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
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Autoantibodies / blood*
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Demyelinating Diseases / blood
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Demyelinating Diseases / immunology*
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Demyelinating Diseases / physiopathology
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Enzyme-Linked Immunosorbent Assay
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Fingers / innervation
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Humans
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Immunoglobulin M / blood
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Immunoglobulin kappa-Chains / blood
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Immunoglobulin lambda-Chains / blood
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Male
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Middle Aged
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Myelin Proteins / immunology*
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Myelin-Associated Glycoprotein
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Paraproteinemias / blood
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Paraproteinemias / complications
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Paraproteinemias / immunology*
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Paresthesia / blood
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Paresthesia / immunology*
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Paresthesia / physiopathology
Substances
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Autoantibodies
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Immunoglobulin M
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Immunoglobulin kappa-Chains
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Immunoglobulin lambda-Chains
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Myelin Proteins
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Myelin-Associated Glycoprotein