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先天性竖毛肌错构瘤。1例病例报告及贝克痣与毛发平滑肌错构瘤谱系的文献复习

Congenital arrector pili hamartoma. A case report and review of the spectrum of Becker's melanosis and pilar smooth-muscle hamartoma.

作者信息

Slifman N R, Harrist T J, Rhodes A R

出版信息

Arch Dermatol. 1985 Aug;121(8):1034-7. doi: 10.1001/archderm.121.8.1034.

Abstract

Congenital pigmented arrector pili hamartomas are unique malformations of epidermis and pilar apparatus usually appearing as localized, lightly pigmented, hairy plaques. Characteristic microscopic features include smooth-muscle proliferation similar to irregularly disposed arrectores pilorum, and slight elongation of epidermal rete with hypermelanosis of the basal unit. An otherwise normally developed child who had this hamartoma at birth is described in an attempt to clarify the relationship between pilar smooth-muscle hamartomas and Becker's melanosis. We propose that these two entities belong at different poles of the same developmental spectrum of hamartomatous change.

摘要

先天性色素性立毛肌错构瘤是一种独特的表皮和毛囊器官畸形,通常表现为局限性、色素沉着较轻的多毛斑块。特征性的显微镜下表现包括类似于不规则排列的立毛肌的平滑肌增生,以及表皮嵴轻微延长伴基底细胞黑素沉着增多。本文描述了一名出生时即患有这种错构瘤但其他方面发育正常的儿童,旨在阐明毛囊平滑肌错构瘤与贝克尔黑素沉着症之间的关系。我们认为这两种病变属于错构瘤性改变同一发育谱系的不同极端情况。

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