ArticleCureus2024
Unique Magnetic Resonance Imaging Findings in Opsoclonus-Myoclonus Syndrome Secondary to the West Nile Virus.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
4 authors.
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Abstract
Opsoclonus-Myoclonus syndrome is a rare neurological disorder that presents with oculomotor dysfunction and is associated with immunological triggers such as an infection. We present a patient with Opsoclonus-Myoclonus syndrome secondary to a West Nile virus (WNV) infection and focus on a unique series of magnetic resonance imaging findings. The following is a case report based on experience taking care of the patient as a member of the primary team in the hospital, chart review, and imaging findings obtained and reported through the department of radiology. A 61-year-old male presented with fatigue, ataxia, dysarthria, and fever after a recent cabin visit in the summer. The initial workup ruled out meningitis and stroke. The patient's condition deteriorated despite empiric treatment. Repeat magnetic resonance imaging (MRI) revealed patchy fluid-attenuated inversion recovery (FLAIR) hyperintensities in the cerebellar hemispheres. Further evaluation confirmed West Nile virus infection through positive immunoglobulin M (IgM) and immunoglobulin G (IgG) antibodies. This case underscores the importance of neuroimaging in evaluating encephalopathy, especially in the presence of multiple comorbidities. These findings contribute to the broader knowledge of West Nile virus encephalitis.
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