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Takayasu 动脉炎合并结核性脑梗死:一例不常见的儿科病例报告。

Stroke in Takayasu arteritis with concomitant tuberculosis: an unusual pediatric case report.

机构信息

Department of Pediatric Tuberculosis, Shenyang Tenth People's Hospital, Shenyang Chest Hospital, Shenyang, 110044, Liaoning, China.

出版信息

BMC Pediatr. 2022 Jan 20;22(1):50. doi: 10.1186/s12887-022-03125-4.

Abstract

BACKGROUND

Stroke is a lethal complication of polyarteritis in children. Takayasu arteritis is a rare disease with an unknown etiology and is known to mainly affect young women. In this report, we present the case of a Chinese boy diagnosed with TA results in stroke, originally presenting in the context of latent tuberculosis infection and then developing active tuberculosis.

CASE PRESENTATION

The patient was a 14-year-old child who developed a latent tuberculosis infection at age 5 after coming in close contact with his grandfather, who had tuberculosis. However, he did not receive any anti-tuberculosis medications at that time. At age 9, he was hospitalized for symptoms of "dizziness and headache" and was diagnosed with Takayasu arteritis and hypertension; however, tuberculosis was not diagnosed. Only antihypertensive drugs were administered without considering the possible pathogenic factors of tuberculosis infection. At age 14, he was rehospitalized for "fever and cough" and was diagnosed with active pulmonary tuberculosis as an analysis of his fiberoptic bronchoscopy sample using the Gene-Xpert assay was positive for Mycobacterium tuberculosis. However, after 2 months of taking oral anti-tuberculosis drugs, his blood pressure continued to rise, and he presented with numbness and weakness of the right limb and a deviation of the right side of his mouth. Computed tomography angiography of his head and neck revealed that the walls of the left subclavian artery and bilateral vertebral arteries were thickened, and the lumen was significantly narrowed. In a recent examination, magnetic resonance imaging and diffusion-weighted imaging of the head showed infarctions in the right basal ganglia area close to the left lateral ventricle. Our patient was treated with methotrexate, tocilizumab and glucocorticoids to control he continued active vasculitis.

CONCLUSIONS

The possible association of tuberculosis and Takayasu arteritis complicated by stroke needs to be considered, especially in children who had prior contact with a family member with tuberculosis infection. The temporal relationship between TA and infection with Mycobacterium tuberculosis in our patient suggests a compelling link that demands further investigation.

摘要

背景

儿童多发性动脉炎可导致中风,是一种致命的并发症。Takayasu 动脉炎是一种罕见的疾病,病因不明,主要影响年轻女性。本报告介绍了一例中国男孩,最初表现为潜伏性结核感染,随后发展为活动性结核,导致 Takayasu 动脉炎并发中风。

病例介绍

患者为 14 岁男孩,5 岁时与患有肺结核的祖父密切接触后感染潜伏性结核。但当时他并未接受任何抗结核药物治疗。9 岁时,他因“头晕头痛”住院,被诊断为 Takayasu 动脉炎和高血压;然而,未诊断出结核病。仅给予了降压药物治疗,并未考虑到可能存在结核感染的致病因素。14 岁时,他因“发热咳嗽”再次住院,纤维支气管镜样本 Gene-Xpert 检测结果阳性,诊断为活动性肺结核。然而,在口服抗结核药物治疗 2 个月后,他的血压持续升高,并出现右侧肢体麻木无力和口角歪斜。头颈部 CT 血管造影显示左侧锁骨下动脉和双侧椎动脉壁增厚,管腔明显狭窄。最近的检查显示,头部磁共振成像和弥散加权成像显示右侧基底节区靠近左侧侧脑室的梗死灶。我们的患者接受了甲氨蝶呤、托珠单抗和糖皮质激素治疗,以控制持续的活动性血管炎。

结论

需要考虑结核病和 Takayasu 动脉炎并发中风之间的可能关联,特别是在与结核病感染的家庭成员有过接触的儿童中。在我们的患者中,TA 和结核分枝杆菌感染之间的时间关系提示存在强烈关联,需要进一步调查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e11d/8772212/59fd61b81062/12887_2022_3125_Fig1_HTML.jpg

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