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痣样局限性血管角化瘤:1例罕见疾病的病例报告

Angiokeratoma circumscriptum naeviforme: a case report of a rare disease.

作者信息

Ghosh Sudip Kumar, Bandyopadhyay Debabrata, Ghoshal Loknath, Haldar Susmit

机构信息

Department of Dermatology, Venereology, & Leprosy, R G Kar Medical College, Kolkata, India.

出版信息

Dermatol Online J. 2011 Sep 15;17(9):11.

PMID:21971276
Abstract

Angiokeratomas are relatively rare vascular lesions characterized by ectasias of the papillary dermal blood vessels with secondary epidermal changes in the form of acanthosis and/or hyperkeratosis. Amongst the several variants of angiokeratomas, angiokeratoma circumscriptum is the least common one. Angiokeratoma circumscriptum naeviforme (ACN) is a still rarer type of angiokeratoma, which is typically seen at birth. We report here a case of linear, unilateral, verrucous plaques on the leg of a young man, diagnosed as ACN.

摘要

血管角化瘤是相对罕见的血管性病变,其特征为乳头层真皮血管扩张,并伴有棘层增厚和/或角化过度形式的继发性表皮改变。在血管角化瘤的几种变体中,局限性血管角化瘤是最不常见的一种。痣样局限性血管角化瘤(ACN)是血管角化瘤中更为罕见的一种类型,通常在出生时即可见到。我们在此报告一例年轻男性腿部出现的线状、单侧、疣状斑块病例,诊断为ACN。

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