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Congenital Peritoneal Encapsulation: A Literature Review of a Rare Pathology

Congenital peritoneal encapsulation (CPE) is a rare, congenital entity in which an accessory peritoneal membrane surrounds the small bowel. This condition is usually asymptomatic and rarely causes intestinal obstruction. Despite the rare cause of intestinal obstruction, it has excellent post-operati...

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Detalles Bibliográficos
Autores principales: Chowdhury, Ashim, Tata, Ravi Chandra, Shah, Ankur, Allu, Veera Jaya Chandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772582/
https://www.ncbi.nlm.nih.gov/pubmed/36569734
http://dx.doi.org/10.7759/cureus.31765
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author Chowdhury, Ashim
Tata, Ravi Chandra
Shah, Ankur
Allu, Veera Jaya Chandra
author_facet Chowdhury, Ashim
Tata, Ravi Chandra
Shah, Ankur
Allu, Veera Jaya Chandra
author_sort Chowdhury, Ashim
collection PubMed
description Congenital peritoneal encapsulation (CPE) is a rare, congenital entity in which an accessory peritoneal membrane surrounds the small bowel. This condition is usually asymptomatic and rarely causes intestinal obstruction. Despite the rare cause of intestinal obstruction, it has excellent post-operative recovery. There is no gold standard approach for investigating CPE; however, a computerized tomography scan of the abdomen might be helpful. Furthermore, diagnostic laparoscopy could be considered an adjunct. This report highlights the rare congenital anomaly as a cause of intestinal obstruction.
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spelling pubmed-97725822022-12-23 Congenital Peritoneal Encapsulation: A Literature Review of a Rare Pathology Chowdhury, Ashim Tata, Ravi Chandra Shah, Ankur Allu, Veera Jaya Chandra Cureus General Surgery Congenital peritoneal encapsulation (CPE) is a rare, congenital entity in which an accessory peritoneal membrane surrounds the small bowel. This condition is usually asymptomatic and rarely causes intestinal obstruction. Despite the rare cause of intestinal obstruction, it has excellent post-operative recovery. There is no gold standard approach for investigating CPE; however, a computerized tomography scan of the abdomen might be helpful. Furthermore, diagnostic laparoscopy could be considered an adjunct. This report highlights the rare congenital anomaly as a cause of intestinal obstruction. Cureus 2022-11-21 /pmc/articles/PMC9772582/ /pubmed/36569734 http://dx.doi.org/10.7759/cureus.31765 Text en Copyright © 2022, Chowdhury et al. https://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 author and source are credited.
spellingShingle General Surgery
Chowdhury, Ashim
Tata, Ravi Chandra
Shah, Ankur
Allu, Veera Jaya Chandra
Congenital Peritoneal Encapsulation: A Literature Review of a Rare Pathology
title Congenital Peritoneal Encapsulation: A Literature Review of a Rare Pathology
title_full Congenital Peritoneal Encapsulation: A Literature Review of a Rare Pathology
title_fullStr Congenital Peritoneal Encapsulation: A Literature Review of a Rare Pathology
title_full_unstemmed Congenital Peritoneal Encapsulation: A Literature Review of a Rare Pathology
title_short Congenital Peritoneal Encapsulation: A Literature Review of a Rare Pathology
title_sort congenital peritoneal encapsulation: a literature review of a rare pathology
topic General Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772582/
https://www.ncbi.nlm.nih.gov/pubmed/36569734
http://dx.doi.org/10.7759/cureus.31765
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