Pemphigus Vulgaris Associated with Acquired Hemophilia A due to
Factor VIll lnhibitor
Ishikawa O, Tamura A, Ohnishi K, Miyachi Y
DOI: 10.2340/0001555573229230
Abstract
A rare case of pemphigus vulgaris associated with acquired hemophilia A is reported. The presence of factor VIII inhibitor is confirmed, and the co-existence of two autoimmune diseases is discussed.
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