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Solitary Granular Cell Tumor of Cecum: A Case Report

Granular cell tumor (GCT) was first described by Abrikossof in 1926. This tumor is a benign neoplasm of unclear histogenesis that is generally believed to be of nerve sheath origin. GCT is not common and most often affects the tongue, skin, and soft tissue, although it may occur anywhere in the body...

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Autores principales: Znati, Kaoutar, Harmouch, Taoufiq, Benlemlih, Amal, Elfatemi, Hinde, Chbani, Laila, Amarti, Afaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168574/
https://www.ncbi.nlm.nih.gov/pubmed/21991536
http://dx.doi.org/10.5402/2011/943804
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author Znati, Kaoutar
Harmouch, Taoufiq
Benlemlih, Amal
Elfatemi, Hinde
Chbani, Laila
Amarti, Afaf
author_facet Znati, Kaoutar
Harmouch, Taoufiq
Benlemlih, Amal
Elfatemi, Hinde
Chbani, Laila
Amarti, Afaf
author_sort Znati, Kaoutar
collection PubMed
description Granular cell tumor (GCT) was first described by Abrikossof in 1926. This tumor is a benign neoplasm of unclear histogenesis that is generally believed to be of nerve sheath origin. GCT is not common and most often affects the tongue, skin, and soft tissue, although it may occur anywhere in the body. Gastrointestinal tract involvement, and especially that of the colon, is very rare. This usually benign tumor appears as a submucosal nodule, measuring less than 2 cm in diameter and is often found incidentally during colorectal examinations. We describe the case of a 27-year-old man with a GCT in the cecum that was detected after a screening colonoscopy. Endoscopic examination revealed a yellowish submucosal tumor, 0.7 cm in diameter. An endoscopic mucosal polypectomy was done for histological confirmation and treatment.
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spelling pubmed-31685742011-10-11 Solitary Granular Cell Tumor of Cecum: A Case Report Znati, Kaoutar Harmouch, Taoufiq Benlemlih, Amal Elfatemi, Hinde Chbani, Laila Amarti, Afaf ISRN Gastroenterol Case Report Granular cell tumor (GCT) was first described by Abrikossof in 1926. This tumor is a benign neoplasm of unclear histogenesis that is generally believed to be of nerve sheath origin. GCT is not common and most often affects the tongue, skin, and soft tissue, although it may occur anywhere in the body. Gastrointestinal tract involvement, and especially that of the colon, is very rare. This usually benign tumor appears as a submucosal nodule, measuring less than 2 cm in diameter and is often found incidentally during colorectal examinations. We describe the case of a 27-year-old man with a GCT in the cecum that was detected after a screening colonoscopy. Endoscopic examination revealed a yellowish submucosal tumor, 0.7 cm in diameter. An endoscopic mucosal polypectomy was done for histological confirmation and treatment. International Scholarly Research Network 2011 2010-11-04 /pmc/articles/PMC3168574/ /pubmed/21991536 http://dx.doi.org/10.5402/2011/943804 Text en Copyright © 2011 Kaoutar Znati et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Znati, Kaoutar
Harmouch, Taoufiq
Benlemlih, Amal
Elfatemi, Hinde
Chbani, Laila
Amarti, Afaf
Solitary Granular Cell Tumor of Cecum: A Case Report
title Solitary Granular Cell Tumor of Cecum: A Case Report
title_full Solitary Granular Cell Tumor of Cecum: A Case Report
title_fullStr Solitary Granular Cell Tumor of Cecum: A Case Report
title_full_unstemmed Solitary Granular Cell Tumor of Cecum: A Case Report
title_short Solitary Granular Cell Tumor of Cecum: A Case Report
title_sort solitary granular cell tumor of cecum: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168574/
https://www.ncbi.nlm.nih.gov/pubmed/21991536
http://dx.doi.org/10.5402/2011/943804
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