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Bilateral ureteral triplication: A case report.

Irfan Wahyudi1, Muhammad Fahri1, Gerhard Reinaldi Situmorang1

  • 1Department of Urology, Cipto Mangunkusumo General Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.

Urology Case Reports
|October 26, 2020
PubMed
Summary

Bilateral ureteral triplication, a rare congenital urinary tract anomaly, was diagnosed in an infant with recurrent urinary tract infections. Surgical intervention was performed to correct the condition.

Keywords:
BilateralLaparoscopicUreteral tailoringUreteral triplication

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Area of Science:

  • Urology
  • Pediatric Surgery
  • Congenital Abnormalities

Background:

  • Ureteral triplication is an exceptionally rare congenital disorder of the urinary tract, with limited documented cases globally.
  • Bilateral ureteral triplication is even rarer, presenting unique diagnostic and management challenges.

Observation:

  • A female infant presented with a history of recurrent febrile urinary tract infections (UTIs) since birth.
  • Computed tomography urography revealed bilateral ureteral triplication.
  • Contrast studies and endoscopic procedures confirmed the diagnosis.

Findings:

  • The patient was diagnosed with bilateral ureteral triplication.
  • Management options range from conservative approaches to surgical intervention.
  • This specific case involved laparoscopic left ureteroneocystostomy and ureteral tailoring.

Implications:

  • This case highlights the rarity and diagnostic considerations for bilateral ureteral triplication.
  • It underscores the importance of prompt diagnosis and tailored surgical management for such anomalies.
  • Further research into long-term outcomes of surgical interventions for rare congenital urinary tract disorders is warranted.