Kari Jameela A, Roebuck Derek J, Tullus Kjell
Department of Paediatric Nephrology, Great Ormond Street Hospital for Children NHS Foundation Trust, Great Ormond Street, London WC1N 3JH, United Kingdom. Tel. +44 (20) 7405 9200 Ext. 0292. Fax. +44 (20) 7829 8841. E-mail.
Saudi Med J. 2014 Oct;35(10):1264-6.
To describe 8 cases of renal artery stenosis (RAS) in children with congenital anomalies of the renal tract.
We conducted a retrospective chart review of 78 children with RAS who were followed up at Great Ormond Street Hospital, London, United Kingdom between 2003 and 2012. We used an interventional radiology database to identify all patients who had RAS confirmed by digital subtraction angiography and examined all cases of congenital anomaly of the renal tract that had been diagnosed during childhood.
We documented the following renal anomalies: multicystic dysplastic kidney (n=2), renal hypoplasia (n=1), congenital solitary kidney with hydronephrosis (n=1), and unilateral vesicoureteric reflux with poorly functioning kidneys (n=2). The anomaly was unknown in 2 cases. Seven children had unilateral nephrectomy at a median age of 2.5 years (range, 0.4-10 years) for various urological abnormalities. All children were confirmed to have RAS after presentation with hypertension at a median age of 10 (3.5-16.2) years. Angioplasty was performed in 7 children, of which 6 achieved control of their blood pressure on reduced medications.
We highlight the association between RAS and other renal anomalies, which indicates that they could share a common genetic background.
描述8例患有泌尿系统先天性异常的儿童肾动脉狭窄(RAS)病例。
我们对2003年至2012年期间在英国伦敦大奥蒙德街医院接受随访的78例RAS儿童进行了回顾性病历审查。我们使用介入放射学数据库来识别所有经数字减影血管造影确诊为RAS的患者,并检查所有在儿童期诊断出的泌尿系统先天性异常病例。
我们记录了以下肾脏异常情况:多囊性发育不良肾(n = 2)、肾发育不全(n = 1)、先天性孤立肾伴肾积水(n = 1)以及单侧膀胱输尿管反流伴肾功能不佳(n = 2)。2例异常情况不明。7名儿童因各种泌尿系统异常在中位年龄2.5岁(范围0.4 - 10岁)时接受了单侧肾切除术。所有儿童在中位年龄10(3.5 - 16.2)岁出现高血压后被确诊为RAS。7名儿童接受了血管成形术,其中6名通过减少药物用量实现了血压控制。
我们强调了RAS与其他肾脏异常之间的关联,这表明它们可能具有共同的遗传背景。