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获得性血友病甲是一种少见的出血性疾病,是因非血友病患者后天自身产生抗凝血因子Ⅷ(F.Ⅷ)抗体引起凝血功能障碍而致,其临床表现与典型血友病甲相似。现对16年来我们遇到的4例报道如下。
Acquired hemophilia A is a rare hemorrhagic disease caused by non-hemophilia patients with anti-coagulation factor Ⅷ (F. Ⅷ) antibodies caused by coagulation disorders caused by its clinical manifestations and typical hemophilia A similar disease. Here are the 4 cases we encountered in 16 years.