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小兒 腹壁遠心性 脂肪萎縮症 1例 A Case of Lipodystrophia Centrifugalis Abdominalis Infantilis

대한피부과학회지 1975년 13권 2호 p.151 ~ 158
李康雨, 趙伯紀, 許沅,
소속 상세정보
李康雨 (  ) 
가톨릭醫科大學 皮膚科學敎室

趙伯紀 (  ) 
가톨릭醫科大學 皮膚科學敎室
許沅 (  ) 
가톨릭醫科大學 皮膚科學敎室

Abstract


Lipodystrophia centrifugalis abdominalis infantilis(LCAI), an atypical form of progressive lipodystrophy, is a disease named by Imamura et al in 1971, and reported a few cases in Japan. We report a case who has been diagnosed as LCAI.
The patient is 5 and half year old boy. He had 2cm by 7cm sized, linear depressed lesion with surrounding erythema on the right inguinal region which was noticed 5 months prior to first diagnosis. There was no family history, no physical abnormality. except skin lesion.
Complete blood cell count, urinalysis, stool examination, liver function test and chest X-ray were within normal limit. Biopsy specimens from the depressed lesion and surrounding erythematous area revealed slight atrophy of the epidermis, a mild lymphocyte infiltration around the vessels and eccrine glands in the upper part of dermis, markedly decreased amount of subcutaneous adipose tissue with mild lymphocyte infiltration in depressed area and marked lymphocyte infiltration, intermingled with histiocyte in surrounding erythematous area, but normal amount of adipose tissue.

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