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A Rare Case of Eosinophilic Gastroenteritis Isolated in the Muscularis Propria of the Small Bowel

Eosinophilic gastroenteritis (EG) is an autoimmune disorder that involves infiltration of eosinophils in the bowel wall of the stomach and/or intestine, resulting in various gastrointestinal symptoms. The majority of cases are diagnosed by findings of increased eosinophils on mucosal biopsies. We de...

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Autores principales: Kim, Seo Hyun, Kesar, Varun, Grider, Douglas, Nguyen, Vu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8592308/
https://www.ncbi.nlm.nih.gov/pubmed/34804656
http://dx.doi.org/10.7759/cureus.18790
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author Kim, Seo Hyun
Kesar, Varun
Grider, Douglas
Nguyen, Vu
author_facet Kim, Seo Hyun
Kesar, Varun
Grider, Douglas
Nguyen, Vu
author_sort Kim, Seo Hyun
collection PubMed
description Eosinophilic gastroenteritis (EG) is an autoimmune disorder that involves infiltration of eosinophils in the bowel wall of the stomach and/or intestine, resulting in various gastrointestinal symptoms. The majority of cases are diagnosed by findings of increased eosinophils on mucosal biopsies. We describe a rare type of eosinophilic gastroenteritis with eosinophilic infiltration involving only the muscularis propria layer. This elusive diagnosis was made after a full-thickness intestinal wall biopsy. This predominantly muscular type eosinophilic gastroenteritis can cause intestinal obstruction or perforation. Similar to the predominantly mucosal type eosinophilic gastroenteritis, this type of eosinophilic gastroenteritis responds to low-dose or topical corticosteroids.
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spelling pubmed-85923082021-11-18 A Rare Case of Eosinophilic Gastroenteritis Isolated in the Muscularis Propria of the Small Bowel Kim, Seo Hyun Kesar, Varun Grider, Douglas Nguyen, Vu Cureus Internal Medicine Eosinophilic gastroenteritis (EG) is an autoimmune disorder that involves infiltration of eosinophils in the bowel wall of the stomach and/or intestine, resulting in various gastrointestinal symptoms. The majority of cases are diagnosed by findings of increased eosinophils on mucosal biopsies. We describe a rare type of eosinophilic gastroenteritis with eosinophilic infiltration involving only the muscularis propria layer. This elusive diagnosis was made after a full-thickness intestinal wall biopsy. This predominantly muscular type eosinophilic gastroenteritis can cause intestinal obstruction or perforation. Similar to the predominantly mucosal type eosinophilic gastroenteritis, this type of eosinophilic gastroenteritis responds to low-dose or topical corticosteroids. Cureus 2021-10-14 /pmc/articles/PMC8592308/ /pubmed/34804656 http://dx.doi.org/10.7759/cureus.18790 Text en Copyright © 2021, Kim 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 Internal Medicine
Kim, Seo Hyun
Kesar, Varun
Grider, Douglas
Nguyen, Vu
A Rare Case of Eosinophilic Gastroenteritis Isolated in the Muscularis Propria of the Small Bowel
title A Rare Case of Eosinophilic Gastroenteritis Isolated in the Muscularis Propria of the Small Bowel
title_full A Rare Case of Eosinophilic Gastroenteritis Isolated in the Muscularis Propria of the Small Bowel
title_fullStr A Rare Case of Eosinophilic Gastroenteritis Isolated in the Muscularis Propria of the Small Bowel
title_full_unstemmed A Rare Case of Eosinophilic Gastroenteritis Isolated in the Muscularis Propria of the Small Bowel
title_short A Rare Case of Eosinophilic Gastroenteritis Isolated in the Muscularis Propria of the Small Bowel
title_sort rare case of eosinophilic gastroenteritis isolated in the muscularis propria of the small bowel
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8592308/
https://www.ncbi.nlm.nih.gov/pubmed/34804656
http://dx.doi.org/10.7759/cureus.18790
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