Vakilzadeh F, Rose I
Hautklinik, Städtíschen Krankenhaus GmbH, Hildesheim.
Hautarzt. 1991 Oct;42(10):634-7.
An unusual type of erythrokeratodermia in an 11-year-old boy is presented. It can be distinguished from the well-known classic types of erythrokeratodermia by clinical criteria, such as the persisting, very slowly migrating, annular lesions, and also by immunohistochemical and ultrastructural findings. In view of the distinct clinical features of this new genodermatosis, the term erythrokeratodermia annularis migrans is proposed.
本文报告了一名11岁男孩患有一种罕见类型的红斑角化病。它可以通过临床标准，如持续存在、迁移非常缓慢的环形皮损，以及免疫组织化学和超微结构检查结果，与众所周知的经典类型的红斑角化病相鉴别。鉴于这种新的遗传性皮肤病的独特临床特征，建议使用“移行性环状红斑角化病”这一术语。
