Szugye Heidi S, Zeft Andrew S, Spalding Steven J
Cleveland Clinic Children's, Cleveland, Ohio, USA.
Center for Pediatric Rheumatology, Cleveland Clinic Children's, Cleveland, Ohio, USA.
Pediatr Rheumatol Online J. 2014 Jun 4;12:21. doi: 10.1186/1546-0096-12-21. eCollection 2014.
Takayasu Arteritis is an idiopathic, chronic, large vessel vasculitis involving the aorta and its primary branches. Few studies have been done in pediatric patients to date with the largest case series of US patients published in 2003 consisting of only 6 patients.
A retrospective chart review was performed on all patients seen at Cleveland Clinic Children's up until 2012 who met EULAR/PRINTO/PRES classification criteria for childhood Takayasu Arteritis.
Twenty-one patients with a mean follow up of 2.3 years were studied. Weight loss, fatigue, and anorexia were the most common presenting complaints. 57.1% of patients were hypertensive at first visit. The most common examintation finding was diminished pulses (61.9%), followed by bruits, and then murmurs. Thoracic aorta stenosis was the most common vascular abnormality. Seven of twenty-one patients responded well to methotrexate and prednisone alone. Ten of twenty-one patients required an additional medication for symptom and disease control (infliximab most commonly). About two-thirds of patients required at least one anti-hypertensive medication. Eight of the twenty-one patients required surgical intervention for severe disease refractory to medications (renal artery stenosis being the most common indication). Almost all patients reported symptomatic improvement after surgical intervention. Two of the eight patients required a second surgery for return of symptoms. Disease sequelae included arterial aneurysms, resolved heart failure, and hypertensive emergencies.
Our study emphasizes that constitutional symptoms coupled with objective findings of diminished pulses, bruits, and hypertension should raise clinical suspicion for Takayasu Arteritis in pediatric patients. Pharmacologic therapy alone can be successful in controlling disease progression, however surgery was successful in minimizing symptoms when medical therapies failed.
大动脉炎是一种特发性、慢性、累及主动脉及其主要分支的大血管血管炎。迄今为止,针对儿科患者的研究较少,美国最大的病例系列发表于2003年,仅包括6例患者。
对克利夫兰诊所儿童医院截至2012年符合儿童大动脉炎欧洲抗风湿病联盟/儿童风湿病国际试验组织/儿科风湿病欧洲学会分类标准的所有患者进行回顾性病历审查。
对21例患者进行了研究,平均随访2.3年。体重减轻、疲劳和厌食是最常见的就诊主诉。57.1%的患者初诊时患有高血压。最常见的检查发现是脉搏减弱(61.9%),其次是血管杂音,然后是心脏杂音。胸主动脉狭窄是最常见的血管异常。21例患者中有7例对甲氨蝶呤和泼尼松单药治疗反应良好。21例患者中有10例需要额外用药以控制症状和疾病(最常用英夫利昔单抗)。约三分之二的患者需要至少一种抗高血压药物。21例患者中有8例因药物难治性重症疾病需要手术干预(最常见的指征是肾动脉狭窄)。几乎所有患者术后症状均有改善。8例患者中有2例因症状复发需要再次手术。疾病后遗症包括动脉瘤、已缓解的心力衰竭和高血压急症。
我们的研究强调,小儿患者若出现全身症状,同时伴有脉搏减弱、血管杂音和高血压等客观体征,应提高对大动脉炎的临床怀疑。单独药物治疗可成功控制疾病进展,然而当药物治疗失败时,手术可成功减轻症状。