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补骨脂素加紫外线A疗法诱发的大疱性类天疱疮

Bullous pemphigoid induced by PUVA therapy.

作者信息

Perl S, Rappersberger K, Födinger D, Anegg B, Hönigsmann H, Ortel B

机构信息

Division of Special and Environmental Dermatology, University of Vienna, Austria.

出版信息

Dermatology. 1996;193(3):245-7. doi: 10.1159/000246255.

Abstract

An 80-year-old psoriatic patient developed a blistering eruption during oral PUVA therapy. The diagnosis of bullous pemphigoid (BP) was established by routine histopathology, which demonstrated subepidermal blistering, and direct immunofluorescence, which revealed linear deposits of IgG, IgM and C3 along the basement membrane zone. Indirect immunofluorescence using normal human split skin revealed binding of IgG antibodies to the epidermal side, thus confirming a subepidermal blistering disorder. These proteins were identified by the immunoblotting technique as BP antigens I and II. Clinically, the lesions could be reproduced by phototesting using topical 8-methoxypsoralen. Again, the histopathological and immunopathological findings were consistent with the diagnosis of PUVA-induced BP. To the best of our knowledge, this is the first report demonstrating psoriasis-associated BP, in which the clinical diagnosis of BP is confirmed by immunoblotting analysis. The exact role of UV light in precipitating bullous lesions, particularly the question whether UV light may represent an unspecific epidermal injury leading to further attraction of autoantibodies to the basement membrane zone, as suggested recently by an experimental study in rodents, remains to be clarified in future studies.

摘要

一名80岁的银屑病患者在口服补骨脂素加长波紫外线(PUVA)治疗期间出现水疱性皮疹。通过常规组织病理学检查(显示表皮下水疱形成)和直接免疫荧光检查(显示IgG、IgM和C3沿基底膜带呈线性沉积)确诊为大疱性类天疱疮(BP)。使用正常人分层皮肤进行间接免疫荧光检查显示IgG抗体与表皮侧结合,从而证实为表皮下水疱性疾病。通过免疫印迹技术将这些蛋白质鉴定为BP抗原I和II。临床上,使用外用8-甲氧基补骨脂素进行光试验可再现皮损。同样,组织病理学和免疫病理学结果与PUVA诱导的BP诊断一致。据我们所知,这是第一份证明银屑病相关BP的报告,其中BP的临床诊断通过免疫印迹分析得到证实。紫外线在引发水疱性皮损中的确切作用,特别是紫外线是否可能代表一种非特异性的表皮损伤,导致自身抗体进一步吸引至基底膜带,正如最近一项啮齿动物实验研究所表明的那样,仍有待未来研究予以阐明。

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