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伴有LGI1抗体的边缘叶脑炎的临床特征。

Clinical features of limbic encephalitis with LGI1 antibody.

作者信息

Wang Meiling, Cao Xiaoyu, Liu Qingxin, Ma Wenbin, Guo Xiaoqian, Liu Xuewu

机构信息

Department of Neurology, Qilu Hospital of Shandong University, Jinan.

Department of Neurology, Binzhou Medical University Hospital, Binzhou.

出版信息

Neuropsychiatr Dis Treat. 2017 Jun 16;13:1589-1596. doi: 10.2147/NDT.S136723. eCollection 2017.

Abstract

OBJECTIVE

The objective of this study was to analyze the clinical manifestation, course, evolution, image manifestation, and treatments of LGI1 limbic encephalitis (LE).

PATIENTS AND METHODS

Studies confirmed that LE with the complex antibody of voltage-gated potassium channels is LGI1 LE. Since then, LE cases have been reported. In this study, 10 typical LE cases were searched in PubMed. These cases and one additional case, which we reported herein, were retrospectively analyzed.

RESULTS

All the patients suffered from recent memory deterioration. The following cases were observed: eight with faciobrachial dystonic seizures (FBDS), six with different kinds of epileptic seizures (four complex partial seizures, one myoclonus seizure, and one generalized tonic-clonic seizure), four with FBDS and different kinds of epileptic seizures at the same time, five with mental disorders (one visual hallucination, one paranoia, one depression, one anxiety, and one dysphoria), five with hyponatremia, and two with sleep disorder. The brain MRI of nine patients revealed abnormalities in the mediotemporal lobe and the hippocampus. The LGI1 antibodies in the blood and/or cerebrospinal fluid (CSF) were positive. The content of the CSF protein of two patients increased slightly. The tumor marker of all the patients was normal, but capitate myxoma was detected in the combined pancreas duct of one patient. Gamma globulin and hormone treatments were administered to nine patients. Of these patients, six received a combination of antiepileptic drugs. The clinical symptoms of all the patients improved.

CONCLUSION

LGI1 LE is an autoimmune encephalitis whose clinical manifestations are memory deterioration, FBDS, epileptic seizure, mental disorders, and hyponatremia. Brain MRI shows that this autoimmune disease mainly involves the mediotemporal lobe and the hippocampus. This condition can also be manifested with other autoimmune encephalitis cases but can be rarely associated with tumors. After patients with LGI1 LE receive gamma globulin and hormone treatments, their clinical prognosis is good.

摘要

目的

本研究旨在分析LGI1边缘叶脑炎(LE)的临床表现、病程、演变、影像表现及治疗方法。

患者与方法

研究证实,伴有电压门控钾通道复合抗体的LE为LGI1 LE。此后,陆续有LE病例报道。本研究在PubMed上检索了10例典型的LE病例。对这些病例以及本文报道的另外1例病例进行回顾性分析。

结果

所有患者均有近期记忆力减退。观察到以下情况:8例有面臂肌张力障碍性癫痫发作(FBDS),6例有不同类型的癫痫发作(4例复杂部分性发作、1例肌阵挛发作和1例全身强直阵挛发作),4例同时有FBDS和不同类型的癫痫发作,5例有精神障碍(1例视幻觉、1例偏执狂、1例抑郁、1例焦虑和1例烦躁不安),5例有低钠血症,2例有睡眠障碍。9例患者的脑部MRI显示中颞叶和海马区异常。血液和/或脑脊液(CSF)中的LGI1抗体呈阳性。2例患者的CSF蛋白含量略有升高。所有患者的肿瘤标志物均正常,但1例患者的胰腺导管合并有头状黏液瘤。9例患者接受了γ球蛋白和激素治疗。其中,6例患者联合使用了抗癫痫药物。所有患者的临床症状均有改善。

结论

LGI1 LE是一种自身免疫性脑炎,其临床表现为记忆力减退、FBDS、癫痫发作、精神障碍和低钠血症。脑部MRI显示,这种自身免疫性疾病主要累及中颞叶和海马区。这种情况也可能与其他自身免疫性脑炎病例表现相似,但很少与肿瘤相关。LGI1 LE患者接受γ球蛋白和激素治疗后,临床预后良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb1/5481279/2c3401fa0116/ndt-13-1589Fig1.jpg

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