The spectrum of IgM monoclonal gammopathy in 430 cases

Mayo Clin Proc. 1987 Aug;62(8):719-31. doi: 10.1016/s0025-6196(12)65225-2.

Abstract

IgM monoclonal gammopathy consists of a broad spectrum of diseases, ranging from apparently benign to malignant conditions. In a long-term follow-up study of 430 patients in whom a monoclonal IgM serum protein had been identified, 242 (56%) had monoclonal gammopathy of undetermined significance, 71 (17%) had Waldenström's macroglobulinemia, 28 (7%) had lymphoma, 21 (5%) had chronic lymphocytic leukemia, 6 (1%) had primary amyloidosis, and 62 (14%) had other malignant lymphoproliferative diseases. More than two-thirds of the patients died, and the most common cause of death was a lymphoid malignant process. Almost a fifth of the patients with an apparently benign monoclonal gammopathy subsequently had a lymphoid malignant lesion (in one patient, more than 20 years after the detection of the serum M protein). The median duration of time from the recognition of the M protein until the development of a malignant lymphoid disease ranged from 4 to 9 years. An increased number of lymphocytes or plasma cells on bone marrow examination was not a reliable indicator of the likelihood of such an outcome. Thus, follow-up of these patients should be conducted indefinitely.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Female
  • Follow-Up Studies
  • Humans
  • Hypergammaglobulinemia*
  • Immunoglobulin M / analysis*
  • Leukemia, Lymphoid / immunology
  • Male
  • Middle Aged
  • Monoclonal Gammopathy of Undetermined Significance* / mortality
  • Multiple Myeloma / immunology
  • Waldenstrom Macroglobulinemia / immunology

Substances

  • Immunoglobulin M