Mesalazine-associated severe aplastic anemia successfully treated with antithymocyte globulin, cyclosporine and granulocyte colony-stimulating factor

Int J Hematol. 1998 Dec;68(4):445-8. doi: 10.1016/s0925-5710(98)00082-6.

Abstract

A 20-year-old male with ulcerative colitis complicated by mesalazine-associated severe aplastic anemia is described. The patient developed aplastic anemia four months after the start of mesalazine therapy. He was treated with antithymocyte globulin, cyclosporine, and granulocyte colony-stimulating factor (G-CSF) and responded well. Hematological complications of mesalazine are rare, but if bone marrow suppression is detected, immediate cessation of the drug and intensive immunosuppressive treatment with G-CSF should be considered.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Anemia, Aplastic / chemically induced*
  • Anemia, Aplastic / drug therapy*
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects*
  • Antilymphocyte Serum / therapeutic use*
  • Cyclosporine / therapeutic use*
  • Drug Therapy, Combination
  • Granulocyte Colony-Stimulating Factor / therapeutic use*
  • Humans
  • Male
  • Mesalamine / adverse effects*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Antilymphocyte Serum
  • Granulocyte Colony-Stimulating Factor
  • Mesalamine
  • Cyclosporine