APRIL, 1905.

XANTHO-ERYTHRODERMIA PERSTANS.

By H. RADCLIFFE-CROCKER.

The above provisional clinical title was suggested to me by my coadjutor

at University College Hospital, Mr. George Pernet, for a well-defined

affection of the skin, of which I have met with ten instances during the

last three years, all but one of them in private practice. I am not

aware that the disease in question has been described before, unless it

can be brought under Brocq’s “erythrodermies pityriasiques en plaques

disseminées,” with which it will be closely compared when the cases

themselves have been considered.

A case which I showed at the Dermatological Society of London in

October, 1904, when Drs. Hallopeau, Gastou, Jacquet and Pautrier were

present, was not regarded by them as a case of Brocq’s disease, with

which they were presumably familiar, but as an entirely new affection in

their experience.

The following description is drawn up from nine of the cases, all males,

which, in the main features, closely resemble each other. The remaining

case, a lady, had some important differences which will be discussed

later.

So far, all the cases have been adults, though some of them were young.

The lesions are evolved in patches of a pale pink or yellowish hue on

the limbs and trunk, the uncovered parts, such as the face and hands,

being free or very slightly affected. Generally, the patches come out

very gradually and in small numbers and, in the main, symmetrically, but

as the older patches never go away spontaneously, while fresh ones are

continually evoluting at short or long intervals, large areas are

involved, and in the course of years (in one case, months) the whole

trunk and limbs are crowded with lesions, though there are always spaces

of normal skin intervening, or sometimes completely enclosed by the

diseased process, where the original patches have coalesced. For the

most part the original patches are discrete and enlarge but little after

their formation, unless they merge into adjoining patches, when

hand-sized or larger areas may be formed.

With regard to individual patches, they are usually of oval or elongated

form, arranged symmetrically in oblique lines on the back in the

direction of the ribs, probably in the lines of fission, more or less

horizontal in direction in front, and often, but not always, in vertical

lines on the limbs. On the latter, especially the thighs, they not

infrequently present the appearance of streaks formed by the finger, the

upper part of the stroke being abrupt, and the lower shading off. This

may sometimes also be seen on the trunk. The majority of the single

patches range from one to three inches in their longest diameter; the

borders are not very well-defined nor raised above the rest, but there

is no difficulty in discerning the morbid from the healthy skin. They

are not raised above the surface, but may be rather deep in the cutis.

Infiltration can often be distinctly felt when the patch is pinched up

in comparison with the adjoining healthy tissues, but in the more recent

and smaller patches it is imperceptible, and occasionally they look like

mere stains. Their colour is either pale pink or yellowish; in some

cases the yellowish hue is pronounced, in others absent or nearly so; on

the lower limbs the pink hue predominates. The surface is smooth on the

trunk, but is often slightly rough on the arms and thighs, and below the

knees maybe distinctly rough or even in branny scales. The patches are

never so marked on the upper as on the lower limbs, the palms are always

free, and the backs of the hands are generally unaffected, but sometimes

there are a few small patches below the wrist. The face is nearly always

free, though I have seen faint patches in one case. There is very little

to suggest that the disease is inflammatory, and itching is quite absent

in most of the cases; a few patients said they had some itching when

hot, but only in one case was it really complained of, and that only in

the early evoluting stage of the patches. The initial site for the

lesions varies; the thighs are the most frequently first affected, the

legs next in frequency, and then the trunk. The lower limbs, too, are

generally more crowded with lesions than other parts.

The duration of the disease may be very long. My first case had been

developing for over ten years, others had been only for a few months;

but in the case of a medical man, over 50 when I saw him, he said that

patches first appeared on his legs when he was a house-surgeon, and had

been slowly evolving ever since, so that after thirty years he was

pretty thickly covered, as none as far as he knew had gone entirely

away, though they had temporarily disappeared when he had rubbed in

chrysarobin ointment, but had gradually returned to their old site.

The disease is compatible with perfect health; and even when there was

any departure from the normal there was no reason to suppose that the

abnormality was in any way connected with the skin lesions, while the

majority of the patients had above the average health for their age.

While there appears to be no tendency in the disease to spontaneous

involution, they are not, as the case narratives show, altogether

rebellious to treatment, and in at least two cases a cure appears to

have been effected and in others some improvement, while in a residue no

improvement could be noted. The agents which appeared to have a good

effect are salicin in 15-grain doses at least three times a day, which

by itself entirely cured a recent case (Case 5) of only two months’

duration and of rather acute development, and vasogen iodine 10 per

cent. rubbed in is a useful supplement and materially aided in the cure

of Case 4. In some cases, salicin has failed to make any marked

impression on the lesions, while in others the patient has not gone on

with it sufficiently long to test its merits. As might be expected, it

has been most successful when the disease has been present for a short

time.

The only female case, a lady aged 47 years, resembled the other cases in

its gradual evolution, long duration, absence of itching, in the

persistence of the old patches with continual evolution of new ones, in

its limitation to the covered parts, and in the general good health of

the patient. The differences were in the patches being distinctly scaly

all over the body; though the scales were small and even powdery in most

parts of the body, they were, as usual, rather larger and more abundant

on the legs. The patches were also more decidedly red than in the other

cases; while there was some spontaneous improvement in the summer, in

winter the patches cracked and smarted. This patient, who had been

affected with the disease for ten years, had had the most varied drug

and spa treatment, including cacodylate of soda injections for three

months without any material effect; but after nine exposures to the

Röntgen rays, the part exposed entirely cleared up, while the disease

was unchanged on the inner side of the leg which the rays had not

reached. I intend, therefore, to make use of the rays wherever

practicable.

As regards to _etiology_, it is chiefly negative. There is a large

preponderance of males, and all the cases have been over 20 years old,

while 56 years is the oldest I have met with. In no case could an

exciting cause be made out; two of the patients had had syphilis, but it

did not appear to have any etiological importance, and in one of them

antisyphilitic treatment was tried vigorously for twelve months without

effect.

* * * * *

CASE 1.—Mr. O——, draper, aged 30 years, was first seen by me on March

5th, 1902. The disease had been present ten years. From the commencement

none of the patches had gone away. They appeared simultaneously inside

the arms and thighs. They increased in numbers very slowly for a long

time, and were confined to the limbs until three years ago, when they

attacked the trunk, and during the last year have greatly increased in

number; in fact, most of them have appeared in the last twelve months.

His father was drowned and his mother died of fatty heart at the age of

51 years. When first seen by me the disease was in yellowish patches

which commenced four inches above the nipples, but were not abundant

till the line of the nipples, and they were less numerous below the

umbilicus than above it. They were rather thickly arranged in horizontal

elongated patches from 1 to 3 inches long, and 1/2 inch wide, as if

streaked by the finger, pale, pink, or yellowish in tint, rather

well-defined, but the edges were not sharp, and when the patch was

pinched up a slight infiltration or thickening could be felt in the

skin. The longer patches were formed by coalescence of some of the

smaller ones. The surface was quite smooth. On the sides, the patches

inclined slightly downwards and forwards, but they were practically

horizontal in front. On the back they were sparse, and faintly developed

in the interscapular region, and not nearly so numerous as in front; but

on the lower half of the back and sides they were in the form of

yellowish red stains, without elevation or roughness, and they were more

numerous than on the upper part of the back. Forearms: The patches were

on the inner side chiefly, more numerous on the right side than the

left, and thickly arranged between the wrist and elbow. They were not

elongated, but roundish, oval, or irregular, about three quarters of an

inch in diameter, and somewhat brighter in tint than on the trunk. The

surface was faintly rough, and on pinching up a patch it was slightly

thicker than usual. There were about eight to ten patches on the right

upper arm, while the left was almost free, and there were not nearly so

many patches on the left forearm as there were on the right. On the

thighs: They were most abundant on the inner side, and many more on the

right side than on the left. There were scarcely any patches on the

front of the thigh, but there were a few on the outer side. The patches

sloped downwards and inwards, were oval and broader than the trunk

patches, but still like finger-streaks. The legs were much more densely

covered with coalesced irregular patches, some enclosing healthy skin,

and the surface was rougher than the lesions on the rest of the body. On

the neck, there were a few ill-defined spots about one inch square in

area. There was slight blotchy redness of a not very obvious kind on the

face, scarcely perceptible on the forehead. There was some seborrhœa

capitis, but not so much as formerly, as he uses brilliantine. The

patches seldom itched unless he got very hot. No illness preceded the

eruption; in fact, he has never had any illness; his tongue was clean,

and he looked and has always been perfectly healthy. The general aspect

was somewhat that of a general orbicular seborrhoic eczema, except that

for the most part the surface was smooth.

He has consulted dermatologists and others, but nothing he has taken or

used has done him any good. I only saw him once.

* * * * *

CASE 2.—Mr. H——, aged 37 years, manager of a factory, came to me on

April 2nd, 1902. His general health was very good. The disease had been

present five years, and began on the right fore-arm and a little later

attacked the left. He has never been free since it first appeared, but

thinks some patches have faded and others come out. In the last winter

he had been decidedly worse, for the patches had certainly increased

during the last few months. On the fore-arms, they were nearly

symmetrical, and were quite so at an earlier stage. The lesions were

yellowish or pale red patches; the simple ones were elongated, but the

compound ones irregular in outline; they were from 3/4 to 1-1/2 inches

long. The surface, with a lens, could be seen to be very slightly

roughened, but this was not perceptible to the finger—but when pinched

up there was decided thickening, though they were not raised. There were

no patches on the back of the arms or fore-arms and none on the trunk,

but there were similar patches on the inside of the thighs and on the

legs, some of them larger than the arm-lesions but less distinctly

patchy. There was a large, irregular area on the back of each thigh, and

a few roundish ones scattered about the limbs. The face was quite free,

there was no seborrhœa capitis and there was no itching or other sensory

symptoms in the patches. He was one of ten brothers and sisters who were

in good health, except one who died of syphilitic paralysis. His father

died aged 71 years, and his mother, aged 63 years, was alive and well.

He was given salicin, gr. xv _ter die_, and a lotion of glycerine of

lead and liquor carbonis detergens. I saw him again on July 3rd, when

the eruption had cleared up considerably, much of it having faded,

leaving only a slight stain, but here and there it was still yellow and

slightly rough. He was much better when he took the medicine regularly,

but when he stopped it some of the eruption returned. The salicin was

increased to 20 grains. I did not see him again until July 23rd, 1904.

He then said he took the medicine for three months from July 3rd, 1902,

and then stopped it. He had used the lotion a little longer. On the back

of the legs there were large patches nearly covering the entire area,

but not much in front. It was more distinctly red here than elsewhere,

and there was very little thickening. There were only one or two patches

on the left thigh, but a dozen or more on the left. The trunk still

remained free. The initial patch was on the right wrist seven and a half

years previously, but had disappeared. Some few fresh ones still

developed occasionally. He was told to continue the salicin and rub on

10 per cent. vasogen iodine.

* * * * *

CASE 3.—Mr. H——, aged 56 years, butcher, came to me with skin lesions of

which he had only been aware three weeks, but they may have been there

longer as he had to get up so early to attend the markets that he rarely

saw his own skin. He was a stout healthy-looking man, but he had

syphilis in 1879 and had then suffered from iritis; he was under

treatment for two years. He suffered from constipation and had done so

since he had enteric fever as a young man. Urine had no albumen nor

sugar. He came of a long-lived family, his father having died at 86 and

his mother at 74. He had seven brothers and sisters alive out of

thirteen. The lesions were few in number and situated symmetrically over

the lower ribs on each side, the patches sloping obliquely downwards

from the back to the front. One on each side was 6 or 7 inches long and

compound. There was a single one much smaller (2-3 inches) symmetrically

situated in a line with the large patch, and there were three or four

others above the major patch on the back. There was one distinct patch

over the left scapula and about half a dozen fainter ones about the

back; a few faint ones were present on the back of each arm and forearm.

The lower limbs were free. The patches were erythematous in aspect, the

larger ones brightish red, the others paler. The surface was very

faintly roughened to the touch, and there was very distinct thickening

when the skin was pinched up, but they were not raised above the

surface. The borders of some of the patches were well defined, while

others shaded off gradually.

He was given salicin internally and, to rub in, 10 per cent. vasogen

iodine.

On February 11th there was decidedly less thickening on the left side

but no noticeable difference on the right. He complained of indigestion,

so the salicin was stopped and bicarbonate of soda given him, with

tincture of nux vomica. On March 17th the thickening was much less and

the patch on the left forearm was gone. On May 8th it had all cleared up

and only left slight staining. As he has not come again he has probably

remained well. The resolution of the patches was in this case probably,

to be chiefly attributed to the vasogen iodine.

* * * * *

CASE 4.—Mr. M——, aged 54 years, a gentleman in good circumstances, was

brought to me on June 2nd, 1903, by Dr. Lovell. All his family were

long-lived. His grandfather was killed by an accident aged 93 years, but

his father died of cardiac disease, aged 67 years. The disease the

patient suffered from commenced early in April, _i.e._ two months before

I saw him, on the right leg, and by June had extended all over the lower

limbs and on the trunk, nearly all over the back, but there was scarcely

any on the front. On the forearms, the patches were more on the extensor

than the flexor surface. The eruption consisted of irregular, pale,

erythematous patches from a square inch to the palm in size, with

distinct infiltration in most of them. On the back, they were arranged

symmetrically in the direction of the ribs, _i.e._ sloping downwards and

forwards from back to front. In the early stage, on the back, they could

be traced to commence as minute papules at the hair-follicles, and

gradually the intervals between were filled up until infiltrations with

a uniform surface were formed. Some itched, but none severely, and many

did not itch at all.

Salicin 15 grains three times a day, with 5 minims of tincture of nux

vomica, was prescribed. On June 23rd I saw him again, and there was then

distinctly less thickening on the thighs and legs and the eruption was

somewhat less bright in some parts. The longitudinal patches over the

scapula were still thickened, but there was less infiltration in the

patches on the upper limbs and on the forearms they were yellower.

In response to my inquiry Dr. Lovell wrote me on November 29th, 1904,

that he saw the patient on July 19th, 1903, and the eruption appeared to

be gradually fading away. He next saw him for a sore throat in January,

1904, and the patient told him that the skin affection had gradually

left him. He had had no other treatment than taking the salicin which I

prescribed. This case is the most satisfactory and rapid in its

involution under treatment, as it was also the most rapid in its

evolution, and came earlier under my observation than any of the others.

* * * * *

CASE 5.—Dr. D——, aged 53 years. In 1876, while a house-surgeon, he first

noticed a patch on one calf; since then the patches have gradually

increased in number, and some of them in size. Chrysarobin kills them

down for a time, but they re-form in the same place. In his family

history a sister died of Addison’s disease, and one daughter is slightly

phthisical. His own health is good and he is well nourished.

When seen by me on February 4th, 1904, there was a large irregular

lesion occupying nearly the whole of the interscapular region and

numerous others on the back, abdomen, and thighs. They were of a dull

pale lemon colour; some were distinctly thickened when the skin was

pinched up; in others this was not recognisable. On the thighs, they

were pinkish and slightly roughened. On the body they were smooth,

elongated, oblong, oval, and well defined, symmetrically placed, and on

the back in oblique lines sloping down and out from the spine in the

lines of cleavage, _i.e._ corresponding to the rib slope. They seldom

itched or gave any trouble.

* * * * *

CASE 6.—Mr. H——, aged 37 years, a draper. The disease had been present

two years. When seen on April 26th, 1904, he had numerous patches on the

calves and front of the legs, some three or four inches across, with

distinct thickening. They were round, well-defined, and when pinched up

were hard as compared with the adjoining healthy skin. Besides these

there were more recent superficial irregular patches symmetrically

arranged on both thighs. In the interscapular region and in front under

the breasts were slightly yellowish stains, but no other alteration of

the skin could be seen or felt, the surface being quite smooth. There

was occasionally some itching, but never severe. There was constipation

present, but no other symptom of ill health.

He was ordered fifteen grains of salicin three times a day, and to rub

in ten per cent. vasogen iodine. He was seen again on June 1st, when

there was less thickening in some of the patches, but no other change.

* * * * *

CASE 7.—Mr. D——, aged 34 years, was seen first on November 3rd, 1904, in

consultation with Dr. Payne. He had had a chancre in 1896. He had a

severe sore throat and a rash, which only lasted a short time. He was

treated with mercury for eighteen months.

The present eruption began from three to four years ago, and for the

last twelve months he had been treated by Dr. Payne with the biniodide

of mercury mixture, 1/16 grain three times a day, and also with

mercurial inunctions, but without making any material effect upon the

present lesions. When I saw him the trunk was only slightly affected.

There were a few pale yellow patches below the nipples, elongated and

nearly horizontal. On the back, there were one or two commencing

yellowish spots in the interscapular region, but in the lumbar and

sacral regions they were fairly numerous, and also yellowish and

elongated horizontally. On the thighs, the patches were very abundant in

vertical elongated streaks about half an inch wide, as if the finger had

been wiped down the limb in two- or three-inch pale yellow streaks. On

the legs, the patches were larger, irregular in outline from

coalescence, and of a yellowish-pink colour. The eruption was very

symmetrical, many of them, especially on the thighs, were slightly but

distinctly thickened when pinched up. On the anus and forearms there

were a good many patches, but not so many as on the thighs, where,

arranged in the line of the limb, they were of a paler yellow colour.

The patient said that they itched very decidedly almost always at night

and very often in the day. Sometimes they were sore. They did not itch

when they first came out. The eruption began on the thighs, and although

fresh ones were coming out from time to time, none, so far as he knew,

had faded or gone away.

He was ordered to rub in vasogen iodine and take salicin 15 grains three

times a day. I heard about two months later by letter that there was no

material change, but he had not used the iodine local application.

* * * * *

CASE 8.—Charles C——, aged 32 years, tailor, came to University College

Hospital on October 4th, 1904. He stated that the skin lesions had

commenced four years previously, appearing first on the thighs, then on

the legs, and a little later on the forearms. He did not remember when

the body was first affected. Fresh patches have appeared from time to

time, but none have gone away. The lesions consisted of irregular

patches from half to several inches in diameter symmetrically

distributed over the trunk and limbs. On the back, they were in

elongated or oval patches, symmetrically arranged in oblique lines

corresponding to the direction of the ribs. They are well defined from

the healthy skin, not raised above the normal skin, and the border was

not raised above the central portion either to sight or touch. In front,

there were large areas due to coalescence of several patches, but the

smaller patches were elongated and horizontally placed. On the thighs

near the groin the patches ran obliquely round the limb, but lower down

were vertical. The general colour was yellowish pink, but in some the

yellow, in others the pink predominated. When pinched up, many of the

patches were distinctly thickened, but in the more recent this could not

be felt, and some appeared as mere stains. The surface was smooth on the

trunk, but on the lower limbs there was some roughness of the surface,

more marked below the knee, but not actually scaly. The patches on the

trunk were larger than on the limbs, and healthy areas of skin were

sometimes completely enclosed by the diseased patches. The upper part of

the chest, neck, and face were free, except a small patch on the lower

lip. There were also large spaces of unaffected skin on the thighs, but

only small ones on the upper limbs. On the back of the hands near the

wrists, there were some small patches. The mucous membrane of the mouth

was normal. There was no itching nor other subjective sensation. There

was a history of phthisis in his mother and brother, but the patient was

well nourished and healthy, except that he was liable to bronchitis, and

had some enlarged post sterno-mastoid glands on the left side. He was

put upon salicin gr. xv _ter die_, and vasogen iodine rubbed on the

forearms, but so far no decisive result has been obtained. Mr. Pernet

has obtained a piece of skin from the right forearm, where the lesion

was apparently superficial. His report is appended.

* * * * *

CASE 9.—A gentleman, aged 29 years, in whom the disease has been present

for four and a half years, was seen with Mr. George Pernet, who showed

him at the Dermatological Society of London in November, 1904, and the

notes of his case were published in the December number of the _British

Journal of Dermatology_, vol. xvi, p. 457.

* * * * *

There remains only the case of the lady, which requires separate

consideration.

* * * * *

CASE 10.—Mrs. H—— was sent to me by Dr. Vassie on January 18th, 1902.

She had suffered from the disease for nine or ten years, had seen other

dermatologists, and visited sulphur and other spas. The disease had

begun with a single patch on the arm, and after remaining single for a

few months, had spread and extended almost all over the body and limbs.

When I saw her, the lesions were practically all over the trunk and

limbs with ill-defined pale red patches with powdery roughness and

decided thickening of the whole cutis of the patches, most marked in a

3-inch patch, situated high up on the right loin. The thigh patches were

also thickened, but on the arms and forearms the thickening was less

marked. On the front of the legs, the patches were irregular and more

decidedly scaly, but not like either eczema or psoriasis. The eruption,

as a whole, was like a seborrhoic eczema but less defined, and in parts

the lesions were very pale and shaded off into the healthy skin. The

neck, face, and hands were free. It smarted in cold weather, but did not

itch.

The catamenia were regular, and her general health when seen was

excellent, but a year previously she had had a fibroid removed after it

had begun to be troublesome for a month from hæmorrhage. Before that the

catamenia were twice a month. There was slight seborrhœa capitis.

Salicin, 15 grains three times a day, was given. On July 17th she was

seen again, and the eruption on the legs was somewhat paler, and that on

the arms was much paler, but over the scapula the lesions were thickened

but paler; but she attributed the improvement to the warmer weather

during the last month, as there was generally some improvement in the

summer, while in the winter it fell back, cracked, and smarted. She was

not seen again until May 12th, 1904, having meanwhile had other advice,

but without any improvement, and none of the patches had gone away. At

Wiesbaden she had subcutaneous injections of cacodylate of soda in the

month while she was there, and once a fortnight for twelve weeks after,

but without benefit. It was noted that the leg’s were distinctly red and

scaly. On the rest of the limbs and body the patches were red and scaly

but without thickening, except on the forearms, the patches on the left

being distinctly thickened. The patches were large, many being

palm-sized and in the aggregate covered three fourths of the body, but

the face and hands were quite free, and the neck nearly so. There was no

itching. As every previous treatment had failed, the possibility of the

disease developing into Mycosis fungoides being entertained, although

itching was absent, it was resolved to try the effect of the Röntgen

rays on a portion of one leg. Nine exposures of ten minutes each at a

distance of eight inches were given, and a month after there was slight

improvement where the rays had been used, but it was not very decided;

but on the left arm where vasogen iodine had been rubbed in there was

decided improvement, the lesions being pale, less scaly, and there was

some clearance as compared with the right side, which had not been

treated. I did not see her again until February 7th, 1905, and she then

told me that the improvement where the X-rays had been applied had

continued, and in a few weeks after I last saw her, in August, 1904, the

disease had entirely disappeared from the outer side of the leg below

the knee, and the skin when I examined it was quite white and smooth on

the part exposed and had been so for four months, while the inner side

of the leg where the rays had not reached remained unaltered. She had

not continued the vasogen iodine to the arm, and it had become scaly

again.

General Remarks on the Disease.

From the above description and the cases related in support of it, what

inference may be drawn as to the nature of the disease and its relation

to other skin affections? Frankly, at present I am quite unable to even

conjecture its pathology, or to suggest, with one exception, any

relation to other dermatoses. In my first cases I supposed that it was

an early stage of Mycosis fungoides, though the absence or trifling

character of the subjective symptoms did not lend this any support. I

clung to this theory, however, _faute de mieux_, for a long time, but it

received its _coup de grace_ when I met with a case of over thirty

years’ duration without any such malign development.

At the Dermatological Society of London, where Mr. George Pernet and

myself have shown three cases, among other suggestions, that of a

possible seborrhoïde or Urticaria pigmentosa have been made. Against the

former, the absence of scaliness in a large proportion of the patches,

that the patches are in the skin, not raised above, and that itching is

an exceptional feature, together with the unchanging character of the

lesions, effectually bar the diagnosis of a seborrhoïde. Neither can I

find anything beyond the yellowish tint frequently, but not always,

present to support the idea of Urticaria pigmentosa. The absence of

itching in nearly all the cases of Urticaria factitia, while the patches

are level with the normal skin, and their unchanging character, are all

strongly against such a diagnosis, to say nothing of the extreme rarity

of adult Urticaria pigmentosa and the improbability of one man meeting

with nine cases of it. The histology also negatives this.

I can therefore, at present, only regard it as a dermatosis

_sui-generis_, of which the pathology must be left an open question, as

Mr. George Pernet’s report on the histology of the portion of skin

removed from Case 8 does not throw much light upon the pathology. There

remains only the affection described by Brocq, to which, certainly,

there are closer resemblances than to any other affection.

Brocq[1] divides the group which he calls parapsoriasis into three

groups:

First variety (very closely related to psoriasis), Parapsoriasis

guttata. Jadassohn’s case is probably to be referred to it.

Second variety (intermediate between Lichen and psoriasis),

Parapsoriasis lichenoides, including Parakeratosis variegata of Unna,

and Lichen variegatus (Crocker).

Third variety (closely allied to Seborrhœa psoriasiformis),

Parapsoriasis in patches, corresponding to Erythrodermie pityriasique en

plaques disseminées of Brocq, and of which cases have also been reported

by J. C. White and C. J. White.

It is only with the third variety that comparison need be made, the deep

colour and very small pattern, like a mosaic of the first two, sharply

contrasting with the broad effects as of colour dashed on, in

Xantho-erythrodermia perstans.

For the whole group Brocq gives the following characteristics:

(1) An almost complete absence of pruritus.

(2) A very slow evolution.

(3) A distribution in circumscribed, sharply defined patches, whose

dimensions are from 2 cm. to 6 cm. in diameter, and which are scattered

here and there over the integument.

(4) An almost complete absence of infiltration of the derma.

(5) A pale redness (pinkish coloured).

(6) A fine pityriasic desquamation.

(7) An extraordinary resistance to the local applications usually

employed in the treatment of psoriasiform or pityriasic seborrhœa, in

fact, only yielding slowly and imperfectly to the most energetic

application of pyrogallic acid.

The special features of the third variety he describes as:

(1) Being in patches, circumscribed, sharply defined from 2 cm. to 6 cm.

in diameter.

(2) They are scattered irregularly over the skin without any apparent

system.

(3) The colour varies from a pale red to a brownish or livid red,

according to the part affected.

(4) There is always present a fine pityriasic desquamation more or less

marked in different cases.

(5) There are at times in some of these cases, aggregations of small

flattened papules which may be considered as links connecting it with

the second variety.

(6) There is no infiltration of the integument appreciable to the eye or

touch.

(7) The face is rarely affected, and there is the same extremely slow

evolution, great resistance to local treatment, and few or no subjective

symptoms.

Referring to the whole group, he says: “We know nothing very definite

about the etiology or pathology of these affections. They may appear at

any age, but seem more frequent in youths or adults. He has observed

cases in men and women and in all classes of society. They seem to be

slightly more frequent in women than in men.”

It must be confessed that there are many points of resemblance of this

third variety to Xantho-erythrodermia perstans, and, as regards the

lady, Case 10, it is probably what Brocq has described as “Erythrodermie

pityriasique en plaques disseminées,” although I should say there was

distinct infiltration in a large proportion of the lesions, and many of

the patches far exceeded the limits in size that Brocq lays down.

With regard to the other nine cases, the differences are somewhat more

marked, and they should, at least for the present, be either kept apart

or treated as a distinct variety.

The differences are:

(1) The patches are frequently much larger, 3 and 4 inches or more in

their long diameter, and the margin is not very sharply defined.

(2) A distinct arrangement in lines in direction varying with the

topography is observable in most cases.

(3) The colour is either pale red or distinctly yellowish.

(4) Instead of a fine pityriasic desquamation being always present, this

is only distinct on the legs, sometimes just recognisable on the thighs

and arms, while on the trunk it is absent, the surface being usually

quite smooth.

(5) The presence of papules I have not observed, except at the

commencement of Case 4.

(6) There is distinct infiltration in a large proportion of the patches,

perceptible to the touch, though not to the eye.

The resemblances are: the absence of conspicuous pruritus, and there is

often none; the occurrence in patches; the slow evolution; a pale

redness; in many cases an extraordinary resistance to treatment. These

are not enough to establish identity, but I confess that in my opinion

they show greater resemblance to the affection I am describing than they

do to psoriasis, and certainly my nine male cases would never suggest to

any one a resemblance to psoriasis, and I should strongly demur to class

them under parapsoriasis as a covering term.

Histological Note by George Pernet.

A piece of skin was removed from the extensor surface of the right

forearm of the male case, aged 32 years (a Jewish tailor), where the

more recent patches had appeared. Clinically there was practically no

infiltration to be felt in that situation. The specimen was hardened in

alcohol, cut in celloidin, and stained in various ways. The

microscopical appearances were as follows:

_Epidermis._—The stratum granulosum was either atrophied or absent. The

stratum lucidum was absent except for traces here and there. The

epidermis generally showed a slight amount of œdema.

_Corium._—The vessels were dilated, with some cellular infiltration

about them. The collagen appeared to be normal, with the exception of

slight œdema, but the elastin was apparently reduced in quantity,

especially in the papillary layer, and it was to some extent fragmented

in places. It should be mentioned that the specimen was stretched on a

small piece of cork in the process of hardening. The elastin stained,

however, much as in the normal condition.

Altogether there was little to be gathered from the histology _quâ_

cause, except that the appearances of the blood-vessels perhaps pointed

to a general blood condition.

Dr. Thiele, Pathologist to University College Hospital, kindly

examined the blood and reported: Total red corpuscles per c.mm.,

6,560,000; total whites per c.mm., 21,878. Hæmoglobin, 84%. C.T.,

65. Differential count of whites: Small lymphocytes, 18·2%; large

lymphocytes, 9·4%; neutrophiles, 60·7%; oxyphiles, 1·6%: hyaline

cells, 2·1%.

Footnote 1:

_Amer. Journ. Cut. Dis._, vol. xxi, 1903, p. 315.

IDIOPATHIC MULTIPLE PIGMENT SARCOMA (IDIOPATHIC MULTIPLE HÆMORRHAGIC

SARCOMA) OF KAPOSI.

By F. PARKES WEBER, M.D., F.R.C.P., AND PAUL DASER, M.D.

The patient, Jakob Z——, is a Polish Jew, aged 46 years, from Galicia,

who has lived nine years in England, and says he has enjoyed good

health. There is no evidence of previous alcoholism or syphilis. The

patient was brought by Dr. Weber before the Dermatological Society of

London on February 8th, 1905.

The present illness commenced about three years before, when he chanced

to wound the sole of his right foot with a nail. A pedunculated growth,

about the size of a cherry, arose from the wound. This description

reminds one of the strawberry-like granulation tumours sometimes growing

from small wounds or ulcers on the fingers, which have been termed

“botryomycosis,” or rather “botryomycomata,” because at one time they

were supposed to be caused by the “botryomyces.”[2] The growth was

removed by a doctor. Afterwards small bluish nodules developed from time

to time on the feet and legs. Some of these nodules apparently undergo

the following series of changes: They slowly increase in size, and after

about three months constitute little pendulous tumours, which ultimately

fall off spontaneously or else are knocked off or pulled off by chance;

in this way local healing occurs, but fresh nodules form elsewhere.

Though, as stated, some of the nodules become pedunculated growths,

others appear to atrophy and merely leave brownish pigment in the skin,

whilst others seem to undergo very little change, and, at all events,

persist for a long time in their primitive form, namely, as hard bluish

lumps under the epidermis. Treatment has been as yet without result.

_Present condition_ (January, 1905).—On _the hands_ about the knuckles

and backs of the fingers are a few minute slightly elevated bluish

nodules. On the sole of the _right foot_, especially on the inner part,

there are nodules in various stages of development. The minute ones,

those in an early stage of development, are slightly elevated and of a

bluish colour, similar to those on the hands. Others, further advanced

in development, are small, sessile, or pedunculated hard outgrowths,

without bluish colour and sometimes covered by thickened epidermis.

There is a large patch of pigmented (brown) skin on the dorsal surface

of the right foot, and in the neighbourhood of this pigmented area are

some minute nodules of similar character to those already described. It

is possible that the pigmented skin has been the site of minute growths

which have undergone spontaneous involution, and have, as frequently

happens in Lichen planus, left pigmentation of the skin behind them. The

right thigh and leg are not affected.

The _left lower extremity_ is the part most affected by the disease, and

there is chronic, rather firm, œdema of the left foot and ankle. The

nodules on the left foot are similar to those on the right, but are more

widely distributed, and the left foot differs from the right in the

absence of the pigmented area and in the presence of the œdema to which

we have just alluded. Of the little sessile or pedunculated tumours on

the back of the left foot and in the neighbourhood of the ankle-joint

(see Fig. 1) the biggest are of the size of a large pea. There are

likewise little tumours of various sizes—that is, in various stages of

development—on the inner aspect of the left popliteal region (see Fig.

2) and in the neighbourhood of the patella, the smaller ones being

bluish and slightly elevated, the larger ones being reddish,

lentil-sized, sessile outgrowths.

There are no nodules or growths on other parts of the limbs, trunk, or

head, with the exception of four or five minute purplish or bluish

papules on the _glans penis_ and neighbouring skin.

[Illustration: Figure 1.]

There is no evidence of any disease of the thoracic or abdominal

viscera. The patient is not strongly built, but looks well nourished. He

complains of various pains, but whether these are related to the disease

or not is doubtful.

[Illustration: Figure 2.]

_Microscopic examination._—One of the growths, of the size of a large

pea, was removed from the left ankle, and a smaller one (lentil-sized)

from the left knee. Sections of both were stained with hæmatoxylin and

eosin-hæmatoxylin. The growths are seen to be situated in the corium,

and are circumscribed. The epidermis over one of them is thickened. They

consist of oval and spindle cells, which, in some parts, are more or

less grouped into strands or bundles, and are cut in various directions.

In some parts of the sections there are empty spaces (? lymph spaces)

and in some parts there is homogeneous substance between the cells; in

other parts there is extravasated blood. The cells in the larger and

older of the two nodules are decidedly more elongated and

fibrous-looking than in the smaller and more recently developed one. Dr.

J. M. H. MacLeod is kindly going to make a further report of the

microscopical features.

_Remarks._—It seems to us clear that the case is a typical but

relatively early one of the so-called idiopathic multiple pigment

sarcoma (idiopathic multiple hæmorrhagic sarcoma) of Kaposi and later

writers. For the literature on the subject we refer to the English

summaries of Dr. J. H. Sequeira[3] and Dr. Radcliffe-Crocker.[4] The

patient in our case is a male, as in nearly all other recorded cases of

this disease; he is of the favourite age (between 40 and 50), and it may

likewise be noted that he is a Galician Jew, as the patient of Sir

Stephen Mackenzie[5] and Dr. J. J. Pringle was. The minute bluish

nodules in the corium may be regarded as the primary feature of the

disease. They either remain for a long time without undergoing much

obvious change, or they undergo spontaneous involution and completely

atrophy, leaving behind them only a little brownish cutaneous

pigmentation; or else (thirdly) they may increase in size, become much

elevated, and form definite sessile tumours, which, later on, become

pedunculated, and finally drop off. This is the cycle in regard to the

development of the little pendulous tumours which constitutes one of the

most characteristic features of the disease. Another characteristic

feature of the disease, probably sooner or later present in every case,

is the œdema which occurs in the parts most affected, especially in the

lower extremities. It is persistent œdema, and results in an

elephantiasis-like condition. It is well marked in the left foot and

ankle of our case. The striking blue or purple colour of the small

nodules (which is absent in the pendulous tumours) seems, as in other

cases, to be due to the venous blood contained in the blood-vessels or

extravasated. What pigment there is in the growths is probably derived

from blood. In our patient there is no evidence of gout as in certain

cases described by Mr. Hutchinson.[6]

The prognosis in the present case is not altogether unfavourable,

considering that the patient’s general health is good, that the disease

is probably seldom of itself fatal, and that in some cases improvement

or spontaneous care has, apparently, occurred after the disease has

lasted twenty years or more.

Footnote 2:

_Vide_ X. Delore, _Lyon Médicale_, July 16th, 1899, p. 376; J.

Sabrazès and A. Laubée, _Arch. Gén. de Méd._, Paris, November, 1899,

p. 515; R. von Baracz, _Wien. klin. Wochenschr._, 1901, No. 14; G.

Carrière and G. Potel, _Presse Médicale_, Paris, May 17th, 1902, p.

471; and L. Legroux, “La Botryomycose,” _Thèse de Paris_, 1904. The

botryomyces appears to have owed its supposed existence to a mistaken

interpretation of microscopic appearances. H. Bichat (_Arch. Gén. de

Méd._, February 2nd, 1904, p. 281) thinks there is nothing specific in

the growths, but V. Ball (_Arch. Gén. de Méd._, August 2nd, 1904, p.

1921) concludes that that botryomycosis, though it owes its name to an

error, is nevertheless a pathological entity and is a special

staphylococcal affection. Dr. Weber possesses a microscopic section of

one of these little growths, which was removed from the finger (close

to the nail) of a woman in 1890, when he was a house-surgeon at St.

Bartholomew’s Hospital for Sir William Savory. It was a typical

strawberry-like “botryomycoma” with quite a narrow pedicle. Dr. J. M.

H. MacLeod, who has kindly examined the section in question, tells us

he regards such growths as “septic granulomata,” septic organisms

producing very various effects according to their degree of virulence

and naturally according to the nature of the living soil on which they

grow.

Footnote 3:

_British Journal of Dermatology_, June, 1901, p. 201.

Footnote 4:

_Diseases of the Skin_, third edition, 1903, p. 963.

Footnote 5:

_British Medical Journal_, June 4th, 1890. Amongst foreign accounts

_vide_ Radaeli’s report of five cases in _Lo Sperimentale_, December,

1904, p. 1023.

Footnote 6:

_Archives of Surgery_, vol. v, p. 237, and vol. vi. p. 132. See also

Mr. Hutchinson’s _Smaller Atlas of Clinical Surgery_, Plate 61, where

he refers to the case figured by Hebra and Kaposi as “Sarcoma

melanodes”; also his remarks on “Sarcoma melanodes” in the _British

Medical Journal_, January 7th, 1905, and the case shown by him at the

Polyclinic in December, 1904, which was also shown by Dr. Ormerod at

the Dermatological Society of London, July 8th, 1903.

SOCIETY INTELLIGENCE.

THE DERMATOLOGICAL SOCIETY OF LONDON.

An Ordinary Meeting of the above Society was held on March 8th, 1905, at

5.15 p.m., Dr. J. H. STOWERS in the chair.

The following cases were demonstrated:

* * * * *

Dr. JAMES GALLOWAY showed the case of a young lady presenting an

eruption on the left arm of unusual character. The lesion in some

respects resembled those of granulomatous origin, but no definite

diagnosis was given. This case will be subsequently noted in full.

* * * * *

Dr. T. J. P. HARTIGAN (introduced) showed a case of _atrophy of the

nails_, a description of which will be found on page 147.

* * * * *

Dr. GRAHAM LITTLE showed: (1) A case of a _corymbose syphilide_ in a man

aged 44 years, with a history suggestive of a double infection with

syphilis. The patient had been in the Army and had contracted syphilis

in India, twelve years ago. He then had a chancre on the top of the

glans penis, the scar of which was still visible. He was taken into the

Military Hospital and treated for exactly ninety-seven days, his

treatment ceasing entirely after this period. He had no secondary

eruption and no further symptoms. Eight years later he had another

chancre, also on the glans penis, but near the frænum. This was,

according to his description, a deep ulcer, which was seven weeks in

healing. He had no bubo following and no secondary eruption. Ten weeks

ago he began to have the present eruption, which was the only general

rash he had ever had. With the exception of the treatment during the

actual presence of the two chancres, he had had no specific treatment

whatever.

The eruption as seen on exhibition consisted of numerous groups of

fairly large papules arranged in a somewhat herpetiform manner, with

here and there a central larger papule surrounded by smaller ones, in

the manner described as corymbose, but for the most part the groups were

composed of papules equal in size; these groups were scattered over the

back especially, the chest, the arms, the thighs, and the face, with

individual large papules here and there upon the arms and legs. The

mucous membranes were not affected.

The history seemed to point to a double infection, the interval between

the two chancres being eight years.

(2) A case of _dermatitis artefacta_ in a young lady, a private patient,

who gave the following history. She was bitten by an old collie dog

twenty-three days ago on the calf, through her dress. She was not seen

by a doctor until a week or more later, and when seen by him she had a

circular “patch upon the calf of vesicating erythema, surrounding the

bite, with a vivid erythematous non-vesicating ring, about half an inch

broad, surrounding the central patch, and separated from it by an

intervening band of healthy skin, about a quarter of an inch broad.”

Four days later an exactly similar condition was noted on the lower part

and inner aspect of the same leg, “a patch of vesicating erythema the

size of a florin, surrounded immediately by healthy skin and then a ring

of vivid erythema half an inch wide.” The patient did not appear to be

in any way neurotic. There was no apparent animus against the owners of

the dog, who were old and intimate friends, and no breach of relations

between them had taken place. She led a healthy active life and was, in

fact, in robust health at the time. The ointment used in the first

instance was obtained from a chemist; her doctor had prescribed carbolic

ointment. The method of production was not ascertained and no adequate

motive could be assigned.

(3) A case which was shown as _syringomyelia_ with trophic ulcers on the

upper arm and shoulder in a woman who had been under Mr. Ernest Lane’s

care for about twelve years, and had had numerous operations performed

for a continually ascending necrosis of bone accompanied by trophic

ulcers on the skin.

Some divergences of opinion were expressed as to the diagnosis, and

this being at any rate a rare and interesting case, a more detailed

report will be subsequently submitted for publication in this

journal.

* * * * *

Dr. J. M. H. MACLEOD showed a case of _grouped comedones_ associated

with acneiform lesions on the chest of a boy aged 2 years. The comedones

were present chiefly on the sternal region, but several isolated groups

occurred around the nipple and umbilicus. Only a few of the comedones

had become inflamed or transformed into acne pustules. The mother had

noticed the comedones about a month before exhibition. There was a

definite history of local irritation in the case, for since the child

was a few months old he had worn a piece of flannel over the chest in

the affected region, and as the mother believed that he had a delicate

chest the flannel had been frequently saturated with camphorated oil.

The exhibitor intended to make a bacterial examination of the lesions

with the object of trying to find the acne bacillus, and hoped to report

the result at a subsequent meeting of the Society. Another point of

interest in connection with the case was the fact that it occurred in a

boy, as the large majority of reported cases have been in boys. Dr.

MacLeod referred also to another case in an infant boy of about a year

old, which he had seen on the afternoon of the meeting, but

unfortunately had been unable to bring up, in which the comedones were

grouped on the forehead and cheeks and in which there was no history of

local irritation to account for the lesions.

* * * * *

Mr. MALCOLM MORRIS showed a case of early _Parakeratosis variegata_, a

full report of which will be published in a future issue of the journal.

* * * * *

Dr. ORMEROD showed: (1) A case of _Lupus erythematosus telangiectodes_.

The patient was a woman, aged 44 years, who stated that she had suffered

from an eruption on the cheeks for the last eighteen months. On

exhibition, there was a large red area situated symmetrically on either

check, the redness being due to dilatation of the small vessels. Within

these areas there were islets of paler and shiny skin, which showed

superficial atrophy. A small area in each patch was covered with a crust

which was difficult to remove, and when detached showed little tags and

prominences on the under surface. The appearance of the eruption had not

materially altered since the patient was first seen fourteen months ago.

All the members present agreed with the diagnosis of the exhibitor.

(2) A woman, aged 38 years, suffering from a curious _eruption

associated with obscure nerve symptoms_. The history showed that four

years ago she had suffered from some chest affection, accompanied by the

expectoration of blood and offensive matter. She was ill three months,

and during her convalescence she scratched her right thumb, and a

lymphangitis of the arm, with axillary abscess, resulted. She next

developed a painful swelling of the right elbow, which was opened and

drained, and she thought a piece of bone came away; the arm was put up

in splints. The right elbow had been stiff since that time, and during

its healing she had developed pricking sensations in the fingers, which

became contracted. There was then an interval of nine months’ good

health, after which, two years ago, she developed an abscess in front of

the right thigh, which eventually broke, and laid her up for four

months. Subsequently, about eighteen months ago, the rash appeared, at

first round the site of the abscess, then spreading towards the buttock

and loin, and finally extending down the leg.

On exhibition, the patient showed an extensive anæsthetic area over the

right side extending up into the axilla, curving down both in front and

behind at the level of about the sixth rib, and embracing the whole of

the right arm and leg, with the exception of small islands on the palm,

sole, and gluteal region, where sensation still persisted. The rash

followed a similar distribution, but did not affect the arm, and tailed

off on the leg with the appearance of isolated spots. The rash

developed, according to the patient’s history, in the form of red spots,

on which a blister full of clear fluid formed. The fluid then became

mattery, and an ulcer resulted. The development of an ulcer was heralded

by a pricking sensation. On exhibition, the striking characteristics

were the presence of patches of excoriated skin and white scars,

surrounded by pigmentation. The patches were oval in shape, with the

long axis running down the limb or transversely on the trunk. The more

recent lesions consisted of red, raised papules with an excoriation on

the summit. In spite of bandaging with boric acid ointment in the

hospital a few lesions formed beneath the dressings, though more

appeared outside. Examination of the supposed affected joints showed

nothing abnormal; the reactions of the atrophied muscles to electricity

were also normal. The anæsthesia was shown to be of psychical nature,

and the exhibitor therefore considered most, if not all, of her

disabilities to be of an hysterical nature. He asked the opinion of the

Society as to the nature of the eruption.

Most members, including the exhibitor, considered that the eruption

was artificially produced by the patient.

* * * * *

Dr. J. J. PRINGLE Showed a case of _Lupus erythematosus associated with

Raynaud’s disease_ in a highly neurotic woman, aged 44 years. The

symptoms of Raynaud’s disease apparently first manifested themselves in

1895, but were first recognised as such in 1896. Associated with the

typical phenomena of recurrent local syncope and asphyxia of the

extremities, more especially of the hands, there were attacks of severe

griping abdominal pain. The exact nature of these attacks had never been

accurately determined, but there were evidences of some chronic

intestinal obstruction, which could not, however, be located. The

exhibitor had witnessed several occurrences of typical Raynaud symptoms

in the hands, and the nutrition of all the fingers was impaired, their

tips being stumpy and atrophied, but no gangrene had ensued. The first

manifestations of Lupus erythematosus showed themselves in 1900, in the

temporal regions and scalp. They were regarded as “gouty psoriasis,” and

were treated by a physician professing the cult of homœopathy by

repeated painting with pure oil of cade (!), under which they progressed

rapidly, but in the wrong direction. She was also advised to winter in a

high, cold, and dry locality, but she suffered terribly from this

experience, which was carried out last winter in Switzerland.

The Lupus erythematosus was of severe inflammatory type and occupied a

great portion of the scalp, denuding it of hair, and giving rise to a

large atrophic scar which was the seat of peculiarly obstinate recurrent

attacks of suppuration, probably referable to a dirty toupet, worn for

cosmetic purposes. Symmetrical patches were also present behind the

ears, inside the pinnæ, and in the zygomatic regions, while there were

present over the whole face a large number of telangiectatic spots

averaging nearly the size of a pea. The nasal and buccal mucous

membranes were healthy. The urine contained neither albumen nor

blood-pigment, nor was there any history pointing towards

hæmoglobinuria. The exhibitor asked the experience of members as to the

value of treatment of such a condition by Finsen’s method, X-rays, and

especially by high-frequency currents, which he was inclined to try as

of possible value in both the associated conditions present.

Dr. Pringle’s suggestion, that treatment by high-frequency currents

afforded the best prospect of benefiting the patient, especially

with regard to the Raynaud phenomena, was generally accepted.

Dr. DORE was of opinion that the disease would thereby be

considerably ameliorated and possibly even arrested, but the

attitude of the majority of members present was somewhat sceptical.

* * * * *

Dr. H. RADCLIFFE-CROCKER showed a case of _tuberculous gummata_ (or

gummatous tuberculides). The patient was a well-grown and

well-nourished, healthy-looking girl, aged 18 years, who first came

under observation on February 17th, when the following notes were made:

The disease began at the age of 7 years, when a crop of lesions made

their appearance. One of these occurred on the abdomen, near the right

ilium, where a large scar, about 3 inches (over 7 centimetres) in

diameter, was present. This condition lasted for a few months. Then very

few lesions appeared up to the age of 15, when they became more numerous

and had gone on ever since without any interval of freedom. For three

years the patient had been subject to flat circumscribed infiltrations

of the skin varying from a shilling to a crown in size. These lesions

all broke down more or less into superficial ulcers, which healed in

from two to three weeks. On the legs and thighs up to the crest of the

ilium there were a large number of more or less circular scars varying

in size, but most of them about as large as half a crown (3

centimetres). On the thighs, however, some were over 2 inches in

diameter (about 5 centimetres). On the right thigh near the knee there

was a recent lesion (two weeks old), which was about 2-1/2 inches by 1

inch (6 centimetres by 2 centimetres), dull red, with great thickening;

it presented on its surface a pea-sized ulceration, which had formed

within twenty-four hours of the time when the patient was first seen. A

similar lesion, with a more advanced ulceration, on the right calf, had

been present three weeks. Below the left knee there was a flat

infiltration, slightly raised and well defined, about the size of a

shilling (about 2 centimetres). On the right temple there was a small

circular scar of 1/4 inch, which had resulted from a similar lesion to

those already described. The patient’s lungs were unaffected, but the

history was strongly tuberculous on the father’s side, a large number of

his relations having died of consumption, whilst some others were dying

of the same disease at the present moment. The patient had lost one

sister, aged 21 years, of phthisis, and a brother and another sister of

“consumption of the bowels.”

* * * * *

Dr. SEQUEIRA showed a case of _Lupus vulgaris_ to illustrate the value

of Dr. A. E. Wright’s recent work upon opsonins. The patient, a Jewess,

aged 20 years, was first seen at the London Hospital in the summer of

1900. The whole of the face and part of the neck were then much

infiltrated and in parts ulcerated. The feet also were affected, parts

of several toes having been destroyed. Owing probably to the fact that

she was unable to walk, the patient was not seen again until February,

1905. Fortunately, photographs of the condition in 1900 were preserved,

and these showed that the disease had extended very little in the four

years and a half, although the patient had had no treatment whatever in

the interval. The general health had improved, but the lupoid

infiltration of the face and neck were well marked and there was still

considerable ulceration, the ulcers being covered with dirty scab. The

destructive ulceration of the toes had slightly increased. There were no

physical signs pointing to tuberculosis of the internal organs. The

glands were slightly enlarged, but this was not a marked feature.

Dr. Sequeira took the patient into the hospital, intending to use

tuberculin. Before doing this, the blood was examined by Dr. Wm.

Bulloch, who found that the opsonic index was 1·3, normal blood being 1.

A high opsonic index, it may be mentioned, has been found by Dr. Bulloch

in a certain proportion of the cases of Lupus attending the London

Hospital, and particularly in the chronic cases doing well under the

light treatment. As the opsonic index was already high in this case, it

was deemed unnecessary to raise it by the injection of tuberculin, and

fomentations were applied to the affected areas, to bring the opsonins

to the diseased parts. The result was very striking. In a few days the

lesions were paler, flatter, and clean. When shown at the meeting, after

a fortnight’s treatment with fomentations, the infiltration had markedly

diminished, the raised margin being flatter and paler, and the ulcerated

areas healed up, except upon the stumps of the toes.

The fomentations were of boracic lint soaked in hot water and covered

with oil silk frequently changed. It may be mentioned that the

improvement was much more rapid than had been seen in similarly

extensive cases treated by fomentations, the only known difference being

the high opsonic index. The case is of importance as supporting Wright’s

work, and also as showing the value of examining the blood before

injecting tuberculin. It also explains why some apparently severe cases

do well under simple treatment.

Dr. GRAHAM LITTLE was able to confirm Dr. Sequeira’s observations in

this case from one at St. Mary’s Hospital, in which a similar

improvement had been noticed with fomentations in a patient whose

opsonic index was as high as 2.

* * * * *

Mr. GERALD SICHEL (introduced) showed, on behalf of Sir Cooper Perry:

(1) The boy, aged 8 years, who was shown at the February meeting as a

case for diagnosis, and in whose case the chronic nodular annular

patches had gradually increased in size; fresh, hard, painless, and but

slightly tender, shotty nodules had also developed in the periosteum of

the left temporal region. Dr. Galloway recognised the case as identical

with one he had described in this journal as _Lichen annularis_. Dr.

Pringle also had seen similar cases.

(2) A boy, aged 13 years, presenting symmetrical, painless

_callosities_, covering in size an area of between a shilling and a

two-shilling piece, on the back of each heel, and which he had noticed

for the past eight or nine months.

The British Journal of Dermatology, April 1905 · 第 3 / 20 题