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A massive sinonasal psammomatoid variant of juvenile ossifying fibroma: Report of a rare entity

Juvenile ossifying fibroma (JOF) is an uncommon, benign, bone-forming neoplasm with an aggressive local growth that is distinguished from other fibro-osseous lesions primarily by its age of onset, clinical presentation and aggressive behaviour. JOF is considered as a variant of the ossifying fibroma...

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Autores principales: Guttikonda, VR, Taneeru, S, Gaddipati, R, Madala, J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830247/
https://www.ncbi.nlm.nih.gov/pubmed/24250099
http://dx.doi.org/10.4103/0973-029X.119751
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author Guttikonda, VR
Taneeru, S
Gaddipati, R
Madala, J
author_facet Guttikonda, VR
Taneeru, S
Gaddipati, R
Madala, J
author_sort Guttikonda, VR
collection PubMed
description Juvenile ossifying fibroma (JOF) is an uncommon, benign, bone-forming neoplasm with an aggressive local growth that is distinguished from other fibro-osseous lesions primarily by its age of onset, clinical presentation and aggressive behaviour. JOF is considered as a variant of the ossifying fibroma (OF) and the former includes psammomatoid JOF (PsJOF) and Trabecular JOF (TrJOF). Both variants involve the craniofacial bones with the trabecular variant being more common in the jaws and the psammomatoid variant being more common in the craniofacial skeleton. PsJOF is an unique variant of JOF that has a predilection for the sinonasal tract and the orbit particularly centered on the periorbital, frontal, and ethmoid bones. We report a rare case of massive PsJOF involving the maxillary sinus in a 20-year-old female.
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spelling pubmed-38302472013-11-18 A massive sinonasal psammomatoid variant of juvenile ossifying fibroma: Report of a rare entity Guttikonda, VR Taneeru, S Gaddipati, R Madala, J J Oral Maxillofac Pathol Case Report Juvenile ossifying fibroma (JOF) is an uncommon, benign, bone-forming neoplasm with an aggressive local growth that is distinguished from other fibro-osseous lesions primarily by its age of onset, clinical presentation and aggressive behaviour. JOF is considered as a variant of the ossifying fibroma (OF) and the former includes psammomatoid JOF (PsJOF) and Trabecular JOF (TrJOF). Both variants involve the craniofacial bones with the trabecular variant being more common in the jaws and the psammomatoid variant being more common in the craniofacial skeleton. PsJOF is an unique variant of JOF that has a predilection for the sinonasal tract and the orbit particularly centered on the periorbital, frontal, and ethmoid bones. We report a rare case of massive PsJOF involving the maxillary sinus in a 20-year-old female. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3830247/ /pubmed/24250099 http://dx.doi.org/10.4103/0973-029X.119751 Text en Copyright: © Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Guttikonda, VR
Taneeru, S
Gaddipati, R
Madala, J
A massive sinonasal psammomatoid variant of juvenile ossifying fibroma: Report of a rare entity
title A massive sinonasal psammomatoid variant of juvenile ossifying fibroma: Report of a rare entity
title_full A massive sinonasal psammomatoid variant of juvenile ossifying fibroma: Report of a rare entity
title_fullStr A massive sinonasal psammomatoid variant of juvenile ossifying fibroma: Report of a rare entity
title_full_unstemmed A massive sinonasal psammomatoid variant of juvenile ossifying fibroma: Report of a rare entity
title_short A massive sinonasal psammomatoid variant of juvenile ossifying fibroma: Report of a rare entity
title_sort massive sinonasal psammomatoid variant of juvenile ossifying fibroma: report of a rare entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830247/
https://www.ncbi.nlm.nih.gov/pubmed/24250099
http://dx.doi.org/10.4103/0973-029X.119751
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