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一名老年男性自身免疫性脑炎的非典型表现:抗LG1边缘叶脑炎。

Atypical presentation of an elderly male with autoimmune encephalitis: anti-LG1 limbic encephalitis.

作者信息

Bhandari Binita, Basyal Bikash, Sendil Selin, Khanal Resha, Neupane Sunita, Nookala Vinod

机构信息

Department of Medicine, UPMC Pinnacle, Harrisburg, PA, USA.

Department of Medicine, Abington Jefferson Health, Abington, PA, USA.

出版信息

J Community Hosp Intern Med Perspect. 2020 Aug 2;10(4):377-379. doi: 10.1080/20009666.2020.1785160.

DOI:10.1080/20009666.2020.1785160
PMID:32850103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7427439/
Abstract

INTRODUCTION

We present a case of an elderly male with anti-LG1 limbic encephalitis involving hypothalamus presenting with acute changes in mental status and persistent hyperthermia.

CASE REPORT

A 74-year-old male presented to the hospital with fever and chills. He had also been evaluated by his PCP for changes in his mental status, trouble remembering things, and following directions while driving. A lumbar puncture was performed, and empiric meningitis coverage was initiated. His LP results were not suggestive for any infectious process. An MRI showed bilateral hippocampal edema. As an infectious workup was non-revealing and other causes were ruled out, with the concern for paraneoplastic or autoimmune encephalitis, patient was started on high dose steroids and plasma exchange while results of antibodies for autoimmune and paraneoplastic encephalitis were awaited. After plasmapheresis and a course of steroids, the patient's mental status began to slowly improve. He was discharged from the hospital and on subsequent neurology office visit, his serum autoimmune encephalitis panel returned positive for anti-LGI 1 antibodies. Further management consisted of outpatient rituximab infusion.

DISCUSSION

Diagnosis of limbic encephalitis can be challenging and can present with symptoms of limbic dysfunction. A modest index of suspicion of limbic encephalitis should be kept in adults with altered mental changes. Early recognition and initiation of therapy can be crucial in the management of patients with autoimmune encephalitis and can prevent permanent cognitive impairment and damage.

摘要

引言

我们报告一例老年男性抗LGI1边缘叶脑炎累及下丘脑,表现为精神状态急性改变和持续高热。

病例报告

一名74岁男性因发热和寒战入院。他还因精神状态改变、记忆困难以及驾驶时听从指示困难而接受其初级保健医生的评估。进行了腰椎穿刺,并开始经验性覆盖脑膜炎治疗。他的腰椎穿刺结果不提示任何感染性过程。磁共振成像显示双侧海马水肿。由于感染性检查未发现异常且排除了其他病因,考虑到副肿瘤性或自身免疫性脑炎,在等待自身免疫性和副肿瘤性脑炎抗体结果的同时,患者开始接受大剂量类固醇和血浆置换治疗。经过血浆置换和一个疗程的类固醇治疗后,患者的精神状态开始缓慢改善。他出院了,在随后的神经科门诊就诊时,他的血清自身免疫性脑炎检测结果显示抗LGI1抗体呈阳性。进一步的治疗包括门诊利妥昔单抗输注。

讨论

边缘叶脑炎的诊断可能具有挑战性,可表现为边缘叶功能障碍的症状。对于精神状态改变的成年人,应保持对边缘叶脑炎的适度怀疑指数。早期识别和开始治疗对于自身免疫性脑炎患者的管理至关重要,可预防永久性认知障碍和损害。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0f7/7427439/a3ba8f9a881d/ZJCH_A_1785160_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0f7/7427439/a04f4fa46b35/ZJCH_A_1785160_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0f7/7427439/a3ba8f9a881d/ZJCH_A_1785160_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0f7/7427439/a04f4fa46b35/ZJCH_A_1785160_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0f7/7427439/a3ba8f9a881d/ZJCH_A_1785160_F0002_B.jpg

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Anti-NMDA receptor encephalitis associated with atrial fibrillation and hearing loss.抗N-甲基-D-天冬氨酸受体脑炎伴心房颤动和听力损失
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Anti-LGI1 Limbic Encephalitis Presented with Atypical Manifestations.抗 LGI1 边缘性脑炎的不典型表现。
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What should you know about limbic encephalitis?关于边缘叶性脑炎你应该了解些什么?
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Anti-N-methyl-D-aspartate receptor encephalitis: an emerging cause of centrally mediated sinus node dysfunction.抗 N-甲基-D-天冬氨酸受体脑炎:一种中枢介导窦房结功能障碍的新病因。
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