Guttate hypopigmentation in Darier disease: A rare presentation

Aradhana Rout, A. Pandey, Karthi Kishore
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引用次数: 0

Abstract

Darier disease (DD) is an autosomal dominant genodermatosis attributed to ATP2A2 gene mutation which encodes the sarco/endoplasmic reticulum Ca2+ATPase isoform 2. Due to variable gene expressivity, the clinical manifestations are often atypical and of varied severity. The classical feature of DD is the presence of firm yellowish brown flat to hyperkeratotic papules in a seborrheic distribution. Cobblestoning of oral mucosa and V shaped nicking of nails are also important associated findings of DD. Herein, we report a 35-year-old male patient with guttate leukoderma as a presenting feature of Darier disease with its clinical, histopathological, and dermoscopic findings.
达里尔病的齿状色素沉着:一种罕见的表现
达里尔病(Darier disease,DD)是一种常染色体显性遗传性皮肤病,由编码肌浆/内质网 Ca2+ATPase 同工酶 2 的 ATP2A2 基因突变引起。由于基因表达能力不同,临床表现往往不典型,严重程度也各异。DD 的典型特征是脂溢性分布的黄褐色扁平至角化过度的坚实丘疹。口腔粘膜糜烂和指甲 V 形抠破也是 DD 的重要相关表现。在此,我们报告了一名 35 岁男性患者的临床、组织病理学和皮肤镜检查结果。
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19
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27 weeks
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