Spontaneous Retroperitoneal Hemorrhage Caused by Idiopathic Acquired Hemophilia A Misdiagnosed as a Delayed Traumatic Hematoma: A Case Report
10.17479/jacs.2019.9.2.72
- Author:
Seon Hee KIM
1
;
Sung Jin PARK
;
Chan Ik PARK
;
Seon Uoo CHOI
;
Jae Hun KIM
Author Information
1. Department of Trauma Surgery, Pusan National University Hospital, Busan, Korea. psjtrauma@gmail.com
- Publication Type:Case Report
- Keywords:
autoantibodies;
blood coagulation disorders;
factor VIII;
hematoma;
hemophilia A
- MeSH:
Autoantibodies;
Blood Coagulation Disorders;
Blood Coagulation Factors;
Diagnosis, Differential;
Factor VIII;
Hematoma;
Hemophilia A;
Hemorrhage;
Humans;
Male;
Middle Aged;
Rare Diseases
- From:
Journal of Acute Care Surgery
2019;9(2):72-75
- CountryRepublic of Korea
- Language:English
-
Abstract:
Acquired hemophilia A (AHA) is a rare disease where typically coagulation factor VIII is inhibited by autoantibodies. It occurs in patients with no personal or familial history of bleeding. In this case study a 61-year-old male presented with a huge psoas hematoma. He had no history of bleeding disorders. He was initially diagnosed with delayed traumatic hematoma. Despite conservative and surgical treatments, coagulopathy was not resolved and postoperative bleeding continued. Consequently, coagulation factor tests were performed and showed reduced activity of factor VIII (2.7%). In addition, factor VIII inhibitor was detected. The patient was diagnosed with AHA and administered recombinant factor VIII for 3 days which resulted in the cessation of bleeding. AHA can lead to a life-threatening hemorrhage, and needs to be considered in differential diagnoses in any patients presenting with unexplained and repeated bleeding, where there is no personal or familial history of bleeding disorders.
