Congenital Pouch Colon associated with Pseudoexstrophy: Report of Two Cases
This report describes two newborn girls with single perineal opening (cloaca), and pseudoexstrophy in the form of divergent pubic bones and rectus muscles, and a low-set umbilicus. Both patients had a type II congenital pouch colon (CPC) with one hemiuterus and vagina on each side in the pelvis. In...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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EL-MED-Pub
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715891/ https://www.ncbi.nlm.nih.gov/pubmed/26814054 |
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author | Jhanwar, Praveen Shinde, Nand Kishor Patel, Jigar N Pant, Nitin Chadha, Rajiv |
author_facet | Jhanwar, Praveen Shinde, Nand Kishor Patel, Jigar N Pant, Nitin Chadha, Rajiv |
author_sort | Jhanwar, Praveen |
collection | PubMed |
description | This report describes two newborn girls with single perineal opening (cloaca), and pseudoexstrophy in the form of divergent pubic bones and rectus muscles, and a low-set umbilicus. Both patients had a type II congenital pouch colon (CPC) with one hemiuterus and vagina on each side in the pelvis. In one patient, a Meckel’s diverticulum was present 5 cm from the ileocecal junction. In both girls, a diverting proximal ileostomy was the initial surgery. |
format | Online Article Text |
id | pubmed-4715891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | EL-MED-Pub |
record_format | MEDLINE/PubMed |
spelling | pubmed-47158912016-01-26 Congenital Pouch Colon associated with Pseudoexstrophy: Report of Two Cases Jhanwar, Praveen Shinde, Nand Kishor Patel, Jigar N Pant, Nitin Chadha, Rajiv APSP J Case Rep Case Report This report describes two newborn girls with single perineal opening (cloaca), and pseudoexstrophy in the form of divergent pubic bones and rectus muscles, and a low-set umbilicus. Both patients had a type II congenital pouch colon (CPC) with one hemiuterus and vagina on each side in the pelvis. In one patient, a Meckel’s diverticulum was present 5 cm from the ileocecal junction. In both girls, a diverting proximal ileostomy was the initial surgery. EL-MED-Pub 2016-01-01 /pmc/articles/PMC4715891/ /pubmed/26814054 Text en Copyright © 2016 AJCR http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Jhanwar, Praveen Shinde, Nand Kishor Patel, Jigar N Pant, Nitin Chadha, Rajiv Congenital Pouch Colon associated with Pseudoexstrophy: Report of Two Cases |
title | Congenital Pouch Colon associated with Pseudoexstrophy: Report of Two Cases |
title_full | Congenital Pouch Colon associated with Pseudoexstrophy: Report of Two Cases |
title_fullStr | Congenital Pouch Colon associated with Pseudoexstrophy: Report of Two Cases |
title_full_unstemmed | Congenital Pouch Colon associated with Pseudoexstrophy: Report of Two Cases |
title_short | Congenital Pouch Colon associated with Pseudoexstrophy: Report of Two Cases |
title_sort | congenital pouch colon associated with pseudoexstrophy: report of two cases |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715891/ https://www.ncbi.nlm.nih.gov/pubmed/26814054 |
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