| Autor: |
Takahashi W; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine., Ichikawa M; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine., Furuichi S; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine., Nagasawa F; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine., Iso H; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine., Arai H; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine., Tsurumi S; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine., Handa T; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine., Tadokoro J; Department of Hematology, Shinmatsudo Central General Hospital., Nakamura Y; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine., Nakamura Y; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine., Sasaki K; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine., Mitani K; Department of Hematology and Oncology, Dokkyo Medical University School of Medicine. |
| Abstrakt: |
A 56-year-old man who sustained a right waist injury 1 month ago, reported to our department complaining of pain in the right waist and femur for 1 day. In a computed tomography examination, hematoma of the right iliopsoas muscle was revealed, and arterial embolization was immediately performed but was not effective. Laboratory findings showed hemoglobin levels as 5.4 g/dl, platelet of 20.2×10 4 /µl, prothrombine time of 13.1 s, partial thromboplastin time (APTT) of 81.1 s, and a convex upward curve of the APTT cross-mixing test. The activity of the coagulation factor VIII was <1.0%, but its amount was 120%, and the level of factor VIII inhibitor was 130 Bethesda Unit/ml. Disseminated intravascular coagulation was not noted. Under the diagnosis of acquired hemophilia A, treatment with prednisolone and recombinant activated factor VII was initiated. However, APTT remained prolonged, and intubation and mechanical ventilation were required because of right hemothorax. After steroid pulse therapy and plasma exchange, APTT returned to its normal range, and the inhibitor disappeared. Thus, we finally succeeded in extubation. This case indicated that intensive care may be necessary in the early phase treatment for acquired hemophilia A. |
