Objective: To assess the outcome after pyeloplasty in children with an ante-natal diagnosis of hydronephrosis, shown on post-natal renography to be due to pelvi-ureteric junction (PUJ) obstruction, and in particular to review the outcome of those who had initially been managed expectantly.
Patients And Methods: Between 1984 and 1995, 321 patients were diagnosed as having PUJ obstruction, after investigating ante-natal hydronephrosis. Of these, 47 had undergone pyeloplasty and also had a normal contralateral kidney; 26 patients had early pyeloplasty because of impaired function and 21 underwent surgery after a period of expectant management. Renal function was assessed renographically before and at least one year after surgery.
Results: Relative renal function was stabilized in those patients who underwent early pyeloplasty (mean differential function 28.1% before and 32.7% after surgery). In patients who underwent pyeloplasty after a period of expectant management, the mean relative function decreased from 44.8% initially to 30.5% before surgery; this recovered to 37.5% at the post-operative reassessment, representing a statistically significant loss of function (P < 0.01).
Conclusion: In patients born with PUJ obstruction and impaired renal function, pyeloplasty failed to significantly improve function. Possibly because of cortical loss. In patients with ante-natal PUJ obstruction managed expectantly there is a small but significant risk of a modest loss of renal function.
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http://dx.doi.org/10.1046/j.1464-410x.1998.00519.x | DOI Listing |
J Surg Case Rep
December 2024
Accident and Emergency Department, Provincial Hospital Malangwa, Balmandir Chowk, Malangwa, Sarlahi 45800, Nepal.
A 16-year-old male presented to OPD with right-sided flank pain associated with lower urinary tract symptoms. CT scan and ultrasound findings demonstrated a 12.9 mm renal stone in the lower calyx and moderate hydronephrosis, respectively.
View Article and Find Full Text PDFJ Minim Access Surg
November 2024
Department of Urology, All India Institute of Medical Sciences, New Delhi, India.
Introduction: To evaluate the feasibility, safety, and effectiveness of different pyeloplasty procedure approaches for pelvicureteric junction (PUJ) obstruction in kidney anomalies. The presence of difficult, unfamiliar and anomalous anatomy makes pyeloplasty challenging in these conditions.
Patients And Methods: We conducted a retrospective review of pyeloplasty in patients with congenital anomalous kidneys at our national tertiary referral centre.
J Indian Assoc Pediatr Surg
August 2024
Department of Pediatric Surgery, Mazumder Shaw Medical Center, Bengaluru, Karnataka, India.
Inflammatory myofibroblastic tumor (IMT) is a very rare tumor with still rare occurrence in the genitourinary system, presenting as a pelvic-ureteric junction (PUJ) obstruction (PUJO). We report a case of IMT at the PUJ mimicking congenital PUJO and review the relevant literature.
View Article and Find Full Text PDFArch Ital Urol Androl
June 2024
Urologic Department, Sisters of Charity Hospital and Urologic Praxis, Wien.
Children (Basel)
March 2024
Pediatric Surgery Unit, Salesi Children's Hospital, 60123 Ancona, Italy.
Introduction: In children, the association of ipsilateral pyeloureteral junction obstruction (PUJO) and ureterovesical junction obstruction (UVJO) is a rare malformation with a non-standardized treatment. We report a case of PUJO and UVJO treated by a combined minimally invasive surgical treatment to resolve the double urinary obstruction. The current literature was also reviewed.
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