汉森病的肢端角变性:一个新的认识

V. Shah, K. Rambhia, J. Mukhi, R. Singh
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摘要

acrokeratoelasteidosis (AKE)于1953年由Costa首次描述,其特征是小而坚硬的角化丘疹,沿手和脚的边缘呈中央脐状。它是一种掌足底边缘丘疹性角化病,需要与其他边缘丘疹性角化病鉴别。AKE可遗传或散发性,易感因素为过度日晒、多汗症和重复性创伤。我们在这里描述一个病例的AKE在麻风病患者可能继发于重复性慢性创伤由于感觉功能丧失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acrokeratoelastoidosis in hansen's disease: A new insight
Acrokeratoelastoidosis (AKE), first described by Costa in 1953, is characterized by small, firm, keratotic papules with central umbilication along the borders of the hands and feet. It is a type of palmoplantar marginal papular keratoderma and needs to be differentiated from other marginal papular keratodermas. AKE can be inherited or sporadic, with predisposing factors being excessive sun exposure, hyperhidrosis, and repetitive trauma. We here describe a case of AKE in a leprosy patient with probably secondary to repetitive chronic trauma due to loss of sensory function.
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