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A congenital case of circumscribed acral hypokeratosis.

机译:一例先天性外接性角化不全。

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摘要

Circumscribed acral hypokeratosis is a disorder characterized by areas of erythematous depressed skin with distinct histopathological findings typically found on the palmar and plantar surfaces. Most patients are middle-aged women who report a multiyear history. We present an 10-year-old African American boy who had an asymptomatic, irregularly shaped erythematous lesion on his left medial foot that had been present since birth. A biopsy showed an abrupt, well-demarcated decrease in the thickness of the stratum corneum layer, with no parakeratosis, that was consistent with a diagnosis of circumscribed hypokeratosis. This represents the first pediatric and congenital case of circumscribed hypokeratosis reported. We review the literature and discuss the ramifications of a congenital case on understanding the etiology of circumscribed hypokeratosis.
机译:周围性肢端性角化病是一种以皮肤红斑凹陷为特征的疾病,通常在手掌和足底表面发现明显的组织病理学发现。大多数患者是中年妇女,有多年病史。我们介绍了一个10岁的非洲裔美国男孩,他的左内侧脚有无症状,形状不规则的红斑病变,此病变自出生以来就一直存在。活检显示,角质层厚度突然减少,界限清楚,无角化不全,这与确诊为角化不全的角质病相符。这是报道的首例小儿和先天性角化不全的病例。我们回顾了文献,讨论了先天性病例对了解外切性角化病病因的影响。

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