Neurology:LGI-1自身免疫性脑炎患者3个不同阶段的18F-FDG-PET/SPM分析

2019-12-24 zyx 神经科病例撷英拾粹

50岁女性,睡眠时出现面臂肌张力障碍样发作约50天。

50岁女性,睡眠时出现面臂肌张力障碍样发作约50天(图A)。最初的MRI扫描正常,但FDG-PET可见基底节(BG)和颞叶内侧(MTL)高代谢(图B)。临床症状高度怀疑LGI-1自身免疫性脑炎的诊断,经LGI-1抗体滴度检测(血清和CSF)证实。复发后,患者再次表现为先前的PET异常模式。

LGI-1自身免疫性脑炎的早期诊断对于进一步治疗是必需的。PET上BG和MTL的代谢异常变化比MRI上病灶出现早。



(图:A:患者FBDS症状出现后的事件顺序;B:入院诊断,复发,出院和复查的3个不同时间阶段的代表性MRI和18F-FDG-PET/SPM[p <0.01]图像;BG=基底神经节;IVIg=静脉注射免疫球蛋白;IVMP=静脉注射甲强龙;MTL =颞叶内侧;VPA=丙戊酸)

原始出处:Shan W, Liu X, Wang Q. Teaching NeuroImages: 18F-FDG-PET/SPM analysis in 3 different stages from a patient with LGI-1 autoimmune encephalitis.Neurology. 2019 Nov 12;93(20):e1917-e1918.

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    2020-06-05 xugumin
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    2020-02-29 feather89
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    2020-01-04 hb2008ye
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