Psammomatoid Juvenile Ossifying Fibroma: Report of Three Cases with a Review of Literature

Psammomatoid juvenile ossifying fibroma (PJOF), a variant of juvenile ossifying fibroma (JOF), is a locally aggressive neoplasm of the children and young adults. This entity has predilection for the sinonasal region. It forms a differential diagnosis for many bone neoplasms. We report three cases of...

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Autores principales: Rao, Shilpa, Nandeesh, Bevinahalli N., Arivazhagan, Arimappamagan, Moiyadi, Aliasgar V., Yasha, T. Chickabasaviah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890560/
https://www.ncbi.nlm.nih.gov/pubmed/29675079
http://dx.doi.org/10.4103/jpn.JPN_78_17
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author Rao, Shilpa
Nandeesh, Bevinahalli N.
Arivazhagan, Arimappamagan
Moiyadi, Aliasgar V.
Yasha, T. Chickabasaviah
author_facet Rao, Shilpa
Nandeesh, Bevinahalli N.
Arivazhagan, Arimappamagan
Moiyadi, Aliasgar V.
Yasha, T. Chickabasaviah
author_sort Rao, Shilpa
collection PubMed
description Psammomatoid juvenile ossifying fibroma (PJOF), a variant of juvenile ossifying fibroma (JOF), is a locally aggressive neoplasm of the children and young adults. This entity has predilection for the sinonasal region. It forms a differential diagnosis for many bone neoplasms. We report three cases of PJOF, in young patients whose biopsy showed the presence of psammomatoid bodies in a cellular fibrous stroma. The diagnosis of JOF indicates requirement of extensive surgery due to its locally aggressive nature.
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spelling pubmed-58905602018-04-19 Psammomatoid Juvenile Ossifying Fibroma: Report of Three Cases with a Review of Literature Rao, Shilpa Nandeesh, Bevinahalli N. Arivazhagan, Arimappamagan Moiyadi, Aliasgar V. Yasha, T. Chickabasaviah J Pediatr Neurosci Case Report Psammomatoid juvenile ossifying fibroma (PJOF), a variant of juvenile ossifying fibroma (JOF), is a locally aggressive neoplasm of the children and young adults. This entity has predilection for the sinonasal region. It forms a differential diagnosis for many bone neoplasms. We report three cases of PJOF, in young patients whose biopsy showed the presence of psammomatoid bodies in a cellular fibrous stroma. The diagnosis of JOF indicates requirement of extensive surgery due to its locally aggressive nature. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5890560/ /pubmed/29675079 http://dx.doi.org/10.4103/jpn.JPN_78_17 Text en Copyright: © 2018 Journal of Pediatric Neurosciences 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Rao, Shilpa
Nandeesh, Bevinahalli N.
Arivazhagan, Arimappamagan
Moiyadi, Aliasgar V.
Yasha, T. Chickabasaviah
Psammomatoid Juvenile Ossifying Fibroma: Report of Three Cases with a Review of Literature
title Psammomatoid Juvenile Ossifying Fibroma: Report of Three Cases with a Review of Literature
title_full Psammomatoid Juvenile Ossifying Fibroma: Report of Three Cases with a Review of Literature
title_fullStr Psammomatoid Juvenile Ossifying Fibroma: Report of Three Cases with a Review of Literature
title_full_unstemmed Psammomatoid Juvenile Ossifying Fibroma: Report of Three Cases with a Review of Literature
title_short Psammomatoid Juvenile Ossifying Fibroma: Report of Three Cases with a Review of Literature
title_sort psammomatoid juvenile ossifying fibroma: report of three cases with a review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890560/
https://www.ncbi.nlm.nih.gov/pubmed/29675079
http://dx.doi.org/10.4103/jpn.JPN_78_17
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