Colorectal epithelial neoplasm associated with gut-associated lymphoid tissue

Background Colorectal epithelial neoplasm extending into the submucosal gut-associated lymphoid tissue (GALT) can cause difficulties in the differential diagnosis. Regarding GALT-associated epithelial neoplasms, a few studies favor the term “GALT carcinoma” while other studies have mentioned the ter...

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Main Authors: Yo Han Jeon, Ji Hyun Ahn, Hee Kyung Chang
Format: Article
Language:English
Published: Korean Society of Pathologists & the Korean Society for Cytopathology 2020-03-01
Series:Journal of Pathology and Translational Medicine
Subjects:
Online Access:http://jpatholtm.org/upload/pdf/jptm-2019-11-06.pdf
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author Yo Han Jeon
Ji Hyun Ahn
Hee Kyung Chang
author_facet Yo Han Jeon
Ji Hyun Ahn
Hee Kyung Chang
author_sort Yo Han Jeon
collection DOAJ
description Background Colorectal epithelial neoplasm extending into the submucosal gut-associated lymphoid tissue (GALT) can cause difficulties in the differential diagnosis. Regarding GALT-associated epithelial neoplasms, a few studies favor the term “GALT carcinoma” while other studies have mentioned the term “GALT-associated pseudoinvasion/epithelial misplacement (PEM)”. Methods The clinicopathologic characteristics of 11 cases of colorectal epithelial neoplasm associated with submucosal GALT diagnosed via endoscopic submucosal dissection were studied. Results Eight cases (72.7%) were in males. The median age was 59 years, and age ranged from 53 to 73. All cases had a submucosal tumor component more compatible with GALT-associated PEM. Eight cases (72.7%) were located in the right colon. Ten cases (90.9%) had a non-protruding endoscopic appearance. Nine cases (81.8%) showed continuity between the submucosal and surface adenomatous components. Nine cases showed (81.8%) focal defects or discontinuation of the muscularis mucosae adjacent to the submucosal GALT. No case showed hemosiderin deposits in the submucosa or desmoplastic reaction. No case showed single tumor cells or small clusters of tumor cells in the submucosal GALT. Seven cases (63.6%) showed goblet cells in the submucosa. No cases showed oncocytic columnar cells lining submucosal glands. Conclusions Our experience suggests that pathologists should be aware of the differential diagnosis of GALT-associated submucosal extension by colorectal adenomatous neoplasm. Further studies are needed to validate classification of GALT-associated epithelial neoplasms.
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spelling doaj.art-6f364f04279e4c77ac9775f9f4debedb2022-12-22T02:38:28ZengKorean Society of Pathologists & the Korean Society for CytopathologyJournal of Pathology and Translational Medicine2383-78372383-78452020-03-0154213514510.4132/jptm.2019.11.0616889Colorectal epithelial neoplasm associated with gut-associated lymphoid tissueYo Han Jeon0Ji Hyun Ahn1Hee Kyung Chang2 Department of Pathology, Kosin University College of Medicine, Busan, Korea Department of Pathology, Kosin University College of Medicine, Busan, Korea Department of Pathology, Kosin University College of Medicine, Busan, KoreaBackground Colorectal epithelial neoplasm extending into the submucosal gut-associated lymphoid tissue (GALT) can cause difficulties in the differential diagnosis. Regarding GALT-associated epithelial neoplasms, a few studies favor the term “GALT carcinoma” while other studies have mentioned the term “GALT-associated pseudoinvasion/epithelial misplacement (PEM)”. Methods The clinicopathologic characteristics of 11 cases of colorectal epithelial neoplasm associated with submucosal GALT diagnosed via endoscopic submucosal dissection were studied. Results Eight cases (72.7%) were in males. The median age was 59 years, and age ranged from 53 to 73. All cases had a submucosal tumor component more compatible with GALT-associated PEM. Eight cases (72.7%) were located in the right colon. Ten cases (90.9%) had a non-protruding endoscopic appearance. Nine cases (81.8%) showed continuity between the submucosal and surface adenomatous components. Nine cases showed (81.8%) focal defects or discontinuation of the muscularis mucosae adjacent to the submucosal GALT. No case showed hemosiderin deposits in the submucosa or desmoplastic reaction. No case showed single tumor cells or small clusters of tumor cells in the submucosal GALT. Seven cases (63.6%) showed goblet cells in the submucosa. No cases showed oncocytic columnar cells lining submucosal glands. Conclusions Our experience suggests that pathologists should be aware of the differential diagnosis of GALT-associated submucosal extension by colorectal adenomatous neoplasm. Further studies are needed to validate classification of GALT-associated epithelial neoplasms.http://jpatholtm.org/upload/pdf/jptm-2019-11-06.pdfhumanscolorectal neoplasmslymphoid tissueadenomatous polyps
spellingShingle Yo Han Jeon
Ji Hyun Ahn
Hee Kyung Chang
Colorectal epithelial neoplasm associated with gut-associated lymphoid tissue
Journal of Pathology and Translational Medicine
humans
colorectal neoplasms
lymphoid tissue
adenomatous polyps
title Colorectal epithelial neoplasm associated with gut-associated lymphoid tissue
title_full Colorectal epithelial neoplasm associated with gut-associated lymphoid tissue
title_fullStr Colorectal epithelial neoplasm associated with gut-associated lymphoid tissue
title_full_unstemmed Colorectal epithelial neoplasm associated with gut-associated lymphoid tissue
title_short Colorectal epithelial neoplasm associated with gut-associated lymphoid tissue
title_sort colorectal epithelial neoplasm associated with gut associated lymphoid tissue
topic humans
colorectal neoplasms
lymphoid tissue
adenomatous polyps
url http://jpatholtm.org/upload/pdf/jptm-2019-11-06.pdf
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AT jihyunahn colorectalepithelialneoplasmassociatedwithgutassociatedlymphoidtissue
AT heekyungchang colorectalepithelialneoplasmassociatedwithgutassociatedlymphoidtissue