Pathology and Oncology Research (Jun 2022)

Case Report: A Child With Hemophilia A Serves as Donor for Hematopoietic Stem Cell Transplantation to Cure His Brother’s Severe Aplastic Anemia

  • Gabriella Kertész,
  • Krisztián Kállay,
  • Csaba Kassa,
  • Csaba Kassa,
  • Marianna Zombori,
  • Imre Bodó,
  • Csongor Kiss,
  • István Szegedi,
  • Gergely Kriván,
  • Gergely Kriván

DOI
https://doi.org/10.3389/pore.2022.1610171
Journal volume & issue
Vol. 28

Abstract

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The first-line treatment of severe aplastic anemia is allogeneic hematopoietic stem cell transplantation with a matched sibling donor. However, co-morbidities of the identical donor can make donation difficult. We present a transplantation where in parallel with the patient’s conditioning treatment, the preparation of the donor with severe hemophilia A required a special management with perioperative factor VIII substitution. Donation was successful without complications, and 18 months after transplantation, the patient and his donor are well without any long-term sequelae. To our knowledge, this is the first reported succesfull transplantation with hemophilic child serving as a bone marrow donor. The procedure did not mean a significant risk to donor health, so donors with hemophilia should not be excluded from donation.

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