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混合性免疫性大疱病:这是线状IgA疾病吗?

Mixed immunobullous disease: is this linear IgA disease?

作者信息

Sheridan A T, Kirtschig G, Wojnarowska F

机构信息

Department of Dermatology, Oxford Radcliffe Hospitals, United Kingdom.

出版信息

Australas J Dermatol. 2000 Nov;41(4):219-21. doi: 10.1046/j.1440-0960.2000.00440.x.

Abstract

We report five patients who demonstrated clinical, histological and direct immunofluorescence (IF) features typical of linear IgA disease (LAD), but who also displayed IgG anti-basement membrane zone (BMZ) antibodies on indirect IF. The presence of circulating IgG anti-BMZ antibodies is often said to exclude the diagnosis of LAD. Unable to confidently classify these patients, we reviewed their clinical progress for unifying features. This revealed an almost universal benefit from dapsone therapy. We therefore propose that when strong linear IgA deposition is observed at the BMZ, a first line trial of dapsone is indicated, irrespective of the presence of circulating IgG. The class of antibody fixed in vivo appears to influence the clinical picture more than the class of circulating antibody.

摘要

我们报告了5例患者,他们表现出具有线性IgA疾病(LAD)典型的临床、组织学及直接免疫荧光(IF)特征,但在间接免疫荧光检查中也显示出IgG抗基底膜带(BMZ)抗体。通常认为循环中存在IgG抗BMZ抗体可排除LAD的诊断。由于无法对这些患者进行确切分类,我们回顾了他们的临床病程以寻找统一特征。这显示出氨苯砜治疗几乎对所有患者都有益。因此,我们建议,当在基底膜带观察到强烈的线性IgA沉积时,无论循环中是否存在IgG,均应首先试用氨苯砜进行试验。体内固定的抗体类别似乎比循环抗体类别对临床症状的影响更大。

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