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Background: Ureteral anomalies distal to the uretero-pelvic junction (UPJ) belong to the wide spectrum of congenital anomalies of the kidney and urinary tract (CAKUT). They can cause severe obstruction requiring a detailed anatomical depiction to define the surgical approach. Up to date, ultrasonography, voiding cystourethrography and scintigraphy are considered the gold-standard diagnostic tools to study obstructive anomalies of the urinary tract; however, they do not provide accurate ureteral anatomical details. The aim of our study was to evaluate the concordance between functional magnetic resonance urography (fMRU) and intraoperative findings to define ureteral anomalies distal to UPJ.
Methods: Pediatric patients with ureteral anomalies distal to the UPJ who underwent surgery after performing fMRU were retrospectively collected. Surgical data were compared with radiological results. The concordance was assessed considering both pathological and non-pathological urinary tracts and was calculated by means of the Cohen's kappa coefficient. fMRU diagnostic accuracy was defined by sensitivity, specificity, and binomial exact confidence intervals.
Results: We included 46 patients. The sensitivity and specificity of fMRU were 98.0% and 83.3%; positive predictive value 90.4%, negative predictive value 96.2%. The concordance between surgical findings and fMRU was 92.3%, with a Cohen's k coefficient of 0.83 (excellent).
Conclusions: Our study demonstrates the excellent agreement between fMRU and surgical findings in the definition of ureteral anomalies distal to the UPJ in children. Thus, it could be considered a valid imaging technique in the preoperative planning as it provides the surgeon with important information regarding the etiology and site of the obstruction.
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http://dx.doi.org/10.23736/S2724-5276.22.06462-X | DOI Listing |
J Nephrol
September 2025
Italian Society of General Medicine (SIMG), COMEGEN Primary Care Physicians Cooperative, Naples, Italy.
Background: Kidney stone formation is driven by an imbalance between lithogenic substances and crystallization inhibitors. Current guidelines recommend a 24-h urine collection in patients with kidney stone disease to assess the risk of stone formation and monitor therapy compliance. However, real-world data on adherence to these guidelines remain limited and outdated.
View Article and Find Full Text PDFInt J Surg Case Rep
September 2025
Department of Urology, Shandong Provincial Third Hospital, Shandong University, Jinan, 250012, China; Shandong Stone Disease Prevention and Treatment Center, Jinan, 250012, China. Electronic address:
Introduction: The Multiple primary malignant tumors (MPMT) refers to the occurrence of two primary malignant tumors in the same organ or organs in the same patient at the same time. However, MPMT is rare in the urinary system. Congenital urinary tract anomalies (e.
View Article and Find Full Text PDFIntroduction: Bladder cancer in patients with ureteral anomalies presents unique surgical challenges, particularly regarding urinary diversion. This case highlights a novel approach to uretero-ileal anastomosis in a patient with duplicated right ureters undergoing radical cystectomy.
Case Presentation: A 65-year-old man with cT2N0M0 bladder cancer underwent transurethral resection of the bladder tumor, revealing a complete duplex right ureter.
BMC Urol
September 2025
Department of Urology, University Medical Center Goettingen, Robert-Koch-Str. 40, Goettingen, 37075, Germany.
INTRODUCTION AND IMPORTANCE: "Congenital anomalies of the kidney and urinary tract" (CAKUT) represent a heterogeneous and rare group of disorders affecting the urinary tract. Despite the widespread availability of ultrasound, the diagnosis of congenital urinary tract malformations is often made in adulthood. As a result, CAKUT are typically incidental findings during imaging investigations.
View Article and Find Full Text PDFCureus
July 2025
Paediatric Surgery, San Fernando Teaching Hospital, San Fernando, TTO.
Proximal ureteral atresia is an exceedingly rare presentation of congenital or neonatal hydronephrosis. We report the case of a full-term, female neonate born with an abdominal mass. On palpation, the mass occupied the right flank, and CT showed features suggestive of multicystic dysplastic kidney (MCDK).
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