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免疫功能低下宿主中模仿自身免疫性纹状体脑炎的塞拉托分枝杆菌脑炎:首例病例报告

Mycobacterium celatum encephalitis in an immunocompromised host mimicking autoimmune striatal encephalitis: the first case report.

作者信息

Taweephol Thanapoom, Pongpitakmetha Thanakit, Anukoolwittaya Prakit, Marukatat Chayoot, Rattanawong Wanakorn, Hemachudha Pasin, Vanichanan Jakapat, Rotcheewaphan Suwatchareeporn, Saraya Abhinbhen W

机构信息

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, 10330, Thailand.

Department of Pharmacology, Faculty of Medicine, Chulalongkorn University, Bangkok, 10330, Thailand.

出版信息

BMC Infect Dis. 2025 Mar 6;25(1):321. doi: 10.1186/s12879-025-10602-5.

Abstract

BACKGROUND

Encephalitis is rarely caused by nontuberculous mycobacteria (NTM), which is generally not considered a highly virulent pathogen. However, NTM encephalitis in immunocompromised hosts occurs with varied clinical presentations, posing a diagnostic challenge in clinical practice. This study aims to describe an atypical case of NTM encephalitis caused by Mycobacterium celatum, which has not previously been reported to infect the central nervous system of immunocompromised hosts, mimicking autoimmune striatal encephalitis (ASE).

CASE PRESENTATION

A 35-year-old immunosuppressed woman presented with prolonged fever for 4 months and rapidly progressive cognitive decline for 3 months. Neurological examination showed impaired cognition and parkinsonism. Laboratory testing was unremarkable. Her brain imaging on T2-weighted fluid-attenuated inversion recovery (T2/FLAIR) exhibited lesions involving basal ganglia and subcortical white matter in both hemispheres, mimicking ASE. Cerebrospinal fluid (CSF) analysis revealed mild pleocytosis with normal glucose and protein levels. CSF comprehensive microbiological studies and autoimmune panels were negative. ASE was suspected, and immunotherapies were given. Despite immunotherapies, her condition worsened with seizures, warranting a stereotactic brain biopsy to achieve a definite diagnosis. Her brain tissue pathology result was non-specific. However, we identified M. celatum from her brain tissue. Thus, the final diagnosis was M. celatum encephalitis. Therefore, we discontinued immunotherapies and started anti-NTM treatment, including isoniazid, rifampicin, ethambutol, and levofloxacin. After completing a 16-month treatment course, her clinical condition was stable, afebrile, and seizure-free.

CONCLUSIONS

We proposed that NTM invades the central nervous system and also triggers immune dysregulation, developing features resembling ASE. In case of suspicious autoimmune encephalitis with poor response to immunotherapies, a tissue biopsy should be performed to exclude chronic infection.

摘要

背景

脑炎很少由非结核分枝杆菌(NTM)引起,NTM通常不被认为是高毒力病原体。然而,免疫功能低下宿主中的NTM脑炎临床表现多样,给临床实践中的诊断带来挑战。本研究旨在描述一例由塞拉分枝杆菌引起的非典型NTM脑炎病例,此前尚未有该菌感染免疫功能低下宿主中枢神经系统的报道,该病例酷似自身免疫性纹状体脑炎(ASE)。

病例报告

一名35岁免疫功能低下的女性,持续发热4个月,认知功能迅速进行性下降3个月。神经系统检查显示认知障碍和帕金森综合征。实验室检查无异常。她的脑部T2加权液体衰减反转恢复序列(T2/FLAIR)成像显示双侧基底节和皮质下白质有病变,酷似ASE。脑脊液(CSF)分析显示轻度细胞增多,葡萄糖和蛋白质水平正常。CSF综合微生物学研究和自身免疫检查均为阴性。怀疑为ASE并给予免疫治疗。尽管进行了免疫治疗,她的病情仍因癫痫发作而恶化,因此需要进行立体定向脑活检以明确诊断。她的脑组织病理结果无特异性。然而,我们从她的脑组织中鉴定出了塞拉分枝杆菌。因此,最终诊断为塞拉分枝杆菌脑炎。于是,我们停止了免疫治疗并开始抗NTM治疗,包括异烟肼、利福平、乙胺丁醇和左氧氟沙星。完成16个月的治疗疗程后,她的临床状况稳定,无发热且无癫痫发作。

结论

我们提出NTM侵入中枢神经系统并引发免疫失调,从而出现类似ASE的特征。对于疑似自身免疫性脑炎且对免疫治疗反应不佳的病例,应进行组织活检以排除慢性感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e06e/11884120/9f8464f28566/12879_2025_10602_Fig1_HTML.jpg

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