Department of Neurology, Shengjing Hospital of China Medical University, Sanhao Street 36, Shenyang, Liaoning, China.
Neurol India. 2022 Jan-Feb;70(1):384-386. doi: 10.4103/0028-3886.338681.
Anti-leucine-rich glioma-inactivated 1 (LGI1) encephalitis is a rare type of non-paraneoplastic limbic encephalitis (LE) mainly characterized by seizures, cognitive disorder, faciobrachial dystonic seizures (FBDS), hyponatremia, insomnia, and autonomic dysfunction. Here, we report the case of an elderly female patient who tested positive for antibodies against LGI1 and was initially thought to have Hashimoto encephalopathy (HE) due to its similar clinical features and the patient's high titers of antithyroid antibody. Interestingly, during the course of the disease, the patient exhibited typical FBDS and brain magnetic resonance imaging (MRI) showed a hyperintense signal evolution from T2/Fluid attenuated inversion recovery (FLAIR) to T1-weighted image in the bilateral basal ganglia (BG), which have rarely been reported previously.
抗亮氨酸丰富胶质瘤失活 1 型 (LGI1) 脑炎是一种罕见的非副肿瘤性边缘叶脑炎 (LE),主要表现为癫痫发作、认知障碍、面臂肌张力障碍发作 (FBDS)、低钠血症、失眠和自主神经功能障碍。在这里,我们报告了一例老年女性患者,其 LGI1 抗体检测呈阳性,最初由于其相似的临床特征和患者高滴度的抗甲状腺抗体,被认为是桥本脑病 (HE)。有趣的是,在疾病过程中,患者出现了典型的 FBDS,脑部磁共振成像 (MRI) 显示双侧基底节区 (BG) 从 T2/FLAIR 到 T1 加权图像的高信号演变,这在以前很少有报道。