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多发性大动脉炎合并颈动脉闭塞患儿的临床特征及预后

[Clinical features and prognosis of children with multiple Takayasu's arteritis complicated with carotid artery occlusion].

作者信息

He B P, Lai J M

机构信息

Affiliated Hospital of Inner Mongolia Medical University, Hohhot010010, China.

Children's Hospital Affiliated to Capital Institute of Pediatrics, Beijing100020, China.

出版信息

Zhonghua Yu Fang Yi Xue Za Zhi. 2024 Dec 6;58(12):2033-2037. doi: 10.3760/cma.j.cn112150-20240602-00444.

Abstract

This study aimed to analyze the clinical characteristics and prognosis of Takayasu's arteritis (TA) with carotid artery occlusion in children. This study collected clinical data and follow-up information on the first diagnosis and treatment of c-TA combined with carotid artery occlusion in pediatric patients at the Children's Hospital affiliated with the Capital Institute of Pediatrics and Inner Mongolia Medical University Affiliated Hospital from 2013 to 2023. This study included four female patients with a mean age of (13.25±1.71) years old. The time from onset to diagnosis was (8.14±11.19) months. Their main clinical symptoms and signs were dizziness, headache, chest discomfort, aphasia, dyskinesia, impaired mobility of the limbs, hypertension, asymmetry of blood pressure in the limbs, vascular murmurs or tremors, weakened radial artery pulsation, and decreased muscle strength. All four children showed elevated levels of C-reactive protein and erythrocyte sedimentation rate. The medical imaging results showed that among the four patients, three had bilateral carotid artery occlusion, and one had unilateral carotid artery occlusion. There were three cases of cerebrovascular involvement, accompanied by arterial involvement in multiple parts of the body, mainly involving bilateral subclavian arteries, cephalic trunk arteries, bilateral renal arteries, bilateral iliac arteries, and middle cerebral arteries. Four children were effectively treated with glucocorticoids and immunosuppressants. These children were followed up for a period of (42.25±52.54) months, which showed that the original affected artery still had varying degrees of occlusion, with no progression from the pre-treatment period and no new arterial involvement. The condition of three children with pre-existing physical and language disorders gradually improved. In summary, children with c-TA combined with carotid artery occlusion can cause involvement of multiple blood vessels. Their clinical manifestations are mostly systemic symptoms and ischemia of corresponding supply organs caused by vascular lesions, which are prone to be combined with cerebral infarction, and their occluded blood vessels are difficult to recover.

摘要

本研究旨在分析儿童大动脉炎(TA)合并颈动脉闭塞的临床特征及预后。本研究收集了2013年至2023年期间首都儿科研究所附属儿童医院及内蒙古医科大学附属医院收治的小儿c-TA合并颈动脉闭塞患者首次诊断及治疗的临床资料和随访信息。本研究纳入4例女性患者,平均年龄为(13.25±1.71)岁。从发病到诊断的时间为(8.14±11.19)个月。其主要临床症状和体征为头晕、头痛、胸部不适、失语、运动障碍、肢体活动受限、高血压、四肢血压不对称、血管杂音或震颤、桡动脉搏动减弱及肌力下降。4例患儿C反应蛋白和红细胞沉降率均升高。医学影像结果显示,4例患者中3例为双侧颈动脉闭塞,1例为单侧颈动脉闭塞。有3例脑血管受累,同时伴有身体多个部位动脉受累,主要累及双侧锁骨下动脉、头臂干动脉、双侧肾动脉、双侧髂动脉及大脑中动脉。4例患儿接受糖皮质激素和免疫抑制剂治疗有效。对这些患儿随访了(42.25±52.54)个月,结果显示原受累动脉仍有不同程度的闭塞,与治疗前相比无进展,也无新的动脉受累情况。3例原有肢体及语言障碍的患儿病情逐渐好转。综上所述,小儿c-TA合并颈动脉闭塞可导致多血管受累。其临床表现多为全身症状及血管病变引起的相应供血器官缺血,易合并脑梗死,且闭塞血管难以恢复。

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