Literature DB >> 21216673

Ureteral triplication: a rare anomaly with a variety of presentations.

N Kokabi1, N Price, G H H Smith, P J Gibbons, A J A Holland.   

Abstract

Ureteral triplication remains a very rare congenital malformation of the urinary tract with a wide spectrum of presentation. The sporadic nature of this condition and its association with other anomalies makes evidence-based management difficult. We report two cases of triplication in association with the VACTERL syndrome, one developing pelvi-ureteric junction obstruction and the other vesico-ureteric reflux. Crown
Copyright © 2010. Published by Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21216673     DOI: 10.1016/j.jpurol.2010.12.006

Source DB:  PubMed          Journal:  J Pediatr Urol        ISSN: 1477-5131            Impact factor:   1.830


  2 in total

1.  An extremely rare case of unilateral renal arterial and venous multiple deformity, combined with duplex pelvis and malrotation.

Authors:  Liang Gao; Siyuan Bu; Fan Wan; Fei Zhao; Qiang Wei; Ping Han; Tianyong Fan; Lu Yang
Journal:  Int Urol Nephrol       Date:  2013-02-01       Impact factor: 2.370

2.  Percutaneous and Endoscopic Management of Nephrolithiasis in a Patient with Five Native Ureters (Trifid Right and Bifid Left Collecting System).

Authors:  Neel H Patel; Mark J Ferretti; Jonathan B Bloom; Suraj Parikh; Michael Iorga; Nikil Uppaluri; David Schwalb; Majid Eshghi; Andrew Fishman
Journal:  J Endourol Case Rep       Date:  2018-03-01
  2 in total

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