Abstract
Pure red cell aplasia was observed in a 28 year old woman following a major ABO mismatched allogeneic bone marrow transplant for chronic lymphocytic leukemia. No evidence of red blood cell production was observed for more than one year following transplant despite the absence of high isohemagglutinin titers. Treatment with antithymocyte globulin resulted in prompt restoration of reticulocytosis. Therapy with antithymocyte globulin should be considered in these instances when red cell aplasia follows mismatched allogeneic marrow transplantation.
MeSH terms
-
ABO Blood-Group System* / genetics
-
Adult
-
Antilymphocyte Serum / therapeutic use*
-
Antineoplastic Combined Chemotherapy Protocols / therapeutic use
-
Bone Marrow Transplantation / adverse effects*
-
Chlorambucil / administration & dosage
-
Combined Modality Therapy
-
Female
-
Histocompatibility*
-
Humans
-
Isoantibodies / immunology
-
Leukemia, Lymphocytic, Chronic, B-Cell / drug therapy
-
Leukemia, Lymphocytic, Chronic, B-Cell / surgery*
-
Nuclear Family
-
Prednisone / administration & dosage
-
Red-Cell Aplasia, Pure / etiology*
-
Red-Cell Aplasia, Pure / therapy
-
T-Lymphocytes / immunology*
-
Transplantation, Homologous / adverse effects
Substances
-
ABO Blood-Group System
-
Antilymphocyte Serum
-
Isoantibodies
-
Chlorambucil
-
Prednisone