Pathology and Oncology Research (May 2024)

Case Report: Effective management of adalimumab-induced acquired hemophilia A with the CyDRI protocol

  • Andrea Ceglédi,
  • Andrea Ceglédi,
  • Andrea Ceglédi,
  • Árpád Bátai,
  • János Dolgos,
  • Mónika Fekete,
  • László Gopcsa,
  • Viktória Király,
  • Gergely Lakatos,
  • György Nagy,
  • György Nagy,
  • György Nagy,
  • Zsuzsanna Szemlaky,
  • Andrea Várkonyi,
  • Beáta Vilimi,
  • Gábor Mikala,
  • Gábor Mikala,
  • Imre Bodó,
  • Imre Bodó

DOI
https://doi.org/10.3389/pore.2024.1611720
Journal volume & issue
Vol. 30

Abstract

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IntroductionAcquired Hemophilia A (AHA) is a rare autoimmune disorder characterized by the emergence of inhibitors that specifically target coagulation Factor VIII, frequently resulting in severe bleeding episodes.MethodsWe conducted a retrospective analysis of the medical records of a 68-year-old male patient who presented with adalimumab-induced AHA.ResultsThe patient received adalimumab, a tumor necrosis factor inhibitor antibody, as part of his treatment for rheumatoid arthritis. The patient’s clinical journey, characterized by intense bleeding and coagulopathy, was effectively managed with the application of recombinant Factor VIIa (rFVIIa) and the CyDRi protocol.DiscussionThe case emphasizes the importance of prompt coagulation assessment in patients with bleeding symptoms receiving disease-modifying therapy for rheumatoid arthritis that includes adalimumab therapy, considering the rare yet life-threatening nature of AHA. Additionally, this report provides an extensive review of the existing literature on drug-induced AHA, with a special emphasis on cases linked to immunomodulatory medications. Through this two-pronged approach, our report aims to enhance understanding and awareness of this severe complication among healthcare providers, promoting timely diagnosis and intervention.

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