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Multinucleated stromal giant cells in the gastroesophageal junctional and gastric mucosa: a retrospective study

BACKGROUND: Atypical multinucleated stromal giant cells (MSGCs) are occasionally encountered in the esophagogastric mucosa. This study aims to investigate the origin and clinical association of MSGCs in the upper gastrointestinal tract. METHODS: Three hundred sixty-one contiguous biopsies and 1 rese...

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Autores principales: Sachak, Taha, Frankel, Wendy L., Arnold, Christina A., Chen, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661083/
https://www.ncbi.nlm.nih.gov/pubmed/31351475
http://dx.doi.org/10.1186/s13000-019-0860-y
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author Sachak, Taha
Frankel, Wendy L.
Arnold, Christina A.
Chen, Wei
author_facet Sachak, Taha
Frankel, Wendy L.
Arnold, Christina A.
Chen, Wei
author_sort Sachak, Taha
collection PubMed
description BACKGROUND: Atypical multinucleated stromal giant cells (MSGCs) are occasionally encountered in the esophagogastric mucosa. This study aims to investigate the origin and clinical association of MSGCs in the upper gastrointestinal tract. METHODS: Three hundred sixty-one contiguous biopsies and 1 resection specimen from the stomach and gastroesophageal junction (GEJ) were identified from archives for morphologic and immunohistochemical studies. RESULTS: MSGCs were identified in 22 cases (6%: 7 gastric, 15 GEJ). Patients’ average age was 53 years. There was no sex predilection. 77% cases had only 1 or 2 MSGCs per 10 high power fields. MSGCs were located in the lamina propria of the gastric or GEJ mucosa, with an accentuation in the subepithelial zone. The median number of nuclei in a MSGC was 5 (ranging from 3 to 16). The nuclei were touching/overlapping, often arranged into “wreath”, “caterpillar”, or “morula” configurations. MSGCs expressed smooth muscle actin, desmin, while negative for cytokeratin AE1/3, CD68, S100, chromogranin, and CD117. The most common clinical history was epigastric pain, gastroesophageal reflux, and Barrett esophagus. The most common associated pathologic diagnoses included reactive (chemical) gastropathy (71% gastric biopsies) and gastroesophageal reflux (73% GEJ specimens). CONCLUSIONS: MSGCs in the esophagogastric mucosa show smooth muscle/myofibroblast differentiation by immunohistochemistry and likely represent a reactive/reparative stromal reaction associated with gastroesophageal reflux and reactive (chemical) gastropathy.
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spelling pubmed-66610832019-08-01 Multinucleated stromal giant cells in the gastroesophageal junctional and gastric mucosa: a retrospective study Sachak, Taha Frankel, Wendy L. Arnold, Christina A. Chen, Wei Diagn Pathol Research BACKGROUND: Atypical multinucleated stromal giant cells (MSGCs) are occasionally encountered in the esophagogastric mucosa. This study aims to investigate the origin and clinical association of MSGCs in the upper gastrointestinal tract. METHODS: Three hundred sixty-one contiguous biopsies and 1 resection specimen from the stomach and gastroesophageal junction (GEJ) were identified from archives for morphologic and immunohistochemical studies. RESULTS: MSGCs were identified in 22 cases (6%: 7 gastric, 15 GEJ). Patients’ average age was 53 years. There was no sex predilection. 77% cases had only 1 or 2 MSGCs per 10 high power fields. MSGCs were located in the lamina propria of the gastric or GEJ mucosa, with an accentuation in the subepithelial zone. The median number of nuclei in a MSGC was 5 (ranging from 3 to 16). The nuclei were touching/overlapping, often arranged into “wreath”, “caterpillar”, or “morula” configurations. MSGCs expressed smooth muscle actin, desmin, while negative for cytokeratin AE1/3, CD68, S100, chromogranin, and CD117. The most common clinical history was epigastric pain, gastroesophageal reflux, and Barrett esophagus. The most common associated pathologic diagnoses included reactive (chemical) gastropathy (71% gastric biopsies) and gastroesophageal reflux (73% GEJ specimens). CONCLUSIONS: MSGCs in the esophagogastric mucosa show smooth muscle/myofibroblast differentiation by immunohistochemistry and likely represent a reactive/reparative stromal reaction associated with gastroesophageal reflux and reactive (chemical) gastropathy. BioMed Central 2019-07-27 /pmc/articles/PMC6661083/ /pubmed/31351475 http://dx.doi.org/10.1186/s13000-019-0860-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Sachak, Taha
Frankel, Wendy L.
Arnold, Christina A.
Chen, Wei
Multinucleated stromal giant cells in the gastroesophageal junctional and gastric mucosa: a retrospective study
title Multinucleated stromal giant cells in the gastroesophageal junctional and gastric mucosa: a retrospective study
title_full Multinucleated stromal giant cells in the gastroesophageal junctional and gastric mucosa: a retrospective study
title_fullStr Multinucleated stromal giant cells in the gastroesophageal junctional and gastric mucosa: a retrospective study
title_full_unstemmed Multinucleated stromal giant cells in the gastroesophageal junctional and gastric mucosa: a retrospective study
title_short Multinucleated stromal giant cells in the gastroesophageal junctional and gastric mucosa: a retrospective study
title_sort multinucleated stromal giant cells in the gastroesophageal junctional and gastric mucosa: a retrospective study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661083/
https://www.ncbi.nlm.nih.gov/pubmed/31351475
http://dx.doi.org/10.1186/s13000-019-0860-y
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