Decoding Multiple Antibody Positivity: Lessons from Paraneoplastic Sensory Ataxia

Paraneoplastic neurologic syndromes are cancer-associated, immune-mediated neurologic manifestations that may involve any part of the nervous system. They usually present with characteristic neurologic features and should be considered in high-risk phenotypes such as limbic encephalitis, encephalomyelitis, rapidly progressive cerebellar syndrome, opsoclonus-myoclonus, sensory neuronopathy, enteric neuropathy, and Lambert-Eaton myasthenic syndrome. The diagnosis is made by antibody positivity in the serum or cerebrospinal fluid, in the presence of an appropriate clinical phenotype. Findings on antibody testing by immunoblot should always be verified by immunofluorescence. We report a rare case of sensory neuronopathy with triple paraneoplastic antibody positivity (anti-Hu, anti-collapsing response-mediator protein 5, and anti-amphiphysin) on immunoblot but only anti-Hu positivity on immunofluorescence. The presence of lower facial dyskinesias should raise the possibility of an immune-mediated neurologic syndrome in the appropriate clinical context.

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Publication Details

Journal
Annals of Indian Academy of Neurology
Published
2024-08-21
DOI
https://doi.org/10.4103/aian.aian_307_24
Primary Topic
Autoimmune Neurological Disorders and Treatments
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article
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article

Decoding Multiple Antibody Positivity: Lessons from Paraneoplastic Sensory Ataxia

Awadh Kishor Pandit, Divyani Garg, Divya Madathiparambil Radhakrishnan, S. Sidharth et al.
Annals of Indian Academy of Neurology
Autoimmune Neurological Disorders and Treatments
article

Decoding Multiple Antibody Positivity: Lessons from Paraneoplastic Sensory Ataxia

Awadh Kishor Pandit, Divyani Garg, Divya Madathiparambil Radhakrishnan, S. Sidharth, Achal Kumar Srivastava, Pranjal Gupta, Shamim Ahmed Shamim, Anita Mahadevan, Ayush Agarwal
article en

Abstract

Paraneoplastic neurologic syndromes are cancer-associated, immune-mediated neurologic manifestations that may involve any part of the nervous system. They usually present with characteristic neurologic features and should be considered in high-risk phenotypes such as limbic encephalitis, encephalomyelitis, rapidly progressive cerebellar syndrome, opsoclonus-myoclonus, sensory neuronopathy, enteric neuropathy, and Lambert-Eaton myasthenic syndrome. The diagnosis is made by antibody positivity in the serum or cerebrospinal fluid, in the presence of an appropriate clinical phenotype. Findings on antibody testing by immunoblot should always be verified by immunofluorescence. We report a rare case of sensory neuronopathy with triple paraneoplastic antibody positivity (anti-Hu, anti-collapsing response-mediator protein 5, and anti-amphiphysin) on immunoblot but only anti-Hu positivity on immunofluorescence. The presence of lower facial dyskinesias should raise the possibility of an immune-mediated neurologic syndrome in the appropriate clinical context.

Annals of Indian Academy of NeurologyVol. 27(5)
All India Institute of Medical Sciences Raipur (IN), Wayne State University (US), All India Institute of Medical Sciences Bhopal (IN), All India Institute of Medical Sciences (IN), National Institute of Mental Health and Neurosciences (IN)
Good health and well-being
Openalex Percentile: Top 78%
Autoimmune Neurological Disorders and Treatments
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