Epidermolysis bullosa acquisita

The article describes present-day information on the pathogenesis, clinical picture, treatment and differential diagnostics of epidermolysis bullosa acquisita, an autoimmune skin disease caused by the production of anti-Type VII collagen autoantibodies and manifested mainly by subepidermal blisters...

全面介紹

書目詳細資料
發表在:Vestnik Dermatologii i Venerologii
Main Authors: V. V. Chikin, L. F. Znamenskaya, M. A. Nefedova, V. A. Charikov
格式: Article
語言:英语
出版: State Scientific Center of Dermatovenereology and Cosmetology 2017-08-01
主題:
在線閱讀:https://www.vestnikdv.ru/jour/article/view/148
實物特徵
總結:The article describes present-day information on the pathogenesis, clinical picture, treatment and differential diagnostics of epidermolysis bullosa acquisita, an autoimmune skin disease caused by the production of anti-Type VII collagen autoantibodies and manifested mainly by subepidermal blisters and erosions. The authors present the results of a case study of a rare form of epidermolysis bullosa - epidermolysis bullosa acquisita in a male patient aged 53. A combined therapy with peroral prednisolone and subcutaneous injections of methotrexate had a positive effect in the form of epithelialization of most of the erosions.
ISSN:0042-4609
2313-6294