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

• Published in: Pathology oncology research Vol. 28
• Main Authors: Kertész, Gabriella, Kállay, Krisztián, Kassa, Csaba, Zombori, Marianna, Bodó, Imre, Kiss, Csongor, Szegedi, István, Kriván, Gergely
• Format: Journal Article
• Language: English
• Published: Frontiers Media S.A 08.06.2022
• Subjects: children; hematopoietic stem cell transplantation (HSCT); hemophilia a; hepatitis associated bone marrow failure (HABMF); Pathology and Oncology Archive; severe aplastic anemia (SAA)
• ISSN: 1532-2807; 1219-4956; 1532-2807
• DOI: 10.3389/pore.2022.1610171

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.