Deng Lan, Li Bing-Hu
Department of Neurology, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, China.
J Int Med Res. 2025 Jun;53(6):3000605251350961. doi: 10.1177/03000605251350961. Epub 2025 Jun 25.
Anti-leucine-rich glioma-inactivated-1 (LGI1) autoimmune encephalitis is one of the most prevalent forms of autoantibody-associated limbic encephalitis. Brain magnetic resonance imaging of patients with anti-LGI1 encephalitis often presents as fluid-attenuated inversion recovery hyperintensities of the medial temporal lobe. We report the case of a man in his early 60s who suddenly experienced involuntary movement of the right limbs. Brain magnetic resonance imaging revealed normal T1 signal and T2 hyperintensity in the left caudate nucleus, with corresponding fluid-attenuated inversion recovery hyperintensity, diffusion-weighted imaging hyperintensity, and apparent diffusion coefficient hypointensity. The patient was ultimately diagnosed with anti-LGI1 autoimmune encephalitis. For patients with unilateral involuntary movement accompanied by restricted diffusion in the basal ganglia region, anti-LGI1 encephalitis should be considered.
抗富含亮氨酸胶质瘤失活蛋白1(LGI1)自身免疫性脑炎是自身抗体相关性边缘性脑炎最常见的形式之一。抗LGI1脑炎患者的脑磁共振成像常表现为内侧颞叶的液体衰减反转恢复序列高信号。我们报告了一例60岁出头的男性患者,他突然出现右肢不自主运动。脑磁共振成像显示左侧尾状核T1信号正常,T2高信号,相应的液体衰减反转恢复序列高信号、扩散加权成像高信号及表观扩散系数低信号。该患者最终被诊断为抗LGI1自身免疫性脑炎。对于伴有基底节区扩散受限的单侧不自主运动患者,应考虑抗LGI1脑炎。