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一名儿科患者的遗传性棘状角化病:病例报告及文献综述

Hereditary Spiny Keratoderma in a Pediatric Patient: A Case Report and Literature Review.

作者信息

Erize Herrera Joyce Andrea, Pacheco Santiago Lexli Danae, Pérez Rojas Diego Olin, Guevara Sanginés Esther Guadalupe

机构信息

Dermatology, Institute for Social Security and Services for State Workers Regional Hospital "Lic. Adolfo Lopez Mateos", Mexico City, MEX.

Internal Medicine, Institute for Social Security and Services for State Workers Regional Hospital "Lic. Adolfo Lopez Mateos", Mexico City, MEX.

出版信息

Cureus. 2024 Nov 29;16(11):e74789. doi: 10.7759/cureus.74789. eCollection 2024 Nov.

Abstract

A 14-year-old male with disseminated superficial porokeratosis and a family history of the same lesions on his maternal side presented with spiny keratoderma. Spiny keratoderma is a dermatosis characterized by multiple punctate keratotic neoformations on the palms and soles. It is considered a rare disease, with fewer than 84 cases reported in the world medical literature to date.

摘要

一名14岁男性患有播散性浅表性汗孔角化症,其母系家族有相同皮损的病史,现出现棘状角化病。棘状角化病是一种皮肤病,其特征是手掌和脚底出现多个点状角化性新生物。它被认为是一种罕见疾病,迄今为止,世界医学文献报道的病例少于84例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1852/11683159/b3b0ed6ba958/cureus-0016-00000074789-i01.jpg

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