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Updated: Jun 30, 2025

Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis
Published on: September 9, 2022
Paraneoplastic/autoimmune myelopathies
Mayra Montalvo1, Eoin P Flanagan2
1Department of Neurology, University of Florida, Gainesville, FL, United States.
Abstract:
Paraneoplastic myelopathies are a rare but important category of myelopathy. They usually present with an insidious or subacute progressive neurologic syndrome. Risk factors include tobacco use and family history of cancer. Cerebrospinal fluid analysis usually shows lymphocytic pleocytosis with elevated protein. MRI findings suggest that paraneoplastic myelopathies include longitudinally extensive T2 hyperintensities that are tract-specific and accompanied by enhancement, but spinal MRIs can also be normal. The most commonly associated neural antibodies include amphiphysin and collapsin-response-mediator-protein-5 (CRMP5/anti-CV2) antibodies with lung and breast cancers being the most frequent oncologic accompaniments. The differential diagnosis of paraneoplastic myelopathies includes nutritional deficiency myelopathy (B12, copper) as well as autoimmune/inflammatory conditions such as primary progressive multiple sclerosis or spinal cord sarcoidosis. Patients treated with immune checkpoint inhibitors for cancer may develop myelitis, that can be considered along the spectrum of paraneoplastic myelopathies. Management of paraneoplastic myelopathy includes oncologic treatment and immunotherapy. Despite these treatments, the prognosis is poor and the majority of patients eventually become wheelchair-dependent.
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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