Abstract
BackgroundPyelo-ureteral junction syndrome (PUJS) is a frequent congenital malformation. We report the surgical management of PUJS by pyeloplasty according to Anderson-Hyne-Kuss’s procedure at the Zinder National Hospital..MethodsThis was a retrospective study from January 2013 to December 2016 (4 years), including patients who have undergone surgery for PUJS.ResultsTwelve (12) cases of PUJS had a surgery among which 66.7% were men with an average age of 32.5 ± 7.6 years. The clinical symptomatology was lumbar pain or renal colic in 92.3% of cases. This pain had evolved for more than 2 years for 58.3% of the cases. Ultrasound coupled with intravenous urography or CT-scan was performed to confirm the diagnosis of PUJS in 58.3 and 41.7% of cases. The average serum creatinine level at admission was 181.25 ± 67.3 μmol/L [Lab reference range: 53–97 μmol/L]. The Anderson-Hynes non dismembered pyeloplasty is used for all the patients. The release of a crossing lower pole vessel was performed in 25%, pyelolithotomy in 16.7%. The average surgery time was 118.3 ± 20.7 min. The average hospital length of stay was 10.8 ± 3 days. Immediate postoperative complications were recorded in 33.3% (n = 4). Postoperative outcomes were considered good by disappearance of clinical, biological and radiological signs.ConclusionThe Anderson-Hynes non dismembered pyeloplasty gives good results and provides a successful alternative in an environment where laparoscopy and robotic surgery are not developed.
Highlights
IntroductionWe report the surgical management of Pyelo-ureteral junction syndrome (PUJS) by pyeloplasty according to Anderson-Hyne-Kuss’s procedure at the Zinder National Hospital
Pyelo-ureteral junction syndrome (PUJS) is a frequent congenital malformation
PUJS may result from an intrinsic, functional, congenital abnormality of the ureteral wall or extrinsic compression more often by a lower polar vessel [2, 3, 6]
Summary
We report the surgical management of PUJS by pyeloplasty according to Anderson-Hyne-Kuss’s procedure at the Zinder National Hospital. Pyelo-ureteral junction syndrome (PUJS), known as primary hydronephrosis, is a common cause of urinary malformation in the upper urinary tract [1,2,3,4]. It is characterized by a narrowing of the junction between the pelvis and the ureter [1, 2, 4,5,6]. We hereby report the surgical management of PUJS by pyeloplasty according to Anderson-HyneKuss’s procedure at the Zinder National Hospital
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.