Lowe Gregory J, Canon Stephen J, Jayanthi Venkata R
Section of Urology, Columbus Children's Hospital, The Ohio State University, Columbus, OH 43205, USA.
BJU Int. 2008 Jan;101(2):227-30. doi: 10.1111/j.1464-410X.2007.07106.x. Epub 2007 Sep 13.
To present our initial experience of laparoscopic reconstructive surgery in children with upper urinary tract obstruction associated with duplex anomalies, as although there is much information on ablative procedures such as laparoscopic heminephrectomy, there is little available about minimally invasive reconstructive options for duplex renal anomalies in children.
We retrospectively reviewed four consecutive patients (aged 6-11 years) with duplex anomalies and laparoscopic reconstruction for obstructed, dilated segments treated at our institution. The port placement and surgical exposure were analogous to that for transperitoneal laparoscopic pyeloplasty. A JJ stent was placed retrogradely into the ureter immediately before each procedure. The procedures performed were pyelo-ureterostomy for incomplete duplication and lower pole pelvi-ureteric junction (PUJ) obstruction, lower pole pyeloplasty for lower pole PUJ obstruction and complete duplication, and ipsilateral uretero-ureterostomy and distal ureterectomy for an obstructed, ectopic upper pole. Foley catheters were left indwelling for 36-48 h and stents were removed at 4-6 weeks. Postoperative imaging included either ultrasonography or intravenous urography.
Three children presented with intermittent flank pain due to lower pole PUJ obstruction. The other child presented with pyonephrosis and purulent drainage from her vagina due to an ectopic ureter associated with a functioning upper pole segment. All procedures were successfully completed. The only complication was in the first patient (pyelo-ureterostomy) who had transient urinary extravasation that resolved with bladder decompression for 10 days. With a follow-up of 6-18 months, all had resolution of symptoms with improvement in radiographic variables.
This series shows that children with duplex anomalies and obstruction can undergo successful reconstruction using techniques learned with laparoscopic pyeloplasty.
介绍我们对患有上尿路梗阻并伴有重复畸形的儿童进行腹腔镜重建手术的初步经验,因为尽管有很多关于诸如腹腔镜半肾切除术等消融手术的信息,但关于儿童重复肾畸形的微创重建选择的信息却很少。
我们回顾性分析了在我院接受治疗的连续4例(年龄6至11岁)患有重复畸形且因梗阻、扩张节段接受腹腔镜重建手术的患者。端口放置和手术暴露类似于经腹腹腔镜肾盂成形术。每次手术前立即经逆行将一根双J支架置入输尿管。所施行的手术包括针对不完全重复和下极肾盂输尿管连接部(PUJ)梗阻的肾盂输尿管吻合术、针对下极PUJ梗阻和完全重复的下极肾盂成形术,以及针对梗阻性、异位上极的同侧输尿管输尿管吻合术和远端输尿管切除术。留置Foley导尿管36至48小时,支架在4至6周时取出。术后影像学检查包括超声检查或静脉肾盂造影。
3例儿童因下极PUJ梗阻出现间歇性胁腹痛。另一例儿童因与功能正常的上极节段相关的异位输尿管出现肾积脓和阴道脓性引流。所有手术均成功完成。唯一的并发症发生在第一例患者(肾盂输尿管吻合术),出现短暂性尿外渗,经膀胱减压10天后缓解。随访6至18个月,所有患者症状均缓解,影像学指标改善。
本系列研究表明,患有重复畸形并伴有梗阻的儿童可以使用从腹腔镜肾盂成形术中学到的技术成功进行重建手术。