Retroiliac ureter is a rare congenital anomaly. In this paper, we present a case in which retroiliac double ureters were incidentally found during a retroperitoneoscopic nephroureterectomy procedure in a 5-year-old boy with dysplastic right kidney in duplex system and ureterocele. Ureters were both in the retroiliac artery position. The nephroureterectomy procedure was completed retroperitoneoscopically. After a literature review, this case appeared to be the first report of retroiliac double ureters in a duplex system. © Mary Ann Liebert, Inc.

Retroiliac double ureters in duplex system: incidental retroperitoneoscopic diagnosis / Cobellis, Giovanni; Mastroianni, L; Noviello, C; Cruccetti, A; Martino, A; Amici, Giuseppe. - In: JOURNAL OF LAPAROENDOSCOPIC & ADVANCED SURGICAL TECHNIQUES. - ISSN 1092-6429. - 17(4):(2007), pp. 517-518. [10.1089/lap.2006.0118]

Retroiliac double ureters in duplex system: incidental retroperitoneoscopic diagnosis.

COBELLIS, GIOVANNI
Writing – Review & Editing
;
AMICI, Giuseppe
Supervision
2007-01-01

Abstract

Retroiliac ureter is a rare congenital anomaly. In this paper, we present a case in which retroiliac double ureters were incidentally found during a retroperitoneoscopic nephroureterectomy procedure in a 5-year-old boy with dysplastic right kidney in duplex system and ureterocele. Ureters were both in the retroiliac artery position. The nephroureterectomy procedure was completed retroperitoneoscopically. After a literature review, this case appeared to be the first report of retroiliac double ureters in a duplex system. © Mary Ann Liebert, Inc.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11566/50918
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