Ishikawa O, Tamura A, Ohnishi K, Miyachi Y
Department of Dermatology, Gunma University School of Medicine, Maebashi, Japan.
Acta Derm Venereol. 1993 Jun;73(3):229-30. doi: 10.2340/0001555573229230.
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.
报告了1例寻常型天疱疮合并获得性血友病A的罕见病例。证实了Ⅷ因子抑制剂的存在,并讨论了两种自身免疫性疾病的共存情况。