兄妹同患残毁性掌跖角皮症  

Mutilating Palmoplantar Keratoderma (Vohwinkel syndrome) in Two Siblings

作　　者：杜红霞[1] 邹勇莉[1] 郑博文[1] 柴艳杰[1] 

机构地区：[1]昆明医学院第一附属医院皮肤科,云南昆明650032

出　　处：《中国皮肤性病学杂志》2010年第2期162-163,共2页The Chinese Journal of Dermatovenereology

摘　　要：患者男,27岁。掌跖红斑角化20余年,指、趾可见纤维缩窄环,关节功能障碍12年;其妹症状相似。均诊断为残毁性掌跖角。The patient, 27 aged, presented to our hospital with erythema, hyperkeratosis on palms and soles for 20 years ;constricting fibrous bands on the digits and arthr-dysfunction for 12 years. His younger sister has similar symptom. The two siblings were diagnosed as keratoderma hereditarium mutilans .

关 键 词：掌跖角皮症残毁性 Vohwinkel综合征 

分 类 号：R739.5[医药卫生—肿瘤] R758.5[医药卫生—临床医学]