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 .
出处
《中国皮肤性病学杂志》
CAS
北大核心
2010年第2期162-163,共2页
The Chinese Journal of Dermatovenereology
