Multiple myeloma complicated by autoimmune hemolytic anemia

Intern Med. 2004 Jul;43(7):595-8. doi: 10.2169/internalmedicine.43.595.

Abstract

A 57-year-old man was admitted with severe anemia and hypergamma globulinemia. After a diagnosis of multiple myeloma and autoimmune hemolytic anemia was made, chemotherapy rapidly decreased the M-protein level and improved his anemia with normalization of the direct Coombs test. The immunoglobulin binding to the patient's red cells was immunoglobulin G kappa chain like the myeloma M-protein. However, monoclonal immunoglobulin G derived from short-term culture of the patient's bone marrow mononuclear cells did not bind to a panel of red cells. Therefore, the relationship between the M protein produced by his myeloma cells and hemolysis remained unclear.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Anemia, Hemolytic, Autoimmune / complications*
  • Anemia, Hemolytic, Autoimmune / diagnosis*
  • Biomarkers, Tumor / analysis
  • Blood Chemical Analysis
  • Disease Progression
  • Fatal Outcome
  • Humans
  • Japan
  • Male
  • Middle Aged
  • Multiple Myeloma / complications*
  • Multiple Myeloma / diagnosis*
  • Myeloma Proteins / analysis*
  • Risk Assessment
  • Severity of Illness Index

Substances

  • Biomarkers, Tumor
  • Myeloma Proteins
  • multiple myeloma M-proteins