海岸端角化弹性体病:零星病例报告

L. Ochoa, Melissa María Velilla Contreras, Jaime Avila Cárdenas, J. Ríos-Yuil
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引用次数: 0

摘要

哥斯达黎加的肢端角蛋白弹性样变性是一种罕见的常染色体显性遗传的遗传性皮肤病。它的特征是手和/或脚的边缘区存在多个角化性丘疹,主要出现在儿童和成年早期。它通常是无症状和慢性的。其与其他角化病的鉴别诊断对医生来说是一个挑战;然而,弹性变形的组织学发现使我们能够对其进行分类。我们提出一个散发病例的年轻女性患者,临床和组织病理学特征的典型疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acroqueratoelastoidosis de Costa: reporte de un caso esporádico
The acrokeratoelastoidosis of Costa is a rare genodermatosis of autosomal dominant inheritance with variable expressivity. It is characterized by the presence of multiple hyperkeratotic papules in the marginal zone of the hands and / or feet, which appears predominantly in childhood and early adulthood. It is generally asymptomatic and chronic. Its differential diagnosis from the rest of acrokeratodermias is a challenge for the physician; however, the histological finding of elastorhexis allows us to categorize it. We present a sporadic case of a young female patient, with clinical and histopathological characteristics typical of the disease.
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