格罗弗病:关于一过性和持续性棘层溶解性皮肤病的现代观点。

Ksenia Olegovna Chepushtanova, Alexandr V. Patrushev, Yuri Gennadievich Gorbunov, Irena Eduardovna Belousova
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引用次数: 0

摘要

格罗弗氏病是一种丘疹泡状瘙痒性皮肤病,其特征是病程短暂、持续或无症状。我们分析了1970年至2022年期间在PubMed和RSCI科学文献数据库中发现的文献。其中描述了格罗弗氏病的临床表现、可能的定位、病因以及该病的组织学和皮肤镜图像。根据文献资料,该病的发病可能与多种因素有关,包括日晒、妊娠、血液透析、化疗、出汗、多种皮肤病以及恶性肿瘤和器官移植史。也有人描述了这一过程的季节性。迄今为止,已描述了该病的 9 种组织学模式,其中最常见的是棘层溶解性角化不良。在本综述中,我们纳入了对格罗弗氏病患者的观察结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Grover's disease: modern ideas about transient and persistent acantholytic dermatosis.
Grover's disease is a papulo-vesicular pruritic dermatosis characterized by a transient, persistent, or asymptomatic course. We have analyzed the publications found in the PubMed and RSCI scientific literature databases between 1970 and 2022. The clinical manifestations of Grover's disease, possible localization, etiological factors, and the histological and dermatoscopic picture of the disease are described. According to the literature, the putative associations with disease onset are highly variable and include insolation, pregnancy, hemodialysis, chemotherapy, sweating, a number of dermatoses, and a history of malignancy and organ transplantation. Seasonality of the process has also been described. To date, 9 histologic patterns of the disease have been described, the most common being acantholytic dyskeratosis. In this review, we have included our observations of patients with Grover's disease.
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