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Incomplete bladder duplication with multiple congenital anomalies: A rare presentation
We report a rare case of incomplete bladder duplication associated with multiple congenital malformation. The patient presented with a symptomatic left pelvi-ureteric junction obstruction which was surgically managed. To the best of our knowledge, this type of bladder duplication with such syndromic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310127/ https://www.ncbi.nlm.nih.gov/pubmed/25657553 http://dx.doi.org/10.4103/0974-7796.148628 |
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author | Awasthi, Nipun Kumar Goel, Hemantkumar Mahapatra, Rajkumarsingha Pal, Dilipkumar |
author_facet | Awasthi, Nipun Kumar Goel, Hemantkumar Mahapatra, Rajkumarsingha Pal, Dilipkumar |
author_sort | Awasthi, Nipun Kumar |
collection | PubMed |
description | We report a rare case of incomplete bladder duplication associated with multiple congenital malformation. The patient presented with a symptomatic left pelvi-ureteric junction obstruction which was surgically managed. To the best of our knowledge, this type of bladder duplication with such syndromic association is not yet reported in literature. |
format | Online Article Text |
id | pubmed-4310127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43101272015-02-05 Incomplete bladder duplication with multiple congenital anomalies: A rare presentation Awasthi, Nipun Kumar Goel, Hemantkumar Mahapatra, Rajkumarsingha Pal, Dilipkumar Urol Ann Case Report We report a rare case of incomplete bladder duplication associated with multiple congenital malformation. The patient presented with a symptomatic left pelvi-ureteric junction obstruction which was surgically managed. To the best of our knowledge, this type of bladder duplication with such syndromic association is not yet reported in literature. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4310127/ /pubmed/25657553 http://dx.doi.org/10.4103/0974-7796.148628 Text en Copyright: © Urology Annals http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Awasthi, Nipun Kumar Goel, Hemantkumar Mahapatra, Rajkumarsingha Pal, Dilipkumar Incomplete bladder duplication with multiple congenital anomalies: A rare presentation |
title | Incomplete bladder duplication with multiple congenital anomalies: A rare presentation |
title_full | Incomplete bladder duplication with multiple congenital anomalies: A rare presentation |
title_fullStr | Incomplete bladder duplication with multiple congenital anomalies: A rare presentation |
title_full_unstemmed | Incomplete bladder duplication with multiple congenital anomalies: A rare presentation |
title_short | Incomplete bladder duplication with multiple congenital anomalies: A rare presentation |
title_sort | incomplete bladder duplication with multiple congenital anomalies: a rare presentation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310127/ https://www.ncbi.nlm.nih.gov/pubmed/25657553 http://dx.doi.org/10.4103/0974-7796.148628 |
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