Acquired hemophilia is generally curable with aggressive treatment, but the specifics vary from person to person.
Acquired hemophilia is not a congenital hereditary disease, but is generally a secondary bleeding disorder caused by various reasons such as autoimmune diseases, malignant tumors, and infections. The disease may cause bleeding manifestations such as muscle hematomas, skin petechiae, vaginal bleeding, bloody stools, black stools, etc., which may affect normal life, and in severe cases, death may occur due to intracranial hemorrhage.
It can be treated by supplementing coagulation factors, immunosuppressive therapy, such as human factor VIII products, cyclophosphamide and other drugs, and actively treating the primary disease.
Acquired hemophilia patients must investigate the cause of the disease, under the guidance of a professional doctor for treatment, avoid using drugs alone.