Complete cloacal duplication imaged before and during pregnancy

Authors

  • Omar Ragab
  • Melanie Landay
  • Jabi Shriki

DOI:

https://doi.org/10.3941/jrcr.v3i11.305

Keywords:

Complete genitourinary duplication, uterine anomalies, complete cloacal duplication, genitourinary duplication, cloacal duplication, caudal duplication syndrome, caudal duplication

Abstract

The authors describe a 31 year-old female who presented emergently with abdominal pain and was found at CT to have complete genitourinary duplication including separate urinary bladders, uteri, cervices, and vaginas, and also duplication of the rectum. No etiology for abdominal pain was identified. The patient was referred to urology for further evaluation, and an intravenous urographic study was obtained, which confirmed complete lower urinary tract duplication. The patient presented emergently 9 months later during a subsequent pregnancy for further evaluation of abdominal pain.  A second CT scan was ordered to rule out appendicitis.  Findings consistent with cloacal duplication were again noted. There was also dilatation of the urinary collecting systems, more prominently on the right side. A Cesarean section was performed and confirmed total genitourinary and rectal duplication.

Author Biographies

Omar Ragab

MS4, Medical student

University of Southern California

Keck School of Medicine

Melanie Landay

Maternal and Fetal Medicine Fellow, Department of Obstetrics and Gynecology, University of Southern California, Keck School of Medicine

Jabi Shriki

Assistant Professor

Associate Program Director, Diagnostic Radiology Residency

Published

2009-10-04

Issue

Section

Obstetric & Gynecologic Radiology