CD79A and bullous pemphigoid: Thirty patients (81.1%) were eventually diagnosed clinically and immunopathologically with subepidermal autoimmune bullous diseases (SAIBD); 23 patients (62.2%) with bullous pemphigoid (BP), of whom one patient had coexisting psoriasis, 4 patients (10.8%) with mucous membrane pemphigoid, 2 patients (5.4%) with linear IgA bullous dermatosis (had IgA intercellular antibodies), and one patient (2.7%) with lichen planus pemphigoides.