Tuberculoma development in tuberculosis immune reconstitution inflammatory syndrome in an infant

Alexandria E. Melendez-Zaidi, Fábio A. Nascimento, Nikita M. Shukla, Thierry A. G. M. Huisman
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Abstract

A 14-month-old girl presented to the emergency department (ED) with two weeks of fever, vomiting, and new onset focal and generalized seizures and was diagnosed with tuberculosis (TB) meningitis based on imaging and serum studies, later confirmed by a TB-specific culture of the cerebral spinal fluid (CSF, acid-fast bacilli culture). She was started on anti-TB combination therapy (rifampin, isoniazid, pyrazinamide, and levofloxacin). One month later she returned to the ED with 10 days of fussiness, beginning after receiving scheduled vaccinations. Neuroimaging revealed intraparenchymal and leptomeningeal tuberculomas surrounding the anterior and posterior circulation (middle panel), which were absent from prior imaging (left panel). Repeat CSF cultures were negative for TB or other infections, leading to a diagnosis of paradoxical TB immune reconstitution inflammatory syndrome (TB-IRIS). She was started on steroids, and tuberculomas resolved within six months (right panel). She has remained seizure-free but has persistent delays in communication.

Paradoxical TB-IRIS is a severe immune response that causes clinical worsening of TB lesions following initiation of appropriate treatment.1 Though rare, neurological symptoms from TB-IRIS develop at a median of 60 days after treatment.1, 2 Imaging classically demonstrates tuberculomas and/or meningitis. Patients are at a high risk of stroke given the tendency to develop lesions within the basal cisterns. Young children may be at higher risk of complications because their symptoms are often nonspecific (e.g., fussiness), leading to a delay in diagnosis (Figure 1).

Alexandria E. Melendez-Zaidi: Conceptualization; writing—original draft; writing—review and editing. Fábio A. Nascimento: Writing—review and editing. Nikita M. Shukla: Resources; writing—review and editing. Thierry A. G. M. Huisman: Resources; supervision; writing—original draft; writing—review and editing. All authors accept responsibility for conduct of the research.

The authors declare no conflicts of interest.

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婴儿结核免疫重建炎性综合征中结核瘤的发展
一名14个月大的女婴以两周的发热、呕吐和新发局灶性和全局性癫痫就诊于急诊科(ED),根据影像学和血清检查诊断为结核性脑膜炎(TB),后来通过脑脊液结核特异性培养(CSF,抗酸杆菌培养)确诊。她开始接受抗结核联合治疗(利福平、异烟肼、吡嗪酰胺和左氧氟沙星)。一个月后,她回到急诊科,在接受了预定的疫苗接种后,她开始了10天的焦虑。神经影像学显示肺实质内和轻脑膜结核瘤环绕前后循环(中图),先前影像学未见(左图)。重复脑脊液培养结核或其他感染呈阴性,导致诊断为矛盾结核免疫重建炎症综合征(TB- iris)。她开始使用类固醇,结核瘤在6个月内消退(右图)。她一直没有癫痫发作,但在沟通方面一直存在延迟。矛盾的结核病- iris是一种严重的免疫反应,在开始适当治疗后会导致结核病病变的临床恶化虽然罕见,但结核- iris的神经系统症状在治疗后中位数为60天出现。影像学典型表现为结核瘤和/或脑膜炎。患者中风的风险很高,因为有在基底池内发展病变的倾向。幼儿可能有更高的并发症风险,因为他们的症状通常是非特异性的(例如,大惊小怪),导致诊断延误(图1)。原创作品草案;写作-审查和编辑。Fábio A. Nascimento:写作、审查和编辑。尼基塔·m·舒克拉:资源;写作-审查和编辑。豪氏威马:资源;监督;原创作品草案;写作-审查和编辑。所有作者都对研究行为负责。作者声明无利益冲突。
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