Patrizi A, Neri I, Di Lernia V, Varotti C
Department of Dermatology, University of Bologna, Italy.
Acta Derm Venereol. 1993 Dec;73(6):459-60. doi: 10.2340/0001555573459460.
Congenital symmetrical interdigital hyperkeratosis is a rare disorder described by Frei in 1923, characterized by localized hyperkeratosis of the interdigital spaces of the hands and feet. The authors report the case of a 7-year-old girl affected by this condition. The skin hyperkeratotic lesions appeared localized exclusively to the interdigital spaces of the hands. Histologic examination showed orthokeratotic hyperkeratosis, hypergranulosis and acanthosis. Keratolytics failed to improve the clinical picture.
先天性对称性指间角化过度症是一种由弗赖于1923年描述的罕见疾病,其特征为手足指间部位局限性角化过度。作者报告了一名患有这种疾病的7岁女孩的病例。皮肤角化过度性病变仅出现在手部指间部位。组织学检查显示为正角化性角化过度、颗粒层增厚和棘层肥厚。角质松解剂未能改善临床表现。