Ureteropelvic Junction Obstruction by a Long Intraluminal Polyp and a Concurrent Crossing Vein in a Symptomatic

Daniel M Carter Ramirez1, Hin Yu Vincent Tu2, Luis H Braga3

  • 1McMaster University, Hamilton, Ontario, Canada.

Urology
|July 23, 2015
PubMed

Insights

A rare case of ureteropelvic junction obstruction in an 8-year-old boy was caused by a fibroepithelial polyp. This condition, often diagnosed later, highlights the importance of considering unusual causes for flank pain and hydronephrosis.

Area of Science:

  • Pediatric Urology
  • Surgical Innovation
  • Medical Imaging

Background:

  • Ureteropelvic junction (UPJ) obstruction can be intrinsic or extrinsic, with extrinsic causes typically presenting later in childhood with symptoms.
  • Antenatal ultrasonography frequently detects intrinsic UPJ obstruction.
  • Symptomatic presentation in older children often suggests extrinsic causes or less common intrinsic pathologies.

Observation:

  • An 8-year-old boy presented with acute severe left flank pain and grade 3 hydronephrosis on ultrasonography.
  • No signs of infection were present.
  • Diagnostic imaging revealed significant left hydronephrosis.

Findings:

  • Laparoscopic dismembered pyeloplasty identified the cause as a large fibroepithelial polyp in the proximal ureter.
  • An anterior crossing vein was also noted, potentially contributing to the obstruction.
  • This case represents a rare cause of UPJ obstruction in a pediatric patient.

Implications:

  • Fibroepithelial polyps are an uncommon but significant cause of ureteropelvic junction obstruction in children.
  • This case underscores the need for thorough intraoperative evaluation to identify all contributing factors, such as crossing vessels.
  • Successful laparoscopic management demonstrates the efficacy of minimally invasive techniques for complex UPJ obstruction.

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