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播散性浅表性光化性汗孔角化症并发鳞状细胞癌1例 被引量:9

A Case of Disseminated Superficial Actinic Porokeratosis combined with Squamous Cell Carcinoma
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摘要 患者男,55岁。全身泛发环状丘疹,中央呈轻度萎缩,边缘呈堤状隆起的棕色皮损40年,3年前左踝部出现一菜花样增生,反复多次发生溃疡。左踝增生处皮损组织病理:表皮可见两个充满角蛋的凹陷及角化不全柱,下方颗粒层消失,棘层肥厚:真皮内大量鳞状细胞团块,小血管周围大量以淋巴细胞为主的单核细胞浸润。诊断:播散性浅表性光化性汗孔角化症;鳞状细胞癌。本病属常染色体显性遗传,有恶变倾向。 A case of disseminated superficial actinic porokeratosis combined with squamous cell carcinoma was reported. The patient, male, 55-year-old, presented with generalized annular brown dermal injure, characterized by light dermal atrophy in the centre with dam-like eminence around it, on his whole body for 40 years. There was a cauliflower-like proliferation and ulceration on his left ankle in the recent 3 years, which was diagnosed as disseminated superficial actinic porokeratosis combined with squamous cell carcinoma. Disseminated superficial actinic porokeratosis was an autosomal dominant disease and inclinable to be malignant.
作者 陈梅 王飞
出处 《中国皮肤性病学杂志》 CAS 北大核心 2009年第9期587-588,共2页 The Chinese Journal of Dermatovenereology
关键词 汗孔角化症 鳞状细胞癌 遗传 恶变 Porokeratosis Squamous cell rcinoma Heredity Cancer.
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参考文献3

  • 1WILLIAM D J,TIMOTHY G B,DIRK M E.安德鲁斯临床皮肤病学[M].北京:科学出版社,2008:595-596.
  • 2HAPPLE R.Cancer proneness of linear porokeratosis may be explained by allelic loss[J].Dermatology,1997,195(1):20-25.
  • 3MAGEE J W,MCCALMONT T H,LEBOIT P E.Overexpression of p53 tumor suppressor protein in porokeratosis[J].Arch Dermatol,1994,130(2):187-190.

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