Abstract
Inflammatory neuropathies constitute a collection of prevalent and manageable pathologies resulting from a humoral or cellular immune response directed towards distinct components of the peripheral nervous system. These pathologies can manifest acutely, as exemplified by Guillain-Barré syndrome (GBS) and its subtypes, or chronically, as seen in the case of chronic inflammatory demyelinating polyneuropathy (CIDP), multifocal motor neuropathy, or nodal-paranodal disorders. Diagnosis primarily relies upon clinical manifestations and electromyographic studies, aimed at facilitating timely initiation of treatment.
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