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홍남수,임춘평 대한피부과학회 1977 大韓皮膚科學會誌 Vol.15 No.4
Xeroderma pigmentosum is a genodermatosis characterized by extreme sun sensitivity, photophobia, freckly hyperpigmentation, atrophy, telangiectases, keratoses and finally malignant degeneration of the skin. It is rare and prebobly inherrited as a recessive trait, Photosensitive cutaneous symptoms developed in complication with squamous cell ca is presented. A 20-year-old male were studied. Routine laboratory examinations were within normal limits including hemogram, urinalysis, blood urea nitrogen, serum creatinina, liver function tests(including bromsulphalaein excretion) and serum electrolytes, chest X-Ray. The histopathological picture showed characteristic xeroderma pigmentosum and squamous cell ca. Clinical, histopathological and biochemical features of this disease are also discussed.
乾癬治療를 爲한 副腎皮質 Hormone 長期間 使用으로 倂發된 醫因性 Cushing氏 症候群 治驗一例 報告
金又烈,林春平 順天鄕大學校 1977 의대논문집 Vol.2 No.-
A case of iatrogenic Cushing's syndrome in a 42-year-old male pntient was experienced. Physical findings revealed central obesity, moon face, Purplish striae in lower abdomen. The patient had a history of corticosteroid treatment for the management of psoriasis for several years. The diagnosis was confermed by patient's history, physical finding, biochemical and hormonal assay. On admission, the hormonal studies revealed as follows;urinary 17 Hydroxycortico steroidslevel was decreased to a range of 5㎎/day and urinary 17-ketosteroid level was within normal limit. After A.C.T.H. stimulation test, the urinary 17-hydroxycorticosteroid level was not elevated also. Our case was reported and the current literatures about cushing's syndrome wers reviewed