1.A Case of Hyperkeratosis of the Nipple and Areola Aggravated During Pregnancy.
Sun Young MOON ; Joo Heung LEE ; Seung Chull LEE
Korean Journal of Dermatology 1994;32(6):1111-1113
We report a case of hyperkeratosis of the nipple and areola occuing in 33 year old woman. She did not have a history of endocriruipathy, horrnonal therapy and other ceatoses, so this case seems to be the nevoid form by Levy-Franckel classification. Interestingly, however the lesion which had developed before marriage suddenly aggr avated during pregnancy. This may be a unique feature which has not been reported elsewhere. Histapathologic findings are compatible with breviously reported eases. There was no response to topical steroid and retinoic acid treatrnent.
Adult
;
Classification
;
Female
;
Humans
;
Marriage
;
Nipples*
;
Pregnancy*
;
Tretinoin
2.Clinical Study on Psoriasis.
Jai Il YOUN ; Joo Heung REE ; Yoo Shin LEE
Korean Journal of Dermatology 1988;26(6):839-845
In study of 360 psoriatic patients between June 1982 and May 1987 in Seoul National University Hospital, psoriasis was classified according to the severity based on the extent of involvement. The guideline of the extent of involvement was as follows, 1) mi1d less than 5% involvement of whole surface area 2) moderate : 5% 30% involvement of whole surface area 3) severe: over 30% involvement of whole surface area This study was done to evaluate the distribution and clinical features of psoriasis according to the extent, of involvement. Among 360 psoriatics, 180(50.0%) patients had mild psoriasis, 140(38.9%) patients had moderate psoriasis and 40(11.1%) patients presented as severe psoriasis. The duration of psoriasis seemed longer in moderate and severe groups than in mild group but the difference was not signifcant. There was also a tendency that patients developing psoriasis before the age of 20 were more prevalent in severe group.
Humans
;
Psoriasis*
;
Seoul
3.Hyalinosis Cutis et Mucosae: Report of 4 Cases.
Joo Heung REE ; Kyung Chan PARK ; Yoo Shin LEE
Korean Journal of Dermatology 1989;27(6):741-747
We report four cases of hyalinosis cutis et mucosae. They developed hosrseness in their infancy and all had past history of frequent skin infections with accompanying varioliform scars. On physical examination, all the patients had beaded papules along their eyelid margins, hoarseness, varioliform scars and various skin and mucous membrane infiltrations. Pathologic examinations performed on skin infiltrations and eyelid papules revealed diastase resistant periodic acid Schiff positive materials deposited mainly in upper dermis. We have given three of four patients 1g/day of dimethyl sulphoxide from 6 to 12 months with no significant side effects nor remarkable clinical improvement.
Amylases
;
Cicatrix
;
Dermis
;
Dimethyl Sulfoxide
;
Eyelids
;
Hoarseness
;
Humans
;
Lipoid Proteinosis of Urbach and Wiethe*
;
Mucous Membrane
;
Periodic Acid
;
Physical Examination
;
Skin
4.Three Cases of Giant Hydronephrosis.
Yong Joo KIM ; Yeng Sik YOON ; Yun Heung LEE
Korean Journal of Urology 1969;10(4):191-195
Three cases of giant hydronephrosis containing 9,800 cc, 3,800cc, and 1,300cc, Developed in the Korean soldiers are presented. The important clinical, laboratory and x-ray features are discussed. Brief review of literature was also made.
Humans
;
Hydronephrosis*
;
Military Personnel
5.A Case of Papillary Eccrine Adenoma.
Sung Pil YOON ; Seong Hun LEE ; Joo Heung LEE ; Seung Chul LEE ; Joon Mee KIM
Annals of Dermatology 1997;9(2):163-166
Papillary eccrine adenoma is a rare sweat gland tumor with a characteristic histopathological appearance and has a benign clinical course. Five cases were reported in Korea since a report by Song et al. in 1988. We report a case of papillary eccrine adenoma in a 38-year-old male who had a firm, dark brown nodule on the medial surface of the left thigh. Microscopically, the tumor was composed of multiple dilated ducts lined by two or more layers of epithelial cells and the luminal cells showed papillary projections into the lumen in some tubules. Immunoperoxidase staining was positive for CEA, S-100, and EMA. We excised the lesion completely and no evidence of recurrence was observed for 6 months.
Adenoma*
;
Adult
;
Epithelial Cells
;
Humans
;
Korea
;
Male
;
Music
;
Phenobarbital
;
Recurrence
;
Sweat Glands
;
Thigh
6.Interleukin-4 as a New Index of Disease Severity in Atopic Dermatitis.
Seong Hun LEE ; Joo Heung LEE ; Seung Chul LEE ; Young Keun KIM
Korean Journal of Dermatology 1998;36(1):95-102
BACKGROUND: Interleukin-4(IL-4) from the Th2 subset of lymphocytes has been known to have a key role in the pathogenesis of atopic dermatitis. Blood levels of IgE, often reflecting the severity of allergic diseases, are not always elevated in patients with atopic dermatitis due to its homocytotrophic characteristics. OBJECTIVE: We propose that IL-4 can substitute or at least complement the role of IgE as an index of disease severity of atopic dermatitis. METHODS: Eleven patients with atopic dermatitis and five normal controls were included in this study. Before treatment, we evaluated the clinical severity of atopic dermatitis by the method described elsewhere with some modification which employed extent, duration, and intensity of skin lesions. Based on this criteria, we divided patients into 'severe and mild groups. With blood samples drawn from patients and normal controls, we measured IL-4 and IgE values. After a treatment period of I to 2 months, when all of the patients became free of symptoms and signs of atopic dermatitis, patients in each group were re-evaluated for ehanges of IL-4 and IgE values. IL-4 values were determined with a Predicata human interleukin-4 kit from Genzyme diagnostics (Predicta IL-4 kit) and ELISA reader (CRES UV900, Biotek). IgE values were measured .with IMx total IgE assay system from Abott laboratories (model 8389-0). RESULTS: l. Of eleven patients, six were mild and five were severe in clinical severity. 2. IL-4 levels were decreased from the pre-treatment average value of 57.149+/- 40.079 pg/ml to a post-treatment average value of 32.072+/- 16.912 pg/ml (p<0.05) which was similar to average normal control value, 36.690+/- 24.451 pg/ml. 3. IgE levels were similarly decreased from an average value of 230.2 86.4 IU/ml before treatment to one of 171.S+/-79.4 IU/ml after treatment (p<0.05). 4. This tendency of post-treatment lowering of values became more apparent in severe groups (p<0.05) but less obvious in mild groups both in terms of IL-4 and IgE (p>0.1). CONCLUSION: We conclude that IL-4 is not only involved in the pathogenesis but can also be used as a main index of disease severity in atopic dermatitis especially when the clinical severity is more than mild.
Complement System Proteins
;
Dermatitis, Atopic*
;
Enzyme-Linked Immunosorbent Assay
;
Humans
;
Immunoglobulin E
;
Interleukin-4*
;
Lymphocytes
;
Skin
7.A Case of Eosinophilic Pustular Folliculitis (Ofuji's Disease) in a Newborn.
Eil Soo LEE ; Nark Kyoung RHO ; Suk Jin CHOI ; Joo Heung LEE ; Eil Soo LEE
Annals of Dermatology 2002;14(2):117-120
We describe a case of eosinophilic pustular folliculitis in a 1-month-old Korean male infant. The patient was suffering from erythematous papules and pustules affecting the scalp, trunk, and extremities, detected at birth. The flare was accompanied by leukocytosis and eosinophila. Histopathology revealed folliculitis with a predominant eosinophilic infiltrate. Lesions showed partial response to topical steroid and disappeared in four weeks. Three months after the resolution of the lesions, he presented a similar clinical picture as the previous episode.
Eosinophils*
;
Extremities
;
Folliculitis*
;
Humans
;
Infant
;
Infant, Newborn*
;
Leukocytosis
;
Male
;
Parturition
;
Scalp
8.A Case of Cryptococcosis with Cutaneous Manifestation.
Seong Hun LEE ; Sun Young MOON ; Joo Heung LEE ; Seung Chul LEE ; Young KIM
Korean Journal of Dermatology 1995;33(5):935-939
Cryptococcosis is a disease caused by the Cryptococcus neoformans, occcuring most frequently in immunocompromised hosts. Cutaneous involvement is seen in 10-15 % of disseminated cases and its manifestation is variable. A 52 year old man presented with a subcutaneous neck mass and severe headache which had lasted for 2 months and 1 month respectively. Initially cutaneous involvement was monomorphic and localized and a CSF study failed to reveal any organisms. After several weeks of herb medication, however, multiple skin lesions occurred with varied morphology and a CSF study confirmed cryptococcosis by culture. The Urine cortisol was markedly elevated, suggesting an exogenous intake of steroid.
Cryptococcosis*
;
Cryptococcus neoformans
;
Headache
;
Humans
;
Hydrocortisone
;
Immunocompromised Host
;
Middle Aged
;
Neck
;
Skin
9.A case of erythropoietic protoporphyria.
Ha Wook BONG ; Joo Heung LEE ; Yoo Shin LEE ; Jung Ho KIM
Korean Journal of Dermatology 1993;31(5):817-822
Erythropoietic protoporphyria, sometimes also called erythrohepitic protoporphyria or simple protoporphyria, is a heritable detect of heme synthesis in which the last enzyme of the heme synthetic pathway, ferrochelatase(or heme synthetase), is functioning subopt,imally. A 23-year-old male has experi nced erythema and edema on the fae and hands during or immediately after sun exposure, since 3 years of age. The skin lesions have been accompanied by severe itching, a buring sensation and pain. Severe episodes were followed hy head iche and vomiting. We have seen a case of erythropoietic protoporphyria presenting clinically and histo athologically, wit.h a skin lesion on the sun exposured area, and free erthrocyte protoporphyrin serologically.
Edema
;
Erythema
;
Hand
;
Head
;
Heme
;
Humans
;
Male
;
Protoporphyria, Erythropoietic*
;
Pruritus
;
Sensation
;
Skin
;
Solar System
;
Vomiting
;
Young Adult
10.A Case of Dermatomyofibroma in a 2-year-old Boy.
Soo Hong KIM ; Jeong Joon OH ; Joo Heung LEE ; Eil Soo LEE
Annals of Dermatology 2003;15(2):68-70
Dermatomyofibroma is a rare benign dermal tumor, mainly found in young women. Clinically it can be confused with keloid or dermatofibrosarcoma protuberans. Typical histopathologic features of dermatomyofibroma are sufficiently distinctive to alert histopathologists to consider dermatomyofibroma in the diagnostic process. We report a case of dermatomyofibroma, presenting as reddish plaques and nodules on the buttock of a 2-year-old boy. Histopathologic examination showed fascicles of uniform spindle cells in the reticular dermis, predominantly oriented parallel to the epidermal surface. Immunohistochemical study and electron microscopy confirmed its myofibroblastic nature.
Buttocks
;
Child
;
Child, Preschool*
;
Dermatofibrosarcoma
;
Dermis
;
Female
;
Humans
;
Keloid
;
Male*
;
Microscopy, Electron
;
Myofibroblasts