Complete duplication of the urinary bladder: An extremely rare congenital anomaly

A case of complete bladder duplication with urethra duplication, diphallus, anorectal malformation and rightsided renal agensis with ipsilateral gonadal agenesisis was reported because of its rarity. Possible deranged embryology resulting in these anomalies has been reviewed with relevant hypothesis...

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Autores principales: Gajbhiye, Vishal, Nath, Sasanka, Ghosh, Priya, Chatterjee, Argha, Haldar, Dipanjan, Das, Sukanta K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310128/
https://www.ncbi.nlm.nih.gov/pubmed/25657554
http://dx.doi.org/10.4103/0974-7796.148629
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author Gajbhiye, Vishal
Nath, Sasanka
Ghosh, Priya
Chatterjee, Argha
Haldar, Dipanjan
Das, Sukanta K.
author_facet Gajbhiye, Vishal
Nath, Sasanka
Ghosh, Priya
Chatterjee, Argha
Haldar, Dipanjan
Das, Sukanta K.
author_sort Gajbhiye, Vishal
collection PubMed
description A case of complete bladder duplication with urethra duplication, diphallus, anorectal malformation and rightsided renal agensis with ipsilateral gonadal agenesisis was reported because of its rarity. Possible deranged embryology resulting in these anomalies has been reviewed with relevant hypothesis. The patient underwent several investigations and undergoing multistage surgical intervention.
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spelling pubmed-43101282015-02-05 Complete duplication of the urinary bladder: An extremely rare congenital anomaly Gajbhiye, Vishal Nath, Sasanka Ghosh, Priya Chatterjee, Argha Haldar, Dipanjan Das, Sukanta K. Urol Ann Case Report A case of complete bladder duplication with urethra duplication, diphallus, anorectal malformation and rightsided renal agensis with ipsilateral gonadal agenesisis was reported because of its rarity. Possible deranged embryology resulting in these anomalies has been reviewed with relevant hypothesis. The patient underwent several investigations and undergoing multistage surgical intervention. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4310128/ /pubmed/25657554 http://dx.doi.org/10.4103/0974-7796.148629 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
Gajbhiye, Vishal
Nath, Sasanka
Ghosh, Priya
Chatterjee, Argha
Haldar, Dipanjan
Das, Sukanta K.
Complete duplication of the urinary bladder: An extremely rare congenital anomaly
title Complete duplication of the urinary bladder: An extremely rare congenital anomaly
title_full Complete duplication of the urinary bladder: An extremely rare congenital anomaly
title_fullStr Complete duplication of the urinary bladder: An extremely rare congenital anomaly
title_full_unstemmed Complete duplication of the urinary bladder: An extremely rare congenital anomaly
title_short Complete duplication of the urinary bladder: An extremely rare congenital anomaly
title_sort complete duplication of the urinary bladder: an extremely rare congenital anomaly
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310128/
https://www.ncbi.nlm.nih.gov/pubmed/25657554
http://dx.doi.org/10.4103/0974-7796.148629
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