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局限于先天性贝克尔痣的ILVEN样持续性银屑病样皮炎。

ILVEN-like persistent psoriasiform dermatitis confined to a congenital Becker nevus.

作者信息

Abbasi Naheed, Fangman William L, Rosenman Karla S, Schaffer Julie V

机构信息

Department of Dermatology, New York University School of Medicine, New York, New York 10016, USA.

出版信息

Pediatr Dermatol. 2008 May-Jun;25(3):390-1. doi: 10.1111/j.1525-1470.2008.00690.x.

Abstract

A 10-year-old boy presented with a 5-year history of an intractably pruritic, recalcitrant psoriasiform plaque in a broad vertical band on the left buttock, with histologic as well as clinical features suggestive of an inflammatory linear verrucous epidermal nevus. This lesion was completely superimposed upon a congenital Becker nevus. We postulate that the restricted distribution and persistence of the psoriasiform plaque reflected an inflammatory response limited to the aberrant clone of cells composing the Becker nevus, a manifestation of cutaneous mosaicism that could be characterized as an "inflammatory Becker nevus."

摘要

一名10岁男孩左侧臀部有一广泛垂直条带分布的顽固性瘙痒、难治性银屑病样斑块,病史5年,组织学及临床特征提示为炎症性线状疣状表皮痣。该病变完全叠加于先天性贝克痣之上。我们推测,银屑病样斑块的局限性分布和持续存在反映了一种炎症反应,该反应局限于构成贝克痣的异常细胞克隆,这是一种皮肤镶嵌现象的表现,可被描述为“炎症性贝克痣”。

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