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

Ureteral duplication associated with ectopic ureteral insertion is a rare congenital anomaly clinically more common in females. Early urinary incontinence the main symptom of ectopy first childhood these patients. Contrast computed tomography and magnetic resonance imaging are most effective methods to rule out or confirm diagnosis duplication. In cases where significant surgical functions performed, reconstructive approach reimplantation unit technique choice. We present case 6-year-old female patient who was diagnosed bilateral complete ureteropielocalicial duplicity confirmed by intravenous pyelography. Confirmation only occurred intraoperatively. The correction consisted patient's bladder, since preserved renal evidenced scintigraphy DMSA. After performed procedure, remained asymptomatic normal patterns. For accomplishment study, we used as data source medical records, useful for realization clinical history from definitive treatment that concluded case. should be perfectly understood had possible recurrent infections. Investigation through detailed physical examination use appropriate tests may help early detection this genitourinary tract.