Korean J Dermatol.  2016 Jul;54(6):464-467.

A Case of Epidermolysis Bullosa Acquisita Associated with Psoriasis

• Moon KR
• Yun SJ
• Kim SJ
• Lee SC
• Won YH
• Lee JB

Abstract

Epidermolysis bullosa acquisita (EBA) is an autoimmune subepidermal blistering disease characterized by the presence of circulating IgG autoantibodies to type VII collagen. Various types of autoimmune blistering disease have been reported in association with psoriasis. A 58-year-old man with a 5-year history of psoriasis vulgaris presented with painful and mildly pruritic erythematous multiple bullae and vesicles. Histopathologically, there was a subepidermal bulla with infiltration of inflammatory cells composed of neutrophils and eosinophils. The salt-split skin indirect immunofluorescence test showed IgG binding to the dermal side of the separation, and immunoblotting using normal human dermal extract revealed antibodies directed against a 290-kDa polypeptide. He was diagnosed with EBA and started medication of oral prednisolone and mycophenolate mofetil. Skin lesions were continuously regressed. Of all the autoimmune blistering diseases coexisting with psoriasis, bullous pemphigoid is the most frequent. However, a few cases of EBA associated with psoriasis have been reported in the literature. We report a rare case of EBA coexisting with psoriasis vulgaris.

Keyword

Epidermolysis bullosa acquisita; Psoriasis vulgaris

MeSH Terms

Antibodies
Autoantibodies
Blister
Collagen Type VII
Eosinophils
Epidermolysis Bullosa Acquisita*
Epidermolysis Bullosa*
Fluorescent Antibody Technique, Indirect
Humans
Immunoblotting
Immunoglobulin G
Middle Aged
Neutrophils
Pemphigoid, Bullous
Prednisolone
Psoriasis*
Skin
Antibodies
Autoantibodies
Collagen Type VII
Immunoglobulin G
Prednisolone