代谢亢进
自身免疫性脑炎
医学
边缘脑炎
效价
脑炎
病理
基底神经节
基础(医学)
放射科
抗体
内科学
免疫学
中枢神经系统
病毒
胰岛素
作者
Wei Shan,Xiao Liu,Qun Wang
出处
期刊:Neurology
[Lippincott Williams & Wilkins]
日期:2019-11-12
卷期号:93 (20): e1917-e1918
被引量:6
标识
DOI:10.1212/wnl.0000000000008473
摘要
A 50-year-old woman presented with faciobrachial dystonic seizures for about 50 days during sleeping (figure, A). Initial MRI scan was normal, but FDG-PET showed hypermetabolism in the basal ganglia (BG) and medial temporal lobes (MTLs) (figure, B). Clinical symptoms raised a strong suspicion of LGI-1 autoimmune encephalitis (AE) diagnosis, and LGI-1 antibody titer examination (serum and CSF) confirmed the suspicion.1,2 After relapse, the patient showed a previous PET abnormal pattern.
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