MOGAD（MOG antibody–associated disease）の画像的特徴

森 雅裕

doi:10.15082/jsnt.40.4_594

Neurological Therapeutics

Online ISSN : 2189-7824
Print ISSN : 0916-8443
ISSN-L : 2189-7824

Radiological features of MOGAD

Masahiro Mori

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Keywords: myelin oligodendrocyte glycoprotein antibody–associated disease, aquaporin–4 antibody–associated disease, multiple sclerosis, neuromyelitis optica spectrum disorders, magnetic resonance imaging

JOURNAL FREE ACCESS

2023 Volume 40 Issue 4 Pages 594-597

DOI https://doi.org/10.15082/jsnt.40.4_594

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Abstract

MOGAD (myelin oligodendrocyte glycoprotein antibody–associated disease) has been recognized as a new disease entity which predominantly involves optic nerves, spinal cord, and brain including brainstem and cerebral cortex. The clinical and radiological features of MOGAD has been elucidated comparing with the ones of aquaporin–4 antibody–associated disease (AQPAD) and multiple sclerosis. In this review, I summarize the clinical and radiological features of MOGAD.

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