Suppr超能文献

抗LGI1自身免疫性边缘叶脑炎:一种易漏诊的疾病。

Anti-LGI1 Autoimmune Limbic Encephalitis: An Easy-To-Miss Diagnosis.

作者信息

Freitas Henriques Carolina, Fernandes Rui, Neves Leonor, Miranda Rubina, Noronha Duarte, Aguiar Teresa Carolina, Faria Teresa

机构信息

Internal Medicine Department, Hospital Central do Funchal, Funchal, Portugal.

Internal Medicine Department, Hospital Prof. Doutor Fernando Fonseca, Amadora, Portugal.

出版信息

Eur J Case Rep Intern Med. 2024 Nov 19;11(12):005025. doi: 10.12890/2024_005025. eCollection 2024.

Abstract

BACKGROUND

Autoimmune limbic encephalitis (ALE) is a rare inflammatory disorder characterised by a subacute onset, usually within weeks. The presence of multiple neuropsychiatric symptoms such as seizures, short-term memory deficits, anxiety and depression often leads to misdiagnosis as another medical condition, contributing to poor prognosis and reduced long-term survival.

CASE DESCRIPTION

A 60-year-old man, with no chronic illnesses, presented at the emergency department with daily episodes of palpitations, shivering, piloerection and a sense of impending doom lasting two months. Initially diagnosed with anxiety disorder and treated with venlafaxine 50 mg daily, he showed no improvement and developed memory loss. Hospitalised three months later, he exhibited both temporal and spatial disorientation, along with short-term memory loss. Key findings included elevated serum sedimentation rate, hyponatraemia, increased cerebrospinal fluid (CSF) protein levels and cranial magnetic resonance imaging evidence of bilateral temporal intra-parenchymal lesions, suggesting limbic encephalitis. After ruling out alternative diagnoses, screening of autoantibodies in the CSF was requested, which was positive for anti-LGI1 antibodies. The diagnosis of anti-LGI1 ALE was assumed, and treatment was initiated with significant clinical and imaging improvement.

CONCLUSIONS

ALE's broad clinical spectrum contributes to underdiagnosis. Therefore, in patients with new onset of neuropsychiatric symptoms and no prior psychiatric history, ALE should be considered, as prompt diagnosis and treatment are pivotal to achieve a good prognosis.

LEARNING POINTS

Autoimmune limbic encephalitis is a rare inflammatory neurological disease that affects the limbic system particularly the hippocampus, leading to memory impairment and neuropsychiatric symptoms.Due to its wide range of neuropsychiatric symptoms, the diagnosis of autoimmune limbic encephalitis may go unnoticed, leading to misdiagnosis as another medical disorder.Early diagnosis is essential to prevent potential neurological sequelae through appropriate treatment.

摘要

背景

自身免疫性边缘叶脑炎(ALE)是一种罕见的炎症性疾病,通常在数周内呈亚急性起病。癫痫发作、短期记忆缺陷、焦虑和抑郁等多种神经精神症状的存在,常常导致误诊为其他疾病,从而导致预后不良和长期生存率降低。

病例描述

一名60岁男性,无慢性疾病史,因每日发作心悸、寒战、竖毛及濒死感达两个月就诊于急诊科。最初被诊断为焦虑症,每日服用50mg文拉法辛治疗,症状无改善且出现记忆力减退。三个月后住院,表现为时间和空间定向障碍以及短期记忆丧失。主要检查结果包括血清沉降率升高、低钠血症、脑脊液(CSF)蛋白水平升高以及头颅磁共振成像显示双侧颞叶脑实质内病变,提示边缘叶脑炎。排除其他诊断后,要求对脑脊液进行自身抗体筛查,结果抗LGI1抗体呈阳性。考虑诊断为抗LGI1 ALE,并开始治疗,临床和影像学均有显著改善。

结论

ALE广泛的临床谱导致诊断不足。因此,对于新发神经精神症状且无既往精神病史的患者,应考虑ALE,因为及时诊断和治疗对于获得良好预后至关重要。

学习要点

自身免疫性边缘叶脑炎是一种罕见的炎症性神经疾病,影响边缘系统尤其是海马体,导致记忆障碍和神经精神症状。由于其广泛的神经精神症状,自身免疫性边缘叶脑炎的诊断可能被忽视,导致误诊为其他疾病。早期诊断对于通过适当治疗预防潜在的神经后遗症至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e394/11623357/4efefb2b87f6/5025_Fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验