Author/Authors :
Kitamura, Tomohisa Department of Oral and Maxillofacial Surgery - Saitama Medical University, Japan , Sato, Tsuyoshi Department of Oral and Maxillofacial Surgery - Saitama Medical University, Japan , Ikami, Eiji Department of Oral and Maxillofacial Surgery - Saitama Medical University, Japan , Fukushima, Yosuke Department of Oral and Maxillofacial Surgery - Saitama Medical University, Japan , Yoda, Tetsuya Department of Maxillofacial Surgery -Tokyo Medical and Dental University, Tokyo, Japan
Abstract :
Background. Acquired hemophilia A (AHA) is a rare disorder which results from the presence of autoantibodies against blood
coagulation factor VIII. The initial diagnosis is based on the detection of an isolated prolongation of the activated partial
thromboplastin time (aPTT) with negative personal and family history of bleeding disorder. Definitive diagnosis is the
identification of reduced FVIII levels with evidence of FVIII neutralizing activity. Case report. We report a case of a 93-year-old
female who was diagnosed as AHA after tooth extraction at her home clinic. Prolongation of aPTT and a reduction in factor
VIII activity levels were observed with the presence of factor VIII inhibitor. AHA condition is mild. However, acute subdural
hematoma of this patient occurred due to an unexpected accident in our hospital. Hematoma was gradually increased and the
patient died 13 days after admission. Discussion. Although AHA is mild, intracranial bleeding is a life-threatening condition. We
also should pay attention to the presence of AHA patients when we extract teeth.
Keywords :
Mild Acquired , Hemophilia A , Tooth Extraction , Hematoma , Head Injury