Focal Cerebral Arteriopathy and Stroke Secondary to Tuberculous Meningitis

Mahesh Chikkannaiah, Sarah G. Yu, Laura D. Fonseca, Ajay Goenka, Gogi Kumar
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引用次数: 0

Abstract

In countries where tuberculosis (TB) is endemic, children with tuberculous meningitis (TBM) commonly present with cerebrovascular complications such as stroke [1]. Herein, we present a patient from the United States with stroke associated with focal cerebral arteriopathy (FCA) secondary to TBM.

This 11-month-old girl presented with left hemiparesis and seizure. About 1.5 weeks before presentation, her parents noticed fatigue and decreased appetite and that she was not crawling as usual. Two days before presentation, her parents noticed decreased strength in her left arm and leg. Computed tomography of the head showed an area of hypoattenuation in the right basal ganglia and loss of gray and white matter differentiation in the right frontal cortex. While en route to our hospital, she had a seizure described as bilateral upper extremity shaking lasting 1 min, which self-resolved. On examination, she had right preferential gaze and left hemiparesis. Laboratory findings were significant for hyponatremia of 126 mEq/L. Magnetic resonance imaging of the brain (Figure 1) showed a right middle cerebral artery (MCA) distribution ischemic stroke. Magnetic resonance angiography (Figure 2) showed decreased flow in the right supraclinoid portion of the right internal carotid artery (ICA), A1 segment of the right anterior cerebral artery (ACA), and M1 segment of the right MCA and mild narrowing involving the petrous portion of the right carotid artery and carotid siphon. Her evaluation included cerebrospinal fluid (CSF) evaluation, which showed pleocytosis (235 cells/μL) with hypoglycorrhachia (11 mg/dL) and an elevated CSF protein (272 mg/dL).

Additional evaluation included CSF testing (bacterial culture, viral meningitis/encephalitis panel, herpes simplex virus polymerase chain reaction [PCR], and varicella virus PCR and antibodies) and respiratory panel for COVID-19, which were all negative. Chest computed tomography showed mediastinal and right hilar lymphadenopathy as well as nodular opacities in bilateral upper lobes with a miliary pattern.

Further family history included exposure to grandfather 1 month before his diagnosis of active TB; her grandfather had recently traveled to his native country, where TB is endemic. An interferon-gamma release assay and gastric aspirate culture were positive for Mycobacterium tuberculosis. The TB skin test was also positive. A CSF acid-fast bacilli culture was negative. She was diagnosed with FCA with right MCA stroke secondary to TBM and disseminated TB. She was treated with steroids and antitubercular therapy. Her seizures were controlled with levetiracetam and phenobarbital, which were weaned off as an outpatient. Upon the most recent follow-up at 3 years of age, she had spastic left hemiplegia, and she was able to sit independently but was not walking yet.

TB affects 1.2 million children worldwide, with an estimated 4% of TB diagnoses progressing to TBM [1-3]. The peak incidence of TBM in children is 2–4 years, with presentation ranging from nonspecific symptoms such as fever and headache to more progressive symptoms including cranial nerve palsies, focal neurological deficits, and stroke [1, 3, 4]. In the VIPS study, distal ICA was typically involved in individuals with an infection-related FCA like meningitis, as in our patient, compared with proximal MCA involvement in FCA related to other etiologies [5]. Infection should be considered in FCA involving the distal ICA, although MCA and ACA involvement is not uncommon [6]. In our patient, the imaging findings were suspicious for an infection-related FCA, which prompted an evaluation. Hyponatremia, CSF findings, and a history of exposure to a grandfather with TB guided our diagnosis for this patient.

Our patient emphasizes the imaging characteristics of an infection-related FCA. With increasing international travel and global immigration, clinicians, even in non-endemic countries, should consider TB in their differential diagnosis.

Mahesh Chikkannaiah: conceptualization, investigation, writing – original draft, writing – review and editing, methodology, visualization, supervision. Sarah G. Yu: investigation, writing – original draft, writing – review and editing. Laura D. Fonseca: writing – original draft, writing – review and editing, project administration. Ajay Goenka: writing – review and editing. Gogi Kumar: writing – review and editing, supervision.

A consent-to-disclose form was obtained from the legal guardian of the patient, authorizing the publication of the information included in this article. This case report was acknowledged by the institutional review board of the hospital (Study #2023-003, IRB# 2002722) and determined as a non-research activity.

The authors declare no conflicts of interest.

Abstract Image

继发于结核性脑膜炎的局灶性脑动脉病变和中风
在结核病流行的国家,患有结核性脑膜炎(TBM)的儿童通常伴有脑血管并发症,如脑卒中。在此,我们报告了一位来自美国的脑卒中伴局灶性脑动脉病变(FCA)继发于TBM的患者。这个11个月大的女孩表现为左偏瘫和癫痫。大约在分娩前1.5周,她的父母注意到她的疲劳和食欲下降,并且她不像往常那样爬行。在就诊前两天,她的父母注意到她左臂和左腿的力量有所下降。头部计算机断层扫描显示右侧基底节区低衰减,右侧额叶皮层灰质和白质分化丧失。在去我们医院的途中,她癫痫发作,描述为双侧上肢颤抖,持续1分钟,并自行消退。经检查,患者有右倾凝视和左偏瘫。实验室结果对126 mEq/L的低钠血症有显著意义。脑磁共振成像(图1)显示右脑中动脉(MCA)分布缺血性卒中。磁共振血管造影(图2)显示右侧颈内动脉(ICA)、右侧大脑前动脉(ACA) A1段和右侧MCA M1段血流减少,轻度狭窄累及右侧颈动脉岩部和颈动脉虹吸。脑脊液(CSF)检查显示细胞增多(235个细胞/μL),低糖血症(11 mg/dL)和脑脊液蛋白升高(272 mg/dL)。其他评估包括脑脊液检测(细菌培养、病毒性脑膜炎/脑炎面板、单纯疱疹病毒聚合酶链反应[PCR]、水痘病毒聚合酶链反应和抗体)和COVID-19呼吸道面板,均为阴性。胸部电脑断层显示纵隔及右侧肺门淋巴结病变及双侧上叶结节性混浊,呈军事征状。进一步的家族史包括在祖父诊断出活动性结核病前1个月与祖父接触;她的祖父最近回到了肺结核流行的祖国。干扰素释放试验和胃抽吸培养均为结核分枝杆菌阳性。结核菌皮肤试验也呈阳性。脑脊液抗酸杆菌培养阴性。她被诊断为FCA,右MCA中风继发于TBM和播散性结核病。她接受了类固醇和抗结核治疗。她的癫痫发作由左乙拉西坦和苯巴比妥控制,这两种药物在门诊时停用。在3岁时的最近一次随访中,她患有痉挛性左偏瘫,她能够独立坐着,但还不能走路。结核病影响全世界120万儿童,估计有4%的结核病诊断进展为结核性结核[1-3]。TBM在儿童中的发病率高峰为2-4岁,表现从发热、头痛等非特异性症状到更进行性的症状,包括脑神经麻痹、局灶性神经功能缺损和中风[1,3,4]。在VIPS研究中,与近端MCA受累与其他病因相关的FCA相比,远端ICA通常累及感染相关的FCA(如脑膜炎),就像我们的患者一样。尽管累及MCA和ACA并不罕见,但累及远端ICA的FCA应考虑感染。在我们的患者中,影像学结果怀疑是感染相关的FCA,这促使我们进行了评估。低钠血症、脑脊液检查结果以及与患有结核病的祖父接触史指导了我们对该患者的诊断。我们的病人强调了感染相关FCA的影像学特征。随着国际旅行和全球移民的增加,即使是非流行国家的临床医生也应在其鉴别诊断中考虑结核病。Mahesh Chikkannaiah:概念化,调查,写作-原稿,写作-审查和编辑,方法论,可视化,监督。Sarah G. Yu:调查,写作-原稿,写作-审查和编辑。劳拉·d·丰塞卡:写作-原稿,写作-审查和编辑,项目管理。阿杰伊·葛印卡:写作——评论和编辑。高基库马尔:写作-审查和编辑,监督。从患者的法定监护人处获得了一份同意披露表格,授权发布本文中包含的信息。该病例报告得到了医院机构审查委员会的认可(研究#2023-003,IRB# 2002722),并被确定为非研究活动。作者声明无利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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