Delayed appearance of anti-myelin-associated glycoprotein antibodies in a patient with chronic demyelinating polyneuropathy

Ann Neurol. 1993 Sep;34(3):394-6. doi: 10.1002/ana.410340314.

Abstract

A patient who had a polyneuropathy compatible with a chronic inflammatory demyelinating polyneuropathy and was initially negative for anti-myelin-associated glycoprotein (MAG) antibodies developed a double monoclonal gammopathy, IgM kappa and IgM lambda, two years after the diagnosis. The IgM kappa, but not the IgM lambda, exhibited strong anti-MAG antibody activity. The late appearance of the anti-MAG immunoreactivity suggests that in patients with an initial diagnosis of chronic inflammatory demyelinating polyneuropathy, the search for anti-MAG antibodies should be repeated during the course of the neuropathy.

Publication types

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

MeSH terms

  • Autoantibodies / blood*
  • Demyelinating Diseases / blood
  • Demyelinating Diseases / immunology*
  • Demyelinating Diseases / physiopathology
  • Enzyme-Linked Immunosorbent Assay
  • Fingers / innervation
  • Humans
  • Immunoglobulin M / blood
  • Immunoglobulin kappa-Chains / blood
  • Immunoglobulin lambda-Chains / blood
  • Male
  • Middle Aged
  • Myelin Proteins / immunology*
  • Myelin-Associated Glycoprotein
  • Paraproteinemias / blood
  • Paraproteinemias / complications
  • Paraproteinemias / immunology*
  • Paresthesia / blood
  • Paresthesia / immunology*
  • Paresthesia / physiopathology

Substances

  • Autoantibodies
  • Immunoglobulin M
  • Immunoglobulin kappa-Chains
  • Immunoglobulin lambda-Chains
  • Myelin Proteins
  • Myelin-Associated Glycoprotein