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Solitary Intra-Osseous Myofibroma of the Jaw: A Case Report and Review of Literature

Myofibroma is a rare benign spindle cell neoplasm in children that usually affects both soft tissue and bone in the head and neck region. Approximately one third of these cases are seen within jaw bones as solitary lesions. Solitary intra-osseous myofibroma of the jaw bone shares its clinical, radio...

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Autores principales: Dhupar, Anita, Carvalho, Karla, Sawant, Poonam, Spadigam, Anita, Syed, Shaheen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664021/
https://www.ncbi.nlm.nih.gov/pubmed/29064415
http://dx.doi.org/10.3390/children4100091
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author Dhupar, Anita
Carvalho, Karla
Sawant, Poonam
Spadigam, Anita
Syed, Shaheen
author_facet Dhupar, Anita
Carvalho, Karla
Sawant, Poonam
Spadigam, Anita
Syed, Shaheen
author_sort Dhupar, Anita
collection PubMed
description Myofibroma is a rare benign spindle cell neoplasm in children that usually affects both soft tissue and bone in the head and neck region. Approximately one third of these cases are seen within jaw bones as solitary lesions. Solitary intra-osseous myofibroma of the jaw bone shares its clinical, radiographic and histological features with other spindle cell tumors. The rarity of this lesion can make diagnosis difficult for clinicians and pathologists. We report a case of a solitary intra-osseous myofibroma in the mandible of a nine-year-old child.
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spelling pubmed-56640212017-11-06 Solitary Intra-Osseous Myofibroma of the Jaw: A Case Report and Review of Literature Dhupar, Anita Carvalho, Karla Sawant, Poonam Spadigam, Anita Syed, Shaheen Children (Basel) Case Report Myofibroma is a rare benign spindle cell neoplasm in children that usually affects both soft tissue and bone in the head and neck region. Approximately one third of these cases are seen within jaw bones as solitary lesions. Solitary intra-osseous myofibroma of the jaw bone shares its clinical, radiographic and histological features with other spindle cell tumors. The rarity of this lesion can make diagnosis difficult for clinicians and pathologists. We report a case of a solitary intra-osseous myofibroma in the mandible of a nine-year-old child. MDPI 2017-10-24 /pmc/articles/PMC5664021/ /pubmed/29064415 http://dx.doi.org/10.3390/children4100091 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Dhupar, Anita
Carvalho, Karla
Sawant, Poonam
Spadigam, Anita
Syed, Shaheen
Solitary Intra-Osseous Myofibroma of the Jaw: A Case Report and Review of Literature
title Solitary Intra-Osseous Myofibroma of the Jaw: A Case Report and Review of Literature
title_full Solitary Intra-Osseous Myofibroma of the Jaw: A Case Report and Review of Literature
title_fullStr Solitary Intra-Osseous Myofibroma of the Jaw: A Case Report and Review of Literature
title_full_unstemmed Solitary Intra-Osseous Myofibroma of the Jaw: A Case Report and Review of Literature
title_short Solitary Intra-Osseous Myofibroma of the Jaw: A Case Report and Review of Literature
title_sort solitary intra-osseous myofibroma of the jaw: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664021/
https://www.ncbi.nlm.nih.gov/pubmed/29064415
http://dx.doi.org/10.3390/children4100091
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