成人起病的格雷瑟氏病:罕见的两例报告

H. Khan, Ayesha Sharmeen, S. Amin, Bushra Siddiqui
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引用次数: 0

摘要

遗传性掌跖角化皮病(PPKs)在婴儿期晚期或儿童早期发病,并有积极的家族史。散发性病例和成年发病病例很少报告。我们描述了两例女性PPK变性和前变性,在成年期发病,具有格雷特病(GD)的临床和组织学特征。文献中仅报道过一例成人发病的GD。所有表现为掌跖角化病的患者都应该进行彻底的评估,因为它可能是一种迟发性遗传性疾病,它增加了迟发性ppk的症状范围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adult-Onset greither's disease: A rare report of two cases
Inherited palmoplantar keratodermas (PPKs) have onset in the late infancy or early childhood and have a positive family history. Sporadic cases and cases with onset in adulthood have been rarely reported. We describe two female cases with transgradiens and progradiens PPK, with onset in adulthood having clinical and histological features of Greither's disease (GD). Only a single report of adult-onset GD has been reported in the literature. All patients presenting with palmoplantar keratoderma should be thoroughly evaluated, as it may be a late-onset inherited disorder, it adds to the spectrum of conditions to presenting with PPKs of late-onset.
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