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Oral Bilateral Collagenous Fibroma: A previously unreported case and literature review
Collagenous fibroma, also known as desmoplastic fibroblastoma, is a rare benign slow growing tumor particularly uncommon in the oral cavity. The aim of this study was to analyze the clinical and histopathological features of an oral collagenous fibroma as well as to compare this data with those repo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medicina Oral S.L.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899808/ https://www.ncbi.nlm.nih.gov/pubmed/29670724 http://dx.doi.org/10.4317/jced.54123 |
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author | Vasconcelos, Ana-Carolina Gomes, Ana-Paula Tarquinio, Sandra Abduch-Rodrigues, Eduardo Mesquita, Ricardo Silva, Karine |
author_facet | Vasconcelos, Ana-Carolina Gomes, Ana-Paula Tarquinio, Sandra Abduch-Rodrigues, Eduardo Mesquita, Ricardo Silva, Karine |
author_sort | Vasconcelos, Ana-Carolina |
collection | PubMed |
description | Collagenous fibroma, also known as desmoplastic fibroblastoma, is a rare benign slow growing tumor particularly uncommon in the oral cavity. The aim of this study was to analyze the clinical and histopathological features of an oral collagenous fibroma as well as to compare this data with those reported in an English-literature review. The thirteenth case of collagenous fibroma in the oral cavity and the first to present clinically as a bilateral mass was described. A 48-years-old female patient was referred to a School of Dentistry, complaining about an asymptomatic swelling on the hard palate, lasting around ten years. The intraoral examination revealed two well-defined mass, bilaterally in the hard palate. An excisional biopsy was performed. Microscopically, the connective tissue consisted of dense collagen bundles in which were seen scarcely distributed spindle-shaped to stellate fibroblastic cells. Blood vessels were few, as well as inflammatory cells. Immunohistochemical staining was positive for vimentin, α-smooth muscle actin and factor XIIIa and negative for S-100, CD68, CD34, HHF35, desmin and AE1/AE3. The patient remains disease-free 24 months after excision. In conclusion, oral collagenous fibroma should be included in the differential diagnosis of bilateral sessile nodules in the oral cavity. Key words:Connective tissue, mouth diseases, mouth neoplasms, oral diagnosis, oral pathology. |
format | Online Article Text |
id | pubmed-5899808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medicina Oral S.L. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58998082018-04-18 Oral Bilateral Collagenous Fibroma: A previously unreported case and literature review Vasconcelos, Ana-Carolina Gomes, Ana-Paula Tarquinio, Sandra Abduch-Rodrigues, Eduardo Mesquita, Ricardo Silva, Karine J Clin Exp Dent Case Report Collagenous fibroma, also known as desmoplastic fibroblastoma, is a rare benign slow growing tumor particularly uncommon in the oral cavity. The aim of this study was to analyze the clinical and histopathological features of an oral collagenous fibroma as well as to compare this data with those reported in an English-literature review. The thirteenth case of collagenous fibroma in the oral cavity and the first to present clinically as a bilateral mass was described. A 48-years-old female patient was referred to a School of Dentistry, complaining about an asymptomatic swelling on the hard palate, lasting around ten years. The intraoral examination revealed two well-defined mass, bilaterally in the hard palate. An excisional biopsy was performed. Microscopically, the connective tissue consisted of dense collagen bundles in which were seen scarcely distributed spindle-shaped to stellate fibroblastic cells. Blood vessels were few, as well as inflammatory cells. Immunohistochemical staining was positive for vimentin, α-smooth muscle actin and factor XIIIa and negative for S-100, CD68, CD34, HHF35, desmin and AE1/AE3. The patient remains disease-free 24 months after excision. In conclusion, oral collagenous fibroma should be included in the differential diagnosis of bilateral sessile nodules in the oral cavity. Key words:Connective tissue, mouth diseases, mouth neoplasms, oral diagnosis, oral pathology. Medicina Oral S.L. 2018-01-01 /pmc/articles/PMC5899808/ /pubmed/29670724 http://dx.doi.org/10.4317/jced.54123 Text en Copyright: © 2018 Medicina Oral S.L. http://creativecommons.org/licenses/by/2.5/ 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 | Case Report Vasconcelos, Ana-Carolina Gomes, Ana-Paula Tarquinio, Sandra Abduch-Rodrigues, Eduardo Mesquita, Ricardo Silva, Karine Oral Bilateral Collagenous Fibroma: A previously unreported case and literature review |
title | Oral Bilateral Collagenous Fibroma: A previously
unreported case and literature review |
title_full | Oral Bilateral Collagenous Fibroma: A previously
unreported case and literature review |
title_fullStr | Oral Bilateral Collagenous Fibroma: A previously
unreported case and literature review |
title_full_unstemmed | Oral Bilateral Collagenous Fibroma: A previously
unreported case and literature review |
title_short | Oral Bilateral Collagenous Fibroma: A previously
unreported case and literature review |
title_sort | oral bilateral collagenous fibroma: a previously
unreported case and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899808/ https://www.ncbi.nlm.nih.gov/pubmed/29670724 http://dx.doi.org/10.4317/jced.54123 |
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