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偶发性棘层松解

Incidental acantholysis.

作者信息

Sánchez Yus E, Requena L, Simón P, de Hijas C M

机构信息

Department of Dermatology, Facultad de Medicina, Universidad Complutense, Madrid, Spain.

出版信息

J Cutan Pathol. 1993 Oct;20(5):418-23. doi: 10.1111/j.1600-0560.1993.tb00664.x.

Abstract

The incidental finding of microscopic foci of acantholytic dyskeratosis, reproducing the histological pattern of Darier's disease, has been the subject of a number of papers in the last few years. In contrast, the incidental finding of other types of acantholysis has not been mentioned in the literature. In the last 5 years, we have noticed such a microscopic finding in 14 biopsy specimens (0.15% of our cutaneous specimens). they were from 13 patients (7 men and 6 women); their ages ranged from 37 to 79 years (mean, 63). Three lesions were located on the head, 7 on the trunk, and 4 on the limbs. The histological diagnoses were basal cell carcinoma (6 cases), keratoacanthoma (2 cases), psoriasis (2 cases), elastolytic granuloma, acral arteriovenous angioma, tinea corporis, and leukocytoclastic vasculitis (1 case each). The histological patterns of the acantholytic foci simulated pemphigus vulgaris (9 cases), superficial pemphigus (1 case), Hailey-Hailey disease (3 cases), and unclassifiable acantholysis (1 case). None of the patients had familial or personal history of acantholytic disorders. We propose a classification of the primary acantholytic disorders based on both their acantholytic pattern and their clinical extent.

摘要

近年来,棘层松解性角化不良的微小病灶偶然发现,重现了 Darier 病的组织学模式,这一情况已成为多篇论文的主题。相比之下,文献中未提及其他类型棘层松解的偶然发现。在过去 5 年中,我们在 14 份活检标本(占我们皮肤标本的 0.15%)中注意到了这种微观发现。它们来自 13 名患者(7 名男性和 6 名女性);年龄范围为 37 至 79 岁(平均 63 岁)。3 个病变位于头部,7 个位于躯干,4 个位于四肢。组织学诊断为基底细胞癌(6 例)、角化棘皮瘤(2 例)、银屑病(2 例)、弹性组织溶解性肉芽肿、肢端动静脉血管瘤、体癣和白细胞破碎性血管炎(各 1 例)。棘层松解灶的组织学模式模拟寻常型天疱疮(9 例)、浅表性天疱疮(1 例)、Hailey-Hailey 病(3 例)和无法分类的棘层松解(1 例)。所有患者均无棘层松解性疾病的家族史或个人史。我们基于棘层松解模式及其临床范围提出了原发性棘层松解性疾病的分类。

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