Sustained and full fetal hemoglobin production after failure of bone marrow transplant in a patient homozygous for beta 0-thalassemia: a clinical remission despite genetic disease and transplant rejection.
Am J Hematol
; 84(6): 372-3, 2009 Jun.
Article
en En
| MEDLINE
| ID: mdl-19373892
An adult patient affected by beta(0)-thalassemia major underwent allogeneic bone marrow transplant (BMT) from a matched related donor. Forty days after transplant, allogeneic engraftment failure and autologous beta(0)-thalassemic bone marrow recovery were documented. Red blood cell transfusions were required until 118 days post-transplant. Thereafter, the haemoglobin (Hb) levels stabilized over 11.8 gr/dl throughout the ongoing 34-month follow-up, abolishing the need for transfusion support. The Hb electrophoresis showed 100% Hb Fetal (HbF). This unexplained case suggests full HbF production may occur in an adult patient with beta(0)-thalassemia major.
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Hemoglobina Fetal
/
Trasplante de Médula Ósea
/
Talasemia beta
/
Rechazo de Injerto
Límite:
Adolescent
/
Humans
Idioma:
En
Revista:
Am J Hematol
Año:
2009
Tipo del documento:
Article
Pais de publicación:
Estados Unidos