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박의수(Eui Soo Park),이원석(Won Seok Lee),송준영(Joon Young Song) 대한피부과학회 1989 대한피부과학회지 Vol.27 No.5
Benign symmetric lipomatosis is characterized by massive symmetric fat deposition, predominantly in the neck and shoulder girdle ares. We present a case of benign symmetric lipomatosis with alcoholic liver cirrhosis in a 54-year-old man. About two years ago, solitary skin-colored, non-tender swelling on the right upper arm was developed. The lesion had been aggravsted abruptly and rapidly in size and distribution since about one month ago. Histopathologic findings showed completely replaced reticular dermis and invaded subcutaneous tissue by mature fat cells.
김석주,이원석,박의수,이규석,송준영 啓明大學校 醫科大學 1989 계명의대학술지 Vol.8 No.2
Statistical observation was made on 936 patients who had been referred to the Department of Dermatology during hospitalization in Keimyung Universty School of Medicine Dongsan Hospital from September 1986 to August 1989. The results were as follows: The consulted patients were 936 among 57,524 inpatients(1.6%). The most frequent age group was 3rd decaed and the highest incidence of seasonal distribution was summer. The ratio of the departmental consulted patients to the departmental inpatients was the most highest in Neurosurgery. The most common 5 dermatoses were eczema gruop, drug eruption, fungal infection, viral infection, skin manifestations of systemic diseases. The frequrent causes of consultation were as follows: the dermatologic diseases or conditions 57.3%, the diseases related to the treatment 20.1%, the skin lesions of systemic diseases 10.8%, the dermatologic tests 3.4%, and admitted to other departments with dermatologic diseases 2.1%, resectively.
이원석,송준영,김용대,박의수 啓明大學校 醫科大學 1988 계명의대학술지 Vol.7 No.2
We report a case of lupus erythematosus profundus in a 16-year old male. He had multiple pea-nut to bean sized subcutaneous nodules with dark brownish colored overlying skin was present on the upper arm, trunk & other systemic disease. Histologically, deep dermis & subcutaneous layer had dense patch lymphocytic infiltration and homogenized hyaline fat necrosis. Direct immunofluorescene studies showed IgM and C?? deposit on the vessel wall. We treated him with chloroquine and corticosteroid.
송준영,박의수,이원석,김석주 啓明大學校 醫科大學 1990 계명의대학술지 Vol.9 No.3
We report a case of twenty-nail dystrophy accompanied by alopecia universalis in a 45-year old woman. She had developed dystrophic nail changes on her all finger and toe nails for 26 years and alopecia universalis for 10 years. On examination, 20 nails were affectedwith opalescent, thickening, longitudinal ridging, and total hair loss were in scalp, eyebrow, axilla, and pubic area. Mycologic study of involved nails was performed, but negative results were obtained. Histologic findings of dystrophic nails revealed prominent hyperkeratosis, acanthosis, and mild infiltration of mononucler cells in the upper dermis. The histologic findings of scalp showed a few atrophic hair follicle, thining of epidermis, and slightly hyperkeratosis. All of these clinical and histologic findings were considered as twenty-nail dystrophy accompanied by alopecia universalis. She was treated with intralesional injection of triamcinolone acetonide and topical application of dinitrochlorobenzene, but no significant improvement was made. The further observation is being conducted.
Cutis Marmorata Telangiectatica Congenita 의 1예
김용대,송준영,이원석,박의수 啓明大學校 醫科大學 1988 계명의대학술지 Vol.7 No.2
Cutis marmorata telangiectatica congenita is a rare congenital vascular anomaly, characterized by congenital cutis maromrata, phlebectasia, opider nevi, ulceration, and in most instances, steady improvement from birth. We report a case of cutis marmorata telangiectatica congenita in 3-month-old boy who has developed localized, dark red reticulated mottling with shiny atrophic scars on the inner side of the left leg. Diagnosis was confirmed by clinical and histopathologic features.
송준영,박의수,이원석,최윤애 啓明大學校 醫科大學 1990 계명의대학술지 Vol.9 No.3
Acute febrile neutrophilic dermatosis, which was introduced to the dermatologic literature by Sweet in 1964, is characterized by persistent higt fever and preceding upper respiratory infection like symptom, polymorphonuclear leukocytosis in the peripheral blood, raised painful plaque on the face, neck and limbs, histologically a dense dermal infilteration with polymorphonuclear leukocytosis, dramatic reponse to corticosteroids, and the absence of scarring. A 41 year-old female who had suffered from malaise, arthragia, upper respiratory tract infection like symptoms one month before the each episode of the cutaneous manifestation. Erythematous, well demarcated, slight scaly plaque appeared on the face with tendency of recurrences. Histologically a dense inflammatory cell infilteration, composed predominantly of polymorphonuclear leukocyte, lymphocytes and histiocytes were seen in dermis. The skin lesion and general symptoms were well controlled with orally administered corticosteroid.