Rheumatoid arthritis and pure red cell aplasia

Ann Intern Med. 1984 Feb;100(2):202-6. doi: 10.7326/0003-4819-100-2-202.

Abstract

Three patients with severe, deforming, and long-standing rheumatoid arthritis developed pure red cell aplasia that did not remit after withdrawal of medications, ran a chronic course, and in two patients remitted only after cytotoxic immunosuppressive treatment. An IgG inhibitor of autologous erythroid colony-forming and burst-forming unit growth in vitro was found in the serum of one patient. This specific erythropoietic inhibitor persisted in lower titer in the patient's serum even after an azathioprine-induced remission of pure red cell aplasia, indicating the possible need for maintenance immunosuppressive therapy. Chronic pure red cell aplasia may be another extra-articular manifestation of rheumatoid arthritis and should be considered when severe anemia develops in the absence of blood loss or hemolysis.

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Anemia, Aplastic / etiology*
  • Anemia, Aplastic / immunology
  • Arthritis, Rheumatoid / blood
  • Arthritis, Rheumatoid / complications*
  • Arthritis, Rheumatoid / immunology
  • Bone Marrow Examination
  • Colony-Forming Units Assay
  • Erythropoiesis
  • Female
  • Humans
  • Immunoglobulin G
  • Middle Aged

Substances

  • Immunoglobulin G