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Granular cell tumour of the tongue in a 14-year-old boy: case report

Granular cell tumour is a rare soft tissue neoplasm that can virtually affect any site of the body. Its histological origin is controversial, since several studies have shown that different cells are involved. Granular cell tumour was initially described as myoblastoma, but, at present, a neural ori...

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Autores principales: BARBIERI, M., MUSIZZANO, Y., BOGGIO, M., CARCUSCIA, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pacini Editore SpA 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185822/
https://www.ncbi.nlm.nih.gov/pubmed/22058595
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author BARBIERI, M.
MUSIZZANO, Y.
BOGGIO, M.
CARCUSCIA, C.
author_facet BARBIERI, M.
MUSIZZANO, Y.
BOGGIO, M.
CARCUSCIA, C.
author_sort BARBIERI, M.
collection PubMed
description Granular cell tumour is a rare soft tissue neoplasm that can virtually affect any site of the body. Its histological origin is controversial, since several studies have shown that different cells are involved. Granular cell tumour was initially described as myoblastoma, but, at present, a neural origin is supported by most Authors, due to the immunohistochemical pattern. Even if the biological behaviour of granular cell tumours is usually benign, accurate histological examination is mandatory, because in a small number of cases they can be malignant. Here, a case is described of granular cell tumour in a 14-year-old boy, which is a very rare occurrence, since these tumours typically manifest in subjects between the third and sixth decade. Histopathological features, differential diagnosis and therapeutic implications of granular cell tumour are discussed, together with a brief review of the recent literature.
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spelling pubmed-31858222011-11-04 Granular cell tumour of the tongue in a 14-year-old boy: case report BARBIERI, M. MUSIZZANO, Y. BOGGIO, M. CARCUSCIA, C. Acta Otorhinolaryngol Ital Case Report Granular cell tumour is a rare soft tissue neoplasm that can virtually affect any site of the body. Its histological origin is controversial, since several studies have shown that different cells are involved. Granular cell tumour was initially described as myoblastoma, but, at present, a neural origin is supported by most Authors, due to the immunohistochemical pattern. Even if the biological behaviour of granular cell tumours is usually benign, accurate histological examination is mandatory, because in a small number of cases they can be malignant. Here, a case is described of granular cell tumour in a 14-year-old boy, which is a very rare occurrence, since these tumours typically manifest in subjects between the third and sixth decade. Histopathological features, differential diagnosis and therapeutic implications of granular cell tumour are discussed, together with a brief review of the recent literature. Pacini Editore SpA 2011-06 /pmc/articles/PMC3185822/ /pubmed/22058595 Text en © Copyright by Società Italiana di Otorinolaringologia e Chirurgia Cervico-Facciale http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License, which permits for noncommercial use, distribution, and reproduction in any digital medium, provided the original work is properly cited and is not altered in any way. For details, please refer to http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Case Report
BARBIERI, M.
MUSIZZANO, Y.
BOGGIO, M.
CARCUSCIA, C.
Granular cell tumour of the tongue in a 14-year-old boy: case report
title Granular cell tumour of the tongue in a 14-year-old boy: case report
title_full Granular cell tumour of the tongue in a 14-year-old boy: case report
title_fullStr Granular cell tumour of the tongue in a 14-year-old boy: case report
title_full_unstemmed Granular cell tumour of the tongue in a 14-year-old boy: case report
title_short Granular cell tumour of the tongue in a 14-year-old boy: case report
title_sort granular cell tumour of the tongue in a 14-year-old boy: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185822/
https://www.ncbi.nlm.nih.gov/pubmed/22058595
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