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本文引用的文献

1
Renovascular hypertension--is it fibromuscular dysplasia or Takayasu arteritis.肾血管性高血压——是纤维肌性发育不良还是 Takayasu 动脉炎。
Pediatr Nephrol. 2013 Feb;28(2):191-6. doi: 10.1007/s00467-012-2151-7. Epub 2012 Mar 28.
2
Genetic testing in renal disease.遗传性肾脏病的基因检测。
Pediatr Nephrol. 2012 Jun;27(6):873-83. doi: 10.1007/s00467-011-1865-2. Epub 2011 May 27.
3
Renal artery stenosis: is angiography still the gold standard in 2011?肾动脉狭窄:2011 年血管造影术仍是金标准吗?
Pediatr Nephrol. 2011 Jun;26(6):833-7. doi: 10.1007/s00467-010-1757-x. Epub 2011 Jan 30.
4
Severe renovascular hypertension in an infant with congenital solitary pelvic kidney.先天性孤立盆腔肾婴儿的严重肾血管性高血压
Pediatr Nephrol. 2006 Mar;21(3):437-40. doi: 10.1007/s00467-005-2109-0. Epub 2005 Dec 29.
5
Fatal hypertensive encephalopathy in a child with association of multicystic kidney and renal artery stenosis.一名患有多囊肾和肾动脉狭窄的儿童发生致命性高血压脑病。
Klin Padiatr. 2003 Jul-Aug;215(4):205-7. doi: 10.1055/s-2003-41396.
6
Utility of computed tomographic renal angiogram in the management of childhood hypertension.
Pediatr Nephrol. 2002 Sep;17(9):741-7. doi: 10.1007/s00467-002-0921-3. Epub 2002 Jul 30.
7
[Successful autotransplantation of a solitary kidney in a 2-year old girl with malignant hypertension caused by critical renal artery stenosis].[一名2岁患有严重肾动脉狭窄所致恶性高血压的女童单肾成功自体移植]
Pediatr Pol. 1995 Feb;70(2):161-6.
8
Renal artery occlusion and malignant hypertension in polycystic kidney disease.多囊肾病中的肾动脉闭塞与恶性高血压
J Urol. 1980 Aug;124(2):279-80. doi: 10.1016/s0022-5347(17)55407-5.
9
Renovascular hypertension associated with a pelvic kidney and multicystic dysplasia.与盆腔肾和多囊性发育异常相关的肾血管性高血压。
J Urol. 1982 Oct;128(4):794-7. doi: 10.1016/s0022-5347(17)53193-6.
10
Renovascular hypertension with a congenital solitary kidney.先天性孤立肾伴肾血管性高血压
Arch Intern Med. 1966 Dec;118(6):580-3.

肾动脉狭窄合并肾脏和尿路先天性异常。

Renal artery stenosis in association with congenital anomalies of the kidney and urinary tract.

作者信息

Kari Jameela A, Roebuck Derek J, Tullus Kjell

机构信息

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.

出版信息

Saudi Med J. 2014 Oct;35(10):1264-6.

PMID:25316474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4362124/
Abstract

OBJECTIVES

To describe 8 cases of renal artery stenosis (RAS) in children with congenital anomalies of the renal tract.

METHODS

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.

RESULTS

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.

CONCLUSION

We highlight the association between RAS and other renal anomalies, which indicates that they could share a common genetic background.

摘要

目的

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。

方法

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。

结果

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。

结论

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。