Epidermolysis bullosa acquisita (EBA) is a rare, acquired, chronic subepidermal bullous disease of the skin and mucosa characterized by autoantibodies to type VII collagen structures, a major component of anchoring fibrils, that attach the epidermis onto the dermis. The treatment of EBA is based on anecdotal reports in the literature with systemic therapies. We report a case of EBA successfully treated by dapsone.

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Associate Professor, MD-PhD at Nicolae Testemitanu State University of Medicine and Pharmacy,

Chisinau, Republic of Moldova

Member of the Editorial Board of the International Journal of Clinical Dermatology & Research, USA

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