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大动脉炎患儿的临床研究:来自中国单中心的回顾性研究。

Clinical study of children with Takayasu arteritis: a retrospective study from a single center in China.

作者信息

Feng Ye, Tang Xuemei, Liu Mingyue, Zhou Juan, Zhao Xiaodong, Li Qiu

机构信息

Department of Rheumatology and Immunology, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, No. 136, Zhongshan 2nd Road, Yuzhong District, Chongqing, 400014, People's Republic of China.

Chongqing Key Laboratory of Pediatrics, No. 136, Zhongshan 2nd Road, Yuzhong District, Chongqing, 400014, People's Republic of China.

出版信息

Pediatr Rheumatol Online J. 2017 Apr 17;15(1):29. doi: 10.1186/s12969-017-0164-2.

Abstract

BACKGROUND

Delayed diagnosis of childhood Takayasu arteritis (TA) is common due to its atypical symptoms. The objective of the present study was to summarize the clinical features of childhood TA to raise awareness and improve management.

METHODS

Eleven children diagnosed with TA at our hospital were enrolled. Clinical information, diagnosis, treatment, and outcome were then examined retrospectively. The Pediatric Vasculitis Activity Score (PVAS) and the Indian Takayasu Clinical Activity Score (ITAS2010) were used to assess disease activity.

RESULTS

Male-to-female ratio was 4:7. The mean age was 9.4 (1.4-14) years and the average time to diagnosis was 40.6 days (12-90 days). All patients suffered from hypertension and few had immunologic abnormalities. Two patients had low levels of autoantibodies and one had elevated immunoglobulin E levels. Aberrant (elevated) laboratory parameters included erythrocyte sedimentation rate (ESR) (9/10 patients, 90.0%), protein excretion (8/9 patients, 88.9%), renin-angiotensin-aldosterone system (RAAS) activity (5/5 patients, 100.0%), and serum lipid levels (3/5 patients, 60%). The common onset patterns were headache with convulsions (27.2%) and kidney damage (27.2%). The abdominal aorta (81.8%) and renal artery (72.7%) were the most commonly involved vessels. At presentation, the mean PVAS and ITAS2010 scores were 12.1 (6-26)/63 and 9.7 (5-14)/57, respectively. All patients were treated with glucocorticoids and antihypertensive agents; two underwent renal artery stent placement.

CONCLUSION

The diagnosis of TA should be considered in patients with pediatric hypertension and high expression of inflammatory markers or abnormal urine results. Doppler ultrasonography of major vessels may be helpful. PVAS and ITAS2010 both help to evaluate disease activity, and the PVAS is recommended for patients with kidney damage. Glucocorticoid and antihypertensive agents are effective. Interventional therapy can be an option for patients with persistent hypertension.

摘要

背景

儿童高安动脉炎(TA)因其非典型症状,延迟诊断很常见。本研究的目的是总结儿童TA的临床特征,以提高认识并改善管理。

方法

纳入我院诊断为TA的11名儿童。然后回顾性检查临床信息、诊断、治疗及结果。采用儿童血管炎活动评分(PVAS)和印度高安临床活动评分(ITAS2010)评估疾病活动度。

结果

男女比例为4:7。平均年龄为9.4(1.4 - 14)岁,平均诊断时间为40.6天(12 - 90天)。所有患者均患有高血压,少数有免疫异常。2例患者自身抗体水平低,1例免疫球蛋白E水平升高。异常(升高)的实验室指标包括红细胞沉降率(ESR)(9/10例患者,90.0%)、蛋白排泄(8/9例患者,88.9%)、肾素 - 血管紧张素 - 醛固酮系统(RAAS)活性(5/5例患者,100.0%)和血脂水平(3/5例患者,60%)。常见的起病方式为头痛伴惊厥(27.2%)和肾损害(27.2%)。腹主动脉(81.8%)和肾动脉(72.7%)是最常受累的血管。就诊时,平均PVAS和ITAS2010评分分别为12.1(6 - 26)/63和9.7(5 - 14)/57。所有患者均接受糖皮质激素和抗高血压药物治疗;2例接受肾动脉支架置入术。

结论

对于患有儿童高血压且炎症标志物高表达或尿液结果异常的患者,应考虑TA的诊断。主要血管的多普勒超声检查可能有帮助。PVAS和ITAS2010均有助于评估疾病活动度,对于有肾损害的患者推荐使用PVAS。糖皮质激素和抗高血压药物有效。对于持续性高血压患者,介入治疗可以是一种选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3818/5393038/013a49d2eed9/12969_2017_164_Fig1_HTML.jpg

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