Severe case of postpartum-acquired haemophilia A after laparoscopic cholecystectomy
- PMID: 38553018
- PMCID: PMC10982749
- DOI: 10.1136/bcr-2023-258812
Severe case of postpartum-acquired haemophilia A after laparoscopic cholecystectomy
Abstract
Acquired factor VIII inhibitor, also known as acquired haemophilia A, has been associated with the postpartum state in young females. Treatment of acquired haemophilia A is focused on two goals: control of bleeding and eliminating the factor VIII inhibitor. Management requires successful intervention to accomplish both goals. Here, we describe the presentation and management of a case of acquired haemophilia A resulting in particularly severe and protracted intra-abdominal bleeding after routine laparoscopic cholecystectomy in a young and otherwise healthy female at 3 months postpartum. Due to diffuse intra-abdominal bleeding, she required return to the operating room on five occasions for intra-abdominal packing, reassessment of bleeding and ultimate fascial closure. Her abdomen was open for 5 days. She was treated with activated recombinant human factor VIIa to bypass inhibited factor VIII, and with immunosuppression using steroids, cyclophosphamide and anti-CD20 monoclonal antibody rituximab. She achieved remission after 6 weeks of treatment.
Keywords: General surgery; Haematology (drugs and medicines).
© BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ.
Conflict of interest statement
Competing interests: None declared.
References
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- Green D, Lechner K. A survey of 215 non-Hemophilic patients with inhibitors to factor VIII. Thromb Haemost 1981;45:200–3. - PubMed
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