When do you consider testing autoimmune antibodies for axonal polyneuropathies without clear etiology?
Do you routinely test for axonal neuropathy autoimmune antibody panels in patients with slowly progressive idiopathic axonal sensorimotor neuropathy?
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Dr. @Dr. First Last gave an excellent summary of the clinical red flags that should trigger antibody testing in polyneuropathies. I would like to highlight that not all antibodies are pathogenic or cause the same phenotypes/clinical syndromes; therefore, I would like to break it down by antibody group:
Group 1: Non-specific antibodies associated with connective tissue diseases (ANA, SSA, SSB, ANCA, RF, dsDNA, etc.)
Group 2: Paraneoplastic antibodies (Hu, CV2/CRMP5, etc)
Group 3: Ganglioside anti...
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Testing for autoimmune antibodies in axonal polyneuropathies without a clear etiology is considered when the clinical picture, history, or associated features suggest an underlying immune-mediated or paraneoplastic process. Here’s when it would be reasonable to consider antibody testing:
1. Subacute Onset or Rapid Progression
Faster-than-expected progression (weeks to a few months) is suspicious for an immune-mediated cause rather than a classic length-dependent axonal neuropathy from metabolic ...
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