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Research and review articles are invited for publication in September 2026 - Vol. 36, Issue 3 

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Bilateral complete ureteropielocalicial duplicity associated with ectopic ureteral vaginal insertion in childhood: Case report

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  • Bilateral Complete Ureteropielocalicial Duplicity Associated With Ectopic Ureteral Vaginal Insertion In Childhood: Case Report
  • Bilateral complete ureteropielocalicial duplicity associated with ectopic ureteral vaginal insertion in childhood: Case report

Ítalo Grizolia Junqueira de Sousa 1, *, Gustavo Notari de Moraes 2, Gabriela Carvalho Maciel 3 and Luiz Carlos Maciel 4

1 Medical student at the University of Taubaté, City of Taubaté, State of São Paulo, Brazil.
2 Assistant Professor I of the Discipline of Urology at the University of Taubaté, City of Taubaté, State of São Paulo, Brazil.
3 Medical student at the University of Taubaté, Caraguatatuba Campus, City of Caraguatatuba, State of São Paulo, Brazil.
4 Assistant Professor III of the Discipline of Urology at the University of Taubaté, City of Taubaté, State of São Paulo, Brazil. 
 
Research Article
GSC Biological and Pharmaceutical Sciences, 2023, 23(03), 192–197.
Article DOI: 10.30574/gscbps.2023.23.3.0222
DOI url: https://doi.org/10.30574/gscbps.2023.23.3.0222
Received on 27 April 2023; revised on 13 June 2023; accepted on 16 June 2023
Ureteral duplication associated with ectopic ureteral insertion is a rare congenital anomaly clinically more common in females. Early urinary incontinence is the main symptom of ureteral ectopy in the first childhood of these patients. Contrast computed tomography and magnetic resonance imaging are the most effective imaging methods to rule out or confirm the diagnosis of ectopy associated with ureteral duplication. In cases where significant surgical functions are performed, the reconstructive surgical approach with reimplantation of the ureteral unit is the technique of choice.
We present the case of a 6-year-old female patient who was diagnosed with bilateral complete ureteropielocalicial duplicity confirmed by intravenous pyelography. Confirmation of ureteral ectopy only occurred intraoperatively. The surgical correction consisted in reimplantation of the ectopic ureteral unit in the patient's bladder, since preserved renal functions evidenced in renal scintigraphy with DMSA. After performed the procedure, the patient remained asymptomatic and with normal urinary patterns.
For the accomplishment of the present study, we used as data source the patient's medical records, useful for the realization of the clinical history from the diagnosis to the definitive surgical treatment that concluded the case.
Ureteral duplication associated with ectopic ureteral insertion should be perfectly understood and had with a possible diagnosis for cases of urinary incontinence and recurrent urinary infections. Investigation through detailed physical examination and the use of appropriate imaging tests may help in the early detection of this rare anomaly of the genitourinary tract.
Ureteropielocalicial duplicity; Ureteral ectopy; Urinary incontinence; Congenital anomaly
https://gscbps.gsconlinepress.com/sites/default/files/fulltext_pdf/GSCBPS-2023-…

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Ítalo Grizolia Junqueira de Sousa, Gustavo Notari de Moraes, Gabriela Carvalho Maciel and Luiz Carlos Maciel. Bilateral complete ureteropielocalicial duplicity associated with ectopic ureteral vaginal insertion in childhood: Case report. GSC Biological and Pharmaceutical Sciences, 2023, 23(3), 192-197. Article DOI: https://doi.org/10.30574/gscbps.2023.23.3.0222


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