致编辑的信:自身免疫性多腺综合征患者疱疹样皮炎与白癜风共发。

Journal of dermatological case reports Pub Date : 2013-09-30 eCollection Date: 2013-01-01 DOI:10.3315/jdcr.2013.1153
Abby E Macbeth, Kevin Y C Lee, Nick J Levell, Laszlo Igali, George W M Millington
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引用次数: 3

摘要

我们报告一例疱疹样皮炎与节段性白癜风共定位在一个37岁的妇女与自身免疫性多腺综合征2型的背景历史。我们提出遗传嵌合是一种可能的机制。只有一个以前的病例报告,其中肝炎样皮炎共定位在近距离,但不完全是在白癜风患者自身免疫性甲状腺炎。据我们所知,这是第一例报告的疱疹样皮炎共定位专门为节段性白癜风存在自身免疫性多腺综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photoletter to the editor: Dermatitis herpetiformis co-localised with vitiligo in a patient with autoimmune polyglandular syndrome.

We report a case of dermatitis herpetiformis co-localised with segmental vitiligo in a 37-year-old woman with a background history of autoimmune polyglandular syndrome type 2. We propose genetic mosaicism as a possible mechanism. There has only been one previous case report in which dermatitis hepetiformis co-localised in close proximity but not exclusively within vilitigo in a patient with autoimmune thyroiditis. To our knowledge, this is the first case report of dermatitis herpetiformis co-localised exclusively to segmental vitiligo in the presence of autoimmune polyglandular syndrome.

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