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布伦斯汀-佩里瘢痕性类天疱疮:局限性获得性大疱性表皮松解症的一种临床变异型?

Brunsting-Perry cicatricial bullous pemphigoid: a clinical variant of localized acquired epidermolysis bullosa?

作者信息

Joly P, Ruto F, Thomine E, Delpech A, Balguerie X, Tron F, Lauret P

机构信息

Department of Dermatology, Hôpital Charles Nicolle, Rouen, France.

出版信息

J Am Acad Dermatol. 1993 Jan;28(1):89-92. doi: 10.1016/0190-9622(93)70016-m.

Abstract

An 84-year-old man who had the typical clinical features of Brunsting-Perry cicatricial pemphigoid is described. Direct immunofluorescence microscopic examination of salt-split skin revealed linear deposits of IgG and C3 on the floor of the artificial bullae. Direct immunoelectron microscopic examination of peribullous skin showed dermal cleavage level below the lamina densa and granular deposits of IgG and C3 attached to and below the lamina densa in a pattern identical to epidermolysis bullosa acquisita. These findings suggest that Brunsting-Perry cicatricial pemphigoid may represent a clinical variant of epidermolysis bullosa acquisita.

摘要

本文描述了一位具有Brunsting-Perry瘢痕性类天疱疮典型临床特征的84岁男性患者。盐裂皮肤的直接免疫荧光显微镜检查显示,人工水疱底部有IgG和C3的线性沉积。水疱周围皮肤的直接免疫电子显微镜检查显示,真皮分离水平位于致密板下方,IgG和C3的颗粒状沉积物附着于致密板并在其下方,其模式与获得性大疱性表皮松解症相同。这些发现提示,Brunsting-Perry瘢痕性类天疱疮可能是获得性大疱性表皮松解症的一种临床变体。

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