Original Articles (Abstract)drmtl.org/data/068010001E.pdf · 2011-04-28 · cancer, the...

8
Original Articles (Abstract) Supplementary studies on Pigmentation in Nevoid, Neoplastic, and other Diseases of the Skin゛゜ By Hiroshi Tanaka** Pigment anomalies of the foetal skin and of diseased skin were studied by means of the dopa reaction and other routine stains, in an attempt to find some explanation for the increase and decrease of pigments in different diseases. The results are as follows : 1. In the foetal skin, a well-defined picture of the melanocytes is visible without recourse to the dopa reaction, because their cytoplasm is filled with abundant melanin granules. It is characteristic of the foetal skin that the melanocytes are situated at the same level as the basal cell layer or at the somewhat higher level。 2. The hyperfunctional conditions of melanocytes : In Addison's disease. the me^ano- cytes are shown to be in a stimulated condition by the increase of their reactivity. their hypertrophy in size. and the increase of their number as disclosed by the dopa reaction. The author found that the normal rhythm of the pigment formation is maintained in this disease, a fact endorsing Lerner-Shizume's view that the pigment formation in Addisonタs, disease is caused by the hypersecretion of MSH. A similar phenomenon was observed in a patient who had received prolonged treatment with Prednisolone. 3. The findings on the pigmented nevus, nevus spilus, the pigmented macules of Reck- linghausen's phacomatosis. and pigmented spots on palms and soles were studied from the etiological point of view. In the pigmented spots on palms and soles, the difierences・ between nevoid and non-nevoid pigmented spots were pointed out. 4. The findings on Mongolian spot and their allied conditions were described. and it was shown that the pigmented macules in pigmentovascular phacomatosis (Ota) coincide with Mongolian St)Ot. 5. The relation between the proliferation of Malpighian cells and the amount of melanin was investigated. In melanoepithelioma, both the number of ]Malpighian cells and the amount of melanin increased together. But in the precancerous condition and actual cancer, the co-existence of ・Malpighian cells and melanin is disturbed. and the decrease or disappearance of melanin and the decrease, shrinkage or disappearance of melanocytes are observed. In hard nevi, the epidermal pigment sometimes increases and sometimes decreases, apparently owing to different types of proliferation of Malpighian cells. 6. A phenomenon common to incontinentia pigmenti (Bloch-Sulzberger) and histological pigmentary incontinence including fixed drug eruption, multiple macular hyperpigmentation。

Transcript of Original Articles (Abstract)drmtl.org/data/068010001E.pdf · 2011-04-28 · cancer, the...

Page 1: Original Articles (Abstract)drmtl.org/data/068010001E.pdf · 2011-04-28 · cancer, the co-existence of ・Malpighian cells and melanin is disturbed. and the decrease or disappearance

Original Articles

  (Abstract)

Supplementary studies on Pigmentation in Nevoid, Neoplastic,

         andother Diseases of the Skin゛゜

                           By

                       Hiroshi Tanaka**

   Pigment anomalies of the foetal skin and of diseased skin were studied by means of

the dopa reaction and other routine stains, in an attempt to find some explanation for the

increase and decrease of pigments in different diseases. The results are as follows :

   1. In the foetal skin, a well-defined picture of the melanocytes is visible without

recourse to the dopa reaction, because their cytoplasm is filled with abundant melanin

granules. It is characteristic of the foetal skin that the melanocytes are situated at the

same level as the basal cell layer or at the somewhat higher level。

   2. The hyperfunctional conditions of melanocytes : In Addison's disease. the me^ano-

cytes are shown to be in a stimulated condition by the increase of their reactivity. their

hypertrophy in size. and the increase of their number as disclosed by the dopa reaction.

The author found that the normal rhythm of the pigment formation is maintained in this

disease, a fact endorsing Lerner-Shizume's view that the pigment formation in Addisonタs,

disease is caused by the hypersecretion of MSH. A similar phenomenon was observed

in a patient who had received prolonged treatment with Prednisolone.

   3. The findings on the pigmented nevus, nevus spilus, the pigmented macules of Reck-

linghausen's phacomatosis. and pigmented spots on palms and soles were studied from

the etiological point of view. In the pigmented spots on palms and soles, the difierences・

between nevoid and non-nevoid pigmented spots were pointed out.

   4. The findings on Mongolian spot and their allied conditions were described. and it

was shown that the pigmented macules in pigmentovascular phacomatosis (Ota) coincide

with Mongolian St)Ot.

   5. The relation between the proliferation of Malpighian cells and the amount of

melanin was investigated. In melanoepithelioma, both the number of ]Malpighian cells and

the amount of melanin increased together. But in the precancerous condition and actual

cancer, the co-existence of ・Malpighian cells and melanin is disturbed. and the decrease or

disappearance of melanin and the decrease, shrinkage or disappearance of melanocytes

are observed. In hard nevi, the epidermal pigment sometimes increases and sometimes

decreases, apparently owing to different types of proliferation of Malpighian cells.

   6. Aphenomenon common to incontinentia pigmenti (Bloch-Sulzberger) and histological

pigmentary incontinence including fixed drug eruption, multiple macular hyperpigmentation。

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and Riehl's melanosis. is the decrease of epidermal melanin notwithstanding normal or even

enhanced production of the pigment, accompanied with the increase of dermal melanin.

These diseases show complicated histological pictures. due to the difference in degree or

phase of the above mechanism, aad the changes proper to each of the diseases.

   7. Depigmentation : In vitiligo. the melanocytes are seen to suffer suppressed func-

tion and degeneration. In some cases. however, large amounts of melanin was observed

in the dermis. It may be a vestige of past pigmentary incontinence. Leucoderma centri-

fugum acquisitum (Sutton) is also caused by the same mechanism, with pigmented nevi

in its center. so the nevus cells suffer the same changes・

   8. We have hitherto had only scanty description of the leucoderma in Morbus Harada

and sympathetic ophthalmia. The author carried out histological studies on each one case

of the two diseases. and noticed their resemblance to vitiligo.

   9. In nevi depigmentosi, partial albinism and albinoidism, the melanocytes show

pathologic changes in proportion to the degree of their depigmentation. In albinoidism.

however, it was found, contrary to expectation, that the enzymic activity of melanocytes

was still maintained.

  10.1t is generally thought that there is an eti ological resemblance between Addison's

disease and systemic scleroderma. Leucoderma in the both diseases may be considered as

the result of exhaustion of melanocytes caused by the excessive stimulalion of MSH.

  1L The findings on leucoderma in Bourneville-Pringle's phacomatosis and dyschroma-

tosis hereditaria symmetrica (Toyama) were described.

  12. Mongolian cells were found histologically in the skin from two adults and the

significance of the cells was discussed.

 * Full-length report: Japanese section pp. 1~59

** From the Dermato-Urological Clinic (Director: Prof. T. Kawamura), University of Kanazawa,

  Kanazawa

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                     ACase of Para-anthrax*

                           By

          KiheiTanioku, Fujitaka Zenisaka and Masashi Murata**

   A35-year-old farmer was referred to us with the appearance of slightlypruritic,raised。

dark-purple lesions on the extensor surface of right wrist and arm on January 8,1957.

The present skin disorder began in December, 1956. Physical examination revealed good

general health without significantfindings. The lesions consisted of Siχ nodules, which

were sharply demarcated, round, varying in size, 0.5 to 3.5cm in diameter, and were

markedly raised above the skin surface, elastic softon palpation. There were some

vesicles on each nodule.

   Bacteriological and histological studies―Material was obtained from one nodule.

Cultures in simple agar showed a pure culture of a different colony among the colonies

of staphylococcus albus. The organism was observed to be a gram-positive large rod.

It was definitelymotile. There was no capsule noted. Spores were formed with energic

and irregular characteristic. It produced acid, but no gas, in glucose, maltose and

saccharose. Growth in broth resulted formation of sediment but no pellicule。 The rod

did not produce hemolysis on blood agar. There was no pathogenicity for mice. The=

biopsy specimen from one nodule exhibited thin epidermis, slightly edematous superficial

layers of the corium and some large rods in the area from the basal layers of epidermis

to the superficiallayers of corium. These rods is most likelyB. anthracoides.

   Treatment and course―All cutaneous symptoms had completely subsided by the

symptomatic treatment two weeks later.

   Itwas felt that from these characteristics the organism could best be classifiedヽas

Bacillus anthracoides.

   Acase of para-anthrax due to Bacillus anthracoides was reported. The difierentiating

features between anthraχ and para-anthrax were briefly discussed.

 *Full-length report: Japanese section pp. 60~67

** From the Department of Dermatology & Urology (Director: Prof. K. Tanioku), Faculty of

  Medicine, Shiushu University, Matsumoto

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Society Transactions

The 362nd Tokyo Society

   Universityof Tokyo

   September21, 1957

Fumiyuゐj Ishihara ; A Case of Unilateral

  Pringle゛s Disease。

   The patient was a 23-year-old woman, who

had typical lesions of Pringle's disease on the

right side of the face alone. This was proved

to be the fourth case of unilaterally appeared

Pr ingle's disease reported in this country. ca-

nicai and histological studies on Pringle's dis-

ease referring to literatures have also been

done.and several diagnostically important facts

were pointed out.        ∧

S力inichiルlitsuhashiand YoshiWsoYamazaii: A

  Case of Urticaria Caused by Ingestion of

  Flour。

   The patient is a 55-year-old man. who de-

velops lesions of urticaria when he takes food

containing wheat flour. in these 20 years. By

means of patch test and intracutaneous iniec-

tion using several kinds of flour, it was con-

eluded that the component, responsible for the

provocation of the disease, was g】uten.

KunioHanaiand Ma加加 Waianabe: Venereal

  Diseases fro皿the standpoint of Public

  Health Center.

lUuroOtaand UdtaKato:A Case of Throm-

  boangitis Obliterans.           `

   The patient was a man, 42 years of age,

who complained of cold sensation and dullness

in the extremities, and was lame in the right

leg. The pulsation of the right posterior tibial

artery. dorsal artery of the right foot. and right

brachial artery were faint or not perceptible.

however, no necrotic lesions were observed on

the skin. Biopsy of the right posterior tibial

artery showed thromboangitis. Etiological factors

in this case seemed to be the habit of smoking

and syphilis.

Araia Maisui and TanefitroSatio: Enzymatic

 Debridement by Local Applicaation of

 Trypsilin stick。

   The effect of Trypsilin Stick (prepared by

Mochida Seiyaku Co.), consists chiefly of poly-

ethylene glycol containing 10,000 units of trypsin

per cc, was studied both chemically and clin-

ically。It was found that the effect of Trypsilin

Stick lasted for a longer time than trypsin

powder. Proteolytic action of Trypsilin Stick

on egg albumin. casein, and gelatin were also

demonstrated experimentally. When inserted

into the wounds of acute pyoderma and ulcer,

it facilitated markedly the debridement of

necrotic lesions and the secretion of pus.

Noboru Isfttz≪fei and Kazuzo Satoご Studies on

 Chrome Dermatitis。

   Six patients with contact dermatitis due

to chrome were observed. Three of them were

printers and the other three were dye workers.

all having subacute eczematous dermatitis on

the exposed area. such as hands. forearms

and face. Positive patch test was observed in

printers゛group with ammonium bichromate

and in dye workers with sodium bichromate.

Discussion:(rtichiro Harada:l have often Ob-

served similar cases of contact dermatitis in

printers. For the detection of the etiological

factor in these cases. l believe the series of

patch test using various kinds of chromates are

the most valuable, because bichromate is the

very irritating substance in itself.

Kihei Taniofeu, Ryuzo Maisuyama,YoswMfeo Saida。

 YMfetO Nis恒常mra.Kozwhiro Tsurumi and Afejo

 Kaw心μ揖i: studies on Skin Metabolism

 (Fifth Report)。

   The changes of the contents of Sodium,

Potassium, Calcium, Magnesium, Glucose,

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Glycogen, Vitamin C,Vitamin B2,Biotin, Panto-

thenic Acid, Niacin and Cholinesterase in the

skin of rabbits. irradiated with infra-red rays,

were studied. The irradiation was carried out

for five minutes on the clipped skin of one side of

the back, and the other side was used as the

control. Lamp skin distance is about 12 cm.

The measurements were performed at inter-

vals of o min., 1 hr., 2 hrs., 3 hrs., 5 hrs.,

8 hrs., 12 hrs., and 24 hrs. after the irradia-

tion. The changes of their contents in the

skin were observed at period from o min. to

12 hrs. after the irradiation. These observa-

tions were different from the experiments in

which the ultraviolet irradiation on the rabbit-

-skin was employed.

Discussion: TatsuroMasw竹lizM:l should like to

ask you that what a different reaction between

an ultraviolet and infra-red irradiation on the

small vessels of the skin could be observed?

J?yMzoMafSMyama:Theinfluences of ultraviolet

and infra・red irradiation on the blood vessels

have been uncertain・, but l would say that the

infra-red rays reach the deeper tissue of the

・skin, the heat ray of infra・red irradiations

causes the reaction more earlier and the reac-

tion subsides more faster than the ultraviolet

irradiation.

AlsushiKuhita:studies on Melanin Formation。

  with Special Reference to Tyrosinase

  Activity of Hair Melanocytes。

   The tyrosinase activity of hair melanocytes

in the various colored human hairs (black.

red, grey and hairaof albino) and in the chick-

embryos of three different breeds (White Leg-

horn, Rhode Island Red and Black Australorp)

was determined with an autoradiographic tech-

nic using radioactive C14 tagged tyrosine pre・

viously described (Science, 121, 893, 1955; J.

Invest. Dermat・, 26, 173, 1956). Active tyrosin-

ase activity was detected in melanocytes in

black, red and blond hairs. The degree of the

activity was found to be high in the following

descending order: blond hair, red hair and

black hair. No tyrosinase activity was detected

in melanocytes in the grey hair and hair in

albino. In the chick-embryos. no tyrosinase

activity was detected in the melanocytes of the

feather daring the embryonal development of

White Leghorn, but dopa-oxydase activity was

found in melanocytes at the limited period of

the embryonal life (11 day to 15 day). Both

tyrosinase and dopa oxydase were detected at

the limited period of the embryonal life (10

day t0 14 day) in the embryos of Rhode

Island Red and Black Australorp, however, the

activities were not detected in the successive

embryonal life.

Tosfitwfei FunabasM andSadahiko Haれat:A Case

 of Acanthosis Nigricans。

   A 57-year-old male having acanthosis nigri-

cans with no evidence of associated malignancy

was reported. The study on pathogenesis of

this case will appear elsewhere.

R泌垣 Koiima and His(IShi Nishidn: Small

 Nodular Lesions on the Skin。

   Six cases with small nodular lesions were

reported. All cases were examined histologi-

cally, and their diagnoses were as follows :

granuloma having necrosis, thrombosis, epi-

thelial cyst, lesion resembling calcifying epi-

thelioma, granuloma pyogenicum, and capsulat-

ed neurofibroma.

尺anehiko Kiiamu?72: The Eleventh International

 Congress of Dermatology。

 See this journal, 67 : 723. 1957.

    Demonstration of Clinical Cases

Melanoleucoderma and Poliosis observed in

 Carbon Binder Worker (Yamaiiashi Kenritsu

 Hospital)。

   This patient,carbon. binder worker, was a

38-year-old male, who had adiffuseredness and

fever-sensation on the upper part of the chest

and the back of the feet on the firstday of his

employment. On the neχtday. the lamellar

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desquamation and depigmented lesions were

noticed on the upper part of the chest and

back of the feet. Four or five days after that,

numerous freckle-like pigmented spots appeared

in the depigmented lesions, and the lanugos

on the lesions, hairs on the scalp, mustache

and eyelashes started to grey・

Discussion: Koicht Nishida-. l have observed

different kinds of pigmentary disorder in the

other workers of the same factory.

Basal Cell Epithelioma treated with Purified

 Vaccine Lymph (Yokohama City University).

   A patient, 38-year-old woman, was given

local injection of P.V.L・,1 cc a day, for 18

days. The necrosis of the tumor was noted

two days after the treatment was started.

and subsequently the size of the tumor was

reduced.

Discussion: YoihikuniNogwchi; The principle

of this treatment is thought to be due to the

epidermotropic action of small pox virus, and

also the excellent results have been obtained

in the treatment of verruca with the same

mode of P.V.L. administration.

Lichen Pig皿entosus (Yokohama City Univer-

 sity).

   A 45-year-old male has had pigmented

pruritic eruptions on the lateral surface of the

neck, forearms and back of the feet of two

years' duration. Recently the pigmentation of

the lesion hds increased. Histopathologic exam-

ination: Although there was a band-like infiltra-

tion of round cells in the upper part of the

corium in the specimen taken from the dorsum

of the feet, no diagnostic characteristics of

lichen planus were found in the lesion of the

side ・of the neck.

Discussion: KαれehifeoKUa俳話ra:l have observ-

ed frequently the cases of lichen pigmentosus

which have no diagnostic characterstics in the

histological examination like those of Riehl's

melanosis.

Case for Diagnosis (Yokohama City Univer-

sity).

   A 15-year-old girl has had a well-demar-

cated, elevated, erythematous lesion on the left

cheek for siχ months. The redness of the

lesion is increased by the exposure to the sun.

Biopsy was performed, and showed atrophy of

the epidermis, homogenization of the collagen

and loss of the elastic fibers.

Discussion:尺挽≪! Tanioku: l think this patient

has dermatitis atrophicans maculosa idiopa-

thica. KaiashxYo恥部■mo'.l would agree with Dr.

Tanioku゛s opinion. I think the lesion shows

atrophy of the skin clinically, which helps

establish this diagnosis.

Urticaria Pigmentosa in Adult (Branch Hos-

pital, University of Tokyo)。

   A 17-year-old woman has had numerous

flat pigmented spots on the chest. and lower

extremities for several months. Recently the

number of the lesions has been increasing。

however, her subjective symptoms are slight・

Blood examination for syphilis was positive.

Histological examination revealed small num-

bers of mast cells (Rona type)・

Connective Tissue Nevus (Tokyo Medicodental

 University)。

   A 22-year-old woman first noticed milium一一

to rice-sized, white, soft papules distributed

on her breasts, upper abdomen, back and

lumbar region two and a half years ago. NO・

subjective symptoms are complained. Micro-

scopically, the lesion showed swelling and

diminution of the elastic fibres.

Discussion: KoMefiifeoKi拠単瓦ya: l wonder if

the course of two and a half years is enough

to diagnose this lesion as a nevus. Giicfiiro=

Harada: l think this case is nevus tardus.

Case for Diagnosis (Juntendo University。

 Tokyo)。

   A 42-year-old woman suffered from caries.

of the femur two years ago. The present

lesion occurred as a hen-egg-sized induration

on the upper part of the left leg about one

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year ago. The lesion thereafter has spread

to the surrounding skin. At present time, the

lesion shows an ill-defined, firm, pigmented

macule covering the entire left leg. Histological

・examination revealed edema and perivascular

lymphocytic infiltration of the subpapillary

 layer, and proUferation and homogenization

・of the connective tissue in the corium.

Discussion: 召7,・aki Miyazaki: If it is a case

of vasculitis, the distribution of the lesion

should be arranged bilaterally・

A Case of Leucoderma (University of Tokyo)。

   A 17-year-oId girl has had greying of

eyelashes of two months' duration. and f0ll0V7-

ing the sea-bathing this summer, the we11-

demarcated, numerous depigmented spots appe-

ared mostly on the exposed regions, the fore-

head, cheeks, sternal region and extremities.

They vary in size from that of a rice-grain to

a hen-egg. and have irregular, round or oval.

and annular shape. In the lesions on the

forearms and lower legs. the spotty or reticular

normal skin is left which shows a monstrous

picture.

Porokeratosis Systematica (University of To-

  kyo)。

   This patient is a 26-year・old man. The

present skin lesions appeared shortly after his

birth. At present. there are numerous, irregular,

milium- to broad-bean-sized. pigmented lesions

scattered on the chest, the upper abdomen,

and on the flexor surface of the left upper

extremity. Some of them are confluent. form-

ing irregular plaques. The small lesions are

dark-purplish or brownish in hue, slightly

elevated with sharp demarcation. and the larger

lesions have elevated borders and depressed

centers, having normally colored skin or brow-

nish pigmentation. The lesions show linear

Con丘guration and tend to affect the left side of

the body rather than the right. Microscopic・

ally, the typical changes of porokeratosis

were observed in the epidermis.

Precancerosis (University of Tokyo)。

   Aman, aged 33, has had gradually develop-

ing lesions for 10 years. Extremities, espe-

cially forearms, eχtensor aspect of thighs. and

popliteal regions showed well-demarcated,

round, pale pinkish or dark brownish pea-

to coin-sized, slightly scaly lesions. Histology

showed some anaplastic cells in the epidermis.

but no clumping cells.

Discussion:KatasW Yokoyama; Wehave experi-

enced a case of Bowen's disease with multiple

lesions, which had been diagnosed clinically as

psoriasis. I believe the case presented here

is essentially the same as ours.

Parapsoriasis en Plaques (University of To-

  kyo)。

   A girl, aged 15, has had the present con-

d皿on for 4 years. Coin- to palm-sized erythema

with pityriasic scales scattered on both thighs

and on the trunk。 Not pruritic. Histological

findings: Hyperkeratosis, destruction of the ba-

sal layer, exocytosia at the lower part of the

epidermis, spongiosis of the slight degree in the

prickle layer. and perivascular lymphocytic in・

filtration in the corium.

Weber-Christian's Disease (Hitachi Hospital)。

   A woman, aged 54, developed the edematous

erythematous swelling on the face in winter,

15 years ago, which resulted in the formation

of the marked depression of the skin after-

wards. In fall 1956, she suffered from vertigo,

and palpitation, and at the same time subcuta-

neous nodular lesions appeared on both shoulders

which gradually extended to chest and upper

arms. The center of the lesions again became

depressed progressively. She was afebrile dur-

ing the course of the disease. Panniculitis is

a predominant feature histologically・

Discussion: Hitoshi 召''atano: Among various

types of idiopathic lipogranulomas, Rothman-

Makai゛s syndrome is thought to be a favorite

diagnosis because of the absence of marked

general symptoms such as high fever.

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Sqamous Cell Carcino皿a of the Lip (Nippon

 University)。

   A 65-year・old man. 3 years d゙uration. Mi-

liary to bean-sized papules with rough surfaces

were grouped on the right half of the lower

lip, forming a papillomatous, hard, tender no-

dule. Submandibular and submental lymph

nodes were swollen. Histologically, nests of

tumor cells with dark-staining atypical nuclei

were found.

Case for Diagnosis (Poikiloderma Atrophi。

 cans Vasculare?) (Nippon University)。

   A60-year-old man had developed labial and

perioral pigmentation after the topical applica-

tion of an ointment for probable cheilitis.

Later, pruritic erythema a耳d pigmentation had

appeared on the flexor surface of arms and

thighs. Clinical features when the patient was

presented were violaceous pigmentation of the

face, telangiectasis,pigmentation, and atrophy

on the trunk and extremities. Histology:

The epidermis is atrophic. Narrow zones of

pigmentation and depigmentation are observed

in the basal layer. Subepidermal band-like

infiltrationare also found in some parts of the

cutis.

Xantho皿a Disse皿Inatuin (Okubo Hospital, To-

 kyo).

   A 14-year-old boy has had the lesions on

axillae for l year, which gradually increased

in number and became generalized. Thirst

and polyuria were observed. Yellowish brown

papules, with size of a pin-head to a grain of

rice, are located on the face. head, neck, trunk.

genitalia, and thighs. Some of the papules

tend to coalesce forming pea-sized lesions. Con-

sistency is elastic firm. Total cholesterol in

serum: 173 mg/dl. Specific gravity of urine :

1,001. The lesion was found to be typical

xanthoma histologically・

Squamous Cell Carcinoma and Cutaneous Horn

 (OkuboHospital, Tokyo).

 Coincidental occurrence of both dermatoses

in a 79-year-oia man.

Familial Benign Chronic Pemphigus? (Kanto

 Teishin Hospital, Tokyo).

Alopecia Areata, Vitiligo and Arsenical Me-

 lanosis (Kanto Teishin Hospital, Tokyo).

Lupus Erythematosus Discoides Chronicus

 (Kanto Teishin Hospital, Tokyo).