Paraneoplastic/autoimmune myelopathies

Mayra Montalvo1, Eoin P Flanagan2

  • 1Department of Neurology, University of Florida, Gainesville, FL, United States.

PubMed

Insights

Paraneoplastic myelopathies are rare neurological disorders associated with cancer, often presenting with progressive spinal cord symptoms. Early diagnosis and treatment, including immunotherapy, are crucial but prognosis remains poor.

Area of Science:

  • Neurology
  • Oncology
  • Immunology

Background:

  • Paraneoplastic myelopathies are rare neurological disorders affecting the spinal cord, often presenting insidiously or subacutely.
  • Risk factors include tobacco use and a family history of cancer, with common neural antibodies like amphiphysin and CRMP5/anti-CV2.
  • Lung and breast cancers are the most frequent oncologic associations.

Approach:

  • Cerebrospinal fluid analysis typically reveals lymphocytic pleocytosis with elevated protein.
  • Spinal MRI may show tract-specific, longitudinally extensive T2 hyperintensities with enhancement, though normal MRIs can occur.
  • Differential diagnosis includes nutritional deficiencies and other autoimmune/inflammatory conditions like multiple sclerosis or sarcoidosis.

Key Points:

  • Immune checkpoint inhibitor-induced myelitis can be considered within the spectrum of paraneoplastic myelopathies.
  • Management involves addressing the underlying cancer and employing immunotherapy.
  • Despite treatment, the prognosis is generally poor, with most patients becoming wheelchair-dependent.

Conclusions:

  • Paraneoplastic myelopathies represent a significant neurological complication of cancer requiring multidisciplinary management.
  • Understanding associated antibodies and imaging findings aids diagnosis.
  • Further research into more effective treatments is warranted to improve patient outcomes.

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