Abstract
Abnormal brain MRI has been described in up to 60% of patients with NMO patients. However, white matter T2 hyperintensities have been rarely observed. We report the case of a 49-year-old woman with long-lasting neuromyelitis optica (NMO) spectrum disorder and diffuse cerebral white matter T2-weighted hyperintensities. Our case suggests that some NMO patients can progressively develop l extensive cerebral involvement.
Keywords:
Devic’s syndrome; Neuromyelitis Optica; white matter disease.
© The Author(s), 2014.
MeSH terms
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Aquaporin 4 / immunology
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Autoantibodies / blood
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Biomarkers / blood
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Disease Progression
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Female
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Humans
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Immunosuppressive Agents / therapeutic use
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Leukoencephalopathies / diagnosis*
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Leukoencephalopathies / pathology
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Magnetic Resonance Imaging*
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Middle Aged
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Neuromyelitis Optica / blood
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Neuromyelitis Optica / diagnosis*
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Neuromyelitis Optica / drug therapy
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Neuromyelitis Optica / immunology
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Neuromyelitis Optica / pathology
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Predictive Value of Tests
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Time Factors
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Treatment Outcome
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White Matter / pathology*
Substances
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AQP4 protein, human
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Aquaporin 4
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Autoantibodies
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Biomarkers
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Immunosuppressive Agents