医学
视神经脊髓炎
抗体
多发性硬化
髓鞘少突胶质细胞糖蛋白
光谱紊乱
脱髓鞘病
水通道蛋白4
磁共振成像
疾病
少突胶质细胞
免疫学
髓鞘
病理
白质
视神经炎
脊髓炎
横贯性脊髓炎
中枢神经系统
内科学
放射科
实验性自身免疫性脑脊髓炎
精神科
作者
S. Salama,Majid Khan,Mark Levy,Izlem Izbudak
标识
DOI:10.1016/j.msard.2019.11.041
摘要
Myelin Oligodendrocyte Glycoprotein (MOG) antibody and aquaporin-4 (AQP4) antibody seropositive diseases are immunological distinct subtypes of neuromyelitis optica spectrum disorders (NMOSD) with similar clinical presentations. Magnetic resonance imaging (MRI) findings can be instrumental in distinguishing MOG antibody disease from AQP4 antibody NMOSD. This is a retrospective study of 26 MOG and 25 AQP4 seropositive patients in which MRI features of the brain were compared. Brain abnormalities showed some overlap, but cortical grey/ juxtacortical white matter involvement was distinct to MOG patients, while area postrema involvement was a rare feature. Cortical grey/ juxtacortical white matter lesions on brain MRI might help distinguish MOG antibody disease from AQP4 positive NMOSD. These findings could be of value in distinguishing the two entities as early as the first presentation.
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