Congenital ureteral strictures most commonly occur at the proximal and distal segments of the ureter. Congenital midureteral stricture is a rare entity that is usually detected by prenatal ultrasonography and repaired in infants. We present the case and video of a congenital midureteral stricture in a 20-year-old woman who presented with a severe episode of pyelonephritis. The congenital midureteral stricture was successfully managed with robot-assisted laparoscopic excision and ureteroureterostomy.
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UPJO combined with Congenital mid-ureteral stenosis:A rare case.
Asian J Surg
October 2024
Department of Urology, Anhui Provincial Children's Hospital, Hefei, Anhui, 230000, China.
Introduction: Most congenital ureteral strictures occur at the ureteropelvic or ureterovesical junction in children. Mid-ureteral stricture is very rare and can cause congenital hydronephrosis. Only a few studies have reported on coexisting mid-ureteral stricture with ipsilateral atrophic kidney in young adults.
View Article and Find Full Text PDFLong-term, single-center study comparing open and laparoscopic procedures for congenital midureteral obstruction in children.
Pediatr Surg Int
June 2023
Department of Urology and Laboratory of Pelvic Floor Muscle Function, Shenzhen Children's Hospital, Futian District, Shenzhen, 518000, Guangdong, People's Republic of China.
Purpose: To compare the safety and outcomes of open and laparoscopic procedures in the management of congenital midureteral obstruction in children (CMO).
Methods: Between February 2008 and February 2022, a total of 18 patients underwent open ureteroureterostomy (OU group), and 26 underwent laparoscopic ureteroureterostomy (LU group). The operative time, postoperative hospital stay, hospital costs, postoperative complications, and success rates of the two groups were compared.
Congenital midureteral stenosis in children: a 13-year retrospective study based on data from a large pediatric medical center.
BMC Urol
November 2021
Department of Urology, Beijing Children's Hospital Affiliated With Capital Medical University, National Center for Children's Health, No. 56 Nanlishilu Rd, West District, Beijing, 100045, China.
Background: Midureteral stenosis is very rare in children and can cause congenital hydronephrosis. We report our experience treating children with congenital midureteral stenosis at our center, focusing on the differences in preoperative diagnosis and treatment compared with other congenital obstructive uropathies.
Methods: We retrospectively reviewed the medical records of 26 children diagnosed with congenital midureteral stenosis at our center between January 2007 and December 2020, such as preoperative examination methods, intraoperative conditions, and postoperative follow-up results.
Coexisting congenital mid-ureteral stricture and megaureter due to ureterovesical junction obstruction: A case report.
Urol Case Rep
January 2022
Department of Urology, Graduate School of Medicine, University of the Ryukyus, Okinawa, 903-0215, Japan.
Congenital mid-ureteral strictures (CMS) are rare. Most congenital strictures occur at the ureteropelvic junction or ureterovesical junction, with mid-ureteral strictures accounting for only 4-5% of all cases of ureteral obstruction in children. Furthermore, there are very few reports of coexisting mid-ureteral stricture and ureterovesical junction obstruction (UVJO).
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