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Ureteral quadruplication: the fourth case report

S Sourtzis1, N Damry, F Janssen

  • 1Department of Radiology, Hôpital Universitaire des Enfants Reine Fabiola, Brussels, Belgium.

Pediatric Radiology
|January 1, 1994
PubMed
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Ureteral quadruplication, a rare urinary tract abnormality, is exceptionally uncommon in infants. This report details the first documented case of unilateral ureteral quadruplication in a 9-month-old child.

Area of Science:

  • Pediatric Urology
  • Congenital Abnormalities
  • Urinary Tract Development

Background:

  • Ureteral anomalies are common developmental abnormalities of the upper urinary tract.
  • While ureteral duplication is frequent, triplication is rare, and quadruplication is exceedingly unusual.
  • Previous reports of ureteral quadruplication have exclusively involved adult patients.

Observation:

  • This case study presents a unilateral ureteral quadruplication in a 9-month-old infant.
  • The patient's age is significant, as all previously reported cases involved adult individuals.
  • This finding highlights the potential for rare congenital anomalies to manifest early in life.

Findings:

  • The infant presented with unilateral ureteral quadruplication.

Related Experiment Videos

  • Literature review confirmed this is the first reported case of ureteral quadruplication in an infant.
  • This case expands the known spectrum of ureteral anomalies in pediatric patients.

    • Implications:

    • This case underscores the importance of considering rare congenital urinary tract abnormalities even in very young patients.
    • Further research may be needed to understand the embryological basis and clinical course of ureteral quadruplication in infants.
    • Early identification and management of such anomalies are crucial for optimal patient outcomes.