Bone-marrow transplantation for severe aplastic anaemia using histocompatible unrelated volunteer donors.

نویسندگان

  • E C Gordon-Smith
  • S M Fairhead
  • P M Chipping
  • J Hows
  • D C James
  • A Dodi
  • J R Batchelor
چکیده

Two patients with severe aplastic anaemia received bone-marrow transplants from unrelated donors selected for HLA compatibility. Graft-versus-host disease occurred in both patients but responded to treatment. Both patients had stormy courses after grafting, but subsequently their conditions improved, and one was not receiving any treatment at follow-up after day 330 while the other had mild chronic graft-versus-host disease at day 150. These results show that unrelated, histocompatible volunteers may successfully donate marrow for the treatment of severe aplastic anaemia, though many problems remain to be solved.

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Histocompatible unrelated volunteer donors compared with HLA nonidentical family donors in marrow transplantation for aplastic anemia and leukemia.

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Histocompatible Unrelated Volunteer Donors Compared With HLA Nonidentical Family Donors in Marrow Transplantation for Aplastic Anemia and Leukemia

We treated 1 4 patients by transplantation of marrow from unrelated volunteer donors. Eight patients had severe aplastic anemia, 3 had chronic granulocytic leukemia, and 3 had Fanconi’s anemia. The results are compared with those of a group of 1 4 similar patients transplanted concurrently from human leukocyte antigen (HLA)-mismatched family members: Sustained engraftment was achieved in 8 of 1...

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Selection of patients for bone marrow transplantation in severe aplastic anemia.

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Increased incidence of neurological complications in patients receiving an allogenic bone marrow transplantation from alternative donors.

OBJECTIVE To compare the frequency and type of neurological complications after bone marrow transplantation (BMT) with an HLA identical unrelated donor or a mismatched related donor (alternative donors) to the neurological complications after matched sibling BMT for standard and high risk leukaemia or myelodysplastic syndromes. METHODS Retrospective analysis of consecutively treated patients ...

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عنوان ژورنال:
  • British medical journal

دوره 285 6345  شماره 

صفحات  -

تاریخ انتشار 1982