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米贝利型汗孔角化症伴毁形:病例报告

Porokeratosis of Mibelli with mutilation: a case report.

作者信息

Handjani Farhad, Shahbaz Shima, Aslani Fatemeh Sari, Gheisari Farshid, Mozaffarian Kamran, Kasraee Behrooz

机构信息

Department of Dermatology, Shiraz University of Medical Sciences, Iran.

出版信息

Cutis. 2010 Aug;86(2):77-80.

Abstract

Porokeratosis is a rare keratinization disorder of the skin characterized by annular plaques with an atrophic center surrounded by a raised keratotic wall that spreads centrifugally. We report a case of porokeratosis of Mibelli with mutilation. A 30-year-old woman presented with atrophic plaques on the index fingers of both hands with a keratotic ridge in some margins of the plaques. There was loss of the distal phalanx of the left index finger. In the right hand, shortening of the right distal phalanx and flexion contracture of the distal interphalangeal joint were noted in the index finger.

摘要

汗孔角化症是一种罕见的皮肤角化异常疾病,其特征为环形斑块,中央萎缩,周围有隆起的角化性边缘,并呈离心性扩散。我们报告一例伴有毁形的米贝利汗孔角化症病例。一名30岁女性,双手示指出现萎缩性斑块,部分斑块边缘有角化性嵴。左手示指远节指骨缺失。右手示指可见右远节指骨缩短及远侧指间关节屈曲挛缩。

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