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Ectopic ureter associated with uterine didelphys and obstructed hemivagina: preoperative diagnosis by MRI

Uterine didelphys with obstructed hemivagina and ipsilateral renal anomalies is a rare congenital malformation of the female urogenital tract. While the urinary anomalies almost always involve renal agenesis, we report a rare case of a 17-year-old girl with the malformation associated with ectopic u...

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Autores principales: Wang, Zhen J., Daldrup-Link, Heike, Coakley, Fergus V., Yeh, Benjamin M.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2817805/
https://www.ncbi.nlm.nih.gov/pubmed/19924410
http://dx.doi.org/10.1007/s00247-009-1454-8
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author Wang, Zhen J.
Daldrup-Link, Heike
Coakley, Fergus V.
Yeh, Benjamin M.
author_facet Wang, Zhen J.
Daldrup-Link, Heike
Coakley, Fergus V.
Yeh, Benjamin M.
author_sort Wang, Zhen J.
collection PubMed
description Uterine didelphys with obstructed hemivagina and ipsilateral renal anomalies is a rare congenital malformation of the female urogenital tract. While the urinary anomalies almost always involve renal agenesis, we report a rare case of a 17-year-old girl with the malformation associated with ectopic ureteral insertion into the obstructed hemivagina, which was diagnosed preoperatively by MR imaging. To the best of our knowledge, preoperative MR imaging diagnosis of the ectopic ureter associated with this syndrome has not been previously reported. Accurate preoperative diagnosis of ectopic ureteral insertion associated with this syndrome is important for surgical planning.
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spelling pubmed-28178052010-02-13 Ectopic ureter associated with uterine didelphys and obstructed hemivagina: preoperative diagnosis by MRI Wang, Zhen J. Daldrup-Link, Heike Coakley, Fergus V. Yeh, Benjamin M. Pediatr Radiol Case Report Uterine didelphys with obstructed hemivagina and ipsilateral renal anomalies is a rare congenital malformation of the female urogenital tract. While the urinary anomalies almost always involve renal agenesis, we report a rare case of a 17-year-old girl with the malformation associated with ectopic ureteral insertion into the obstructed hemivagina, which was diagnosed preoperatively by MR imaging. To the best of our knowledge, preoperative MR imaging diagnosis of the ectopic ureter associated with this syndrome has not been previously reported. Accurate preoperative diagnosis of ectopic ureteral insertion associated with this syndrome is important for surgical planning. Springer-Verlag 2009-11-19 2010 /pmc/articles/PMC2817805/ /pubmed/19924410 http://dx.doi.org/10.1007/s00247-009-1454-8 Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Case Report
Wang, Zhen J.
Daldrup-Link, Heike
Coakley, Fergus V.
Yeh, Benjamin M.
Ectopic ureter associated with uterine didelphys and obstructed hemivagina: preoperative diagnosis by MRI
title Ectopic ureter associated with uterine didelphys and obstructed hemivagina: preoperative diagnosis by MRI
title_full Ectopic ureter associated with uterine didelphys and obstructed hemivagina: preoperative diagnosis by MRI
title_fullStr Ectopic ureter associated with uterine didelphys and obstructed hemivagina: preoperative diagnosis by MRI
title_full_unstemmed Ectopic ureter associated with uterine didelphys and obstructed hemivagina: preoperative diagnosis by MRI
title_short Ectopic ureter associated with uterine didelphys and obstructed hemivagina: preoperative diagnosis by MRI
title_sort ectopic ureter associated with uterine didelphys and obstructed hemivagina: preoperative diagnosis by mri
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2817805/
https://www.ncbi.nlm.nih.gov/pubmed/19924410
http://dx.doi.org/10.1007/s00247-009-1454-8
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