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皮肤黑素细胞增多症:一种临床谱

Dermal melanocytosis: a clinical spectrum.

作者信息

Stanford D G, Georgouras K E

机构信息

Dermatology Centre, Liverpool Hospital, New South Wales, Australia.

出版信息

Australas J Dermatol. 1996 Feb;37(1):19-25. doi: 10.1111/j.1440-0960.1996.tb00989.x.

Abstract

While most dermal melanocytoses are congenital or have an onset in early childhood, there is a group which is clearly acquired, with an onset in adult life. While the Mongolian spot typically disappears in childhood, other dermal melanocytoses persist for life. A brief review of the clinical spectrum of the dermal melanocytoses is undertaken and three illustrative cases are described: a case of congenital naevus of Ota, a case of acquired bilateral naevus of Ota-like macules, and an unusual case of a congenital dermal melanocytotic lesion on the left had which began to spread in adulthood. The possibilities regarding the pathogenesis of this intriguing group of disorders are considered.

摘要

虽然大多数皮肤黑素细胞增多症是先天性的或在儿童早期发病,但有一组显然是后天获得性的,在成年期发病。蒙古斑通常在儿童期消失,而其他皮肤黑素细胞增多症会终生持续存在。本文简要回顾了皮肤黑素细胞增多症的临床谱,并描述了三个典型病例:一例太田痣先天性痣、一例后天性双侧太田痣样斑痣,以及一例左侧先天性皮肤黑素细胞增多性损害在成年期开始扩散的罕见病例。文中还考虑了这一有趣疾病组发病机制的可能性。

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