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首页> 外文期刊>BMC Neurology >Clinical characteristics and short-term prognosis of LGI1 antibody encephalitis: a retrospective case study
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Clinical characteristics and short-term prognosis of LGI1 antibody encephalitis: a retrospective case study

机译:LGI1抗体脑炎的临床特征和短期预后:回顾性病例研究

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摘要

Recently, most reports of Leucine-rich glioma-inactivated 1 (LGI1) antibody encephalitis are from Europe and the US, while the short term outcome and clinical characteristics of Chinese patients are rarely reported,we study the clinical manifestations, laboratory results and brain magnetic resonance images (MRI) of eight patients who were recently diagnosed with LGI1 antibody encephalitis in our hospital to improve the awareness and knowledge of this disease. Eight patients (five males and three females; mean age, 63.4) with LGI1 antibody encephalitis who were diagnosed and treated in the Department of Neurology of Shengjing Hospital of China Medical University from September 2016 to June 2017 were recruited for the current study. Their general information, clinical manifestations, treatment regimens, and short-term prognoses were retrospectively analyzed, as were the results from MRI and laboratory findings. Overall, patient symptoms included cognitive impairment, which manifested primarily as memory deficits (8/8), seizures (including faciobrachial dystonic seizure, (FBDS)) (8/8), psychiatric and behavioral disorders (7/8), sleep disorders (4/8), and autonomic abnormalities (3/8). Five patients also had abnormal findings on brain MRI, mainly involving the hippocampus, basal ganglia and insula. Hyponatremia occurred in six cases. All patients tested positive for LGI1 antibodies in their serum/cerebrospinal fluid (CSF)and patients were negative for tumors. Symptoms rapidly improved after treatment with immunoglobulin and/or steroid therapy. The patients were followed up for 4–13?months after discharge, and two patients relapsed. Primary symptoms of LGI1 antibody encephalitis include memory impairments, seizures, FBDS, and mental and behavioral abnormalities. Increased titers of LGI1 antibodies are also present in the serum/CSF of patients. Patients often have hyponatremia, and MRIs show abnormalities in various brain regions. Finally, immunotherapy shows good efficacy and positive benefits, although patients may relapse in the short-term.
机译:近年来,有关富含亮氨酸的神经胶质瘤灭活1(LGI1)抗体脑炎的报道大多来自欧洲和美国,而中国患者的短期结局和临床特征很少报道,我们研究其临床表现,实验室检查结果和脑磁图最近在我院诊断为LGI1抗体脑炎的八例患者的磁共振图像(MRI),以提高对该疾病的认识和知识。招募了2016年9月至2017年6月在中国医科大学附属盛京医院神经内科诊治的8例LGI1抗体脑炎患者(男5例,女3例;平均年龄63.4)。回顾性分析他们的一般信息,临床表现,治疗方案和短期预后,以及MRI和实验室检查结果。总体而言,患者症状包括认知障碍,主要表现为记忆力减退(8/8),癫痫发作(包括面臂臂肌张力性惊厥(FBDS))(8/8),精神病和行为障碍(7/8),睡眠障碍( 4/8)和自主神经异常(3/8)。五名患者在脑部MRI上也有异常发现,主要涉及海马,基底神经节和岛状。低钠血症发生6例。所有患者的血清/脑脊液(CSF)中LGI1抗体均呈阳性,而肿瘤呈阴性。免疫球蛋白和/或类固醇治疗后,症状迅速改善。出院后对患者进行了4-13个月的随访,两名患者复发。 LGI1抗体脑炎的主要症状包括记忆力减退,癫痫发作,FBDS以及精神和行为异常。患者的血清/ CSF中也存在LGI1抗体效价升高的情况。患者常患有低钠血症,MRI显示大脑各个区域异常。最后,尽管患者可能在短期内复发,但免疫疗法显示出良好的疗效和积极的益处。

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