Clinical Case Reports (Jan 2024)

Combined life‐threatening internal organ bleeding and postpartum hemorrhage associated with acquired hemophilia A

  • Chanakarn Kanitthamniyom,
  • Pharit Siladech,
  • Natchaya Polpichai,
  • Maireigh McCullough,
  • Sakditad Saowapa

DOI
https://doi.org/10.1002/ccr3.8399
Journal volume & issue
Vol. 12, no. 1
pp. n/a – n/a

Abstract

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Key Clinical Message Acquired hemophilia A (AHA) can present as life‐threatening bleeding during the postpartum period. Prompt treatment allows patients with AHA to achieve complete remission and have normal subsequent pregnancies. Abstract Acquired hemophilia A (AHA) is a rare bleeding disorder caused by the production of autoantibodies against factor VIII (FVIII). AHA can present with severe bleeding, especially in postpartum patient. We report a 38‐year‐old woman who presented in an emergency department with severe postpartum hemorrhage 2 weeks after cesarean section. Her investigation showed an isolated prolongation of partial thromboplastin time (PTT), low factor VIII assay and a factor VIII inhibitor test, resulting in abnormal Bethesda units which consistent with AHA. This case report highlights the importance of early diagnosis and treatment of AHA. With timely and appropriate management, most patients can achieve a good outcome.

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