Abstract
Bilateral single system ectopic ureter (BSSEU) is a rare congenital malformation. We report a case of BSSEU with a rare association of ectopic ureter with contralateral ectopic sphinctero-stenotic ureterocele with agenesis of one seminal vesicle with normal urinary continence and fertility presenting in adulthood as a case of chronic kidney disease. Diagnosis of ureterocele was missed even after detailed radiological investigations, so concurrent endoscopic evaluation is important for final diagnosis and operative intervention. As renal functions were markedly deranged, so transurethral incision of the right ureterocele with double J stenting was done as a preliminary procedure. Renal functions improved subsequently. Patient is planned for left nephroureterectomy and if necessary right ureteric reimplantation as a secondary major surgery in the follow-up period. World J Nephrol Urol. 2014;3(2):103-105 doi: http://dx.doi.org/10.14740 /wjnu162w
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
