Epidermolysis Bullosa Acquisita Localized to the Face
Gwang Seong Choi, Eun‐So Lee, Soo‐Chan Kim, Sungnack Lee
Abstract
Gwang Seong Choi, Eun‐So Lee, Soo‐Chan Kim, Sungnack Lee
Abstract
A 39-year-old woman had a three-year history of recurrent bullous eruption localized to her left cheek. The diagnosis of epidermolysis bullosa acquisita was confirmed by means of direct immunofluorescence and direct immunoelectron microscopic studies performed on the perilesional salt-split skin. Topical corticosteroid treatment reduced pruritus and bullae formation. This case of localized epidermolysis bullosa acquisita on the face is reminiscent of Brunsting-Perry cicatricial pemphigoid. We also review the previously reported cases of localized epidermolysis bullosa acquisita.
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A 39-year-old woman had a three-year history of recurrent bullous eruption localized to her left cheek. The diagnosis of epidermolysis bullosa acquisita was confirmed by means of direct immunofluorescence and direct immunoelectron microscopic studies performed on the perilesional salt-split skin. Topical corticosteroid treatment reduced pruritus and bullae formation. This case of localized epidermolysis bullosa acquisita on the face is reminiscent of Brunsting-Perry cicatricial pemphigoid. We also review the previously reported cases of localized epidermolysis bullosa acquisita.
Key concepts: Epidermolysis bullosa acquisita, Dermatology, Medicine, Cicatricial pemphigoid, Epidermolysis bullosa, Bullous pemphigoid, Immunoelectron microscopy, Direct fluorescent antibody