Bone marrow transplantation for severe aplastic anemia. A report of 9 cases

Acta Haematol. 1979;62(3):121-7. doi: 10.1159/000207557.

Abstract

9 patients with severe aplastic anemia (SAA) were treated with bone marrow transplantation (BMT). 5 were conditioned with cyclophosphamide and received and HLA-identical graft (4 patients) or a mismatched graft (1 patient): 1 rejected the graft on day 30 and died on day 34 during conditioning for a second transplant; 1 died on day 15 with acute and severe graft versus host disease (GvHD) in the absence of haemopoietic engraftment; 3 are alive and complete chimeras at 1,069, 490 and 332 days after transplantation. GvHD developed in 4 patients and was treated successfully in 3 with high dose methylprednisolone and/or antilymphocytic globulin (ALG). 4 patients were conditioned with ALG and received bone marrow from a haploidentical sibling or parent: 1 patient was refractory; 3 patients showed evidence of hematologic reconstitution, but 2 of these required a second course of ALG. 3 patients in this group are alive between 60 and 490 days; 1 patient died on day 121 of HBSAg-negative acute hepatitis.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Anemia, Aplastic / therapy*
  • Antilymphocyte Serum / therapeutic use
  • Bone Marrow Transplantation*
  • Child
  • Cyclophosphamide / therapeutic use
  • Female
  • Graft Enhancement, Immunologic
  • Graft Rejection
  • Graft vs Host Reaction
  • Humans
  • Male
  • Middle Aged
  • Transplantation, Isogeneic

Substances

  • Antilymphocyte Serum
  • Cyclophosphamide