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Ureteroinguinal Herniation with Consecutive Ureteral Stricture in a 2-Month-Old Infant: Case Report
Carlos Delgado-Miguel1, Antonio Jesus Muñoz-Serrano2, Pablo Aguado2
1Department of Pediatric Surgery, Hospital Universitario La Paz, Madrid, Spain.
Insights
Ureteroinguinal hernia, a rare condition in children, can cause obstructive uropathy. Early suspicion of ureteral obstruction in inguinal hernia cases is crucial for timely diagnosis and management.
Area of Science:
- Pediatric Urology
- Surgical Case Reports
- Abdominal Wall Abnormalities
Background:
- Inguinal herniation of the ureter is a rare pediatric condition.
- It can lead to significant obstructive uropathy if not identified.
Observation:
- A 2-month-old infant presented with antenatal hydronephrosis and an inguinal mass.
- Ultrasound suggested bladder herniation or a dilated ureter in the inguinal canal.
- Surgical exploration revealed a paraperitoneal ureteroinguinal hernia.
Findings:
- Initial surgical repair involved sac ligation and ureter replacement.
- Recurrent hydronephrosis and obstruction necessitated ureteral segment removal and reimplantation.
- The patient remained asymptomatic with normal renal function post-reimplantation.
Implications:
- Hydronephrosis in infants with inguinal hernias warrants suspicion for ureteroinguinal hernia.
- Prompt diagnosis and appropriate surgical intervention are vital for preventing long-term renal damage.
- This case highlights the importance of preoperative diagnostic suspicion in managing rare urological anomalies.
Abstract:
Inguinal herniation of ureter is an uncommon finding among children, with scarce reported cases in the literature to date, that can potentially lead to obstructive uropathy. We report a case of ureteroinguinal herniation discovered during an inguinal hernia repair in a patient with antenatally ultrasound finding of hydronephrosis. A 2-month-old infant with antenatal left hydronephrosis presented with left inguinal mass. Preoperative ultrasound showed an anechoic tubular image producing a mass effect on the left testicle, with suspected bladder herniation and/or dilated ureter toward the inguinal canal. An open surgical inguinal exploration was performed, where the left inguinal canal revealed a peritoneal sac and sliding of the dilated left ureter behind the sac, with a significant change in diameter, corresponding to the paraperitoneal variant of ureteroinguinal herniation. Ligation of the sac and replacement of the ureter into the retroperitoneum were performed, with improvement in the hydronephrosis observed on the ultrasound 1 month after the intervention. However, 6 months later, hydronephrosis worsening as well as the obstructive pattern observed in the diuretic renogram required removal of the stenotic ureteral segment and reimplantation of the healthy proximal segment in the bladder by open approach (Cohen's reimplantation). Follow-up ultrasound of the renal tract showed no dilatation of the upper renal tract and the renal function tests were normal. Currently, the patient is 2 years old and he remains asymptomatic. In conclusion, s igns of ureteral obstruction such as hydronephrosis in patients with inguinal herniation may suggest the possibility of an ureteroinguinal hernia. Preoperative diagnostic suspicion is essential.
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