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Granular Cell Tumor of Cecum: A Common Tumor in a Rare Site with Diagnostic Challenge

Granular cell tumor (GCT) also known as Abrikossoff’s tumor is a benign neoplasm that is usually seen in the fourth to sixth decades of life with slight female preponderance. It is most frequently seen in the oral cavity, skin, and subcutaneous tissue. Gastrointestinal tract involvement is uncommon,...

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Autores principales: Rajagopal, Meyyappa Devan, Gochhait, Debasis, Shanmugan, Dasarathan, Barwad, Adarsh Wamanrao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617916/
https://www.ncbi.nlm.nih.gov/pubmed/28975016
http://dx.doi.org/10.4081/rt.2017.6420
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author Rajagopal, Meyyappa Devan
Gochhait, Debasis
Shanmugan, Dasarathan
Barwad, Adarsh Wamanrao
author_facet Rajagopal, Meyyappa Devan
Gochhait, Debasis
Shanmugan, Dasarathan
Barwad, Adarsh Wamanrao
author_sort Rajagopal, Meyyappa Devan
collection PubMed
description Granular cell tumor (GCT) also known as Abrikossoff’s tumor is a benign neoplasm that is usually seen in the fourth to sixth decades of life with slight female preponderance. It is most frequently seen in the oral cavity, skin, and subcutaneous tissue. Gastrointestinal tract involvement is uncommon, in which esophagus is the most commonly affected site. There are case reports of GCT in stomach, appendix, colon and rectum. In this article, we report a case of GCT involving cecum. The cell of origin in GCT is controversial. There are various pools of thoughts regarding its histogenesis, the details of which are reviewed in this article with emphasis on the diagnostic difficulties encountered in this tumor.
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spelling pubmed-56179162017-10-03 Granular Cell Tumor of Cecum: A Common Tumor in a Rare Site with Diagnostic Challenge Rajagopal, Meyyappa Devan Gochhait, Debasis Shanmugan, Dasarathan Barwad, Adarsh Wamanrao Rare Tumors Case Report Granular cell tumor (GCT) also known as Abrikossoff’s tumor is a benign neoplasm that is usually seen in the fourth to sixth decades of life with slight female preponderance. It is most frequently seen in the oral cavity, skin, and subcutaneous tissue. Gastrointestinal tract involvement is uncommon, in which esophagus is the most commonly affected site. There are case reports of GCT in stomach, appendix, colon and rectum. In this article, we report a case of GCT involving cecum. The cell of origin in GCT is controversial. There are various pools of thoughts regarding its histogenesis, the details of which are reviewed in this article with emphasis on the diagnostic difficulties encountered in this tumor. PAGEPress Publications, Pavia, Italy 2017-08-29 /pmc/articles/PMC5617916/ /pubmed/28975016 http://dx.doi.org/10.4081/rt.2017.6420 Text en ©Copyright M.D. Rajagopal et al., 2017 http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Rajagopal, Meyyappa Devan
Gochhait, Debasis
Shanmugan, Dasarathan
Barwad, Adarsh Wamanrao
Granular Cell Tumor of Cecum: A Common Tumor in a Rare Site with Diagnostic Challenge
title Granular Cell Tumor of Cecum: A Common Tumor in a Rare Site with Diagnostic Challenge
title_full Granular Cell Tumor of Cecum: A Common Tumor in a Rare Site with Diagnostic Challenge
title_fullStr Granular Cell Tumor of Cecum: A Common Tumor in a Rare Site with Diagnostic Challenge
title_full_unstemmed Granular Cell Tumor of Cecum: A Common Tumor in a Rare Site with Diagnostic Challenge
title_short Granular Cell Tumor of Cecum: A Common Tumor in a Rare Site with Diagnostic Challenge
title_sort granular cell tumor of cecum: a common tumor in a rare site with diagnostic challenge
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617916/
https://www.ncbi.nlm.nih.gov/pubmed/28975016
http://dx.doi.org/10.4081/rt.2017.6420
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