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Solitary fibrous tumor of the tongue
Solitary fibrous tumor (SFT) is a benign mesenchymal neoplasm originally described in pleura with a rare presentation in the oral cavity. Herein, we report a case of a 28-year-old male patient who presented an asymptomatic slow-growing mass in the anterior part of the tongue. Intraoral examination r...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hospital Universitário da Universidade de São Paulo
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675090/ https://www.ncbi.nlm.nih.gov/pubmed/36426115 http://dx.doi.org/10.4322/acr.2021.405 |
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author | Siqueira, Juliana Mota Heguedusch, Daniele Aguiar, Emília Maria Gomes dos Santos, Anaeliza Figueiredo Alves, Fabio Abreu Nunes, Fabio Daumas |
author_facet | Siqueira, Juliana Mota Heguedusch, Daniele Aguiar, Emília Maria Gomes dos Santos, Anaeliza Figueiredo Alves, Fabio Abreu Nunes, Fabio Daumas |
author_sort | Siqueira, Juliana Mota |
collection | PubMed |
description | Solitary fibrous tumor (SFT) is a benign mesenchymal neoplasm originally described in pleura with a rare presentation in the oral cavity. Herein, we report a case of a 28-year-old male patient who presented an asymptomatic slow-growing mass in the anterior part of the tongue. Intraoral examination revealed a well-circumscribed mass covered by normal mucosa with a fibrous consistency. Due to non-specific clinical findings, the initial diagnostic hypotheses include benign submucosal neoplasms such as leiomyoma, neurofibroma, SFT, and others. An excisional biopsy was performed. Microscopically, the tumor was surrounded by a thick fibrous capsule; hypo and hypercellular areas were arranged in a storiform pattern with a stroma formed by collagen and abundant vascularization. Tumor cells showed immunopositivity for CD34 and STAT-6 and no expression of CD99, AML, S-100, and Ki-67. According to these findings, the diagnosis of SFT was established. After 24 months, the patient is asymptomatic and has no evidence of recurrence. Although oral involvement is rare, SFT should be included in the differential diagnosis of oral submucosal lesions. |
format | Online Article Text |
id | pubmed-9675090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hospital Universitário da Universidade de São Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-96750902022-11-23 Solitary fibrous tumor of the tongue Siqueira, Juliana Mota Heguedusch, Daniele Aguiar, Emília Maria Gomes dos Santos, Anaeliza Figueiredo Alves, Fabio Abreu Nunes, Fabio Daumas Autops Case Rep Clinical Case Report Solitary fibrous tumor (SFT) is a benign mesenchymal neoplasm originally described in pleura with a rare presentation in the oral cavity. Herein, we report a case of a 28-year-old male patient who presented an asymptomatic slow-growing mass in the anterior part of the tongue. Intraoral examination revealed a well-circumscribed mass covered by normal mucosa with a fibrous consistency. Due to non-specific clinical findings, the initial diagnostic hypotheses include benign submucosal neoplasms such as leiomyoma, neurofibroma, SFT, and others. An excisional biopsy was performed. Microscopically, the tumor was surrounded by a thick fibrous capsule; hypo and hypercellular areas were arranged in a storiform pattern with a stroma formed by collagen and abundant vascularization. Tumor cells showed immunopositivity for CD34 and STAT-6 and no expression of CD99, AML, S-100, and Ki-67. According to these findings, the diagnosis of SFT was established. After 24 months, the patient is asymptomatic and has no evidence of recurrence. Although oral involvement is rare, SFT should be included in the differential diagnosis of oral submucosal lesions. Hospital Universitário da Universidade de São Paulo 2022-11-17 /pmc/articles/PMC9675090/ /pubmed/36426115 http://dx.doi.org/10.4322/acr.2021.405 Text en Copyright © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Case Report Siqueira, Juliana Mota Heguedusch, Daniele Aguiar, Emília Maria Gomes dos Santos, Anaeliza Figueiredo Alves, Fabio Abreu Nunes, Fabio Daumas Solitary fibrous tumor of the tongue |
title | Solitary fibrous tumor of the tongue |
title_full | Solitary fibrous tumor of the tongue |
title_fullStr | Solitary fibrous tumor of the tongue |
title_full_unstemmed | Solitary fibrous tumor of the tongue |
title_short | Solitary fibrous tumor of the tongue |
title_sort | solitary fibrous tumor of the tongue |
topic | Clinical Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675090/ https://www.ncbi.nlm.nih.gov/pubmed/36426115 http://dx.doi.org/10.4322/acr.2021.405 |
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