儿童慢性大疱性皮肤病。

S Kárpáti, E Török, Z Vajda, I Répay, I Kósnai
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引用次数: 0

摘要

对16例儿童慢性大疱性皮肤病(CBDC)进行了研究。他们被随访了0.5到4.5年。每例患者均行皮肤组织学和免疫荧光(IF)检查,局部皮肤病变行Trafuril试验,12例患者行肠道活检。4例患者皮肤基底膜有IgG, 3例有IgA。9例患者未检测到免疫球蛋白;这些IF阴性病例似乎是假阴性。反复的皮肤活检和免疫电镜检查可能是有帮助的。在根据皮肤IF研究分类的三组患者中,临床和组织学表现、曲福瑞试验反应和治疗结果均无差异。12例患者中有3例小肠黏膜异常。在两名患者中引入无麸质饮食对疾病的病程没有影响。CBDC伴IF阴性或阳性、幼年类天疱疮和IgA线性皮肤病似乎是一种常见的临床实体,其严重程度不同且存在个体差异。此病与杜氏疱疹样皮炎不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic bullous dermatosis of childhood.

A study of 16 patients with chronic bullous dermatosis of childhood (CBDC) is reported. They were followed up for 0.5 to 4.5 years. Histological and immunofluorescent (IF) study of the skin and local provocation of skin lesions by Trafuril test were carried out in every case, intestinal biopsy in twelve cases. Four patients were found to have IgG, and three IgA, along the skin basement membrane. In nine patients, no immunoglobulins were detectable; these IF negative cases seemed to be pseudonegative. Repeated biopsy and immunoelectronmicroscopic study of the skin may be helpful. In the three patient groups classified on the basis of skin IF studies, there was no difference in the clinical and histological picture, in reaction to Trafuril test and in the result of treatment. The small intestinal mucosa was abnormal in three of twelve patients. A gluten-free diet introduced in two patients had no effect on the course of the disease. CBDC with negative or positive IF, juvenile pemphigoid and IgA linear dermatosis seem to be a common clinical entity, different in severity and with individual variations. The condition is not identical with dermatitis herpetiformis Duhring.

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