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Upper gastrointestinal tract involvement of pediatric inflammatory bowel disease: A pathological review
Upper gastrointestinal (UGI) tract involvement of inflammatory bowel disease (IBD) is commonly seen in pediatric patients. Upper endoscopy is included in the routine workup of children with suspected IBD to enhance the diagnosis and management of these patients. Currently, childhood IBD is classifie...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487385/ https://www.ncbi.nlm.nih.gov/pubmed/31086461 http://dx.doi.org/10.3748/wjg.v25.i16.1928 |
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author | Abuquteish, Dua Putra, Juan |
author_facet | Abuquteish, Dua Putra, Juan |
author_sort | Abuquteish, Dua |
collection | PubMed |
description | Upper gastrointestinal (UGI) tract involvement of inflammatory bowel disease (IBD) is commonly seen in pediatric patients. Upper endoscopy is included in the routine workup of children with suspected IBD to enhance the diagnosis and management of these patients. Currently, childhood IBD is classified into ulcerative colitis (UC), atypical UC, Crohn’s disease (CD) and IBD unclassified. Histologic confirmation of UGI tract involvement, in particular the presence of epithelioid (non-caseating) granulomas, is helpful in confirming the diagnosis of IBD and its classification. Herein, we reviewed selected IBD-associated UGI tract manifestations in children. Lymphocytic esophagitis, seen predominantly in CD, is histologically characterized by increased intraepithelial lymphocytes (> 20 in one high-power field) in a background of mucosal injury with absence of granulocytes. Focally enhanced gastritis is a form of gastric inflammation in pediatric IBD marked by a focal lymphohistiocytic pit inflammation with or without granulocytes and plasma cells in a relatively normal background gastric mucosa. Duodenal inflammation seen in children with IBD includes cryptitis, villous flattening, increased intraepithelial lymphocytes, and lamina propria eosinophilia. Finally, epithelioid granulomas not associated with ruptured gland/crypt are a diagnostic feature of CD. The clinicopathologic correlation and differential diagnosis of each microscopic finding are discussed. Clinicians and pathologists should be cognizant of the utility and limitations of these histologic features. |
format | Online Article Text |
id | pubmed-6487385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-64873852019-05-13 Upper gastrointestinal tract involvement of pediatric inflammatory bowel disease: A pathological review Abuquteish, Dua Putra, Juan World J Gastroenterol Minireviews Upper gastrointestinal (UGI) tract involvement of inflammatory bowel disease (IBD) is commonly seen in pediatric patients. Upper endoscopy is included in the routine workup of children with suspected IBD to enhance the diagnosis and management of these patients. Currently, childhood IBD is classified into ulcerative colitis (UC), atypical UC, Crohn’s disease (CD) and IBD unclassified. Histologic confirmation of UGI tract involvement, in particular the presence of epithelioid (non-caseating) granulomas, is helpful in confirming the diagnosis of IBD and its classification. Herein, we reviewed selected IBD-associated UGI tract manifestations in children. Lymphocytic esophagitis, seen predominantly in CD, is histologically characterized by increased intraepithelial lymphocytes (> 20 in one high-power field) in a background of mucosal injury with absence of granulocytes. Focally enhanced gastritis is a form of gastric inflammation in pediatric IBD marked by a focal lymphohistiocytic pit inflammation with or without granulocytes and plasma cells in a relatively normal background gastric mucosa. Duodenal inflammation seen in children with IBD includes cryptitis, villous flattening, increased intraepithelial lymphocytes, and lamina propria eosinophilia. Finally, epithelioid granulomas not associated with ruptured gland/crypt are a diagnostic feature of CD. The clinicopathologic correlation and differential diagnosis of each microscopic finding are discussed. Clinicians and pathologists should be cognizant of the utility and limitations of these histologic features. Baishideng Publishing Group Inc 2019-04-28 2019-04-28 /pmc/articles/PMC6487385/ /pubmed/31086461 http://dx.doi.org/10.3748/wjg.v25.i16.1928 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Minireviews Abuquteish, Dua Putra, Juan Upper gastrointestinal tract involvement of pediatric inflammatory bowel disease: A pathological review |
title | Upper gastrointestinal tract involvement of pediatric inflammatory bowel disease: A pathological review |
title_full | Upper gastrointestinal tract involvement of pediatric inflammatory bowel disease: A pathological review |
title_fullStr | Upper gastrointestinal tract involvement of pediatric inflammatory bowel disease: A pathological review |
title_full_unstemmed | Upper gastrointestinal tract involvement of pediatric inflammatory bowel disease: A pathological review |
title_short | Upper gastrointestinal tract involvement of pediatric inflammatory bowel disease: A pathological review |
title_sort | upper gastrointestinal tract involvement of pediatric inflammatory bowel disease: a pathological review |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487385/ https://www.ncbi.nlm.nih.gov/pubmed/31086461 http://dx.doi.org/10.3748/wjg.v25.i16.1928 |
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