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Polyneuropathy in nonmalignant IgM plasma cell dyscrasia: a morphological study
Annals of Neurology
|July 1, 1983
Summary
Peripheral neuropathy associated with IgM plasma cell dyscrasia has varied causes. Some cases involve antibodies targeting myelin-associated glycoprotein, while others show primary axonal damage, suggesting heterogeneous pathogenesis.
Area of Science:
- Neurology
- Immunology
- Pathology
Background:
- Peripheral neuropathy can be associated with plasma cell dyscrasias.
- IgM plasma cell dyscrasia is a nonmalignant condition that can present with neurological complications.
Purpose of the Study:
- To investigate the underlying mechanisms of peripheral neuropathy in patients with IgM plasma cell dyscrasia.
- To determine if monoclonal immunoglobulins play a role in nerve damage.
Main Methods:
- Immunological studies to identify monoclonal immunoglobulin targets.
- Sural nerve biopsy for morphological examination.
- Analysis of clinical and pathological findings in six patients.
Main Results:
- Two patients had monoclonal immunoglobulin reacting with myelin-associated glycoprotein, with primary myelin sheath damage.
- Four patients showed primary axonal injury, with two having monoclonal IgMK reactive with chondroitin sulfate C.
- Heterogeneous patterns of nerve damage were observed.
Conclusions:
- The pathogenesis of peripheral neuropathies in IgM plasma cell dyscrasia is diverse.
- Monoclonal IgM paraproteins may interact with peripheral nerve autoantigens, contributing to neuropathy in some cases.