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分枝杆菌性弓形体脉络膜视网膜炎伴发中枢神经系统病变:病例报告及文献复习。

Mycobacterium chimaera chorioretinitis preceding central nervous system lesions: a case report and review of the literature.

机构信息

Department of Ophthalmology, University of Kansas School of Medicine, 7400 State Line Rd, Prairie Village, Kansas, KS, 66208, USA.

出版信息

BMC Ophthalmol. 2022 Jul 22;22(1):316. doi: 10.1186/s12886-022-02528-2.

Abstract

BACKGROUND

Mycobacterium chimaera ocular infection is a rare disease that is linked to bypass devices used during cardiothoracic surgeries. Reported cases in the literature of ocular involvement preceding CNS involvement are based on clinical exam with no neuroimaging. Here we present a case of M. chimaera ocular infection with no CNS M. chimaera lesions on brain magnetic resonance imaging (MRI).

CASE PRESENTATION

A 59-year-old female presented with altered mental status and blurred vision in February 2021. Her past medical history was significant for aortic valve replacement and ascending aortic aneurysm repair in 2017 complicated by known M. chimaera infection. She had been receiving azithromycin, ethambutol, rifampin, and amikacin as systemic anti-mycobacterium treatment. Her dilated fundus exam showed numerous yellow placoid circular lesions scattered throughout the macula and peripheral retina in both eyes with associated vitritis. Systemic workup, including brain MRI showed no acute infectious lesions. Her infections workup was unremarkable except for a positive toxoplasma IgM, for which she was treated with sulfamethoxazole/trimethoprim. One month later, a head computed tomography showed new numerous scattered round foci of hyperdensity throughout the cerebrum and brainstem thought to be foci of M. chimaera infection. Clofazimine was added per culture and sensitivity. MRI brain 1 month later showed mild decrease in conspicuity and number of these intensities while on anti-mycobacterium treatment. Her cognition had improved at that time as well. She was seen in retina clinic 2 months later where her exam showed similar retinal lesions with no associated vitritis or anterior chamber cell in bilateral eyes, suggesting a lack of active infection. Optical coherence tomography macula showed parafoveal cystoid macular edema bilaterally. She was started on steroidal and non-steroidal anti-inflammatory eye drops.

CONCLUSIONS

To the best of our knowledge, this is the first case in the literature to report M. chimaera chorioretinitis with concomitant negative neuroimaging. Chorioretinal M. chimaera lesions should motivate high suspicion of CNS involvement prompting early neurological work up.

摘要

背景

分枝杆菌属奇美拉眼部感染是一种罕见疾病,与心胸外科手术中使用的旁路装置有关。文献中报道的眼部受累先于中枢神经系统受累的病例是基于无神经影像学检查的临床检查。在这里,我们报告了一例分枝杆菌属奇美拉眼部感染,而脑部磁共振成像(MRI)无中枢神经系统分枝杆菌属奇美拉病变。

病例介绍

一名 59 岁女性于 2021 年 2 月出现精神状态改变和视力模糊。她的既往病史包括 2017 年主动脉瓣置换和升主动脉瘤修复,期间发生了已知的分枝杆菌属奇美拉感染。她一直在接受阿奇霉素、乙胺丁醇、利福平、阿米卡星等全身性抗分枝杆菌治疗。她的眼底检查显示双眼黄斑区和周边视网膜有许多黄色盘状圆形病变,伴有葡萄膜炎。全身检查,包括脑部 MRI,未显示急性感染性病变。她的感染检查除了弓形虫 IgM 阳性外无其他异常,为此她接受了磺胺甲恶唑/甲氧苄啶治疗。一个月后,头部 CT 显示大脑和脑干有许多新的散在圆形高密度灶,被认为是分枝杆菌属奇美拉感染灶。根据培养和药敏结果,加用氯法齐明。一个月后,脑部 MRI 显示在抗分枝杆菌治疗期间,这些强度的可见度和数量略有下降。此时,她的认知功能也有所改善。两个月后,她在视网膜诊所就诊,双眼视网膜病变相似,无相关葡萄膜炎或前房细胞,提示无活动性感染。光学相干断层扫描黄斑显示双侧黄斑区旁中心性囊样水肿。她开始使用皮质类固醇和非甾体抗炎眼药。

结论

据我们所知,这是文献中首例报告分枝杆菌属奇美拉脉络膜炎同时伴有阴性神经影像学的病例。脉络膜视网膜分枝杆菌属奇美拉病变应引起对中枢神经系统受累的高度怀疑,促使早期进行神经学检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aaf/9308188/6295c7a22f78/12886_2022_2528_Fig1_HTML.jpg

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