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疱疹样皮炎和大疱性类天疱疮混合型患者皮肤中IgA的超微结构定位

The ultrastructural localization of IgA in skin of a patient with mixed form of dermatitis herpetiformis and bullous pemphigoid.

作者信息

Dabrowski J, Chorzelski T P, Jabłońska S, Kraińska T, Jarzabek-Chorzelska M

出版信息

J Invest Dermatol. 1978 Feb;70(2):76-9. doi: 10.1111/1523-1747.ep12541207.

Abstract

A case with mixed features of dermatitis herpetiformis and bullous pemphigoid was investigated by immuno-electron microscopy. There were clinical, histological, and ultrastructural characteristics of both diseases, the response to sulfapyridine was dramatic at the beginning, but intestinal lesions were absent. Direct immunofluorescence tests were made 6 times in the 4 year period and demonstrated in all biopsies exclusively linear IgA deposits. The IgA deposits were shown to occupy the entire lamina lucida and to adhere to the basal cell membranes and lamina densa, very much like IgG deposits in bullous pemphigoid. Antibodies against the basement membrane zone could not be demonstrated in the serum.

摘要

对一例具有疱疹样皮炎和大疱性类天疱疮混合特征的病例进行了免疫电子显微镜检查。该病例具有这两种疾病的临床、组织学和超微结构特征,起初对磺胺吡啶反应显著,但无肠道病变。在4年期间进行了6次直接免疫荧光试验,所有活检均显示仅存在线性IgA沉积。IgA沉积物占据整个透明板,并附着于基底细胞膜和致密板,与大疱性类天疱疮中的IgG沉积物非常相似。血清中未检测到针对基底膜带的抗体。

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