进行性对称性红斑角化症：一家系报告。

Progressive symmetric erythrokeratoderma: report of a Chinese family.

机构信息

Department of Dermatology, Wuhan General Hospital of Guangzhou Command, and Biological Research Center of Huazhong University of Science and Technology, Wuhan, China.

出版信息

Indian J Dermatol Venereol Leprol. 2011 Sep-Oct;77(5):597-600. doi: 10.4103/0378-6323.84070.

DOI:10.4103/0378-6323.84070

PMID:21860161

Abstract

A large pedigree of progressive symmetric erythrokeratoderma is reported. The proband was a 22-year-old male with generalized asymptomatic lesions characterized by symmetrical well-demarcated erythematous hyperkeratotic plaques mainly distributed on the extremities. The proband's parents were also affected, and they were first cousins. Thus, a case of familial progressive symmetric erythrokeratoderma is described.

摘要

现报道一个进行性对称性红斑角化病的大型家系。先证者为 22 岁男性，全身无症状皮损，表现为对称性边界清楚的红斑角化性斑块，主要分布于四肢。先证者父母也受影响，他们是表亲。因此，描述了一个家族性进行性对称性红斑角化病病例。