Brief Report.) LB. 

Pilsbuby, Journ. Amer. Med. Assoc., 1914, lxiii, Oct. 10, p. 1274. 

The results obtained in eleven cases are here described and tabu¬ 
lated. Six showed improvement in some respect not necessarily 
clinical, one is no better, and four are dead. 


A. Ninian Bruck. 



ABSTRACTS 


503 


RESULTS OF ONE HUNDRED INJECTIONS OF SALVAR8ANISED 

(617) SERUM. C. Eugene Riggs and Ernest H. Hammes, Joum. 
Amer. Med. Assoc., 1914, Ixiii., Oct. 10, p. 1277. 

The 100 injections were administered to twenty-four cases, and in 
all the cases who received over four combined injections the 
Wassermann reaction in the blood became negative, except in one 
case. Only four of the cases are recorded, but the author states 
that the results in paresis have not been so good as in tabes. One 
case of syphilitic meningomyelitis in a tabetic developed an aseptic 
chemical meningitis after the fourth intraspinal injection, but 
recovered and improved. The paper is followed by a discussion. 

A. Ninian Bruce. 

KORSAKOW’S PSYCHOSIS OCCURRING DURING PREGNANCY. 

(618) D. E. Henderson, Johns Hopkins Hasp. Bull., 1914, xxv., p. 261. 

Henderson quotes several illustrative cases, including the following 
two personal ones:— 

1. A woman, aged 31, during the first month of her second 
pregnancy, began to suffer from vomiting and rapidly lost weight. 
Symptoms of multiple neuritis developed, and she became 
depressed, disoriented, and showed a tendency to fabricate. 
Considerable improvement occurred under treatment in hospital. 

2. A woman, aged 37, whose previous pregnancies had been 
normal, had uncontrollable vomiting in her fourth pregnancy, and 
during the last two months developed a psychosis characterised 
by apathy, forgetfulness, suspiciousness, and later by a pseudo- 
hallucinatory state and a tendency to fabricate. There was no 
polyneuritis. She was discharged unimproved. 

J. D. Rolleston. 

THE PSYCHOSIS OCCURRING DURING THE COURSE OP 

(619) PERNICIOUS ANAjMIA. G. H. Williams, Joum. Amer. Med. 
Assoc., 1914, Ixiii., Sept. 12, p. 936. 

Two cases are described in men, aged 52 and 55 respectively, who 
showed definite evidence of pernicious ansemia associated with an 
abnormal mental condition, which developed during the course of 
the disease, and thus was not to be regarded as a final complica¬ 
tion. The mental signs were lack of orientation, attention, and 
appreciation, undue happiness, loss of accuracy for recent and 
remote events in one case, and numerous physical signs, such as 
parasthesias, diminished sensibilities, vertigo, speech disturbances, 
loss of functions of the arms and legs, ankle clonus, unequal 
patellar reflexes, Romberg sign, and unsteady gait. The author 
considers the condition might best be classified amongst the 
intoxication psychoses. A. Ninian Bruce. 



504 


REVIEWS 


■Reviews. 

SfcMIOLOGIE DBS AFFECTIONS DU SYSTEMS NERVEUX. Prof. 

(620) J. D£j£bine. Pp. xxvi. +1212, avec 560 figures en noir et en couleura, 
et 3 planches hors-texte en conleurs. 1914 Masson A Cie., Paris. 

Prof. D£j£rine points out in his introduction that this book is a 
second edition of the volume which appeared under the same title 
in 1900. It then formed part of Prof. Bouchard’s “Traits de 
Pathologic gdndrale.” It is now published separately, having been 
re-written, extended, and brought thoroughly up to date. It is 
written with that charm of style which we are accustomed to look 
for in Prof. Dejdrine’s books. The book, however, is of special 
value because of the excellence of the illustrations of which two 
separate series particularly call for remark. The first of these is 
concerned with the relationship between the clinical symptoms and 
pathological lesions present in the medulla oblongata, pons, and mid¬ 
brain. These are represented and explained by a series of diagrams 
which consist of two parts, an upper part in which the clinical 
symptoms are roughly sketched in, and a lower part in which the 
actual lesion is marked out. It is thus possible to see at a glance 
the relationship they bear to each other. 

The second series consists of a number of large coloured figures 
which demonstrate in a remarkably clear manner the paths taken 
by various systems or groups of nerves. For instance, in one 
figure the whole pathway of the peripheral sensory neurones are 
traced out from their distribution in the skin to their termination 
in the medulla oblongata; in another the nerve supply to the 
bones is shown ; in another the visual fibres and the nerve supply 
to the ocular muscles are all represented, and so on. A great 
many different colours have been used in these diagrams, and 
thus allow the different pathways to be easily distinguished. 

The type is large and clear and the paper good. The text 
illustrations are carefully chosen and well reproduced. References 
to literature are not given. The book, which is large, is one which 
may be safely recommended to anyone wishing a good up-to-date 
work on the nervous system, and even those who do not read 
French will find much of value in the excellence and variety of 
the illustrations and diagrams. 

THE MUSICAL FACULTY: ITS ORIGINS AND PROCESSES. 

(621) William Wallace. Pp. vi.+228. Macmillan A Co., Ltd., London, 
1914. Pr. 5a net. 

This book deals with the mechanism of the musical sense. Its 
aim is psychological rather than musical, and it records in outline 



REVIEWS 


505 


the mental processes concerned with the creation and production 
of music. It is a subject which the psychologist has up till now 
rather tended to avoid. Music is a spontaneous act of creation. 
The gift may be inherent and spontaneous, or it may be an 
acquisition deliberately cultivated to such a point as to pass for 
genuine creative ability. Music is limited by the absence of any 
standard of excellence. In music we have a form of thought, 
which, in its evolution, presents marked crises, one large and 
spacious period being followed by a new kind of music absolutely 
repellent to the adherents of the older dispensation, and the 
process becomes repeated when this new style in its turn yields 
to its successor. It is interesting to note that the earliest piece 
of musical notation extant, known as the Delphic Hymn to Apollo, 
is ascribed to the year 278 b.c., and it took the musical faculty 
700 years to bring harmony from its embryonic state to the 
maturity upon which our modern music is based. 

Precocity in the arts is seen in its most highly organised state 
in music. No matter how musical the child’s parents may be, 
they can do little more than instruct him in technique. He has 
to develop himself from within. In the prodigy we find a highly 
receptive and sensitive musical faculty, but one which seems to be 
largely unconscious. The act of performing is mainly reflex, and 
independent of direct thought and concentration. He does not 
realise the magnitude of his performance. There is evidently a 
hypersesthesia of the sensori-motor tracts when connected with the 
reflex-auditory centres, and this tends to become exhausted unless 
the tracts and centres are brought into circuit with volitional 
centres. The whole problem is elaborated here with great skill 
and clearness. The chapter on heredity is most interesting, while 
that headed “A Clinical Study” takes the form of a strong 
criticism of Nisbet’s “ Insanity of Genius.” 

The analysis of the mental acts giving rise to the production 
of music, and its effect upon the hearers, is here presented in a 
most carefully thought-out manner, which forms a valuable con¬ 
tribution to musical science, and which ought to give food for 
much thought to all those who are interested in the psychological 
side of this question. 

MIND AND ITS DISORDERS. W. H. B. Stoddabt. Second Edition, 
(622) with 74 illustrations. Pp. xvi. +518. H. E. Lewis, London. 

Pr. 12s. 6d. net. 

Thb first edition of this work, which appeared in 1908, has already 
been reviewed in this journal ( v . Review, 1909, vii., p. 219). It 
is thus not necessary for us to do more than to draw attention 
to the main additions which have been made. The previous three 
divisions into normal psychology, abnormal psychology, and mental 



506 


BOOKS AND PAMPHLETS RECEIVED 


diseases have been retained. Most of the chapters have been 
altered or added to in some way, while two fresh chapters have 
been added to Part II., the first on the “ Psychopathology of the 
Freudian School,” where psycho-analysis is briefly discussed and 
a list of 200 stimulus words for use by the association method 
is given, and the second on “ Anomalies of the Sexual Instinct.” 
Part III. has been rearranged in such a way as to establish more 
clearly the similarity of the various toxic psychoses. 


BOOKS AND PAMPHLETS RECEIVED. 

Babinski, J. “Expose des Travaux Scientifiquea.” Masson «fe Cie., 
Paris, 1913. 

Boring, Edwin Q. “Introspection in Dementia Praecox” (Amer. Journ. 
Psychol., 1913, xxiv., pp. 145-170). 

Boring, Edwin Q. “ Learning in Dementia Praecox ” ( The Psychological 
Monographs, Psychological Review Publications, 1913). 

Flexner, Simon, and Amoss, Harold L. “ Localisation of the Virus and 
Pathogenesis of Epidemic Poliomyelitis,” (Journ. Exp. Med., 1914, xx., p. 249). 

Flexner, Simon, and Amoss, Harold L. “ Penetration of the Virus of 
Poliomyelitis from the Blood into the Cerebro-spinal Fluid ” ( Joum. Exp. 
Med., 1914, xix., p. 411). 

Flexner, Simon, and Lewis, Paul A. “ Experimental Epidemic Polio¬ 
myelitis in Monkeys ” (Joum. Exp. Med., 1910, xii., p. 227). 

Simpson, Sutherland. “The Motor Areas and Pyramid Tract in the 
Canadian Porcupine (Erethizon dorsatus, Linn).” (Quart. Joum. Exp. 
Physiol., 1914, viii., p. 79). 

Simpson, Sutherland. “The Physiology of the Hypophysis Cerebri” 
(N. Y. State Joum. of Med., 1913, Sept.). 

Simpson, Sutherland. “The Pyramid Tract in the Red Squirrel 
(Sciurus hudsonius, Loquax) and Chipmunk (Tamias striatus, Lysteri )” 
(Joum. Comp. Neurol, 1914, xxiv., April, p. 137). 

Swift, Walter B. “ A Voice Sign in Chorea " (Amer. Joum. Dis. Child., 
1914, vii., pp. 422-427). 

Swift, Walter B. “Further Analysis of the Voice Sign in Chorea” 
(Amer. Joum. Dis . Child., 1914, xii., pp. 279-282). 

Thorne, Frederic H. “Some of the Histological Changes found in 
Tabes” (Joum. of Med. Soc. of New Jersey, 1914). 

Turner, William Aldren. “The Outlook in Epilepsy” (Brit. Med. 
Joum., 1914, Oct 17). 

Wollstein, Martha. “Parameningococcus and its Antiserum” (Joum. 
Exp. Med., 1914, xx., p. 201). 

The Training School Bulletin, 1914, xi., Oct. 

“ Forty-fourth Annual Report of the Resident Medical Superintendent 
of the Down District Lunatic Asylum, Downpatrick,” 1914. 

“Eighty-seventh Annual Report of James Murray’s Royal Asylum, 
Perth,” 1914. 



IRevtew 

of 

IReuroloGS anfc> IPs^cbiatn? 


©riglnal articles 


STUDIES IN NEUROLOGICAL TECHNIQUE.—NO. 
2: 1 INDICATION AND METHOD FOR THE 
USE OF THE ELECTRICAL RE-ENFORCE¬ 
MENT FOR THE ELICITATION OF THE 
ABSENT REFLEXES. 

By WALTER B. SWIFT, M.D., Boston, Mass., U.S.A., 

Formerly Assistant to Physicians for Nervous Diseases, Boston City Hospital; 
in charge Voice Clinic, Psychopathic Hospital; Instructor in Neuropathology, 
Tuft’s College, Medical School, Boston. 

At the Atlantic City meeting of the American Medical Associa¬ 
tion last June I presented in a preliminary note (1)—and as far as 
I know for the first time—a new method of reflex elicitation by 
electricity. I wish now to amplify that presentation somewhat, 
and mention the indications for the use of the method. By 
no means do I intend to convey the idea that electricity should 
be applied in every case where we try the reflexes, any more 
than Jendrassik’s hand grasp should be applied to reinforce the 
elicitation of every knee jerk. But there are certain cases of 
absent reflexes where “electrical reinforcement” is applicable, 

1 “ Studies in Neurological Technique.—No. 1: The Points in Jendrassik’s 
Method of Eliciting the Patella Reflex.” Alienist and Neurologist, 1913, xxxiv., 
No. 3, August. 

4i 



508 


WALTER B. SWIFT 


and in fact has been proven (1) to be the only method known 
for such elicitation. Those cases are few as compared with all 
the cases whose reflexes we take, and in just the same way that 
the cases are few where the Jendrassik method of reflex 
elicitation is applied. In fact, electrical reinforcement need 
not be applied as frequently as others, and should be reserved, 
as it were, for a last resort. The situation demands this for two 
reasons: First, electrical reinforcement should be resorted to 
lastly because other methods are good, and in the majority of 
cases suffice. Secondly, electrical reinforcement, while sometimes 
the only method that meets with success, is nevertheless clumsy, 
inconvenient, and takes considerable time. 

I should therefore posit that we arrive finally plumb up 
against the indications for electrical reinforcement by making 
the reflex test in its usual way first; then if absent, secondly try 
some convenient method of reinforcement such as relaxation, and 
in case of the knee jerk the Jendrassik hand grasp (of course 
according to the most approved method (2); and lastly, when 
the reflex is still absent, employ this new method—the electrical 
reinforcement. 

In a word, then, absent reflexes unelicited by the employment 
of milder forms of reinforcement, indicate the electrical method. 
Many will justifiably feel that a still further limitation is 
necessary. When other symptoms call for absent reflexes, such 
as advanced cases of tabes, old cases of anterior poliomyelitis, 
or other known breaks in the reflex arc, most of us will be 
satisfied with the older methods of reinforcement. This would 
designate the electrical method as strongly indicated where an 
absent reflex stands out as an irrelevant sign, where absent 
reflexes seem uncalled for to complete the otherwise unified 
details in the picture of our symptom complex—as where it 
vitiates our neurological chiaroscuro—or where it alone may 
turn a diagnosis. In such, I might almost say sport, cases the 
electrical reinforcement is unquestionably indicated. Naturally 
those interested in research will broaden this field, as there are 
still many problems here unsolved. 

In the preliminary report (1) upon the value of using the electric 
current in the elicitation of reflex action the technique of that 
method was omitted. 

Now I wish to present briefly that method of applying 



STUDIES IN NEUROLOGICAL TECHNIQUE 509 


electricity to various parts of the body in the elicitation of those 
reflexes. 

In general, it makes little difference in which direction the 
current passes as long as it does pass the mechanism that causes 
the reflex act; it also makes little difference as to whether that 
current is faradic or galvanic. It makes a great difference whether 
there is a strong, medium, or weak current. It makes a great 
difference whether that current gives pain or not. If pain results 
from too strong a current, the reflex elicitation is interfered with 
by muscle contractions. These contractions move the leg or arm 
away, so that the current is interrupted, or cause such marked 
motion that the reflex action cannot be judged. 

Therefore the first requisite in the technique of the applica¬ 
tion of the current is to have it as strong as possible up to the 
point of causing pain. Then for the elicitation of the reflexes the 
following electrode positions have been found of good service. 
Patient seated. 

The knee jerk: one electrode under upper leg, the other on 
anterior aspect of lower leg, about the middle third. These 
positions secure the following advantages:—By placing the 
electrode under the leg the operator does not need to hold it, and 
is thus left free to handle the other electrode, and to tap for the 
knee jerk. The position of the other electrode upon the anterior 
aspect of the lower leg (middle third) prevents interruption of 
current at the appearance of the reflex, and is convenient for the 
single operator. 

The ankle jerk may be elicited by placing one electrode upon 
the anterior aspect of lower leg (patient kneeling); and the other 
electrode pressing gently upon the ball of the same foot. This 
allows the action again of a single operator, and prevents inter¬ 
ruption of current as the reflex appears; and also secures good 
pressure for the electrical contact. 

For the elicitation of the triceps reflex, place the upper 
electrode under the patient’s arm, instructing him to adduct; 
and the lower electrode can be held by the operator’s hand upon 
the lower arm about its centre. 

For the elicitation of the wrist jerk, the upper electrode is 
placed low behind the upper arm, and the lower electrode held by 
the operator in the hand of the patient. 

The writer will gladly receive any reports of success or failure 



ABSTRACTS 


510 


in using this new method of reflex reinforcement, and to any 
interested will gladly send reprints of the preliminary report 

Summary .—The electrical method of reflex reinforcement is 
indicated where reflexes are absent; and where, at the same 
time, other methods have failed and that absence is doubled, 
irrelevant, inexplicable, or may turn a diagnosis. As for method, 
avoid pain, and place electrodes above and below the point of 
reflex stimulation, in such a way that reflex action may not 
interrupt the current. 


References. 

(1) Swift, Walter B. “A New Method of Reflux Elicitation.” Preliminary 

Note. Juurn . Amtr. Afeef. Assoc. , 1914, Oct. 31. 

(2) Swift, Walter B. See No. 1 of this series. 


abstracts 

ANATOMY. 

A RACIAL PECULIARITY IN THE POLE OF THE TEMPOEAL 
(623) LOBE OF THE NEGRO BRAIN. Robert Bennett Bean, Anal. 

Record , 1914, viii., Nov., p. 479. 

The material studied consisted of 127 brains of negro males, 
53 of negro females, and 53 of white males (no white females), 
and measurements were made on each temporal lobe in two 
planes. 

The general conclusions are:—The size of the pole of the 
temporal lobe is less in the negro than in the white, and less 
in the negro female than in the male. The differences are more 
pronounced in measurements taken below the hippocampus than 
in those which pass through that structure. Hence it is probable 
that the hippocampus is larger in the negro than in the white, and 
larger in the negro female than in the male. The shape of the 
pole of the temporal lobe is different in the two races, being 
slightly more slender in the negro, and almost the same size in 
the two races antero-posteriorly. The differences are not only 
absolute, but also relative to the weight and size of the entire 
cerebral hemispheres. A. Ninian Bruce. 



ABSTRACTS 


511 


A NOTE ON THE DEGENERATION OF THE FAS0I0ULU8 
(624) CEREBRO-8PINALI8 IN THE ALBINO EAT. S. Walter 
Ran SON, Joum. Comp. Neurol., 1914, xxiv., Oct, p. 603. 

Thb cerebro-spinal or pyramidal tracts of the rat decussate in 
the medulla, and run through the spinal cord in the ventral part 
of the posterior columns. They consist of fine and medium-sized 
medullated fibres, and of great numbers of non-medullated axons. 
The medullated fibres are of cortical origin. The non-medullated 
fibres are now proved to be also of cortical origin, since they were 
found degenerated in rats in whom all the cortex of the upper and 
lateral surfacee of the anterior half of the hemisphere had been 
destroyed without injuring the underlying structure. These non- 
medullated fibres in the area occupied by the pyramidal tract in 
the cord are thus true pyramidal fibres, since they come from the 
motor cortex. The method used was the pyridine-silver method 
( v. Review, 1914, xii., p. 467). A. Ninian Bruce. 


THE COMPARATIVE DISTRIBUTION OF MITOCHONDRIA IN 
(626) SPINAL GANGLION CELLS OF VERTEBRATES. E. V. 

Cowdry, Amer. Joum. Anat., 1914, xviL, Nov., p. 1 (14 figs.). 

Mitochondria occur in the spinal ganglion cells of man, monkey, 
guinea-pig, white rat, pigeon, snake, turtle, frog, and necturus, in 
which they are characterised by the constancy of their morphology, 
distribution, relative amount, and microchemical properties. There 
is a reciprocal relation between the amount of mitochondria and 
lipoid granules in the spinal ganglion cells of these vertebrates. 
The coagulability of the Nissl substance, on fixation, increases 
progressively in the gradation which exists between the small 
and the large spinal ganglion cells of man, monkey, guinea-pig, and 
white rat. A. Ninlan Bruce. 


PHYSIOLOGY. 

STUDIES ON THE CEREBRO-SPINAL FLUID.-I. INTRODUO- 

(626) TION. Harvey Cushing, Joum. Med. Research, 1914, xxxi., 
Sept., p. 1. 

STUDIES ON THE CEREBRO-SPINAL FLUID. — IL THE 

(627) THEORIES OF DRAINAGE OF CEREBRO SPINAL FLUID, 
WITH AN ANALYSIS OF THE METHODS OF INVESTIGA¬ 
TION. Lewis H. Weed, Joum. Med. Research, 1914, xxxi., Sept, 

p. 21. 



512 


ABSTRACTS 


STUDIES ON THE OEREBBO-SPINAL FLUID.—HI. THE PATH- 

(628) WATS OF ESCAPE FROM THE SUBARACHNOID SPACES, 
WITH PARTICULAR REFERENCE TO THE ARACHNOID 
VILLI. Lewis H. Weed, Journ. Med. Research, 1914, xxxi., Sept, 
p. 51. 

STUDIES ON THE CEREBRO SPINAL FLUID.-IV. THE DUAL 

(629) SOURCE OF CEREBRO SPINAL FLUID. Lewis H. Weed, 
Journ. Med. Research, 1914, xxxi., Sept., p. 93 (with 6 plates). 

II. The observations of previous investigators have, in fairly 
definite fashion, established the fact that cerebro-spinal fluid 
escapes chiefly by way of the venous system, and to a lesser 
extent along lymphatic pathways. No exact pathway of escape 
has been agreed upon. The injection methods of past investiga¬ 
tions have been such that any deductions made from them are 
open to adverse criticism. The intravital injection of the cerebro¬ 
spinal spaces with true solutions, and the subsequent precipitation 
of the chemical body in situ, affords a new and satisfactory method 
of studying the manner of escape of the cerebro-spinal fluid from 
the subarachnoid spaces. For the purpose, solutions of potassium 
ferrocyanide and iron ammonium citrate are recommended. 

III. The chief method of return of cerebro-spinal fluid to the 
general circulation is by a process of filtration through arachnoid 
villi into the great sinuses. In addition to the major return of 
cerebro-spinal fluid by the arachnoid villi, there is also an accessory 
drainage of the fluid into the lymphatic system. This plays a 
comparatively insignificant part in absorption, except from the 
isolated spinal-subarachnoid space. No evidence was found of the 
escape of cerebro-spinal fluid into the cerebral veins or capillaries. 
Absorption from the cranial-subarachnoid space is much more 
rapid and much greater in amount than from the spinal portion. 

IV. Cerebro-spinal fluid appears to be derived from two 

sources: (a) the choroid plexuses in the cerebral ventricles; (6) 
the perivascular systems of the nervous tissues. No evidence is 
afforded by these observations of any absorption of cerebro-spinal 
fluid into the cerebral capillaries. Under certain pressure 
conditions an extensive injection of the perivascular system 
from the subarachnoid spaces can be secured by the ferrocyanide 
method. A. Ninian Bruce. 


STUDIES ON CEREBRO-SPINAL FLUID.—V. THE DRAINAGE 
(630) OF INTRA-OCULAR FLUIDS. Paul Wegefarth, Jovm. Med. 
Research, 1914, xxxi., Sept., p. 119 (with 3 plates.). 



ABSTRACTS 


513 


STUDIES ON CEREBROBPINAL FLUID.—VI. THE ESTABLISH¬ 
ED MENT OF DRAINAGE OF INTRAOCULAR AND INTRA¬ 
CRANIAL FLUIDS INTO THE VENOUS SYSTEM. Paul 
Wegbfabth, Joum. Med. Research, 1914, xxxi., Sept, p. 149 (with 
1 plate). 

STUDIES ON CEREBRO SPINAL FLUID —VH THE ANALOGOUS 
(632) PROCESSES OF THE CEREBRAL AND OCULAR FLUIDS. 

Paul Wbgbfabth, Joum. Med. Research, 1914, xxxi., Sept, p. 167. 

V. In the process of elimination of the aqueous fluid at the 
so-called filtration angle, the fluid gains access to the scleral 
sinuses in the lower animals (cat, dog, rabbit) by a passage through 
“ pectinate villi,” which are analogous in structure and function to 
the arachnoid villi of the cerebral meninges. The process in man 
is the same as in lower animals, except that the pectinate ligament 
tufts extend in an unbroken chain round the periphery of the 
anterior chamber. The large neurones of the retina possess peri¬ 
cellular spaces which communicate with the aqueous reservoir, 
and by means of these communications the waste products of the 
cells appear to be in all likelihood eliminated. In the rabbit, and 
probably in other animals as well, the ocular and cranial fluids 
come into direct contact around the central vessels and in the 
tissue of the optic nerve. The anterior chamber can be injected 
from the veins after aqueous decompression. Neither the choroid, 
ciliary body, nor cornea play any part in aqueous absorption, 
whereas the function of the iris in this respect is still a doubtful 
problem. 

VI. A direct communication between the sinuses of the sclera 
and the fluid reservoirs in the canine eye has existed for at least 
forty-eight hours without haemorrhage into the ocular cavity. A 
direct communication between the superior longitudinal sinus and 
the subarachnoid space of normal dogs has remained patent during 
observations up to seven days in length, without haemorrhage into 
the fluid spaces. Sino-ventricular punctures in the cause of a hydro¬ 
cephalic kitten were followed by improvement in the animal’s 
general condition. No intraicranial bleeding was occasioned by 
these punctures. 

VII. The almost complete anatomical and physiological corre¬ 
spondence of the fluid relations in the eye and cranium are pointed 
out here, the secretion, the course of the fluid, and the ultimate 
return to the major circulation being wholly similar processes. 

A Ninian Bkuce. 



514 


ABSTRACTS 


PSYCHOLOGY. 

THE BINET MEASURING SCALE OF INTELLIGENCE. Henry 
(633) H. Goddard, The Training School Bulletin , 1914, zL, Oct, p. 86. 

The use of this scale upon thousands of children proves it to be, 
without doubt, the most satisfactory and accurate method of 
determining a child’s mental development available. Roughly 
accurate results can be obtained by anyone who applies the scale 
intelligently, but to determine a child’s mental level with precision 
and certainty, the examiner should be an expert in child 
psychology, who has gained experience in the use of the tests. 
Persons who use the tests should conform strictly to the standard 
method of giving them. People who use some of the tests, making 
their own modifications or variations of others, are not really 
using the Binet scale at all, and have no standard with which to 
compare their results. W. B. Drummond. 


PATHOLOGY. 

PATHOLOGICAL CHANGES IN THE ADRENAL GLANDS. T. R. 

(634) Elliot, Quart. Joum. Med., 1914, riii, Oct., p. 47. 

The normal adrenal gland of an adult man weighs between 
4 and 5 g., and contains from 4 to 5 mg. adrenalin. There is no 
proof that the store of adrenalin in the medulla is increased in 
any disease. The adrenaliu is lessened in many infective diseases, 
but probably not to such a degree as to endanger the circulation. 
The greatest loss was observed in examples of afebrile acute cardiac 
failure, associated with mental distress in the struggle to live. 
The lipoid of the cortex is stored and lost under conditions entirely 
different from those which govern the other fats of the body. 
It does not disappear in extreme bodily emaciation. The cortical 
lipoid vanishes with great rapidity in all acute febrile infections. 
There is a tendency for it to appear in excess in chronic renal 
disease, especially in conjunction with athero-sclerosis. 

A. Ninian Bruce. 

CLINICAL NEUROLOGY. 

THE BEHAVIOUR OF THE ABDOMINAL CUTANEOUS 

(635) REFLEXES IN ACUTE CONDITIONS WITHIN THE 
ABDOMEN AND PELVIS. R. R. Smith, Surgery, Gynecology, 
and Obstetric», 1914, xix., p. 604. 

From examination of 175 cases which came to operation, includ¬ 
ing appendicitis, acute cholecystitis, pelvic inflammation, ectopic 



ABSTRACTS 


515 


gestation, perforated gastric or duodenal ulcer, and acute intestinal 
obstruction, Smith concludes that the abdominal cutaneous reflex 
has a distinct though limited diagnostic value in acute conditions 
within the abdomen (cf. Review, 1906, iv., p. 582). 

J. D. Rolleston. 


GENERALISED HERPES ZOSTER. Q. Fernet, Brit. Joum. Derm., 

(636) 1914, xxvi., p. 399. 

Man, aged 80. In addition to characteristic lesions of herpes 
zoster occupying the areas of the third, fourth, and fifth dorsal 
nerves on the left side, there were a very large number of discrete 
vesicles scattered over the trunk and limbs, very few, however, 
being found below the knees. There were also a few lesions on 
the face and scalp. 

Recovery was uneventful J. D. Rolleston. 

GENERALISED NEUROFIBROMATOSIS (VON RECKLING- 

(637) HAUSEN’S DISEASE). Report of a case showing a superficial 
resemblance to Hodgkin’s Disease. C. A. Elliot and A F. 
Beifeld, Joum. Amer. Med. Auoe., 1914, lxiii., p. 1356. 

A record of a case in a boy, aged 16, with no congenital, 
hereditary, or familial history. The condition first developed at 
about 10 years of age, when “lumps” first appeared in both 
cervical regions, and subsequently became generalised. He was 
at first regarded as a case of Hodgkin’s disease, but on examina¬ 
tion, in addition to general lymphadenitis and enlargement of the 
spleen, tumours of the skin and nerves and pigment patches were 
found. 

The writers hold that von Recklinghausen’s disease is closely 
related to the status lymphaticus and that the ductless glands 
play a part in the production of both. J. D. Rolleston. 

MTATONIA CONGENITA (Miatonia congenita.) F. Schwkizer, 

(638) Rev. Soe. Mid. Arg., 1914, xxii., p. 637. 

An exhaustive monograph, with an account of three original cases 
and a table of all the cases on record down to December 1913. 

J. D. Rolleston. 

NERVOUS FORMS OF MALTA FEVER. (Formas nervioeas de la 

(639) melitococcia.) R. V. Barber!, PolieUniea , 1914, ii., p. 929. 

Nervous complications in Malta fever are not rare, but compara¬ 
tively little is known about them. Barberd records four cases. 



516 


ABSTRACTS 


1. Diffuse subacute myelitis in a man, aged 40, ending in recovery. 

2. Left spastic hemiplegia in a woman, aged 50, following osteitis 
of the frontal and parietal bones. In four months the exostosis 
and hemiplegia disappeared. 3. Mixed infection of paratyphoid 
B and Malta fever. Headache and double sciatica occurred during 
the acute stage, and mental confusion in convalescence. Recovery 
in four months. 4. Woman, aged 52. Violent headache, intense 
neuralgia, and psychasthenia. Recovery in four months. 

J. D. Rollkston. 


LATE DEFORMITIES OF THE VERTEBRAL COLUMN FOLLOWING 

(640) TRAUMA (HUMMELS DISEASE). (Deformazione tardiva 
della colonna vertebrale consecutive a trauma (Morbo di Ktbnmel.) 
N. Capriole, Giom. intemaz. di Set. mtd ., 1914, xxxvL, p. 769. 

Severe deformity, either in the nature of kyphosis or less 
frequently of scoliosis or kypho-scoliosis, may follow after a long 
or short interval direct or indirect trauma of the vertebral 
column. The pathological change is a rarefying osteitis, especially 
of the spongy tissue of the body of the vertebra. 

This process very often follows a fracture that has escaped 
notice, but in many cases there has been merely a contusion of 
the spine. There is little or no probability of complete recovery. 

The paper contains the records of fifty-four cases, including an 
original one. A bibliography is appended. J. D. Rolleston. 

POST-TYPHOID POLYNEURITIS OF QUADRIPLEGIC FORM. 

(641) (Polineuritis postlflca k forma quadripllgica.) C. B. Udaondo and 
M. M. Casteiots, Rev. Soc. Mid. Arg ., 1914, xxii., p. 851. 

A man, aged 22, in convalescence from severe typhoid fever, 
developed sensory and motor troubles in all four limbs. The 
sphincters were not affected, and the cerebro-spinal fluid was 
normal. 

Under treatment by injections of strychnine and hot baths 
complete recovery took place (cf. Review , 1912, x., p. 336). 

J. D. Rolleston. 


ACUTE MYELITIS, SECONDARY TO PERIRECTAL ABSCESS, 
(643) DEVELOPING A FEW HOURS AFTER SEVERE FRIGHT. 

William G. Spiller, Journ. Atner. Med. Assoc., 1914, lxiii., Oct 31, 
p. 1546. 

A railroad conductor, aged 35, developed a right facial paralysis 
after sitting at an open window. Complete recovery took place. 



ABSTRACTS 


517 


Three years later he was attacked by three men in an eating- 
house, who tried to rob him. He drove them off, and is certain 
he was not injured in any way. Two days later he saw from a 
window the man who had assisted him in driving off the robbers, 
and noticed suddenly that both legs had gone asleep. They 
became numb, and later completely paralysed. A double Babinski’s 
sign developed, with absence of both knee jerks, loss of sensation 
from a line about two inches below the umbilicus, and incontinence. 

At the autopsy pus was found round the rectum with cellulitis 
extending as high as the pleura, and involving the nerves to the 
spinal cord. The Streptococcus pyogenes was cultivated from it. 
The spinal cord showed softening in the lower dorsal and lumbar 
regions, and numerous haemorrhages. 

It is pointed out that Orr and Rows’ work upon inflammation 
of the central nervous system following the infection of the 
ascending lymph stream of nerves may explain this case. At the 
subsequent discussion the question of fright as a cause of organic 
nervous disease was considered, and the possibility that the fright 
was not an important factor in producing the cord lesion in this 
case. A. Ninian Bruce. 


MAGNESIUM SULPHATE IN PURULENT CEREBRO SPINAL 
(643) STREPTOCOCCIC MENINGITIS. History of a case complicat¬ 
ing acute otitis media, complicated by paralysis of external and 
internal recti oculi. W. Sohibb Bryant, Boston Med. and Surg. 
Joum., 1914, clxxi., Nov. 26, p. 812. 

Man, aged 22, was seized with pain in the left ear and slight 
deafness. Ten days later he passed into a typhoidal state, with 
severe headache, stupor, slight delirium, rigid neck, slight Kemig 
reflex, altered Babinski, and descending optic neuritis of the left 
eye. Lumbar puncture showed the fluid under high tension, 
containing pus and cocci. As he became comatose, with marked 
signs of meningitis and double optic neuritis, decompression was 
performed with local drainage. He improved immediately. A 
cerebral hernia protruded about half an inch, and the cerebro¬ 
spinal fluid drained freely. He was given as much magnesium 
sulphate as possible to combat toxaemia, and by the seventh day all 
symptoms of meningitis had entirely disappeared. 

Unfortunately infection of the cranial wound followed con¬ 
tamination of the dressings, and the patient died on the 190th day 
from encephalitis and toxaemia. The author claims that this case 
lived longer after the onset of the disease than any other case 
hitherto reported. A. N. Bruce. 



ABSTRACTS 


518 

ACQUIRED HYDROCEPHALUS DUE TO THE MENINGITIS OF 
(644) MUMPS. (Hydrocdphalie acquise par mdnin^ite ourlienne.) 

J. A. SicaRD, Jiev. Neurol. , 1914, i., p. 706. 

A hoy, aged 15 years, showed well-marked hydrocephalus which 
had followed an attack of mumps, complicated by meningitis two 
years previously. Lumbar puncture performed at that time 
allowed abundant lymphocytosis without any micro-organisms. 
The meningeal symptoms soon subsided, but a few weeks later the 
boy suffered from headache and vertigo. The gait became spastic, 
and hydrocephalus developed. Within the last few months 
considerable obesity had set in, being possibly due to a pituitary 
reaction caused by the hydrocephalus. This is the first case on 
record of hydrocephalus following the meningitis of mumps. 

J. D. Rollestos. 


INFANTILE PARALY8IS OF THE SMALL MUSCLES OF THE 
(645) HAND. W. F. Lk ukield, Med. Jonrn. Australia, 1914, i., Oct 10, 
p. 347. 

A girl, aged 12, suddenly became feverish, went to bed, and two 
days later lost the use of the right hand. The thenar and hypo- 
thenar wasted; the fingers could not be moved in any direction, 
except for the slightest ilexion of the tips; the wrist could neither 
lie flexed nor extended; pronation and supination of the forearm 
were very weak; flexion of the forearm was strong, but extension 
weak, and the deltoid and muscles of the shoulder girdle were 
unaffected. There were no sensory changes. The limb was put 
at rest with daily massage, but the only improvement was some 
increase of power in the triceps. 

The interest of the case is the unusual involvement of the 
small muscles of the hand without paralysis of the upper arm. 

A. Ninian Bbuce. 


LANDRY’S PARALYSIS. Report of & case, with necropsy. Edward 
(646) D. Fisher, Joum. Amer. Med. Assoc., 1914, lxiii, Nov. 21, p. 1845. 

A boy, aged 15, complained of pain and weakness in the lower 
limbs. This increased in severity until they became paralysed, 
with loss of reflexes and tenderness over the larger nerve trunks, 
but no anaesthesia. This weakness gradually extended to the 
upper extremities, with loss of power, which soon became complete 
in the hands and anns. This was followed by difficulty in 
swallowing, and by complete paralysis of the muscles of the right 



ABSTRACTS 


519 


eye and of the superior oblique of the left eye. He died from 
respiratory failure after about six weeks’ illness. 

The cord showed intense congestion to the naked eye, but 
nothing else. Microscopically there was an interstitial neuritis 
of the sciatic nerve and congestion of the anterior horns, without 
perivascular infiltration or meningeal involvement. The medulla 
oblongata showed involvement of the cranial nerve nuclei and 
degeneration of the axis cylinders for a short distance from the 
cell body. The whole picture differentiated it from poliomyelitis. 
The brain was not examined. No micro-organisms could be found, 
and injection of emulsified cord into a monkey was not performed. 

A. Ninian Bruce. 

•A CASE OF MULTIPLE VISCERAL HYDATID CYSTS (HEART, 
(647) BRAIN, KIDNEYS), RUPTURE OF ONE OF THE HEART 
CYSTS IN THE LEFT AURICLE. DISCOVERY, POST 
MORTEM, OF FREE DAUGHTER CYSTS IN THE LEFT 
CARDIAC CAVITIES. INTEGRITY OF THE LIVER AND 
LUNGS. (Un cas de cystes hydatiques visclraux multiples 
(cqbut, cerveau, reins). Rupture de l’un des cystes du coeur dans 
l’oreillette gauche. Constatation h l’autopsie des v6sicules-fllles 
libres h l’intdrieur des cavitds cardiaques gauches. Intdgritd du 
foie et des poumons.) C. B. Foresti and J. Bonaba, Bull, et 
mtrn. Soc. mdd. h6p. de Parity 1914, xxxviii., p. 262. 

A girl, aged 17, was admitted to hospital for headache, con¬ 
vulsions, and complete left hemiplegia. The convulsions and 
headache had started five years previously, but the hemiplegia 
had been present for only two months. Death from coma 
occurred about a month after admission. The necropsy showed 
four cysts in the middle portion of the convexity of the right 
cerebral hemisphere, including the motor zone. The whole of 
the right corona radiata was destroyed. In the left hemisphere 
there was a cyst in the occipital region. The cerebellum, pons, 
and medulla were not affected. 

The cerebral lesions were regarded as embolic, the primary 
lesions being situated in the heart. J. D. Rollrston. 

A VOICE SIGN IN CHOREA. (Preliminary report.) Waltxb B. 
(646) Swift, Amer. Joum. Pit. Child., 1914, vii., pp. 422-427. 

FURTHER ANALYSIS OF THE VOICE SIGN IN CHOREA. 

(649) Walter B. Swift, Amer. Joum. Pit. Child., 1914, viii, pp. 279-282. 

Examination of vocal utterance on the kymograph demonstrates a 
fairly constant voice change, consisting of a rise in pitch and 



520 


ABSTRACTS 


increase in intensity, accompanying choreic movements. The 
most marked change is in the rendering of the vowel a as in 
around. These changes so constantly accompany choreic con¬ 
tractions as to deserve recognition as a new sign in chorea. 

An analysis of twenty cases of chorea, with over 500 obser¬ 
vations on the voice, show a change of pitch and intensity in 
two cases out of three—a change that deserves recognition as a 
new sign in chorea—the choreic voice sign. 

A. Ninian Bruce. 

EPILEPSY AND OEBEBBAL TUMOUR. William Aldrkn Turner, 
(660) Brit. Med. Joum., 1914, Dec. 6, p. 969. 

Tumours involving the cortex and subcortical white matter of a 
cerebral hemisphere may give rise to seizures having features 
characteristic of idiopathic epilepsy. These attacks may precede 
the onset of the symptoms and signs of intracranial tumour by 
many years, and render the diagnosis of the true cause of the 
attacks well-nigh impossible. The existence of certain signs, 
however, favours the presence of an organic lesion; such are a 
well-defined local warning, the presence of some degree of post- 
convulsive hemiplegia, inequality of the deep reflexes on the two 
sides, unilateral abolition or impairment of the abdominal reflexes, 
and, above all, the development of an extensor plantar response. 
Eventually, more decided evidence of a destroying lesion is shown 
in hemiplegia, hemiamesthesia, hemianopsia, or aphasia, especially 
if accompanied by optic neuritis. It is therefore important in all 
cases of epilepsy to examine the reflexes and the optic discs from 
time to time, especially if a decided change occurs in the character 
of the fits, or a new symptom develops. A Ninian Bruce. 

TUMOUR OF THE ORUS CEREBRI. John H. W. Rhein, Joum. 
(651) Amer. Med. Astoc., 1914, lxiii., Nov. 7, p. 1662. 

A girl, 12 years of age, developed gradual loss of power in the 
right side of the face and the right arm and leg, with left-sided 
ptosis and convulsive seizures confined to the right face, arm, and 
leg. Later, paralysis of associated movements of the eyeballs, 
upwards, downwards, and laterally, developed. The pupils did not 
react to light nor to accommodation. Weakness of the left arm 
then occurred, and a double Babinski’s sign was present without 
ankle-clonus and with equal and exaggerated knee jerks. Later, 
the pupils became unequal. Intense swelling of the nerve-head 
and surrounding retina, with a few scattered haemorrhages, was 
found. A diagnosis of tumour of the upper part of the pons was 
made on the strength of the paralysis of associated movements. 



ABSTRACTS 


521 


At the necropsy a large tubercular mass was found, involving 
the left crus cerebri, extending to the upper limit of the pons below 
and the basal ganglia above. The internal capsule was somewhat 
implicated in its anterior limb, and the optic thalamus in its 
anterior third. The focus in the pons extended to the opposite 
side to a slight degree. 

In a review of the literature only seventeen cases of tumour of 
the crus cerebri were found, in which the diagnosis was verified by 
autopsy. These are briefly described here. The characteristic 
symptoms of such tumours is said to be hemiplegia on the opposite 
side to the lesion, associated with oculomotor palsy on the same 
side. The close proximity of the two oculomotor nuclei, however, 
usually leads to involvement of both third nuclei. 

A. Ninian Bruce. 

OPERATIVE INTERVENTION IN CYST OF THE LEFT CERE 
(652) BEAL HEMISPHERE, WITH A CONSIDERATION OF THE 
PREOPERATIVE AND SUBSEQUENT SYMPTOMS. Chablbs 
M. Rkmsen, Joum. Amer. Med. Attoc., 1914, lxiii., Nov. 7, p. 1649. 

A man, aged 59, seven years previously, suddenly became uncon¬ 
scious while in the middle of a conversation, and could not remember 
the right words to express himself afterwards. Slight improve¬ 
ment was followed by regression. He was found in July 1913 
to be suffering from aphasia, but with no evidence of motor or 
sensory changes. He could repeat phrases, and sign his name, and 
write from dictation slowly, but not legibly and not spontaneously. 
A diagnosis of haemorrhage into the cortex of the angular gyrus 
and Broca’s area was made. In March 1914 his blood pressure 
was 195 mm., and in addition to his previous symptoms there were 
spells of convulsive jerking of the fingers on the right side, with 
numbness. The Jacksonian attacks increased, involving the hand, 
the forearm, and then the right leg; apraxia, ataxia, and stereog- 
nosis developed rapidly. There was no optic neuritis, and the 
Wassermann reaction in the cerebro-spinal fluid was negative. 
As there was thus evidence of a progressive lesion, he was 
trephined and a pale yellow area exposed, which on puncture 
proved to be a cyst. About half an ounce of fluid was removed, 
which was under great pressure. The brain tissue below was of 
quite a jelly-like consistency. There was no cyst wall, and the 
wound was closed without drainage owing to the risk of infection. 
He made a good recovery, the Jacksouian attacks and dragging of 
the right foot completely disappeared, the aphasia diminished 
markedly, and the sensory, stereognostic, apraxia, ataxia, and 
position-sense disturbances all improved. 


A. Ninian Bruce. 



522 


ABSTRACTS 


OTST OF THE PITUITARY GLAND. W. N. Robertson and 
(663) E. D. Ahern, Med. Joum. Australia, 1914, i, Oct. 17, p. 372. 

A man, aged 28, came to hospital complainiug of severe and 
persistent headaches, without vomiting or giddiness, and localised 
mainly between the eyes. When 3 years old, he had “slight 
infantile paralysis.” Four years ago he had scarlet fever, 
followed by a “relapse,” which was diagnosed as meningitis. 
This lasted two months, and was followed by severe headaches, 
which disappeared after four months. He had had concussion 
three times, accompanied by about half-an-hour’s unconsciousness 
each time. 

On examination he was stunted, being 5 ft. 4 in. in height, 
and weighed 11 st. 7 lbs. His apparent age was about 17, and 
his build was feminine. Wassermarm’s reaction was negative. 
The eye condition was reported as “optic atrophy on both 
sides. Marked limitation of visual acuity. Midline bi-temporal 
hemianopsia.” An X-ray showed no enlargement of the sella 
turcica. A pituitary tumour was diagnosed, and operation was 
performed by the nasal route. A pearly cyst was found about 
the size of a hazel nut. About one drachm and a half of glairy 
fluid escaped on opening the cyst The cavity was gently 
curetted, and as much as possible of the sac wall removed with 
forceps, the cavity swabbed with iodine, and lightly packed with 
gauze. Recovery was uneventful. The headache disappeared, and 
although the eyesight has not improved much, he is able to earn 
his living as a music teacher. A. Ninian Bruce. 


000LU8I0N OF THE POSTERIOR INFERIOR CEREBELLAR 
(664) ARTERY. Andrew C. Qillis, Joum. Amer. Med. Assoc., 1914, 
lxiii., Oct. 31, p. 1660. 

The symptom complex produced by occlusion of the posterior 
inferior cerebellar artery is as follows: Sudden onset with 
giddiness, and marked tendency to fall to the affected side; no loss 
of consciousness; difficulty with swallowing and occasionally with 
phonation; loss of appreciation of pain, heat, and cold over part or 
the whole of the trigeminal area on one side of the face (usually 
the side of the lesion), and a corresponding loss of pain and 
temperature sense over the opposite side of the body from the 
face down; touch, tactile discrimination, deep pressure, and 
muscular sense are intact; paralysis of the sympathetic on the side 
of the lesion, causing retraction of the eyeball, contraction of the 
pupil, and drooping of the eyelid, and ataxia of the arm and leg, 
usually on the side of the lesion. In the course of from two to six 



ABSTRACTS 


523 


months practically all symptoms disappear, other than the sensory 
charges, which usually are permanent. 

Two cases are here described, the first in a woman, aged 40, 
in which the symptoms appear to have been due to thrombosis, 
and the second in a man, aged 39. A short discussion of the 
paper took place. A. Ninian Bruce. 


TOTAL DEAFNESS, ASSOCIATED WITH THE SYMPTOM COM- 
(655) PLEX DESCRIBED BY BAkANY IN WHICH COMPLETE 
RESTORATION OP HEARING OCCURRED. Robert Barany, 
Joum. of Laryngol., Rhxnoland Otol., 1914, Jau. 

A girl, aged 20, was seen in May 1911. She had had an acute 
inflammation in the right ear in December 1910, which healed up, 
but had left some giddiness, pain in the back of the head on the 
right side, deafness, and tinnitus. The drumhead was normal, 
there was slight tenderness on the mastoid process, and some 
nerve deafness. The caloric reaction was present, but impaired on 
the right side. There was deviation of the right hand outwards. 
The diagnosis of a localised collection of fluid at the cerebello¬ 
pontine angle was made. Lumbar puncture performed. Three 
c.cm. withdrawn. Following upon this the headache on the right 
side became much worse. Vomiting continuous, giddiness intense 
and persistent, and remained so for six days. Operation per¬ 
formed : the dura of the posterior fossa was exposed, and over the 
region of the internal auditory meatus it was massaged with a 
swab. The effect was startling, as headache, giddiness, and 
vomiting had disappeared. Before operation whisper and con¬ 
versational voice was heard at 0 - 25 aud 1 m. respectively. Patient 
not seen till middle of August. At that time still quite well, 
and hearing had improved. The caloric reaction was still 
diminished on the right side. Hearing now for whisper and 
conversation 0 75 and 2-3 m. On 29th August the hearing had 
become nojmal on the right side, while the left ear was now 
becoming deaf. For some days the patient had had headache and 
tinnitus on the left side. Within a few days the hearing on the 
left side had become reduced to whisper a.c., conversation 19 cm. 
Lumbar puncture again performed without effect. Some days 
later the dura was exposed on the left side and the symptoms 
improved, but the headache returned after a time and was worse 
than ever. The dura was then slit, and a blunt instrument was 
introduced in the direction of the internal auditory meatus. A 
free flow of cerebro-spinal fluid resulted. The headache and 
giddiness disappeared, but the patient was totally deaf on the left 
side. A year later the patient returned with severe pain behind 
42 



524 


ABSTRACTS 


the left ear, giddiness, and tinnitus. Hearing: conversation 5 m. 
in the left ear. Deviation of left wrist present. Some weeks 
later the patient had improved, so that she could hear a whisper 
at 5 m. No deviation of wrist. 

The case is not one of hysteria, but can be explained by the 
presence of a localised collection of fluid in the cerebello-pontine 
angle. The eighth nerve lies in a definite cisterna pontis lateralis. 

J. K. Milne Dickie. 


CEREBELLAR SYMPTOMS AND CEREBELLAR LOCALISATION, 
(656) including kmem&togr&phic observations on cerebellar phenomena. 

Charles K. Mills and Theodore H. Wbisbnborg, Journ. Amer. 

Med. Assoc., 1914, lxiii., Nov. 21, p. 1813. 

The authors emphasise the fact that asynergy is the fundamental 
symptom of cerebellar disease, and tabulate their views on cere¬ 
bellar symptoms as follows:— 

Fundamental symptom in cerebellar disease— 

Asynergy. 

Special symptomatic manifestations of asynergy— 
Hypermetry. 

Adiadokocinesis. 

Tremor. 

Symptoms resulting from asynergic efforts— 

Asthenia. 

Atonia. 

Ataxia. 

Whether vertigo and nystagmus are cerebellar or vestibular 
symptoms must be largely determined by a thorough study of 
each case. 

In studying the focal symptoms of cerebellar disease, hyper¬ 
metry, adiadokocinesis, and tremor at times indicate not only the 
presence of cerebellar asynergy, but give the clue to the part of 
the cerebellum most involved, as when exhibited in the trunk, 
head, arms, legs, or eyes. These facts of localisation may be 
emphasised by kinematographic investigation and rendered easy to 
analyse. They may be tabulated as follows:— 

Focal symptoms indicated by localised asynergic movements— 
Eye movements. 

Attitude and movements of head. 

Movements of jaw, face, tongue, larynx, etc. (Distur¬ 
bances of speech, emotional expression, etc.) 

Position and movements of trunk. 

Special movements of upper extremity. (Disturbances 
in fine movements, including writing.) 



ABSTRACTS 


525 


Movements of trunk and upper extremity (shoulder- 
girdle movements). 

Special movements of lower extremity. 

Movements of trunk and lower extremity (pelvic-girdle 
movements). 

The question of cerebellar localisation is then discussed. The 
authors agree with Rothmann that the cerebellar cortex is 
excitable to the electric current, although a stronger current 
is required than for the cerebral cortex. The fact that the cere¬ 
bellum as a whole and in subdivision is concerned with synergy, 
indicates that movements in which various parts of the body are 
at the same time concerned, cannot be fully represented by a 
centre or area for one of the parts. In the human cerebellum 
there must be centres for synergically simple movements, and 
centres and zones for more and more complex synergic move¬ 
ments. Each simple synergic movement has, however, its special 
cortical representation. The fact that the representation in 
certain parts of each hemisphere may be homolateral, contra¬ 
lateral, or bilateral makes it more difficult to draw an inference 
or reach a conclusion as to the localisation of function, and 
therefore as to the results of focal lesions. Two diagrams are 
given representing the zones and centres of the superior and of 
the inferior surface of the cerebellum. Trunkal movements, and 
those movements of the limbs which must act with them to 
preserve static and dynamic equilibrium, must involve the vermis 
in whole or in part. The association involvement of one lateral 
lobe in the vermal lesions will be largely determined by unilateral 
dysmetric phenomena, the extent of the antero-posterior involve¬ 
ment of the inferior vermis by the preponderance of asynergy in 
either the lower or the upper limbs. A. Ninian Bruce. 


A NOTE ON THE INCREASE OF TOTAL NITROGEN AND 
(657) UREA NITROGEN IN THE CEREBRO SPINAL FLUID IN 
CERTAIN CASES OF INSANITY, WITH REMARKS ON 
THE URIC ACID CONTENT OF THE BLOOD. H. M. 

Adler, Boston Med. and Surg. Joum. t 1914, clxxi., Nov. 19, p. 769. 

One hundred and ten cases were examined. The cerebro-spinal 
fluid was examined within twenty-four hours after withdrawal. 
Out of twenty-four cases of general paralysis the average total 
nitrogen per 100 c.c. was 27 2 mg., with a minimum of 15 5 mg. 
and a maximum of 55*3 mg., whereas the normal variations are 
from 15 to 20 mg. in 100 e.c. This observation coincides with the 
increase in albumen and globulin in this condition. The unclassified 



526 


ABSTRACTS 


dementias included several which showed high total nitrogen 
content. 

Concentration of uric acid in the blood of insane patients, 
however, varies within normal limits. 


A CASE OF TETANUS, WITH RECOVERY, TREATED BY 
(668) CARBOLIC ACID INJECTIONS. J. T. Fotheringham, 
Canadian Med. Assoc. Joum., 1914, iv., Oct., p. 902. 

A man, aged 18, wounded the sole of his foot. There was a little 
suppuration, and he did not return to work. On the thirteenth 
day stiffness of the muscles of the neck and jaw set in, and five 
days later he was admitted to hospital. There was no fever, no 
convulsions, and no opisthotonus. Lumbar puncture caused general 
spasticity and tension of muscles, especially of the limbs, but no 
convulsions. He was given, under chloroform, 10 c.c. of antitetanic 
serum into the spinal canal. Next day he had very severe 
headache. Smears from the wound gave B. tctani. A second 
dose of 20 c.c. of antitetanic serum was given under chloroform 
16£ hours after the first, and no more. As the headache was so 
severe he was given chloral hydrate 10 gr., and pot. bromide 
20 gr., four-hourly, and hypodermic injection of one drachm of 
pure carbolic acid in one drachm of glycerin. This was injected 
alternately into (1) the left pectoral region, (2) the right pectoral 
region, (3) the left thigh, and (4) the right thigh, and so on, with 
the white cell count taken at the time of each injection. The 
parts looked as if local sloughing were going to take place, but 
always healed completely, and no carboluria occurred. The 
leucocytosis rose rapidly to 24,000. His convalescence was rapid 
and uneventful. 

Whether the carbolic acid injections aided the recovery is 
doubtful, as the case was a favourable one for recovery at any 
rate, especially as the symptoms were localised and did not spread, 
and the interval between injury and onset of symptoms was 
thirteen days. A. Ninian Bruce. 


UNFAVOURABLE COMPLICATION FOLLOWING AN INTRA- 
(659) DURAL INJECTION OF NEOSALVARSAN. Alfred Gordon, 
Joum. Amer. Med. Assoc., 1914, lxiii., Nov. 21, p. 1851. 

A man, aged 35, with typical symptoms of tabes dorsalis, includ¬ 
ing pain in the lower extremities, ataxia, incontinence of urine, 
and constipation, and with a positive Wassermann reaction in the 
serum and in the cerebro-spinal fluid, improved greatly after one 
injection with autosalvarsanised serum. After two months the 



ABSTRACTS 


527 


bladder symptoms returned, and it was decided to give him a 
direct intradural injection of neosalvarsan. The solution used 
was 6 per cent, of neosalvarsan in distilled water, and as each 
drop contained 3 mg. of neosalvarsan, only two drops were injected. 
A small quantity of the spinal fluid was allowed to flow out, the 
two drops were mixed with this, and then it was all gently returned 
to the spinal canal. The patient was placed in Trendelenburg’s 
position. Half an hour later severe pain in the lower limbs set 
in, followed by vomiting, retention of urine, incontinence of faeces, 
and gangrenous patches developed on the sacrum and scrotum. 
His condition grew gradually more and more alarming, the pain in 
the limbs became agonising, and he died shortly after. There was 
no necropsy. 

This case strongly contraindicates the direct intradural use of 
neosalvarsan. A. Ninian Bruce. 

SOME MANIFESTATIONS OF CONGENITAL SYPHILIS. Leonard 

(660) Findlay and Madge E. Robertson, Glasgow Med. Joum ., 1914, 
vi., Dec., p. 401. 

As the result of an examination of thirty-three cases of spastic 
diplegia (Little’s disease) at the out-patient department of the Glas¬ 
gow Children’s Hospital, 45 per cent, showed evidence of congenital 
syphilis, as evidenced by a positive Wassermann reaction, while 
out of twenty-two cases of mentally deficient and epileptic 
children, 60 per cent, also showed similar evidence. 

A. Ninian Bruce. 

OVARIAN GRAFT IN HYPERTHYROIDISM. (Ingerto ovarico en 

(661) el hypertiroidismo.) A. F. Celesia, Rev. Soc. Mid. Arg., 1914, 
xxii., p. 843. 

A woman, aged 23, was admitted to hospital for Graves’ disease. 
After all other treatment had failed, an ovary removed 1 from 
a patient at a hysterectomy was grafted into the cellular tissue of 
the abdominal wall. At first there was no change in her condition, 
but in a month improvement began, and three months after the 
operation all the symptoms of hyperthyroidism had disappeared. 

J. D. Rolleston. 


PSYCHIATRY. 

INTRATHECAL TREATMENT OF GENERAL PARALYSIS. E. 

(662) Mapother and T. Beaton, Joum. of Mental Set., 1914, Oct., p. 691. 

An account of four cases treated by this method, together with a 
review of the previous work done in this direction. The authors 



528 


ABSTRACTS 


point out that injection of salvarsan intrathecally has been fol¬ 
lowed by grave results in many cases, and they have therefore 
followed the plan adopted by Swift and Ellis of injecting the drug 
first intravenously, and an hour later removing some blood and 
injecting intrathecally the serum obtained from it. One of their 
four cases deteriorated, and the other three have shown slight 
clinical improvement and a marked diminution in the Wassermann 
reaction. The authors discuss the view that the sub-arachnoid 
space is a closed one, unconnected with the cerebral lymph 
channels, and think that to this fact, if it is a fact, may be 
ascribed the relative unsuccess of the treatment. The possibility 
of spore formation by the spirochaetes, with a consequent latent 
period, accompanied by remission of the symptoms, is also discussed. 

W. D. Wilkins. 

INTRASPINAL INJECTIONS OF NEOSALVARSAN IN TABES 
(G63) AND OENERAL PARALYSIS. (Les injections intrarachi- 

diennes de neosalvarsan dans le tabes et la paralysis gdnlrale.) 

L. Lort at-Jacob and J. Paraf, Bull, et mim. Soc. mid. H6p. de 

Paris , 1914, xxxviii., p. 272. 

One case of tabes, two of general paralysis, and one case of 
tuberculous meningitis in an old syphilitic patient were treated 
with intraspinal injections of 3-5 mg. of neosalvarsan. None 
showed the slightest improvement, but, on the other hand, the 
injection in one case was followed by a gastric crisis and re¬ 
tention of urine, and in another by severe pain in the lower 
limbs. J. D. Rolleston. 

THE WASSERMANN REACTION AND THE MALE INSANE. 

(664) J. C. Wootton, Joum. of Mental Set., 1914, Oct., p. 679. 

An account of an investigation into the reactions of 550 specimens 
of serum and 65 specimens of cerebro-spinal fluid. The author 
gives a description of his technique, and summarises the results 
obtained by previous authors. Of 66 cases of male adult epileptics, 
5, or 7’6 per cent., gave a positive reaction, this result comparing 
well with that obtained by other observers. In all the cases of 
general paralysis that have died since the reaction was observed, 
the post-mortem findings have confirmed the diagnosis, and the 
author has not had any case of undoubted general paralysis which 
has not given a positive reaction. However, there were a number 
of cases which had been looked upon as chronic general paralysis, 
and which gave a negative reaction. These cases the author 
considers to be cases of Eorsakow’s syndrome, or alcoholic insanity. 
Further investigations were made of the serum of the relatives of 



ABSTRACTS 


529 


some general paralytics, and a positive reaction was commonly 
obtained. 

To find the incidence of syphilis among the ordinary chronic 
asylum population, 150 cases were taken at random from the male 
incurables of some years’ standing, and 8 per cent, gave a positive 
reaction, a result which agrees closely with that obtained in the 
epileptic series. Lastly, 284 consecutive male admissions were 
examined, and of these 31 per cent, gave a positive reaction, but 
when general paralytics are excluded, the percentage drops to 
12*5 per cent., which is still, however, higher than that obtained 
among the chronic patients. W. D. Wilkins. 

THE ELIMINATION OF NITROGEN AND URIC ACID IN STATES 

(665) OF EXCITEMENT AND STUPOR. (L’eiimin&zione dell’ 
azoto e dell’ acido urico in stati di ecdtamento e di stupore.) 
D. Valtorta, II Manicomio , 1913, xxviii., p. 167. 

From examination of thirteen cases Valtorta came to the following 
conclusions:— 

In states of excitement, maniacal or catatonic, the excretion of 
nitrogen and uric acid was more marked than in cases of stupor, 
circular or catatonic. The difference between the quantity of 
urinary nitrogen and uric acid excreted appeared greater in the 
same individual in the passage from the stuporous stage to the 
stage of excitement, or vice versa, than in various individuals 
suffering from the same affection. J. D. Rollestox. 

ANALYSIS OF A CASE OF PS YOH ASTHENIA. Hrxri Flournoy, 

(666) John* Hopkins Hosp. Bull., 1914, xxx., Nov., p. 328. 

A man, aged 28, suddenly developed the idea he would have to 
kill his child. After five months this idea vanished, and was 
replaced by the thought of killing himself. An analysis is given 
here, in which, amongst other points, the fact that the patient was 
going to have a second child whom he could not well afford to 
keep, is shown, the change in his fears coinciding with the birth 
of the second child. The obsession disappeared as soon as it was 
explained to him, although an uneasy feeling towards the children 
without fear arises at times when he is depressed. 

A Ninian Bruce. 

TWO OASES OF ANERGIC STUPOR TREATED WITH THYROID 

(667) GLAND EXTRACT. B. S. Bhiday, Indian Med. Gat., 1914, 
Nov., p. 429. 

As some cases of anergic stupor and melancholia recover rapidly 
after an acute physical illness, e.g., erysipelas, Stoddart advises the 



530 


ABSTRACTS 


induction of hyperthyroidism, giving six 5 gr. tabloids of thyroid 
extract the first day, then rising by two tabloids each day to the 
fourth, then falling by two tabloids daily to the seventh day, at 
suitable intervals. Bhiday subjected two cases to this treatment: 
one patient was a Brahman, the other a Mussulman. The result 
was that thyroid treatment failed to produce any physical illness 
or change in their mental condition: but further trial is suggested 
by the writer. Leonard J. Kidd. 

THE WET PACK IN THE TREATMENT OF INSOMNIA AND 

(668) MENTAL DISORDERS. H. Rayner, Joum. of Mental Set., 
1914, Oct, p. 672. 

The author endeavours to recover for this method of treatment 
a greater measure of popularity than it at present enjoys, so far 
as asylum work is concerned, and he traces its disuse, with great 
probability, as the result of its being classed by the Lunacy 
Commissioners as a form of mechanical restraint. He shows 
that its first effect is the production of a cold state, with shivering 
and a falling temperature. This is followed quickly by the stage 
of reaction, in which the temperature rises and there is profuse 
sweating due to dilatation of the cutaneous vessels, with sub¬ 
sequent sleep. There is probably considerable elimination of 
toxins in the sweat. He lays stress on the point that as soon 
as the temperature reaches the normal the coverings should be 
diminished, as it is not desirable that pyrexia should be produced, 
and he adds other practical points to be observed. The author 
considers that the use of the wet pack is extremely beneficial, 
both in acute delirious mania and in the ordinary acute form, and 
also in melancholia and other forms of mental disease accompanied 
by insomnia, and he strongly urges the revision of the existing 
rules regarding its employment. W. 1). Wilkins. 

ON LETHARGY. K. Agadjaniantz, Joum. of Mental Set., 1914, Oct, 

(669) p. 620. 

An interesting communication which emanated from the troubled 
city of Warsaw before the outbreak of hostilities.. Consideration 
of two cases of lethargy leads to a discussion of the nature and 
etiology of the condition. One case was that of a girl of 18, who 
passed into a lethargic state during an attack of measles, remaining 
in it for two days. In the second case, that of a woman of 40, 
there were frequent attacks, lasting for several hours each. The 
physiological changes resembled those of natural sleep, and the 
state of consciousness was undoubtedly greatly obscured, the 
patients being unable, after the attacks, to remember anything 



ABSTRACTS 


531 


that happened around them during the attacks. The question of 
the connection between lethargic attacks and hypnotism and 
hysteria is a vexed one. Lethargy is not an independent disease, 
but a symptom complex which may occur as the result of the 
suggestion of hypnotism or hysteria, but may also occur quite 
independently of either. W. D. Wilkins. 

THE USE OF SCOPOLAMINE HYDROBROMIDE OB HYOSGINE 

(670) IN THE TREATMENT OF MENTAL DISORDERS. A. W. 

Daniel, Joum. of Mental Set ., 1914, Oct., p. 611. 

An account of the symptoms which follow repeated dosage with 
hyoscine. The drug was given in some cases for weeks or months, 
and it was found necessary to gradually increase the dose, as 
immunity was quickly established. The maximum dosage was 
Jjy gr. twice a day hypodermically. Unfavourable symptoms 
generally commenced after three or four weeks, and consisted of 
rapid emaciation, ataxia, and paresis of various muscles. But by 
far the most characteristic symptom was vivid hallucinosis of a 
terrifying character, leading to extreme restlessness, agitation, and 
aggressiveness. All the symptoms rapidly subsided on withdrawal 
of the drug. The author considers that hyoscine may still be 
looked upon as a most useful sedative for occasional use. 

W. D. Wilkins. 

OBSERVATIONS ON CASES OF ENCEPHALITIS. E. F. Reeve 

(671) and Geobge A. Watson, Jowm. of Mental Sci. , 1914, Oct., p. 616. 

An important preliminary communication concerning some 
anomalous cases which have been found to present distinctive 
pathological changes in the nervous system, together with clinical 
symptoms of a uniform character, but not corresponding exactly 
to any generally recognised type. The symptoms consist chiefly 
of a rapidly increasing paresis, accompanied in a large proportion 
of the cases by gastro-intestinal symptoms, vomiting being 
common and often severe. In a few cases there have been 
eczematous rashes of the exposed parts. The mental symptoms 
were usually suggestive of dementia prsecox. The cortical 
changes consisted of a well-marked lesion of the Betz cells, of 
which great numbers showed advanced degeneration of a special 
type, this affecting also other cells, both of the cortex, the basal 
ganglia, and the cord. The diagnosis is at present uncertain, but 
there is some resemblance to pellagra, and it may, on the other 
hand, be possible that the cases may belong to a form of dementia 
pnecox, accompanied by changes of a much more widespread 
character than is usually observed. W. D. Wilkins. 



532 


REVIEWS 


THE DETECTION OF ▲ DYSENTERY CARRIER. H. S. Gettings 
(672) and Ethel Wald eon, Joum. of Mental Set., 1914, Oct., p. 606. 

The patient in question was a female who for four years hid 
had daily loose stools, not at all of a dysenteric character. 
Her health was otherwise quite good. Bacteriological examina¬ 
tion of the stools resulted in the isolation of B. dysenteries, 
after some preliminary negative attempts, their numbers being 
evidently small. On investigation it was found that a number of 
other cases could be ascribed with great probability to infection 
from this patient. W. D. Wilkins. 


■Reviews. 

THE MODERN TREATMENT OF NERVOUS AND MENTAL 
(673) DISEASES, by American and British Authors. Edited by 

William A. White and Smith Ely Jelliffe. Illustrated. 

2 vols. 1913. Henry Kimpton, London. Pr. £3 net. 

These two immense volumes view nervous and mental diseases 
from quite a different standpoint from the usual text-book. The 
nervous system is here regarded as a whole, and as inclusive of 
the mind. The ordinary text-book is concerned too much with 
the details of nervous disease such as disorders of gait, loss of 
sensation, &c., to the neglect of the larger problem of the individual 
as a whole and his relation to his environment. They are, as it 
were, more concerned with the cure of nervous disease than with 
its prevention, and nervous and mental diseases offer the widest 
possible opportunities for preventive medicine. The book thus 
lays great importance upon the psychical side of life, and sets forth 
doctrines of nervous and mental hygiene, reconstructive factors in 
social organisation, eugenic problems, questions of education and 
of heredity, the applications of legal measures in their remedial 
bearings, the functions of the hospital in nervous and mental 
disorders, and other important points of the above nature. This 
work is not addressed to the medical practitioner alone, but 
also to the educator, the legislator, the lawyer, the student of 
criminology and of dangerous trades, the social worker, and all 
those who come intimately in contact with their fellows and are 
concerned with their well-being. The aim has been to focus 
attention as far as possible upon the processes, to differentiate 
between closely related ones, to outline as clearly as possible their 
etiology, and show finally how best to overcome and remove the 



REVIEWS 


533 


main features of the disorders. This may be illustrated by a 
reference to tabes and general paresis, two diseases generally 
olassified separately because they show an entirely different 
clinical picture, but the underlying process is the same in both 
cases, only in the one case it is the spinal cord which is attacked, 
and in the other the brain. 

As the result of the attention here paid to the prevention of 
nervous and mental disease, the question of l>orderland conditions 
is discussed at some length, especially as the psychoneuroses form 
a natural avenue of approach to the understanding of the more 
profound and widespread disturbances met with in the psychoses. 
It is emphasised that the word “ insanity ” should be eliminated 
both from medicine and from law, and regarded as a relic of that 
time when all brain disorders with predominant mental symptoms 
were considered as one disease. 

The two volumes of this book are so large and cover so much 
ground that considerable time is required for their study. There 
are thirty-six chapters in all, each of which is written by a 
recognised authority. They are so arranged that any single 
chapter may be read independently, and thus the book is of the 
nature of an encyclopaedia. The aim of each chapter has been 
therapeutics, and only as much clinical and pathological data have 
been introduced as to make the diagnosis certain, while chapters 
on Buch subjects as diet, massage, &c., have been omitted altogether. 
The value of the different chapters varies considerably, some being 
treated on very conventional lines, while others are most original 
and suggestive. The books will form a valuable addition to all 
neurological libraries. 


THE INTENSIVE TREATMENT OF SYPHILIS AND LOCOMOTOR 
(674) ATAXIA BY AACHEN METHODS. Reginald Haves. Pp. 
iv.+64. Baillifere, Tindall A Cox, London, 1914. Pr.3s.6d.net. 

In spite of the discovery of salvarsan and neosalvarsan, the use of 
mercury for syphilis has in no way diminished, and it is generally 
recognised that treatment by salvarsan should be accompanied by 
a course of mercury. 

Of all the means of administering mercury, inunction is the 
best, and the method employed at Aachen is the most satisfactory. 
This consists in the inunction of a mercurial ointment by the 
bare hand of skilled rubbers under medical supervision, and, in 
addition, the use of sulphur water internally and externally. The 
method is fully described here, and the advantages which it 
possesses over other methods of administration clearly pointed out, 
together with a description of the precautions taken to prevent 



534 


REVIEWS 


the occurrence of salivation and gingivitis and other effects 
obtained by intensive mercurialisation. The book appears at an 
appropriate moment, and should prove of considerable use. 

MODERN PROBLEMS IN PSYCHIATRY. Ernesto Lugaro. 

(675) Translated by David Orr and R. Q. Rows. With a foreword 
by Sir T. S. Clouston. Second Edition. 1913. Pp. vii.+305. 
Pr. 7a 6d. net. 

We have reviewed the first edition of this valuable work when it 
appeared (r. Review, 1909, vii., p. 792). This, the second edition, 
does not present any radical alterations. The authors have 
taken the opportunity of making a large number of small changes, 
including the correction of several errors, typographical and 
otherwise, which appeared in the original issue. They are to be 
congratulated on the success which has necessitated the issuing of 
a second edition. 

HYPNOTISM AND SUGGESTION. C. Lloyd Tuckey. Sixth Edition, 

(676) revised and enlarged. Pp. xxviii.+431. 1913. Baillifere, Tindall 
<fe Cox, London. Pr. 10s. 6d. net. 

Six years have now elapsed since the fifth edition of this book 
was published, and the author points out how the important 
progress made in psychotherapy during the last few years has 
induced him to publish this sixth, and probably final, edition. 
He is strongly convinced of the importance of psycho-analysis, 
and considers that in many obscure cases it may take the place 
of hypnotic suggestion, although there is room for both, and 
possibly for their combination. We reviewed the fifth edition 
fully in an earlier number of this journal ( v. Review, 1907, v., 
p. 577), and will content ourselves with again pointing out that, 
for those interested in this subject, Dr Tuckey’s book will be 
found an admirable text-book, and should do much to arouse an 
interest in the mind of the general practitioner on this subject. 

MENINGOCOCCUS MENINGITIS. Henry Hkiman and Samuel 

(677) Frldstein. With introduction by Henry Koplik. Pp. xiv.+ 
313. With 4 plates, 31 figures (2 in colour), and 4 charts. J. B. 
Lippincott Co., London. Pr. 12s. 6d. net. 

This monograph is founded on a study of cases of meningococcus 
cerebro-spinal meningitis which have been treated in the children’s 
wards of the Mount Sinai Hospital, New York, and reflects the 
methods of study of the symptoms, diagnosis, and treatment in 
vogue there. As its purposes are practical, and as it is intended 
for the use of students and physicians engaged in clinical work, 



REVIEWS 


535 


only so much of technical detail has been included as can be 
carried out with ordinary laboratory facilities. 

A short history of the condition is first given, followed by 
chapters on the bacteriology, epidemiology, mode of dissemina¬ 
tion, and pathological anatomy of the disease. The clinical types 
are then discussed with the symptomatology, complications, and 
differential diagnosis, including chapters on the eerebro-spinal fluid 
and laboratory diagnosis. The book concludes with chapters on 
prognosis and treatment. 

The authors have succeeded in producing a most readable 
book. The subject is carefully and systematically studied, each 
chapter being followed by a separate bibliography. The chapter 
on the mode of dissemination concludes as follows: “ The present 
state of our knowledge permits us to state that there is some 
evidence, but no conclusive proof, that the meningococcus primarily 
invades the blood and secondarily the meninges.” The onset of 
blindness from pressure on the optic nerves from the pituitary is 
not referred to, with subsequent amelioration of the symptoms 
when the pressure is removed. The subject of internal hydro¬ 
cephalus is clearly explained. The chapter on treatment has been 
brought quite up to date, and the different methods of preparing 
the sera of Flexner, Kolle and Wassermann, Dopter, and Jochmann, 
is described, together with the results of their use. The book 
forms a very complete monograph on this subject, the references 
to the literature being most useful. 


DREAMS. Henri Bergson. Translated, with an Introduction, by 
(878) Edwin E. Slosson. Pp. 62. T. Fisher Unwin, London. Pr. 
2s. 6d. net. 

ON DREAMS. Prof. Sigm. Freud. Only authorised English Translation, 
(678) by M. D. Eder, from the Second German Edition, with an Intro¬ 
duction by W. Leslie Mackenzie. Pp. xxxii. + llO. William 
Heinemann, London. Pr. 3s. 6d. net 

THE INTERPRETATION OF DREAMS. Prof. Sigm. Freud. 
(680) Authorised Translation of Third Edition, with Introduction, by 
A A. Brill. Pp. xiL+510. George Allen «k Co., London. 1913. 

These books should be read in the above order. Both authors 
base their views on the theory that no conscious experience is 
entirely lost. According to Freud, “ what seems to have vanished 
from the current consciousness has really passed into a sub¬ 
consciousness, where it lives on in an organised form as real as if 
it were still part of the conscious personality.” 

Bergson carries this still further; he believes “ that all our 
past life is there, preserved even to the infinitesimal details, that we 



536 


REVIEWS 


forget nothing, and that all that we have felt, perceived, thought, 
willed from the first awakening of our consciousness survives 
indestructibly.” Dreams are the expression of these subconscious, 
dormant complexes. Bergson, who does not believe in the 
parallelism of mental and nervous activities, considers that all 
these memories are packed away in the subconscious mind, under 
pressure, like steam in a boiler. He regards the brain as the 
organ of attention, whose function is to concentrate the entire 
accumulated experience, i.e., memory, upon any sensation, and to 
interpret it correctly. Sleep is to be regarded as a condition of 
“disinterestedness.” One sleeps to the extent one becomes dis¬ 
interested, and thus, during sleep, these subconscious memories 
throng forth and express themselves as dreams. 

Freud analyses the dream at great length. Dreams, being the 
awakening of dormant complexes, are transfigured experiences, 
and are a manifestation of ordered mental processes. They are 
largely the expression of unfulfilled desires. They may be divided 
into three classes, according to their relation towards the realisation 
of desires: first, those which exhibit non-repressed, non-concealed 
desire ; these are best seen in children, where the sleeping ex¬ 
perience differs very little from the waking experience, and the 
dream thus takes the form of the ungratified desires of the day. 
Second, dreams may express in veiled form some repressed desire ; 
these constitute by far the greater number of adult dreams. Freud 
considers that painful experiences tend to be repressed, ie., to 
disappear from conscious memory, but persist subconsciously, 
and if they reappear as dreams, they usually require a psycho¬ 
analysis to be understood, i.e., they are concealed realisations of 
repressed desires. Third, dreams where repression exists, but 
without or with but slight concealment. Such dreams usually are 
accompanied by a feeling of dread, which brings them to an end. 

The dream work denotes the transference of the dream thought 
to the dream content, and thus is not creative; it judges nothing, 
it decides nothing, and it develops no new fancies. Four stages 
may be traced in this dream work. First, condensation, because 
a single dream is representative of many waking experiences. 
Second, displacement, by which emotional emphasis is transferred 
from its right place in the train of dream ideas to some trivial 
element in the dream content, owing to the fact that a psychical 
censorship exists, which tends to suppress everything unpleasant 
or impossible. Third, dramatisation or figurative imagination; and 
fourth, elaboration from the necessity for regard to intelligibility. 

Freud’s work on dreams is of great value, and is clearly 
explained in these two books, the first of which is an introduction 
to the second, where the whole subject is treated at great length. 
All the translations have been well done. 



REVIEWS 


537 


OLANDES SUBRfcNALES ET ORGANES OHBOMAFFINES. 

(681) M. Lucibn and J. Pabisot. Pp. iv. + 453, avec 100 figures dans le 
text©. F. Gittler, Paris, 1913. Pr. Fr. 14 

The increasingly important subject of the internal secreting 
glands has, within recent years, led to the production of excellent 
English ( v . Review, 1913, xi., p. 176) and German ( Ibid ., 1914, 
xil, p. 173) text-books on this subject. 

We have here the French contribution, where, instead of 
including all the different internal secreting glands in one volume, 
it has been decided to issue a separate volume for each gland, and 
this, the first of the series, deals with the suprarenal glands and 
the chromaffine tissue system. 

The book is divided into four parts, the first anatomical, 
the second physiological, the third pathological, and the fourth 
clinical. 

The suprarenal glands in man consist of two portions, a cortex 
and a medulla. In the first, however, these two portions form 
distinct and separate organs, and all stages can be traced between 
this and man. Developmen tally, these two portions are found to 
have separate origins. The cortex appears to be related in some 
way to the reproductive organs, the medulla is part of the 
chromaffine tissue system. This system is so called because the 
cells stain yellow with bichromate solutions, and such cells always 
contain adrenalin. These chromaffine cells are derived from the 
same cells which also give rise to the nerve cells of the sympathetic 
ganglia, and thus are really part of the nervous system. Most of 
them disappear about birth, the medulla of the suprarenals being 
the largest remnant. 

In Part I. comparative anatomy, embryology, anatomy, and 
histology is described. Part II. deals with physiology, and 
discusses the effects of removal of one and both suprarenal glands, 
the effects of injection of extracts prepared from them, especially 
upon the circulatory system and on general nutrition, the action 
of adrenalin, the antitoxic functions of the suprarenals, and the 
physiology of the accessory glands. Part III. is related to 
pathology, and describes, in turn, atrophy, hypertrophy, vascular 
lesions, inflammatory conditions, and tumours. Part IV. discusses 
suprarenal syndromes in acute, chronic, and inflammatory condi¬ 
tions, pluriglandular syndromes, and the symptomatology of 
suprarenal tumours. It is suggested that the presence of 
adrenalin in the suprarenals is of definite medico-legal value in 
determining if death has been sudden or slow. The last chapter 
deals with suprarenal opotherapy. 

The account given here of the suprarenal glands is most 
complete, and forms a valuable contribution to the subject. 



538 


BOOKS AND PAMPHLETS RECEIVED 


LEAD POISONING : from the industrial, medical, and social points 
(682) of view. Sir Thomas Oliver. Pp. x. + 294. Crown 8vo. H. K. 

Lewis, London, 1914. Pr. 6s. net. 

This book consists of the lectures delivered by the author at the 
Royal Institute of Public Health, and forms an excellent illustra¬ 
tion of the good which may be done by suitable inspection and 
control in reducing an industrial disease. 

The book opens with a description of the methods of lead 
smelting and of manufacturing red and white lead, and points out 
the dangers of lead poisoning arising at various stages. House 
painters are next considered, and there seems to be little doubt 
that the acute illness house painters suffer from is not always 
plumbism, but is the result of the inhalation of vapours given off 
by the materials with which the pigments are mixed. Pottery 
work is next considered, and a striking contrast is given between 
the condition in this country and in Hungary. 

Lead may enter the body in food or drinking water, or as 
fume or dust, or through the skin; probably most enters by the 
alimentary canal. It is dissolved by the hydrochloric acid of the 
gastric juice, and is absorbed unless proteid food is being digested 
at the same time, when it forms an insoluble albuminate. The 
symptoms are pallor, anaemia (basophilia is not constant), blue line 
on gums, colic and constipation, headache, loss of vision, and 
numerous nervous symptoms, such as weakness of the wrists, with 
or without tremor, extensor paralysis, sensory changes, and mental 
symptoms. The presence of a positive Wassermann reaction must 
not be considered certain evidence of syphilis. The chapter upon 
“ what constitutes lead poisoning ” is most interesting, great stress 
being laid upon the presence of lead in the urine. The injurious 
effects of lead upon pregnancy is clearly shown, and after discussing 
treatment, both preventive and curative, the book finishes with 
the Factory and Workshop Orders relating to lead poisoning. 


BOOKS AND PAMPHLETS RECEIVED. 

Bergson, Henri. “ DreamB.” Translated with an Introduction by 
Edwin E. Slosson. T. Fisher Unwin, London. 

Hayes, Reginald. “ The Intensive Treatment of Syphilis and Locomotor 
Ataxia by Aachen Methods.” Raillifere, Tindall & Cox, London. 

Kaplan, D. M. “Serology of Nervous and Mental Disease.” W. B. 
Saunders Co. 

Oliver, Sir Thomas. “Lead Poisoning, from the Industrial, Medical, 
and Social Points of View.” H. K. Lewis, London. 

Rebizzi, Renato. “ Osservazioni al Progetto di Manicomio per la 
Provincia di . . . Utopia” {Annali del Manicomio Provinciale di 
Perugia, 1912, vi., Gennaio-Giugno). 



Bibliography 


ANATOMY. 

YAMAKAWA, SHOTARO. Zur Kenntnis der Ventrolateralen Pyremidenbahn 
Barnes’ and der Dreikantenbahn Helwegs. Bemerkungen *ur Frege der Leitungi- 
bahn im laterelen Markfeld der Olive und in der anterolaterelen Rtickenmarks- 
Peripherie. MitteU . a. d. Med. Fakultat d. Kaiserlieh UnivtrtiUU ru Tokyo , 
1913, xi. v Oct. 3, S. 1. 

WEED, LOUIS H. Reconstruction of the nuelear masses in the rhombenoephalon. 
Anal. Record, 1913, vii., Deo. 20, p. 443. 

THOMPSON, C. B. A comparative study of the brains of three genera of ants, with 
special reference to the mushroom bodies. Joum. Comp* Neurol ., 1913, xxiii., 
p. 515. 

LAND ACRE, F. L., and CONGER, A. C. The origin of the lateral line primordia 
in Lepidosteus oueus. Joum. Comp. Neurol ., 1913, xxiii., p. 575. 

HERRICK, C. J., and OEENCHAIN, J. B. Notes on the anatomy of acydostome 
brain: Ichthyomyzon conoolor. Joum. Comp. Neurol ., 1913, xxiii., p. 635. 

NISSL, FRANZ. Die Grossbirnanteile des Kaninchsns. Arckiv. /. Psychiat. u. 
Nervenkr., 1913, liL, S. 867. 

AGUGLIA, ENG. Le alterazioni nuclear! delle cellule radicolari in seguito a resesione 
dello sciatioo. Riv. Ital. di Neuropatol., PsichuU. ed EleUroter., 1913, vi., p. 516. 

KRASSNIG, MAX. Von der Arteria vertebrelis thoracica der S&uger und Vdgel. 
Anal. Hefle , 1913, xlix., S. 523. 

STRANDBERG. Om Musoulus sternalis’ innervation. Upsala Ldkarefbrenings 
Fdrhand., 1913, xix., S. 65. 


PHYSIOLOGY. 


MARINESCO and MINE A. Quelques differences physioo-chimiques entre les cellules 
des ganglions spinaux et leur axone. Compt. Rend. d. L Soe. de Biol., 1913, lxxv., 
Dec. 19, p. 584. 

COLLIN. Les relations des corps de Niasl et des neurofibrilles dans la cellule nerveuse. 
Compt. Rend. d. L Soe. de BioL , 1913, lxxv., Deo. 19, p. 600. 

NAGEOTTE. Structure des nerfs dans les phases tardives de la dAgAnAretion walleri- 
enne. Note additionnelle. Compt. Rena. d. 1. Soe. de Bid ., 1913, lxxv., Dec. 26, 

p. 620. 

D&IERINE. Le syndrome des fibres radiculaires longues des cordons poctArieurs. 
Compt. Rend. d. 1. Soe. de Bid., 1913, lxxv., Dec. 19, p. 554. 

GASSER and LOB VENHART. The mechanism of stimulation of the medullary centres 
by decreased oxidation. Joum. Pharmaed. and Exper. Ther ., 1913, v., Jan., 
p. 239. 

GERHARTZ and LOEWY. Uber die H5he des Muskeltones. PJlUger's Arckiv ., 1913, 
dv.,S. 42. 


CAMUS and ROUSSY. Hypophysectomie et polyurie expArimentales. Compt. Rend. 


MUS and ROUSSY. Hypophysectomie et 
d. 1. Soe. de Bid., 1913, lxxv., Dec. 5, p. 41 


. 483. 

CAMUS and ROUSSY. Polyurie expArimentale par lAaions de la base du cerveau. La 
pd^rurie dite hypophysaire. Compt. Rend. d. 1. Soc. d. Bid. 1913, lxxv., Dec. 26, 




a 



2* 


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ISCOVESCO Contribution k la physiologic du lobe anterieur de rhypophyse. Le 
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CUSHING and GOETSCH. Hibernation and the pituitary body. Proe. Soc. Exp. 
Biol, and Med., 1913, xi., Oct 15,14 (831). 

GOETSCH and CUSHING. The pan anterior and its relation to the reproduction 
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WERSCHININ, N. Uber die Herzwirkung des Pituitrins. PJluger't Archiv , 1913, 
civ., S. 1. 

VOEGTUN, C., and MACHT, D. I. Isolation of a new vasoconstrictor substance from 
the blood and the adrenal oortex. Presenoe of the substance in the blood, and its 
action on the cardiovascular apparatus. Joum. Amor. Med. Assoc., 1913, lxL, 
Dec. 13, p. 2136. 

OTT, I., and SCOTT, J. C. The effect of animal extracts and iodine upon the volume 
of the thyroid gland. Therap. Qaz., 1913, xxix., Nov., p. 781. 

URECHIA and POPEIA. La m4thode d'Abderhalden chez les animaux en dtat de 
tdtanie experimental©. Gompt. Rend. d. 1. Soc. de Biol., 1913, lxxv., Dec. 19, p. 691. 

ISCOVBSCO. Sur les propri^t4s d’un lipoide (II. Bd.) extrait de la partie eorticale des 
capsules aurrlnales. Compt. Rend. d. I. Soc. de Biol. , 1913, lxxv., Deo. 5, p. 510. 

ISCOVESCO. Propri4tds physiologiques d'un lipoide (II. Bd.) extrait de la partie 
mldullaire des capsules surrlnales. Compt. Rend. d. 1. Soc. de Biol., 1913, lxxv., 
Dec. 19, p. 548. 

PSYCHOLOGY. 

MULLER, G. E. Neue Versuohe mit Riickle. ZUch. f. Psychol, 1913, lxviL, S. 193. 

HAZAY, O. v. Gegenstandstheoretische Betrachtungen uber Wahrnehmung und ihr 
Verhaltnis zu anderen gegenstbnden der Psychologic. ZUchr. f. Psychol., 1913, 
lxvii., 8. 214. 

BALEY, S. Uber den Zusammenklang einer groaseren Zahl wenig verschiedener Tone. 
ZUchr. f. Psychol., 1913, lxviL, S. 261. 

PIKLER, J. Empftndung und Vergleioh. I. ZUchr. f. Psychol ., 1913, lxviL, S. 277 

ACKERKNECHT, E. Uber Umfang und Wert des Begriffes “ Gestaltqualitat.’* 
ZUchr. f. Psychol., 1913, lxvii., S. 289. 

KATZ, D., and REVESZ, G. Ein Beitrag zur Kenntnis des Liohtsinns der Nachtvogel. 
ZUchr. f. Sinnesphysiol., 1913, xlviii., S. 165. 

LASAREFF, P. Das Weber-Feehnersohe Gesetz und die Abhangigkeit des Reizwertes 
leuchtender Objekte von ihrer Flachengrosse. ZUchr. j. Sinnesphysiol ., 1913, 
xlviii., S. 171. 

BORCELART, H. Beitrage zur Kenntnis der absoluten Schwellenempfindlichkeit der 
Netzhaut. ZUchr. J. Sinnesphysiol ., 1913, xlviiL, S. 176. 

TRENDELENBURG, W. Versuohe liber binokulare Mischung von Spektralfarben. 
ZUchr. f. Sinnesphysiol., 1913, xlviii., S. 199. 

MINKOWSKI. E. Die Zenkersche Theorie der Far ben perception. ZUchr. f. Sinnes¬ 
physiol., 1913, xlviii., S. 211. 

TRENDELENBURG. W. Eine Beleuohtungsvorrichtung fhr die Anordnung sur 
spektralen Farbenmischung in physiologischen Ubungen naoh v. Kries, Ztschr. f. 
Sinnesphysiol , 1913, xlviii., S. 229. 

YERKES, R. M. Comparative psychology in relation to medicine. Boston Med. and 
Surg. Journ., 1913, oixir., Nov. 27, p. 779. 

SZYMANSKI, J. S. Zur Analyse der sozialen Instinkte. Biol. Ccnlralbl., 1913, 
xxxiii., Nov. 20, S. 649. 

NATZMER, G. v. Zur Psychologic der sozialen Instinkte der Ameisen. Biol. CentrabL, 
1913, xxxiii., Nov. 20, 8. 666. 

SCHILDER, P. Uber das Selbstbewusstsein und seine Storungen. ZUchr. f. d. yes. 
Neurol, u. Psychiat. (Orig.), 1913, xx., Nov. 26, S. 511. 

HEILBRONNER, K. Konstitutionelles Wachtraumen. Als Beitrag zur Pathologic 
des Pertfbnlichkeitsbewusstseins. MonaUsch. f. Psychiat. u. Neurol., 1913, xxxiv., 
Dez., p. 510. 



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3* 


PATHOLOGY. 

CALLISON and MACKENTY. Tumours of the carotid body. Annals of Surg., 1913, 
lviii., Dec., p. 740. 

NOYAK. Uber den Einfluss der Nebennierenausschaltung auf das genitale. Archit 
f. Oynaekol. , 1913, cL, S. 36. 

ABRAMOW and MISCHENNIKOW. Uber die Entgiftung bakterieller Toxine durch 
Adrenalin. Ztschr. f. Jmmunitdtsfor. (Orig. Teil I.), 1913, xx., 8. 263. 

GYENES and STERNBERG. Ueber eine neue und schnelle Methode zum Nacbweis 
der Spirochcete pallida in den Geweben. Berl. klin. Wehnschr., 1913, 1., Der. 
8, S. 2282. 

CLINICAL NEUROLOGY. 

GBJfERAL— 

PARKER, C. H. The nervous system, its origin and evolution. N. Y. Med. 
/oum., 1913, zcviiL, Dec. 13, p. 1167. 

MOLREN, GEORGE A. Metallic Poisons and the Nervous System. Amer. 
Joum . Med. Sci ., 1913, cxlvi., Dec., p. 883. 

SAUER. Uber das Vorkommen einer Lymphoeytose im Blutbild, insbesondere bei 
den funktionell nervosen Leiden und dessen diagnostische und klinische 
Verwertung. Dent. Ztschr. f'. Nervenheilk ., 1913, xlix., S. 447* 

TAYLOR, A. S. Conclusions derived from further experience in the surgical 
treatment of brachial birth palsy (Erb’s type). Amer. Jour. Med. Sci., 1913, 
cxlvi., Dec., p. 836. 


KENNEDY, FOSTER. Myotonia atrophica. Joum. Amer. Med . Auoe., 1913, 
lxi, Nov. 29, p. 1969. 

MORLEY, JOHN. Traumatio intramuscular ossification : its pathology and treat¬ 
ment by excision and autogenous grafting of fascia. Brit. Med . Joum., 1913, 
Dec. 6, p. 1475. 

BOOT, G. W. A case of oongenital myotonia. Joum. Amer. Med. Assoc., 1913, 
lxi., Dec. 20, p. 2237. 

BABONNEIX, M. L. La reaction myotonique. (Rev. g4n.) Qaz. desHdp 1913, 
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SPINAL CORD— 

General.—D’ABUNDO, G. Modificasioni spinali consecutive a lesioni periferiche 
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Fracture, Dislocation, Ac* —ROTH, P. B. The treatment of sooliosis. Med. 
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Herpes Zoster. —LANG WILL H. G. Does Herpes Zoster ever oocur trau- 
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Cervical Rib. —GARDINER, H.— Bilateral cervical ribs. Proe. Roy. Soc. Med., 
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fiplma Bifida. —HOGUET, J. P. Spina bifida. N. Y. Med. Joum., 1913, xcviii. 
Dec. 13, p. 1166. 

Byrlaao-Myelllls.—GARDINER, H.—Case of (?) syringo-myelitio. Proc. Boy. 
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Paraplegia. —SHARPE, WM., and FARRELL, B. P. A new operative treat¬ 
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Tabes Dorsalis.— AUSTREGESILO, A Friihdiagnose der Tabes und der Tabes 
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SIEGRIST. Nervoses Fieber bei Tabes dorsalis. MUnch. Med. Wehnschr., 
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OCZB3AL8KI, K. Bin Fall von Kotbrechen bei gastrischen Krisen. Berl. 
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KAPLAN, D. M. The “ Wassermann-Fast Tabes a serologic precursor of 
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Assoc., 1913, lxi., Dec. 13, p. 2146. 

POGGIO, E. Insufficienza paratiroidea oronica ed innesto di tiroide. Riv. Crit. 
di Clin. Med., 1913, xiv., Deo. 6, p. 769. 

Tetmaws*—MILLION!, LUIGI. Considerazioni e note sulla terapia del tetano. 
Riv. Crit. di Clin. Med., 1913, xiv., Nov. 29, p. 763. 


SPECIAL SEMES AMD CEAMIAL MEEVBS— 

RttBEL, E. Hemianopisches Ringskotom. Klin. Monatsbl. J. Augenheilk. 
1913, li., Dez., S. 706. 

TAKASHIMA, S. Seohs Ffclle der komplizierten heredit&r-famili&ren Opti 
kusatrophie dee Kindes-alters (Behr.). Klin. Monatsbl. f. Augenheilk., 1913, 
1L, Dez., S. 714. 

ASCHER, K. W. Zur Frage nach dem Einfluss von Akkommodation und 
Konvergenz ituf die Tiefeniokalisation und die scheinbare Grouse der Sehdinge. 
Ztschr. f. Biol., 1913, lxii., S. 508. 

MOUGEOT, A. Tachycardie paradoxale des hjpertendus et riflexe oculo- 
oardiaque. Prog. Mid., 1913, xli., Dec. 20, p. 663. 

LOEPER and MOUGEOT. L’absenoe du rdflexe oculo-cardiaque dans le tabes. 
Prog. Mid., 1913, xli., Dec. 27, p. 676. 

ONODI, L. Uber die rhinogenen und otogenen Lttsionen des Okulomotorius, 
Troohlearis, Trigeminus, und Abducens. Ztschr. f. OhrenheUk. u. /. d. Krankh. 
d. Luftwege, 1913, lxix., S. 1. 

STERLING, W. Ueber die Abduoenaltthmungen reflektorisohen und otitieohen 
Ursprungs (Gradenigoeohea Syndrom). Monatssch. f. Psychiat. u. Neurol., 
1913, xxxiv., Dez., S. 668. 

ANTON, W. Uber Mlni&reschen Symptomenkomplex. Prag. Med. Wchnsehr., 
1913, xxxviii., Dez. 11, S. 687. 

MANGOLD, E., and ECKSTEIN, A. Reflektorische Kontraktionen dee Tensor 
tympani beim Mensohen, Internal. Zentralbl. f. OhrenheUk. u. Rhino - 
Laryngol., 1913, xi., S. 603. 

DENKER, A. Uber die Funktion dee akustischen und statischen Apparates bei 
einem Falle von Ageneeie des Kleinhirns. Ztschr . /. Ohrenhetlf. u. f. d. 
Krankh. d. Luftwege, 1913, xx}., S. 173. 

b 



10* 


BIBLIOGRAPHY 


XUCKLUIVMIJ8 SYMPTOMS AMD CASES— 

DANA, CHARLES L. The Future of Neurology. Journ. Nerv. and Merit. Dit., 
1913, xl., Dec., p. 763. 

CLAUDE, H. Defensive Reflexes: their Semeiological and Prognostic Value. 
Med. Prett, 1913, xcvi., Deo. 17, p. 664. 

ZELIONT. Prooede technique pour l’etude de r4flexe musculaires oonditionnels. 
(Premiere com.) Compt. Rena. d. 1. Roe. de Biol., 1918, lxxv., Dec. 26, p. 669. 

BlfSRIEL and DURAND. Bur les paralysies respiratoires. (Suite et fin.) Lyon 
Med., 1913, cxxL, Nov. 30, p. 885. 

BERG MANN, V. Ulcus duodeni und vegeta tives Nervensystem. Berl. klin. 
Wchntchr., 1913, L, Des. 22, S. 2374. 

Mt)NZER, A. Ueber “ Decentralisation ” psyohischer Krankheitserscheinungen. 
Berl. klin. Wchntchr., 1913,1., Dex. 22, S. 2886. 

EISLER Radiologisohe Studien fiber Bexiehungen des Nervensystems xur 
motorischen Funktion des Magens. MUnck. Med. Wchntchr ., 1913, xlix., 
Des. 9, S. 2734. 

REZNICEK. Zur Klinik der posthemiphlegischen Ph&nomene. Dent. Zltckr. f. 
Nervenheilk., 1913, xlix., S. 827. 

BARENNE, J. G. D. D*. Zur Kenntnis der Allofcsthesie. Monatueh. f. 
Ptyckiat. u. Neurol., 1913, xxxiv., Dex., p. 523. 

FAVRE. Zur Frage der Dysbasia angiosclerotioa (“ interznittierendea Hinken ”). 
DetU. Zltckr. f. Nervenheilk., 1913, xlix., S. 293. 

BERTOLOTTI, M. Etude radiologique d’un oas de sol4rodermie. Analogies de 
la sclerodermic avec le syndrome ae Proflchet. Nouv. Icon, de la SalpH., 1913, 
xxvi., p. 291. 

BAGALOGLU and PARHON. Sur un eas de vitiligo k topographie en ceinture. 
Nouv. loon, de la SalpH., 1913, xxvi., p. 309. 

BOKS, D. B. (Edbme congenital familial des extremites inferieures. Nouv. 
loon, de la Salptt., 1913, xxvi, p. 316. 

GEELVINK, P. Ueber Hyperphalangie. Archiv. f. Ptyckiat. u. Nervenkr ., 
1913, lii., S. 1015. 

DZIERZYNSKY, W. Dystrophia periostalix hyperplastioa familiaris. Zltckr. 
f. d. get. Neurol, u. Ptyckiat. (Ong.), 1913, xx., S. 547. 

FLATAU and STERLING. Uber das Symptom der Subpatellardelle. Neurol. 
Gentralbl., 1913, xxxii, Deo. 16, S. 1537. 

REUBEN, M. S., and CLEAVER, E. E. Oxycephaly. Arch, of Ped., 1913, 
xxx., Nov., p. 820. 

LAURAS* G. Les anormaux psyehiques militaires devant la justice. Arckivet. 
d'Antkropol. Grim., 1913, xxviii., Dec, 15, p. 881. 


PSYCHIATRY. 

6IVK1AL PAM ALTSIS— 

NONNE. Der heutige Standpunkt der Lues-Paralysefrage. Deut. Zltckr. f. 
Nervenheilk., 1913, xlix., S. 384. 

SICHEL, MAX. Die progressive Paralyse bei den Juden. Archiv. f. Ptyckiat. 
u. Nervenkr., 1913, m., S. 1030. 

ORTON, S. F. An analysis of the errors in diagnosis in a series of sixty cases of 
paresis. Journ. Nerv. and Ment. Dit., 1913, xl., Dec., p. 779. 

ANTHEAUME and PIQUEMAL. Remission consecutive i un ictus epileptiforme 
et fc une poussee furonouleuse ches un paralytique general taWtique. L'En- 
dphale , 1913, viii., p. 635. 

LEVADITI, MARIE, and MARTEL. Traitement de la paralysie generale par 
injection de serum salvarsanise sous la dure-mfere cerebrals. Compt. Bend , cf. 
1. Soc. de Bid., 1913, lxxv., Deo. 19, p. 567. 



BIBLIOGRAPHY 


11* 


OBREGIA, URBCHIA and POPKIA. Le coefficient ur^^or^toire d’Ambard 
dans la paralysie g^n^rale. Compt. Rend. d. I . See. dt Biol., 1913, lxxv., Dec. 
19, p. 586. 

MARKUS, OTTO. Ueber klinische Diagnoee nnd pathologiaoh-anatomische 
Befande bei Paralyse. Archiv. /. Peyehiat. u. Nervenkr., 1913, lii., S. 1116. 


DEMENTIA PRJECOX— 

TREPSAT. Dessins et Merits d’un dement priooce. L'EnctphaU, 1913, viii., p. 
541. 

ROSS, ELLISON, L. Some forms of urinary nitrogen affeoted by the adminis¬ 
tration of desiccated thyroid to dementia precox patients. Archives I fit. 
Med., 1913, xiL, Dec., p. 746. 


GENEMAIr- 


HTSLOP, THEO. B. The Inheritance of Mental Characters. Joum. State 
Med., 1913, xxi., p. 705. 

PETERY, A. K Some early symptoms of mental disturbances. Med. Record, 
1913, lxxxiv., Dec. 20, p. 1123. 

DAM A YE, H. Demence consecutive k une psychose prolong^. Rev. de 
Ptyehiat ., 1913, xvii., Oct., p. 416. 

PIQUEMAL. Syndrome hypooondriaque ches une debile avant simuie un debut 
de d4menoe senile. Joum. de Neurol., 1913, xviii., p. 421. 

BBSSliSRE, R. Rapports de la paranoia et de la psychose periodique (la 
theorie de Speoht). Rev. de Peyehiat., 1913, xvii., Oct., p. 402. 

SOHNIZER. Die Paranoiafrage. Ztechr. f. d. get. Neurol, u. Peyehiat. (Ref.), 
1913, viii., S. 313. 

BIsINON, R. Manic et idiotie. Nouv. Icon, de la Salptt., 1913, xxvi., S. 358. 


HOOPER, J. W. D. Homoplastic transplantation of one ovary into a woman 
suffering from amenorrhcea associated with insanity. Australian Med. Joum., 
1913, ii., Nov. 15, p. 1297. 

JAHNEL, F. Bin Beitrag zur Kenntnis der geistigen Stdrungen bei der 
Eklampsie. Archiv. f. Peyehiat. u. Nervenkr., 1913, Hi., S. 1095. 


FBRRAND, J., and PIQUEMAL. Delire de persecution avec hallucinations 
auditives cauiees par un etat obsedant ohes un cydothymique. Considera¬ 
tions j^sychiatriques et medioo-iegales. Oaz. dee Hdp., 1913,1 


, lxxxvl., Dec. 30, 


CHAUFFARD. Sur deux oas de saturnisms. Determinations viscerales, 
paralysies fonctionnelles ohes les saturnine. Joum. dee Prat., 1913, xxvii., 
Dec. 20, p. 823. 


ROBEY, W. H. The nervous irritability of chronio renal disease. Boston Med. 
and Surg. Joum., 1913, clxix., Dec. 4, p. 817. 

QENIL-PERRIN, G. La psychiatric olinique dans roBuvre de Felix Pater. 
Rev. de Peyehiat ., 1913, xvii., Oct., p. 424. 

MERCIER, C. A. The oonoept of Insanity. Proe. Roy. Soc. Med., 1913, vii., 
Nov. (Sect. Psychiat.), p. 3. 


SJOBRING, H. Den individualpsykologiska fragestkllingen inom psykiatrien. 
Upeala Lakaref&r. F&rhandl., 1913, xix., S. 1. 

BIRNBAUM, K. Der Konstitutionsbegriff in der Psyohiatrie. Zteehr. J. d. gee . 
Neurol, u. Peyehiat. (Orig.), 1913, xx., S. 520. 

TREADWELL, O. F. N. Oonduot of the feeble-minded criminal. Med. Preee, 
1913, xovi., Dec. 24, p. 695. 

FRIEDMAN, H. M. The criminal’s plaoe in psychiatry. N. Y. Med. Joum., 
1913, xcviii., Nov. 29, p. 1058. 

DECROLY. Examen mental des enfants anormaux. Joum. de Neurol., 1913, 
xviii., pp. 381 et 401. 



12* 


BIBLIOGRAPHY 


MAAS, S. Psychiatrisohe Erfahrungen mit dam Abderhaldenschen Dialitierver- 
fahren. Ztsehr. /. d. gts. Neurol . u. Psychicd. (Orig.), 1913, xz., S. 561. 

FRIEDLANDER. A. Ueber die Anwendung pyrogenetiacher Mittel in der 
Psyehiatrie. Archiv f. Psychiat. u. Nervenkr ., 1913, liL, 8. 981. 

ALZHEIMER, A. 25 Jahre Psychiatric. Bin Ruokblick anlfcsalich dea 25 
ifchrigen Jubilfcums von Prof. Dr Emil Sioli ala Direktor der Frankfurter 
Irrenanstalt. Archiv f. Psychiat. u. Nervenkr ., 1913, lii. t S. 853. 

LUCAS, W. P. Note on aome problema of the adoleecent aa seen in the Psycho- 
patbic Hoapital Out-patient Department, Boaton, Maaaachuaetta. Boston Med . 
and Surg. •fotim., 1913, clxix., Nov. 27, p. 782. 

SOUTHARD, E. E. The Paychopathic Hoapital Idea. Joum. Anver . Med. 
Assoc*. 1913, lxi., Nov. 29, p. 1972. 

HALL, H. J. Hoapital and Aaylum Workshopa: Some poaaibilitiea of handi¬ 
capped labour. Joum* Amer. Med. Assoc., 1913, lxi., Nov. 29, p. 1976. 


TREATMENT.* 

WISZW1ANSKI. Der diagnoetiche und therapeutiache Wert der Nervenmassage. 
Ztcchr. /. Physikal . u. JJidi. Therapie , 1913, xviL, S. 738. 

POST. Die Nervenpunktlehre von Cornelius und die achwediache Massage. Mtinch . 
Med. Wchnschr ., 1913, xlix., Dez. 9, S. 2732. 

OBRRNDORF, C. P. The aoope and technique of psychoanalysis. Med. Record, 1913, 
lxxxiv., Nov. 29, p. 973. 

FRINK, H. W. The Freudian Conception of the Payohoneuroeea. Med. Record , 1913, 
lxxxiv., Nov. 29, p. 967. 

* A number of raferanoea to papers on Treatment are inolaUed in the Bibliography under 
individual dlaaaaaa. 



Bibliography 


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JEFFERSON, S. A note on the sulcus post-centralis superior. A not. Anzcig 1913, 
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LANDAU, E. Uber die Furchen an der Lateralfl&che des Grosshirns bei den Ersten. 
Mit 60 dioptrogr. Abbildungen von 30 Gehirnen. ZUchr . /. Morphol. u. ArUhropd ., 

1913, xvi., 8. 239. 

KURZ. Zwei Ghinesengehirne. Bin Beitrag zur Rassenanatomie. ZUchr . /. MorpkoL 
if. Anthropoid 1913, xvi, S. 281. 

LANDAU, E. Uber verwandtschaftliche Formbildung der Grosshirnwindungen an 
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HOCH8TETTER. F. Uber die Bntwickelung der Plexus ohorioidei der Seitenkammern 
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LAIGNEL-LAVASTINE and JONNE8CO. Sur la structure physique de la oellule 
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MALONE, E. F. Recognition of members of the somatic motor chain of nerve oells bv 
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in oertain regions of the mammalian brain. A not. Record. 1913, vii, March, p. 67. 

WEBER, A. Phlnom&nes de dlglnlreeoence dans les cellules on activity oaryocindtique 
du tube nerveux d’embryons de Slladens. Anal. Anzcig ., 1913, xliv., Aug. 21, 
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LUNA, E. Sulle modifioaxioni dei plastosomi delle oellule nervoee nel trapianto ed in 
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AMIN, M. The oourse of the phrenic nerve in the embryo. Joum. Anat. and Phy$icl. % 

1914, xlviii., Jan., p. 215. 

GRAPBR, L. Die Rhombomeren und ihre Nervenbeziehungen. Arekiv f. mikr. Anal.% 
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BINDEWALD, C. A E. Das Vorderhim von Amblyttoma mcxicanum. Arch. f. 
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WATSON, D. M. 8. Some notes on the Anomodont brain case. Anal. Anzcig ., 1913, 
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DBL8MAN, H. G. 1st das Hirnblaschen des Amphioxus dem Gehirn der Kranioten 
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FRANZ, V. Faserauatomie dee Morayridengehirns. Anal. Anzcig ., 1913, xlv., Dez. 
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BOBKE, J. Die doppelte (motorisohe und sympathische) efferente Innervation der 
quergestreiften Muskelfasern. Anat. Anzcig.. 1913, xliv., Aug., 8. 343. 


PHYSIOLOGY. 

ANDIU&-THOMAS and DURUPT. Lee localisations e4r4belleuses (verification anato- 
mique) fonctions des centres du lobe lat4raL (4 fig.) Rev. Neurol ., 1913, xxi, 
Dec. 30, p. 728. 

CITRON, J., and LESOHKE, E. Ueber den Binfiuss der Ausschaltung des Zwisohen- 
hirns auf das infeotibse und niehtinfeetiose Fieber. ZUchr. f. Exp. Path . u. Thcrap ., 
1913, xiv., 8. 379. 



14* 


BIBLIOGRAPHY 


DITTLER, R , an<l ur>TTllKR t HANS. liber die Aktionssfcrome menschlicher Muakela 
bei naturlicher Innervation, nach Untersuchungen an geaunden und kranken 
Menschcn. Piiujer s Archiv 1914, civ., S. 251. 

FULLE, C. Sulle compensazioni organiche e funziouali della deficienze cerebellari. 
Archivio di FtsioL, 1015, xi., Luglio, p. 370. 

LEEUWKN, W. S. v. Druckfehlerbericlitigung zu der Arbeit “Quantitative pharma* 
kologische Unternuchungen uber die Retfexfunktionen des Riickenxnarkes an Warm* 
bluteru in Band 154 Seite 307." Ptimer's Archiv., 1914, civ., S. 350. 

MARTIN, E. G., and LACEY, W. H. Vasomotor reflexes from threshold stimulation. 
Amcr. Joum. Physiol ., 1914, xxxiii., p. 212. 

EDWARDS, D. J. A study of the anatomy and the vasomotor phenomena of the 
sympathetic neivous system in the turtle. Amcr. Joum. Physiol. , 1914, xxxiii., 
p. 229. 

GRUBER, C. M. Studies in Fatigue. II. The Threshold Stimulus as affected by 
Fatigue and Subsequent Rest. Amer. Joum. Physiol., 1913, xxxii-, p. 438. 

NICE, L. B. Thresholds for faradio stimulation of the respiratory reflex and of the 
phreuic-diaphragm preparation. Amcr. Joum. Physiol 1914, xxxiii., p. 204. 

ASHER, LEON, and PEARCE, R. G. Die sekretorische Innervation der Niere 
Ztschr. f. Biol., 1914, lxiii., S. S3. 

KENT, A. F. S. Neuro-muscular structures in the heart. Proc. Roy. Soc.. 1914, 
Ser. B, Vol. Ixxxvii., p. 198; Journ. Physiol., 1913, xlvii. (Proc. Physiol. Soc,, 
1913, Nov. 15, p. wii.). 

ROSENHEIM, OTTO. The galactosides of the brain—I. Bioehem. Joum., 1913, rii., 
Dec., p. 604. 

CLAUDE, H., and PORAK, RENE. Sur l'action hypotensive de certains extraits 
hypophysaires. Presse Med., 1914, Jan. 10, p. 25. 

ABRAMOW, S. Uber die Veninderungen der Hypophyse bei der experimcntelUn 
Diphtheric. Virchow's Archiv., 1913, ccxiv., S. 408. 

BOUIN and ANCEL. Sur un procede d isolement de la substance active du lobe 
posterieur hypophysaire. Compt. Bend, d . 1. Soc. d. Biol., 1914, lxxvi., pp. 62 
and 110. 

TRENDELENBURG. W. Uber die Beziehung der Nebennieren tur normalen Blut- 
druckhohe. Ztschr. f. Biol., 1914, lxiii., S. 155. 

PICARD. Ueber Jen Einfluss der Muskelarbeit auf den Cholesteringehalt des Blutea 
und der Nebennieren. Archiv. f. Exp. Path, u. Pharm, 1913, lxxiv., 8. 450. 

1SCOVESCO. Sur les proprietes d’un lipoide (II. Bd.) extrait de la partie corticale 
des capsules surrdnales. Compt. Rewi. d. I. Soc. d. Biol., 1914, lxxvi., p. 510. 

JANOSIK, J. Correlations fonctionnclles ontre les capsules surrenales etlesglande* 
gonitales. Arch, de Bio/., 1913, xxviii., p. 627. 

SMITH, E. V., and BRODEltS, A. C. The iodin content of the thyroid gland, with 
especial reference to the pathologic types, and a review of some experimental work. 
Journ. Amer. Med. Assoc., 1914, lxii., Jan. 10, p. 113. 

MARINE. DAVID. Observations on tetany in dogs. Relation of the parathyroid* 
to the thyroid; relation of tetany to age, amount of parathyroid tissue removed, 
accessory parathyroids, pregnancy, lactation, rickets, sulphur and diet; relation of 
parathyroids to sugar tolerance ; effect of calcium salts. Joum. Exp. Med., 1914, 
xix., Jan., p. 89. 

KEETON, R. W. The secretion of the gastric juice during parathyroid tetany. Amer. 
Joum. Physiol., 1914, xxxiii., J an., p. 25. 

STOLAND, O. O. The influence of parathyroid tetany on the liver and the pancreas. 
Amer . Journ. Physiol., 1914, xxxiii., Jan., p. 2^3. 

TSCHIRJEW, S. Elektrische Erscheinungen am tierischen Muskcl- und Nerven- 
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COHN, A. E. The Effect of Morphin on the Mechanism of the Dog’s Heart after 
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COHN, A. E., and LEWIS, T. The Predominant Influence of the Left Vagus Nerve 
upon Conduction between Auricles and Ventricles in the Dog. Joum, Exp . Med ., 
1913, xviii., Dec., p. 739. 


BIBLIOGRAPHY 


15* 


ELIAS, H. Store und Nervenerregbarkeit. Witn. Jdin. Wchnsehr., 1914, xxrii., 
Jon. 8, S. 21. 

OHRWALL, H. Oibt ei viauelle Bewegungsempfindungen ? Skand. Arehiv /. 
Physiol., 1918, xxx., S. 229. 

TIGER8TEDT, CARL, and DONNER, SVEN. Zur Kenntnis der positiven Nach- 
schwankung dee Nervenstromea bei niedrigor Temperatur. Skand. Arehiv f. 
Physiol., 1913, xxx., S. 309. 


PSYCHOLOGY. 

SANFORD, E. C. Psychic research in the animal field : Der klnge Hans and the 
Elberfcld horses. Amer. Joum . Psychol ., 1914, xxv., Jan., p. 1. 

FINKENBINDER. E. O. The remembrance of problems and of their solutions: a 
study in logical memory. Amer. Joum, Psychol ., 1914, xxv., Jan., p. 82. 

POFFENBERGER, A. T. The effects of strychnine on mental and motor efficiency. 
Amer. Journ Psychol., 1914, xxv., Jan., p. 82. 

FERNBERGER, S. W. A simplification of the practice of the method of oonstant 
stimuli. Amer. Joum. Psychol ., 1914, xxv., Jan., p. 121. 

W1LMANNS, KARL Ein Beitrag zur Psychologic der Kinderaussagen vor Gericht. 
Vierteljahrs. f. gcrichtl. Med., 1914, xlvii., Jan., S. 102. 

MARCUSE, H. Psychische Erregung und Hemmung vom Standpunkt der JodTschen 
Psyohologie. Arehiv f. Psychiat., 1914, liii., S. 262. 

TAYLOR, G. H. The emotions and their relation to the mind. Austral. Med. Oaz., 
1913, xxxiv., Oct. 4, p. 315. 

CRAEMER, OTTO. Zur Psychopathologie der religidsen Wahnbildung. Arehiv f. 
Psychiat., 1914, liii., S. 2#6. 

BLOCH, E. Die Intelligenzpriifung nach der Methode von Binet>Simon in ihrer 
Bedeutung zur Erforschung des Schwachsinns bei Schulkindem. Ztschr. f. 
Jugendl. Schwachsinns , 1913, vii., S. 272. 


PATHOLOGY. 

ROUBINOVITCH and BARBE. Un cas d’ag^n&ie partielle du corps calleux. (2 pi.) 
Nouv . Icon. d. 1. Salptt., 1913, xxvi., p. 407. 

STEIN, F. W. Die Bedeutung der mehrkernigen Ganglienzellen. Ztschr. f. d. ges. 
Neurok u. Psychiat., 1914, xxi. (Orig.), S. 461. 

MEYER, OSKAR. Ein besonderer Typus Riesenzellengliom. Frankfurter Ztschr. f. 
Path., 1913, xiv., S. 185. 

HENRICH, ERNST. Ubcr das diffuse Gliom des Pons und der Medulla oblongata. 
Frankfurter Ztschr. f. Path., 1913, xiv., S. 294. 

FRANK, A. Uber subependymtre Gliaknoten. Frankfurter Ztschr. f. Path., 1913, 
xiv., S. 450. 

v. PODMANICZKY. Die faserige Glia bei Arteriosklerose der Kieinhimrinde. 
Frankfurter Ztschr. f. Path., 1913, xiv., S. 395. 

FISCHER, O. Ein Beitrag zur forensischen Bedeutung der histopathologischen Unter- 
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8ARTESCHI, U. La sindrome epifisaria 14 macrogenitosomia preoooe w ottenuta 
sperimentalmente nei mammiferi. Pathdogica, 1913, v., Die., p. 707. 

LtJTTGE. Uber einen besonderen histologischen Befund aus dem Gebiete der 
fruhinfantilen familiftren Erkrankungon des Nervensvstems. Deut. Ztschr. f. 
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MCHLMANN, M. Das Nervenpigment beim Papagei. Virchow*s Arehiv , 1913, 

ocxiv., S. 412. 

PASTINB, C. Valore dell’estensione spontanea dell’alluce nolle lesioni dalle vie 
piramidali. Riv. di Patol. nerv. e ment., 1914, xix., Gennaio, p. 21. 



16* 


BIBLIOGRAPHY 


MARIE, A. Activation de la toxin# t4tanique. Annales de VInstxtut Pasteur, 1914, 
xxnii., Jan., 8. 1. 

VOLPINO, G. Recherche# ear la culture du virus rabique eelon Noguchi. Prtsse 
M, 1914, Jan. 88, p. 79. 


CLINICAL NEUROLOGY. 

RRNBRAL— 

HOWELL, C. M. HINDS. Trauma in relation to oertain aspects of nervous 
dis ease . Lancet, 1914, clxxxvi., Jan. 31, p. 302. 

JONES, D. W. OARMALT. Gait in nervous disease. Practitioner , 1914, xcii., 
Jan., p. 13. 

KAUFFMANN, ELSA. Klinischer und anatomischer Beitrag cur Frage der 
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SCHAFFER, EL Zur anatomischen Wesensbestimmung hereditkrer Nerven- 
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MINGAZZINI, G. Remarque additionnelle k ma note: “ Sur quelques petite 
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WILSON, S. A. KINNIER. A lecture on some oommon errors in the diagnosis 
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MlfftCW- 

SPILLER, WM. G. The relation of the myopathies. Brain, 1913, xxxvi., p. 75. 

BRUCE, A. NINIAN. Spinal changes in pseudo-hypertrophic paralysis. Edin. 
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COURTNEY, J. W., and EATON, H. B. A case of myatoma congenita 
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SCUDERI, ALFIO. Su di un caso di atrofia musoolare da intoesioaxione saturnine. 
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AUSTREGESILO. Sur un oas d’atrophie musculaire chez un n&gre. (1 pi.) 
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•PINAL CORD— 

General. —GROBER. Akute bedrohliohe Erkrankungen dee Rtiokenmarks und der 
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CUIFFINI, P. Klinischer und pathologisch-anatomischer Beitrag sum Studium 
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KIDD, PERCY, and TOZER, E. A. Combined sclerosis of the spinal oord and 
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WARRINGTON, W. B. Acute generalised infective paralyses in adults. Liver¬ 
pool Med.-Chir. Journ., 1914, No. 66, Jan., p. 67. 

Fracture, Dislocation, Ac.— BATTLE, W. H. Bullet wound of the spine. A 
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DESFOSSES, P. Quelques travaux reoents sur la soolioae. Prtsst Mid., 1914, 
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NAGEOTTE-WILBOUCHEWITCH. La scoliose par malformation de la 
cin^ui&me vert^bre lorobaire et son traitement. Arch, de Mid. des Enf., 1914, 
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ENGELMANN, G. Ueber das Liegendtragen der Kinder und die HMuflgkeit der 
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Cervical Rib.—HERTZ, A. F., and JOHNSON, W. Cervical rib with marked 
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Spina RlSda.—STONEY, R. A. Spina bifida. Clin. Journ., 1914, xlUi., Jan. 14, 
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SCHABNKB. Enuresis und Spina bifida ooculta. Archiv f. Psychiat ., 1914, 
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PFANNER, W. Ueber einen Fall von Spina bifida ooculta sacralis mit Blasen- 
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Tabes Dorsalis. —FRUGONI, C. Contributo alio studio delle 1 * crisi ematemetiohe 
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BIELHER, M. DE. Maladie de Heine-Medin, considerations relatives k 
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SUTHERLAND, G. A. Anterior poliomyelitis: paralysis of abdominal muscles; 
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ENGELMANN, GUIDO. Uber ein an Poliomyelitiskranken beobachtetes 
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LOVETT, R. W. Principles of the treatment of infantile paralysis. Journ. 
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WHITMAN, R. Further observations on the operative treatment of paralytic 
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LUST and ROSENBERG. Beitrag zur Aetiologie der Heine-Medinsohen Krank- 
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DUBOIS, NEAL, and ZINGHER. Experimental Studies in Poliomyelitis. 
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Paraplegia.— NORRIE, H. Spastic paraplegia treated by Foerster’s method of 
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MARIE, PIERRE, and FOIX, CHARLES. Sclerose intra-clrlbrale centrolobaire 
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KNAPP, P. C. Two cases of removal of extra-dural tumour of the spinal cord. 
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BRAIN— 

General, —RAUZIER and BAUMEL. Tuberculomes multiples du oerveau et des 
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RENTON, J. C. Clinical Lecture on Cranial Cases. Clin. Journ., 1914, xliii., 
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MEYER, W. Dammerxusthnde mit naohfolgender Amnesic bei leiohter Com¬ 
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Meningitis* —WARRINGTON, W. B. Intracranial serous effusions of inflamma¬ 
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HESS, J. L. Leukocyte counts in pneumonia and oerebro-spinal meningitis. 
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BOECKMANN. Ein Beitrag zur Atiologie der Pachymeningitis interna 
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WOHLWILL, FR. Uber Pachymeningitis hjemorrhagioa interna. Virchow 1 1 
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SNESSAREFF. Du processus de reparation dans le oerreau. Un cas de 
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Hydrocephalus.—THOMAS, W. 8. Experimental hydrooephalus. Journ. Exp. 
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RITTERSHAUS, E. Zur Frags der Hydrooephalie. ZUchr. f. Jugtndl. 
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Hsmorrhage.—MACFARLANE, A. Venesection in cerebral haemorrhage, with 
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Hemiplegia.—JONES, A. WEBB. Two cases of post-operative hemiplegia. 
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Facial Paralysis.—BALLANCE, C. A Facial palsy following a mastoid opera* 
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PITRES and ABADIE. H&nispasmes synoindtiques de la faoe lids au dignement 
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Facial Hemiatrophy.—GRABS, E. Ein Fall von Hemiatrophia faciei progressiva. 
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Cerebral A rterlo-Sclerosis.—SCARPINI, V. Sopra un caso d’arteriosderosi 
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Cerebellar Ataxia.—SPRAWSON, C. A. A family with oerebellar ataxia. Brit . 
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Amaarotlc Family Idiocy.—BIELSCHOWSKY, M. Uber sp&tinfantile familiare 
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Tumours.—ZANELLI, O.-F. Tumeur sons-corticale des lobes prdfrontaux ot du 
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LAS ARE W, W. Uber eine Stoning der Innervation des N. facialis bei Gesch- 
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SCHLESINGER, HERMANN, and SCHILLER, A. Uber die Kombination von 
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COSTANTINI, F. Tumoro della faccia interna dei lobi prefrontali e della parte 
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MINGAZZINI, G. Studi sulla semcjologia dei turnon delle varie tone del lobo 
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SPILLEll, WM. G. Some causes of disappointment in operations on brain 
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CHAMPION, E. Tumour of brain. Australian Med. Journ., 1914, ii, Jan. 3, 
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Fit Hilary Tnmears, Ac.—TAYLOR, A. L. A case of tumour of the pituitary 
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GOETSCH, E. The pituitary body. Critical review. Quart. Journ. Med., 

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HI a betet Insipid ms.—HERRIN GHAM, W. P. A case of diabetes insipidus. 
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ROMER, C. Die Beziehungen zwischen der Funktion der Hypophysis cerebri 
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SIMMONDS. Ueber seknndfcre Geschwiilste des Hirnanhangs und ihre Bezie¬ 
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Aphasia, de,—FROSCHELS, EMIL. Ueber die Behandlung der Aphasien. 
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FROMENT and MONOD. La reeducation des aphasiques moteurs. Lyon mid., 

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FUNK, CASIMIR. Studies on pellagra. I. The influence of the milling of 
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Aehendroplasla.— BEFANI, G. C. Una alienata acondroplasica. Rassegna di 
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SEQUEIRA, J. H., and FILDES, PAUL. Case of syphilis showing Noguchi's 
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POST, ABNE R. Mortality of hereditary syphilis. Boston Med. and Surg. Joum ., 

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M'DONAGH, J. F. R. The biology of syphilis. Med. Press, 1914, Jan. 14, 
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SAUNDBY, R. Syphilitic paralysis of the oesophagus. Brit . Med . Joum., 
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COCKIN, R P. Treatment of yaws by intramuscular injections of salvarsan. 
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Me—alvarian.—FISHER, E. D. Present status of neosalvarsan in the treatment 
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WESSON, M. B. Clinical report of a case of rabies treated with neosalvarsan 
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Cerebre-Splnal Flwtd.— SOPER, W. E„ and GRANAT, S. The urea content of 
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CLARK, L. P., and CALDWELL, E. W. The sella tardea in some epileptice. 
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MAYS, T. J. The therapeutic value of crotalin in the treatment of epilepsy. 
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Megrim.—STEPHENSON, 8. Migraine and Eye-strain. Clin. Joum., 1914, 
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Mysterfla.—NEWMARK, L. Hysteric blindneee of both eyes in elderly men. 

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Cherea.—LANG MEAD, FRED. On the diagnosis, prognosis, and treatment of 
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RICHARDS, JOHN H. Chorea; with report of two cases in which Streptococcus 
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GRACE, JOHN J. Note on the treatment of sciatica. Lancet, 1914, clxxxvi., 
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BRIEGER, L. Die Behandlung der Iechiae mit Bewegungebhdern. Berl. Idin. 
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d 



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24* 


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e 


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BOENNINGHAUS, GEORG. Ein Beitrag sur Kenntnis der Meningitis aerott 
venfcricularis acuta. Ztschr . /. Ohrenheilk , Ac., 1914, Ixx., S. 23. 

SCHRODER. Ein Fall von labyrinthogener Cerebrospinalmeningitis mit 
eigenartigem Verlauf durch Influenzab&zillen. Ztschr. /. Ohrenheilk, Ac., 1914, 
lxx., S. 27. 

AUDRY, CH., and LAVAU. Sur lea mdningites prdrosdoliques. AnnaUs de 
Dermatol, tt Syphil., 1914, v., Jan., p. 29. 

llydroeephalo*.—HEELE. Ueber die chirurgiscbe Bebandlung des Hydro* 

zephalus. Fortsch. d. Med.. 1914, xxxii., Jan., p. 72. 

Abeeess. —DICK, G. F., and EMGE, L. A. Brain abscess caused by fusiform 
bacilli. Journ. Amer. Med. Assoc., 1914, lxii., Feb. 7,p. 446. 

REYNOLDS, C. B. A case of brain abscess. Journ. Amer. Med. Assoc., 1914, 
lxii., Feb. 7, p. 449. 

BERNSTEIN, B. P. Brain abscess due to the bacillus Colt communis. Med. 
Record, 1914, lxxxv., Feb. 7, p. 249. 

ELSCHNTG, A. Der orbitogene Himabezess und seine Operation. Prayer Med. 
Wchnschr 1914, xxxix., Feb. 5., S. 37. 



BIBLIOGRAPHY 


29* 


PIFFL, OTTO. Zur Kazuistik der rhinogenen Stirnhirnabzeese. Prayer Med. 
Wchntehr., 1914, xxxix., Feb. 6, S. 89. 

MARGUUES, A. Znr Frage des orbitogenen Stirnhiraabszesse*. Prayer Med . 
Wchntehr ., 1914, xxxix., Feb. 5, S. 41. 

Haemorrhage.—BAWLING, L. B. Decompression of the brain in intracranial 
haemorrhage: the value of the operation in oases the outcome of aocident or 
disease. Lancet , 1914, clxxxvi., Feb. 21, p. 529. 

SCHEER, W. M. Zur Klinik des Haematoma subdurale nebst Bernerkungen 
tiber das Verhalten desf Babinakischen Zehenph&nomens und liber den Wert 
des Perkussions-Auskultitionsverfahrens am Sch&del, zur Erkennung epi- und 
subduraler Blutungen. Ztschr. f. d. yet. Neurol, u. Ptychiat ., 1914, xxiii. 
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KIRCHNER, KARL. Blutung aus einem Zweig der Arteria meningea media bei 
Paukenhohlentuberkulose. Zttchr. f. Ohrenheilk , dec., 1914, Ixx., S. 85. 

Facial Paralysis.—ZESAS, D. G. Neuere operative Verfahren zur Behandlung 
der peripheren Facialisl&hmung. Centralbl. f. d. Grenzyeb. d. Med. u. Chir. f 
191^ xviii., Feb., S. 141. 

Momoplegla.—STEWART, PURVES. Hysterical brachial monoplegia. Proe. Boy. 
Soc . Med.. 1914, vii., Jan. (Neurol. Sect.), p. 24. 

Hemiplegia.—PALMER, H. S. Congenital heart disease and hemiplegia. Proe . 
Boy. Soc. Med ., 1914, Jan. (Clin. Seot.), p. 48. 

TURNEY, H. G. Sclerodermia; neuropathic oedema; functional hemiplegia. 
Proe. Boy. Soc. Med., 1914, vii., Jan. (Neurol. Sect.), p. 18. 

BARD, L. De la perte hdmiopique du rlflexe palpebral dans les h4mipl4gies. 
Sem. Mid., 1914, xxxiv., Jan. 14, p. 13. 

W1THJLNGTON, C. F. Pneumonic hemiplegias. Amer. Joum. Med. Sei., 
1914, cxlvii., Feb., p. 203. 

Neirtas.—SEQUEIRA, J. H. Multiple neuromata. Proe. Boy. Soc. Med., 1914, 
vii., Jan. (Dermatol. Sect.), p. 67. 

Cerebellar Ataxia.—BUZZARD, E. F. Acute cerebellar ataxia in an adult. 
Proe. Boy. Soc. Med., 1914, vii, Jan. (Neurol. Sect.), p. 22. 

BATTEN, F. E. Cerebellar ataxia. Proe. Boy. Soc. Med., 1914, vii., Jan. (NeuroL 
Sect.), p. 22. 

Taasoars.—OPPENHEIM, H. Bemerkung zu der Mitteilung Lasarews: “Uber 
cine Stoning der Innervation des N. facialis bei Gesoh wills ten der hinteren 
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BATTEN, F. E. Glioma of the oerebeUum; recovery after simple drainage of 
cyst. Proe. Boy. Soc. Med., 1914, vii., Jan. (Neurol. Sect.), p. 23. 

ntaltary Tumears, Ae.—SZILY, A. v. Ueber Hypophysisoperationen. Klin. 
Monaltbl. f. Auyenheilk., 1914, lii., S. 202. 

SIMMONDS, M. Ueber Hypophysfsschwund mit todlichem Ausgang. Deut. 
Med. Wchntchr., 1914, xl., Feb. 12, S. 322. 

llabetei Insipid ms.—JEWETT, D. B. Hypophyseal disease as related to 
diabetes insipidus, with report of two cases. Med. Becord, 1914, lxxxv., 
Feb. 7, p. 242. 

ImfkmUlIsm.—GILFORD, HASTINGS. Infantilism. Lancet, 1914, clxxxvi., 
Feb. 28, p. 587. 

Aphasia, Ac.— FROMENT and MONOD. La reeducation des aphasiques 
moteurs. Lyon mid., 1914, exxii., Feb., pp. 213, 283, et 329. 

SALOMON, E. Motorische Aphasie mit Agrammatismus und sensorisch- 
agrammatisohen Stdrungen. Monatttch. f. Psyehiat. u. Neurol., 1914, xxxv., 
S. 181. 

STERN, HUGO. Die Grundprinzipien der spraoh&rztliehen Behandlung 
Aphasischer. Wien. Med. WchnteKr., 1914, bdv., Feb. 14, S. 247. 

BONHOEFFER, K. Klinischer und anatomischer Befund zur Lehre von der 
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Neurol., 1914, xxxv. (Orig.), S. 118. 




30* 


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BOX, C. R. Clinical lecture on pellagra as it has appeared in Great Britain. 
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Sypfcllls.—PROCA, DANILA, and STROR. Snr les spirochetes “ inter- 
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PROCA, DANILA, and STROE. Spirochetes “ interm&Liares ” et cuti-r&otion 
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CUNNINGHAM, JOHN H. Progress in the diagnosis and treatment of syphilis. 
Boston Med. and Surg. Joum., 1914, clxx., Jan. 29, p. 151. 

Salvarsam.—KOHRS. Ueber einen weiteren Todesfall an akuter Encephalitis 
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M‘ADAMS, P. S. The effect of “ 606 ” on the eye, with the report of seven oases 
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SCHMITT, A. Intramnskulare Salvarsandepots und deren Folgerustknde im 
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SCHUBEL, K. Ueber das Schicksal des Arsens naoh snbkntaner und intra- 
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SMITH, C. M. Have the early olaims of salvarsan been realised? Boston Med. 
and Surg. Joum., 1914, clxx., Feb. 19, p. 269. 

MeesalvarsanL—PURCKHAUER, R., and MAUSS, TH. Bin Fall von Poly¬ 
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Milnch. Med. Wehnschr., 1914, lxi., Feb. 24, S. 423. 

ABELIN. Uber das Vorhalten des Neosalvarsans und des Salvarsans im Or- 
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Watsermamn Reaction.—'THIELE, F. H., and EMBLETON, D. Methods of 
increasing the accuracy and delioaoy of the Wassermann reaction. Lancet, 
1914, olxxxvi., Feb. 21, p. 526. 

LANGER, HANS. Eine durch Watte bedingte FehlerqueUe bei der Wasser- 
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THOMAS, B. A., and IVY, R. H. Use of cholesterinised Antigens in the 
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OLMSTEAD, M. P. The value of absorption methods in the Wassermann 
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CerebrO'&pInAl Field.—MACPHAIL, H. D. The albumen in the cerebrospinal 
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BLOCH and VERNES. Un aigne r^trospectif de la syphilis: hyperalbuminose 
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BABES. La xanthochromie du liquide olphalo-rachidien ohes les asystoliquee. 
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GENERAL AND FUNCTIONAL DISEASES— 

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DONATH, JULIUS. Sedobrol in der Behandlung der Epilepsie. Wien. klin. 
Wehnschr., 1914, xxvii., Feb. 19, S. 182, 



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POPE, CURRAN. Chronic malarial cachexia and its relation to neurasthenoid 
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MAURICE. Le neurasthdnique mdningopathe. Lyon mid., 1914, xxxii, 
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FEVER, C. W. lx. The eyes of the neurotic. N.Y\ Med. Joum ., 1914, 
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CUNNINGHAM, W. P. Dermatoses neurotic*. N.Y. Med. Joum. % 1914, 
xeix., Jan. 31, p. 225. 

Nenritts.—PRIEST, R. C. Some observations upon thirty-one oases of multiple 
peripheral neuritis amongst European troops in India. Joum. Roy. Army 
Med. Corps , 1914, xxii., Feb., p. 178. 

CHAMBERLAIN. W. P. The etiology of Oriental beri-beri. Character of the rioe 
which eausee polyneuritis in man and fowls. N.Y. Med. Joum., 1914, xcix., 
Feb. 7, p. 263. 

HEISER, V. G. Beri-beri: An additional experience at Culion. How oan a 
knowledge as to its prevention best be applied from the standpoint of state 
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SHLBAYAMA, S. The present state of the study of beri-beri in Japan. Med. 
Press, 1914, oxlvii., Feb. 4, p. 119. 

Neuroses.—WALLACE, R. The traumatic neuroses, due to alleged or actual 
injury, from the medicolegal standpoint Med. Record, 1914, lxxxv., Feb. 28, 

CLARK, L. PIERCE, and BUSBY, A. H. Value of Roentgen analysis of gastro¬ 
intestinal tract in some types of so-called functional nervous disorders. Joum. 
Amer. Med. Assoc., 1914, lxii., Feb. 7, p. 440. 

WALTON, G. L. Certain phases of the psychoneuroses and their possible 
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CLARK, L. PIERCE. Some observations upon the etiology of mental tortioollis. 
Med. Record, 1914, lxxxv., Feb. 7, p. 232. 

CLARK, L. PIERCE. A further study upon mental tortioollis as a psycho- 
neurosis. Med. Record, Feb. 28, p. 371. 

Psychoses.—PILOZ, A. Psychosen bci inneren Krankheiten. Med. Klinik, 1914, 
x., Feb. 22, S. 313. 

KASTAN, MAX. Psyohosen, Abbau- und Fermentspaltungsvorginge. Deut. 
Med. Wchnschr., 1914, xL, Feb. 12, S. 819. 

OBR^GIA, URBOHIA, and OIAUSB8CO. Le OMffieient orfe-afcrtftoir. 
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beykthslsile Mile, Cretinism, de.—CHVOSTEK, F. Zur Pathogenese des 
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WERTHEIM, B. Die Basedowsohe Krankheit ala Kontraindikatkm gegen 
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32* 


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WALTER, F. K., and HOSEMAKN, G. Experimentelle Untersuchungen tiber 
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u. Psychiat. , 1914, xxiii. (Orig.), S. 98, 

ROSE, FELIX. Le thymus et la maladie de Basedow. Sem. Mid., 1914, xxxir.. 
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TATHAM, C. C. Symptoms and treatment of hyperthyroidism. Canadian 
Med. Assoc. Joum ., 1914, ir., Feb., p. 108. 

SEHRT. Die Besiehungen der SehilddrtLseninsuffizieni xu den nerrosen Beech- 
werden und der spastischen Obstipation der Frauen. MUnch. Med. Wchnschr. 9 
1914, lxi., Feb. 24, S. 408. 

M'GARRISON, R. Experimental researches on the etiology of cretinism, con¬ 
genital goitre, and oongenital parathyroid disease. Indian Joum. Med . 
Research, 1914, i., Jan., p. 505. 

M‘GARRISON, R. An inquiry into the causation of goitre at the Lawrence 

Military Asylum, Sana war, with a report on the water supply. Indian Joum. 
Med. Research , 1914, i., Jan., p. 586. 

OURSCHMANN, H. Thyreotoxiache Diarrhoea. Arckiv. /. Verdauungs- 
Krankh. y 1914, xx., 8. L 

LAMSON, O. F. Intrathoraoic Goitre. Annals of Surgery , 1914, lix., Feb., 
p. 191. 

WOODBURY. M. S. The technique of outlining the thyroid gland. N*Y. Med. 
Joum 1914, xoix., Feb. 14, p. 333. 

Paralysf s Aglttis.—FRIEDLANDER, R. Zur Uebungsbehandlung der Paralysis 
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GREENWALD, I. The supposed relation between paralysis agitans and 
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SCHIOTZ, O. Die Besiehungen der BlutdrUsen sur Pathogenese der Parkin - 
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Tetany.-CURSCHMANN. Zur Frege der “ Bronchotetanie * der Erwachsenen 
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Feb. 10, S. 289. 

SPECIAL SENSES AND CRANIAL NEE YES— 

FIRTH, A. H. The pupil and its reflexes in insanity. Joum. MenL Set., 
1914, lx., Jan., p. 82. 

GIGNOUX. Paralysis otique du moteur oculaire extern© assooile k l’atteinte du 
trijumeau. Rev. hebd. de Laryngol., d'Otol. et de Rhinal. t 1914, xxxr., Feb., 

p. 61. 

LANGE, W. Aplasie des Ganglion spirale und des Nervus cochlearis als Ursache 
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MISCELLANEOUS SYMPTOMS ANE CASES— 

MILLS, 0. K. Neurology at the Reoent (Seventeenth) International Congress of 
Medicine. N. Y. Med. Joum., 1914, xcix., Jan. 31, p. 205. 

JOLLY, PH. Neuere neurologisohe Arbeiten. (Sammelreferet.) Schmidt's 
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TRIES, A. Ueber die Differentialdiapnose abdomineller Erkrankungen auf 
Grand yon Symptomen des vegetativen Nervensystems, insbeeondere mit 
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COHEN, S. 8. On some angioneural arthroses (periarthroses, pararthroses) 
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THOMPSON, W. G. Occupational diseases. Med. Record 1914, lxxxr., 
Jan. 31, p. 185. 

KING, P. Nerves in illness. Med. Press , 1914, oxlviii., Feb. 25, p. 197. 



BIBLIOGRAPHY 


33 * 


CUNNINGHAM, A. T. R. Report of a case of gradual occlusion of the common 
carotid artery in the treatment of pulsating exophthalmos. Joum. Amer. 
Med. Assoc., 1914, lxin, Jan. 31, p. 873. 

GRECO, F. DEL. La psiooterapia eontemporanea. Riv. Ual. di Neuropaiol., 
Psichiat. ed Elettroter., 1914, vii., p. 11. 

HEILBRONNER. Selbstanklagen und pathologische Gestfcndnisse. Miinch, 
Med. Wcknsch., 1914, lxi., Feb. 17, S. 3&. 


PSYCHIATRY. 

CKXBIAl PARALYSIS— 

ROBERTSON, GEORGE M. The Morison lectures, 1913.—The serum and 
oerobro-spinal fluid reactions and signs of general paralysis. Joum. Merit. 
Set., 1914, lx., Jan., p. 1. 

OBREGIA and PITULESCO. La s&o-reaction d’Abderhalden dans la paralysis 
g6n4rale, lepilepsie et les psychoses p^riodiques. Compt. Rend. d. 1. Soc. de 
Biol., 1914, lxxvi., p. 316. 

MARINESCO, G. De l'emploi des injections do serum salvarsanisl in vivo et 
in vitro sous l'arachnoi'de spinal© et o4r6br&le dans le tabes et la paralysie 
g4n6rale. Compt. Rend. d. 1. Soc. de Biol., 1914, lxxvi., Fdv., p. 211. 

CKISTIANI, A. La cApaoith civile nolle remissioni della Paralisi gene rale 
progressiva. Riv. ited. di Neuropaiol., Psichiat. ed Elettroter, 1914, vii., 
p. 24. 

D’ABUNDO, G. Sui tentativi di speciali sieroterapie nella paralisi general© 
progressiva. Riv. ital. di Neuropaiol., Psichiat. ed Elettroter., 1914, vii., p. 1. 

DEMENTIA PRJ2COX— 

MELLUS, E. The early diagnosis and treatment of dementia prsecox. Boston 
Med. and Surg. Joum ., 1914, clxx., Feb. 26, p. 313. 

FANKHAUSER, E. Ueber die somatische grundlage der Dementia precox. 
Oorrespondenz-Bl. f. Schtceizer Aerzte , 1914, xliv., Jan., 8. 66. 

SCHMIDT. Adrenalinunempfindlichkeit der Dementia prsecox. Miinch. Med. 
Wchnschr., 1914, lxi, Feb. 17, S. 366. 

STELZNER, H. Die Frtthsymptome der Schizophrenic in ihren Beziehungen 
zur Kriminalit&t und Prostitution der Jugendliohen. AUg. Ztschr. f. Psychiat., 
1914, Ixxi., S. 60. 

CEIEKAIr- 

HUGGINS, R. R. The diagnosis and treatment of puerperal insanity. Amer. 
Joum. Obstetrics , 1914, lxix., Feb., p. 244. 

BECKER. Die Behandlung der Melanoholie. F&rtsch. d. Med., 1914, xxxii., 
p. 164. 

BALLET, G., and GEN1L-PERRIN, G. L’examen clinique du fond mental chez 
les dements. Technique d’examen et representation graphique. L'EnctpkaU. 
1914, ix., F4v. 10, p. 101. 

VALLON, C., and BESSI^IRE, RENlL Les troubles mentaux d’origin© 
cocainique. UEnc&phdLe, 1914, ix., Fdv. 10, p. 136. 

FARIS, G. T. The management of disturbed mental cases prior to commitment. 
Therap. Gaz., 1914, xxxviii., Feb., p. 77. 

M'CASKEY, G. W. Insanity occurring in latent Bright’s disease. N. Y. Med. 
Joum., 1919, xeix., Jan. 24, p. 178. 

FUCHS and FREMD. Ueber den Nachweis proteolytischer Abwehrfermente im 
Serum Geisteskranker durch das Abderhaldensohe Dialysierverfahren. Miinch. 
Med. Wchnschr., 1914, lxi., Feb. 10, S. 307. 

STEDMAN, H. R. The extradition of insane persons. Med. Record, 1914, 
lxxxv., Feb. 28, p. 369. 

KNOX, HOWARD A. Mental defectives. N.Y. Med. Joum., 1914, xeix., 
Jan. 31, p. 216. 

f 



34* 


BIBLIOGRAPHY 


GWYN, M. K. The Healy puzzle picture end defective aliens. Med. Record , 
1914, lxxxv., Jan. 31, p. 197. 

KREUSER. Uber Geistesstorungen im htiheren Lebenaalter und ihre Genesungs- 
aussiohten. AUg. Ztechr. f. Peychiat., 1914, lxxL, S. 1. 

MORAVCSIK, E. Klinisohe Mitteilungen. AUg. Ztechr . /. Psychiat ., 1914, 
lxxL, S. 23. 

KLINKE. Arbeiteentlohnung. AUg. Ztechr. f. Ptychiai ., 1914, lxxL, S. 131. 

SCHULTZ. BlutuntersuchuDgen als klinisches Hilfsmittel auf psychiatrischem 
Gebiete mit besonderer BerUcksichtigung der Prognosenstellung. Monateech. 
/. Psychiat. u. Neurol., 1914, xiiv., S. 128. 

ROBERTSON, W. FORD. Vaoeine treatment in asylums. Joum. Merit. Sct. 9 
1914, lx., Jan., p. 17. 

STANSFIELD, T. E. KNOWLES. The villa or colony system for the care and 
treatment of cases of mental disease. Joum. Merit. Sci. 9 1914, lx., Jan., p. 
30. 

GETTINGS, H. S. Dysentery, past and present. Joum . Ment. Sci. 9 1914, lx., 
Jan., p. 39. 

JACKSON, D. J. The clinioal value and significance of leuoocytosis in mental 
disease. Joum. Ment. Set.. 1914, lx., Jan., p. 5G. 

O’DOHERTY, PATRICK. Some features of the recent outbreak of enterio 
fever at Omagh District Asylum. Joum . Ment. Sex ., 1914, lx., Jan., p. 76. 


TREATMENT.* 

CYRIAX, E. F. Die lokale manuelle Nervenbehandlung in Bexiehung xu atonischen 
Zustfcnden dec Mastdarms. Ztechr. f. Phyeik. u. Duet. Therap ., 1914, xviiL, S. 75. 

TANNENBAUM, S. A. Psychanalysis. N.Y. Med. Joum., 1914, x<rix., Feb. 7, p. 
277. 

TANNENBAUM, S. A. A consideration of objections to psychanalysis. Med. Record , 
1914, Ixxxv., Feb. 21, p. 338. 

HOWELL, W. W. Suggestive treatment in diseases of childhood. Boston Med. and 
Surg. Joum.. 1914, clxx., Feb. 12, p. 230. 


* A number of references to papers on Treatment are included in the Bibliography under 
Individual diseases. 



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MUSKENS, L. J. The physiological analysis of the posterior longitudinal fasciole 
Le Ntvraxe , 1913, xiv.-xv., Dec., p. 297. 

WALLENBERG, A. Beitrag zur Kenntnis der Sehbahnen der Knochenfische. Lc 
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WINKLER, C. On the olfactory tract in the rabbit. Le Ntvraxe. 1913, xiv -xv 
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ROULE, L. Nouvelles recherches zur le system© nerveux central normal du lombric 
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MOLHANT, M. Le nerf vague. Etude anatomique et exp^rimentale. lYoisifcme 
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SCOTT, G. G. The percentage of water in the brain of the smooth dog-fish. Anal 
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HOLMGREN, EMIL. Neue Beitr&ge zur Kenntnis der quergestreiften Muskelfasern. 
Le Ntvraxe, 1913, xiv.-xv., Dec., p. 277. 


PHYSIOLOGY. 

BERSOU. Phenom&nes de degenerescenoe et de r6gen£resoenoe nerve use oonsecutifs k 
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LOEWBNTHAL, N. Contribution experimental© k l’etude de la degenerescence retro¬ 
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STEFANI, A. SulTaxione trofica del sistema nervoso. Le Ntvraxe, 1913, xiv -xv 
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ORR, D., and ROWS, R. G. Further observations on the influence of toxins on the 
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SCHREITER, B. Uber die Einwirkung einiger Katiouen auf das Polarisationsbild des 
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TSCHERMAK. Die Lehre von der tonischen Innervation. Wien. Jilin. Wchnschr 
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CREHORE and WILLIAMS. Electric currents in conductors with distributed capacity, 
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B iol, and Med., 1914, xi., 35 (352). 

9 



36* 


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DEJERINE. Paralysies du plexus brachial. Joum. des Prat., 1914, xxviii., 
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Ceaeral.—RUDOLPH, OTTO. Untersuchungen liber Hirngewicht, Hirnvolumen 
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HARTENBERG, M. Lee cbphaleee musculaires ou cellulitiques. Joum. de 
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BARNES, A. E., and KERR, W. S. A case of otitic meningitis and cerebellar 
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Msemorrhagc.—HUTINEL. Hemorragie mbningee. Joum. des Prat., 1914, 
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Monoplegia.— STEWART, PURVES. Farther note upon a case of hysterical 
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Miplegia. —BEULE, FR DE. Deux cas d’operation de Fcerster-Van Gehuchten 
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HUTINEL. Tumeur enobphalique probable. Joum. des Prat., 1914, xxviii, 

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Neosalvarsan.—BERGER, H. Neosalvarsan und Zentralnervensystem. Ztschr. 
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THOMAS, B. A., and MOORHEAD, S. W. Severe cutaneous eruption follow¬ 
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KLEIN u. FRANKKL. Ueber die wirksamen Bestandteile der Wassermann- 
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I'erebro-Hplnal Fluid. —LAUNOIS, FROIN, and LEDOUX. Un cas de syndrome 
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MORSE, M. E. Correlation of oerebro-spinal examinations with psyohiatric 
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MORAES, VIEIRA DE. La tension, les prot4ines et la lymphocytose du liquide 
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fimill AMD mCTIONAL DIftEA&K£— 

Epilepsy*—TURNER, W. ALDREN. An address delivered before the meeting of 
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M ( DOUGALL, ALAN, and PLANT, W. A. Schools for epileptics and the 
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ANTON, G. Die operative Beeinflussung der Entwioklungmtorungen des 
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COLLINS, M. ABDY. The hereditary transmission of epilepsy. Epilepsia , 
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TURNER, W. ALDREN. International league against epilepsy. Epilepsia, 
1914, vi., Jan., p. 369. 

VEIT. Uber epileptische Dammerzust&nde. Epilepsia, 1914, vi., Jan., p. 375. 

AMMANN, R. Uber Epilepsieetatistik. Epilepsia , 1914, vi., Jan., p. 383. 

BENON and DENES. Epilepsie infantile et asthlno-manie. Gaz. des H6p., 
1914, lxxxvii, Jan. 29, p. 183. 

STEINER, G. Uber die familiare Anlage zur Epilepsie. (Ein Beitrag sur noeo- 
logischen Differenzierung bestimmter Epilepsieformen.) Ztschr. /. d. ges. 
Neurol, u. Psychiat., 1914, xxiii. (Orig.), S. 815. 



BIBLIOGRAPHY 


43* 


LESZYNSKY, W. M. Traumatic epilepsy. Report of a case of five years* dura¬ 
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21, p. 612. 

CROOKSHANK, F. G. Epilepsy and epileptics. Med . Press, 1914, cxlviii., 
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ANDERSON, J. F. Danger in the subcutaneous injection of solutions of crotalin, 
with report of a fatal case. Joum. Amcr. Med. Assoc., 1914, lxii., March 21, 
p. 893. 

Chorea.—MARIE, PIERRE, and LHERMITTE, J. Lesions de la choree chronique 
progressive (Chor4e d*Huntington). La d6g4n4ration atrophique oortioo-striee. 
Annates de M6d., 1914, i., Jan., p. 18. 

Megrim. —WATERMAN, G. A. The relationship between epilepsy and migraine. 
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BRAV, AARON. Ophthalmoplegic migraine, with report of a case of recurrent 
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Xearalgla.— EPSTEIN, H. Rasche Heilung der genuinen Neuralgic durch ein 
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GORDON, ALFRED. Experimental study of intraneural injections of alcohol. 
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BERSON. L’injection intra-tronoulaire d’alcool dans les nerfs p4riph4riques. 

Le N&vraxe , 1913, xiv.-xv., Deo., p. 581. 

Nearltl*.— HOWELL, C. M. HINDS. Brachial Neuritis. Practitioner , 1914, 
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AUSTREGESILO, A. Polynevrites scorbutiques. Rev. Neurol., 1914, xxii., 
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ARSIMOLES and LEGRAND. Etude clinique d’un oas de presbyophrenic de 
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HEILE, B. Ueber druckentlastende Operationen bei Ischias. Berl. klin. 
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HUNT, J. RAMSAY. The ischemic lumbago, a further contribution to the 
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Bcrl-Herl.—ARNOLD, W. J. J. The etiology of beri-beri. Brit. Med. Joum., 
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FUNK, CASIMIR. Studien fiber Beri-beri. X. Mitteilung. Experimentelle 
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SCHAUMANN, H. Bemerkungen zu der Verdffentliohung von Casimir Funk : 
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Nearas thenla. —RITCHIE, JAMES. Neurasthenia. Edin. Med. Joum., 1914, 
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Nearoses.— BURROW, T. Character and the neuroses. Psychoanalytic Review, 
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BOUMAN, L. Contribution k l’4tude des dermatoneuroses ftbriles. Le Nivraxe, 
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Alcoholism, Ac.— ROSEBRUGH, A. M. An economical treatment of inebriates. 
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DUPRE and SAVOUREUX. Autod4nonoiation recidivante chez une dipsomane. 

Oaz. des H6p., 1914, IxxxviL, Mars 5, p. 437. 

LAUMONIER, J. Alooolisme et deg^nerescenoe. Gaz. des H6p., 1914, lxxxvii., 
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Exophthalmic Goitre, Cretinism, Ac.—MOSS, M. I. Heredity in exophthalmic 
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STOLOFF, I. A. Surgery in goitre. N. Y. Med. Joum., 1914, xeix., Feb. 28, p. 
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v. GRAFF and NOVAK. Basedow und Geuitale. Archiv f. Gynaskol., 1914, 
cii., S. 18. 

h 



44 * 


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v. GRAFF. Schilddruse und Gen: tale. Artkiv /. GyncekoL, 1914, & 109. 

M CA PRISON, K. Etiology of endemic cretinism, congenital goitre, and eon* 
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raral/aftn Aglfaus.—STIEFLER, GEORG. Kliniacher Beitrag xur genmien 
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Tetanus.—MARTIN, L., and DARRE, H. Traitement du tdtanoa grave par 
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Addlfton'i Disease.—ROLLESTON, H. D.. and BOYD, E, J. Addisoa’s disease 
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HOLMES, A. O. Defaced type of Addison’s disease. Joum. Amer . Med. Assoc., 
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BROOKS, H. Hypernephroma with long standing symptoms of adrenal deficiency, 
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Tetany. —RODMAN, W. L. Gastric tetany. Joum. Amer. Med. Asso c., 1914, 
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ariCUl SEN8E8 AND CBAJVUL NEBVBft— 

SARBO, ARTHUR V. Zur Technik der Pupillenuntersuchvmg und eine nsue, 
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BABINSKI, J., and JARKOWSKI, J. Sur les mouvements oonjuguds. Bee. 
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SPILLER, W. G. Bilateral oculomotorius palsy from softening in each oculo- 
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CANTONNE, A. Les keratites neuro-paralytiques. Joum. da PruL, 1914, 
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NUCEUANEOH8 SYltmNS AND CA8EA— 

PRIESTLEY, JOHN. Nervous diseases of elementary sohool-children—Boy» 
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COSTE, FELIX. Headache. Med. Press, 1914, exlviii., March 25, p. 304. 

JOLLY, PH. Neuere neurologische Arbeiten. Schmidts JahrbUcher d. in- «. 
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FRINK, H. W. What is a complex? Joum. Amer. Med. Assoc., 1914, lxii., 
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RYTHER, M. Neurological Social Service, Massachusetts General Hospital 
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BUSH, A. D. Tobacco smoking and mental efficiency. B.Y. Med* Joum., 
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BECKER and OLSEN, Metabolism during mental work. Skand. Archie f. 
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MUXS, CHARLES K. Silaa Weir Mitchell. Joum. Ntrv. and Ment. Du., 
1914, xii., Feb., p. 65. 




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45* 


BUNNEMANN. Remerkungen mm Schmerzproblem. Neurol. Centroid,., 1914, 
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PSYCHIATRY. 

«uvmi PABUTSU- 

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3INIMTU PBBCOl- 

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SCARPINI, V. Morte improwisa per emorragie bulbari in un oaso di demensa 
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GENERAL— 

KNOX, H. A. A scale, based on the work at Ellis Island, for estimating mental 
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TREATMENT. * 

BERKELEY W. N. The use of pineal gland in the treatment of certain classes of de¬ 
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HABERMAN, J. V. Mental healing. An admonition. Journ. Amer. Med. Assoc., 
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LAPENSKY, MICHAEL. t v ber mechaniaohe Bader in der neurologiachen Praxis 
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Psyekeannlysf s. — DERCUM, F. X. An evaluation of the payobogenic factors in 
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PFISTER, O. Prof. Dr Ernst Durr und seine Stellung zur Psychoanalyse. 
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DUNLAP, K. The pragmatic advantage of Freudo-Analysis. Psychoanalytic 
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JUNG, C. G. The theory of paychoanalyaia. Psychoanalytic Review , 1914, i., 
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JELLIFFE, S. E. The technique of psychoanalysis. Psychoanalytic Review, 
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PUTNAM, J. J. On some of the broader issues of the psychoanalytic movement. 
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RENTERGHEM, A. W. van. Freud et son doole. Nouveaux essais psycho- 
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LAUMONIER, J. Le “ pansexualisme ” de Freud. Oaz. des H6p., 1914, lxxxvii., 
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ASH, E. The law of psychotherapy. Med . Press , 1914, cxlviil, March 25, p. 
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DOUGLAS, A Further notes on mental suggestion by transference. Practi¬ 
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* ▲ number of references to paper* on Treatment are included in the Bibliography under 
individual d is ea ses . 



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47 * 



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CLINICAL NEUROLOGY. 

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1914, liil, April 11, p. 11C7- 

AL^UIEK, L. Basedowisxne on ncrrose vaso-motriee (troubles mo-aoUon 
avcc c<*ur instable st facilement excitable, dyspeptic nemos*, tremblemeai, 
troubles psyahique*). Rev, Neurol 1914, xxii., p. 393. 

PKTTAVKL, C. A. Weiterer Be it rag zur pathologiseheo Anatomic dsi Korku 
Basedowii. Miileil. it. d. Grenzgeb. d, Med. m. Chir 1914, xxrii, S. 694. 

L1KK, E. Zur Fniboperation dee Morbus Basedow. Arehiv. f. Klin. Chit 
1914, oiv., S. 1. 

GKUMMB. Zur Theorie von Morbus Basedowii, Myxodem, Kreturismoi und 
Gebirgskropf, Hyper- und Hypothy reoidismus ? Berl. Win. Wehmchr., 1914, 
li. # S. 737. 

WAGNER, K. Bemerkungen zu den Beziehungen der Rontfenbehandloof dcr 
Ovarien und des Basedow. Wien. Win. Wehruekr ., 1914, xxrii., April 9, 
S. 430. 

SAJOUS, C. E. ns M. Toxemias in the genesis of hyperthyroidism sad their 
treatment. N . IT. Med . Joum., 1914, xcix., p. 724. 

Addison's Macao*.—NAKANO. Hfcmochromatoee unter dsm Bilds dss Morbui 
Addisonii. Munch . Med. Wehntehr., 1914, lxi., S. 919. 

TeUay.—FISCHER, J., and TRIEBENSTEIN, O. Untersuehungen iiber Tetania 
und Alterstar. Klin. Afonatibl. f. A ugenhtilk ., 1914, lii., Mtrz-April, S, 441. 

TANBERG, A. Ueber die chronische Tetanie nach Exstirpation ron 01. pars* 
th> reoidece. Mitteil. a. d. Qrenzyeb. d. Med. u. Chir., 1914, xxrii, S, 575. 

Tela a as.—JOFFE, M. Zur Behandlung des Tetanus mit Phenoliajcktionen nach 
Bacelli. St Petersburger Med. Zt$chr., 1914, xxxix., Feb., S. 45. 


SPECIAL SENSES AND CRANIAL NEB YES— 

BERG, V. Ungewohnlich ausgedehnte markhaltige Nerrsnfasern bci hoch- 
gradiger Myopie und Amblyopia. Klin . MonaUU. /. Augenheilk 1914, lii, 
Marz-April, S. 495. 

1GERSUEIMER, J. Ueber Nystagmus. Klin. MonaUbl. f. Au§enktUk. t Mi 
lii., Mart-April, S. 337. 

JESS, A. Kopfschmerz und Auge. Berl. Win. Wehn$ehr. % 1914, H., & 629. 

LAYTON, T. B. Examination of the intornal ear and hind-brain by itimulstion 
of the vestibular nerve. Clin. Joum., 1914, xliii., April 6, p. 193. 

SCHMIDT, C. J. M. Ein Fall von progredienter Thrombophlebitis dsr Hinainui 
nach Otit. mod. acuta. Septische Verlaufsform. Oj*ration nach 
Monatsschr. f. Ohrenheilk . u . Lnryngo-Bhinol 1914, xlviii., S. 270. 

MIStELLANEBL* SYMPTOMS AND CASES— 

NICCOLAI, N. Contribute clinico alio studio delle sindromi epifisaric e funiioni 
endocrine. Biv. ciut. di Clin. Med., 1914, xv., S. 241 und 257. 

BELING, C. C. A case of dystonia musculorum deformans. Joum. Nerv. and 
MetU. Die., 1914, xli., March, p, 148. 

LEVIN, H, C. Organic and psychogenic delirium. N. Y. Med. Joum., 1914, 
xcix., p. 631. 

LEVY, D. J. Etiology and symptomatology of nervousness in infancy. Architet 
of Fed., 1914, xxxi., April, p. 270. 

EDEN, R., and REHN, B. Die autoplastische Fetttransplantation xur Nturolyiii 
und Tendolysis. Arehiv f. klin . Chir., 1914, dv., S. 66. 

KRETSCHMER, M. Zur Neuropathie des kindliehen Alters. ZUchr.f. Phptikol. 
u. Dmt. Therapie, 1914, xviii., S. 206, 

ANTON, G. Ueber familiar# Dysostose beginnend in dsr Gescbleehtsrslfe 
(Pubertats-dysostose). Arehiv f. PsychuU. u. Nenwitr., 1914, Ur., S. 76. 



BIBLIOGRAPHY 


55* 


FRANKL-HOCHWART, L. v. Uber die nervtisen Erkrankungen der Taba- 
krancher mit besonderer Berttoksiohtigung dee Kindesalters. Med. Blatter, 
1914, xxxvi., Mfcrz, 8. 37. 

BODE, P. Zur Kenntnis der Ktinstliohen Atmung bei zentraler Atemlahmung. 
St Petenburger Med, Zttchr ., 1914, xxxix., April, 8. 86. 

FISCHER, H. Bin Fall von Dercumscher Krankheit and seine Beziehangen 
zu den Blutdrttsen. MoncUttchr. f. Ptychiat. u. Neurol ., 1914, xxxv. f April, 
8. 307. 

LISSMANN, P. Zur Behandlung der sexuellen Impotenz. Neurol, CerUralbl ., 
1914, xxxiii., April 1, 8. 417. 

HEISE, W. Ein Beitrag zur Frage dee aknten Ekzems mit psychischer Atiologie. 
Neurol, Centralbl ., 1914, xxxiii., Apri^l6, 8. 499. 

COURBON, PAUL. La convoitise incestueuse dans la doctrine de Freud et les 
conditions du dtair sexael. L'Encephale , 1914, ix., Avril, p. 346. 

ANTON, G. Nachruf auf E. Hitzig anlisslicb der Aufstellung des Hitrig- 
Denkmalea in der Hallenser Klinik fUr Geistes- und Nervenkranke. Archiv f. 
Ptychiat. u, Nervenkr ., 1914, liv., S. 1. 

ANTON, G. Gefahrliohe Menschentypen. Arthiv f, Ptychiat, u, Nervenkr 
1914, liv., 8. 89. 

ROHDE, M. Zur Frage der BerufsnervoeiUt der Volksschullehrer. Monalttchr . 
/. Ptychiat, u, Neurol ., 1914, xxxv., April, 8. 369. 


PSYCHIATRY. 


GENIKAL PARALYSIS— 

FORSTER, E., and TOMASCZEWSKI, E. Untersuchungen uber die Spiroohaete 
des Paralytikergehirns. Deut, Med . Wchntchr., 1914, xl., 8. 694. 

STODDART, W. H. B. Clinical lecture on the curative treatment of general 
paralysis. Med, Prett , 1914, cxlviii., April 1, p. 330. 

MAPOTHER, E., and BEATON, T. Intraspinous treatment (Bwift-Ellis) of 
general paralysis: a preliminary note on four cases treated by this method. 
Lancet , 1914, dxxxvi., April 18, p. 1103. 

MARINESCO, G., and MINE A, J. L’emploi des injections de serum salvarsanisd 
in vitro et in vivo sous l’arachnoide spinale et o4rdbrale dans le tabes et la 
paralysie gdndrale. Rev, Neurol ., 1914, xxii., p. 337. 

SIEBERT, H. Ueber progressive Paralyse. St Petersburger Med, Zttchr 
1914, xxxix., Jan., 8. 20. 

GOLDSTEIN, MANFRED. Adenokarzinom der Hypophyse und progressive 
Paralyse. Archiv f, Ptychiat, u, Nervenkr ., 1914, liv., 8. 211. 

DEMENTIA PKJECOX— 

PELLACANI, G. Rioerohe sulla deviazione del oomplemento nella demenza 
preooce. Riv, di Paid . new, e ment ., 1914, xix., Marzo, p. 164. 

MA8SELON, REN^. Les voies d’inversion de la dlmenoe prfoooe. VEncephalc , 
1914, lx., Avril, p. 312. 

GENERAL— 

BRUCE, LEWIS C. The complement-deviation in cases of manic-depressive 
insanity. Journ, Ment, Sei ., 1914, lx., April, p. 177. 

OBREGIA and PITULESCO. Etude sur les psychoses du cholera. L'EncephaU , 
1914, ix., Mai, p. 39a 

DEVINE, HENRY. The clinical significance of katatonio symptoms. Journ. 
Ment. Sci ., 1914, lx., April, p. 27& 

WILLIGE, HANS. Ueber akute paranoische Erkrankungen. Archiv. /. 
Ptychiat. u. Nervenkr , 1914, liv., 8. 121. 

PRICE, GEORGE E. A sixteenth - oentury paranoiac. N. Y. Med. Journ., 
1914, xoix., p. 727. 

k 



56* 


BIBLIOGRAPHY 


KNAPP, P. C. The treatment of cases of mental disorder in general hospitals. 
Boston Med. and Sun 7 . Joum 1914, dxx., p. 637. 

ALLERS, RUDOLF. Ergebnisse stoffwecbxdpathologischer Unterauchungen b*! 
Psychosen.—III. Das manisch-depressive Irresein. Ztschr, f t d. get. Neurol, 
u. Psychiat. (Ref ), 1914, lx., S. 5S5. 

LOMER, GEORG. Initiate Schriftveranderung bei Paralyse. Ally. Ztschr. /. 
Psychoit %y 1914, lxxi., S. 195. 

ROWS. R. G. The imi>ortancc of disturbances of the personality in mental 
disorders. Joum, Ment. &«., 1914, lx., April, p. 192. 

AUSTREGESILO and ESPOSEL. Les cenesthopathiss, L'EnctphaU, 1914, 
ix. t Mai, p. 425. 

REED, ALFRED C. Insanity in China. Boston Med. and Surg. Journ. , 1914, 
clxx., p. 572. 

FIRTH, A. H. The pupil and its reflexes in insanity. Joum. Ment. Sci , 1914, 
lx., April, p. 224. 

COURBON, PAUL. L’hallucination tdealgesique. L'KnctphdU, 1914, ix„ Mai, 
p. 440. 

LOBB, S. Die AbderhaMenschen Fermentreaktionen und ibre Bedetitung far 
die Psychiatric. Afonatsschr. f. Psychiat. u. tfeurol., 1914, xxxv., April, S, 382. 

STEIN, EMIL. Posttraumatischc Sp&tpsychose oder Dementia arterio-iclerotics. 
Pragtr Med. Wchnschr, 9 1914, xxxix., Marz, S. 116, 

SKHOTT, Aus der Praxis der Entmundigung wegen Trunksucht. Ally. ZUdr. 
/. Psychiat. , 1914, lxxi., S. 213. 

WEBER, L. W. Die Fahigkeit zur freien Selbstbestimmung bei der Wahl des 
Aufenthaltsortes. Ally. Ztschr. /. Psychiat. t 1914, lxxi,, S. 252. 

MULLER, E. Die Kaiser Dotnitian, Commodus, Caracalla und Elagabal, ein 
Beitrag zur Prage des Casarenwahnsinns. AUg. Ztschr . /. Psychiat 1914, 
lxxi., 5. 271. 

STF.MMKR, W. Das Irren- und Siechenhaus Pforzheim nnd seine Ante. AUg. 
Ztschr. f. Psychiat. , 1914, lxxi., S. 289. 

TRUELLK, V. Geistige Storungen bei Tuberkulosa. Med. Blatter, 1914,xxm, 
Marz, S. 49. 

TITIUS. Ein Beitrag zur Kasuistik des Stotterm. AUg. Ztschr./. Psychud., 
1914, lxxi., S. 207. 

KNOX, HOWARD A. A comparative study of the imaginative powers in 
mental defectives. Med. Recordy 1914, lxxxv., April 25, p. 748. 

FOSTER, M. H. Methods of examination of illiterates for mental defectives 
Joum . Amcr. Med. Assoc., 1914, lxii., April 4, p. 1068. 

SIBBBRT, C. Ueber psychiatrische Gutachten vor Gerichi St Petersburger 
Med. Ztschr., 1914, xxxix., S. 7. 


TREATMENT,* 

BUNNEMANN. Worauf beruhen die psychotherapeutischen Erfolge Dubois 1 ? Neurol. 
Centralbl., 1914, xxxiii., April 16, S. 496. 

KAHANE, H. Die Zwangsvorstellungen und ilire psychieche Therapie. Wien. Hin. 
Wchnschr ., 1914, xxvii., April, S. 371. 

WILLIAMS, TOM A. A oomtrast in psychoanalysis: three cases. B. Y. Med. Joum, 
1914, xoix., p. 672. 


• A number of reftrenoes to papers on Treslmeikt are inoluded in the BibUofrsphj and* 
individual diseases 



Bibliography 

ANATOMY. 

8ERGI, SERGIO. Uber die Morphologic and Sjmmetrie des Lobus frontalis beixn 
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LEIDLER, R. Uber die Anatomic und Funktion des Nucleus Bechterew (Mit 4 fig.). 
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SODERBERGH, GOTTHARD. Quelle eat l’innervation radiculaire des muscles 
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FUMAROLA, G., and ZANELLI, C. F. Anatomisch-experimentelle Forschungen 
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PHYSIOLOGY. 

TRENDELENBURG, W. Neuere Methoden und Ergebnisse der Hirnphysiologie. 
Berl. klin. Wchnschr ., 1914, li., Juni 1, S. 1015. 

CAMUS, J., and ROUSSY, G. Polyurie par l&ion de la region opto-pedonculaire de 
la base du cerveau. Mecanisme regulateur de la teneur sn eau de l’organisme. 
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DIXON, W. E., and HALLIBURTON, W. D. The cerebro*spinal fluid. II. Cerebro¬ 
spinal pressure. Joum. Physiol ., 1914, xlviii., p. 128. 

WEED, LEWIS H. Observations upon deoerebrate rigidity. Joum. Physiol., 1914, 
xlviii., p. 205. 

TRIBE, ENID M. Vaso-motor nerves in the lungs. Joum. Physiol., 1914, xlviii., 
p. 154. 

MARTIN, E. G., and STILES, P. G. The influence of curare on vasomotor reflex 
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MOGWITZ, G. Uber das Verhalten des sympathischen Nervensystems des S&uglings 
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PORT and BRUNOW. Der Einfluss des vegetativen Nervensystems auf das Blutbild. 
Archiv. f. exp. Path. u. Phaimakol., 1914, lxxvi., S. 239. 

HOSKINS, R. G., and WHEELON, HOMER. Adrenal deficiency and the sympathetic 
nervous system. Amer. Joum. Physiol ., 1914, xxxiv., May, p. 172. 

SWETSCHNIKOW, W. A. Uber die verschiedenen Bedingungen der Adrenalinwir- 
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WIGGERS, CARL J. Further observations on the constricting action of adrenaline on 
the cerebral vessels. Joum. Physiol ., 1914, xlviii, p. 109. 

I 


57 * 



BIBLIOGRAPHY 


r>s 


>* 


KLEE. Die Magenforvn bei gesteigertem Vague- und Sympatbikustonus. Jfu>icA. 
Med. \Vchnsckr. % 1914, Ixi., Mai 12, S, 1044. 

WOLFSOHN, J. M. The normal and pathologic physiology of the visceral nervous 
system, with especial reference to vagotomy and aympathicotony. Journ . Amr. 
Med. A$soc. f 1914, lxii., May 16, p. 1535. 

KURE, K., HIRAMATSU, T., and NAITO, H. Zwerchfelltonos und Nervi Splanchnid 
Zentralbl. j. Physiol., 1914, xxviii., 8. 130. 

CARLSON, A. J. The nervous control of the gastric hunger mechanism (man, dog). 
Amer. Journ. Physiol., 1914, xxxiv., May, p. 155. 

FROHLICH, ALFRED. Die Pharmakologie der Hypophysensubstanzen. Wien. Med. 
Wchnschr., 1914, Ixiv., Mai 16, 8. 1061. 

WULZEN, R, The anterior lobe of the pituitary body in its relationship to the early 
growth period of birds. Amcr. Journ. Physiol 1914, xxxiv., May, p. 127. 

CA8TELLI, R. Contribution h l’£tude des substances grasses de l*hypophyee humaine. 
Archives de Med. exp., 1914, xxvi., Mars, p. 185. 

FUNK, CASIMIR. Is polished rice plus vitamine a complete food? Journ. Physiol., 
1914, xlviii., p. 228. 


PSYCHOLOGY. 

HALL G. STANLEY. A synthetic genetic study of fear. Amer. Journ. Psychol., 
1914, xxv., April, p. 149. 

FLETCHER, J. M. An experimental study of stuttering. Amcr. Journ. Psychol., 
1914, xxv., April, p. 201. 

CANNON, W. B. The interrelations of emotions as suggested by recent physiological 
researches. Amer. Journ. Psychol. , 1914, xxv., April, p. 256. 

MOORE, J. S. The articulation of the concepts of normal and abnormal psychology. 
Amcr. Journ. Psychol 1914, xxv., April, p. 283. 

LAURENS, HENRY. Uber die raumliche Unter*cheidungg-fahigkeit beim Dimmer* 
ungssehen. Ztschr. f. Stnncsphy&iol ., 1914, xlviii., S. 233. 

GILDEMBISTER, MARTIN. Uber einige Analogien zwiachen den Wirkungenoptischer 
und elektrischer Rcize. Ztschr. /. Smncsphysiol ., 1914, xlviii., S. 252. 

GILDEMEISTER, MARTIN. Uber die Wahrnehinbarkeit von Lichtlucken. Ztschr. 
/. Smncsphysiol., 1914, xlviii., S. 256. 

RUTENBURG, D. Uber die Netzhautrcizung durch Kurzdauernde Lichtb litre und 
Lichtliicken. Ztschr. f. Sinnesphystol., 1914, xlviii., 8. 268. 

JANET, PIERRE. Psychoanalysis. Journ. Abnorm. PsychoL , 1914, ix., April*May, 

p. 1. 

PUTNAM, JAMES, J. Dream interpretation and the theory of psychoanalysis. 
Journ. Abnorm. Psychol ., 1914, ix., April-May, p. 36. 

TERM AN, LEWIS, M. Recent literature on juvenile suicides. Journ. Abnom. 
Psychol ., 1914, ix., April-May, p. 61. 

BENEDICT, A. L. The psychological effect of the fairy story. N. Y. Med. Journ., 
1914, xeix., May 9, p. 925. 

M‘DOUGALL, WM. The definition of the sexual instinct. Proc . Boy. Soc. Med., 
1914, vii., April (Sect, of Psychiat.), p. 65. 

LOEWY, A., and PLACZEK, S. Die Wirkung der Hohe auf das Seelenleben des 
Luftfahrers. Berl. klin. Wcknschr., 1914, li., Juni 1, 8. 1020. 

PATHOLOGY. 

ORR, D. f and ROWS, R. G. Toxi-infection of the oentral nervous system. Proc. Boy. 
Soc. Med., 1914, vii., April (Neurol. Sect.), p. 43. 

BIONDI, GIOSUE. Degenerazioni primarie ed alterazione postmortali dells fibre 
nervose del midollo spinale. Riv. ital. di NcuropatolPtickiatr. ed Stettroter. 
1914, vii., Aprile, p. 158. 



BIBLIOGRAPHY 


59* 


TORRE, P. la. Alterazioni del retioolo neurofibrillar® endooellulare della intossicazione 
saturnina. Pathologica , 1914, vi., Aprile, p. 186. 

LEVADITI, C., DANULESCO, V., and ARZT, L M<$ningite par injeotion de microbes 
pyp^nes dans les nerfs pdriphdriques. Annales de Vlnstitut Pasteur , 1914, xxviii, 

SARTESCHI, V. Sopra le alterazioni del sistema nervoso oentrale nella intossicazione 
difterica sperimentale e nella infedone difteriea umana. Biv. ital. di Neuropatol ., 
Psichiatr . ed Elettroter ., 1914, vii., Aprile, p. 146. 

PALADINO, G. Le eellnle nerve#® sono element! perenni dell* organismo ? ed il potere 
germiu&tivo dell* ependima e limits to al periodo embrionalef Annali di Nevrol., 
1913, xxxi., p. 276. 

ISENSCHMID and SCHNITZLER. Beitrag zur Lokalisation des der Wttrmeregulation 
voratehenden Zentralapparates im Zwisehenbim. Archie. /. exp. Path, u . 
Pharmakol. , 1914, lxxvi., S. 202. 

TODDE, C. Ricerehe sulla fundone e sulla atruttura delle ghiandole seasnali masobili 
nelle malattie men tali. Biv. Sper. di Preniat ., 1913, xxxix., pp. 696-766. 

BONFIGLIO, FRANCESCO. Un metodo rapido per la coloradone delle guaine 
mieliniche nelle sedoni al eongelatore. Biv. Sper. di Preniat. , 1913, xxxix., pp. 
652-668. 

COSTANTINI, B. Osservadoni eliniohe ed anatomopatologiche sulla forma “pro- 
dutfciva” della aifilide cerebral©. Biv . Sper. di Preniat ., 1913, xxxix., pp. 659-o86. 

ROSENHEIM, OTTO. The galactoeidea of the brain. II. The preparation of phrenoain 
with kerasin by the pyridine'method. HI. Liquid crystals and the melting point of 
phrenoain. Biochem. Journ., 1914, viii., April, pp. 110 and 121. 

ABELOUS and SOUL A. Sur la repartition de l’azote et du phoaphore dans le oerveau 
dm lapin8 normaux et anaphylactisea. D&luctions aur le m&amsme de l’anaphylaxie. 
Compt. Bend . d. 1. Soc. de Biol., 1914, lxxvi., Avril, p. 671. 

NICHOLS, H. J. Observations on a strain of Spiroeheeta pallida isolated from the 
nervous system. Journ. Exp. Med ., 1914, xix., April, p. 362. 


CLINICAL NEUROLOGY. 

GENERAL— 

BOX WELL, WM. Disordered bladder function in nervous disease. Dublin 
Journ. Med. Sei., 1914, 8er. iii., No. 609, p. 340. 

VERNET and PETZETAKIS. Le r^flexe ooulo-cardiaque. Gaz. des Hop., 1914, 
Ixxxvii., Mai 2, p. 837. 

AVIRAGNET, DORLENCOURT, and BOUTTIER. Le rlflexe oculo-cardiaque 
au coura de l’intoxication diphteriquo. Compt. Bend . d. 1. Soc. de Biol., 1914, 
lxxvi., Mai 15, p. 771. 

DUPONT, L. lUflexe auriculo-cardiaque et auriculo-vaso-moteur. Compt. Bend, 
d. 1. Soc. de Biol., 1914, lxxvi., Mai 15, p. 731. 

NERVES— 

KENNEDY. F., ELSBERG, C. A., and LAMBERT, C. I. A peculiar un- 
described disease of the nerves of the cauda equina. Amer. Journ. Med. Sci., 
1914, cxlvii., May, p. 646. 

LAURENT, O. Les an^vrysmes et les Measures des nerfs en chirurgie de guerre. 
Bev. de Chir., 1914, xxxiv., Mai, p. 553. 

ZALLA, M. Sui trapianti dei nervi periferici. Biv. di Patol. nerv. e ment ., 
1914, xix., Maggio, p. 193. 

KENNEDY, ROBERT. Experiments on the restoration of paralysed muscles by 
means of nerve anastomosis. Part II. Anastomosis of the nerves supplying 
limb muscles. Proc. Boy. Soc., 1914, Ser. B., Vol. lxxxvii., p. 331. 

SPINAL CRRR— 

General.— VULPIUS, OSCAR. Ueber die Lahmungstherapie an der oberen 
Extremist. Dent. Med. Wchnschr., 1914, xl., Mai 21, S. 1053, 



GO* 


BIBLIOGRAPHY 


Fracture, Dislocation, die.—ADAMS, Z. B. The causes and their relation to 
the treatment of lateral curvature of the spine. Baton Med. and Surg. 
Joum 1914, clxx., May 21, p. 786. 

EVANS, E. L. Scoliosis associated with primary myopathy. Proc. Roy. Soc. 
Med., 1914, vii., April (Surg. Sect.), p. 207. 

EVANS, E. L. Scoliosis of functional character. Proc . Roy. Soc. Med., 1914, 
vii., April (Surg. Sect.), p. 209. 

NASH, J. B. Laminectomy for spinal injury. Australasian Med. Qai., 1914, 
xxxv., April 11, p. 314. 

WENZEL. Ueber einen Fall hochgradigster Ankylose der Wirbelsaule. Munch. 
Med . Wehnsehr. t 1914, Ixi., Mai 12, S. 1060. 

Herpes Zoster.—SOUQUES, A. Zona cervical et paralysis facials. (1 fig.) Ret. 
Neurol ., 1914, xxii., Mai 15, p. 625. 

Tabes Dorsalis.—LUKACS, E. Amyotrophische Tabes mit histologischem Befunde. 
Ztsehr. f. d. get. Neurol, u. Psychiat ., 1914, xxiv. (Orig.), S. 437. 

v. BAEYER. Ein neues Symptom bei der Tabes. Munch. Mtd. Wehnsehr ., 
1914, Ixi., Mai 19, S. 1105. 

MALONEY, W. J. M. A. Note on mechanical support for the feet in locomotor 
ataxia. Med. Record , 1914, lxxxv., May 16, p. 881. 

BERIEL, L., and DURAND, P. Ein serotherapeutischer Versuch beiTibesund 
Paralysis progressiva: arachnoideale Injektion mit Serum von Syphilitikem. 
Nevrol . Centralbl 1914, xxxiii., Mai 16, S. 612. 

Poliomyelitis Anterior Acnta.—ELMSLIE, R. C. Poliomyelitis of extensive 
distribution with dislocation of the left hip. Proc. Roy. Soc. Med., 1914, viL, 
April (Surg. Sect), p. 209. 

JONES, ROBERT. The annual oration on the surgical treatment of infantile 
paralysis. Lancet, 1914, clxxxvi., May 30, p. 1515; Brit. Med . Joum., 1914, 
May 30, p. 1165. 

KERN. Ueber eine Anstaltsendemie von Heine-Medinscher Rrankeit. Miinch. 
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FLEXNER, S., and AMOSS, H. L. Penetration of the virus of poliomyelitis 
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CLARKE, J. MICHELL, and LANSDOWN, R. G. P. Intramedullary tumour of 
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Landry's Paralysis. — DOUGLAS, R. O. A case of Landry's paralysis 
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McMURRAY, S. Miner’s nystagmus. Journ. State Med., 1914, xxii., May, 
p. 303. 

NEIDING, M. Die isolierte Lfchmung des N. trigeminus. Neurol. CcrUralbL , 
1914, xxxiii., Mai 16, S. 615. 

EWING, HARVEY M. Complete bilateral isolated paralysis of the seventh 
nerve developing four months after the primary infection of syphilis. Journ. 
Amer. Med. Assoc., 1914, lxii., May 9, p. 1459. 

PASSOW, A. Neue Mittel gegen Horstorungen und Ohrgerausche. Med. 
Klinik., 1914, x., Mai 3, S. 753. 

WALKER, D. H. Aural vertigo. Boston Med. and Surg. Journ., 1914, clxx., 
May 21, p. 791. 

ABOULKER, HENRI. Resection du l&ryngd sup^rieur dans la dysphagie des 
tuberculeux. Rev. held, de Laryngol., d'Otol., ct de Rhtnol., 1914, xxxv., 
S. 641. 

0 

MISCELLANEOUS SYMPTOMS AND CASES— 

WARRINGTON, W. B. Acute generalised infective paralysis in adults. Clin. 
Journ., 1914, xliii., May 13, p. 296. 

WOERKOM, W. van. La cirrhose hdpatique avec alterations des centres 
nerveux dvoluanfc chez les sujets d’&ge moyen. Nouv. Icon. d. I SalpR., 1914, 
vii., Feb., p. 41. 

CARLILL, H. B. Spastic smile with tremor of the upper extremity and 
defective articulation. Proc. Roy. Soc. Med., 1914, >ii. ( April (Clin. Sect.), 
p. 114. 

COURTNEY, J. W. On territorial autonomy in cerebral circulation, and its 
rdle in the genesis of symptoms in the psychoneuroses. Boston Med. and 
Surg. Journ., 1914, clxx., May 14, p. 745. 

CHAUFFARD, A. Les syndromes tdtaniques. Journ. des Prat., 1914, xxriii., 
Mai 2 et 9, pp. 272 et 290. 

JOURDANET, P. Le r61e du systerae nerveux dans les dermitee professionnellex 
Pressc mtd., 1914, No. 42, Mai 27, p. 402. 



BIBLIOGRAPHY 


67* 


BERTOLOTTI, M. Le syndrome oxydpbalique on syndrome de cranio- 
synostoee patbologique. Presse mid., 1914, No. 35, Mai 2, p. 332. 

OAUTLBY, E. The nenrotie temperament in ohildren. Clin. Joum ., 1914, 
xliiL, May 27, p. 326. 

BOURUIGNON, G. Localisation de l’exdtation dans la mdthode dite“Mono- 
polaire ” ches l'homme, pdles r4els et poles Yirtnels dans deux organee different*. 
(8 fig.) Rev. Neurol ., 1914, xxii., Avril 30, p. 553. 

MALONEY, J. M. A. The co-ordination of movement. Joum. Nerv. and Ment. 
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MOCHI, A. Le asimbolie. Rassegna di Studi Psichiat ., 1914, iv., Gennaio- 
Febbraio, p. 3. 

WESTPHAL. Untersuchungen xnr Frage der nervttsen Entstehung peptischer 
Ulcera. Dent. Arehiv f. klin. Med., 1914, cxiv., S. 327. 

STURSBERG. Zur Kenntnis der nervfisen Erkrankungen bei Leukkmie. Deut. 
Arehiv f. klin. Med., 1914, cxiv., S. 292. 

CALLIYARIS, GIUSEPPE. Ulteriori ricercbe sullelinee entanee iperestesiobe. 
Riv. Sper. di Frenial ., 1913, xxxix., pp. 557-636. 

BITTORF. Bin weiterer Beitrag zur Kenntnis der Muskelkrkmpfe peripheren 
Ursprungs und verwandter Erscheinungen. Deut. Ztschr. f. Nervenkeilk ., 
1914, li., S. 124. 

PICK, A. Perseveration und andere Mechanismen als Ursache agrammatiscber 
Erscheinungen nebst Bemerkungen uber die Beziehungen des “ Yerschreibens 99 
rum “ Versprechen.” Monatsschr. /. Psychiat. u. Neurol., 1914, xxxv., Mai, 
S. 407. 

MEIGE, H. Un hec-de-lifevre en peinture et quelques remarques sur la con¬ 
formation des l&vres. Nouv. Icon. d. 1. Salplt., 1914, vii., Feb., p. 57. 

MENDICINI, A., and ARTOM, G. Sur le spasme k bascube de 1’orbiculaire des 
paupi&res. Nouv. lean. d. I . Salplt. , 1914, vii., Feb., p. 32. 

BERTOLOTTI, M. Poly dactylic et t^ratome hypophysaire. Contribution k 
I’tStude des influences morphog4n4tiques des glandes k secretion interne sur 
l’organog<£ntae. Nouv. Icon. d. 1. Salplt., 1914, vii., Feb., p. 11. 

CHE VALUER, P. Sur un oas d’acrodactylopathie hypertrophiante. Nouv. 
Icon. d. 1. Salplt., 1914, vii., Feb., p. 3. 

SAFFIOTTI, U., and SERGI, S. Sul tempo di reazione remplice nella nevrosi 
traumatica e sua importanza nella valuta* ione della capacity al lavoro. Riv. 
Sper. di Freniat., 1913, xxxix., pp. 686-695. 

NUTT ALL, G. H. F. “ Tick Paralysis” in man and animals. Further published 
records, with oomments. Parasitology , 1914, vii., May, p. 95. 


PSYCHIATRY. 

GENERAL PARALYSIS— 

MYERSON, A. Results of the Swift-EUis intradural method of treatment in 
general paresis. Boston Med. and Surg. Joum., 1914, clxx., May 7, p. 709. 

MEYER, B. Die Stellung der progressiven Paralyse (und Tabes) zur Syphilis 
und die Frage ihrer Behandlung. Berl . klin. Wchnsehr., 1914, li., Mai 25, 
S. 965. 

RUNGE. Salvarsanbehandlung der progressiven Paralyse. Deut. Med. 
Wchnsehr., 1914, xl., Mai 14, S. 998. 

NONNE, M., and WOHLWILL, FR. Uber einen klinisch und anatomisch 
untersuchten Fall von isolierter reflektorischer PupiUenstarre bei Fehlen von 
Paralyse, Tabes, und Syphilis oerebroepinalis. Neurol. Centralbl., 1914, xxxiii., 
Mai 16, S. 611. 

REMENT1A PRJCCOX— 

KAHLMETER, G. Blutuntenuchungen bei einem Fall von Dementia Praecox 
mit periodischem Verlauf. Ztsehr. f. d. ges. Neurol, u. Psychiat., 1914, 
xxiv. (Orig.), S. 483. 



68* 


BIBLIOGRAPHY 


GESKBAls— 

ASTANKOFF, P. Die Phasen der Manic. Arehiv f. PsvchiaL, 1914, lit., 
8. 368. 

ITTEN, W. Zur Kenntnis hkmatologiaoher Befunde bei einigen Piyehoeen 
Ztschr. f. d. get. Neurol, u. Psychiat ., 1914, xxir. (Orig.), S. 341. 

SIGG, E. Versuch einer retroepektiven Diagnostik der aenilen Psy chosen nach 
dem Druaeobefunde. Ztschr. /. d. get. Neurol . u. PtychuU ., 1914, xxir. (Orig.), 
8. 453. 

GOLLA, H. Die Bedeutung der Abderhaldenschen Serodiagnoatik fiir die 
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xx iv. (Orig.), 8. 410. 

EWENS, G. F. W. Insanity from exhaustion. Indian Med. Oat 1914, xlii , 
April, p. 131. 

DEVINE, HENRY. The biological significance of delusions. Proc. Boy Soc. 
Med 1914, vii., April (Sect, of Paychiat.), p. 89. 

KASTAN, MAX. Kriminalitkt und exogene Erregbarkeit bei angeborenen 
paychi»chen Defekten. Arckiv /. PsychiaL, 1914, liy., S. 454. 

MUNDIE, G. S. The mentally defective. Canadian Med. Assoc . Joum., 1914, 
iv.. May, p. 396. 

JOUCHTCHRNKO, A. J. Contribution h la question de I’analyae dea procesius 
de fermentation dans la payehiatrie et la neuropathologie. Compt. Rend. d. I 
Soc. de Biol ., 1914, ixxvi., Avril, p. 609. 

ALEXANDER, R. M. Dermatitia exfoliativa In an insane patient N. Y. Med. 
Jvum ., 1914, xcix., May 2, p. 876. 

SOUTHARD, B. E. Feeble-mindedness aa a leading social problem. Boston 
Med. and Surg. Joum., 1914, elxx., May 21, p. 781. 

STEDMAN, HENRY R. The art of companionship in mental nursing. Boston 
Med . and Surg. Joum., 1914, clxx., April 30, p. 673. 

CONSIGLIO, P. Studii di Paichiatria Militare. Riv. Sper , di Freniat., 1913, 
xxxix., pp. 792-849. 

CAMPBELL, C. MACFIE. The work of the out-patient department of the 
Henry PhippB Psychiatric Clinic. Bullet. Johns Hopkins Hosp 1914, xxv., 
May, p. 153. 


TREATMENT.* 

MAUPKTIT, GEORGES. Lea paycho-ndvrosea hypoaphyxiques. Lear trsitemwi 
Pretie Mid ., 1914, Mai 27, p. 401. 

DARDEL, M. Lea in jectiona d’oxygfene dans lea maladies nerveusea et men tales. Re*, 
mid. d . 1. Suisse Rom., 1914, xxxiv., Mara, p. 192. 

Psyefceanalyala.—SOLOMON, M. Psychoanalysis. N.Y. Med. Jou m., 1914, 
xcix.. May 9, p. 919. 

ENGELEN. Suggestionafaktoren bei der Freudachen Psychoanalyse. Deul. Med. 
Wehnschr ., 1914, xl., Mai 7, S. 958. 

* A number of references to papers on Treatment are included in the Bibliography under 
Individual diseases. 


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70* 


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ONODI, LADISLAUS. The rbinogenic and otogenie leaiona of the third, fourth, fifth, 
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WAHL, H. R. Neuroblastomata; with a study of a case illustrating the three tjpn 
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BOBZANI, GIOVANNI. Note cliniche ed anatomo-patologiohe su di un caso di glioma 
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SALMON, A. Sulla patogenesi della oefalea essenziale. Riv. crit. di Clin. Med., 
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DOPTER and PAUKON. La saturation des agglutinines et des pr^dpitine* appliance 
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1. Soc. dc Biol., 1914, lxxvii., Juin 26, p. 157. 

8EZARY, M. A. Lee tumeurs de la glande pineals. (Rev. gen.) Qaz. des H6p 1914, 
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CIAMPI, L.» and VALDIZAN, H. Lo sviluppo fiaico nei frenastenici. Riv. italdi 
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HANDMANN. Ptosis und Cataracta senilis. Bemerkungen iiber die Pathogeness der 
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WAGNER, R. Uber Nebennierenkephalin und andere Lipoids der Nebeunisrsurinde 
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CLINICAL NEUROLOGY. 

general— 

GORDON, A. Lumbar puncture as a special procedure for controlling headache 
in the oourse of infectious diseases. Therap. Qaz., 1914, xxxviii., Junt, p. 392. 

UIVM- 

LEVERTY, A. S. A clinical study of traumatic nerve paralysis. Med. Record, 
1914, lxxxv., May 30, p. 907. 

Mi/*cua-r 

AIME, HENRI. Considerations bisto-pathogeniques sur la myotonie atrophi^ue. 
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gpnrii cdhd—, 

General* —BEKIEL, M. L. Remarques oliniques sur les syndromss bulbaires 
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Fracture, Dislocation, Ac.—SEVER, J. W. A report of the scoliosis clinic of 
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Cervical Rib.—DUPRE, B. G., and TODD, T. WINGATE. A transitional typo 
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Myelitis.—HOLDEN, WARD A. A fifth case of acute dissemiaated myelitis with 
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FLEISOHMANN. Zur Lehre von der Myelitis funicularis. Uber heilbare und 
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JONES, ROBERT. The surgioal treatment of infantile paralysis. Clin. Joum ., 
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Tabes Dorsalis.—BOGGS, THOMAS R., and SNOWDEN, R. R. The intra 
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BARKAN, HANS. On the simultaneous occurrence and interrelation of 
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BE AIM— 

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Von Beeklliigbansen’s Disease.—LIKE, W. Ueber Neurofibromatose. Ztschr. 
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Meningitis.—NAPIER, A. D. L. Meningitis in infancy and early childhood. 
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F1NKELSTEIN, H. Zur Entstehungsweise seroser Meningitiden bei tuberkulosen 
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LAVAN, M. Sur la mdningite syphilitique metachancreuse et preroseolique. 
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HUBER. Pneumococcic meningitis and meningismus. Archives of Ped., 1914, 
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KRAMER, S. P. Fatal accidents following the injection of antimeningitis serum. 
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DARRE and DUMAS. Nouvelle esp^ce de paramJningocoque. Plurality des 
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Hydroeepkalns.—v. BLOMBBRG, FREIHERR. Ein seltener Fall von Hydro- 
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Abscess.—DICK, G. F., and EMGE. L. A. Brain abscesB caused by fusiform 
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Disseminated Sclerosis.—FLASCHEN, STAN. Ein Beitrag zur Aetiologie der 
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■stmorrbage.—MARIE, PIERRE, aud LEON-KINDBBRG, M. Le coma dans 
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Pella*™.— FRAZER, T. Pellagra with late skin lesions: case report. Journ. 
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Lead P#l*«aln*.^LINENTHAL, HARRY. The early diagnosis of lead-poisoning 
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H A YH UR ST, EMERY R. Critical examination of one hundred painter* for 
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MARTINOTTI, L. Di una particolare propriety del Salvarsan. Suo possibile 
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1 : Orig.), S. 183. 

BIND. La s^reuse sous-arachnoidienne en regard de la syphilis. Influence du 
traitement salvaraanique. Rev. Mtd. de la Suisse Rom., 1914, xxxiv., Mai20. 
p. 320. 

DRKSCH. Salvarsan, mercure et eaux sulfureuses dans le traitement de la 
syphilis. Journ. des Prat., 1914, xxviii., Juin 20, p. 390. 

M'CASKBY, G. W. The autonerosalvarsan treatment of syphilis of the central 
nervous system. Journ. Amer. Med. Assoc., 1914, lxii., May 30, p. 1709. 

BAUM, O., and HERRENHEISER, G. Chemotherapeutische Versuche mit 
salvarsan. Wien. Klin . Wcknschr., 1914, xxvii., Juni 11, S. 843. 

BUBERL. Zur Salvarsanbehandlung des Milzbrandkarbunkles. Munch Mtd. 
Wchnschr., 1914, lxi., Juni 16, S. 1340. 



BIBLIOGRAPHY 


73* 


TAEGB. Bine Methode dor schnellsten Darstellung absolut steriler Kochsabz- 
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SCHMITT. Die Sal varsantodesfalls und ihre Ursachen mit Beriicksichtigung der 
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1337 und 1396. 

Neosalvarsan.—CRAIG, C. B. v and COLLINS, JOSEPH. Four yean' experience 
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syphilis. Joum. Amer. Med. Assoc., 1914, LdL, June 20, p. 1955. 
BLAISDELL, J. HARPER. The use of neoealvarsan from a clinical and 
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p. 868. 

GIRSDANSKY, J. Neoealvarsan in concentrated solution. N. Y. Med. Joum., 
1914, xcix., June 20, p. 1243. 

SEGER, EMIL. Erfahrungen mit Neoealvarsan. Prayer Med. Wchnschr., 1914, 
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RtfHL. Ueber Salvarsan und Neoealvarsan, besonders ambulatorisch angewendet. 
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Lwetftw Reaction. —NANU - MUSCEL, ALRXANDRRSCA - DERSCA, and 
FRIEDMANN. Uber die Luetinreaktion nach Noguchi. Miinch. Med. 
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Wassermann Reaction.—HECHT, H. Zum Wesen der Wassermannschen 
Reaktion. Prayer Med. Wchnschr., 1914, xxxix., Juni 18, S. 316. 
HIERONYMUS, W. Peychiatrische Erfahrungen mit der Wassermannschen 
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ges. Neurol, u. Psychiat ., 1914 xxv. (Orig.), S. 82. 

RAYANT, PAUL. Les erreurs d'interprStation de la reaction de Wassermann. 

Annales de Dermatol, et de SyphUig., 1914, v., Mai, p. 285. 

STERN, M. Zur Theorie und Praxis der Wassermannschen Reaktion. Ztschr. 

f. Immunitatsforsch., 1914, xxii. (Orig.), S. 117. 

THOMPSON, LOYD. The titration of Wassermann reagents. Arch. Ini. Med., 
1914, xiii., June, p. 904. 

STONE, CHESTER T. Sources of error in the Wassermann Technic. N. Y. 

Med. Joum., 1914, xcix., June 20, p. 1242. 

SOUTHARD, E. E. Statistical notes on a series of 6,000 Wassermann tests for 
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Boston Med. and Surg. Joum., 1914, olxx., June 18, p. 947. 

PEASE, M. C. The provocative Wassermann reaction. Med. Record , 1914, 
lxxxv., May 30, p. 982. 

Cerebrw-ftpiMl Field.—GLASER, ARTHUR* Zur ldinisohen Brauchbarkeit 
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xxxiii., Juni 16, S. 748. 

De CRINIS and FRANK. Ueber die Goldsolreaktion im Liquor cerebrospinalis. 

Miinch. Med. Wchnschr ., 1914, lxi., Juni 2, S. 1216. 

BOVERI. Eiue neue Reaktion der Zerebrospinalfliissigkeit. Miinch. Med. 
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WECHSELBAUM and DINKELACKER. Uber die Beziehungen der allgemeinen 
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SPAT, W. Zur Frage der Herkunft des luetischen Reaktionskoipers in der 
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HAUPTMANN. Die Diagnose der “ fruh-luetischen Meningitis" aus dem 
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NONNR. Uber die Bedeutung der Liquoruntersuchung fiir die Prognose von 
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GUTMANN, C. Liquorbefunde bei unbehandelter Friihsyphilis. Dermatol. 

Wchnschr ., 1914. Nr. 25, Juui 20, S. 705. 

BABES, AUREL A. Le liquide cdphalo-raohidien dans les falmorragies craniennes. 
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74* 


BIBLIOGRAPHY 


CLAUDE, H., PORAK, R., and ROUILLARD, J. Recherche* dt manometrie 
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CtKAEBAL AND HNCT10V4L DlftEAHR*— 

Epilepsy.—KELLNER. Die arztliche Versorgung der Anstalten fur Schwacb 
sinnige uml Epileptiker. Ztschr. /. d. Erjvrsch. «. Bthandi d. Jugendl. 
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Hysteria.—LEVY, P.*E. A propos d'un cas d’hystcrie. Le traitement de* 
nrvro»en par 1 education de la volonte. Jourtu dcs Prat, 1914, xxviii.. Juin 
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H ASCII E - KLUNDKR. Ein Fall von degenerativer Hysteria in engem 
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RHEINDORF, A. Hysteroneuraathenie oder cbronisebe appendicitis? Btrl. 
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GRIFFITH, J. P. C. Neurotic, psychasthenic and hysterical children. N.Y 
Med. Journ ., 1914, xcix., June (i, p. 1113. 

C'fearea*—DRAPER, A. P. The relationship between chorea and rheumatism. 
Dublin Journ. Med. Sci ., 1914, Series 111., No. 510, June, p. 416. 

Xemrllls.—THORN VAL, A. Polyneuritis cerebralis menteriformis (t. Fonkl 
Hochwart). Ztschr. /. Ohrenheilk. ti. /. d. Krankh . d. Luftwtge, 1914, Ixxi., 
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Nemralgla*—CAMP, CARL D. The treatment of trifacial neuialgia by the injection 
of alcohol into the Gasserian gauglion. Med. Record , 1914, lxxx?., June 20, 

p. 1110. 

LUCE. Beitrag zur Klinik der Hodeuneuralgie. Dent. Ztschr. /. Nenenheilk., 
1914, li., S. 198. 

Senrastlseala*—HAIG, A., and OXON, D. M. Deficiency of chloride of sodium in 
the etiology of neurasthenia. Med. Record, 1914, lxxxr., June 6, p. 1017 

PaycMaae*.—BLOCK, S. A new psychosis. N.Y. Med. Journ., 1914, xcii., 
May 23, p. 1038. 

MRRCKLIN, A. Die Psychosen imserer kleinst&dtischen Bevolkerung. Ztschr. 
/ d. (je$. Neurol, u. Psychiat., 1914, xxv. (Orig.), S. 142. 

LUTHER, A. Erblichkeitsbeziebungen der Psycbosen. Ztschr. f. d. gts. Neurol 
n. Psychiat., 1914, xxiv. (Orig.), S. 12. 

AleohallsaSy .PERELMANN, A. De la dipsomania. VEnciphale, 1914, lx., 

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SCHNEIDER. Zur Behandlung ties Delirium tremens. Milnch. Med- 
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Kxspbtlialsile Goitre, Cretinism* de. — ABRAHAMS, R. The medical 
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p. 1122. 

SONNE, CARL. Uebt das Antithyreoidin eine spezifische Wirkung gegeniiber 
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PLETNEAV, D. D. Ueber den Basedowsyndrom, ein t re tend mit akuten in- 
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GOETZKY, F., and WB1HE, F. Uber die Bedeutung der Rpiphysenscbatten 
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Telaams. —IRONS, E. E. The treatment of tetanus by antitoxin. Journ. Amer. 
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STEVENS, P, A. Treatment of tetanus by subdural injections of magnesium 
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Tetany.— BEUMER, H. Das Dialysieverfahren Abderhaldens bei Reohitis und 
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MASSLOW, M. Uber Verknderungen der Atmungskurren bei Kindern mit 
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BIBLIOGRAPHY 


75* 


Addison's Mieue.—MUNZER, E. Bin Fall von Morbua Addiionii mit besonderer 
BerUcksichtigong der hfcmodynaraischen VerhSltnisae nebst Berner kungen iur 
Lehre von der Acidose. Ztichr . /. exper. Path. u. Therap., 1914, xiv., 8. 281. 

NlftCELUNRiOIIS SYMPTOMS AND CASES— 

MAKUEN, G. H. A study of 1,000 cases of stammering 9 with special reference to 
the otiology and treatment of the affeotion. Therap. Qaz ., 1914, xxxviii, June, 

p. 386. 

TURAN, F. Uber die neuralgiache Form der Angina pectoris. IPicn. Med. 
Wchnschr., 1914, lxiv., Juni20, S. 1396. 

WEICKSEL. Ueber dystrophia adiposo-genitalis, Afiinch. Med. Wckn$chr. f 
1914, lxi., Juni 2, S. 1227. 

AUER, JOHN. The effeot of intraepinal injections of serums, with and without 
preservatives. Joum. Amer . Afed. Assoc ., 1914, lxii., June 6, p. 1799. 
RABINOWITZ, M. A. Two neurological cases in pediatric practice. Med. 
Record , 1914, lxxxv., June 6, p. 1031. 

ORCHARD, N. G. A case of anorexia nervosa in an infant. Archives of Ptd. % 
1914, xxxi., May, p. 367. 

R08ENSTERN, J. Uber spasmophile Diathese. Zischr. /. d. ges. Neurol . u. 
Psychiat ., 1914, x. (Ref.), 8. 1-32. 

TOMASCHNY. Ein Beitrag zur Frage des PUegerunterrichtes. Zischr . /. d. 

Neurol. u. Psychiat ., 1914, xxv. (Orig.), S. 126. 

SAENGER. Uber Eunuchoidism us. Zteul. Zischr. f. Nervenhcilk., 1914, li., S. 
178. 

SPECIAL SENSES AND CRANIAL N EM YES— 

BOETERS, OSKAR. Vergleiohende Untersnohungen Uber den Drehnachny* 
stagmus und den kalorischen Nystagmus. Zischr. f. Ohrenhcilk. u. /. d. 
Krankh . d. Luftwege , 1914, IxxL, 8. 77. 


PSYCHIATRY. 

GENERAL PARALYSIS— 

BONHOMME. Les acquisitions recentes dans le domains de la paralysis glntode. 

Jfer. Aftrf. de 2a &utue Roto., 1914, xxxiv., Mai 20, p. 338. 

RIGGS, C. E. Juvenile paresis treated by the intraepinal injection of salvarsan- 
ized serum. Report of a case. Joum. Amer. Med . A**oe., 1914, lxii, June 13, 

p. 1888. 

COLLIN, A. Quelle est la forme olinique de la syphilis qui aboutit le plus 
souvent k la paralysis g4n4rale? Gaz. aes H&p., 1914, lxxxvii., p. 1125. 
PASCAL, C. Forme paranoids de la paralysis glnlrale. L'Enctphale , 1914, lx., 
Juin, p. 544. 

BANSE, H., and RODERBURG, H. Bcmerkungen Uber die progressive Paralyse 
mit besonderer BerUcksichtigung der Halluzinafionen. Zischr. /. d. ges. Neurol . 
u. Psychiat ., 1914, xxv. (Ong.), 8. 99. 

LAUSCHNER. Die Frage der leichten Lues und der spfcteren Paralyse. Zischr. 

f. d. ges. Neurol, u. Psychiat ., 1914, xxv. (Orig.), 8. 169. 

LIND, W. A. T. A case of juvenile general paralysis of the insane. Australian 
Med. Joum., 1914, iih, May 23, p. 1567. 

DEMENTIA PRRCOZ— 

MEGGENDORFER. Uber Syphilis in der Asoendenz von Dementia ptaeoox- 
Kranken. Deut. Zischr. f. Nervenhcilk., 1914, li., 8. 443. 

SIMON, C. E. The Abderhalden-Fauser reaction in mental diseases, with special 
reference to dementia prsscox. Joum. Amer. Med. Assoc., 1914, lxii.. May 30, 

p. 1701. 

ROSS, ELLISON L. Metabolism in dementia prseoox. Arch. Int. Med., 1914, 
iii., June, p. 889. 

SCHRODER, M. Todesursachen schizophrener Frauen. Zischr. f. d. ges. Neurol 
u. Psychiat., 1914, xxv. (Orig.), p. 115. 

GENERAL— 

DUFOUR, H. Trois cas de psychoee polynrfvritique ou maladie de Khorsakoff, 
Journ. de M4d. de Paris, 1914, xxxiv., Juin 6, p. 447. 



BIBLIOGRAPHY 


76* 


BURR, C. W. Chronic dementi*, cerebellar ataxia and epileptiform convuliioni 
in a boy canned bv ptomain poisoning from eating canned salmon. Joum, 
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PARHON and ODOBKSCO. Sur un syndrome peycho-endocrimen carseterii* 
par un etat paranoide et dee troubles thyro-ovariens, Relations patfcogenetiquei 
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VEncepkale, 1914, ix., Juin, p. 489. 

WOODBURY. F. The treatment of the insane in the tropics. N.Y. Med 
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ROSENTAL, STEFAN. Zur Methodik der Schadelkapazitatsbestimmimg ©it 
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1914, xxxiii., Juni 16, S. 738. 

FROMMER, K. Ein durch seinen Verlauf und seine Sphtgenesung bsschten- 
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(Orig.), 8. 107. 

KRETSCHMER, E. Wahnbildung und m&nisch-depreasiver 8ymptorakomplex. 
Allg. Ztsc.hr. /. Psychiat., 1914, lxxi., S. 397. 

FISCHER, MAX. Berufsgeheimnis und Herausgabe der Krankengeschichten. 
Allg. Zttehr. /. Psyrhiat.. 1914, lxxi., S. 464. 

ALBRECHT. Kasuiatischcr Beitrag zur Konstanz der Wahnideen und Sinnw- 
tauschungen. Allg. Zttehr. /. Psychiat., 1914, lxxi., S. 493. 

SIEMENS, F. Die Provincial-Heilanstalt Lauenburg in Pommern nsch 25 
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LIND, J. E. Diagnostic pitfalls in the mental examination of negroes. N. Y. 
Med. Joum., 1914, xeix., June 27, p. 1286. 

BISCH, L. E. The recognition of mental deficiency. N. Y. Med. Joum., 1914, 
xeix., May 30, p. 1073. 

DENDY, MARY. Feeble-minded children. Joum. State Med., 1914, nil, 
July, p. 412. 

JAR RETT, MARY C. The function of the social service of the psychopathic 
hospital, Boston. Boston Med. and Surg. Joum., 1914, dxx., June25, p. 987. 

SCHLAPP, MAX G. An economic and social study of feeble-minded women. 
Med. Record, 1914, lxxxv., June 6, p. 1025. 


TREATMENT.* 

LIEBESNY, P. Elektropbysiologische Studien zur Therapie der Lahmungen. Wien. 

Med. Wchntchr ., 1914, lxiv., Juni 27, S. 1450. 

LAPINSKY, MICHAEL. Tiber mechanische Bader in der neurologiachen Praxii 
(hydraulische Massage). Neurol. Ccntralbl., 1914, xxxiii., S. 743. 

ZEUNER, W. Pbenoval als Beruhigungsmittel fur die Nerven. ZentralhL f.d.get . 
Therap ., 1914, xxxii., Mai, S. 227. 

p§ych#*B*Iy»i»«— PUTNAM, JAMES J. The present status of psychoanalytic 
Boston Med . and Surg. Joum., 1914, olxx., June 11, p. 897. 

CLARK, L. PIERCE. Some nersonal results in psychoanalysis and the future of 
psychotherapy. Boston Med. and Surg. Joum., 1914, clxx., June 11, p. 903. 
BURROW, T. The psychanalyet and the community. Joum. Amer Med. 
Assoc., 1914, lxii., June 13, p. 1876. 

HAMBURGER, F. Uber Psychotherapie im Kindesalter. Wien, Med. 

Wchnschr 1914, lxiv., Juni 13, S. 1313. 

GOTT. Psychotherapie in der Kinderheilkunde. Munch. Med. Wchnschr., 
1914, lxi., Juni 23, S. 1377. 

* A number of referenoee to papers on Treatment are inoluded io the Bibliography under 
Individual diseases. 



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CARNOT and COIRRE. Localisation du brome apr&s son administration therapeutique. 
Compt. Rend. d. 1. Soc. de Biol., 1914, lxxvii., p. 197. 

HERRING, P. T. The origin of the active material of the posterior lobe of the pituitary 
bodv. Quart. Journ. Exp. Physid., 1914, viii., p. 245; the physiological activity 
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Ibid., p. 267. 

HILL, R. L, and SIMPSON, 8. The effect of pituitary extract on milk secretion in 
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HEWITT, J. A. The influence on metabolism of administration of small amounts of 
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GARNIER and SCHULMANN. Action des extraits oombin4s de surrtnale et 
d’hypophyse poetcrieure sur la s&r4tion urinaire. Compt. Rend. d. L Soc. de Bid, 
1914, lxxvii., Juillet 24, p. 388. 

ANTONI, N. R. E. Adrenalin und Pupille. Neurd CentralbL, 1914, xxxiii, Juni 1, 
S. 674. 



BIBLIOGRAPHY 


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PSYCHOLOGY. 

WATT, H. J. Psychological analysis and thsory of hearing. Brit. Joum. Psychol., 
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THOMSON, G. H. The aocuracy of the <p (y) process. Brit. Joum. Psychol ., 1914, vii., 
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HOWARD, R. A note on pictorial balance. Brit. Joum. Psychol ., 1914, vii., p. 56. 

CARET,.N, An improved colour wheel. Brit. Joum. Psychol ., 1914, vii., p. 64. 

MYERS, C. S., and VALENTINE, C. W. A study of the individual differences in 
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MYERS, C. S. Two cases of synesthesia. Brit. Joum. Psychol ., 1914, vii., p. 112. 

VALENTINE, C. W. The method of comparison in experiments with musical 
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FERNBERGER, S. W. Note on the affective values of oolours. Amer. Joum. Psychol ., 
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LELESZ, H. L’orientation d’esprit dans le tdmoignage. (5 fig.) Archives dt Psychol ., 
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OD1ER, OH. Apropos d*uncas de contracturehysterique. (2fig.) Archives dePsychol., 
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DEGALLIER, E. Horlogerie et psychologic. Archives de Psychol ., 1914, xiv., p. 202. 

REICHARDT. Ueber die Folgen psyobischer Vorg&nge auf Korper und Seele. 
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BOCCI, B. La psiohe emotive. Rassegna di Studi Psichiat ., 1914, iv., Maggio-Giugno, 
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HAENEL, HANS. Neue Beobachtungen an den Elberfelder Pferden. Neurol. 
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MIDDLEMI3., J. E. Some oases of psychological interest from private practice. 
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HASS ALL, JAMES C. Constitutional psychopathy in children. Pediatrics, 1914, 
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VALLON and FURS AC. La timidity sexuelle au point de vue medicolegal. Archives 
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PATHOLOGY. 

KRAUS, E. J. Uber einen Fall von pigmentiertem Gliom bei mnltiplen Gliomen des 
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MATTIOU, L. Su l’origine della “ Plasmazellen” e la loro nresenza nel sangue 
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SANGUINETI, L. R. Influenza della sostanze nervine su raccrescimento dei nervi 
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BUSCAINO, V. M. Graisses, sterines et lipoides dans le syst&me nerveux central en 
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SHINYA, S. Experimentalversuohe Uber Muskeltransplantation mit BerUcksiehtigung 
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SACQUEPEE and DELATE R. Nouveau milieu do culture pour le mrfningoooque et 
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CLINICAL NEUROLOGY. 

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GUILLAIN and LAROCHE. La fixation dea poiaona but le syst&me nerveux. 
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MUSCLES— 

HERZ, A. F. Three membera of one family Buffering from Myotonia Hyper> 
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GOMBEL, TH. Zur Behandlung der apaatiaohen L&hmungen mit der Foerater’* 
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Tnmoars.— BAILEY, PEAKCK. Painleaa tumours of the spinal cord. Journ. 
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BABIN SKI, J., LECENE, P., and JARKOWSKI, J. Paraplegic crurale par 
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Tabes Dorsalis.—VIX. Der heutige Stand der Tabes-Paralyae-Frage. Fortechr. 
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RICHTER, HUGO. Zur Hiatogeneae der Tabea. Vorl&ufige Mitteilung. 
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DAUWE, F. L’hypers4cr4tion dans lea criaea gaatriquea du tab&s avec eaaai de 
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EXNER, A., and SCHWARZMANN, E. Gaatrische Krisen und Vagotomie. 
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STEW"ART, PURVES. The diagnosis and treatment of oerebro-apinal syphilis, 
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Poliomyelitis Anterior Aenta.—FRASER, FRANCIS R. Clinical observations 
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oxlviii., July, p. 1. 



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BURNETT, ROBERT. Poliomyelitis. Joum. State Med., 1914, xxii., April, 
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BATTEN, F. E. Further note on the use of celluloid splints in the treatment 
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CYRIAX, E. F. The mechano-therapeutics of chronio infantile paralysis (polio* 
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BBAUV— 

Cemerml.—WYNNE, F. E. Tubercle of the crus cerebri simulating enteric fever. 
Lanai, 1914, clxxxvi., June 13, p. 1676. 

STERN, A. Uber eine Schussverletxung des Thalamus opticus nebst Bemerkungen 
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FULPIUS, Q. A propos d’un cas de syndrome thalamique. Rev. mid. d. 1. 
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REIOHARDT, M. Hirn und Korper. B. Das Kdrpertemperatur bei Hirnkrunk- 
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REICHARDT, M. Die physikalischen Eigenschaften und Zustands&nderungen 
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REICHARDT, M. Uber normale und Elrankhafte Vorgange in der Hirnsubstanx. 
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JANICHEWSKY, A. Le rdflexe de prehension dans les affections organiques de 
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Skull Injury, Ac.—SOLIERI, SANTE. Ueber die Stichwunden des Gehirns 
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Yen Recklinghausen's Disease.—SCHOONHEID, P. H. Beitrag xur Kasuistik 
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Disseminated Sclerosis.—STAMM, CARL. Bin Fall von multipler Skleroee 
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(Cerebellar Ataxia.—BLAUNER, S. A. Hereditary cerebellar ataxia. N. Y. 
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Meningitis.-CLARKE, J. MICHELL, SYMES, J. ODERY, and VEALE, P. J., 
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1914, June 13, p. 1286. 

COMBY and CONDAT. M4ningite odr4bro*spinale avec arthrites k mlningo- 
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SMITH, W. M. Meningitis in children. Brit. Med. Joum., 1914, May 2, 
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KERR, CHARLES. Case of chronic primary pneumoooocal oerebro-spinal 
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DUFOUGERE, W. La m^ningite k pneumoooques des tirailleurs rfnlgalais. 
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HUMBERT, G., and ALEXIEFF, W. Contribution k l'dtude de la mlninrite 
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BARTHELEMY, R. Les hlmorragies mfoingles. (Rev. g4n.) Prog, mid., 
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CLEGG, J. G. A case of orbital oellulitis produoed by ethmoidal sinusitis. 
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MILLER, JAMES, and HEWAT, A. FERGUS. A case of tuberculous disease 
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Abscess.—WILKINSON, GEORGE. A caso of paralysis of the external rectus 
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xxix., Aug., p. 409. 



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Tumours. —HOWLAND, G. \V. The diagnosis of subtentorial tumours. With 
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JOHNS* >X. W. A pathological investigation of four cases of pituitary tumour. 
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Aphasia, Ac. —DURUY. EUGENE. A lecture on localisation of motor and speech 
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Lend Poisoning.—STAINTHORPE, \V. W. Observations on 120 cases of lead 
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Syphilis.—STEINER, G. Zur Erzeugung und Histopathologie der experimentellen 
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BAUDOUIN and MARCORELLES. Paralysie radiale et syphilin. (2 fig.) 
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EuetlB Reaction.— KLAUSNER, E. Die Kutireaktionen bei Syphilis mit 
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KALISCHER, S. Die Retiexcpilepsie und ihre chirurgische Behandlnng. 
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BOLTEN, G. C. Ueber Wesen und Beh&ndlung der sogenannten “genuinsn” 
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AUSTREGESILO, A., and AYRES, O. Myoclonia et dpilepsie (syndrome de 
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GORN f W. Uber Myoklonie, Myoklonus-Epiiepsie und verwandte Kiankheiten. 
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PELLACANI, G. Ricerche suila deviazione del oomplemento nelT epUesiia. 
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NIKITIN. Ueber den Einfluss der Schutzimpfungen gegen Lyna auf den 
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ULRICH, A, Beitrag zur Technik der wirksamen Brombebandlung der Bpilepm* 
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Paramyoeloans.—WILLIAMS, E. M. Paramyoclonus multiplex, including a 
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Hysteria.— AMES, T. H. Analysis of blindness as a symptom of hysteria. 
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Chorea.—M‘KINNISS, C. R. The value of eugenics in Huntington’s chorea. 
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Xearltls.— DAVIES, N. Neuritis: treatment by electricity. Practitioner f 1914, 
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Berl-Berl.— SMITH, F. Beri beri on polyneuritis among British troops in India. 
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BRADDON, W. L., and COOPER, E. A. The influence of the total fuel-value 
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KING, H. D. The etiological controversy anent beri-beri, with some remarks as 
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Mearasthenla.—HURRY, J. B. The vicious circles of neurasthenia. Brit. Med. 
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KRONFELD, A. Ueber die psyobologische Entstehung sogenannter Unfall- 
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RHEINDORF, A. Hysteroneurasthenie oder chronische Appendicitis ? Berliner 
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Nearoses.—GRANT, J. W. GEARY. The traumatio neuroses: some points in 
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KNEPPER. Rentenaufhebung bei angeblicher traumatischer Neurose. Fortseh. 
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Psychoses.—MOSHER, J. M. The psychosis of adolescence. Albany Med. 
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MYERSON, A. A note on the relative weight of the liver and brain in 
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Alcoholism, Ac.—LESSEY, Rev. S. S. The management of the male inebriate 
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THORNE, GUY. The inhalation of cigarette smoke and its relation to chronic 
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P 



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COBH, I. G. A case of hypothyroidism in a mala Brit. Mtd. Journ, 1914, 
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VALTORTA, D. Ricerche urologiohe ed ematologiche in frenastenid am sin- 
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Tetaawa.—STROHMEYKR. Zur Magnesium be hand lung des Tetanus. MwL 
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PARK, WM. H., and NICOLL, M. Experiments on the curative vslue of the 
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Tetaay.—MORGKNSTERN, K. Elektrokardiographiscbe Untersuchungen iiher 
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SPECIAL IFASE.4 AMD CKANIAL NEB YES— 

HANSELL, H. F. Acute double optio nerve atrophy. N. Y. Mtd. Joum., 1914, 
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BYERS, W. G. M, Tumours of the optic nerve. Journ. Anur. Med. Auoe., 
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FRANCIS, L. M. Two cases of acute retrobulbar neuritis, associated with 
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GKADLK, H. E. A subjective examination of the papillary reflexes. Archives 
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LOEPER, MOUGBOT, and VAHRAM. Abolition frdquente du rdflexe oculo- 
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SMITH, E. B. Congenital defect, sixth and seventh cranial nerves. Proe. Rof 
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ZALEWSKI, TEOFIL. Quantitative Untersuchungen iiber den kaJoriechea 
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miscellaneous symptoms and cases— 

DAVIES, IVOR J. Carbon monoxide poisoning in the Senghenydd explosion. 
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SCHUSTER* PAUL. Gehkufte postdiphtherische L*bm ungen; ein Beitoag wr 
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ROTHMANN, MAX. Ueber die Ausfallseracheinungen nach Affektionen det 
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NEUGEBAUER, HANS. Beitrag cur klinik der Vagotonic. Wien , klin. 
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M 4 CORD, O. P. The pineal gland in relation to somatic, sexual, and mental 
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STERLING, W. Die trophischen, vegetativen Erkrankungen, Missbildungen 
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WILHELM. M. Bin Beitrag zu den nervosen Aequivalenten im Skuglingsalter. 
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RECKZEH. Ueber die Begutachtung arteriosklerotisoher und konstitutioneller 
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MILLER, R., and DAVIDSON, J. A. The nervous oompUcations of varicella. 
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COLLIE, Sib JOHN. The necessity for a systematic and oomplete examination 
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BERTOLANI, A. Le Paralisi da Fosfato di Creosoto. Riv. Sper. di Freniat., 
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BOYLE, A. HELEN. Some observations on early nervous and mental cases, 
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PSYCHIATRY. 

CDIIKAL PARALYSIS— 

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BEMKNTU PRRCGY— 

SINGER, H. D. Dementia nraecox in the eighth edition of Kraepelin’s text¬ 
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HOLMES, B. The country care of the dementia precox patient. Therap. Oat., 
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HINR1CHSEN, OTTO. Die Demens der Dementia preoox-Kranken. Corre- 
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GENERAL— 

MOTT, F. W. A lecture on the causes of insanity. Lancet, 1914, clxxxvii., 
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ANSALONE, G. Contribute alia istologia patologica deUe forme atipiche di 
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CUNEO, GEROLAMO. Psicosi maniaco-depressiva prodotta da ritenxione di 
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ROSENTAL, STEFAN. Zur Methodik der SohLdelkapasitLtsbestimmung mit 
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88* 


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VALTORTA, DARIO. L’eliminazione dell’ Azoto e dell’ Acido urico in stati di 
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FAUSER. Ueber “passive” Uebertragung der Ferment* von Geisteskranken 
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SCHROEDER. Einige teohnische Neuerungen in der Dialysiermetbode und die 
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EAGER, R. The rftle of hypnotics in mental diseases, with indications for their 
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PETRAZZANI-SAGOOZZI. Sullo stato di mente del soldato Augusto Mawtti 
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TREATMENT.* 

CHARTIRR, M. Lee bains hydrodlectriquee dans le traitement des affections du 
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LAPINSKI, M. Uber mechanische B&der in der neurologisohen Praxis. (Hydraulisobe 
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WILSON, J. HORNE. Neuro-electricity. The electropathology of disease and 
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LAPINSKY, MICHAEL. Uber mechanische Bader in der neurologisohen Praxis. 
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HELLPACH. WILLY. Die elektrischen Heilwerte. Kritische Bemerkungen zu 
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STERN, F. Erfahrungen mit dem neuen Schlaf- und Beruhigungsmittel Dial-Ciba. 
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MAYER, FELIX. Beitrag zur Wirkung eines neuen Sohlafmittels, dee Dial-Ciba. 
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SAYER, ETTIB. Mentally defective children and their treatment. Joum. State 
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BLEULER. Die Behandlung der moralisch Schwachsinnigen. Correspondenz-Blatt. f. 
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Psychoanalysis.—HABERLIN, P. Psychoanalyse und Erziehung. Internal. 
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HATTINGBERG, HANS VON. Analerotik, Angstlust und Eigensinn. Internal. 
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LONG, CONSTANCE E. Psycho-analysis. Practitioner , 1914, xciii., July, 
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TELLING, MAXWELL. A plea for the more systematic employment of treat¬ 
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LADELL, R. G. M‘DONALD. Some practical points in connection with the use 
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# A number of references to papers on Treatment are included in the Bibliography under 
Individual diseases. 



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HELL WIG, ALBERT. Zur Psychologic Kinematographischer Vorfuhrungsn. ZUchr. 
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MADAY, STEFAN v. Heilung durch Kunstgenuss. Ztschr. /. Psychotherap 1911, 
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WILLIAMS, TOM A. A contrast in psychoanalysis: three cases. Joum. Abnorm. 
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SOLOMON, MEYER. The analysis and interpretation of dreams based on various 
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PATHOLOGY. 

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CLINICAL NEUROLOGY. 

tilffIBAL— 

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nrsass- 

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DUNN, C. H. Myatonia congenita, with report #f cases. Boston Mid. and Surg. 
Joum., 1914, olxxi., July 30, p. 191. 

SHAW, A. F. B. Pseudo-hypertrophic muscular dystrophy. (IUustr.) Dublin 
Joum. Med. Set., 1914, No. 512, Aug., p. 115. 

gPHil CBBJt— 

Fmcimrr, Msl#eatl#m, Ac.—RADLEY, J. H. Spinal subluxations. Their 
nature and cause. Med. Record , 1914, lxxxvi., Aug. 1, p. 203. 



BIBLIOGRAPHY 


91* 


Tabes Denali*.—WHITE, 0. J. A statistical study of syphilis. The relation of 
its symptoms to subsequent tabes dorsalis or general paralysis. Joum. Ainer. 
Med. Assoc., 1914, lxiii., July 25, p. 459. 

Poliomyelitis Anterior Acnta.— MENCIERE, LOUIS. Paralysis flasque du 
membre sup4rieur par poliomydite antlrieure (paralysis infantile). Traitment 
orthop4dique et ctururgical. L'EnctphaU , 1914, ix., Juillet, p. 49. 

FRANCIS, E. An attempt to transmit poliomyelitis by the bite of Lyperoeia 
trritans. Joum. Infect. Bit., 1914, xy., July, p. 1. 

Hiematomyella. — BABINSKI. H4matomydie. Joum . dec Prat., 1914, 

xxriii., Aoflt 1, p. 487. 

Neuroma*—MONRO, T. K., and DUNN, J. S. Malignant gaaglio-neuroma of 
left suprarenaL Glasgow Med. Joum., 1914, lxxxii., Aug., p. 81. 

RRAO— 

Disseminated Sclerosis.—HOLLOWAY, T. B. Peripheral pigmentation of the 
oornee, associated with symptoms simulating multiple sclerosis. Amer. Joum. 
Med. Set., 1914, cxlviii, August, p. 235. 

Amaurotic Family Idiocy.—HUME, W. E. A oase of amaurotio family idiocy. 
Review of Neurol, and Psychiat., 1914, xii, p. 281. 

Meningitis. —FABER, H. K. A case of tuberculous meningitis complicated by 
influenzal meningitis. Amer. Joum. Die. Child., 1914, viii., Aug., p. 150. 

Angiospasm.—CORDON, A. Spasmodic dosing of oerebral arteries in its 
relation to apoplexy. Albany Med. Annals, 1914, xxxv., Aug., p. 423. 

Tumours.—GORDON, ALFRED. Mental manifestations in tumours of the brain. 
Amer. Joum. Med. Sei ., 1914, cxlviii., Aug., p. 225. 

Pituitary Tumours, Ate. —DUNN, ALFRED. Pituitary disease: a clinical 
study of three cases. Amer. Joum. Med. Set., 1914, cxlviii, Aug., p. 214. 

Infantilism.— STRAUCH, A. Infantilism. Amer. Joum. Med. Sei., 1914, 
cxlviii., August, p. 247. 

Aphasia, Ac.—CORE, DONALD. Some modern conceptions of aphasia. Med. 
Chron., 1914, lix., Aug., p. 309. 

d£j£rINE, J., and PtiLISSIER, A. Contribution k made de In odoittf verbal, 
pure, (aveo 8 fig.) LEneiphale, 1914, ix., Juillet, p. 1. 

Lead Poisoning —WILLIAMS, E. M. Lead poisoning, with paralysis of the 
external ocular muscles. Joum. Amer. Med. Assoe., 1914, lxiu., Aug. 1, 
p. 403. 

Syphilis. —HUNT, J. RAMSEY. Syphilis of the vertebral column; its sympto¬ 
matology and neural complications. Amer. Joum. Med. Set., 1914, oxlviii., 
Aug., p. 164. 

BOARD MAN, WM. P. Syphilitic heredity and congenital syphilis. Joum. 
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HAZEN, H. H. Syphilis in the Negro. Joum. Amer. Med. Assoc., 1914, 
lxiii., Aug. 8, p. 463. 

NICOLS, H. J. Observations of the pathology of syphilis. Joum. Amer. Med. 
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Salvarsan.*—BEST, WM. H. The use of salvarsan in non-syphilitie diseases. 
Joum. Amer. Med. Assoc., 1914, lxiii, Aug. 1, p. 375. 

LEREDDE. Les aoddents du salvarsan. M4canisme et prophylaxis. Joum. 
des Prat., 1914, xxviii, Aofit, p. 481. 

Neosalvarsan.— HARPER, PHILIP. Treatment of yaws by intravenous and 
intramuscular injections of salvarsan and neosalvarsan. Lancet. 1914, olxxxvii, 
Aug. 8, p. 370. 

Luctin Reaction.—PUSEY, W. A., and STILLIANS, A. W. Noguchi’s luetin 
test for syphilis. Joum. Cut. Bis., 1914, xxxii., Aug., p. 560. 

Wassermann Reaction.— JUDD, C. C. W. A comparison of oholesterinised 
and non-oholesterinised artificial antigens in the Wassermann reaction. Joum. 
Amer. Med. Assoc., 1914, lxiii, July 25, p. 813. 

HIB8CHFBLD, L., and KLINGER, R. Une nouvelle reaction du sdrum 
syphilitique: la ooagulo-rtaction. Semaine mid., 1914, xxxiv., Aofit 5, p. 361. 



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Uvtkrt RpUal FlaHL—FRAZIER, C. H. The ecrebro-spinal fluidisemblem 
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OKNiKii amd mxmewu iuuiM- 

Epilepsy.—STEWART, K. M. The action of adrenalin end epinineon the pupil 
in epilepsy. Review of Neurol . and PsychiaL, 1914, iiL, p. 297. 

Cfcarau—LEOPOLD, S. 8. Eosinophilia in choree. N. 7. Med. Joum., 1914, a, 
Aug. 1, p. 225. 

Psyefceee*. —WILLIAMS, GUY H. An intoxication psychosis Meoeisted with 
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ExeplithalMlc Mtre, CreUsiiM, Ac.—HALSTEAD, WM. 8 The significance 
of the thymus gland in Graves’ diseas e . Bulletin Johns Hopkins Hasp 1914, 
xxv., Aug., p. 223. 

MAYO, C. H. Hyperthyroidism: primary and late results of operation. Lancet, 
1914, clxxxvii., Aug. 1, p. 301. 

SPECIAL 8EMSE4 AN» CEAJflAl MEETEfl— 

HORNE, JOBSON. Gun deafness and its prevention. Lancet , 1914, dxxxtiL, 
Aug. 15, p. 462. 

MlflCELLAMEOl* ITMPTfMfl AMD CAJiEfl— 

DAVIDSON, A. J. Pott’s paralysis. Restoration by Albee’s operation. N.Y. 

Med. Joum. , 1914, c., July 25, p. 174. 

8AVARIAUD. Dee diffc rentes especes de torticolis. Joum. de mid, de Pant, 
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BOEHME, G. F. Pedal tic. Med. Record , 1914, lxxxvl, July 25, p. 159. 

PSYCHIATRY. 

CEIIIAK. PAKALY8I8— 

MEYER, ADOLF. Differential diagnosis of general paralysis. Amer. Joum. 
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SALMON, THOMAS, W. General paralysis as a public health problem. Amer. 
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DEMEMT1A PEJECDX— 

CLARK, 8. N. Atypical inodes of onset in dementia pnsoox. Amer. Joum 
Insanity , 1914, lxxi., July, p. 153. 

HAURY. La “fausee simulation.” Un ddment preoooe catatoniqueoonvsincu 
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ROSANOFF, A. J. A study of brain atrophy in relation to insanity. Amer. 
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BANCROFT, CHARLES P. Is there an increase among the dementing 
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TORREN, J. v. n. Depressieve toestandsboelden. Ncderlandseh Tijdschr. r. 
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BALLET, GILBERT. A propos de la psyohose hallucinatoire chroniqw. 
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ABBOT, E. STANLEY. What is paranoia? Amer. Joum. Insanity , 1914, 
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HAGEMANN, J. A. A rhinologic&l aspect of some mental disturbanoes. Med. 
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WOOD, H. W. The causes of insanity. Boston Mtd, and Surg. Joum., 1914, 
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RICKSHER, CHARLES. Similar and dissimilar psychosis in relatives. Amer. 
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BARKER, L. F. The relations of internal medicine to psychiatry. Amer. 
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The bibliography in this number is greatly curtailed , since, on account 
of the tear, the number of foreign journals reaching this country 
is considerably diminished. 

ANATOMY. 

DUNN, E. H. The pretence of medullated nerve fibre* pasting from the spinal ganglion 
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WULZEN, ROSALIND. The morphology and histology of a oertain structure 
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SMITH, P. E. Some features in the development of the central nervous system of 
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HERRICK, C. JUDSON. The medulla oblongata of larval Amblystoma. (57 figs.) 
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BIONDI, GlOSUfi. Sulla struttura dei glomeruli della oorteooia oerebeliare. Riv. 
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PHYSIOLOGY. 

SIMONELLI, G. Contributo alia oonosoenca delle localiezazioni oerebellari. Riv. di 
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LONG, F. Sur les d4g4n4resoences asoendantes consecutive* k une lesion de la moelle 
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PEARCE, ROY G. Effect of vagus stimulation on the blood flow through the kidney 
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ADRIAN, E. D. The temperature coefficient of the refractory period in nerve. Joum. 
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WOLF, C. L., and HELE, T. S. Gaseous exchange in the decerebrate animal. Journ. 
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PEAR, T. H. The rfile of repression in forgetting. I. Brit. Joum. Psychol ., 1914, 
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WOLF, A. The rile of repression in forgetting. II. Brit. Joum. Psychol, 1914, vii., 
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MITCHELL, T. W. The rile of repression in forgetting. III. Brit. Journ. Psychol., 
1914, vii., Sept, p. 154. 

LOVED AY, T. The rile of repression in forgetting. IV. Brit. Journ . Psychol., 
1914, vii., Sept., p. 161. 

READ, C. The psychology of magic. Brit. Joum. Psychol., 1914, vii., Sept, p. 166, 

WINCH, W. H. Some new reasoning tests suitable for the mental examination of 
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RE AN BY, M. J. The correlation between general intelligence and play ability as 
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PERKINS, N. L. The value of distributed repetitions in rote learning. Brit. Joum. 
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KOLLARITS, J. Observations de psyehologie quotidienne. Arch, dt Psychol., 1914, 
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8AUSSURE, R. d*. Le tamps an general et la tamps Bargsonian an particulier. Arch, 
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PATHOLOGY. 

D ABUNDO, G. Coprioggatti di collodion nella tacnioa microsoopica. Riv. ital. di 
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BIONDI, GIOSUE. Lo stato attuala degli studii istologici soi lipoidi dal sistama 
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NUNNO, R. DE. L’adona del microooooo di Bruoe (melitense) a dalle sue tossina snl 
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COOPER, E. A. The relations of vitamins to lipoids. Biochcm. Joum ., 1914, Tiii. 
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CLINICAL NEUROLOGY. 

GENERA L— 

HAWTHORNE, C. O. On the occurrenoa of a bi-lateral extensor response in 
states of unconsciousness. Practitioner , 1914, xciii., Sept., p. 330. 

KNAUER, ALWYN, and MALONEY, W. J. M. A. The pneumograph. A new 
instrument for recording respiratory movements graphically. Joum. New. 
and Ment. Die., 1914, xfl., Sapt., p. 567. 

MUSCLES— 

ROSENBLOOM, J., and OOHOE, B. A. Clinical and metabolism studies in a 
case of myotonia congenita—Thomsen's disease. Archives of Int. Med., 1914, 
xiv., August, p. 263. 

SPINAL COED— 

Herpes Lester. —DBADERICK, WM. H. Herpes zoster and malaria. Med. 
Record, 1914, lxxxvi., Sept. 5, p. 421. 

Paraplegia.— CO YON and BARR£. Paraplegic “type Babinsld” chez un sujet 
atteint de maladie de Recklinghausen. Absence de d4g4n4ration seoondaire 
des faiscaaux pyramidaux. Nouv. Icon. d. 1. SalpH ., 1914, rii., p. 81. 

Tabes.— JOHNSTON, GEORGE T., BREAKS, L Z., and KNOEFEL, A. F. 
The treatment of tabetic optic atrophy with intraspinal injections of salvar- 
sanised serum. A preliminary report. Joum. Amer. Med. Assoc., 1914, lxiiL, 
Aug. 29, p. 866. 

WILLIAMS, TOM A. The treatment of tabes dorsalis in the light of its recent 
pathology. Med. Press, 1914, cxlix., Sept. 23, p. 327. 

Poliomyelitis Anterior Acute. —GORDINIER, HERMON C. Study of a case 
of the adult type of poliomyelitis. Albany Med. Annals ., 1914, xxxv., Sept., 
p. 48a 

MOORE, J. W. Surgical treatment of infantile paralysis. (20 illust.) N. Y. 
Med. Joum., 1914, c., Aug. 29, p. 404. 

FLEXNER, SIMON, and AMOSS, H. L. Localisation of the virus and 
pathogenesis of epidemic poliomyelitis. Joum. Exp. Med., 1914, xx., Sept. 1, 
p. 249. 

BRAIN— 

Skull Injury, Be.—ROSENBAUM. GEORGE. Rontgen diagnosis in fractures 
of the cranium in ohildren. (3 illust.) N. Y. Med. Joum., 1914, c., Aug. 29, 
p. 414. 

LOFBERG, OTTO. Zur Deckung von Kranialdefekten. Nordiskt Med. 
Arkiv. (Kirurgi), 1913, xlvi., pp. 1-13. 

Disseminated Sclerosis.—SMITH, H. LYON, and STEWART, T. GRAINGER. 
A case of disseminated sclerosis treated by inoculation. Brit. Med. Joum., 
1914, Aug. 22, p. 364. 



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Hereditary Ataxia*—WILLIAMS, E. if. Hereditary ataxia. Amer. Journ. 
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HealaaltU. —BROWNING, CHAS. 0. Report of four oases of what appeared to 
be tuberculous meningitis with apparent permanent arrestment. Med. Record, 
1914 t lxxxvi., Aug. 22, p. 326. 

MAJOR, RALPH H. v and NOBEL, E. The glycl-tryptopban reaction in 
meningitis. Archives of ItU. Med., 1914, xiv., Sept. 15, p. 383. 

Hydrocephalus.— ROUBINOVITCH and BARBE. Contribution k l’etude de 
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Hsemerrhage. —MOTT, WALTER M. Report of a case of cerebral haemorrhage. 
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Axglespasm.—GORDON, ALFRED. Spasmodic closing of cerebral arteries in 
relation to apoplexy. Journ. Nerv. and Ment. Dis., 1914, xli, August, p. 501. 

Cerebellans.—TAFT, A. E., and MORSE, M. E. Hemiatrophy of the cerebellum 
im a case of late catatonia. Journ. Nerv. and Ment. Die., 1914, xli., Sept., 
p. 553. 

Tamoars.—BLAIR, V. P. Treatment of unlocalised intracranial injuries by 
drainage through a subtemporal approach. Journ. Amer. Med. Assoe., 1914, 
lxiii., Aug. 29, p. 863. 

Acromegaly.—ADDA, M. Dystrophies gigantiques sans acromegalic. (3 pL) 
Nouv. Icon. d. 1. SalpH, 1914, vii., p. 90. 

BERGEIM, OLAF, STEWART, F. T., and HAWK, P. B. A study of the 
metabolism of calcium, magnesium, sulphur, phosphorus, and nitrogen in 
acromegaly. Journ. Exp. Med., 1914, xx., Sept., p. 218. 

HyspfltaUarlsni.—FALCONER, A. W. Further note on a case of dyspituitarism. 
Edin. Med. Journ., 1914, xiii., Sept., p. 246. 

ANDERS, J. M., and JAMESON, H. LEON. The relation of glyoosuria to 
pituitary disease and the report of a case with statistics. Amer. Journ. Med. 
Set., 1914, cxlviii., Sept., p. 323. 

rellagra.— BOX, CHARLES R English pellagra in early childhood. Brit. 
Med. Journ., 1914, Aug. 29, p. 397. 

LOWERY, J. R. Pellagra. Med. Record , 1914, lxxxvi., Aug. 29, p. 378. 

YOEGTLIN, CARL. The treatment of pellagra. Journ. Amer. Med. Assoc., 
1914, lxiii., Sept. 26, p. 1094. 

KOZOVSKY, A.-D. Sur la morphologic du sang dans la pellagre. Nouv. Icon, 
d. 1. Salptt., 1914, vii., p. 94. 

LAVINDER, C. H., FRANCIS, E., GRIM, R M., and LORENZ, W. F. 
Attempts to transmit pellagra to monkeys. Journ. Amer. Med. Assoc., 1914, 
lxiii., Sept. 26, p. 1093. 

SILER, J. F., GARRISON, P. E., and MACNEAL, W. J. Further studies of 
the Thomson-M'Fadden Pellagra Commission. A summary of the seoond 
progress report. Journ. Amer. Med. Assoc., 1914, lxiii., Sept. 26, p. 1090. 

SILER, J. F., GARRISON, P. E., and MACNEAL, W. J. Introduction to the 
second progress report of the Thomson-MTadden Pellagra Commission. 
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relation of pellagra to use of certain foods and to location of domiciles in six 
selected industrial communities. Ibid p. 293. 

Syphilis.—Symposium on syphilis, with especial reference to its importance in 
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WILE, V. J., and STOKES, J. H. A study of the spinal fluid with reference 
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1914, xxxii., Sept., p. 607. 

CRAIG, C. BURNS. Cerebral syphilis in the secondary stage. Med. Record, 
1914, lxxxvi,, Sept. 5, p. 422. 

CORBUS, B. C. A second infection with Spirockceta pallida. N.Y. Med. 
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VARNEY, H. R, and MORSE, P. F. The Abderhalden technique as applied 
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ROSTAINE, PAUL. Acquired and hereditary syphilis. Meet Prtu, 1914, 
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A8SINDER, ERIC. Syphilis in the poorer clams: its diagnosis by tbe 
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WILLIAMS, C. M. The present stage in the treatment of syphilis. Med, 
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tel varan.—STILLMAN, E. G. The immediate results of mlvanan treatment of 
syphilis, as judged by the Wassermann reaction, using a obolesterin-fortified 
antigen. Med, Record , 1914, Ixxxvi., Sept. 5, p. 405. 

CROWELL, A. J., and MUNROK, J. P. Sal Terse n in the treatment of syphilis 
—with special reference to the use of salvaraanised serum in cases of syphilis 
of the central nervous system. Med, Record , 1914, lixivi., Sept. 26, p. 543. 

LOMMEN, A. H. M. E. Over salvarssanbebandeliug der syphilis. Nedcr 
landseh Tijdschr . voor Geneeskunde , 1914, Aug. 29, pp. 525 and 593. 

SMYTH, H. C., and PEPPER, G. E. Treatment of syphilis by taWausn in 
Dr Steevens’s Hospital, Dublin. Dublin Joum. Med, Sei ., 1914, No, 513, 
Sept., p. 183. 

Keasalvsrsan.—ASSEN, J. van. Intraveneuse toediening van geconcentreerde 
oplossingen van neoealvaraaan. Nederlaruhch Tijdschr. voor Geneukunde , 
1914, Aug. 8, p. 388. 

Wmaseraaamm Eearilaa.—MACKINNEY, WM. H. How shall the clinician 
interpret the Wassermann reaction? Annals of Surgery, 1914, lx., Sept, 
p. 309. 

DARLING, I. A., and NEWCOMB, P. B. A comparison of the Wassermann 
reaction among the acute and the ohronio insane. Joum . Ntrv . and Afrot 
Die,, 1914, xli., Sept., p. 576. 

HOPKINS, J. G m and ZIMMERMANN, J. B. Cholesterin antigens in the 
Wassermann reaction and the quantitative testing of typhilitic sera. Amer. 
Joum, Med, Sci., 1914, exlviii., Sept., p. 390. 

STONE, W. J. Comparative Wassermann, Cobra, and globulin tests in syphilis 
—with a report of 106 reactions. Med, Record, 1914, Ixxivi, Sept. 26, p. 545. 

FUCHS, B. Luesbehandlung and Wassermann. Dermatol. Wchnschr 1914, 
lix., Juli 11, S. 831. 

Lsftls Reaction.—NOGUCHI, HIDEYO. Practical application of the luetin 
test. N, Y, Med. Joum., 1914, c., Aug. 22, p. 349. 

MATTIROLO, G., and BOTTESELLE, G. B. Sopra la intradermoreazioncalia 
luetina. Pathoiogiea , 1914, vi., Agosto, p. 383. 

Cerebre-Splnal Fin Ml.—CUSHING, HARVEY. Studies on the cerebro-ipinal 
fluid. I. Introduction. Joum. Med. Research , 1914, xxxi., Sept., p. 1. 

WEED, LEWIS, H. Studies on cerebre-spinal fluid. II. The theories of 
drainage of oersbro-spinal fluid, with an analysis of the methods of investiga¬ 
tion. Joum . Med. Research , 1914, xxxi., Sept., p. 21. 

WEED, LEWIS H. Studies on cerebro-spinal fluid. III. The pathways of 
escape from the subarachnoid spaces, with particular reference to the arachnoid 
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WEED, LEWIS H. Studies on cerebro-spinal fluid. IV. The dual source of 
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WEGEFARTH, PAUL. Studies on oerebro-spinal fluid. V, The drainage of 
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WEGEFARTH, PAUL. Studies on oerebro-spinal fluid. VI. The establish¬ 
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WEGEFARTH, PAUL, and WEED, LEWIS H. Studies on oerebro-spinal 
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DUMAS, G., and LAIGNEL-LAVASTINE. Leo variations de pression du 
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6MIBAL Am rvNttmu diseases— 

Epilepsy.—M‘KENNAN, T. M. T., JOHNSTON, GEORGE 0., and 
HENNINGER, 0. H. Observations on epilepsy, chiefly from an X-ray 
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MANSON, J. F., and SHAW, A. L. The pituitary gland in epileptics. 
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CNerea*— D’ANTONA, S. Contributo all’ anatomia patologica della oorea di 
Huntington. Riv. di Paiol. nerv. e ment., 1914, xix., Agosto, p. 321. 

Aleefcellsm, Ac.—SOMERSET, Lady HENRY. The female inebriate. Brit. 
Joum. Inebriety , 1914, xii., July, p. L 

MJEN, JON A. Sociological aspects of recent legislation in Norway relating to 
aloohol and alooholism. Brit. Joum. Inebriety , 1914, xii., July, p. 9. 

DAVIDSON, J. A. A plea for the early treatment of the inebriate. Brit. 
Joum. Inebriety , 1914, xii., July, p. 19. 

AN EX-PATIENT. The psycho-analysis of an inebriate: A record of 
experiences and reflections. Brit. Joum. Inebriety , 1914, xii., July, p. 22. 

VALLOW, H. Aloohol and tuberculosis. Brit. Joum. Inebriety , 1914, xii., 
July, p. 28. 

NEFF, IRWIN H. The modern treatment of inebriety. Boston Med. and Surg. 
Joum., 1914, olxxi., Aug. 6, p. 224. 

DEMOLE, V. Aloool et delirium tremens. L'EncJphale, 1914, ix., p. 6. 

Nearest ben la.—HEAD, GEORGE D. Neurasthenia and tuberculosis. Joum. 
Amer. Med. Assoc., 1914, lxiii., Sept. 19, p. 996. 

Neuroses.—STERN, ADOLPH. Compulsion neurosis. N. Y. Med. Joum., 1914, 
e., Sept. 5, p. 451. 

NEUHOF, SELIAN. Clinical investigation of gastric neuroses with vago- 
eicitative characteristics. N. Y. Med. Joum., 1914, c., Aug. 22, p. 365. 

Fsycbonenroses.—WILLIAMS, TOM A. Quelques considerations sur les 
psychonlvroses professionnelles. Pathogenfcee et exemples de traitement. 
Nouv. Icon. d. 1. Salptt ., 1914, yIL, p. 108. 

FARNELL, FRED. J. The psyohopathic ohild. Archives of Ped., 1914, xxxi., 
Sept., p. 684. 

Sciatica.— MARCUS, HARRY. A case of sciatica entirely cured with three 
weeks’ treatment. N. Y. Med. Joum., 1914, e., Sept. 12, p. 520. 

LLEWELLYN, L. J., and JONES. A. B. Gluteal and crural types of fibrositis: 
their relationship to spurious and genuine sciatica. Edin. Med. Joum., 1914, 
xiii., Sept., p. 225. 

YEOMANS, F. C. Coooygodynia—a new method of treatment by injections of 
aloohol. Med. Record , 1914, lxxxvi., Aug. 22, p. 322. 

Paralysis Agllaas.—CAMP, CARL D. Paralysis agitans syndrome, with syphilis 
of the nervous system. Joum. Nerv. and Ment. 2Rs., 1914, xii., August, 
p. 489. 

AMlten’s Disease.—BROWN, W. H. A case of implantation of the supra-renals 
in Addison’s disease, with fatal results. Med. Joum. Australia, 1914, i., 
Aug. 8, p. 129. 

Exophthalmic Goitre, Crelinisnt, Ac. —DICK, J. LAWSON. On some signs 
and symptoms of hypothyroidism in sohool children. Lancet , 1914, olxxxvii., 
Sept. 5, p. 644. 

ROGERS, JOHN. The course of acquired disessc of the thyroid gland and the 
principles which seem to control its progress. Annals of Surgery, 1914, lx., 
Sept., p. 281. 

HERTOGHE, E Thyroid deficiency. Med. Record , 1914, lxxxvi., Sept 19, 
p. 489. 

SFRCIAJL SENSES AND CRANIAL NERVES— 

MACNAB, ANGUS. The physiology of vision and fusion (excluding the question 
of colour vision). Birmingham Med. Review , 1914, lxxvi., Aug. and Sept., 
pp. 56 and 81. 



98* 


BIBLIOGRAPHY 


WALKER, CLIFFORD B. Further observations on tbe hemiopio papillary 
reaction obtained with a new clinical instrument. Joum. Amer . Med. Assoc., 
1914, lxiii., Aug. 29, p. 846. 

BASTIAANSK, F. S. VAN B. Hemiopische pupilreactic als diagaoethcb 
hulpmiddei. Ntderlandsch Tijdsck . voor (Jeneeskurule, 1914, April, p. 1217. 

WKSTMACOTT, F. H. Oculomotor paralysis of otitic origin. Joum Laryngol,, 
Khinol. , and Otol ., 1914, xxix., Sept., p. 449. 

MARINO, A. A proj>o8ito di una osaervazione fattami dal prof. 0. Bossi nella 
relazione di un mio studio sui movimenti di cotivergenza e lateraliti dei muscoli 
oculari. Kir, di Patol. tierr. e rnent., 1914, xix., Agosto, p. 372. Risyiosta del 
prof. O. Rossi alia uota del prof. A. Marina. Ibid., p. 375. 

BRAUN, ALFRED. The functional tests of the static labyrinth in neurologies! 
diagnosis. N . Y. Med . Joum., 1914, c., Aug. 22, p. 369. 

MHftCBLLANEOUa SYMPTOMS ASM CASES— 

GRECO, FRANCESCO DEL. Sui rapporti tra “ immorality ” e “delinquema’’ 
negl’ individui umani. Kir. ital . di Neuropat ., Psichiat. ed Eletiroter ., 1914, 
vii., p. 289. 

CHARON, K. t and COURBON, P. Influence du milieu et du travail ror lei 
stereotypies. Nouv, Icon. d. I. SalpH ., 1914, vii., p. 103. 

MEIGE, H. 4, Souvent femme varie. n A propos du groupe “tres in una” de 
M. Paul Richer. (2 pi.) Nouv . Icon. d. I. Salptt ., 1914, vii., p. 120. 

PSYCHIATRY. 

CiBJVBBAL PARALYSIS— 

KAPLAN, D. M. General paresis. N. Y. Med, Joum., 1914, c., Aug. 29, p. 397. 

AGUGLIA, EUGENIO. Nota sulla citoarchitettura delle ciroonvoluaonl 
rolandiche in un caso di paralisi progressiva (forme motoria). Riv. ital. di 
Ncuropatol ., Psichiat . ed Eletiroter., 1914, vii., p. 340. 

JACQU1N, G., and LAIGNEL-LAVASTINK, M. Paralysie gdndrale juvenile 
avec autopsic. V Enciphale, 1914, ix., p. 22. 

RESERAL— 

KARP AS. MORRIS J. Kraepelin’s conception of paraphrenia. Joum. Amer. 
Med. Assoc., 1914, lxiii., Aug. 29, p. 766. 

RING, A. H. The early diagnosis and treatment of manic depression, Boston 
Med. and Sury. Joum., 1914, clxxi,, Sept. 3, p. 376. 

HENDERSON, DAVID K. Korsakow’s psychosis occurring during pregnancy. 
Bulletin Johns Hopkins Hotp 1914, xxv., Sept., p. 261. 

WILLIAMS, G. H. The psychosis occurring during the course of pemidoui 
anaemia. Joum. Amer. Med. Assoc 1914, lxiii., Sept. 12, p. 936. 

SAVAGE, Sib G. H. The feeble minded and their care, Clin. Joum., 1914, 
xliii., Sept. 2, p. 545. 

BARKER, LEWELLYS F. The relations of internal medicine to psychiatry. 
Bulletin Johns Hopkins Hosp+ 1914, xxv., Sept., p, 255. 

ROJAS, NERIO A. Homicidio cometido por dos alienados—(Inforine medico¬ 
legal). Kecista de Criminal ., Psiquiat y Med.-Legal, 1914, i., p. 385. 

PETERS, AMOS W. The sterilisation of mental defectives considered from 
the physiological standpoint. Med. Record , 1914, lxxxvi., Aug. 29, p. 370. 

MAY, JAMES V. Modem peychiatry as related to therapeutics. Albany Med. 
Annals, 1914, xxxv., Sept., p. 495. 

TREATMENT.* 

ROBINSON, O. WILSE, The use of celluloid splints in the treatment of diseases of 
the nervous system. Joum. Amer. Med. Assoc., 1914, lxiii., Aug. 29, p. 773. 

REID, EVA CHARLOTTE. Ergother&py in the treatment of mental disorders. 
Boston Med. and Burg. Joum., 1914, clxxi., Aug. 20, p. 300. 

KELLY, T. J. Insomnia. Dublin Joum. Med. Set., 1914, No. 513, Sept., p. 178. 

• A number of references to papers on Treatment are Inoluded in the Bibhograpby under 

Individual d i s ea ses. 




Bibliography 

The bibliography in this number is greatly reduced,\ since , on account 
of the war , the number of foreign journals reaching this country 
is considerably diminished. 


ANATOMY. 


M'KIBBEN, PAUL S. Mast oells in the meninges of Neotnms and their differentiation 
from nerve oells. Anal. Record., 1914, viiL, Oct., p. 475. 

M'KIBBEN, PAUL S. Ganglion cells of the nervus terminals in the dogfish 
(Mustelus canis). Joum. Comp. Neurol., 1914, xxiv., Oct., p. 437. 

RANSON, 8. W. A note on the degeneration of the fasciculus oerebro-spinalis in the 
albino rat. Joum. Comp. Neurol ., 1914, xxiv., Oct., p. 503. 

DOLLEY, D. H. On a law of species identity of the nucleus-plasma norm for 
corresponding nerve oells: the numerical constancy of the nucleus-plasma co¬ 
efficient of the functionally resting Purkinje cell of the dog species. (6 figs.) Joum. 
Comp. Neurol., 1914, xxiv., Oct., p. 445. 

HAYS, Y. J. The development of the adrenal glands of birds. Anat. Record, 1914, 
viii., Oct., p. 451. 


PHYSIOLOGY. 

FRAZIER, 0. H., and PEET, M. M. Factors of influence in the origin and circulation 
of the cerebro-spinal fluid. Amer. Joum. Physiol., 1914, xxxv., Oct., p. 268. 

BROWN, T. GRAHAM. On the ordering of reciprocal innervation. Med. Chron., 
1914, lx., Sept.-Oct., p. 1. 

MAONAB, ANGUS. The physiology of vision and fusion (excluding the question of 
colour vision). (Oontd.) Birmingham Med. Review, 1914, lxxvi., Oct., p. 117. 

ZANDER, EMIL Zur Frage von der Wirkung der extrakardialen Nerven auf den 
automatisch sohlagenden Yentrikel, zugleich ein Be it rag zur Lokalisation im 
Herzen. Nord. Med. Arkiv, 1915, Aid. IL (lure Medicin), Haft 1-2, pp. 1-6. 

WHERLON, H. Extirpation of the testes and vaso-motor irritability. Amer. Joum. 
Physiol ., 1914, xxxv., Oct,, p. 283. 

CROWE, S. J., and WISLOCKI, G. B. Experimental observations on the suprarenal 
glands, with especial reference to the functions of their inter-renal portions, (Illustr.) 
Bulletin Johns Hopkins Hosp ., 1914, xxv., Oct., p. 287. 


PSYCHOLOGY. 

ROGERS, A L, and M'INTYRE, J. L The measurement of intelligence in children 
by the Binet-Simon scale. Brit. Joum. Psychol ., 1914, vii, Oct., p. 265. 

THOMPSON, E. R. An inquiry into some questions connected with imagery in 
dreams. Brit. Joum. Psychol ., 1914, vii., Oct., p. 300. 

WATKINS, S. H. Immediate memory and its evaluation. Bril. Joum* Psychol ., 
1914, vii., Oct., p. 319. 

FLtfGEL, J. C., and M'DOUGALL, WM. Some observations on psychological oontrast. 
Brit. Joum. Psychol ., 1914, vii., Oct., p. 349. 



100* 


BIBLIOGRAPHY 


CLINICAL NEUROLOGY. 

CiENEEAL— 

BROUWER, B. Over dermatomerie, bijdrage tot de kennis der segmentaal- 
anatomie en der sensibele geleidang bij den Meneoh. Nederlandsch Tijdsehr. 
v . Genecsk ., 1914, H. xii., No. 11 and 12, Sept. 12 and 19, pp. 657 and 742. 

SODERBERGH, GOTTHARD. Quelle eat 1 Innervation radiculaire dea muaclea 
abdominaux? Nord. Med. Arkiv f 1914, xlvii., Aid. II. (Inre Med.), Hkft 1-4, 
pp. 1-7. 

MU3CLES— 

OBBISON, T. J. Myopathy: with olinical record* of eight caaea comprising 
various types. Arner. Journ. Med. Sci., 1914, oxlviii., Oct., p. 560. 

OLIVER, PAUL Myoaitia oaaificana following a single trauma. Journ. Arner. 
Med. Assoc ., 1914, lxiii., Oct. 24, p. 1452. 

MURPHY, JOHN B. Myoaitia. Ischemic myoeitis: infiltration myositis: 
cicatricial muscular or tendon fixation in forearm: internal, external, and 
combined compression myositis, with subsequent musculotendinous shortening. 
Journ. Amer. Med. Assoc. , 1914, lxiii., Oct. 10, p. 1249. 

STRAUCH. A. Myatonia congenita of Oppenheim. Amer. Journ. Dis. Child ., 
1914, vii., Oct., p. 298. 


SPINAL CORD— 

Frsetare, Dislocation, Be.—CUMSTON, C. G. Gunshot wounds of the spine. 
N. Y. Med. Journ., 1914, c., Oct. 17, p. 754. 

Herpes Lester.—PERNET, GEORGE. Generalised herpes zoster. Brit. Journ. 
Dermatol ., 1914, xxvL, Oct., p. 399. 

W YNTER, W. E. Clinical lecture on herpes. Med. Press, 1914, xoviii., Oct. 7, 

р. 372. 

ayrlngemyella.—WILDMAN, H. V. Syringomyelia, with report of a case of 
Morran’s type of the disease. Med. Record, 1914, Ixxxvi., Oct. 17, p. 672. 

Twmeur*.—WILKENS, G. D. Bin Fall von Riickenmarkstumor. Nord. Med. 
Arkiv , 1914, xlvii. (Inre Med.), Haft 1-4, pp. 1-10. 

ELSBERG, C. A. Laminectomy for spinal tumour. Annate of Surgery , 1914, 
lx., Oct., p. 454. 

Vra Recklinghausen’s Disease.—ELLIOTT, C. A., and BEIFELD, A. F. 
Generalised neurofibromatosis (von Recklinghausen’s disease). Report of a 
case showing a superficial resemblance to Hodgkin's disease. Journ. Amer . 
Med. Assoc., 1914. lxiii., Oct. 17, p. 1358. 

Pollonayelltls Anterior Acuta.—GORDINIER, HERMON C. The study of a 
case of the adult type of poliomyelitis and of a case of acute ascending paralysis 
of the type of Landry. Journ. Nerv. and Ment. Dis ., 1914, xli., Oct, p. 640. 

M‘GOWAN, J. P., and DAWSON, JAMES W. A comparison of the lesions of 
the nervous system in distemper of the dog with those of human poliomyelitis. 
Archives Int. Med., 1914, xiv., Oct., p. 182. 

BRAIN— 

General.—SOUTHARD, E. E. The association of various hyperkinetio symptoms 
with partial lesions of the optic thalamus. Journ . Nerv . and Ment. Dis., 
1914, xli., Oct, p. 617. 

CRENSHAW, H. Localisation of brain lesions. N.Y. Med. Journ., 1914, 

с. , Oct 17, p. 765. 

LEDUC, STEPHANE. Cerebral electrisation. Archives of the Roentgen Ray, 
1914, xix., Oct., p. 160. 

THORBURN, WM. The present position of cerebral surgery. Med. Press, 
1914, xcviiL, Oct 21, p. 424. 



BIBLIOGRAPHY 


101* 


RHEIN, JOHN H. W. Contusion of the brain. Journ. Nerv. and Ment. 
Dis., 1914, xli., Oct., p. 653. 

Disseminated Sclerosis. —COLLINS, J., and BAEHR, E. Disseminated 
sclerosis : its frequency compared with other organic diseases; its etiology and 
pathogenesis; the types and differential diagnosis of the disease ; its course 
and treatment. A clinical study of ninety-one cases. Amer. Journ. Med. Set., 
1914, cxlviii., Oct., p. 495. 

WILLIAMS, TOM A. Syphilitic multiple sclerosis diagnosed clinically in spite 
of negative laboratory tests. Boston Med. and Surg. Journ., 1914, clxxi., 
Oct. 1, p. 526. 

Meningitis.— HEIMAN, H. Refractory or so-called “fast” oases of meningococcus 
meningitis. Amer. Journ. Dis. Child ., 1914, viii., Oct., p. 307. 

Encephalitis. —REEVE, E. F. t and WATSON, GEORGE A. Observations on 
oases of encephalitis. Journ. Ment. Sci., 1914, lx., Oct., p. 615. 

Abscess.— WRIGLEY, FRANK G. A case of temporo-sphenoidal abscess follow¬ 
ing chronic middle ear suppuration. Med. Chron., 1914, lx., Sept., Oct., p. 10. 

Mssmorrhage.— LEOPOLD, SAMUEL. Spontaneous subarachnoid hemorrhage. 
A contribution to the subject of meningeal haemorrhage. Journ. Amer. Med. 
Assoc., 1914, lxiii., Oct. 17, p. 1362. 

Angiospasm.— BIRT, A. Vascular crises and angiospasm. Canadian Med. 
Assoc. Journ., 1914, iv., Oct., p. 858. 

Progressive Lenticular Degeneration. —CADWALADER, W. B. Progressive 
lenticular degeneration. Journ. Amer. Med . Assoc., 1914, lxiii., Oct. 17, 
p. 1380. 

Facial Paralysis. —THROCKMORTON, T. B. Bilateral peripheral facial palsy, 
with report of case. Journ. Amer. Med. Assoc., 1914, lxiii., Oct. 3, p. 1155. 

Aphasia. —WHITE, H. W. The disorders of speech. Public Health, 1914, xxviii., 
Oct., p. 8. 

Myasthenia. —SMYTH, R. OSBORN. Myasthenia gravis. A short account of 
the disease, with notes on three cases. Dublin Journ. Med. Sci., 1914, Third 
Series, No. 514, Oct., p. 241. 

Pellagra. —BRENGLE, D. R. Pellagra in Minnesota. Journ. Amer. Med. 
Assoc., 1914, lxiii., Oct. 3, p. 1157. 

SILER, J. F., GARRISON, P. E., and MACNEAL, W. J. The relation of 
methods of disposal of sewage to the spread of pellagra. Archives Ini. Med., 
1914, xiv., Oct., p. 453. 


MACDONALD, J. B. Pellagra and its symptoms; the importance of mouth and 
gastro-intestinal lesions. Boston Med. and Surg. Journ., 1914, clxxi., Sept. 
24, p. 458. 

Mongolism. —HULTGREN, E. O. Studien iiber die Httuffgkeit der mongoloiden 
Idiotic in schwedischen Anstalten fiir Schwachsinnige und liber die Atiologie 
dieser Krankheit. Nord. Med. Arkiv, 1915, Afd. II. (Inre Medicin), Haft 1-2, 

pp. 1-10. 

Syphilis.—VEEDER, B. S., and JEANS, P. C. The diagnosis and treatment of 
“late” hereditary syphilis. Amer. Journ. Dis. Child., 1914, Oct., p. 283. 

FORDYCE, J. A. Modern diagnostic methods in syphilis. N. Y. Med. Journ., 
1914, c., Sept. 26, p. 597. 

WATTERS, W. H. The modern treatment of syphilis. Med. Record, 1914, 
lxxxvL, Oct. 24, p. 711. 

M*WALTER, JAS. C. Antimony in syphilis. Med. Press, 1914, xcriii., Oct. 
28, p. 448. 



102* 


BIBLIOGRAPHY 


BAKU, H., and WITH, CARL. Recherches sur U modification ftpportee }iftr 
Herman et l’erutz k la reaction de precipitation an glycocholate de soudt 
spdcialement au point de vue du diagnostic de syphilis. Word. Med. Arkii , 
1915. xlviii. (Inre Medicin), Afd. II., Haft 1-2, pp. 1-62. 

fllco»alvar*i%n.—FINDLAY, LEONARD. The use of neoealvaraan in mental 
deficiency. Glasgow Med. Joum 1914, lxxxii, Oct., p. 241. 

M*UURN, W. J. Observations on the behaviour of neoealvarsan. Botton Mtd. 
and Surg. Joum 1914, clxxi., Oct. 1, p. 524. 

Lneltn Reaction.—WOLFF, L. K., and ZEEMAN, W. P. C. Over de cutiie- 
actie van Noguchi bij lues. Nederlandsch Tijdsch. v . Geneesk., 1914, H. 
xu. t No. 13, Sept. 26, p. 811. 

SCHIPPERS, J. C. De waarde van de luetine-reactie voor Kinderpraktyk, 
Nederlandsch Tijdsch. r. Genet aA., 1914, H. xii., No. 13, 8ept. 26, p. 817. 

Wassrriuann Reaction.—WOOTTON, J. C. The Wassermann reaction and the 

male insane. Joum. Mental Sci., 1914, h., Oct,, p. 579. 

WALKER, I. CHANDLER. The specificity of cholesterin with iyphilitic 
serums and of cholestet in-reinforced heart antigen in the Wasaennann reaction. 
Archives Int. Med ., 1914, xiv., Oct., p. 563. 

ASS1NDER, ERIC. Syphilis in the poorer classes: its diagnosis by the 
Wassermann test, and its incidence as demonstrated thereby. (Contd.) 
Birmingham Med . Review, 1914, lxxvi., Oct., p. 137. 

Orchro ftplnal Fluid.—ROSENBLOOM, JACOB, and ANDREWS, VERNON 

L. The potassium content of cerebro spinal fluid in various diseases. Archiea 
Int. Med., 1H14, xiv., Oct., p. 536. 


(iKNCEAL AXD FUNCTIONAL DISEASES— 

Epilepsy.—SEBARDT, CARL. Alkohol und Epilepsie. Klinische Studie. 
Nord . Med . Arkiv, 1914, Afd. II. (Inre Medicin). Halt 1-4, pp. 1-26. 

TURNER, WM. ALDREN. The outlook in epilepsy. Brit . Med . Joum., 
1914, Oct. 17, p. 665. 

Chorea.— SWIFT, W. B. Further analysis of the voice sign in chorea Amer. 
Joum. Child . Dis., 1914, viii., Oct., p. 279. 

Neuroses.— WILLIAMS, TOM A. The traamatic neurosis. Amer . Joum. Med, 
Sci. 9 1914, cxlviii., Oct., p. 567- 

BILLSTROM, JAKOB. Ein Fall von traumatischer Neurose bei einer vorher 
gesunden Patieutin, durch Symptombildern von sinigen anderen Nenrose* 
patienten beleuchtet. Nord. Med. Arkiv, 1914, Afd. II. (Inre Mediein), Haft 
1-4, pp. 1-5. 

CROTHERS, T. D. Periodicity of the drink neuroses. Med. Record, , 1914, 
lxxxvi., Oct. 10, p. 628. 

Psychoses* —DRYSDALE, H. H. Juvenile psychosis. Report of a casa Joum 
Amer . Med. Assoc., 1914, lxiii., Oot. 10, p. 1283. 

GERRIN, MARY L. Impressions of a general hospital nurse beginning work in 
the psychopathic hospital (Boston, Massachusetts). Boston Med. and Surg. 
Joum., 1914, clxxi., Sept. 24, p. 483. 

CHANNING, W. Improved nursing for the mentally ill. Boston Med. end 
Surg. Joum., 1914, clxxi., Sept. 24, p. 473. 

NUTTING, M. A. The training of the psychopathic nurse. Boston MecL end 
Surg . Joum., 1914, clxxi., Sept. 24, p. 473. 

GREGG, D. A comparison of the drugs used in general and mental hospitals. 
Boston Med . and Surg. Joum., 1914, clxxi,, Sept. 24, p. 476. 



BIBLIOGRAPHY 


103* 


ELIOT, C. W. Remarks at conference on modem development in mental 
nursing, Feb. 16, 1914. Boiton Med. and Burg. Journ 1914, olxxi., Sept. 24, 
p. 477. 

SOUTHARD, E. E. Analysis of recoveries at the psyehopathio hospital. 
Boston. 1. One hundred oases, 1912-13, considered especially from the stand¬ 
point of nuning. Boston Med. and Surg. Journ., 1914, olxxi., Sept. 24, 
p. 478. 

Berl-Berl.—LITTLE, J. M. Beri-beri. Journ. Amer. Med. Assoc., 1914, lxiii., 
Oct. 10, p. 1287. 

DARLING, S. T. The pathologic affinities of beri-beri and scurvy. Journ. Amer . 
Med. Assoc., 1914, mil, Oct. 10, p. 1290. 

Alcoholism, dtc.—COOPER. J. W. A8TLEY. Proposed legislation for inebriates. 
Brit. Journ. Inebriety , 1914, xii., Oct., p. 59. 

SHAW, T. CLAYE. The aloohol problem of to-day. Brit. Journ. Inebriety, 
1914, xii., Oct., p. 66. 

NEILD, T. Chronic alcoholism and reproduction. Brit. Journ . Inebriety, 
1914, xii., Oct., p. 71. 

WAITE, R. Drink in relation to the poor law. Brit. Journ. Inebriety, 1914, 
xii., Oct., p. 78. 

CARTER, D. Alcoholism as a factor in disease. Med. Record, 1914, lxxxvi., 
Oct. 17, p. 666. 

Tetanms. —MacCONKEY, ALFRED. Tetanus: its prevention and treatment by 
means of antitetanio serum. Brit. Med. Journ., 1914, Oct. 10, p. 609. 

FOTHERINGHAM, J. T. A case of tetanus, with recovery, treated by carbolic 
acid injections. Canadian Med. Assoc. Journ., 1914, iv., Oct., p. 902. 

GORDON, M. H. Traumatic tetanus. Lancet, 1914, clxxxvii., Oct. 31, p. 1036. 

Exophthalmic Goitre, Cretinism, Ac.—CROOKSHANK, F. G. Exophthalmic 
goitre: its pathogeny and treatment. Med. Press, 1914, xcviii., Sept. 30, p. 366. 

WALTON, ALBERT J. The operative treatment of exophthalmic goitre. 
(Illustr.) Practitioner, 1914, xciii., Oct., p. 511. 

MAYO, C. H. The surgical treatment of exophthalmos. Journ. Amer. Med. 
Assoc., 1914, lxiii., Oct. 3, p. 1147. 

BALLARD, I. W. Hyperthyroidism. Med. Record , 1914, lxxxvi., Oct. 10, 

p. 626. 

MATLACK, G. T. Goitre, its surgical treatment. Therap. Gaz., 1914, xxxviii., 
Oct., p. 685. 


SPECIAL SEMES AND CRANIAL NERVES— 

MUSKENS, L. J. J. Labyrinthaire invloed op de oogbewegingen; het 
mechanisme der geoonjugeerde deviatie van hootd en oogen. Nederlandsch 
Tijdsck. v. Geneesk, 1914, H. xii., Nos. 14 and 15, pp. 893 and 970. 

BALLON, D. H. Recent investigations on the semicircular canals and their 
olinical applications. Canadian Med. Assoc. Journ., 1914, iv. t Oct., p. 871. 

MEIERHOF, E. L Thrombophlebitis of the sigmoid sinus of otitio origin 
without local manifestations. Journ. Amer. Med. Assoc., 1914, lxiii., Oct. 17, 
p. 1389. 


MISCELLANEOUS SYMPTOMS AND CASES— 

KANAVEL, A. B. Osteoplastic closure of the trifacial foramina. Journ. 
Amer. Med. Assoc., 1914, lxiii., Oot. 10, p. 1245. 

BARTON, W. M. Postdiphtheritio paralysis. N.Y. Med. Journ., 1914, c., 
Oct. 3, p. 660. 

t 



104 * 


BIBLIOGRAPHY 


GORDON, ALFRED. Nervous And mental disturbances following castration in 
women. Journ. Amer. Med . Assoc., 1914, Ixiii., Oct. 17, p. 1345. 

OADELITS, 13. Kn sallaynt form af idioti med karakteristiska utveckling- 
sanoinalicr—akrocephalo-syndaktyli. Aord. Med. Arkie , 1915, xlviiL, Afd, 
II. (Inre Medeciu), H. 1-2, pp. 1-30. 

GETTINGS, H. S.. and WALDRON, ETHEL. The detection of a dywntery 
carrier. Journ. Mental Sci., 1914, lx., Oct., p. 605. 

AGADJANIANTZ, K. On lethargy. Journ. Mental Sci., 1914, lx., Oct., 

p. 620. 


PSYCHIATRY. 


CK*K*AL PAIAIWW- 

MITCHELL, H. W. General paralysis of the insane. N. Y. Med. Journ., 1914, 
c., Sept. 26, p. 605. 

MAPOTHKR, E., and BEATON, T. Intrathecal treatment of general paralysis. 
Journ. Mental Sci ,, 1914, lx., Oct., p. 591. 

PILSBURY, L. B. Paresis patients treated with intraspinal injections of 
salvarsauised serum. A brief report. Journ. Amer. Med . Attoe., 1914, Ixiii., 
Oct. 10, p. 1274. 

RIGGS, C. E., and HAMMES, E. H. Results of one hundred injections of 
ealvarsanised serum. Journ. Amer. Med. Assoc., 1914, Ixiii, Oct. 10, p. 1*277. 

M'CLURE, C. W. Intraspinous use of salvarsanised serum. Boston Med. and 
Surg. Journ., 1914, clxxi., Oct. 1, p. 520. 

iFABKAIr- 

EWENS, G. F. W. The meaning of insanity. Indian Med. Gaz., 1914, xlix., 
Oct., p. 377. 

BERKELEY-HILL, A. R. A comparison between the mental processes in the 
sane and in the insane. Indian Med. Gaz ., 1914, xlix., Oct., p. 382, 

OVERBECK-WRIGHT, A. The prevention of mental and nervous diseases. 
Indian Med. Gaz., 1914, xlix., Oct., p. 387. 

PEEBLES, A. S. M. Ganja as a cause of insanity and crime in Bengal. Indian 
Med. Gaz., 1914, xlix., Oct., p. 395. 

THOMSON, DAVID G. The presidential address on the progress of psychiatry 
during the past hundred years, together with the history of the Norfolk County 
Asylum during the same period. Journ. Mental Sci., 1914, lx., Oct., p. 541. 

BRILL, A. H., and KARPAS, M. J. Insanity among Jews. Med. Record , 1914, 
lxxxvi, Oct. 3, p. 576. 

GORDON, ALFRED. Neurologic and psychiatric aspects of railway accident 
cases. Consideration of some medico-legal problems. Med. Record , 1914, 
lxxxvi., Oct. 24, p. 706. 


TREATMENT. * 

RAYNER, H. The wet pack in the treatment of insomnia and mental disorder*. 
Journ. Mental Sci., 1914, lx., Oct., p. 572. 

DANIEL, A. W. The use of scopolamine hydrobromide, or byoecine, in tbs treat¬ 
ment of mental disorders. Journ. Mental Sci., 1914, lx., Oct., p. 610. 

• A number of references to papers on Treatment are included in the Bibliography under 
individual diseases. 



ffitbUograpb\> 


The bibliography in this number is greatly curtailed\ since, on account 
of the war , the number of Joreign journals reaching this country 
is considerably diminished. 


ANATOMY. 

BEAN, ROBERT BENNET. A racial peculiarity in the pole of the temporal lube of 
the negro brain. Anat. Record, 1914, viii., Nov., p. 479. 

COWDRY, E. V. The comparative distribution of mitochondria in spinal ganglion 
cells of vertebrates. (14 figs.) Amcr. Journ. Anat., 1914, xvii., Nov., p. 1. 

SMITH, P. E. The development of the hypophysis of Amia calm. Anat. Record , 
1914, viii., Nov., p. 499. 


PHYSIOLOGY. 

WHITE, WM. P. f and TITCOMBE, R. H. Observations on the anterior lobe of the 

S ituitary. III. The action of pituitary (anterior lobe) extract on cancer in mice. 
ted. Cnron ., 1914, lx., Nov., p. 73. 


PSYCHOLOGY. 

HAMILTON, G. V. An estimate of Adolf Meyer’s psychology. Amcr. Journ. 
Insanity , 1914, lxxi., Oct., p. 339. 

SOHN, D. L. The psychic complex in congenital deformity. N. Y. Med. Journ., 1914, 
c., Nov. 14, p. 9o9. 


CLINICAL NEUROLOGY. 

GENERAL— 

SWIFT, WALTER B. A new method of refiex elicitation. Preliminary report. 
Journ. Amcr. Med. Assoc., 1914, lxiii., Oct. 31, p. 1668. 


MUSCLES— 

LEON, J. T. Pseudo-hypertrophic paralysis. Proc. Roy . Soc. Med., 1914, vii., 
July (Sect. Study Dis. of Child.), p. 182. 


SPINAL CORD— 

deaeral.—BERGHAUSEN, OSCAR. Intraspinous medication. N.Y. Med. 
Joxtrn., 1914, c., Nov. 21, p. 1006. 

Herpes Eoster.— FINLAY, R. C. Herpes zoster following arsenic. Journ. Cut. 
Dis., 1914, xxxii., Nov., p. 794. 



lOli* 


BIBLIOGRAPHY 


MjcIIIIh.—KFILEEK, \\\ G. Acute myelitis, secondary to perirectal absceo, 
developing a few hours after severe fright. Journ. Amer. Med. A$*or. t 19R 
lxiii. , Oct. 31, p. 1518. 

Tumoin.- Dort SLAS CRAWFORD, D. Note on two cases of intradural spinal 
tumours. I* roc. Jlo//. S<x\ Mrd ., 1914, vii. t July (Surg. Sect.), p. 263. 

Paraplegia.— PAS'TIXK, C. Sopra un caso di paraplegia improwisae raorbo di 
Pott latente. Jin . di Patof. ntrv. r rnent., 1914, xi.v, Sept., p. 53d. 

Poliomyelitis Anterior Acuta.—PIM, ARTHUR A. Epidemic poliomyelitis. 
Jiritish Mai. Journ ., 1914, Nov. 14, p. 831. 

LITCHFIELD, W. F. Infantile paralysis of the small muscles of the hand. 
Med. Journ. of Australia, 11)14, i., Oct. 10, p. 347. 

Progressive Muscular Atrophy.—DANA, CHARLES L. A new (familial) form 
of progressive spinal myopathy. Journ. Ntrv. and Mrnt . Dis., 11)14, ili., 
Nov., p. i;m. 


BBAltf— 

Meningitis*— <JORDON, ALFRED. Some features of pneumococcal meningitis. 
N. Y. Mid. Journ., 1914, c., Oct. 31, p. 851). 

THOMAS. H. M.,and BLACKFAN, K. D. Recurrent meningitis due to lead in 
a cliiid of five years. Atiur. Journ. Dis. Child., 11)14, viii., Nov., p. 377. 

Ilsrinorrtiage.—(’ORE, DONALD E. Spreading or diffuse sub arachnoid hemor¬ 
rhage. Clin. Journ., 1914, xliii., Nov. 4, p. 841. 

SHUMAN, J. W. Intracranial haemorrhage in the iufaut. with history and 
necropsy report of a case. Journ. Amer. Med. Assoc., 1914, lxiii., Nov. 14, 
p. 1788. 

Thrombosis*—GILLLS, A. C. Occlusion of the posterior inferior cerebellar artery. 
Journ, Amer. Mrd. Assoc., 1914, lxiii., Oct. 31, p. 1550. 

Cerebellum*—MARKS, HENRY K. On the cerebellar syndrome of Babiuski, 
with report of a case. Journ. Nerr. and Meat. Dis., 1914, xlL, Nov., p. 709. 

Myasthenia*—M‘KKXDREE, C. A. A case of myasthenia gravis. Journ. Amer. 
Mrd. Assoc., 1914, lxiii., Oct. 31, p. 1553. 

I yst.— RKMSEN, C. M. Operative intervention in cyst of the left cerebral 
hemisphere, with a consideration of the preonerative and subsequent 
symptoms. Journ. Amer. Mrd. Assoc., 1914, lxiii., Nov. 7, p. 1649. 

ROBERTSON, W. N., and AHERN, E. D. Cyst of the pituitary gland. Med. 
Journ. of Australia, 1914, i., Oct. 17, p. 372. 

Tumour*—KUTTNER, H. The results of one hundred operations performed on 
the diagnosis of brain tumour. Journ. Amer. Med. Assoc., 1914, lxiii., Oct. 
31, p. 17 m0. 

RHEIN, JOHN H. W. Tumour of the crus cerebri. Journ. Amer. Med 
A ssoc. , 1914, lxiii., Nov. 1, p. 1882. 

Pituitary Tnmoir. —HALSTED, T. H. Intranasal operation in tumour of the 
hypophysis. N. Y. Med. Journ., 1914, c., Oct. 31, p. 870. 

CUSHING, HARVEY. The Weir Mitchell Lecture. Surgical experiences with 
pituitary disorders. Journ . Amer. Med. Assoc., 1914, lxiii., Nov. 7, p. 1515. 

Acromegaly*—BLORE, W. ROY. A case of acromegaly, associated with 
glycosuria. Med. Chron., 1914, lx., Nov., p. 92. 

Diabetes Insipidus* —FITZ, R. A case of diabetes insipidus. Archives of M 
Med., 1914, xiv., Nov., p. 708. 

DyspltnitarlHiu.—MATTIROLO, G, Contribute alia conoscenza della distrofi* 
ipofiao genitale. Riv. di Palol. nerv. c nu'nt., 1914, xix., Sept., p. 513. 



BIBLIOGRAPHY 


107* 


Pellagra*—LITTLE, E. G. G. Pellagra with akin eruptions, troc. Roy. Soc. 
Med., 1914, Tii., July (Dermatol Sect.), p. 288. 

HUNTER, G. G., and WILLIAMS, E. H. The widening pellagra zone. Med. 
Record , 1914, lxxxvi., Oct. 81, p. 757. 

■•agollsm.—MIDELTON, W. J. Mongolism with alopecia. Proc. Roy. Soc. 
Med ., 1914, vii., July (Sect. Study Dis. of Child.), p. 184. 

Syphilis*—MTNTOSH, JABIES, and FILDES, PAUL. A comparison of the 
lesions of syphilis and “parasyphilis,” together with evidence in favour of the 
identity of these two conditions. Brain, 1914, xxxvii., p. 141. 

SACHS, B.. STRAUSS, I., and KALISKI, D. J. Modem methods of treatment 
of syphilis of the nervous system. Amer. Journ. Med . Sci., 1914, oxlviii., 
Nov., p. 693. 

STOLL, H. F. The late manifestation of inherited syphilis, with especial 
referenoe to arterial disease. Journ. Amer. Med. Assoc., 1914, lxiii., Oct. 31, 
p. 1558. 

GRULEE, C. G. Laboratory diagnosis in the early stages of congenital syphilis. 
Amer. Journ. Med. Sci., 1914, cxlviii., Nov., p. 688. 

Wssiensan Reaction.— HEAD, HENRY, and FEARNSIDES, E. G. The 
elinioal aspects of syphilis of the nervous system in the light of the Wassermann 
reaction and treatment with neosalvarsan. Brain, 1914, xxxvii., p. 1. 

TEDDER, E. B., and BORDEN, W. B. A comparison of the Wassermann 
and luetin reactions in seven hundred and forty-four individuals. Journ . 
Amer. Med. Assoc., 1914, lxiii., Nov. 14, p. 1750. 

LUSK, W. C. A case of thrombo-angiitis, whose Wassermann was for a long 
time negative, but is now positive. Med. Record, 1914, lxxxvi., Nov. 14, p. 833. 

Lvetln Reaction. —SQUIRES, J. W. Noguchi’s cutaneous reaction for syphilis. 
Med. Press, 1914, oxlix., Nov. 25, p. 540. 

Cerebrospinal Flnid.—MITCHELL, H. W., DARLING, IRA A., and 
NEWCOMB, P. B. Observations upon spinal fluid oell count in untreated 
cases of cerebro-spinal syphilis. Journ. Nerv. and Ment. Dis., 1914, xli., 
Nov., p. 686. 


GENERAL AND FUNCTIONAL DISEASES— 

Epilepsy.—CLARK, L. PIERCE. A clinical contribution to the diagnosis of 
epilepsy. Journ. Amer. Med. Assoc., 1914, lxiii., Nov. 1, p. 1652. 

CLARK, L. P. A personality study of the epileptic constitution. Amer. Journ. 
Med. Sci., 1914, cxlviii., Nov., p. 729. 

JENKINS, C. L., and TENDLETON, A. S. Crotalin in epilepsy. Journ. 
Amer. Med. Assoc., 1914, lxiii., Nov. 14, p. 1749. 

Hysteria*—HEFFERNAN, P. Notes on two oases of hysteria in males. Indian 
Med. Gaz., 1914, xlix., Nov., p. 427. 

Psychoses.—O’MALLEY, MARY. Psychoses in the coloured race : A study in 

comparative psychiatry. Amer. Journ. Insanity, 1914, lxxi., Oct., p. 809. 

GREEN, E. M. Psychoses among negroes. Journ. Nerv. and Ment. Dis., 1914, 
xli., Nov., p. 697. 

Nenroses. — MASOIN, M. E. Ncvroses et psychoses d’originc otopathique. 
Bulletin de VAcad. Roy. de Med., 1914, xxviii., p. 321. 

PARKER, S. M. Neurosis and purpose. Med. Record, 1914, lxxxvi., Nov. 14, 
p. 840. 

Nearalgla*—HARRIS, WILFRED. Some experiences with aloohol injection in 
trigeminal and other neuralgias. Journ. Amer. Med. Assoc., 1914, lxiii., Nov. 
14, p. 1725. 



108 * 


BIBLIOGRAPHY 


Tetaau.— DOYEN. Traitemeut du tetanos par lea injectioni intraraohidienna 
da serum antitetaniquc a haute dose, suivies de renvcrsemeiit da troac en 
position de declivity bulbaire. Compt . Rend. d. L Soc, de BioL, 1914, ixivii, 
p. 504. 

WALTHER, C. Etiologie et prophylaxie du tetanoe chez les blesses de guerTe, 
Presse Mid., 1914, No. 70, Oct 8, p. 042. 

Exapfctkalmlc Csllre, frcllitiM, Ac. —FOWLER, R. S. Exophthalmic goitre. 
N. Y. Med . Jonm., 1914, c., Nov. 14, p. 949. 

SMITH, O, hi'CALL. A case of acute exophthalmic goitre simulating sente 
obstruction. Lancet, 1914, dxxxvii., Oct. 10, p. 894. 

MOORHEAD, T. O. Treatment of Graves's disease by X-rays. DuUin Journ . 
Med. Sci., 1914, Scr. III., No. 515, p. 332. 

FRAZIER, C. H. A review of one hundred consecutive operations for goitre, 
with ee]>ecial reference to the treatment of hyperthyroidism. Annals of 
Surgery, 1914, lx., Nov., p. 583. 

M AMOUR!AN, M ARCUS. Our present knowledge of the thyroid gland. With 
a preliminary report on a case of thyroid grafting. (Illust.) British Mel 
Journ ., 1914, Nov. 14, p. 824. 

HPMIAL SENSES ASM iKANUl NUVB8— 

MAYOU, M. T. Optic neuritis with symmetrical loss of the lower portion of the 
field associated with diabetes. Proc. Roy. Soc . Med., 1914, vil, July (Sect of 
Ophthalmol.), p. 148. 

HENDERSON, E. E. Rupture of the optic nerve at the lamina cribrosa. Proc. 
Roy. Soc. Med., 1914, vii., July (Sect, of Ophthalmol.), p. 158. 

WESTMACOTT, F. H. Oculo motor paralysis of otitic origin. Lancet, 1914, 
clxxxvii., Nov. 14, p. 1143. 


MISCELLANEOUS SYMPTOMS AltB CASES— 

FISHER, E. D. Toxic diseases of the nervous system, with report of case* 
Med. Record, 1914, lxxxvi., Nov. 14, p. 825. 

AUDENINO, E. Studio radiografico delle ossa negli arti paralitici. far. di 
Patol. nen\ t meat., 1914, xix., Sept., p. 543. 

WILLIAMS, TOM A. Some common errors in neurological diagnosis and 
treatment. Med. Press, 1914, cxlix., Nov. 11 and 18, pp. 494 and 516. 

RUBENSTONE, A. I. Meningococcic empyema. N. Y. Med. Journ., 1914, c., 
Nov. 14, p. 975. 

THOMSON, W. H. Vasomotor disorders. Med . Record , 1914, lxxxvi., Oct. ill, 
p. 753. 

HELLER, J. A study of one hundred and fifty cases of twilight sleep. Med . 
Record, 1914, lxxxvi., Nov. 7, p. 797. 

GRANT, Sib JAMES. Nerve block, public health and tuberculosis. iV.L 
Med. Journ., 1914, c., Oct. 31, p. 849. 


PSYCHIATRY. 

general paralysis— 

DUNLOP, C. B. The pathology of general paralysis. Amr. Journ. Insanity, 
1914, Lxxi., Oct., p. 249. 

VIDONI, G. Ricerche sul comportamento del ricambio nella cura della paraliii 
progressiva con la tubercolina. Riv. di Patol . nerv. e ment., 1914, xix., Sepi, 
p. 537. 



BIBLIOGRAPHY 


109* 


NOGUCHI, HIDEYO. On some of the recent advances in the field of micro¬ 
biology ; with demonstrations of the pore cultures of various spiroohates, of 
the viruses of rabies and poliomyelitis, and of Treponema pallidum in the brains 
of general paralytics. Proc. Boy. Soc. Med., 1914, vii., July (occasional 
lecture), p. 3. 


lEMiim fejwox— 

SOUTHARD, E. E. On the topographical distribution of cortex lesion, and 
anomalies in dementia pneoox, with some account of tlieir functional 
significance. Amer. Joum. Insanity, 1914, lxxi., Oct., p. 383. 

KIRBY, G. H. Dementia prsecox, paraphrenia, and paranoia: review of 
Kraepelin’s latest conception. Amer. Joum. Insanity, 1914, lxxi., Oct., 
p. 349. 


GENERAL— 

HASKELL, R. H. Mental disturbances associated with acute articular 
rheumatism. Amer. Joum. Insanity , 1914, lxxi., Oct., p. 361. 

AUER, MURRAY. The psychical manifestations of disease of the glands of 
internal secretion. Amer. Joum. Insanity, 1914, lxxi., Oct., p. 405. 

HEFFERNAN, P. Asylum dysentery. Indian Med. Qaz., 1914, xlix., Nov., 
p. 417. 

ZILOOOHI, ALBERTO. Le pieghe del cuoio oapelluto negli alienati. Rassegna 
di Studi Psichiat., 1914, iv., Sett.-Ott., p. 569. 

BHIDAY, B. S. Two oases of anergic stupor treated with thyroid gland extract. 
Indian Med. Qaz., 1914, xlix., Nov., p. 429, 

CARLISLE, C. L. The translation of symptoms into their mechanism. Amer. 
Joum. Insanity, 1914, lxxi, Oct., p. 279. 

GORDON, ALFRED. Insanity and divorce. N.Y. Med. Joum., 1914, c., 
Nov. 21, p. 997. 

BROWN, SANGER. Applied eugenics. Amer. Joum. Insanity, 1914, lxxi., 
Oct., p. 269. 

GRINKER, JULIUS. The neurologic examination of mental cases. Joum. 
Amer. Med. Assoc., 1914, lxiii, Nov. 14, p. 1754. 

WI LLIAM S L. L. The medical examination of mentally defective aliens: its 
scope and limitations. Amer. Joum. Insanity , 1914, lxxi., Oct., p. 257. 

MOORE, ROSS. The present teaohing of psychiatry in American medical 
schools. Joum. Amer. Med. Assoc., 1914, lxiii., Nov. 7, p. 1643. 

GRAVES, W. W. Some factors tending toward adequate instruction in nervous 
and mental diseases. Joum. Amer. Med. Assoc., 1914, lxiii., Nov. 14, p. 1707. 

SINGER, H. D. The ideal course in psychiatry for medical schools. Joum. 
Amer. Med. Assoc., 1914, lxiii., Nov. 7. p. 1644. 

BOND, C. HUBERT. Introductory address on the position of psychiatry and 
the rdle of general hospitals in its improvement. Lancet, 1914, dxxxvii., 
Oct. 17, p. 935. 

SHAW, W. 8. JAGOE. Some generalisations on the scope, construction, and 
administration of oentral asylum in India. Indian Med. Qaz., 1914, xlix., 
Nov., p. 424. 

JACKSON, J. ALLEN. Need of more state hospitals for the insane. N.Z. 
Med. Joum., 1914, o, Nov. 21, p. 1013. 

STEARNS, A. W. Out-patient work in the Massachusetts State Hospital for 
the insane. Boston Med. and Swrg. Joum., 1914, clxxi., Nov. 5, p. 712. 



110* 


BIBLIOGRAPHY 


TREATMENT.* 

Psycb+aaalysls.—BURR, CHARLES B. A criticism of psychoanalysis. Aim. 
Journ . Insantty, 1U14, lxxi., Oct, p. 233. 

FLOURNOY, HENRI. Analysis of a case of peychaathenia. Bullrtin Johni 
Hopkins Hosp ., 1914, xxv., Nov., p. 328. 

MILLER, H. CRICHTON. The psychic factor in insomnia. Practitiontr, 1914, 
xciii., Nov., p. G20. 

• A number of references to papers on Treatment are included in the Bibliofrsphy nadir 
individual diseases 



Jnbtces. 

SUBJECT INDEX. 

Page Reference* to Original Article* are indicated by Henry Type Figure*. 


Abducbns : vide Nerves, Cranial 
Abscess: Otitic Meningitis and Cerebellar, 
with Recovery, 158 ; Brain, caused by 
Fusiform Bacilli, 216; Brain, 216; 
Orbital Brain, and its Operation, 313 ; 
in Apex of Petrous Pyramid. Death 
from Basal Meningitis, 500; Acute 
Myelitis secondary to Perirectal, de¬ 
veloping a Few Hours after Severe 
Fright, 516 

Acetonuria : Two Cases of Acute Retro¬ 
bulbar Neuritis, associated with 
marked, 390 

Achondroplasia: Does it correspond to 
Partial Hypopituitarism? 40; and 
Chondrohypoplasia, 41 ; Fresh Con¬ 
tribution to Study of, 41 ; with Manic- 
Depressive Psychosis, 86 
Acromegaly : Circulatory System in, 494 
Addison’s Disease: in a Boy, with 
Calcification of Adrenals with Remarks, 
167 ; Defaced Type of, 277 ; Case of, 
observed in 1902, considered as Cured. 
Death from Gastric Cancer in 1913. 
Autopsy, 422 ; Case of Implantation of 
Suprarenale in, with Fatal Result, 461 
Adiposity: due to a Juxta-Pituitary 
Sarcoma, 123: Familial, with Endo- 
crinal Disturbances, 124 
Adiposo - Genital Sjmdrome : Experi¬ 
mental Contribution to Hypophy* 
sectomy and Genital Atrophy, 64 
Adrenal: vide Suprarenal 
Adrenalin: Further Observations on 
Constricting Action of, on Cerebral 
Vessels, 207; Action of, and Epinine 
on Pupil in Epilepsy, 287 ; and the 
Pupils, 306 

Agitans, Paralysis: vide Paralysis 

Agitans 

Alcohol: Histological Observations on 
Nervous System of Progeny of Animals 
subjected to Chronic Poisoning, 26; 
Effect of Administration of, on 


Wassermann’s Reaction, 43; and 
Delirium Tremens, 274 ; Experi¬ 
mental Study of Intruneural Injections 
of, 274 

Alcoholism : Pathological Inebriety : its 
Causation and Treatment (Review), 136; 
Measurement of Blood-Pressure in. and 
Functional Neuroses, excluding Circu¬ 
latory Disturbances, 166 ; Heredo- 
Alcoholic Degeneration, 3S8 
Alkaptonuria : Wassernmnn Re action in 
Blood in Cases of, 223 
All-or-None Principle : in Nerve, 110 
Alzheimer’s Disease : and its Relation 
to Senile Dementia, 327 
Amaurotic Family Idiocy; Case of, 281 
Amblyopia : Unusually Extensive Medul- 
lated Nerve Fibres in High Myopia 
and, 324 

Amyosis : Notes on Sunlight and 
Flashlight Reactions and on Con¬ 
sensual, to Blue Light, 131 
Amyotonia Congenita : Case of. 3X4 
Amyotrophy, Progressive Spinal: Trau¬ 
matic Lesion of Distal Segments of 
Spinal Cord followed by, 376 
Antenna : Familial Case of Splenomegalie, 
with Infantilism, 419 
Anaemia, Pernicious: Psychosis occur¬ 
ring during Course of, 503 
Anaesthesia : General, Absence of Oculo¬ 
cardiac Keflex in, 25S 
Anarthria : Case of Subcortic al or Pure 
Motor Aphasia (Dcjcrine) or, 2o6 
Aneurysm : Subclavian, Nervous Symp¬ 
toms caused by, 71 ; of Vessels of 
Brain, 382 

Angeioma : in Cerebellar Peduncle. 

Fatal Intracranial Hteinori huge, 3X2 
Angina: Vincent’s, Local Treatment 
with Salvarsan, 81 

Angiospasm : Spasmodic Closing of 
Cerebral Arteries in its Relation to 
Apoplexy. 418 


112* 


INDICES 


A«»rtir 1 >is«\iw: Wa>-*ei maim s Reaction 
in, 420 

Aphasia : R«*|x>rt of two Cases exhibiting 
L<->jons of Special Interest for Loralisu- 
lion of, 46 ; Contribution to Study of 
Loc alisations in, 47 : Left Prefrontal 
tilioma with, 47 : C ase from Lesion in 
Lwt Hemisphere in a I^eft-Handed 
Individual. (’tossed Aphasia and Dis¬ 
sociated Aphn.-iu, 82 ; Case of Sub¬ 
cortical or Pure Motor (l)ejerine)> 
or Anarthria (Marie), 260; Articu¬ 
late Language in Normal Man and 
in, 4<>7 ; Cliideally Negative Cases 
of, 4*4 ; Some .Modern Conc eptions of, 

4 it I 

Apoplexy : /*nfr Haemorrhage. 

Apraxia : Clioma of Corpus Callosum 
and Left Parietal Lolx*: Bilateral, 
if if i 

Areuate Nucleus : in Man. the Anthro¬ 
poid Apes and the Microoephalie Idiot, 

51 

Argvll Hohertson Pupil : in Absence of 
(.eneral Paralysis, Talies and Cerebro¬ 
spinal Syphilis, 477 
Arsenic : Myelitis, 490 
Arterv : Constrictmg Act ion of Adrenalin 
oil " Cerebral Vessels, ‘207 ; Nerve 
Arborisations of Blood-Vessel Walls, 
2dl ; 1 list ri hut ion of Nerves to, of 

Arm. Clinical Value of Results, 470 ; 
Hole, of Carotid, in Causation of Vas¬ 
cular fusions of Brain, with Remarks 
on Certain Features of Symptoma¬ 
tology, 4IS ; Spasmodic Closing of 
Cerebral, in Relation to Apoplexy, 418 ; 
Occlusion of Posterior Inferior Cere¬ 
bellar, 522 ; ride Hemorrhage 
AsymWoly : 401 

Asystole : Xanthochromia of Cerebro¬ 
spinal fluid in, 27*2 

Ataxia: and Fear, 118; Family with 
Cerebellar, 160 ; Case of Hereditary, 
with Paramyoclonus Multiplex, 161 ; 
Hereditary Cerebellar, 380; Acute, in 
Convalescence from Measles, 414 j 

Athetosis: Double, Inhibitory Action of [ 
Ocular Compression on Abnormal | 
Movements in Case of, 258 j 

Atrophy : Neural, of Muscles of Hand 
without Sensory Disturbances, 137; 
Muscular, from Lead Poisoning, 220 
Atropine : Constant Suppression of 
Oeulo-Cardiac Keflex by, 250 | 

Auditory Nerve: ride Nerves, Cranial 
Auricle: Local Action of Nicotine on ! 

Dog s Right Cardiac, 63 j 

Axon: Differential Stain, Structure of j 
Vagus Nerve of Man as demonstrated J 
by, 402 


Babin ski : “Second Sign” of Organic 
Hemiplegia in Hemichorea, and its 
Bearing on Organic Nature of Chorea, 

260 

BnrMus colt cnmmuni*: Brain Abscess 
due to, 149 

Bar any: Significance for Differential 
Diagnosis of Pointing-Test of, 3)9; 
Total Deafness associated with 
Symptom Complex described by, in 
which Comnlete Restoration of Hear 
ing oeeurrea, 424 

Basedow's Disease: ride Exophthalmic 
Goitre 

Beehterewhs Nude us: Anatomy and 
Function of, 4il3 

Beri-lx'ri : Relationship of, to (4Lands of 
Internal Secretion, 111; rid* Poly¬ 
neuritis 

Binet Test: of Intelligence, 414 
Birth Palsy: Brachial, Conclusions 
derived from Farther Experience in 
Surgical Treatment of, 78 
Blindness: as Symptom of Hysteria,388 
Blood : Relation of Virus of Epidemic 
Poliomyelitis to, 119: Wassermaim 
Reaction in, in Alkaptonuria, 223; 
Penetration of Virus of Poliomyelitis 
from, into Cerehro-spinal Fluid, 4S8: 
Kosinophilia in Chorea, 419 ; Uric Acid 
Content in, in Insanity, 424; riU 
Leucocytosi8 

Blood-Pressure: High Frequency Current 
in High, 49; Measurement of, in Alco¬ 
holism and Functional Neuroses, ex¬ 
cluding Circulatory Disturbances, 16*i 
Bonaparte : Louis, King of Holland. 
Case of, 154 

Bradycardia: Oculo-Cardiac Reflex in 
Normal Subject-8 without, 245 
Brain: Anatomical: Parietal Area, 64 ; 
Structure of, and Interpretation of 
Mental Phenomena in Relation to Lav, 
170; of Black Monkey. Relative 
Prominence of Different Oyri, 370; 
Racial Peculiarity in Pole of Temporal 
Lobe of Negro, 510. Pathology : Study 
of, Atrophy in Insanity, 430; vidt 
Tumour, Ac. 

Brown Sequards Syndrome: Transitory. 

at Onset of Spinal Syphilis, 261. 

Bulb : Alterations of Cells of, in Case 
of Dementia Pnecox, 48 ; Syndrome 
Hthni-Bulbaire, 78; Sudden Death 
from Hemorrhage in Dementia Pra 
cox, 170 

Bulbar Nuclei: with Special Reference 
to Existence of a Salivary Centre in 
Man, 106 

Bulbo-Pontine Glioma : Case of, 481 
Bullet Wound : of Spine, 154 



INDICES 


113* 


Cabbon Monoxide Poisoning : in Seng- 
henydd, 389 

Cataract: Researches on Senile, and on 
Tetany, 320 

Catatonia: and its Relation to Manic- 
Depressive Insanity, 132; Clinical 
Significance of, 278 

Cauaa Equina: Glioma of, Report of 
Case with Seoondary Gliosis of Spinal 
Cord, 121; Giant Tumours of (xmus 
and, 375 ; Rare Case of Spina Bifida, 
with Subsequent Development of 
Symptoms referable to Involvement of 
Conus Meduliaris and Epiconus, 375; 
Peculiar Undescribed Disease of Nerves 
of, 416 

Celluloid: Splints in Acute Cases of 
Poliomyelitis, 415; in Treatment of 
Diseases of Nervous System, 453 

Cemesthopathies, 253 

Cephalograph: a New Instrument for 
Recording and Controlling Head 
Movements, 253 

Cerebellum: Experimental Researches 
on Function of, 60; Embolism, 123; 
Abscess, 158; Family with, Ataxia, 
160; Hereditary Ataxia, 380; Symp¬ 
toms and Localisation, 524 

Corebro-spinal Fluid: Drop Methods of 
Counting the Cells of the, the Relation 
of the Cell Count to the Wassermann 
Reaction, 333; Urea Content of, with 
Special Reference to its Diagnostic and 
Prognostic Significance ; a Series of 97 
Cases, 82; and Special Method of 
Treatment of Essential Epilepsy, 129 ; 
in General Paralysis, 169; Albumen 
in, in Cases of Mental Disease, 171; 
Syndrome of Xanthochromia and 
Coagulation en masse of, 221 ; Correla¬ 
tions of, Examinations with Psychiatric 
Diagnosis, 227 ; Aseptic Leuoocytosis 
of, with Subacute Meningeal Syndrome 
in Course of Cerebral Haemorrhage, 
Xanthochromia and Polynucleosis, 
271; Prognostic and Diagnostic Value 
of Sign of Isolated Hyperalbuminosis 
in, 271; Retrospective Sign of Syphilis. 
Pure Hyperalbuminosis of, without 
Leucocytosis and without Wassermann, 
271 ; Xanthochromia of, in Asystolic 
Patients, 272 ; Albumen Content of, in 
Relation to Disease Syndromes, 318 ; 
Colloidal Gold Reaction in, 319, 459; 
Method by which Remedial Agents 
may bo mingled with, 387; Practical 
Study of Albumin in, in Syphilis, 421; 
Penetration of Virus of Poliomyelitis 
from Blood into, 488 ; Studies on,—I. 
Introduction. II. Theories of Drainage 
of, with Analysis of Methods of In¬ 


vestigation. III. Pathways of Escape 
from Subarachnoid Spaces, with Par¬ 
ticular Reference to Arachnoid Villi. 
IV. Dual Source of, 512. V. Drainage 
of Intra-Ocular Fluids. VI. Establish¬ 
ment of Drainage of Intra-Ocular and 
Intra - Cranial Fluids into Venous 

S stein. VII, Analogous Processes of 
rebral and Ocular Fluids, 513; In¬ 
crease of Total Nitrogen and Urea 
Nitrogen in, in Certain Cases of In¬ 
sanity, with Remarks on Uric Acid 
Content of Blood, 525. 

Cerebro spinal Pressure : 204 ; General 
Effects of Increasing, 371 
Chagas’ Disease : Nervous Varieties of 
New Form of Trypanosomiasis, 41 
Chemotherapy : Vital Staining and, 203 
Children : Typhoid Cerebro - spinal 

Meningitis in, 32; Respiratory Form 
of Encephalo-Meningeal Reactions in 
Typhoid Fever in, 77; R61e which 
Heredity Plays in inducing Epilepsy in, 
suffering from Infantile Cerebral Palsy, 
120; Addison’s Disease in, with Calci¬ 
fication of Adrenals, with Remarks, 
167 ; Nervous Diseases of Elementary 
School, 210 ; Occurrence of Wasser¬ 
mann Reaction in Serum of, of Poorer 
Classes, 272; Epilepsy in, 321, 322 ; 
X-Rays in Fractures of Cranium in, 
417 ; vide Poliomyelitis, Ac. 
Chondrohypoplasia: Achondroplasia and, 
41 

Chorea: Babinski’s “Second Sign” of 
Organic Hemiplegia in Hemichorea, and 
its Bearing on Organic Nature of, 350; 
Eosinophilia in, 419; Voice Sign in, 591 
Chromaffin Tissue: and Suprarenal 
Glands (Review), 537 
Cinematograph: Observations of Cere¬ 
bellar Phenomena, 524 
Coccygeal Ganglion: Mechanical Stimula¬ 
tion of Contribution to Physiology of 
Sympathetic Nervous System, 207 
Cteliac Reflex : Hypotensive, 305 
Colchicine : Chronic Palsy of Limbs due 
to Prolonged Use of, 324 
Colloid: Structure of Nerve Cell, 152; 
Gold Reaction in Cerebro-spinal Fluid, 
319, 459 

Colony System: for Care and Treatment 
of Cases of Mental Disease, 172 
Congenital : Facial Paralysis, 36; 
Hemiatrophy, 122; Goitre, 167; 
Syphilis, Manifestations of, 527 
Contracture : Considerations on Physio¬ 
logical Pathology of, 61 ; Mechanism 
of Muscular Tonus of Reflexes and of, 
252 ; Case of Hysterical, 485 
Conus Meduliaris: Giant Tumours of, 



114* 


INDICES 


375; Rare Oase of Spina Bifida, with 
subsequent Development of Symptoms 
referable to Involvement of, #75 
Oord, Spinal: t*ide Myelitis, Tumours, Ac. 
Cornea: Contribution to Study of So- 
called Pseudo-sclerosis with Changes 
in Liver and, 270 

Cornu Ammonia: Note on Circulation of, 
202 

Corpus Callosum : Partial Agenesis of, 
209; Glioma of, and Left Parietal 
Lobe : Bilateral Apraxia, 266 
Corpus Striatum: Phylogenetio Evolution 
of, 200 ; vide Lenticular Degeneration, 
Progressive 

Coverslips : Collodion, in Microsoopical 
Technique, 486 

Cranial Nerves : vide Nerves, Cranial 
Cretinism : Etiology of Endemic, Con¬ 
genital Goitre, and Congenital Para¬ 
thyroid Disease, 167 
Crista Acustica : Fourth, 22 
Crural: Neuritis, 130, 275; Paraplegia 
from Extra - Dural Spinal Tumour. 
Operation, Recovery, 452 
Crus Cerebri : Tumour of, 520 
Cyst: Is there a Cystic Variety of 
Disseminated Sclerosis? 380; Operative 
Removal of Pineal, 382; Multiple 
Visceral Hydatid (Heart, Brain, 
Kidneys), Rupture of Heart Cyst in 
Left Auricle, 519 ; of Left Cerebral 
Hemisphere, with Consideration of Pre- 
operative and Subsequent Symptoms, 
5zl; of Pituitary Gland, 522 


Decompression : Sellar, in Case of Pitui¬ 
tary Tumour, 162 

Defectives, Mental: Industries for 
(Review), 49; Pineal Gland in Treat¬ 
ment of, 173 ; Are they Lacking in 
Moral Qualities ? 308 ; Mental De¬ 
ficiency (Review), 330; Physical De¬ 
velopment in, 392, 423; The Training 
School Bulletin (Review), 431 ; Binet 
Measuring Scale of Intelligence, 514 

Degeneration: Structure of Myelin 
Sheath and its Alteration in Secondary, 
25 

Delirium Tremens: Alcohol and, 274 

Dementia Paralytica: vide General 
Paralysis 

Dementia Prtecox: Alterations of Cells 
of Bulb found in, 48 ; Reflexes in, 85 ; 
Researches on Genital Glands in, 
86; Sudden Death from Bulbar 
Haemorrhage in Case of, 170; Meta¬ 
bolism in, 327 ; Somatic Disturbances 
in, 392; in Eighth Edition of Krae- 
pelin’s Text-book, 427 


Dementia, Senile: Alzheimer’s Disease 
and its Relation to, 327 

Diabetes Insipidus: Oase of, 163; and 
Infantilism, 218 

Diabetes Mellitus: Facial Paralysis, 267; 
Talalgia in, 451 ; Optic Neuritis with 
Symmetrical Loss of Lower Portion of 
Ineld associated with, 501 

Diphtheria: Post-Diphtheritic Abducens 
Paralysis, 33; On Changes in Hypo¬ 
physis in Experimental, 68; On 
Treatment and Nature of, Paralysis, 
72; Pathogeny and Symptomatology 
of Post-, Polyneuritis, 118; Ocute- 
Cardiac Reflex in, 311 ; Case of Hemi¬ 
plegia in, 314; Changes in Central 
Nervous System in Experimental and 
Human, 372 ; Organic Hemiplegia of, 
379; Intramuscular Injections of 
Antitoxin in, 379; High Incidence of 
Post-, Paralysis : Contribution to Ques¬ 
tion of Neurotropism of Certain In¬ 
fective Agents, 492 

Diplegia: Cerebral, Oculo-Cardiac Re¬ 
flex in, 312 

Dipfococcus Crcuwt#: Septicaemia with 
Cerebro spinal Localisation, 116 

Disseminated Sclerosis : Anatomical Ex¬ 
amination of Case of, from Dissemin¬ 
ated Syphilitic Myelitis, 67 ; Is there 
a Cystic variety of ? 380 ; with Crossed 
Hemiplegia, 455 

Diuresis : Suprarenal Bodies and, 449 
. Dog: Problem of Thinking Dog of 
Mannheim, 208, 208 

Dreams : (Review), 535 ; Analysis and 
Interpretation of, based on various 
Motives, 67, 410 ; Inventonal Record 
Forms of Use in Analysis of, 309 

Ductless Glands : tide Pituitary, Supra¬ 
renal, Thyroid, Ac. 

Dysentery Carrier : Detection of, 532 

Dyspituitarism: Three Cases of, 40; 
vide Pituitary, Ac. 

Dystonia Musculorum Deformans : Case 
of, 314 


Ear : vide Hearing, Labyrinth 
Electric Shook : Hysterical Monoplegia 
following, 45, 161 

j Electrical Treatment: for Neuritis, 328 
I Embolism : Cerebellar, 123 
| Encephalic Puncture: by Orbital Route. 
Its Clinical and Therapeutic Indica¬ 
tions, 123 

Encephalitis: in Mumps, 158; Observa¬ 
tions on Cases of, 531 
Endocardium: Directly Excitable Region 
in the Human, 63 
' Eosinophilia: in Chorea, 419 



INDICES 


115* 


Ependymitis: Serosa or Meningitis— 
Meningism, Intra - Cranial Serous 
Effusions of Inflammatory Origin. 
With Note on “ Pseudo-Tumours ” of 
Brain, 114 

Epilepsy: The Nature and Treatment 
of So>called Genuine, 231; Aotion of 
Adrenalin and Epinine on Pupil in, 

287 

Epilepsy : Spasmophilia and, 44 ; Alter- 
nans, 47; Mental Manifestations of, 
65; Progressive, Myoclonus, 84; 
Cerebrospinal fluid and Special 
Method of Treatment of Essential, 129; 
Brain of Macrocephalic, 129; Role 
which Heredity Plays in inducing, in 
Children suffering from Infantile 
Cerebral Palsy, 120; Effect on Mental 
State of Minor and Major Attacks in. 
Insanity, 167; Reflex, of Therapeutic 
Origin, 274 ; Changes in Reflexes pro¬ 
duced by Ocular Compression in, 256 ; 
Stoppage of Heart by Oculo-Cardiac 
Reflex in, 257 ; Exaggeration of Oculo- 
Cardiac Reflex in, 287 ; in Childhood, 
321; True Idiopathic, in Children, 322; 
and Tuberculosis, 460; Theory of 
Causation founded upon Clinical Mani¬ 
festations and Therapeutic and Patho¬ 
logical Data, 460; Outlook in, 498; 
and Cerebral Tumour, 520 

Epinine: Action of Adrenalin and, on 
Pupil in Epilepsy, 287 

Etiology: of Epidemic Poliomyelitis, 
156; of Endemic Cretinism, Congenital 
Goitre, and Congenital Parathyroid 
Disease, 167 

Exophthalmic Goitre: Polyneuritis of 
Pregnancy with Symptoms of, 45; in 
the Male Sex, 45; and Sclerodermia, 
46; Case of, successfully treated with 
Milk of Thyroidectomised Woman, 47; 
Oculo-Cardiac Reflex in, 254; Relations 
between, and Puerperal State, 276; 
and Glycosuria, Failure of Pituitary 
Opotherapy, 276; Case of, simulating 
Acute Obstruction, 495; Tuberculosis 
and, 496 


Familial Disease : Two Families with 
Several Members in each suffering from 
Optic Atrophy, 42; Nervous Symptoms 
associated with Optic Atrophy of 
Familial Type, 43; Adiposity with 
Endocrinal Disturbances, 124 
Fear : and Ataxia, 118 
Forearm Sign, 451 

Freud : The Teaching of, and his School, 
84; Neuroses and Sexuality, 84; vide 
Dreams, Psychoanalysis, &c. 


u Friction” : Technique of Nerve Palpa¬ 
tion by Nerve, 148 

Friedreich’s Disease; Sensory Changes 
in, 122; First Observed (jases of, in 
America, 155 


Galactosides : of Brain, 69 

Ganglion: Structure of Otic, 22; Study 
of, Cells in Sympathetic Nervous 
System, with Special Reference to 
Intrinsic Sensory Neurones, 302; 
Comparative Distribution of Mito¬ 
chondria in Spinal, Cells of Vertebrates, 
511; vide Gasserian 

Ganglio-Neuroma: Malignant, of Left 
Suprarenal, 421 

Gaseous Exchange: in Decerebrate 
Animal, 449 

Gasserian Ganglion: Tumour of Middle 
Cranial Fossa, involving, 217 

General Paralysis: Treatment of, with 
Sodium Nucleinate and Salvarsan, 48 ; 
Suprarenal Apoplexy in, Sudden Death, 
85 ; Analysis of Errors in Diagnosis in 
Series of Sixty Cases of, 131 ; Serum 
and Cerebro-spinal Fluid Reactions 
and Signs of, 169; Intraspinal Injection 
of Salvarsanised Serum in Paresis, 225, 
225; Treatment of, with Salvarsan, 226; 
On Attempts at Special Serotherapy 
in, 226; Civil Capacity in Remissions 
from, 227; Arachnoid Injections with 
Serum of Syphilitics in Tabes and, 326; 
Treatment of, 327 ; Trauma and, 392; 
and Pregnancy, 424 ; Focal Symptoms 
in, 424 ; Differential Diagnosis of, 425 ; 
Precocious, Three Years after Chancre 
treated by “606,” 501; Rapidly 
aggravated by “ 606,” 502 ; Results of 
Specific Treatment in, at Salpetrifere, 
1912-1914, 502; treated with Intra- 

K il Injections of Salvarsanised 
m, 502, 503 ; Intrathecal Treat¬ 
ment of, 527 ; Intraspinal Injections of 
Neosalvarsan in, 528 
Glands: vide Suprarenal, &o. 

Glioma; left Prefrontal, with Aphasia, 
37 ; of Cauda Equina. Report of Case 
with Secondary Gliosis of Spinal Cord, 
121; of Corpus Callosum and Left 
Parietal Lobe : Bilateral Apraxia, 266; 
Clinical and Ana tomo-Pathological 
Notes on Case of Bulbo-Pontine, vSl 
Glycosuria: Hypophysectomy and Ex¬ 
perimental, 110; Exophthalmic Goitre 
and, Failure of Pituitary Opotherapy, 
276; Albuminuria, Polyuria and, caused 
by Ocular Compression, 261 
Glycyl-Tryptophan Reaction : in Menin¬ 
gitis, 454 



116* 


indices 


Goitre: Observations and Experiment* » Case of, in Diphtheria, 314, 379; 

on, in Brook Trout, 66; Etiology of Late, of Central Origin with Peripheral 

Congenital, of Congenital Parathyroid Homolateral Paralysis of Tongue from 

Disease, and of Congenital Endemic Cerebral Tumour with Double Localisa- 

Cretinism, 167 , tion, 381 ; Crossed, in Disseminated 

Cold Reaction: Colloidal, in Cerebro- Sclerosis, 455 

spinal Fluid, 319; Critical Study of Heredity: Role played by, in inducing 
1-ange‘s Colloidal, in Cerebro-spinal Epilepsy in Children suffering from 

Fluid, 459 . Infantile Cerebral Palsy, 1*20; Ataxia 

Craves* Disease: ridt Exophthalmic with Paramyoclonus Multiplex, 161; 

Goitre On Pedigree showing both Insanity 

Grooves; Causation of Large Vascular, and Complicated Eye Disease; Antici* 

found on Inner Aspect of Os Parietale, pation of Mental Disease in Successive 

203 | Generations, 325; Orel>ellar Ataxia, 

Growth : Influence of Adrenals on. 111 I ,*180; Unusual Type of, Disease of 

Gummala: of Thyroid, 49ft 1 Nervous System, 455; Persistent 

Gynecology : Thyroid Opotherapy in, , (Edema of Legs (Milroy’s Disease), 

49ft I with Acute Exacerbations. Two Cases, 

I 490 

Heredo-Alcoholic Degeneration, 388 

H.kmatomykma : Traumatic, 34; Trau- j Hero: Myth of Birth of, 464 
matic, without Vertebral Lesion, 265 i Herpes Zoster: Etiology of, in Cerebro- 
Hiemorrhage: into Left Supramarginal ! spinal Meningitis, 75; Oticus, 113; 

and Angular Gyri, 38; Cerebral, in j (5m, ever occur Traumatieally? 114; 

Chronic Myeloid Leuca-mia, 122; j of Dental Origin, 211; in a Patient 

Venesection in Cerebral, with Report i with Spinal Cord Syphilis, -11; 

of Cases, 160; Sudden Death from j Salvarsan in Ophthalmic, 387; wid 

Bulbar, in Case of Dementia Pr.venx, Malaria, 489 ; Conjugal, 489; General- 

170; Diagnosis of Cerebral, by Means i ised, 515 . 

of Lumbar Puncture, 219; Aseptic j Hiccough: Favourable Action of Ocular 
Leueoeytosis of Cerebro-spinal Fluid j Compression on Certain Nervous Mam* 

with Subacute Meningeal Syndrome in ; festations, especially, 260 

Course of Cerebral, Xanthochromia I High Frequency Current: in Treatment 
and Polynucleosis, 271 ; Angeioma in I of High Blood Pressure, 49 
Cerebellar Peduncle. Fatal Intra- j Horses : of Elberfeld once more, 111 
cranial, 382; Spasmodic Closing of I Hydrocephalus: “ Idiopathic,’’ in iorm 
Cerebral Arteries in Relation to of Weber’s Syndrome. R&pid Uj ir ® 

Apoplexy, 418 ; Meningeal Syndrome i Lumbar Puncture, 39; Acquired, due 

in Course of Cerebral, 454 to Meningitis of Mumps, 518 

Hair : Folds of Skin Hair in Insane, 501 I Hyperalbuniinosis; t*idt Cerebro-spina 
Hand : Neural Atrophy of Muscles of, I Fluid . , 

without Sensory Disturbances, 1S7 Hyperostoses : Combination of Crania , 

Headache : Lumbar Puncture as Special | and Cerebral Tumours, 218 

Procedure for Controlling, in Course Hyperplasia: Nodular,of Liverassocia 
of Infectious Diseases, 415 with Brain changes, 26 

Hearing : New Theory of, 483 Hypnotics : Role of, in Mental Disease., 

Heart: Local Action of Nicotine on with Indications for their Selec m 

Dog’s Right Cardiac Auricle, 63 ; A and Employment, 463 

Directly Excitable Region in the Hypnotism; and Suggestion (Kevi /i 
Human Endocardium, 63 534 

Hemianopsia : Binasal, occurring in Hypophysis ; f'idt 
Course of Tabetic Optic Atrophy, 212 Hypopituitarism ; 

Hemiatrophy': Case of Congenital, 122; correspond to a ~~- - , 

Case of Progressive Facid, 219 ; Case and Metabolic Studies of a Case o » 

of Facial, 267 to Cyst of the Hypophysis, » 

Hemiplegia: Two Cases of Tabes com- Infantilism of the Lorain type. ’ 

plicated by, 72; Two Cases of Post- vide Pituitary, &c. • 

Operative, 79; Late, Neosalvarsan, Hysteria : The Bradshaw Lecture » 

Death, 164; Pneumonic, 216; and Some of its Aspects, 44Gwe » 
Prostatectomy, 266 ; Ocuio-Cardioc Monoplegia following Electric * 

Reflex in, ancl Cerebral Diplegia, 312 ; f 45; Psychoanalytic Study ot 


Pituitary Body 
Does Achondmplasia 

Partial ? 40: Clinical 


INDICES 


Case of, 66; Defects of Field of 
Vision in, 323; Psychopathology of, 
(Review), 331 ; Analysis of Blindness 
as Symptom of, 388; Case of, Con¬ 
tracture, 485 


Idiot, Microckphalic : with Malforma¬ 
tion of Brain, 412 

Impact: Remarks on Histopathological 
Changes in Spinal Cord due to Impact. 
Experimental Study, 310 
Industries : for Feeble-minded and 

Imbecile (Review), 49 
Inebriety : ride Alcoholism 
Infantilism; 456; Hypophyseal, 40; of 
Lorain Type due to Cyst of Hypophysis, 
Clinical and Metabolic Studies m, 80 ; 
Retrogressive, 80 ; Diabetes Insipidus 
and, 218 ; Familial Cose of Sp] ieno- I 
megalic Anremia with, 419 
Infantile Paralysis : ride Poliomyelitis 
Infantilism, 456; Hypophyseal, 40; 
Retrogressive, 80; Diabetes Insipidus 
and, 218 

Insomnia: Wet Pack in, and Mental 
Disorders, 530 

Insular Sclerosis: vide Disseminated 
Sclerosis 

Iridoplegia : Experimental Production of 
Reflex, 62 

Ischaemia: Peripheral Neuritis from, 84 
Iscovesco’s Experimental Researches on 
Lipoids of Organs, 100 


“ Jaw-Winking Phenomenon”: Associ¬ 
ated Movement of Jaw and Upper Lid, 
412 


Knock-out: Physiological Mechanism of. 
69 

Kiimniel’s Disease : Late Deformities of 
Vertebral Column following Trauma, 


Labyrinth : Suppuration, 87; Mem¬ 
branous, Fourth Crista Acustica, 22; 
An Aid to the Study of Inflammations 
of the Internal Ear (Review), 135 ; In¬ 
flammation of, after Injection of Neo- 
salvarsan, 164 ; Activity, 391 
Landry’s Paralysis : Case of, 265, 518 
Langes Colloidal Cold Reaction: in 
Cerebro spinal Fluid, 319, 459 
Laryngeal fSac: True, Formation in Man 
and its Operative Treatment, 422 
Lead Poisoning: (Review), 538 ; Mus¬ 
cular Atrophy from, 220: Critical Ex- 


amin&tion of 100 Painters for Evidence 
of, 385 ; Observations on 120 Cases of 
Lead Absorption from Drinking 
Water, 385; with Paralysis of Ex¬ 
ternal Ocular Muscles, 420; Electro¬ 
lytic Treatment of, 455 
Lenticular Degeneration, Progressive: 
Case of, 83, 124, 383, 494 ; Westphal- 
Striim pell’s Pseudosclerosis and, 161 ; 
vide Liver 
Lethargy: 530 

Leucocytosis: Clinical Value and Signi- 
ficance in Mental Disease, 171 : ride 
Cerebro-spinal Fluid 
Leukiemia: Cerebral Haemorrhage in 
Chronic Myeloid, 122 
Lipoids : Isoovesco’s Experimental Re¬ 
searches on, of Organs, 100; Fats, 
Stearines and, in the Normal and 
Pathological Central Nervous System, 
69 

Lipoma: Herpetic Facial Paralysis in 
Patient with Symmetrical, 312 ; Sub¬ 
fascial, of Foot causing Symptoms of 
Sciatic Neuralgia, 495 
Lissauer: Tract of, and Substantia 
Gelatinosa Rolandi, 198 
Liver : Nodular Hyperplasia of, associ¬ 
ated with Brain Changes, 26 ; Contri¬ 
bution to Study of so-called Pseudo- 
Sclerosis, with Changes in Cornea and, 
270; Intoxication Psychosis associated 
with Cirrhosis of, 430; vide Lenticular 
| Degeneration, Progressive 
Luetin Reaction : Noguchi’s, in Syphilis, 
80, 222 

Lumbar Puncture : Case of “ Idiopathic 
Hydrocephalus” in form 9 f Weber’s 
Syndrome. Rapid Cure by, 39 ; Diag¬ 
nosis of Cerebral Ha'morrhage by 
Means of, 219; Sudden Death follow¬ 
ing, 318; as Special Procedure for 
Controlling Headache in course of 
Infectious Diseases, 415 
Lung: Vaso-Motor Nerves in, 205; 
Hypotensive Action of Pituitary 
Posterior Lobe Extract on Circulation 
in, 206 


Macrocephaly : Brain of, Epileptic, 129 
Macro-Genito-Somatic Syndrome: Pre¬ 
cocious, Experimental Production, 23 
Magnesium Sulphate: in Purulent 
Cerebro spinal Streptococcic Menin¬ 
gitis, 517 

Maize: Influence of Milling of, on 
Chemical Composition and Nutritive 
Value of, Meal, 24 

Malachite Green: Vital Staining of 
Nerve Centres by, 112 



118* 


INDICES 


Malari.i : Herpes Zoster and, 489 
Malta Fever: Nervous Forms of, 5 15 
Manic-Depressive Psychosis: On the 
Mechanism of Some Cases of, 175; 
Mechanism of Periodic Mental Depres¬ 
sions as shown in Two Cases, and the 
I hempen tic Advantaged such ‘Studies, 
433 ; Achondroplasia with, 86; CaU- 
tonic Syndrome and its Relation to, 
P12; Complement Deviation in Cases 
of, 278 

Mannheim : Thinking Dog of, 208 
Mast Cells : in Meninges of Neeturus, 
easily mistaken for Nerve Cells, 481 
Mater, Pia: Clinical Observations on 
Tumours of, 38 

Measles : ThromUjsis of Cerebral Sinuses 
alter, 78 : Acute Ataxia in Con¬ 
valescence from, 413 
Meiostagmine Reaction: in Mental 
Disease, 49 

Meningitis: Ccrihro-»pinaJ: Etiology of 
Herpes in, 74 ; Chronic Forms of 
Epidemic, 116; Serotherapy of, 262; 
Meningococcus (Review), 534 
Parnm* mmjococnU: Case of Fulminating, 
313 ; Case of. Serotherapy. Recovery, 
414 ; and its Antiserum, 487 
Pnntmorocrn/: Primary, 75; in Sharp¬ 
shooters of Senegal, 492 
TuIwch/oh# : with Association of Menin¬ 
gococcus, 75 ; Differential Diagnosis of 
Syphilitic and, in Adult, 116 
Typhoid: in Infant, 32; On Meningo- 
Typhoid, 76; Respiratory Form of 
Encephalo - Meningeal Reaction in 
Child, 77 

Streptococcic : Case of Tuberculous Disease | 
of Vertebra?, complicated by Acute | 
Meningitis, 378 ; Magnesium Sulphate 
in Purulent, 517 | 

Syphilitic: Differential Diagnosis of, and i 
Tuberculous in Adult, 116; Basal, 
Five Months after Infection, 159; 
Preroseolar, 213; On Metachancral 
and Preroseolar, 493 
After Follicular Tonsillitis, 31; Hyper¬ 
trophic Cervical, 31 ; Case of Purulent 
Aseptic, after Intranasal Interference, 

31; Parotitis complicated by, 76; Men¬ 
ingeal Form of Poliomyelitis, 30, 30; 
Meningo-Cerebellar Symptom Complex 
in Febrile Diseases occurring in Tuber¬ 
culous Individuals, 32; Intracranial ! 
Serous Kflusions of Inflammatory I 
Origin. Ependymitis Serosa—Menin- 
gism. With Note on ‘‘Pseudo- 
Tumours ” of Brain, 114; Otitic, and 
Cerebellar Abscess, with Recovery, 

158 ; Aseptic Reactions of Meninges 
and their Diagnosis, 214, 493; in 


Mumps, 214; Cerebral Complications 
of Whooping-Cough. With Special 
Reference to “Pachymeningitis Pro- 
ductiva Interna,” 215; Maladies des 
Meninges (Review), 279; Recurrent 
Fever and Meningeal Syndrome, 313, 
(in Greece, 1912 13), 262, (in North 
Africa), 378; Cerebral Rheumatism 
explained by Haemorrhagic Meningitis 
occurring in Course of Acute Articular 
Rheumatism, 262 ; Two Cases of Sup¬ 
purative Otogenic, with Recovery, 263; 
Medullary Cavities and Cervical, 411; 
Meningeal States in Scarlet Fever and 
Scarlatinal Ura?mia, 414; Glycyl* 
Tryptophan Reaction in, 454; Memn- 

f eal Syndrome in Course of Cerebral 
faMnorrhage, 454; Abscess in Apex of 
Petrous Pyramid. Death from Basal, 
j 500 ; Acquired Hydrocephalus due to, 

j of Mumps, 518 

Meningococcus; Tuberculous Meningitis 
I with Association of, 75; Pulmonary 

! Localisations of, 414; Meningitis 

| (Review), 534; vide Parameningo¬ 

coccus 

l Metabolism: in Hypopituitarism with 
! Infantilism of Lorain Type, 80; in 

I Dementia Prarcox, 327; Studies in 

1 Case of Myasthenia Gravis, 457 

| Metallic Poisons: and Nervous System, 
70 ; ride Lead 

; Metatyphoid: Myelitis, 33; vide Typhoid 
Microcephalic idiot: Arcuate Nucleus 
in Man, the Anthropoid Apes, and the, 
51; with Malformation of Brain, 412 
i Migraine: Pathology of, 165 
I Milroy’s Disease : Persistent Hereditary 
| (Edema of Legs, with Acute Exacerba¬ 
tions. Report of Two Cases, 490 
Mitochondria; Comparative Distribution 
of, in Spinal Ganglion Cells of V erte* 
brates, 511 

Moiluscum Gravidarum: vide Neuro¬ 
fibromatosis M 

Monoplegia: Hysterical, following 

Electric Shock, 45, 161 ■ 

Moriz Weisz Reaction: in Menta 


Di seases 462 

Mumps: Nervous Complications of, in 
Child, 117; Encephalitis m, 158; 
Meningitis in, 214; Acquired Hydro* 
cephalus due to Meningitis of, 518 

- Traumatic Intramuscular 


Ossification, 29 . 

Musical Faculty: Its Origin and Pro¬ 
cesses (Review), 504 
Myasthenia Gravis: Contribution 
Pathology, 112; Pathogenesis of, 584 , 
Suprarenal and Pituitary Opotherapy 
in, 384 ; Metabolism Studies in, 45/ 


INDICES 


119* 


Myatonia: Congenita (Oppenheim), 

Case of, 113, 515 

Myelin Sheath : Structure of, and 
Alteration in Secondary Degeneration, 
25; Peculiar Alterations of, in De¬ 
generating Nerve Fibres, 373 
Myelitis : Metatvphoid, and Spinal Cord 
Phenomena of Typhoid Fever, 33; 
Anatomical Examination of a Case of 
Multiple Sclerosis from Disseminated 
Syphilitic, 67; Pneumococcal, 378; 
Arsenical, 490; Acute, Secondary to 
Perirectal Abscess, developing a few 
hours after Severe Fright, 516 
Myoclonus : Idiopathic Varieties of, 28 ; 

Progressive Epileptic Myoclonus, 84 
Myopathies: Relation of, 113 
Myotonia : Theory of, 71 


Name-Forgetting : Three Examples of, 
308 

Neosalvarsan: Death following Two 
Injections of, at Onset of Syphilis, 
125; Late Hemiplegia. Death, 164; 
Inflammation of Labyrinth after 
Injection of, 164 ; Technic of Intra¬ 
dural Injections of, in Syphilis of 
Nervous System, 223 ; Present Status 
of, in Treatment of Parasyphilis of 
Nervous System, 274; Syphilitic 
Reinfection after Treatment with, 
421; Unfavourable Complication 
following Intradural Injection of, 526; 
Intr&spinal Injections of, in Tabes and 
General Paralysis, 52S 

Nerve Cell: Colloidal Structure of, 
152 

Nerves, Cranial: Optic: Neuritis with 
Acetonuria, 390; in Diabetes 501. 

Oculomotor: Notes of a Case of Recur¬ 
rent Paralysis of, 58 ; Bilateral Palsy 
from Softening in each. Nucleus, 154; 
Paralysis of Otitic Origin, 499 

Abducens: Lead Poisoning with Par¬ 
alysis of External Ocular Muscles, 
420; Paralysis of External Rectus 
from Abscess in Apex of Petrous 
Pyramid. Death from Basal Menin- 


pher&l Distribution of Issuing Fibres, 
107 ; Structure of Roots, Trunk, and 
Branches of, 109; Structure of, of 
Man as demonstrated by Differential 
Axon Stain, 302 

Nerve Fibre: Degeneration: Structure 
of Myelin Sheath and its Alteration in 
Secondary, 25 

Regeneration: of Medullated Nerves in 
Absence of Embryonio Nerve Fibres, 
following experimental Non-Traumatic 
Degeneration, 152 

Nerve Tracts: Tract of Lissauer and 
Substantia Gelatinosa Rolandi, 198; 
Nervous Terminalis, 201, 202; Pyra¬ 
mid Tract in Red Squirrel and Chip¬ 
munk, 370; Degeneration of Fascicul- 
ous Cerebro-spinalis in Albino Rat, 
511 

Nervus Terminalis: in Man and 
Mammals, 201 ; in Adult Man, 202; 
Ganglion Cells of, in Dog-Fish, 481 

Neurasthenia: Analysis of So-called, and 
Allied States, 308 

Neuritis: Peripheral, from IsohsBmia, 
84 ; Anterior Crural, 130, 275 ; Treat¬ 
ment of, by Electrical Methods, 328 ; 
vide Optic Neuritis 

Neurofibromatosis, 377, 413; Multiple, 
of Skin, 490; Generalised, 515; 
Recklinghausen’s Disease, 159, 314; 
Incomplete Forms of, 30; Fibrosar¬ 
coma of Leg on Woman suffering from, 
281 ; Clinical Note of Fibroma 
Moliuscum Gravidarum, 213, 213 

Neuroses: Freud’s Theory of (Review), 
330; and Sexuality, 84 

Neurotropism : High Incidence of Poet- 
Diphtheritic Paralysis: Contribution 
to Question of, of Certain Infective 
Agents, 492 

Nicotine: Local Action of, on Dog's 
Right Cardiac Auricle, 63 

Nose: Meningitis Purulenta Aseptica 
after Intranasal Interference, 31 

Nucleinate of Soda: and Salvarsan in 
Treatment of General Paralysis, 48; 
in Paralysis Agitans, 220 

Nucleus Intercalatus: of Stederini, 1 


gitis, 500 I Nystagmus, 323 ; Analysis of, 109 

Facial: Alleged Sensory Cutaneous tone 
of, of Man, 393 ; Congenital Paralysis, 

36 ; Syphilitic Paralysis, 81, 273; Oculo-Cardiac Reflex : 254, 255, 374, 
Diabetic Paralysis, 267 ; Herpetic 374; Absence of, in Tabes, 29, 260 ; in 

Paralysis with Symmetrical Lipo- Graves’ Disease, 254; in Normal 

roatosis, 312; Zoster with Trophic and Subjects without Bradycardia, 255 ; 

Sensory Changes in Lingual Mucosa, producing Stoppage of Heart, 256 ; 

312 Constant Suppression of, by Atropine, 

Vagus: Anatomical and Experimental 256; Changes in, in Epilepsy; Stoppage 

Study of Peripheral Ganglia: Local- i of Heart by, in Epileptic, 257 ; 

isation of Sensory Ganglia and Peri- I Exaggeration of, in Epilepsy, 257; 



120* 


INDICES 


Persistence of, in General Anaesthesia, 
258 ; Inhibitory Action of, on Abnormal 
Movements inCase of Double Athetosis, 

258 : in Patients suffering from Various 
Tremors, 259 ; and Paralysis Agitans, 

259 ; Frequent Abolition of, in Syphilis, 

259 ; Abolition and Inversion of, in 
Pseudo-Bulbar Paralysis, 260 ; Favour¬ 
able Action of, on Certain Nervous 
Manifestations, especially Hiccough, 

260 ; Glycosuria, Albuminuria, and 
Polyuria caused by, 261; in Diph¬ 
theritic Intoxication, 311 ; in Hemi¬ 
plegia and Cerebral Diplegia, 312; 
Changes in, in Pregnancy, 488 

(Esophagus : Two Rare Complications of 
Foreign Bodies in, 316 
Optic Atrophy: Two Families with 
Several Memoers in each suffering from, 
42; Nervous Symptoms associated 
with, of Familial Type, 43; Binasal 
Hemianopsia occurring in Course of 
Tabetic, 212; Treatment of Tabetic, 
with Intraspinous Injections of 
Salvarsanised Serum, 491 
Optic Neuritis: Acute Retrobulbar, 
associated with Marked Aoetonuria, 
390 ; with Symmetrical Loss of Lower 
Portion of Field associated with 
Diabetes, 501 

Ossification : Traumatic Intramuscular, 
29 

Otic: Ganglion, Microscopic Structure of, 

22 

Ovary: Extirpation and Vasomotor 
Irritability, 484; Graft of, in Hyper¬ 
thyroidism, 527 

Oxycephaly : and the Oxycephalic 
Syndrome, 219 

Oxygen : Hypodermically in Nervous and 
Mental Diseases, 329 


Pancreas ; Weight of, in Insane, 172 
Paralysis Agitans: Pathology of, 25 ; 
Supposed Relations between, and 
Insufficiency of Parathyroid Glands, 
220; Nucleinotherapy, 220; Oculo- 
Cardiac Reflex in, 259 
Parameningococcus : and its Antiserum, 
487; tide Meningitis 
Paramyoclonus Multiplex: Case of 
Hereditary Ataxia with, 161 
Paranoia: What is ? 426 
Paraplegia: Heredo-Syphilitic {Spastic, 
264; Crural from Extra-Dural Spinal 
Tumour. Operation, Recovery, 452 
Parathyroid Glands : Congenital Disease 
of, Etiology of, 167; Supposed 
Relation between Paralysis Agitans 
and Insufficiency of, 220 ; Tetany and, 


277 ; Sympathetic Irritability and. 
Deficiency, 307 
Parietal Area, 54 

Parietal Bone: Causation of Large 
Vascular Grooves on Inner Aspect of, 
203 

Parietal Lobe, 54; Glioma of Left, and 
of Corpus Callosum: Bilateral Apraxia, 
266 

Parotitis : Complicated with Meningitis, 
76 

Pellagra: Notes on Case of, 244 ; In¬ 
fluence of Milling of Maize on Chemical 
Composition and Nutritive Value of 
Maize Meal, 24 ; Pathology of, 168 ; 
Zeism or, 168 ; English, in Early 
Childhood, 457 ; Attempt to Transmit, 
to Monkeys, 457; Occurrence of, in 
England, 495 ; ride Maize 
Personality: Importance of Disturb¬ 
ances of, in Mental Disorders, 279 
Phobia: Psychopathology of Case of, 
Clinical Study, 308 

Pineal: Experimental Production in 
Mammals of the Precocious Macro- 
Genito-Somatic Syndrome, 23; in 
Treatment of Certain Classes of De¬ 
fective Children, 173; Tumours of, 
320 ; in Relation to Somatic, Sexual, 
and Mental Development, 372, 449 ; 
Operative Removal of, Cyst, 382 ; New 
Researches on Function of, 448 
Pituitary : Anatomy: Analysis of Juxta 
Neural Epithelial Portion of, with 
Embryological and Histological 
Account of Hitherto Undescribed 
Part of Organ, 200; Morphology 
and Histology of Certain Structure 
connected with Pars Intermedia of 
Ox, 448 

Physiology: Hypophysectomy and 

Genital Atrophy, 64; Hvpotensive 
Action of Posterior Lobe Extract on 
Pulmonary Circulation, 206 
Palholoyy: Changes in Experimental 
Diphtheria, 68; Histological Re¬ 
searches in Psychopaths, 69 ; Tuber¬ 
culosis of, Necropsy Findings, 390 
Clinical: Failure of Opotherapy in Ex¬ 
ophthalmic Goitre and Glycosuria, 
276; Opotherapy in Myasthenia 
Gravis, 384; Cyst of, 522; vide 
Acromegaly, Ac. 

Pneumococcus : Hemiplegia, 216 ; mye¬ 
litis, 378 ; tide Meningitis 
Pointing Test: Bdrdny’s, Significance 
for Differential Diagnosis of, 209 
Poliomyelitis Anterior Acuta : Men in- 

f eal Syndrome in, 30; Meningeal 
'orm of, 30; Note on Etiology of 
Epidemic, 156; Contribution to 



INDICES 


121* 


Epidemiology of, 156 ; Epidemic, 491; 
Unusual Manifestations of, 158; 
Clinical Observations on 90 Cases of 
Acute Epidemic, 452; Atrophy of 
Pelvis in, and its Obstetrical Conse¬ 
quences, 459; of Small Muscles of 
Hand, 518; Further Note on Use of 
Celluloid Splints in Treatment of 
Acute Cases of, 415, 453 ; Contribution 
to Pathology of Epidemic, 157 ; Intra- 
spinous Infeotionin Experimental, 157; 
Attempt to Transmit by Bite of 
Lyperosia irritant , 415 ; Relation to 
Blood of Virus of Epidemic, 119; 
Localisation of Virus, and Pathogenesis 
of Epidemic, 487; Penetration of 
Virus of, from Blood into Cerebro¬ 
spinal Fluid, 488 

Polyneuritis : of Pregnancy with 
Symptoms of Graves* Disease, 45 ; On 
Pathogeny and Symptomatology of 
Post-Diphtheritic, 118; Scorbutic, 
322; Post-Typhoid, of Quadriplegio 
Form, 616 

Polyuria : from Experimental Lesion of 
Optoped uncular Region of Base of 
Brain. Regulating Mechanism of 
Water-Content of Organism, 204; 
Glycosuria, Albuminuria and, caused 
by Ocular Compression, 261 ; Ana¬ 
tomical Localisation in Base of Brain 
of Lesions which provoke, in Dogs, 305 

Pott*s Disease: Tertiary Syphilitic 
Fever and Syphilitic, 163 

Pregnancy: Polyneuritis of, with 

Symptoms of Graves* Disease, 45; 
General Paralysis and, 424; Changes 
in Oculo-Cardiac Reflex in, 488: 
Korsakow’s Psychosis occurring 
during, 503 

Prodigy: Arithmetical, 112 

Profichet’s Syndrome : Sclerodermia and 
its Relations to, 46 

Progeria: Case of Supposed (Premature 
Senility) in Girl of Eight Years, with 
remarks, 389 

Prostatectomy : and Hemiplegia, 266 

Pseudo-Bulbar Paralysis : Abolition and 
Inversion of Oculo-Cardiac Reflex in, 
260 

Pseudo-Hypertrophio Muscular Dys¬ 


trophy : Two Cases with Plates, 413 
Pseuaosclerosis: Familiar Forms of 

Wilson’s Lenticular Degeneration and 
Westphal-Strlimpeirs, 161 ; Contribu¬ 
tion to Study of So-called, with 
Changes in Cornea and in Liver, 270 
Psychasthenia : Analysis of Case of, 529 
Psycho-analysis: of Severe Case of 

Hysteria, 66; and Interpretation of 
Dreams based on Various Motives, 67 ; 


Some of Broader Issues of, Movement, 
228 ; and Interpretation of Dreams, 
410 ; Contrast in, Three Cases, 411 
Psycho-pathology : of Case of Phobia, 
308 ; of Everyday Life (Review), 465 ; 
Significance of Unconscious in, 474 
Psychopaths: Histological Researches 
on Hypophysis of, 69 
Psychosis : History of Prison (Review), 
133; in Typhoid Fever, 48 ; Treatment 
of Syphilitic, 170 ; Similar and Dis¬ 
similar, in Relatives, 429 ; Intoxica¬ 
tion, with Cirrhosis of Liver, 430 ; Is 
there an Increase among the Dement¬ 
ing ? 430 ; occurring during Course of 
Pernicious Anaemia, 503 
Psychosis, Korsakow’s: occurring during 
Pregnancy, 503 

Puerperium : Relations between Exoph¬ 
thalmic Goitre and, 276 
Pupil; Action of Adrenalin and Epinine 
on, in Epilepsy, 287; and its Reflexes 
in Insanity, 278 ; Adrenalin and, 306 
Pyramid Tract: in Red Squirrel and 
Chipmunk, 370 

Pyridine-Silver Method : With Note on 
Afferent Spinal Non-Medullatcd Nerve 
Fibres, 467 


Reflexes: Indication and Method for 
Use of Electrical Re-enforcement for 
Elicitation of Absent, 507: Experi¬ 
mental Production of Iridoplegia 62 ; 
in Dementia Pnecox, 85; Mechanism 
of Muscular Tonus of, 252 ; Hypo¬ 
tensive Oeliac, 305; New Vaso-Dilator, 
in Dog’s Hind Limb, 306; Contralateral 
Oppenheim and Gordon, 311 ; Contra¬ 
lateral Periosteal, of Arm, 311 ; 
Absence of Radial, and of Pronation 
of Forearm and Conservation of Reflex 
of Biceps Tendon from Lesion of 6th 
Cervical Root, 451; Bilateral Extensor 
Response in States of Unconsciousness, 
489 ; Behaviour of Abdominal Cutane¬ 
ous, in Reflex Conditions within 
Abdomen and Pelvis, 514 ; vide Oculo- 
Cardiac 

Religion : Psychology of, 307 

Retina: Vascular and other, Changes 
associated with General Disease, 43 

Reviews: (Bickmore) Industries for 

Feeble - Minded and Imbecile, 49; 
(Nitsche and Wilmanns) History of 
Prison Psychoses, 133; (Braun and 
Friesner) Labyrinth. An Aid to .Study 
of Inflammations of Internal Ear, 135; 
(Coopei) Pathological Inebriety: its 
Causation and Treatment, 136; (Biedl) 
The Internal Secretory Organs: their 


x 



122* 


INDICES 


Physiology and Pathology, 173 ; 
(Horncn) Arbeiten aus dera Patho- 
logischen Institut der Universitat 
Helsingfors (Finland), 228 ; (Hutinel) 
Maladies des M6ninges, 279; (Tredgold) 
Mental Deficiency, 330 ; (Hitchmann) 
Freud’s Theories of the Neuroses, 330; 
(Fox and Badger) Psychopathology of 
Hysteria, 331; (Goddard) The Train¬ 
ing School Bulletin, 1913-14, 431 ; 
(Lohmann) Disturbances of the Visual 
Functions, 432; (Rank) Myth of the 
Birth of the Hero, 404; (Freud) Psycho¬ 
pathology of Everyday Life, 464; 
(Bolton) Brain in Health and Disease, 
405; (l)6j£rine) S&niologie des Affec¬ 
tions du Syst^me Nerveux, 504; 
(Wallace) Musical Faculty: Its Origins 
and Processes, 504 ; (Stoddart) Mind 
and its Disorders (Second Edition), 
505; (White and Jeiliffe) Modem 
Treatment of Nervous and Mental 
Diseases, 532; (Hayes) Intensive 
Treatment of Syphilis and Locomotor 
Ataxia by Aachen Methods, 533; 
(Lugaro) Modem Problems in Psychiatry 
(Second Edition), 534; (Tuckey) 
Hypnotism and Suggestion (Sixth 
Edition), 534 ; (Heimanand Feldstein) 
Meningococcus Meningitis, 534; (Berg¬ 
son) Dreams, (Freud) On Dreams, 
(Freud) Interpretation of Dreams, 535; 
(Lucien and Parisot) Glandes Sur- 
renales et Organes Chromaffincs, 537 ; 
(Oliver) Lead Poisoning, 538 

Rheumatism: Acute Polyarticular, 

localised to a Limb affected with 
Recent Paralysis of Brachial Plexus, 
118; Cerebral, explained by Ha*mor- 
rhagic Meningitis occurring in Course 
of Acute Articular, 262 

Rice: is Polished, plus Vitamine a 
Complete Food ? 208 

Right-Brainedness : in Right -Handed 
Individuals, 383 

Rigidity: Observations on Decerebrate, 
205 


Salivaby Centre ; On the Bulbar Nuclei, 
with 8pecial Reference to Existence of, 
in Man, 106 

Salvarsan: and Sodium Nucleinate in 
Treatment of General Paralysis, 48 ; 
Local Treatment of Vincent’s Angina 
with, 81 ; Have Early Claims been 
recognised ? 120; Tabes aggravated 
by, 154: Treatment of Syphilitic 
Diseases of Central Nervous System 
by Intravenous Injections of, 224; 
Treatment of Tabes Dorsalis and 


General Paralysis with, 226; in Oph¬ 
thalmic Zoster, 387; Precocious General 
Paralysis Three Years after Chancre 
treated by, 501 ; General Paralysis 
rapidly aggravated by, 502 
SalvarsanisSi Serum: in Syphilitio 
Diseases of Central Nervous System, 
163, 224; Intraspinal Injection of, in 
General Paralysis, 225, 22§, 226, 502, 
503; Treatment of Tabetic Optic 
Atrophy with Intraspinal Injections 
of, 491 

Satellite Cells : Iron Infiltration in 
Fixed and Wandering Cells of Central 
Nervous System, 209: Study of, in 
Fifty Selected Cases of Mental 
Disease, 411 

Scarlet Fever : Meningeal States in, and 
Scarlatinal Uraemia, 414 
Sciatica: Notes on Treatment of, 132; 
Case of, entirely Cured in Three 
Weeks’ Treatment, 461 ; Subfascial 
Lipoma of Foot, causing Symptoms of, 
495 

Sclerodermia; and Graves’ Disease, 
46 ; and its Relations to the Syndrome 
of Profichet, 46 

Sclerosis, Disseminated : vide Dissemin¬ 
ated Sclerosis 

Scopolamine Hydrobromide: Use of, or 
Hyoscine in Treatment of Mental 
Disorders, 531 
Scurvy: Polvneuritis, 322 
Sensation: Nature of Cutaneous, with 
Instrument for its Measurement, 374 
Septicaemia: Diplococcus crasstM, with 
Cerebro-spinal Localisation, 116 
Sexuality : and Neuroses, 84 
Sinuses : Cerebral, Thrombosis of, after 
Measles, 78; Case of Progressive 
Thrombophlebitis of Brain, following 
Acute Otitis Media, 315 
Sleep: Problem of, 267 
Skull: Syphilitic Bone Disease of, 125; 
Roentgen Diagnosis of Fracture of, in, 
417 

Spasm: Varieties of Facial, and their 
Treatment, 165 

Spasmophilia : and Epilepsy, 44 
Speech : Relation of Function of, to In¬ 
tonation, Tone, and Rhythm, 383 
Spina Bifida : Rare Case of, with Sub¬ 
sequent Development of Symptoms 
referable to Involvement of Cauda 
Equina, Conus Medullaris, and Epi¬ 
conus, 375 

Spirocha'ta pallida: Observations on 
Strain isolated from Nervous System, 
223; vide Syphilis, Ac. 

Staderini: Nucleus Intercalatus of, 1 
St Hildegard ; 160 



INDICES 


123* 


Stupor: Elimination of Nitrogen and 
Uric Acid in States of Excitement and, 
529; Two Cases of Anergio, treated 
with Thyroid Gland Extract, 529 
Substantia Gelatinosa Rolandi: Tract of 
Lissauer and, 198 

Suggestion: and Hypnotism (Review), 

Suicides: Reoent Literature on Juvenile, 
309 

Sulcus : Post-Centralis Superior, 21 
Suprarenal: Glandes Surr£nales et 
Organes Chromaffines (Review), 537 
Anatomy: Development in Birds, 482, 
Physiology: Activity in Thyroidecto- 
mised Animals, 65 ; Action of Thyroid 
Extract and of Organic Extracts in 
General on Secretion of, 65 ; Influence 
on Growth, Ill ; Deficiency and 
Sympathetic Nervous System, 206; 
Effects of Removal in Guinea-Pigs, 
207; and Diuresis, 449; Experi¬ 
mental Observations with Special 
Reference to their Inter-renal Portions, 
484 

Pathology : Tumour in Cow, 310; Malig¬ 
nant Gangiio-Neuroma of Left, 421 ; 
Pathological Changes in, 514 
Clinical : Sudden Death in General 
Paralysis, 85; Two Deaths due to 
Suprarenal Insufficiency, 221; Virilism 
321; Syphilis and, 386; Opotherapy 
in Myasthenia Gravis, 384; wae 
Addison’s Disease 

Sympathetic Nervous System: and 
Chronic Trophcedema, 81 ; Anatomy 
and Vasomotor Phenomena in Turtle, 
109; and Adrenal Deficiency, 206; 
Study of Ganglion Cells of, with 
Special Reference to Intrinsic .Sensory 
Neuron©8, 302; Parathyroid Deficiency 
and Irritability of, 307 
Synesthesia : Case of, 66 ; Unusual Type 
of, 66 

Syphilis: Noguchi Luetin Reaction in, 
80, 222; facial Paralysis, 81 ; Bone 
Disease of Skull, 125; Fever as 
Solitary Symptom of Latent, 125; 
Tertiary Fever and Syphilitic Pott’s 
Disease, 163; Psychoses, 170; Frequent 
Abolition of Oculo - Cardiac Reflex 
in, 259 ; Transitory Brown-Stfquard’s 
Syndrome at Onset of Spinal, 261 ; 
Heredo-Syphilitio Spastic Paraplegia, 
264 ; Biological Reactions in, of 
Central Nervous System, 273; Late, 
Facial Paralysis associated with 
Chronic Pulmonary, 273 ; Intramenin- 
ge&l Treatment of Cerebro-spinal, 315 ; 
Tests in Latent and Treated, 386; 
and Adrenals, 386: Experimental, of 


Central Nervous System in Rabbits, 
387; Treatment of Parenchymatous, 
by Intracranial Medication, 387 ; of 
Vertebral Column, Symptomatology 
and Neural Complications, 458; 
Cerebral in Secondary Stage, 497; 
Manifestations of Congenital, 527; 
Intensive Treatment by Aachen 
Methods (Review), 533; vide Sal- 
varsan, General Paralysis, Ac. 

Syphilophobia, 497 

Syringomyelia: with Autopsy Findings 
in Two Cases, 73; following a Peri¬ 
pheral Infection, 264; Medullary 
Cavities and Cervical Meningitis, 411 


Tabes : Intensive Treatment of Syphilis 
And, by Aachen Methods (Review), 
533; Absence of Oculo-Cardiac Reflex 
in, 29, 260; Two Cases, complicated 
by Hemiplegia, 72; Report of Case of 
Juvenile, 119; Aggravated by “606,” 
154 ; Diagnosis of, 154 ; with Unusual 
Distribution of Deep-Pain Loss, 155; 
Binasal Hemianopsia occurring in 
Course of Optic Atrophy of, 212; 
Treatment with Salvarsan, 226 ; Intra- 
meningealTreatinentof, 315; Arachnoid 
Injection with Serum of Syphilitics in, 
326; Feminine, Comparative Study at 
Bicetre and Salpetnere, 376; Treat¬ 
ment of Optic Atrophy with Intraspinal 
Injections of Salvarsanised Serum, 491; 
Some Histological Changes in, 486; 
Results of Specific Treatment in, at 
the Salpetri^re, 1912-14, 502; Intra¬ 
spinal Injections of Neosalvarsan in, 
528 

Talalgia : in Diabetes, 451 
Tetanus: Subacute, cured by Antitetonic 
Serum, 131; Serotherapy with Massive 
Doses in, 420; Its Prevention and 
Treatment by means of Antitetanic 
Serum, 498; with Recovery treated by 
Carbolic Acid Injections, 526 
Tetany: in Adult and its Parathyroid 
Origin, 277 ; Researches on, and Senile 
Cataract, 320 

Thrombophlebitis: Case of Progressive, 
of Brain Sinuses following Acute Otitis 
Media, 315 

Thrombosis: of Cerebral Sinuses after 
Measles, 78; of Posterior Inferior 
Cerebellar Artery, 522 
Thyroid: Relation to Antitoxin, 47; 
Physiological Activity of Adrenal of 
Thyroidectomised Animals, 65 ; Action 
of, Extract and of Organic Extracts in 
General on Adrenal Secretion, 65; 
Observations and Experiments on 



124* 


INDICES 


Goitre (Thyroid Carcinoma) in Brook 
Trout, 66; Opotherapy and Typhoid 
Spine, 415; Opotherapy in Gynaecology, 
496 ; Gummata of, 496 ; Two Cases of 
Anergic Stupor treated with Extract 
of, 529 ; tide Exophthalmic Goitre 
Tongue-Chewing: 155 
Tonsillitis : Meningitis after Follicular, 
31 

Tonus: Functional Relation between 
Cortical and Subcortical Centres of, 62; 
Mechanism of Muscular, of Reflexes 
and of Contracture, 252 
Toxin: Further Observations on Influence 
of, on Central Nervous System, 252 
Training School Bulletin, 431 
Transference : Some Notes on, 153 
Transvestism, 132 

Trauma : Intramuscular Ossification, 29; 
Hrematomyelia, 34; Can Herpes 
Zoster ever occur from? 114; Haema- 
tomyelia without Vertebral Lesion, 
265; Lesion of Distal Segments of 
Spinal Cord followed by Progressive 
Spinal Amyotrophy, 376 ; and General 
Paralysis, 392; Late Deformities of 
Verteoral Column following, 516 
Trophoedema: Chronic, and Endocrino- 
Sympathetic System, 81 
Trout: Observations and Experiments 
on Goitre (so-called Thyroid Car¬ 
cinoma) in Brook Trout, 66 
Trypanosomiasis : Nervous Varieties of 


New Form of—Chagas’ Disease, 41 
Tuberole: Meningo-cerebellar Symptom 
Complex in Febrile Diseases occurring 
in Individuals with, 32; of Vertebra 
complicated by Extensive Acute 
Suppurative Meningitis, 378 ; Chronic 
Ocular, Necropsy Findings in Case in 
which Death was due to, of Hypo¬ 
physis, 390; Epilepsy and, 460 ; and 
Exophthalmic Goitre, 496 
Tumours: Cerebral: Left Prefrontal 


Glioma with Aphasia, 37; Clinical 
Observations on, of Pia Mater, 38 ; 
Changes in Spinal Cord in, of Posterior 
Cranial Fossa, 35 ; Defect in Innerva¬ 
tion of Facial Nerve from, of Posterior 
Fossa, 217; of Middle Cranial Fossa, 
involving Gasserian Ganglion, 217; 
Combination of Cranial Hyperostoses 
and Cerebral, 218; Pineal, 320; of 
Frontal Region of Brain, 382; Left 
Hemiplegia of Central Origin with 
Peripheral Homolateral Paralysis of 
Tongue from Cerebral, with Double 
Localisation, 381 ; Mental Manifesta¬ 
tions in, 456; Epilepsy and, 520; of 
Crus Cerebri, 520 ; Intracranial Serous 
Effusions of Inflammatory Origin: 


Meningitis or Ependymitis Serosa— 
Meningism. With a Note on “ Pseudo- 
Tumours ” of the Brain, 114 

Pituitary: 39 ; Adiposity due to Juxta- 
Sarcoma, 123; Case of, and Sellar 
Decompression, 162; Pathological 
Investigation of Four Cases of, 456; 
ride Acromegaly, Dyspituitarism, Ac. 

Spinal: Removal of Intrathecal, from 
Lumbar Region of Spinal Cord, 34; 
Surgical Treatment of, 35 ; Two Cases 
of Removal of Extra-Dural, 265; 
Painless, 374 ; Giant Tumours of Conus 
and Cauda Equina, 375; Crural Para¬ 
plegia from Extra-Dural, Operation, 
Recovery, 452; Two Cases of Intra¬ 
dural, 490 

Turtle : Study of Anatomy and Vaso¬ 
motor Phenomena of Sympathetic 


Nervous System in, 109 
’Tweenbrain : and Midbrain of Reptiles, 


201 


Typhoid: Cerebro-spinal Meningitis in 
an Infant, 32 ; Spinal Cord Phenomena 
in, especially Metatyphoid Myelitis, 
33; Psychosis occurring in, 48 ; Men- 
ingo-typhoid, 76; Respiratory Form 
of Encephalo-Meningeal Reactions in, 
in the Child, 77; Respiratory Dis¬ 
orders of Nervous Origin in, 77 ; Post- 
Polyneuritis of Quadriplegic Form, 516 
Typhoid Spine : Report of Case com¬ 
plicated t>y Thrombophlebitis of Left 
Femoral Vein, 118; Ckwe of, 160, 379; 
and Thyroid Opotherapy, 415 


Uremia : Meningeal States in Scarlet 
Fever and Scarlatinal, 414 
Urea: Content of Cerebro-spinal Fluid, 
with Special Reference toits Diagnostic 
and Prognostic Significance: a Series 
of 97 Cases, 82 

Uric Acid : Elimination of Nitrogen and, 
in States of Excitement and Stupor, 
529 


Vaccine Treatment : in Asylums, 172 
Vagus Nerve : tide Nerves, Cranial 
Varicella : Nervous Complications of, 73 
Vasomotor: Nerves in Lungs, 205; 
Apparatus in Pneumonia, 483 ; Ovarian 
Extirpation and, Irritability, 484 
Vertebral Column : Tuberculous Disease 
of, complicated by Extensive Acute 
Suppurative Meningitis, 378 ; Syphilis 
of, its Symptomatology and Neural 
Complications, 458 ; Late Deformities 
of, following Trauma (KiimmeVs 
Disease), 516 



INDICES 


125* 


Vincent’s Angina: Local Treatment of, 
with Salvarsan, 81 
Virilism: Adrenal, 321 
Vital Staining: of Nerve Centres by 
Malachite ureen, 112; and Chemo¬ 
therapy, 203 

Vitamine: Is Polished Rice plus, a 
Complete Food ? 208 ; vidt Ben-beri 
Von Recklinghausen’s Disease: ride 
N eurofibromatosis 


Wasskkmann Reaction : Drop Methods 
of Counting the Cells of the Cerebro¬ 
spinal Fluid—the Relation of the 
Cell Count to the, 833; Effect of 
Administration of Alcohol on, 43 ; and 
its Application to Neurology, 127; 
Methods of Increasing the Accuracy 
and Delicacy of, 128 ; Positive, after 
Forty-six Years of Syphilis, Syphilitic 
Varicose Ulcers, 164 ; Technique of, 
165; in Blood in Cases of Alkaptonuria, 
223 ; Some Observations on Occurrence 
of, in Serum of Children of Poorer 
Classes, 272; Retrospective Sign of 
Syphilis—Pure Hyperalbuminosis of 
derebro-spinal Fluid without Leuco- 
cytosis and without, 271 ; in Aortic 
Disease, 420; Observations on, 459; 


Errors in Interpretation of, 497; and 
Male Insane, 528 

Weber’s Syndrome: Case of “ Idiopathic 
Hydrocephalus” in Form of, Rapid 
Cure by Lumbar Puncture, 39 

Weigert-ral: Counterstain in, Prepara¬ 
tions, 373 ; Paraffin Methods for Stain¬ 
ing of Nervous Tissue, with some new 
Modifications, 450 

Whooping-Cough: Cerebral Complica¬ 
tions of; with Special Reference to 
“Pachymeningitis Productiva In¬ 
terna,215 


Xanthochbomia : Syndrome of, and 
Coagulation tn masse of Cerebro-spinal 
Fluid, 221 ; and Polyuucleosis, Aseptic 
Leucocytosis of Cerebro-spinal Fluid 
with Subacute Meningeal Syndrome in 
Course of Cerebral Hfemorrhago, 271 ; 
of Cerebro-spinal Fluid in Asystolic 
Patients, 272 


X-Rays: in Fractures of Cranium in 
Children, 417 


Zeism : or Pellagra, 168 



12tj* 


INDICES 


INDEX OF AUTHORS. 

Pay: Rtb retires to OrigauU Articles are indicated hy Heary Type Figwx*. 


Ai.rot, E. Stam.ky. What is Paranoia ? 
426 

AUiin-Delthiel, Raynaud, M., Coudray, 
am! Derrien. Meningeal Syndrome in 
North African Recurrent Fever, 378 
Abrahams, Adolphe. The Analysis of 
Nystagmus, ](><J 

Abramow, S. On Changes in the Hvjkj- 
physis in Experimental Diphtheria, 68 
Acker, G. N. Parotitis Complicated 
with Meningitis, 76 

Adler, H. M. A Note on the Increase 
of 1 otal Nitrogen and Urea Nitrogen 
in the Cerebro spinal Fluid in Certain 
Cases of Insanity, with Remarks on the 
Unc Acid Content of the Blood, 522 
Agadjaniantz, K. On Lethargy, 530 
Agadschanianz. On the Relation of the 
Function of Speech to Intonation, 
lone, and Rhythm, 383 
Ahern, R. D., and Robertson, W. N. 

Cyst of the Pituitary (Hand, 522 
Alderson, H. E. Herpes Zoster in a 
Patient with Spinal Cord Syphilis, 211 
Allen, A. R. Remarks on the Histo- 
pathological Changes in the Spinal 
Cord due to Impact—an Experimental 
Study, 310 

Am&ndrut, J. (de Laval), and Gendron, 

A. (de Nantes). Aseptic Leucocytosis 
of the Corebro-spinal Fluid, with Sub¬ 
acute Meningeal Syndrome in the 
Course of Cerebral Hemorrhage. 
Xanthochromia and Polynucleosis, 271 
Ames, 1. H. Analysis of Blindness as a 
Symptom of Hysteria, 388 
Amosa, Harold L. A Note on the Eti- 
ology of Epidemic Poliomyelitis, 156 
A moss, Harold L., and Flexner, Simon. 
Localisation of the Virus and Patho¬ 
genesis of Epidemic Poliomyelitis, 487; 

I enetration of the Virus of Polio¬ 
myelitis from the Blood into the 
Cerebro spinal Fluid, 488 
Amoss, Harold L., Flexner, Simon, and 
Clark, Paul F. A Contribution to the 
Epidemiology of Poliomyelitis, 156; 

A Contribution to the Pathology of 
Epidemic Poliomyelitis, 157 


Amoss, Harold, L, and Clark, Paul F. 
Intraspinous Infection in Experi- 
1 mental Poliomyelitis, 157. 

Amoss, Harold L., Clark, Paul F.,and 
Fraser, Francis R. The Relation to 
j the Blood of the Virus of Epidemic 
Poliomyelitis, 119 

Andr^-Thomas and Roux, J. C. The 
Hypotensive Codiac Reflex, 305 
Antoni. Adrenalin and the Pupils, 306 
Archambault, La Salle. Report of Two 
Cases Exhibiting Lesions of Special 
j Interest for the Localisation of Aphasic 
Disorders, 36; Contribution to the 
Study of the Localisations in Aphasia, 
37 

Argaud, R. A Directly Excitable 
Region in the Human Endocardium, 63 
Arian, E. D. The All-or-None Principle 
in Nerve, 110 

Audry, C. Conjugal Zoster, 489 
Audry C., and Lavau. On Preroseolar 
Meningitis, 213 

Auer, E. M. A Case of Progressive 
Lenticular Degeneration, 383 
Austregesilo. Scorbutic Polyneuritis, 
322 

Austregesilo and EsposeL The Cenas* 
thopathies, 253 , 

Aviragnet, E. C., Dorlenoourt, H., and 
Bouttier, H. The Oculo-Caidiac Re¬ 
flex in Diphtheritic Intoxication, 311 
Ayala. Chronic Trophcedema and the 
Endocrino-Sympathetic System, 81 
Ayer, James B. Salvarsanised 

( 4 4 Swift Ellis Treatment ”) in bvphibtio 
Diseases of the Central ifervou 
System, 224 

Babes, A. Xanthochromia of the 
Cerebro-spinal Fluid in Asystob 
Patients, 272 ,, 

Babinski, Jumentte, and J* 1 *? 1 ™* 
Hypertrophic Cervical Meningitis, 
Babinski, J., Lecfcne, P., and J* 1 *?,*®* * 
J. Crural Paraplegia from Extra- 
Dural Spinal Tumour. Operation, 
Recovery, 452 


9 


INDICES 


127* 


Bachmacknicoff, Mile. N. Pneumo¬ 
coccal Myelitis, 378 

Bailey, Pearce. Painless Tumours of 
the Spinal Cord, 374 

Ballance, Charles A. A Method by 
which Remedial Agents may be 
Mingled with the Cerebrospinal 
Fluid, 387 

Ballet and Genil-Perrin. Clinical Ex¬ 
amination of the Mental State of 
Dements, 328 

Banceis, J. Larguier des, and Claparede, 
Ed. The Mannheim Dog, 208 

Bancroft, Charles P. Is there an In¬ 
crease among the Dementing Psycho¬ 
ses? 430 

Bar&ny, Robert. Total Deafness, asso¬ 
ciated with the Symptom Complex 
described by Brirany, in which Com¬ 
plete Restoration Occurred, 523 

Barbe and Roubiuovitch. Partial Agen¬ 
esis of the Corpus Callosum, 209 

Barbera, R. V. Nervous Forms of 
Malta Fever, 515 

Barnes, A. E., and Kerr, W. S. A Case 
of Otitic Meningitis and Cerebellar 
Abscess, with Recovery, 158 

Basta and Haskovec. Contribution to 
the Pathology of Paralysis Agitans, 
25 

Bates, Gordon, Strathy, George S., and 
M ‘Vicar, C. S. The Treatment of 
Tabes Dorsalis and General Paresis 
with Salvarsan, 226 

Batten, F. E. Unusual Manifestations 
of Poliomyelitis, 158; Further Note 
on the Use of Celluloid Splints in the 
Treatment of Acute Cases of Polio¬ 
myelitis, 415 

Batten, Frederick E., and Wilkinson, 
Douglas. Unusual Type of Heredi¬ 
tary Disease of the Nervous System, 
455 

Battle, W. H. Bullet Wound of the 
Spine: ACase of Medico-Legal Interest, 

154 

Baumel and Margarot. Does Achondro¬ 
plasia Correspond to a Partial Hypo¬ 
pituitarism? 40 

Bean, Robert Bennett. A Racial Peculi¬ 
arity in the Pole of the Temporal Lobe 
of the Negro Brain, 510 

Beaton, Thomas, and Mapother, Edward. 
Intraspinous Treatment (Swift-Ellis) 
of General Paralysis, 225; Intrathe¬ 
cal Treatment of General Paralysis, 
527 

Beaufils, R. Gummata of the Thyroid, 
496 

Befani, G. C. Achondroplasia with 
Manic-Depressive Psychosis, 86 


Beifeld, A. F., and Elliot, C. A. General¬ 
ised Neurofibromatosis (von Reckling¬ 
hausen’s Disease), 515 
Beling, C. C. A Case of Dystonia Muscu¬ 
lorum Deformans, 314 
Beling, C. E. A Case of Amyotonia 
Congenita, 384 

Benech, J., and Legris, A. A Case of 
Early Spinal Syphilis W'ith Bulbar 
Phenomena, 211 

Benigni, P. The Meiostagmine Reaction 
in some Cases of Mental Disease, 49 
Benjamins, C. E. Contribution to the 
Knowledge of the Membranous Laby¬ 
rinth. On a Fourth Crista Acustiea, 
22 

Berg. Unusually Extensive Medullated 
Nerve Fibres in High Myopia with 
Amblyopia, 324 

Bergson, Henri. Dreams (Review ), 535 
Berguer, Georges. Psychology of Reli¬ 
gion, 307 

Beriel and Delachnal. Anatomical Ex¬ 
amination of a Case of Multiple 
Sclerosis from Disseminated Syphilitic 
Myelitis, 67 

Beriel, L. Encephalic Puncture by the 
Orbital Route. Its Clinical and Thera¬ 
peutical Indications, 123 
Beriel, L., and Durand, P. Tuberculous 
Meningitis with Association of the 
Meningococcus, 75 ; Arachnoid Injec¬ 
tion with the Serum of Syphilitics in 
Tabes and General Paralysis, 326 
Berkeley, W. N. Pineal Gland in Treat¬ 
ment of Certain Classes of Defective 
Children, 173 

Bernhardt. A Further Contribution to 
the Subject of Traumatic Hanna to- 
myelia, 34 

Bernstein, E. P. Brain Abscess due to 
t lie Bar if l iff* col i com //i u n i '*■, 159 
Bertein, P. On the Incomplete Forms 
of Recklinghausen’s Disease, 30 
Bertolani, A. A New Method of Pro¬ 
ducing Experimental Lesions of the 
Nerve Centres, 450 

Bertoiotti. A Case of Selerodcrmia and 
its Relations to the Syndrome of Pro- 
tichet, 46 

Bhiday, B. S. Two Cases of Anergic 
Stupor Treated with Thyroid Gland 
Extract, 529 

Bickel. Clinically Negative Cases of 
Aphasia, 383 

Bickmore, A. Industries for the Feeble- 
Minded and Iml>ecile (Review ), 49 
Biedl, Artur. The Internal Secretory 
Organs : Their Physiology and Path¬ 
ology (Review'), 173 
Bien, G. Encephalitis in Mumps, 158 



128* 


INDICES 


Bigelow, Oliver P. The Diagnosis of 
(Cerebral Hemorrhage by Means of 
Lumbar Puncture, 219 
Biondi, G. Traumatic Lesion of the 
Distal Segments of the - Spinal Cord, 
followed by Progressive Spinal Amyo¬ 
trophy, 376 

Blauner, S. A. Hereditary Cerebellar 
Ataxia, 380 

Biscons. Diplococcm crassm Septi¬ 
cemia with Cerebro-spinal Localisa¬ 
tion, lib 

Bloch, M., Foix, and Halle, J. A. Case 
of Hemiplegia in Diphtheria, 314 
Bloch, M., and Vernes, A. A Retro¬ 
spective Sign of Syphilis — Pure 
Hyperalbuminosis of the Cerebro¬ 
spinal Fluid without Leucocytosis and 
without Wassermann, 271 
Blumenfeld, Mile. S. On Suprarenal 
and Pituitary Opotherapy in Myas¬ 
thenia Gravis, 384 

Blumzweig, M. Talalgia in Diabetes, 451 
Bobrie, J. General Paralysis Rapidly 
Aggravated by “ 606,” 502 
Boez and Du hot. Transitory Brown- 

Sequard’s Syndrome at the Onset of 
Spinal Syphilis, 261 

Boggs, Thomas R., and Snowden, R. R. 
The Intrameningeal Treatment of 
Tabes and Cerebro-spinal Syphilis, 315 
Boisroux, L. The Relations between 
Exophthalmic Goitre and the Puerperal 
State, 276 

Bolten, G. C. The Nature and the 
Treatment of the so-called “Genuine 
Epilepsy,” 231 

Bolton, Joseph Shaw. The Brain in 
Health and Disease (Review), 465 
Bolzani, G. Clinical and Anatomo- 
Pathological Notes on a Case of Bulbo- 
Pontine Glioma, 381 

Bonaba, J., and Foresti, C. B. A CaBe 
of Multiple Visceral Hydatid Cysts 
(Heart, Brain, Kidneys), Rupture of 
one of the Heart Cysts in the Left 
Auricle, 519 

Borel, A. On the Reflexes in Dementia 
Praecox, 85 

Boschi, Gaetano. A Case of Hereditary 
Ataxia with Paramyoclonus Multi¬ 
plex, 161 

Boudon, L., and Laignel-Lavastine. 
Adiposity Due to a Juxta-Pituitary 
Sarcoma, 123 

Bourgeois, R. Aseptic Enoephalo- 
Meningeal Reactions, 493 
Bouttier, H., Aviragnet, E. C., and 
Dorlencourt, H. The Oculo-Cardiac 
Reflex in Diphtheritic Intoxication, 
311 


Box, Charles R. English Pellagra in 
Early Childhood, 457 
Boyd, E. J., and Rolleston, H. D. 
Addison s Disease in a Boy, with 
Calcification of the Adrenals, with 
Remarks, 167 

Boyle, Helen A. Some Observations on 
Early Nervous and Mental Cases, with 
Suggestions as to Possible Improve¬ 
ments in our Methods of Dealing with 
them, 463 

Braude, Morris, and Kuh, Sydney. A 
Contribution to the Pathology of 
Myasthenia Gravis, 112 
Braun, Alfred, and Friesner, Isidore. 
The Labyrinth: An Aid to the Study 
of Inflammations of the Internal Ear 
(Review), 135 

Breaks, L. Z., and Johnson, George T. 
The Treatment of Tabetic Optic 
Atrophy w ith Intraspinal Injections of 
Salvarsanised Serum, 491 
Brinckner, S. M. Fibroma Molluscum 
Gravidarum, 213 

Brookover, C. The Nervus Terminalis 
in Adult Man, 202 

Brown, W. H. A Case of Implantation 
of Suprarenale in Addison's Disease, 
with Fatal Result, 461 
Browning, Carl H. The Technique of 
the Wassermann Reaction, 165 
Bruce, A. Ninian. The Arcuate Nucleus 
in Man, the Anthropoid Apes, and the 
Microcephalic Idiot, 61 
Bruce, Lewis C. The Complement 
Deviation in Cases of Manic-Depres¬ 
sive Insanity, 278 

Bryant, W. Sohier. Magnesium Sulphate 
in Purulent Cerebro-spinal Meningo¬ 
coccal Meningitis, 517 
Bu'ia, I. N. Nucleinotherapy in Paralysis 
Agitans, 220 

Burrow, Trigant. Analysis of so-called 
Neurasthenic and Allied States, 308 
Buscaino, V. M. On the Functional 
Relation between the Cortical and 
Subcortical Centres of Tonus, 62; 
Fats, Stearines, and Lipoids in the 
Normal and Pathological Central 
Nervous System, 69 

Busquet, H. A New Vaso-Dilator 
Reflex in the Dog’s Hind Limb, 306 
Buzzard, E. Farquhar. Varieties of 
Facial Spasm and their Treatment, 
165 

Byrnes, C. M. Anterior Crural Neuritis, 
130, 275. 


Cadwalader, Williams B. Progres¬ 
sive Lenticular Degeneration, 494 



INDICES 


129* 


Camp, Carl D. A Contribution to the 
Study of Hereditary Degeneration, 
71 

Campbell, C. Maofie. On the Mechan¬ 
ism of some Cases of Manic-Depressive 
Excitement, 175; Focal Symptoms in 
General Paralysis, 424 

Campbell, Harry. The Treatment of 
Syphilis of the Nervous System by 
Intrathecal Injections, 163; The Treat¬ 
ment of Parenchymatous Syphilis by 
Intracranial Medication, 387 

Campora, G. Absence of the Radial 
Reflex and of the Reflex of Pronation 
of the Forearm, and Conservation of 
the Reflex of the Biceps Tendon from 
Lesion of the 6th Cervical Root, 451 

Camus, J., and Roussy, G. Hypo- 
physectorny and Genital Atrophy: 
An Experimental Contribution to tne 
Study of the Adiposo-Genital Syn¬ 
drome, 64 ; Hypophvsectomy and Ex¬ 
perimental Glycosuria, 110; Polyuria 
from Experimental Lesion of the 
Ch)to-peduncular Region of the Base 
ot the Brain. The Regulating Mechan¬ 
ism of the Water-Content of the 
Organism, 204 ; The Anatomical Local¬ 
isation in the Base of the Brain of the 
Lesions which provoke Polyuria in 
Dogs, 305; Medullary Cavities and 
Cervical Meningitis, 411. 

Cappell, G. Tertiary Syphilitic Fever 
and Syphilitic Pott’s Disease, 163. 

Carle. Neosalvarsan—Late Hemiplegia 
—Death, 164 

Carpenter, F. W., and Conel, J. L. 
A Study of Ganglion Cells in the 
Sympathetic Nervous System, with 
8pecial Reference to Intrinsic Sensory 
Neurones, 302 

Capriole, N. Late Deformities of the 
Vertebral Column following Trauma 
(Kummel’s Disease), 516 

Casali, R. Subfacial Lipoma of the 
Foot causing Symptoms of Sciatic 
Neuralgia, 495 

Casa major, L. Case of Cerebellar 
Embolism, 123 

Cassirer. A Case of Progressive 
Lenticular Disease, 83 

Casteigts, M. M., and Udaondo, C. B. 
Post-Typhoid Polyneuritis of Quadri¬ 
plegic Form, 516 

Castro, Aloysio de. Congenital Facial 
Paralysis, 36 

Caux, P. Respiratory Disorders of 
Nervous Origin in Typhoid Fever, 77 

Celesia, A. F. Ovarian Graft in Hyper¬ 
thyroidism, 527 

Chagas, Carlos. The Nervous Varieties 


of a New Form of Trypanosomiasis— 
Chagas’ Disease, 41 

Charles, J. R. The Pathology of 
Migraine, 165 

Charon and Courbon. Oxycephaly and 
the Oxycephalio Syndrome, 219 
Chakhine, B. Thyroid Opotherapy in 
Gynaecology', 496 

Chase, M. R., and Ranson, S. W. 
Structure of the Roots, Trunk, and 
Branches of the Vagus Nerve, 109 
Chauvet and Fouques. Hypophyseal 
Infantilism, 39 

Christiani, A. Civil Capacity in Re¬ 
missions from General Paralysis, 227 
Ciuffini. Clinical Observations on 
Tumours of the Pia Mater, 38 
Ciarla, E. Haemorrhage into the Left 
Supramarginal and Angular Gyri, 38 
Ciampi, L., and Valdizan, H. Physical 
Development in the Mentally Defective, 
423 

Clapar&le, Ed. The Horses of Elberfeld 
Once More, 111; Does the Motor 
Verbal Image Exist ? 308 
Claparede, Ed., and Bancels, J. Larguier 
des. The Mannheim Dog, 208 
Clark, Elberd. Regeneration of Medul- , 
la ted Nerves in the Absence of 
Embryonic Nerve Fibres, following 
Experimental Non-Traumatic De¬ 
generation, 152 

Clark, L. Pierce, and Sharp, E. A. The 
Role which Heredity Plays in Inducing 
Epilepsy in Children Suffering from 
Infantile Cerebral Palsy, 120; The 
Mechanism of Periodic Mental Depres¬ 
sions as shown in Two Cases, and 
the Therapeutic Advantages of such 
Studies, 434 

Clark, Paul F., Amoss, Harold L., and 
Flexner, Simon. A Contribution to 
the Epidemiology of Poliomyelitis, 156, 
157 

Clark, Paul F., and Amoss, Harold L. 
Intraspinous Infection in Experimental 
Poliomyelitis, 157 

Clark, Paul F., Fraser, Francis R., and 
Amoss, Harold L. The Relation to 
the Blood of the Virus of Epidemic 
Poliomyelitis, 119 

Clarke, J. Michell, and Morton, C. A. 
Removal of Intrathecal Tumour from 
Lumbar Region of Spinal Cord, 34 
Claude and Loyez. Traumatic Haemato- 
myelia without Vertebral Lesion, 265 
Cockayne, E. A. Associated Movement 
of the Jaw and Upper Lid: “The 
Jaw-Winking Phenomenon,” 412 
Coen, Bernard. A Communication as to 
the Causation of Large Vascular 



130* 


INDICES 


Grooves Found on the Inner Aspect of 
the Os Parietale, 203 
Coghill, G. E. Correlated Anatomical 
and Physiological Studies of the 
Nervous System of Amphibia, 202 
Collins, Joseph, and Elsberg, Charles A. 
Giant Tumours of the Conus and 
Cauda Equina, 375 

Conel, J. L., and Carpenter, F. W. A 
Study of Ganglion Cells in the 
Sympathetic Nervous System, with 
Special Reference to Intrinsic Sensory 
Neurones, 302 

Conklin, C. B. Typhoid Spine. With 
Report of a Case Complicated by 
Thrombo-Phlebitis of the Left Femoral 
Vein, 118 

Conos, B. Disseminated Sclerosis with 
Crossed Hemiplegia, 455 
Conto. A Case of “ Idiopathic Hydro¬ 
cephalus” in the Form of Weber’s 
8yndrome: Rapid Cure by Lumbar 
Puncture, 39 

Cooper, J. W. Astley. Pathological 
Inebriety: Its Causation and Treat¬ 
ment (Review), 136 

Core, Donald. Some Modem Concep¬ 
tions of Aphasia, 420 
Coriat, Isador H. A Case of Synesthesia, 
66 ; An Unusual Type of Synesthesia, 
66 

Corson-Whyte, E. P., and Ludlum, S. D. 
Syphilitic Tests in Latent and Treated 
8yphilis, 386 

Coskinas, G. S. Recurrent Fever and 
Meningeal Syndrome (Epidemic of Re¬ 
current Fever in Greece during and 
after the Two Wars of 1912-13), 262 
Coudray, Derrien, Abdin-Delthiel, and 
Raynaud, M. Meningeal Syndrome in 
North African Recurrent Fever, 378 
Coulet, G. Two Cases of Suppurative 
Otogenic Meningitis, with Recovery, 
263 

Courbon and Charon. Oxycephalic Syn¬ 
drome, 219 

Courtney, J. W., and Eaton, H. B. A 
Case of Myotonia Congenita (Oppen- 
heim), 113 

Cow, Douglas. The Suprarenal Bodies 
and Diuresis, 449 

Cowdry, E. V. The Comparative Dis¬ 
tribution of Mitochondria in Spinal 
Ganglion Cells of Vertebrates, 511 
Craig, C. B. Cerebral Syphilis in the 
Secondary Stage, 497 
Crooq. The Mechanism of Muscular 
Tonus, of the Reflexes, and of Con¬ 
tracture, 252 

Crowe, 8. J., and Wislocki, G. B. Ex¬ 
perimental Observations on the Supra¬ 


renal Glands, with Especial Reference 
to their Inter-Renal Portions, 484 
Cushing, Harvey. Studies on the Cere- 
bro-spinal Fluid—I. Introduction, 511 
Cutting, J. A., and Mack, C. W. The 
Intraspinal Injection of Salvarsanised 
Serum in Paresis, 225 
Cyriax, Edgar F. On the Technique of 
Nerve Palpation by Nerve “ Friction,” 
148 

Cyriax, E. F. and R. V. Mechanical 
Stimulation of the Coccygeal Ganglion: 
A Contribution to the Physiology of 
the Sympathetic Nervous System, 207 


Dabney, Virginius. Herpes Zoster 
Oticus. A Critical Review, with Re¬ 
port of a Case, 113 

D*Abundo, G. Changes in the Spinal 
Cord following Peripheral or Cerebral 
Lesions, Isolated and Combined, 120; 
On Attempts at Special Serotherapy 
in General Paralysis, 226; Collodion 
Coverslips in Microscopical Technique, 
486 

Damaye, H. The Treatment of Syphi¬ 
litic Psychoses, 170; Treatment of 
General Paralysis, 327 
Daniel, A. W. The Use of Scopolamine 
Hydrobromide or Hyoscinc in the 
Treatment of Mental Disorders, 531 
Dardel, M. Oxygen Hypodermically in 
Nervous and Mental Diseases, 329 
Davidson, J. A., and Miller, R. The 
Nervous Complications of Varicella, 
73 

Davies, Ivor J. Carbon Monoxide Poison¬ 
ing in the Senghenydd, 389 
Deaaerick, W. H. Herpes Zoster and 
Malaria, 489 

Debat and Jacquet, L. Subacute Tetanus 
Cured by Antitetanic Serum, 131 
Debr£, R., Hints, E., and Netter. A 
Case of Addison’s Disease derived in 
1902, considered as Cured. Death from 
Gastric Cancer in 1913. Autopsy, 422 
Decroly and Henrotin, E. A Case of 
Motor Imbecility, 163 
De Jassy, Parhon, C., and Zugravu, G. 
The Weight of the Pancreas in the 
Insane, 172 

Dejerine, Professor J. Semiologie des 
Affections du Systerae Nerveux (Re¬ 
view), 504 

Delachanal and Beriel. Anatomical Ex¬ 
amination of a Case of Multiple Scle¬ 
rosis from Disseminated Syphilitic 
Myelitis, 67 

De Lange. The ’Tweenbrain and Mid¬ 
brain of Reptilia, 201 



INDICES 


131* 


Demole, V. Alcohol and Delirium 
Tremens, 274; The Reaction of Moriz 
Weisz in Mental Diseases, 462 
Dercum, F. X. A Case of Suboortical 
or Pure Motor Aphasia (Dejerine) or 
Anarthria (Marie), 266 
Derrien, Abdin-Delthiel, Raynaud, M., 
and Coudray. Meningeal Syndrome in 
North African Recurrent Fever, 378 
Descceudres, Alice. Are Defective Chil¬ 
dren Lacking in Moral Qualities ? 308 
Despujols, B. On the Chronic Form of 
Cerebro-spinal Meningitis, 116 
Devine, Henry. The Clinical Signific¬ 
ance of Kata tonic Symptoms, 278 
De Vries. A Case of Epilepsia Alternans, 
47 

De Witt Stetten and Rosen bloom, J. 
Clinical and Met&bolio Studies of a 
Case of Hypopituitarism due to Cyst 
of the Hypophysis, with Infantilism of 
the Lorain Type, 80 

Dick, G. F., and Emge, F. A. Brain 
Abscess caused by Fusiform Bacilli, 
216 

Diller, Theodore, and Miller, R. T. 
Tumour of Frontal Region of Brain, 
382 

Diller, Theodore, and Rosen bloom, Jacob. 
Metabolism Studies in a Case of Myas¬ 
thenia Gravis, 457 

Dixon, W. E., and Halliburton, W. D. 
The Cerebro-spinal Fluid.—II. Cere¬ 
brospinal Pressure, 204; III. The 
General Effects of Increasing the Cere¬ 
bro-spinal Pressure, 371 
Donald, R. Drop-Methods of Counting 
the Cells of the Cerebro-spinal Fluid— 
The Relation of the Cell-Count to the 
Wassermann Reaction, 333 
Dorlencourt, H., Bouttier, H., and 
Aviragnet, E. C. The Oculo-Cardiac 
Reflex in Diphtheritic Intoxication, 
311 

Douglas, R. 0. A Case of Landry’s 
Paralysis, 265. 

Douglas-Craw ford, D. Note on Two 
Cases of Intradural Spinal Tumour, 
490 

Douglas, Mackenzie, and Funk, Casimir. 
Studies on Beri-Beri.—VIII. The Re¬ 
lationship of Beri-Beri to Glands of 
Internal Secretion, 111 
Dubois, S., and GuilUin, G. Acute Poly¬ 
articular Rheumatism Localised to a 
Limb Affected with Recent Paralysis 
of the Brachial Plexus, 118 ; Abolition 
and Inversion of the Oculo-Cardiac 
Reflex in Pseudo-Bulbar Paralysis, 
260; Syringomyelia following a Peri¬ 
pheral Infection, 264 


Dufouger6, W. Pneumococcal Menin¬ 
gitis in the Sharpshooters of Senegal, 
492 

Dufour, H. On Reflex Epilepsy of Thera¬ 
peutic Origin, 274 

Dufour and Legras. Oculo-Cardiac Re¬ 
flex producing Stoppage of the Heart. 
Ventricular Automatism and Auriculo- 
Ventricular Dissociation. Ovarian In¬ 
sufficiency associated with Thyroid 
Overactivity. Epileptiform Attacks, 
256 

Duhot. Syndrome H£mi-Bulbaire, Ac., 
78 

Duhot and Boez. Transitory Brown- 
Sequard’s Syndrome at the Onset of 
Spinal Syphilis, 261 

Duhot and Hallez. Exophthalmic Goitre 
and Glycosuria, Failure of Pituitary 
Opotherapy, 276 

Duhot, Pier ret, and Verhaeghe. Peri¬ 
pheral Neuritis from Ischaemia, 84 

Dunn, J. S., and Monro, T. K. Malig¬ 
nant Ganglio-Neuroma of Left Supra¬ 
renal, 421 

Durand, P. Etiology of Herpes in Cere¬ 
bro-spinal Meningitis, 74 

Durand, P., and Beriel, L. Tuberculous 
Meningitis, with Association of the 
Meningococcus, 75; Arachnoid Injec¬ 
tion with the Serum of Syphilitics in 
Tabes and General Paralysis, 326 

Durupt and Thomas, Anar6. Experi¬ 
mental Researches on Cerebellar Func¬ 
tion, 60 


Eager, Richard. The Role of Hypno¬ 
tics in Mental Diseases, with Indica¬ 
tions for their Selection and Employ¬ 
ment, 463 

Eaton, H. B., and Courtney, J. W. A 
Case of Myotonia Congenita (Oppen- 
heim), 113 

Edwards, D. J. A Study of the 
Anatomy and the Vasomotor Pheno¬ 
mena of the Sympathetic Nervous 
System in the Turtle, 109 
Elliot, C. A., and Beifeld, A. F. 
Generalised Neurofibromatosis (von 
Recklinghausen’s Disease), 515 
Elliot, T. R. Pathological Changes in 
the Adrenal Glands, 514 
Elliott, W. M. Some Observations on 
the Occurrence of the Wassermann 
Reaction in the Serum of the Children 
of the Poorer Classes, 272 
Elsberg, Charles A., and Collins, Joseph. 
Giant Tumours of the Conus and Cauda 
Equina, 375 

Elsberg, Charles A,, Lambert, C. I., and 



132* 


INDICES 


Keunedy, Foster. A Peculiar Unde¬ 
scribed Disease of the Nerves of the 
Cauda Equina, 416 

Elsohing. The Orbital Brain Abscess 
and its Operation, 313 

Embletpn, Dennis, and Thiele, Francis 
H. Methods of Increasing the Accu¬ 
racy and Delicacy of the Wassermanu 
Reaction, 128 

Emerson, L. E. A Psycho-Analytic 
Study of a Severe Case of Hysteria, 
66 

Emge, F. A., and Dick, G. F. Brain 
Abscess Caused by Fusiform Bacilli, 
216 

Esposel and Austregcsilo. The Cemes- 
thopathies, 253 

Euzi&re, J. On Aseptic Reactions of 
the Meninges and their Diagnosis, 214 

Eversole, E. E., and Myerson, A. Notes 
on Sunlight and Flashlight Reactions, 
and on Consensual Amyosis to Blue 
Light, 131 


Fabkk and Petzetakis. Persistence of 
Oculo-Cardiac Reflex in (General Anes¬ 
thesia, 258 

Falconer, A. W. Three Cases of Dys- 
pituitarism, 40 

Farise, C. An Adrenal Tumour in a 
Cow, 310 

Farrant, Rupert. The Relation of the 
Thyroid to Antitoxin, 46 
Faure-Beaulieu, Vaucher, and Lere- 
boullet. Diabetes Insipidus and In¬ 
fantilism, 218 

Fearnsides, E. G., and Head, Henry; 
M'Intosh, James, and Fildes, Paul. 
Paralysis of the Nervous System, 126 
Feiling, Anthony. On the Bulbar 
Nudei, with Special Reference to 
the Existence of a Salivary Centre in 
Man, 106 

Feldstein, Samuel, and Heiman, Henry. 
Meningococcus Meningitis (Review), 

534 

Fenoglietta, Perrero v. On a Case of 
Polyneuritis of Pregnancy with Symp¬ 
toms of Graves* Disease, 45 
Ferrari, M. Histological Observations 
on the Nervous System of the Progeny 
of Animals Subjected to Chronic 
Alcoholic Poisoning, 26 
Fildes, Paul, and M*Intosh, James; 
Head, Henry, and Fearnsides, E. G. 
Paralysis of the Nervous System, 126 
Fildes, Paul, and MTntosh, James. 
The Wassermann Reaction and its 
Application to Neurology, 127 
Findlay, Leonard, and Robertson, Madge 


E. Some Manifestations of Congeni¬ 
tal Syphilis, 527 

Fischer, Walther, and Yokoyama, Yugo. 
A Peculiar Form of Nodular Hyper¬ 
plasia associated with Brain Changes, 
26 

Fisher, E. D. Present Status of Neo- 
salvarsan in the Treatment of Para- 
syphilis of the Nervous System, 274; 
Landry’s Paralysis, 518 
Fleming, Robert A. Notes of a Case of 
Recurrent Paralysis of the Third 
Cranial Nerve, 58 

Flexner, Simon, and Amoss^ Harold L. 
Localisation of the Virus and Patho¬ 
genesis of Epidemic Poliomyelitis, 487 ; 
Penetration of the Virus of Polio- 
1113 'elitiB from the Blood into the 
Cerebro-spinal Fluid, 488 
Flexner, Simon, Clark, Paul F., and 
Amoss, Harold L. A Contribution to 
the Epidemiology of Poliomyelitis, 
156 ; A Contribution to the Pathology 
of Epidemic Poliomyelitis, 157 
Flournoy, Henri. Analysis of a Case of 
Psychasthenia, 529 

Fofc, C. Now Researches on the Func¬ 
tion of the Pineal Gland, 448 
Foereter. A Meningo-Cerebellar Symp¬ 
tom - Complex in Febrile Diseases 
Occurring in Tuberculous Individuals, 
32 

Foix, Halle, J., and Block, M. A Case 
of Hemiplegia in Diphtheria, 314 
Fon-agtes, C. Arsenical Myelitis, 490 
Foresti, C. B., and Bonaba, J. A Case 
of Multiple Visceral Hydatid Cysts 
(Heart, Brain, Kidneys), Rupture of 
one of the Heart Cysts in the Left 
Auricle, 519 

Forster, George B. The Noguchi Luetin 
Reaction in Syphilis, 80 
Fotheringham, J. T. A Case of Tetanus, 
with Recovery, Treated by Carbolic 
Acid Injections, 526 

Foucque, A. Practical Study of the 
Albumin in the Cerebro-Bpinal Fluid 
in Syphilis, 421 

Fox, Charles D. The Psychopathology 
of Hysteria (Review), 331 
Francis, Edward. An Attempt to trans¬ 
mit Poliomyelitis by the Bite of 
Lyperosia irrilam , 415 
Francis, E., Grimm, R. M., Lorenz, W. 
F., and Lavinder, C. H. Attempts to 
Transmit Pellagra to Monkeys, 4o7 
Francesco, Bandettini di Pog^io. Left 
Hemiplegia of Central Origin with 
Peripheral Homolateral Paralysis of 
the Tongue from a Cerebral Tumour, 
with Double Localisation, 381 



INDICES 


133 * 


Fraaer, Francis R. Clinical Observa¬ 
tions on Ninety Cases of Acute 
Epidemic Poliomyelitis, 452 

Fraser, Francis R., Amoss, Harold L., 
and Clark, Paul F. The Relation to 
the Blood of the Virus of Epidemic 
Poliomyelitis, 119 

Fraser, J. S. Labyrinth Suppuration: A 
Review, 87 

Fredericq, L6on. The Local Action of 
Nicotine on the Dog’s Right Cardiac 
Auricle, 63 

Freud, Sigmund. Psychopathology of 
Everyday Life (Review), 464; On 
Dreams (Review), 535; The Interpre¬ 
tation of Dreams (Review), 535 

Frey, Rameix, and Morichau-Beauchant, 
R. Acute Ataxia in Convalescence 
from Measles, 413 

Friesner, Isidore, and Braun, Alfred. 
The Labyrinth : An Aid to the Study 
of Inflammations of the Internal Ear 
(Review), 135 

Frink, H. W. Three Examples of Name- 
Forgetting, 308 

Frith, A. H. The Pupil and its Reflexes 
in Insanity, 278 

Froment, J., and Monod, O. Articulate 
Language in the Normal Man and in 
the Aphasic, 307 

Funk, Casimir. Studies on Pellagra.— 
I. The Influence of the Milling of 
Maize on the Chemical Composition 
and the Nutritive Value of Maize- 
Meal, 24; Is Polished Rice plus 
Vitamine a Complete Food ? 208 

Funk, Casimir, and Douglas, Mackenzie. 
Studies on Beri-Beri.—VIII. The Re¬ 
lationship of Beri-Beri to Glands of 
Internal Secretion, 111 


Gaitz, Sarah. Diabetic Facial Paraly¬ 
sis, 267 

Ganeau and Giroux. Tabes Aggravated 
by “606,” 154 

Gantz, Mieczyslaw. Two Rare Compli¬ 
cations of Foreign Bodies in the JEao- 
phagus, 316 

Garnier, M., and Levi-Franckel, G. 
Changes in the Oculo-Cardiac Reflex 
under the Influence of Pregnancy, 488 

Gatti, L. Trauma and General Paralysis, 
392 

Gautrelet. The Oculo-Cardiac Reflex, 
254 

Gauthier, G. On the Spinal Cord 
Phenomena of Typhoid Fever, and 
Especially Metatypnoid Myelitis, 33 

Gebb, H. Salvarsan in Ophthalmic 
Zoster, 387 


Gendron, A. (de Nantes), and Amandrut, 
J. (de Laval). Aseptic Leucocytosis 
of the Cerebro-spinal Fluid with Sub¬ 
acute Meningeal Syndrome in the 
course of Cerebral Haemorrhage. 
Xanthochromia and Polynucleosis, 271 
Genil-Perrin and Ballet. Clinical ex¬ 
amination of the Mental State of 
Dements, 328 

Gettings, H. 8., and Waldron, Ethel. 
The Detection of a Dysentery Carrier, 
532 

Gillis, Andrew C. Occlusion of the 
Posterior Inferior Cerebellar Artery, 
522 

Giroux and Ganeau. Tabes Aggravated 
by “606,” 154 

Glaser. The Nerve Arborisations of the 
Blood-Vessel Walls, 251 
Gley, E. The Physiological Activity of 
the Adrenal of Tnyroidectomiaed 
Animals, 65 

Gley, E., and Quinquaud, A. Contribu¬ 
tion to the Study of Humoral Inter- 
Relations.—I. The Action of Thyroid 
Extract and of Organic Extracts in 
General on Adrenal Secretion, 65 
Glynn, T. R. The Bradshaw Lecture on 
Hysteria in some of its Aspects, 44 
Goddard, Henry H. The Binet 
Measuring Scale of Intelligence, 514 
Goebel, 0. Labyrinth Activity, 391 
Goldmann, Professor. Vital Staining 
and Chemotherapy, 203 
Goldstein and Marinesco. Graves* 
Disease and Sclerodermia, 45 
Goldstein and Reichmann. Somatic 
Disturbances in Dementia Prajcox, 392 
Gonnet and Levy, L. Meningeal 
Syndrome in the Course of Cerebral 
Haemorrhage, 454 

Gordon, Alford. Mental Manifestations 
in Tumours of the Brain, 456 
Gordon, Alfred. The Cerebro-Spinal 
Fluid and a Special Method of Treat¬ 
ment of Essential Epilepsy, 129; 
Experimental Study of Intraneural 
Injections of Alcohol, 274; Contra¬ 
lateral Oppenheim and Gordon Re¬ 
flexes, 311; Lumbar Puncture as a 
Special Procedure for Controlling 
Headache in the Course of Infectious 
Diseases, 415; Spasmodic Closing of 
Cerebral Arteries in its Relation to 
Apoplexy, 418 ; Unfavourable Compli¬ 
cation following an Intradural Injec¬ 
tion of Neosalvarsan, 526 
Grabs. A Case of Progressive Facial 
Hemiatrophy, 219 

Grace, John J. Notes on the Treatment 
of Sciatica, 132 





INDICES 


Oraetz. Spasmophilia ami Epilepsy, 43 

Graham, Cecil, ami Harris, Wilfml. A 
Cane of Pituitary Tumour and Sellar 
Decompression, 162 

Grand, Selma, and Soper, Willard B. 
The Urea Content of the Spinal Fluid, 
with Special Reference to its Diag¬ 
nostic and Prognostic Significance. A 
Series of Ninety-seven Cases, 82 

Green wald, J. The Sup|x>sed Relation 
between Paralysis Agilans and In- 
suthciency of the Parathyroid (Hands, 
220 

Gregor and Schilder. The Theory of 
M yotonia, 71 

Gregory, M. S., and Karpas. M. J. 
Syphilitic Bone Disease of the Skull, 
125 

Grellier, G. The Circulatory System in 
Acromegaly, 494 

Grimm, R. M., Lorenz, W. F., Lavinder, 
C. H., and Francis, K. Attempts to 
Transmit Pellagra to Monkeys, 457 

Guichot, H. Primary Pneumococcal 
Cerebro-spinal Meningitis, 75 

Guidi, Feruccio. On the Structure of 
the Myelin Sheath and its Alteration 
in Secondary Degeneration, 25 

Guillain, G. Inhibitory Action of 
Ocular Compression on the Abnormal 
Movements in a Case of Double 
Athetosis, 258 

Guillain, G., and Dubois, S. Acute 
Polyarticular Rheumatism Localised 
to a Limb Affected with Recent 
Paralysis of the Brachial Plexus, 118 ; 
Abolition and Inversion of the Oculo- 
Cardiac Reflex in Pseudo-Bui l »ar 
Paralysis, 2(50; Syringomyelia follow¬ 
ing a Peripheral Infection, 284 ; 

Guillaumont, B. The Oculo-Cardiac 
Reflex in Graves’ Disease, 254 


Hada, B. On the Cerebral Complications 
of Whooping Cough. With Special 
Reference to “ Pachymeningitis Pro¬ 
ductive Interna,” 215 
Hale, Worth. The Cause of Death from 
Subdural Injections of Serum, 388 
Halle, J., Bloch, M., and Foix. A Case 
of Hemiplegia in Diphtheria, 314 
Hallezand Duhot. Exophthalmic Goitre 
and Glycosuria. Failure of Pituitary 
Opotherapy, 276 

Halliburton, W. I)., and Dixon, W. 
E. The Cerebro-Spinal Fluid.—H. 
Cerebro-Spinal Pressure, 204.—III. 
The General Effects of Increasing the 
Cerebro-spinal Pressure, 371 
Hallion, L. The Hypotensive Action of 


Pituitary Posterior Lobe Extract on 
the Pulmonary Circulation, 206 
Handmann and Striimpell. A Contribu- 
' tion to the Study of So-called Pseudo- 
sclerosis, with Changes in the Cornea 
and in the Liver, 270 
Hammes, Ernest H., and Riggs, C. 
i Eugene. Results of One Hundred 
I Injections of Salvarsanised Serum. 503 
Harris, Wilfred, and Graham, CeciL 
A Case of Pituitary Tumour and 
Sellar Decompression, 162 
Haskovec and Basta. Contribution to 
the Pathology of Paralysis Agitans, 25 
Hawthorne, C. 0. On the Occurrence uf 
a Bilateral Extensor Response instates 
of Unconsciousness, 489 
Hayes, Reginald. The Intensive Treats 
ment of Syphilis and Locomotor Ataxia 
by Aachen Methods (Review), 533 
Hayhurst, Emery R. Critical Examina¬ 
tion of One Hundred Painters for 
Evidence of Lead Poisoning, 38o 
Havs, Victor J. The Development of 
the Adrenal Glands of Birds, 482 
Head, Henry, and Fearnsute, t‘ 
M'Intosh, James, and Fildes, P«L 
Paralysis of the Nervous System, l* 
Heed, Charles R., and Price, Georg. * 
Binasal Hemianopsia occurring 
Course of Tabetic Optic Atrophy. 
Heiman, Henry, and Feldstem ^ 
Meningococcus Meningitis (B«™ ' 
534 , t 

Hele, T. S., and Wolf, Charlesitj 
Gaseous Exchange in the Decere 
Animal, 449 , „. l, k ; s 

Henderaon, D. K. KoraakowsP^hnsi 
Occurring during Pregnancy, . 

Henning-Hounc. SomeOasM J 
cal Defect of the Field of \ 
Henrotin, K., and Decroly. A C 

Atw 

■MJfr. Babinski'. •£* 
Sign ” of Organic Henuplepa n‘» 
chorea, and its Bearing on the Organ 
Nature of Chorea, 2*0 q„ 

Herxheimer, G., and Kotn, • 
Recklinghausen’s Neurofibroma! 

Hesnard and Regis. The Teaching of 
Freud and his School, 84 j am «. 

Hewat, Fergus A., and MdJ* the 
A Case of Tuberculous 
Vertebrae, complicated ty j-g 

Acute Suppurative Menmp ikon's 
Higier, H. Familial Forms of ^ 

Lenticular Degenerationand t P u< “ 

Strilmpell’s Pseudosclerosis, m 


INDICES 


135* 


Hinton, W. A., and Lee, Roger 1. A 
Critical Study of Lange’s Colloidal 
Gold Reaction in Cerebro-spinal Fluid, 
459 

Hirtz, E., Debr£, R., and Netter. A 
Case of Addison’s Disease observed in 
1902, considered as Cured. Death 
from Gastric Cancer in 1913 ; Autopsy, 
422 

Hitschmann, Eduard. Freud’s Theories 
of the Neuroses (Review), 330 

Holmes, A. O. Defaced Type of Addison’s 
Disease, 277 

Holmes, Gordon. The Diagnosis of 
Tabes Dorsalis, 154 

Holmes, Gordon M., and Taylor, James. 
Two Families with Several Members in 
Each Suffering from Optic Atrophy, 
42; Nervous Symptoms associated 
with Optic Atrophy of the Familial 
Type, 42 

Hom£n, E. A. Arbeiten aus dem Patho- 
logischen Institut der Universitat 
Helsingfors (Finland) (Review), 228 

Hornowski, J. Two Deaths Due to 
Suprarenal Insufficiency, 221 

Horton, Lydia H. Inventorial Record 
Forms of Use in the Analysis of 
Dreams, 309 

Hoskins, R. G., and Wheelon, Homer. 
Adrenal Deficiency and the Sympa¬ 
thetic Nervous System, 20b; Para¬ 
thyroid Deficiency and Sympathetic 
Irritability, 307 ; Ovarian Extirpation 
and Vasomotor Irritability, 484 

Humo, W. E. A Case oi Amaurotic 
Family Idiocy, 282 

Hunt, J. Ramsay. The Neurol Atrophy 
of the Muscles of the Hand, without 
Sensory I)isturl>ances, 187 ; the Role 
of the Carotid Arteries in the Causation 
of Vascular Lesions of the Brain, with 
Remarks on Certain Special Features 
of the Symptomatology, 418 ; Syphilis 
of the Vertebral Column : Its 

Symptomatology and Neurol Com¬ 
plications, 458 

Hutinel, Professor. Maladies des 

Meninges (Review), 279 


Ige9HKImer, J. On Nystagmus, 323 
Ivy, Robert H., and Thomas, B. A. 
Observations on the Wassermann 
Reaction, 459 


Jacksox, D. J. The Clinical Value and 
Significance of Leucocytosis in Mental 
Disease, 171 

Jacquet, L., and Debat. Subacute 


Tetanus Cured by Antitetanic Serum, 
131 

Jacquin and Marchand. Progressive 
Epileptic Myoclonus, 84 
Jarkowski, Babinski, and Jumenti. 

Hypertrophic Cervical Meningitis, 31 
Jarkowski, J., Babinski, J., ana Lecfcne, 
P. Crural Paraplegia from Extra¬ 
dural Spinal Tumour. Operation. 
Recovery, 452 

Jefferson, Geoffrey. A Note on the 
Sulcus Post-Centralis Superior, 21 ; 
the Parietal Area, 54 
Jelliffe, Smith Ely. Some Notes on 
44 Transference, 153 
Job, E. A Case of Typhoid Spine, 379 
Johnston, J. B. TheNervus Terminalis 
in Man and Mammals, 201 
Johnson, George T., and Breaks, L. Z. 
The Treatment of Tabetic Optic 
Atrophy with Intraspinal Injections 
of Salvarsanised Serum, 491 
Johnson, W. A Pathological Investi¬ 
gation of Four Cases of Pituitary 
Tumour, 456 

Jolowicz. The Treatment of General 
Paralysis with Sodium Nucleinate and 
Salvarsan, 48 

Joltrain, E., and Rouffiac, P. Meningeal 
Syndrome of the Poliomyelitis Type, 

Joltrain, E., Milian, and Sicard. Death 
following two Injections of Neosal- 
varsan at the Onset of Syphilis, 125 
Jones, A. Webb. Two Cases of Post¬ 
operative Hemiplegia, 79 
Jones, Ernest. The Case of Louis Bona¬ 
parte, King of Holland, 153; The 
Significance of the Unconscious in 
Psychopathology, 474 
Jonnescoand Laignel-Lavastine. Histo¬ 
logical Researches on the Hypophysis 
of Psychopaths, 69 

Jumenti^, Jarkowski, and Babinski. 
Hypertrophic Cervical Meningitis, 31 


Karp as, M. J., and Gregory, M. S. 
Syphilitic Bone Disease of the Skull, 
125 

Karplus and Kreidl. The Experimental 
Production of Reflex Iridoplegia, 62 
Kellqg, J. H. The First Observed Cases 
of Friedreich’s Ataxia in America, 155 
Kennedy, Foster, Elsberg, Charles A., 
and Laml>ert, C. J. A Peculiar Un¬ 
described Disease of the Nerves of the 
Cauda Equina, 416 

Kerr, W. S., and Barnes, A. E. A Case 
of Otitic Meningitis and Cerebellar 
Abscess, with Recovery, 158 



136* 


INDICES 


Kidd, Leonard J. The Nucleus Inter - 
c&l&tus of Staderini, 1; Isoovesoo’s 
Experimental Researches on Lipoids 
of Organs, 100; The Alleged Sensory 
Cutaneous Zone of the Facial Nerves 
of Man, 393 

Kilgore, Alson R. The Luetin Cutaneous 
Reaction for Syphilis, 222 
Kirby, George H. The Catatonic Syn¬ 
drome ana its Relation to Manic- 
Depressive Insanity, 132 
Klotz, Oscar. Syringomyelia: With 
Autopsy Findings in Two Cases, 73 
Knapp, Philip Coombs. Two Cases of 
Removal of Extra-dural Tumour of 
the Spinal Cord, 265 
Knauer, A., and Maloney, W. J. The 
Cephalograph, a New Instrument for 
Recording and Controlling Head Move- 

vnAn f o 

Knowles’, T. E. The Villa or Colony 
System for the Care and Treatment of 
Qkses of Mental Disease, 172 
Kobylinsky, Moissey. The Psychosis 
Occurring in Typhoid Fever, 48 
Kramer, J. G., and Todd, T. Wingate. 
The Distribution of Nerves to the 
Arteries of the Arm, with a Discussion 
of the Clinical Value of Results, 370 
Kraus, H. Fever as a Solitary Symptom 
of Latent Syphilis, 125 
Kreidl and Karplus. The Experimental 
Production of Reflex Iridoplegia, 62 
Kuh, Sydney, and Braude, Morris. A 
Contribution to the Pathology of Myas¬ 
thenia Gravis, 112 


Ladame. Neuroses and Sexuality, 84 
Lafforgue. The Meningeal Syndrome in 
Recurrent Fever, 313 
Lahy, J. M. An Arithmetical Prodigy, 
112 

Laignel-Lavastine and Boudon, L. 
Adiposity Due to a Juxta-Pituitary 
Sarcoma, 123 

Laignel - Lavas tine and Jonnesco. 

Histological Researches on the Hypo¬ 
physis of Psychopaths, 69 
Laignel - Lavastine and Levy - Valensi. 
Glioma of the Corpus Callosum and 
Left Parietal Lobe: Bilateral Apraxia, 
266 

Laignel - Lavastine and Pitulesco. 

familial Adiposity with Endocrinal 
Disturbances, 124 

Laignel-Lavastine and Romme. Herpetic 
Facial Paralysis in a Patient with 
Symmetrical Lipomatosis, 312 
Lagane, L. Typhoid Cerebro-spinal 
Meningitis in an Infant, 32 


Lambert C. I., Kennedy, Foster, and 
Elsberg, Charles A. A Peculiar Un¬ 
described Disease of the Nerves of the 
Cauda Equina, 416 

Lange, De. The Phylogenetio Evolution 
of the Corpus Striatum, 200 
Langwill, H. G. Can Herpes Zoster 
ever Occur Traumatically ? 114 
Lasarew. A Defect in Innervation of 
the Facial Nerve from Tumours of the 
Posterior Fossa, 217 

Laubry, C. Cerebral Haemorrhage in 
Chronic Myeloid Leucaemia, 122 
Lavan. On Metachancral and Pre- 
roeeolar Meningitis in Syphilis, 493 
Lavau and Audry, C. On Preroseolar 
Meningitis, 213 

Lavergne, J. de B. de. General Par¬ 
alysis and Pregnancy, 424 
Lavinder, C. H., Francis, E., Grimm, 
R. M., and Lorenz, W. F. Attempts 
to Transmit Pellagra to Monkeys, 457 
Leo&ne, P., Jarkowski, J., and Babinski, 
J. Crural Paraplegia from Extra- 
Dural Spinal Tumour. Operation. 
Recovery, 452 

Ledoux, P. Tuberculosis and Exoph¬ 
thalmic Goitre, 496 

Lee, Roger I., and Hinton, W. A. A 
Critical Study of Lange’s Colloidal 
Gold Reaction in Cerebro-spinal Fluid, 
459 

Legendre, G. C. J. The Results of 
Specific Treatment in Tabes and 
General Paralysis at the Salp6trifcre, 
502 


Legras and Dufour. Oculo - Cardiac 
Keflex producing Stoppage of the 
Heart. Ventricular Automatism and 
Auriculo - Ventricular Dissociation. 
Ovarian Insufficiency associated with 
Thyroid Overactivity. Epileptiform 
Attacks, 256 


Legris, A., and Benech, J. A Case of 
Early Spinal Syphilis with Bulbar 
Phenomena, 211 

Leidler, R. The Anatomy and Function 
of Bechterew's Nucleus, 303 

Lelesz, Helfcne. Mental Tendency in 
Testimony, 485 

Lempert, L. Herpes and Zoster of 
Dental Origin, 211 

Leopold, Simon S. Eosinophilia in 
Chorea, 419 

Lereboullet, Faure - Beaulieu, and 
Vaucher. Diabetes Insipidus and 
Infantilism, 218 

Lesier, C., Vernet, M., and Petzetakis. 
Changes in the Reflexes Produced by 
Ocular Compression in Epilepsy, 256; 
Stoppage of the Hoart by the Oculo- 



INDICES 


137* 


Cardiac Reflex in an Epileptic, 257; 
Exaggeration of the Oculo - Cardiac 
Reflex in Epilepsy. Its Variations 
under the Influence of Medicinal and 
Toxic Causes, 257 ; The Oculo-Cardiac 
Reflex in Patients Suffering from 
Various Tremors, 259; The Oculo- 
Cardiac Reflex and Paralysis Agitans, 

259 ; On the Frequent Abolition of the 
Oculo-Cardiac Reflex in Tabes, 260; 
Glycosuria, Albuminuria, and Polyuria 
caused by Ocular Compression, 261 

Leszynsky, William M. Glioma of the 
Cauda Equina. Report of a Case with 
Secondary Gliosis of the Spinal Cord, 
121 

Levi-Franckel, G., and Gamier, M. 
Changes in the Oculo-Cardiac Reflex 
under the Influence of Pregnancy, 
488 

Levy, L., and Gonnet. Meningeal 
Syndrome in the Course of Cerebral 
Haemorrhage, 454 

Levy, Robert L., and Miller, Sydney R. 
The Colloidal Gold Reaction in the 
Cerebro spinal Fluid, 319 

Levv-Valensi, J. A Case of Congenital 
Hemiatrophy, 122 

Levv-Valensi and Laignel-Lavastine. 
Glioma of the Corpus Callosum and 
Left Parietal Lobe: Bilateral Apraxia, 
266 

Lichfield, W. F. Infantile Paralysis of 
the Small Musoles of the Hand, 518 

Lidbetter, E. I., and Nettleship, E. On 
a Pedigree showing both Insanity and 
Complicated Eye Disease; Anticipation 
of the Mental Disease in Successive 
Generations, 325 

Lier, W., On Neurofibromatosis, 413 

LifBchitz, Mile. R. Tetany in the Adult 
and its Parathyroid Origin, 277 

Lloyd, James H. Epilepsy in Childhood, 
321 

Loeper, M., and Mongeot, A. Absence 
of the Oculo-Cardiac Reflex in Tabes, 
29 

Loeper, Mongeot, andVahram. Frequent 
Abolition of the Oculo-Cardiac Reflex 
in Syphilis, 259 

Loeper and Wiel. Favourable Action of 
Ocular Compression on Certain Nervous 
Manifestations, especially Hiccough, 

260 

Lohraann, Professor W. Disturbances 
of the Visual Functions (Review), 432 

Long. A Case of Aphasia from a Lesion 
in the Left Hemisphere in a Left- 
Handed Individual: Crossed Aphasia 
and Dissociated Aphasia, 82 

Lorenz, W. F., Lavinder, C. H., Francis, 

y 


E., and Grimm, R. M. Attempts to 
Transmit Pellagra to Monkeys, 457 
Lortat-Jacob, L., and Paraf, J. Intra- 
spinal Injections of Neosalvarsan in 
Tabes and General Paralysis, 528 
Loumeau. Hemiplegia and Prostatec¬ 
tomy, 266 

Loyez and Claude. Traumatic Heemato- 
myelia without Vertebral Lesion, 265 
Loygue, G. Pulmonary Localisations of 
the Meningococcus, 414 
Lucien, M., and Parisot, J. Glandes 
Surrenales et Organes Chromaffines 
(Review), 537 

Ludlum, S. D., and Corson-White, E. P. 
Syphilitic Tests in Latent and Treated 
Syphilis, 386 

Lugaro, E. A Biogenetic Principle, 28 ; 
Modem Problems in Psychiatry (Re¬ 
view), 534 

Lyon-Caen, L., and Robin, A. Cerebral 
Rheumatism Explained by Haemor¬ 
rhagic Meningitis occurring in the 
Course of Acute Articular Rheumatism, 
262 


M‘Carrison, Robert. Etiology of En¬ 
demic Cretinism, Congenital Goitre, 
and Congenital Parathyroid Disease, 
167 

M‘Carthy, D. J. Iron Infiltration in the 
Fixed and Wandering Cells of the 
Central Nervous System, 209 
MacConkey, Alfred. Tetanus: its 
Prevention and Treatment by Means 
of Antitetanio Serum, 498 
M‘Cord, Carey Pratt. The Pineal Gland 
in Relation to Somatic, Sexual, and 
Mental Development, 372, 449 
Macfarlane, A. Venesection in Cerebral 
Haemorrhage, with Report of Cases, 160 
M‘Intosh, James, and Fildes, Paul; 
Head, Henry, and Fearnsides, E. G. 
Paralysis of the Nervous System, 126 
M‘Intosh, James, and Fildes, Paul. The 
Wassermann Reaction and its Applica¬ 
tion to Neurology, 127 
Mack, C. W., ana Cutting, J. A. The 
Intraspinal Injection of Salvarsanised 
Serum in Paresis, 225 
Mackenzie, William. The Problem of 
the Thinking Dog of Mannheim, 208 
M‘Kibben, Paul S. Mast Cells in the 
Meninges of Necturus, easily Mistaken 
for Nerve Cells, 481 ; Ganglion Cells 
of the Nervus Terminalis in the Dog- 
Fish {Mu8telus caiiis), 481 
Macleod, C., and Rolleston, J. D. Intra¬ 
muscular Injections of Antitoxin in 
the Treatment of Diphtheria, 379 



138* 


INDICES 


MacPh&il, H. D. The Albumen in the 
Cerebro-spinal Fluid in Cases of 
Mental Disease, 171 

M‘Vicar, C. S., Bates, Gordon, and 
Strathy, George S. The Treatment 
of Tabes Dorsalis and General Paresis 
with Salvarsan, 226 

Magaudda, Paolo. The Nervous 
Symptoms caused by Subolavian 
Aneurysm, 71 

Major, Ralph H., and Nobel, Edmund. 
The Glycyl-Tryptophan Reaction in 
Meningitis, 454 

Maloney, W. J. M. Fear and Ataxia, 
118 

Malone v, W. J., and Knauer, A. 
The Cephalograph, a New Instrument 
for Recording and Controlling Head 
Movements, 253 

Mapother, Edward, and Beaton, Thomas. 
Intraspinous Treatment (Swift-EUis) 
of General Paralysis, 225; Intra¬ 
thecal Treatment of General Paralysis, 
527 

Marchand and Jaoquin. Progressive 
Epileptic Myoclonus, 84 

Marcus, Henry. A Case of Sciatica 
Entirely Cured in Three Weeks* 
Treatment, 461 

Marfan, A. B. Heredo-Syphilitic 
Spastic Paraplegia, 264 

Margarot and Baumel. Does Achon¬ 
droplasia Correspond to a Partial 
Hypopituitarism? 40 

Marie, A., and Morax, V. Effects of 
Adrenalectomy on Guinea-Pigs, 207 

Marine, David. Observations and 
Experiments on Goitre (so-called 
Thyroid Carcinoma) in Brook Trout, 
66 

Marinesco, G. On the Colloidal Structure 
of Nerve Cells, 152 

Marinesco and Goldstein. Graves 1 
Disease and Sderodermia, 45 

Marinesco and Noica. Two Cases of 
Tabes Complicated by Hemiplegia, 
72 

Marinesco and Radovici. The Syndrome 
of Xanthochromia and Coagulation 
en masse of the Cerebro-spinal Fluid, 
221 

Martin, J., and Rebattu, J. A Case 
of Recklinghausen*8 Disease, 159 

Matlauschek. Peculiar Alterations of 
the Myelin Sheaths in Degenerating 
Nerve Fibres, 373 

Mauriac, P., and Philip, P. Meningeal 
States in Scarlet Fever and Scarlatinal 
Uremia, 414 

Mayou, M. S. Optic Neuritis with 
Symmetrical Loss of the Lower Portion 


of the Field Associated with Diabetes, 
501 

Mendel. On Right-Brained ness in 
Right-handed Individuals, 383 
Menael and Tobias. Graves’ Disease 
in the Male Sex, 45 

Meneau. Inflammation of the Labyrinth 
after Injection of Neosalvarsan, 164 
Mercier, F., and Nobecourt. Respiratory 
Form of the Encephalo-Meningeal 
Reactions in Typhoid Fever in the 
Child, 77 

Meyer. Differential Diagnosis of Gene¬ 
ral Paresis, 425 

Middlemiss, J. E. Some Cases of 
Psychological Interest from Private 
Practice, 450 

Milian, Sicard, and Joltrain, E. Death 
following Two Injections of Neo¬ 
salvarsan at the Onset of Syphilis, 
125 

Miller, James, and Hewat, Fergus A. 
A Case of Tuberculous Disease of the 
Vertebre, oomplicated by an Exten¬ 
sive Acute Suppurative Meningitis, 
378 

Miller, R., and Davidson, J. A. The 
Nervous Complications of Varicella, 
73 

Miller, R. T., and Diller, Theodore. 
Tumour of Frontal Region of Brain, 
382 

Miller, Sydney R., and Levy, Robert L. 
The Colloidal Gold Reaction in the 
Cerebro-spinal Fluid, 319 
Milian. Syphilitic Reinfection after 
Treatment with Neosalvarsan, 421 
Mills, Charles K., and Weisenburg, 
Theodore H. Cerebellar Symptoms and 
Cerebellar Localisation, 524 
Minet, J. Sudden Death following 
Lumbar Puncture, 318 
Mira, Ferreira de. The Influence of the 
Adrenals on Growth, 111 
Missimilly, E. The Nervous Complica¬ 
tions of Mumps in the Child, 117 
Mochi, A. Asymboly, 391 
Modern Treatment of Nervous 
Mental Diseases, by American 
British Authors (Review), 532 
Moleen, George A. Metallic Poisons 
and the Nervous System, 70 
Molhant, M. The Vagus Nerve: 
Anatomical and Experimental Study. 
Part III. — The Peripheral Vagus 
Ganglia: Localisation of the Sensory 
Ganglia and Peripheral Distribution 
of their Issuing Fibres, 107 
Mollet, A. Organic Hemiplegia of 
Diphtheritic Origin, 379 
Mongeot, A. Constant Suppression of 


and 

and 



INDICES 


139* 


the Oculo-Cardiao Reflex by Atropine, 
256 

Mongeot, A., and Loeper, M. Absence 
of the Oculo-Cardiao Reflex in Tabes, 
29 

Mongeot, Vahram, and Loeper. Fre- 

C it Abolition of the Oculo-Cardiac 
ex in Syphilis, 259 

Monod, 0., ana Froment, J. Articulate 
Language in the Normal Man and in 
the Aphasic, 307 

Monro, T. K., and Dunn, J. S. Malig¬ 
nant Ganglio-Neuroma of Left Supra¬ 
renal, 421 

Montgomery, D. W. Syphilophobia, 
497 

Morax, V., and Marie, A. Effects of 
Adrenalectomy in Guinea-Pigs, 207 
Morestin, H. Fibrosarcoma of the Leg 
in a Woman Suffering from Reckling¬ 
hausen’s Disease, 261 
Moricand, I. Wassernmnn’s Reaction in 
Aortic Disease, 420 

Morichau-Beauchant, R., Frey, and 
Rameix. Acute Ataxia in Convales¬ 
cence from Measles, 413 
Morley, John. Traumatic Intramus¬ 
cular Ossification, 29 
Morse, Mary E. Correlations of 
Cerebro - spinal Fluid Examinations 
with Psychiatric Diagnoses, 227 
Morton, C. A., and Clarke, J. MichelL 
Removal of Intrathecal Tumour from 
Lumbar Region of Spinal Cord, 34. 
Mouiz. The Idiopathic Varieties of 
Myoclonus, 28 

Myers, Bernard. Tongue Chewing, 155 
Myerson, A. Contralateral Periosteal 
Reflexes of the Arm, 311; The Albumin 
Content of the Spinal Fluid in its 
Relation to Disease Syndromes, 318 
Myerson, A., and Eversole, E. E. Notes 
on Sunlight and Flashlight Reactions, 
and on Consensual Amyosis to Blue 
Light, 131 


Neiding and Raimiste. Changes in the 
Spinal Cord in Tumours of the Posterior 
Cranial Fossa, 35 

Netter, Arnold. The Meningeal Form 
of Poliomyelitis, 30 

Netter, Hirtz, E., and Debr£, R. A Case 
of Addison’s Disease observed in 1902, 
considered as Cured. Death from 
Gastric Cancer in 1913. Autopsy, 422 

Nettleship, E., and Lid better, E. J. 
On a Pedigree showing both Insanity 
and Complicated Eye Disease: Antici¬ 
pation of the Mental Disease in Succes¬ 
sive Generations, 325 


Neue. Biological Reactions in Syphilitic 
Diseases of the Central Nervous System, 
273. 

Neustaedter, M. A Case of Facial 
Hemiatrophy, 267 

New, G. B., and Plummer, W. A. 
Tumour of the Middle Cranial Fossa, 
involving the Gasserian Ganglion, 217 

Newburgh, L. H. and I., and Porter, W. 
T. The State of the Vasomotor 
Apparatus in Pneumonia, 483 

Nichols, Henry J. Observations on a 
strain of Spirochceta pallida Isolated 
from the Nervous System, 223 

Niekans, A. On the Pathogeny and 
Symptomatology of Post-Diphtheritic 
Polyneuritis, 118 

Nightingale, P. A. Zeism or Pellagra, 
108 

Nitsche, Paul, and Wilmanns, Karl. 
The History of the Prison Psychosis 
(Review), 133 

Nob^court and Mercier, F. Respiratory 
Form of the Encephalo-Meningeal 
Reactions in Typhoid Fever in the 
Child, 77 

Noble, Edmund, and Major, Ralph H. 
The Glycyl-Tryptophan Reaction in 
Meningitis, 454 

Noica and Marinesco. Two Cases of 
Tabes Complicated by Hemiplegia, 72 

Nolan, J. N. G. The Recognition and 
Treatment of True Idiopathic Epilepsy 
in Children, 322 

Nonne and Wohlwill. A Clinical and 
Pathological Case of Isolated Argyll 
Robertson Pupils in the Absence of 
General Paralysis, Tabes, and Cerebro¬ 
spinal Syphilis, 377 

Nowicki, G. B. Precocious General 
Paralysis Three Years after a Chancre 
Treated by “606,” 501 

Nurzia, P. On Heredo-Alcoholic Degen¬ 
eration, 388 


Oberndorf, C. P. Slips of the Tongue 
and Pen, 309 

Obregia, Parhon, and Urechia. Re¬ 
searches on the Genital Glands in 
Dementia Praecox, 86 
Odier, Charles. A Case of Hysterical 
Contracture, 485 

Oliver, Sir Thomas. Lead Poisoning: 
from the Industrial, Medical, and 
Social Points of View (Review), 538 
Oppenheini. Is there a Cystic Variety 
of Disseminated Sclerosis ? 380 
Orr, D., and Rows, R. G. Further 
Observations on the Influence of Toxine 
on the Central Nervous System, 252 



140* 


INDICES 


Orticoni, A. The Serotherapy of Cerebro¬ 
spinal Meningitis, 262 

Orton, S. T. An Analysis of the Errors 
in Diagnosis in a Series of Sixty Cases 
of Paresis, 131 ; A Note on the Cir¬ 
culation of the Cornu Ammonis, 202; 
A Study of the Satellite Cells in Fifty 
Selected Cases of Mental Disease, 
411 

Ott, Augusto. Considerations on the 
Physiological Pathology of Contrac¬ 
ture, 61 

Oxley, W. H. F. Electrolytic Treat¬ 
ment of Lead Poisoning, 455 


Pacaud, H. On Meningo-Typhoid, 76 

Paraf, J., and Lortat-Jacob, L. Intra- 
spinal Injections of Neosalvarsan in 
Tabes and General Paralysis, 528. 

Parhon, C., Jassy, de, and Zugravu, G. 
The Weight of the Pancreas in the 
Insane, 172 

Parhon and Schunda. A Fresh Contri¬ 
bution to the Study of Achondroplasia, 

41 

Parhon, Urechia, and Obregia. Re¬ 
searches on the Genital Glands in 
Dementia Pnecox, 86 

Parisot, J., and Lucien, M. Glandes 
Surrenales et Organes Chromatiines 
(Review), 537 

Pawlow, J. The Investigation of the 
Higher Nervous Functions, 27 

Pazzi, M. On the Structure of the Brain 
and the Interpretation of Mental 
Phenomena in Relation to the Law, 
170 

Pellacani, G. A Left Prefrontal Glioma 
with Aphasia, 37 

Pemet, G. Generalised Herpes Zoster, 
515 

Pemet, R. Feminine Tabes. A Com¬ 
parative Study of Tabes at BicStre and 
the Salpetriere, 376 

Petery, Arthur K. A Microcephalic 
Idiot, with Malformation of Brain, 
412 

Petit, L. On the Differential Diagnosis 
of Syphilitic and Tuberculous Menin¬ 
gitis in the Adult, 116 

Petzetakis. The Oculo Cardiac Reflex 
in Normal Subjects, without Brady¬ 
cardia, 255; Circulating and Re¬ 
spiratory Phenomena produced by 
Ocular Compression, 255 

Petzetakis and Fabre. Persistence of 
Oculo-Cardiac Reflex in General Antes- 
thesia, 258 

Petzetakis, M., Lesieur, C., and Vernet, 
M. Changes in the Reflexes produced 


by Ocular Compression in Epilepsy, 
256; Stoppage of the Heart by theOculo- 
Cardiac Keflex in an Epileptic, 257; 
Exaggeration of the Oculo-Cardiac 
Reflex in Epilepsy: Its Variations 
under the Influence of Medicinal and 
Toxic Causes, 207 ; The Oculo-Cardiac 
Reflex in Patients Suffering from 
Various Tremors, 259; The Oculo- 
Cardiac Reflex and Paralysis Agitans, 
259 ; On the Frequent Abolition of the 
Oculo-Cardiac Reflex in Tabes, 260; 
Glycosuria, Albuminuria, and Polyuria 
caused by Ocular Compression, 261 ; 
The Oculo-Cardiac Reflex, 374 
Philibert. A Case of Typhoid Spine, 
160 


Philip, P., and Mauriac, P. Meningeal 
States in Scarlet Fever and Scarlatinal 
Uraemia, 414 

Phillips, J. Persistent Hereditary (Edema 
of the Legs (Milroy’s Disease), with 
Acute Exacerbations. Report of two 
Cases, 490 

Pierret, Verhwghe, and Duhot, Peri¬ 
pheral Neuritis from Ischemia, 84 

Pilsbury, L. B. Paresis Patients Treated 
with Intraspinal Injections of Salvar- 
sanised Serum, 502 

Pim, Arthur A. Epidemic Poliomyelitis, 
491 

PitulescoandLaignel-Lavastine. Familial 
Adiposity witn Endocrinal Disturb¬ 
ances, 124 

Pizzata, C. Thrombosis of the Cerebral 
8inuses after Measles, 78 

Plummer, W. A., and New, G. B. 
Tumour of the Middle Cranial Fossa, 
Involving the Gasserian Ganglion, 
217 


Poirault, H., and Ramond, F. Zoster 
with Facial Paralysis: Trophic and 
Sensory Troubles of the Lingual 
Mucosa, 312 

Porter, W. T , and Newburgh, L. H. 
and I. The State of the Vasomotor 
Apparatus in Pneumonia, 483 
Prel, r. A. Syphilitic Facial Paralysis, 
81 


Price, George E., and Heed, Charles R. 
Bi nasal Hemianopsia occurring in the 
Course of Tabetic Optic Atrophy, 
212 


Priestly, J. Nervous Diseases of 
Elementary School Children — Boys 
and Girls, 210 

Prince, Morton. The Psychopathology 
of a Case of Phobia—A Clinical 8tuny, 
308 


Pussep. Operative Removal of a Pineal 
Cyst, 382 



INDICES 


141* 


Putnam, James J. Some of the Broader 
Issues of the Psycho-Analytic Move¬ 
ment, 228 

Pychlau. A Case of Graves’ Disease 
Successfully Treated with the Milk 
of a Thyroideotomised Woman, 46 


Quinquaud, A., and Gley, E. Contribu¬ 
tion to the Study of Humoral Inter¬ 
relations—I. The Action of Thyroid 
Extract and of Organic Extract in 
General on Adrenal Secretion, 65 


Rablnowitz, M. A. Two Neurological 
Cases in Paediatric Practice, 461 

Radovici and Marinesco. The Syndrome 
of Xanthachromia and Coagulation 
en masse of the Cerebro-spinal Fluid, 
221 

Raff, K. Measurement of the Blood- 
Pressure in Alcoholism and Functional 
Neuroses, Excluding Circulatory Dis¬ 
turbances, 166 

Raimiste and Neiding. Changes in the 
Spinal Cord in Tumours of the Posterior 
Cranial Fossa, 35 

Rameix, Morichau-Beauchant, R., and 
Frey. Acute Ataxia in Convalescence 
from Measles, 413 

Ramond, F., and Poirault, H. Zoster 
with Facial Paralysis: Trophic and 
Sensory Troubles of the Lingual 
Mucosa, 312 

Rand, Carl W. A Case of Supposed 
Progeria (Premature Senility) in a 
Girl of Eight Years. With Remarks, 
389 

Rank, Otto. The Myth of the Birth of 
the Hero (Review), 464 

Ranson, S. Walter. The Tract of 
Lissauer and the Substantia Gelatinosa 
Rolandi, 198; The Structure of the 
Vagus Nerve of Man as Demonstrated 
by a Differential Axon Stain, 302; The 
Pyridine-Silver Method : With a Note 
on the Afferent Spinal Non-Medullated 
Nerve Fibres, 467 ; A Note on the 
Degeneration of the Fasciculus 
Cerebro-spinalis in the Albino Rat, 
511 

Ranson, S. W. f and Chase, M. R. 
Structure of the Roots, Trunk, and 
Branches of the Vagus Nerve, 109 

Rasoh, C. Syphilitic Basal Meningitis 
Five Months after Infection, 159 

Ravaut, P. Errors in the Interpreta¬ 
tion of Wassermann’s Reaction, 497 

Ravenna. Aohondroplasia and Chondro- 
hypoplasia, 41 


Raynaud, M., Coudray, Derrien, and 
Abdin-Delthiel. Meningeal Syndrome 
in North African Recurrent Fever, 
378 

Rayner, H. The Wet Pack in the 
Treatment of Insomnia and Mental 
Disorders, 530 

Rebattu, J., and Martin, J. A Case of 
Recklinghausen’s Disease, 159 

Reeve, E. F., and Watson, George A. 
Observations on Cases of Encephalitis, 
531 

Regis and Hesnard. The Teaching of 
Freud and his School, 84 

Reich, A. True Larvngeal Sac Formation 
in Man, and its Operative Treatment, 
422 

Reich mann and Goldstein. Somatic 
Disturbances in Dementia Praecox, 
392 


lllOy KJA* JL 

r, H. van. The High Frequency 
in the Treatment of High 


A Case of Brain 


Reischig, Leopold. A Case of Meningitis 
Purulenta Aseptica after Intranasal 
Interference, 31 

Remsen, Charles M. Operative Inter¬ 
vention in Cyst of the Left Cerebral 
Hemisphere, with a Consideration of 
the Preoperative and Subsequent 
Symptoms, 521 
Rensselaer, 

Current 

Blood Pressure, 49 
Reynolds, Cecil E. 

Abscess, 216 

Rezza, A. Effect of the Administration 
of Alcohol on Wassermann’s Reaction, 
43; The Alterations of the Cells of 
the Bulb found in Case of Dementia 
Praecox, 48 

Rhein, J. H. W. Cerebral Palsies 
without Demonstrable Anatomical 
Findings, 122; Aneurisms of the 
Vessels of the Brain, 382; Tumour of 
the Crus Cerebri, 520 
Ricksher, Charles. Similar and Dis¬ 
similar Psychosis in Relatives, 429 
Riggs, C. E. Report of a Case of 
Juvenile Tabes, 119 

Riggs, C. Eugene, and Hammes, Ernest 
H. Results of One Hundred Injections 
of Salvarsanised Serum, 503 
Riquier, Carlo. On the Microscopic 
Structure of the Otic Ganglion, 22 
Riser, M. On a Case of Fulminating 
Parameningococcus 
Meningitis, 313 
Robertson, George M. 

Cerebro-spinal Fluid 
Signs of General Paralysis, 169 
Robertson, Madge E., and Findlay, 
Leonard. Some Manifestations of 
Congenital Syphilis, 527 


Cerebro - spinal 

The Serum and 
Reactions and 



142* 


INDICES 


Robertson, W. Ford. Vaccine Treat¬ 
ment in Asylums, 171 

Robertson, W. N., and Ahern, E. D. 
Cyst of the Pituitary Gland, 522 

Robin, A., and Lyon-Caen, L. Cerebral 
Rheumatism Explained by Haemor¬ 
rhagic Meningitis occurring in the 
Course of Acute Articular Rheuma¬ 
tism, 262 

Robinson, G. Wilse. The Use of 
Celluloid Splints in the Treatment 
of Diseases of the Nervous System, 
453 

Rolleston, J. D. Local Treatment of 
Vincent’s Angina with Salvarsan, 81 ; 
The Medical Aspects of the Greek 
Anthology, 325 

Rolleston, J. D., and Macleod, C. 
Intramuscular Injections of Antitoxin 
in the Treatment of Diphtheria, 379 

Rolleston, H. D., and Boyd, E. J. 
Addisons Disease in a Bov, with 
Calcification of the Adrenals, with 
Remarks, 167 

Romaic and Laignel-Lavastine. Herpetic 
Facial Paralysis in a Patient with 
Symmetrical Lipomatosis, 312 

Romer and Viereck. On the Treatment 
and Nature of Diphtheritic Paralysis, 
72 

Rosanoff, A. J. A Study of Brain 
Atrophy in Relation to Insanity, 430 

Rosenbloom, Jacob,and Diller.Theodore. 
Metabolism Studies in a Case of Myas¬ 
thenia Gravis, 457 

Rosenbloom, J., and De Witt Stetten. 
Clinical and Metabolic Studies of a 
Case of Hypopituitarism due to Cyst 
of the Hypophysis, with Infantilism of 
the Lorain Type, 80 

Rosenbaum, George. Roentgen Diagnosis 
inFraoturesof the Cranium in Children, 
417 

Rosenheim, Otto. The Galactosides of 
the Brain, 69 

Ross, D. MaxweU. Notes on a Case of 
Pellagra, 244 

Ross, Ellison L. Metabolism in Dementia 
Prsecox, 327 

Roth, W., and Herxheimer, G. On 
Recklinghausen’s Neurofibromatosis, 
377 

Rother, C. On Post-Diphtheritic Ab- 
duoens Paralysis, 33 

Rothig, Paul. On a Counterstain for 
Weigert-Pal Preparations, 373 

Rothmann. Combined Column-Diseases 
of the Spinal Cord, 71; The Significance 
for Differential Diagnosis of Bdrdny’s 
Pointing-Test, 209; Restitution Phe¬ 
nomena in Cerebral Palsies in Relation 


to Phylogenesis and their Therapeutic 
Influence, 268 

Rotstadt. The Surgical Treatment of 
Cord Tumours, 35 

Roubinovitch and BarbA Partial 
Agenesis of the Corpus Callosum, 209 

Roubinovitch, J., and Soudtere, Reginald 
de la. The Oculo-Cardiac Reflex in 
Hemiplegia and Cerebral Diplegia, 
312 

Roufliac, P., and Joltrain, E. Meningeal 
Syndrome of the Poliomyelitis Type, 

Roussy, G., and Camus, J. Hypophy- 
sectomy and Genital Atrophy: An 
Experimental Contribution to the 
Study of the Adiposo-Genital Syn¬ 
drome, 64 ; Hypophysectomy and Ex¬ 
perimental Glycosuria, 110; Polyuria 
from Experimental Lesion of the Opto- 
peduncular Region of the Base of the 
Brain : The Regulating Mechanism of 
the Water Content of the Organism, 
204; The Anatomical Localisation in 
the Base of the Brain of the Lesions 
which Provoke Polyuria in Dogs, 305 ; 
Medullary Cavities and Cervical Menin¬ 
gitis, 411 

Roux, G. C. Meningitis in Mumps, 
214 

Roux, J. C., and Andr6-Thomas. The 
Hypotensive Cceliac Reflex, 305 

Rows, R. G. The Importance of Disturb¬ 
ances of the Personality in Mental 
Disorders, 279 

Rows, R. G., and Orr, D. Further 
Observations on the Influence of Toxins 
on the Central Nervous System, 252 


Saint-Marc, Mkaux. Wassermann 
Positive after Forty-six Years of 
Syphilis—Syphilitic Varicose Ulcers, 
164 

Sainton. The Oculo-Cardiac Reflex, 374 
Salmon. The Problem of Sleep, 267 
Salmon, P. Vital Staining of Nerve 
Centres by Malachite Green, 112 
Santee, Harris E. The Brain of a Black 
Monkey (Macacos maurus ): The 
Relative Prominence of Different Gyri, 
370 

Sarr&zin, F. E. Serotherapy with 
Massive Doses in Tetanus, 420 
Sarteschi, U. Experimental Production 
in Mammals of the Pineal Precocious 
Macro-Geni to Somatic Syndrome, 23 ; 
On the Changes in the Central Nervous 
System in Experimental Diphtheritic 
Intoxication and Human Diphtheritic 
Infection, 372 



INDICES 


143* 


Saunders, P. W. Sensory Changes in 
Friedreich’s Disease, 122 
Sawyer, James E. H. A Case of Pro¬ 
gressive Lenticular Degeneration, 124 
Sc&rpini, Vincenzo. Sudden Death from 
Bulbar Haemorrhage in a Case of 
Dementia Prsecox, 170 
Schilder and Gregor. The Theory of 
Myotonia, 71 

Schlesinger and Schuller. On the Com¬ 
bination of Cranial Hyperostoses and 
Cerebral Tumours, 218 
Schmidt, C. J. M. A Case of Pro¬ 

gressive Thrombophlebitis of the Brain 
Sinuses following Acute Otitis Media, 
315 

Schmoucher, Mile. G. Atrophy of the 
Pelvis in Infantile Paralysis, and its 
Obstetrical Consequences, 459 
Schoonheid, P. H. Multiple Neuro¬ 

fibromatosis of the Skin, 490 
Schuller and Schlesinger. On the Com¬ 
bination of Cranial Hyperostoses and 
Cerebral Tumours, 218 
Schunda and Parhon. A Fresh Contri¬ 
bution to the Study of Achondroplasia, 
41 

Schuster, P. High Incidence of Post- 
Diphtheritic Paralysis: A Contribu¬ 
tion to the Question of the Neuro¬ 
tropism of Certain Infective Agents, 
492 

Schweizer, F. Myatonia Congenita, 515 
Scuderi, A. On a Case of Muscular 
Atrophy from Lead Poisoning, 220 
Seringes. Retrogressive Infantilism, 80 
Sezary, A. Pineal Tumours, 320; 

Syphilis and the Adrenals, 386 
Sharp, E. A., and Clark, L. Pierce. The 
R&le which Heredity Plays in Inducing 
Epilepsy in Children Suffering from 
Infantile Cerebral Palsy, 120 
Shaw, A. F. Bernard. Pseudo-Hyper¬ 
trophic Muscular Dystrophy: Two 
Cases with Plates, 413 
Shaw, Henry B. The Relation between 
Epilepsy and Tuberculosis, 460 
Shaw, J. J. M. Epilepsy : A Theory of 
Causation Founded upon the Clinical 
Manifestations and the Therapeutic 
and Pathological Data, 460 
Sheldon, Ralph Edward. Paraffin- 
Weigert Methods for the Staining of 
Nervous Tissue, with some New 
Modifications, 450 

Sicard, J. A. Acquired Hydrocephalus 
due to the Meningitis of Mumps, 518 
Sicard, Joltrain E., and Milian. Death 
following Two Injections of Neo- 
salvarsan at the Onset of Syphilis, 
125 


Siemerling, E. Meningitis after Folli¬ 
cular Tonsilitis, 31 

Simchowicz. Alzheimer’s Disease and 
its Relation to Senile Dementia, 327 
Singer, C. St Hildegard, 166 
Singer, Douglas H. Dementia Priecox 
in the Eighth Edition of Kraepelin’s 
Text-Book, 427 

Smith, C. Morton. Have the Early 
Claims of Salvarsan been Realised? 
126 

Smith, G. M‘Call. A Case of Exoph¬ 
thalmic Goitre Simulating Acute 
Obstruction, 495 

Smith, P. E. Some Features in the 
Development of the Central Nervous 
System of D^^mogimthus fusca , 482 
Smith, R. R. The Behaviour of the 
Abdominal Cutaneous Reflexes in 
Acute Conditions within the Abdomen 
and Pelvis, 514 

Snowden, R. R., and Boggs, Thomas R. 
The Intr&meningeal Treatment of 
Tabes and Cerebro-spinal Syphilis, 
315 

Soderbergh. The Wassermann Reaction 
in the Blood in Cases of Alkaptonuria, 
223 

Solomon, Meyer. The Analysis and 
Interpretation of Dreams Based on 
Various Motives, 67 ; On the Analysis 
and Interpretation of Dreams based on 
Various Motives, and on the Theory 
of Psycho-Analysis, 410 
Somen, H. Physiological Mechanism of 
the Knock-out, 69 

Somerville, \V. F. The Treatment of 
Neuritis by Electrical Methods, 328 
Soper, Willard B., and Grand, Selma. 
The Urea Content of the Spinal Fluid, 
with Special Reference to its Diagnostic 
and Prognostic Significance: A Series 
of Ninety-seven Cases, 82 
Soudi&re, Reginald de la, and Roubino- 
vitch, J. The Oculo-Cardiac Reflex in 
Hemiplegia and Cerebral Diplegia, 312 
Souques, A. Chronic Palsy of Limbs due 
to Prolonged Use of Colchicine, 324 
Souques and Chauvet. Hypophyseal 
Infantilism, 39 

Spiller, William G. The Relation of the 
Myopathies, 113; Bilateral Oculo- 
motorius Palsy from Softening in each 
Oculomotorius Nucleus, 154; Acute 
Myelitis, Secondary to Perirectal 
Abscess, Developing a Few Hours after 
Severe Fright, 516 

Spooner, Lesley H. The Treatment of 
Syphilitic Diseases of the Central 
Nervous System by Intravenous Injec¬ 
tions of Salvarsan, 224 



144* 


INDICES 


Spr&wson, C. A. A Family with Cere¬ 
bellar Ataxia, 160 

Stainthorpe, W. W. Observations on 
One Hundred and Twenty Cases of 
Lead Absorption from Drinking Water, 
385 

Steiner. The Production and Histo- 
pathology of Experimental Syphilis of 
the Central Nervous System in Rabbits, 
387 

Stern. The Pathogenesis of Myasthenia, 
384 

Stewart, Purves. A Case of Hysterical 
Monoplegia following Electric Shock, 
44; Further Note upon a Case of 
Hysterical Monoplegia following 
Electric Shock, 161 

Stewart, R. M. The Action of Adrenalin 
and Epinine on the Pupil in Epilepsy, 

287 

Stoddart, W. H. B. Mind and its Dis¬ 
orders (Review), 505 

Strathy, George S., M 4 Vicar, C. S., and 
Bates, Gordon. The Treatment of 
Tabes Dorsalis and General Paresis 
with Salvarsan, 226 

Strauch, August. Infantilism, 456 

Striimpell and Handmann. A Contribu¬ 
tion to the Study of So-called Pseudo¬ 
sclerosis, with Changes in the Cornea 
and in the Liver, 270 

Simpson, Sutherland. The Pyramid 
Tract in the Red Squirrel (Scmrus 
Hudxonianus , Loquax) and Chipmunk 
(Tania* striatus , Lysteri), 370 

Stum, F. P. A New Theory of Hearing, 
483 

Sutton, R. L. A Clinical Note on 
Fibroma Molluscum Gravidarum, 213 

Swift, Walter B. Studies in Neurological 
Technique, 507; A Voice Sign in Chorea, 
519; Further Analysis of the Voice 
Sign in Chorea, 519 


Talmey, B. S. Transvestism, 132 

Taylor, A. L. A Case of Tumour of the 
Pituitary Body, 39 

Taylor, A. S. Conclusions Derived from 
Farther Experience in Surgical Treat¬ 
ment of Brachial Birth Palsy (Erb’s 
Type), 78 

Taylor, James, and Holmes, Gordon M. 
Two Families with Several Members 
in Each Suffering from Optic Atrophy, 
42; Nervous Symptoms Associated 
with Optic Atrophy of the Familial 
Type, 42 

Taylor, James. Vascular and other 
Retinal Changes Associated with 
General Disease, 43 


Terman, Lewis M. Recent Literature 
on Juvenile Suicides, 309 

Teixeira-Mendez. The Forearm Sign, 
451 

Teyssien, De. Suprarenal Apoplexy in 
General Paralysis: Sudden Death, 
85 

Thiele, Francis H., and Embleton, Dennis. 
Methods of Increasing the Accuracy 
and Delicacy of the Wassermann 
Reaction, 128 

Thomas, Andr6, and Durupt. Experi¬ 
mental Researches on Cerebellar 
Function, 60 

Thomas, B. A., and Ivy, Robert H. 
Observations on the Wassermann 
Reaction, 459 

Thome, Frederick H. Some of the 
Histological Changes found in Tabes, 
486 

Tilney, F. An Analysis of the Juxta- 
Neural Epithelial Portion of the 
Hypophysis Cerebri, with an Embryo- 
logical and Histological Acoount of a 
Hitherto Undescribed Part of the 
Organ, 200 

Timme, Walter. The Nature of Cutan¬ 
eous Sensation, with an Instrument 
for its Measurement, 374 

Tobias and Mendel. Graves’ Disease in 
the Male Sex, 45 

Todd, T. Wingate, and Kramer, J. G. 
The Distribution of Nerves to the 
Arteries of the Arm, with a Discus¬ 
sion of the Clinical Value of Results, 
370 

Tredgold, A. F. Mental Deficiency— 
Amentia (Review), 330 

Tribe, Enid M. Vaso-Motor Nerves in 
the Lungs, 205 

Trieben8tein, Otto, and Fischer, Johan¬ 
nes. Researches on Tetany and Senile 
Cataract, 320 

Tuckey, C. Lloyd. Hypnotism and Sug¬ 
gestion, 534 

Tuffier. Adrenal Virilism, 321 

Turner, John. The Biological Concep¬ 
tion of Insanity, 462 

Turner, William Aldren. The Outlook 
in Epilepsy, 498; Epilepsy and 
Cerebral Tumour, 520 

Tutyschkin. A Rare Case of Spina 
Bifida, with Subsequent Development 
of Symptoms Referable to Involve¬ 
ment of the Cauda Equina, Conus 
Medullaris, and Epiconus, 375 


Udaonda, C. B., and Casteigts, M. M. 
Post-Typhoid Polyneuritis of Quadri¬ 
plegic Form, 516 



INDICES 


145* 


Urechia, Parhon, and Obreria. Re¬ 
searches on the Genital Glands in 
Dementia Prseoox, 86 


Vahram, Loeper, and Mongeot. Fre¬ 
quent Abolition of the Oculo-Cardiac 
Reflex in Syphilis, 259 
Valdizan, H., and Ciampi, L. Physical 
Development in the Mentally Defective, 
423 

Vallery-Radot, P. A Case of Para¬ 
meningococcus Cerebro-spinal Menin¬ 
gitis. Serotherapy. Recovery, 414 
Valtorta, D. The Elimination of 
Nitrogen and Uric Acid in States of 
Excitement and Stupor, 529 
Vaucher, Lereboullet, and Faure- 
Beaulieu. Diabetes Insipidus and 
Infantilism, 218 

Verde, E. Late Syphilitic Facial 
Paralysis associated with Chronic 
Pulmonary Syphilis, 273 
Verhaeghe, Duhot, and Pierret. Peri¬ 
pheral Neuritis from Ischaemia, 84 
Verhoeff, F. H. Chronic Ocular 
Tuberculosis. Necropsy Findings in 
a Case in which Death was Due to 
Tuberculosis of the Hypophysis Cerebri, 
390 

Vernes, A. The Prognostic and Diag¬ 
nostic Value of the Sign of Isolated 
Hyperalbuminoeis in the Cerebro¬ 
spinal Fluid, 271 

Vernes, A., and Bloch, M. A Retro¬ 
spective Sign of Syphilis. Pure 
Hyperalbuminosis of the Cerebro¬ 
spinal Fluid without Leucocytosis and 
without Wassermann, 271 
Vernet, M., Petzetakis, and Lesieur, C. 
Changes in the Reflexes Produced 
by Ocular Compression in Epilepsy, 
256; Stoppage of the Heart by the 
Oculo - Camiac Reflex in an Epi¬ 
leptic, 257; Exaggeration of the 
Oculo - Cardiac Reflex in Epilepsy : 
Its Variations under the Influence 
of Medicinal and Toxic Causes, 257 ; 
The Oculo-Cardiac Reflex in Patients 
Suffering from Various Tremors 
259 ; The Oculo - Cardiac Reflex 
and Paralysis Agitans, 259; On the 
Frequent Abolition of the Oculo- 
Caroiac Reflex in Tabes, 260; 
Glycosuria, Albuminuria, and Poly¬ 
uria caused by Ocular Compres¬ 
sion, 261 ; The Oculo-Cardiac Reflex, 
374 

Viegas, L. On Recklinghausen’s Disease, 
314 

Viereck and Romer. On the Treatment 


and Nature of Diphtheritic Paralysis, 
72 

Vitdn, A. Typhoid Spine aud Thyroid 
Opotherapy, 415 


Waldron, Ethel, and Gettings, H. S. 
The Detection of a Dysentery Carrier, 
532 

Wallace, William. The Musical Faculty: 
Its Origins and Processes (Review), 504 

Walshe, S. J A. H. Case with Com¬ 
ments. Effect on the Mental State 
of Minor and Major Attacks in 
Epileptic Insanity, 167 

Warrington, W. B. Acute Generalised 
Infective Paralysis in Adults, 114; 
Intraoranial Serous Effusions of In¬ 
flammatory Origin. Meningitis or 
Ependymitis Serosa — Meningism. 
With a Note on “ Pseudo-Tumours” 
of the Brain, 114 

Watson, George A., and Reeve, E. F. 
Observations on Cases of Encephalitis, 
531 

Watson, George A., and Wiggles worth, 
J. The Brain of a Macrocephalic 
Epileptic, 129 

Weber, F. Parkes. A Familial Case of 
Splenomegalic Anaemia with In¬ 
fantilism, 419 

Weed, Lewis H. Observations upon 
Decerebrate Rigidity, 205 ; Studies on 
the Cerebro-spinal Fluid. —II. The 
Theories of Drainage of Cerebro-spinal 
Fluid, with an Analysis of the Methods 
of Investigation ; III. The Pathways 
of Escape from the Subarachnoid 
Spaces, *ith Particular Reference to 
the Arachnoid Villi; IV. The Dual 
Source of Cerebro-spinal Fluid, 511, 
512 

Wegefarth, Paul. Studies on Cerebro¬ 
spinal Fluid.—V. The Drainage of 
Intra-ocular Fluids; VI. The Establish¬ 
ment of Drainage of Intra-ocular and 
Intra cranial Fluids into the Venous 
System ; VII. The Analogous Pro¬ 
cesses of the Cerebral and Ocular 
Fluids, 512, 513 

Weil and Loeper. Favourable Action of 
Ocular Compression on Certain Nervous 
Manifestations, especially Hiccough, 
260 

Weisenburg, Theodore H., and Mills, 
Charles K. Cerebellar Symptoms and 
Cerebellar Localisation, 524 
1 Westmacott, F. H. Oculomotor Paralysis 
of Otitic Origin, 499 

Wheelon, Homer, and Hoskins, R. G. 
Adrenal Deficiency and the Sympa- 



146* 


INDICES 


thetic Nervous System, 206; Para¬ 
thyroid Deficiency and Sympathetic 
Irritability, 307 ; Ovarian Extirpation 
and Vasomotor Irritability, 484 

Wiggers, Carl J. Further Observations 
on the Constricting Action of Adrena¬ 
line on Cerebral Vessels, 207 

Wigglesworth, J., and Watson, George 
A. The Brain of a Macroeephauc 
Epileptic, 129 

Wile, Udo J. The Technic of the 
Intradural Injections of Neosalvarsan 
in Syphilis of the Nervous System, 
223 

Wilkinson, Douglas, and Batten, Frede¬ 
rick E. Unusual Type of Hereditary 
Disease of the Nervous System, 455 

Wilkinson, George. A Case of Paralysis 
of the External Rectal Muscle due 
to the Presence of an Abscess in the 
Apex of the Petrous Pyramid—Death 
from Basal Meningitis, 500 

Willcocks, R. W. The Occurrence of 
Pellagra in Englaud, 495 

Williams, E. M. Lead Poisoning with 
Paralysis of the External Ocular 
Muscles, 420 

Williams, Guy H. An Intoxication 
Psychosis associated with Cirrhosis of 
the Liver, 430 ; The Psychosis occur¬ 
ring during the Course of Pernicious 
Anaemia, 503 

Williams, Tom A. Tabes with Unusual 
Distribution of Deep-Pain Loss, 155; 
A Contrast in Psycho-Analysis : Three 
Cases, 411 

WilmannB, Karl, and Nitsche, Paul. The 
History of the Prison Psychosis 
(Review), 133 

Wilson, S. A. Kinnier. The Pathology 
of Pellagra, 168 


Wirgman, C. Wynn. Angeioma in 
Ct -ebellar Peduncle: Fatal Intra- 
cr. *•! Haemorrhage, 382 

Wish G. B., and Crowe, S. J. 
Exj lental Observations on the 
Supi mal Glands, with Especial 
Refer* .ce to their Inter-renal Portions, 
484 

Withington, C. F. Pneumonic Hemi¬ 
plegias, 216 

Wohlwill and Nonne. A Clinical and 
Pathological Case of Isolated Argyll 
Robertson Pupils in the Absence of 
General Paralysis, Tabes, and Cerebro¬ 
spinal Syphilis, 377 

Wolf, Charles G. L., and Hale, T. 8. 
Gaseous Exchange in the Decerebrate 
Animal, 449 

Wollstein, Martha. Parameningoooccus 
and its Antiserum, 487 

Wootton, J. C. The Wassermann Reac¬ 
tion, and the Male Insane, 528 

Wulzen, Rosalind. The Morphology and 
Histology of a Certain Structure con¬ 
nected with the Pars Intermedia of 
the Pituitary Body of the Ox, 448 


Yawxjer, N. S. The Mental Manifesta¬ 
tions of Epilepsy, 66 
Yokovama, Yugo, and Fischer, Walther. 
A Peculiar Form of Nodular Hyper¬ 
plasia of the Liver associated with 
Brain Changes, 26 


Zilocchi, Alberto. The Folds of the 
Skin Hair in the Insane, 501 
Zugravu, G., de Jassy, and Parhon, C. 
The Weight of the Pancreas in the 
Insane, 172 


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