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婴幼儿先天性输尿管中段狭窄的腹腔镜修复术

Laparoscopic repair of congenital midureteric strictures in infants and children.

作者信息

Chandrasekharam V V S

机构信息

Pediatric Surgery, Pediatric Urology & MAS, Rainbow Children's Hospitals, Hyderabad, India.

出版信息

J Pediatr Surg. 2015 Nov;50(11):1909-13. doi: 10.1016/j.jpedsurg.2015.07.013. Epub 2015 Jul 26.

Abstract

PURPOSE

Congenital midureteric strictures (CMUS) are an uncommon cause of obstructive uropathy. There are only a few case reports of laparoscopic management of CMUS. We present our experience with laparoscopic repair of CMUS in 7 children.

PATIENTS AND METHODS

The records of all children (n=7, 5 infants) undergoing laparoscopic reconstruction for CMUS were reviewed. Preoperative imaging included ultrasound (US) and diuretic renography (DR) in all children. Intravenous urography or magnetic resonance urography was performed in 3 children when a dilated ureter was seen on the ultrasound. Retrograde pyelography was performed in 6 children before definitive surgery. All children underwent transperitoneal laparoscopic excision of the stricture with ureteroureterostomy. Follow-up included clinical examination and US in all children, with DR in 5 children.

RESULTS

Over a 3-year period, 7 children underwent laparoscopic repair of CMUS. Six children had antenatally diagnosed hydronephrosis, while one child presented with infected hydronephrosis, underwent nephrostomy and was later referred to us. The diagnosis of CMUS was suspected preoperatively in 4 children; in 3 children, diagnosis of CMUS was confirmed on retrograde pyelography. Laparoscopic repair was successfully completed in all children; there were no significant intraoperative or postoperative complications. At a median follow-up of 18months, all children are asymptomatic, with US (7) and DR (5) confirming significant reduction in the hydronephrosis and improved drainage. The cosmetic results have been excellent.

CONCLUSION

To our knowledge, this is the first report of laparoscopic repair of CMUS in children. Laparoscopic repair of CMUS can be safely and successfully performed even in small infants, with good results.

摘要

目的

先天性输尿管中段狭窄(CMUS)是梗阻性尿路病的一种罕见病因。关于CMUS的腹腔镜治疗仅有少数病例报告。我们介绍我们对7例儿童进行CMUS腹腔镜修复的经验。

患者与方法

回顾了所有接受CMUS腹腔镜重建的儿童(n = 7,5例婴儿)的记录。所有儿童术前影像学检查包括超声(US)和利尿肾图(DR)。当超声检查发现输尿管扩张时,3例儿童进行了静脉肾盂造影或磁共振尿路造影。6例儿童在确定性手术前进行了逆行肾盂造影。所有儿童均接受经腹腹腔镜狭窄段切除及输尿管端端吻合术。随访包括所有儿童的临床检查和超声检查,5例儿童进行了利尿肾图检查。

结果

在3年期间,7例儿童接受了CMUS腹腔镜修复。6例儿童产前诊断为肾积水,1例儿童表现为感染性肾积水,接受了肾造瘘术,后来转诊至我们这里。4例儿童术前怀疑为CMUS;3例儿童通过逆行肾盂造影确诊为CMUS。所有儿童均成功完成腹腔镜修复;术中及术后均无明显并发症。中位随访18个月时,所有儿童均无症状,超声(7例)和利尿肾图(5例)证实肾积水明显减轻,引流改善。美容效果极佳。

结论

据我们所知,这是儿童CMUS腹腔镜修复的首例报告。即使是小婴儿,CMUS的腹腔镜修复也能安全、成功地进行,效果良好。

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