Epidermolysis bullosa acquisita responsive to dapsone therapy.

Abstract:

BACKGROUND:Epidermolysis bullosa acquisita (EBA) is a chronic subepidermal blistering disease that is frequently resistant to therapy. OBJECTIVE:A 58-year-old man who had a one-year history of a bullous eruption involving the hands, forearms, trunk, scalp, and oral mucosa. Histopathology revealed a subepidermal bulla, and direct and indirect immunofluorescence studies were consistent with EBA. The patient failed respond to niacinamide and tetracycline and oral prednisone 40 mg per day. METHODS:Complete control of his blistering was achieved within two months of initiating oral dapsone, 150 mg per day. CONCLUSION:Dapsone may be an effective agent for some patients with EBA.

journal_name

J Cutan Med Surg

authors

Hughes AP,Callen JP

doi

10.1007/s10227-001-0008-y

subject

Has Abstract

pub_date

2001-09-01 00:00:00

pages

397-9

issue

5

eissn

1203-4754

issn

1615-7109

journal_volume

5

pub_type

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