作者: Christopher J. Arpey , Boni E. Elewski , Deborah K. Moritz , W. Ray Gammon
DOI: 10.1016/0190-9622(91)70107-D
关键词: Epidermolysis bullosa acquisita 、 Subepidermal blistering disease 、 Disease 、 Epidermolysis bullosa 、 Medicine 、 Dermatology 、 Response to therapy
摘要: Epidermolysis bullosa acquisita is an acquired subepidermal blistering disease with variable clinical, pathologic, and immunologic features. The has been reported infrequently in adults only rarely children. We describe three new cases of childhood epidermolysis acquisita, review previously cases, contrast the features children those adults. results suggest that both have clinical pathologic may mimic other bullous diseases. characterized by a chronic course, poor response to therapy, occasional remissions.