进行性对称性红斑角化症伴肾病综合征：巧合还是新的关联？

Progressive symmetric erythrokeratoderma with nephrotic syndrome: Coincidence or new association?

作者信息

Sacchidanand S, Sahana M S, Kamoji Sushruth G, Asha G S

机构信息

Department of Dermatology, STD and Leprosy, Bangalore Medical College and Research Institute, Bangalore, Karnataka, India.

出版信息

Indian Dermatol Online J. 2013 Oct;4(4):347-9. doi: 10.4103/2229-5178.120680.

DOI:10.4103/2229-5178.120680

PMID:24350023

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3853908/

Abstract

Progressive symmetric erythrokeratoderma (PSEK) is a rare genodermatosis with variable inheritance. It is characterized by symmetrical, erythematous, and hyperkeratotic plaques on the extremities. We report a case of a 15-year-old boy with PSEK of autosomal recessive inheritance associated with nephrotic syndrome.

摘要

进行性对称性红斑角化症（PSEK）是一种罕见的遗传性皮肤病，遗传方式多样。其特征为四肢出现对称性、红斑性及角化过度的斑块。我们报告一例15岁男孩，患有常染色体隐性遗传的进行性对称性红斑角化症，并伴有肾病综合征。