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Prenatal urinary ascites and persistent cloaca: risk factors for poor drainage of urine or meconium

M C Adams1, J Ludlow, J W Brock

  • 1Vanderbilt Children's Hospital, Vanderbilt University, Nashville, Tennessee, USA.

The Journal of Urology
|November 17, 1998
PubMed

Insights

Persistent cloaca in girls can cause abnormal urine and meconium drainage, potentially diagnosed prenatally. Cutaneous vesicostomy effectively diverted urine in infants before definitive repair.

Area of Science:

  • Pediatric Surgery
  • Urology
  • Neonatal Medicine

Background:

  • Persistent cloaca is a complex congenital anomaly.
  • It involves the fusion of the urinary, genital, and gastrointestinal tracts.
  • Aberrant drainage can occur due to the unique anatomical confluence.

Observation:

  • Three female patients with persistent cloaca presented with urinary ascites.
  • This ascites resulted from intraperitoneal urine reflux via the genital system.
  • A long, narrow cloaca with high confluence of urethra, vagina, and rectum was noted.

Findings:

  • Cutaneous vesicostomy was performed in all three patients.
  • This procedure effectively diverted urine away from the cloaca.
  • The intervention was performed prior to definitive surgical repair.

Implications:

  • Persistent cloaca can lead to significant urinary outflow resistance.
  • High confluence in persistent cloaca may cause aberrant urine and meconium drainage.
  • Prenatal identification of these issues suggests a need for postnatal intervention.
Abstract

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