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Juvenile psammomatoid ossifying fibroma of the posterior fossa: a case report and review

BACKGROUND: Ossifying fibroma is a rare benign bone tumor that occurs mostly in the jaw, but also affects paranasal sinuses and fronto-ethmoidal complex. Occipital bone is an extremely rare location for these tumors; only two cases have been reported. METHODS: We present the first case reported as p...

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Autores principales: Cotúa Quintero, Carlos, Saab Mazzei, Anwar, Revuelta Barbero, Juan, Parajon Diaz, Avelino, Ley Urzaiz, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947081/
https://www.ncbi.nlm.nih.gov/pubmed/27468389
http://dx.doi.org/10.1186/s40064-016-2758-4
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author Cotúa Quintero, Carlos
Saab Mazzei, Anwar
Revuelta Barbero, Juan
Parajon Diaz, Avelino
Ley Urzaiz, Luis
author_facet Cotúa Quintero, Carlos
Saab Mazzei, Anwar
Revuelta Barbero, Juan
Parajon Diaz, Avelino
Ley Urzaiz, Luis
author_sort Cotúa Quintero, Carlos
collection PubMed
description BACKGROUND: Ossifying fibroma is a rare benign bone tumor that occurs mostly in the jaw, but also affects paranasal sinuses and fronto-ethmoidal complex. Occipital bone is an extremely rare location for these tumors; only two cases have been reported. METHODS: We present the first case reported as psammomatoid subtype of ossifying fibroma, according to the 2005 WHO classification. An 18 years old male patient with infratentorial tumor, in the occipital bone, that produces mass effect over the cerebellum. CONCLUSIONS: This case may provide a guide to consider these lesions for a more rapid and precise diagnostic in future cases.
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spelling pubmed-49470812016-07-27 Juvenile psammomatoid ossifying fibroma of the posterior fossa: a case report and review Cotúa Quintero, Carlos Saab Mazzei, Anwar Revuelta Barbero, Juan Parajon Diaz, Avelino Ley Urzaiz, Luis Springerplus Case Study BACKGROUND: Ossifying fibroma is a rare benign bone tumor that occurs mostly in the jaw, but also affects paranasal sinuses and fronto-ethmoidal complex. Occipital bone is an extremely rare location for these tumors; only two cases have been reported. METHODS: We present the first case reported as psammomatoid subtype of ossifying fibroma, according to the 2005 WHO classification. An 18 years old male patient with infratentorial tumor, in the occipital bone, that produces mass effect over the cerebellum. CONCLUSIONS: This case may provide a guide to consider these lesions for a more rapid and precise diagnostic in future cases. Springer International Publishing 2016-07-15 /pmc/articles/PMC4947081/ /pubmed/27468389 http://dx.doi.org/10.1186/s40064-016-2758-4 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Study
Cotúa Quintero, Carlos
Saab Mazzei, Anwar
Revuelta Barbero, Juan
Parajon Diaz, Avelino
Ley Urzaiz, Luis
Juvenile psammomatoid ossifying fibroma of the posterior fossa: a case report and review
title Juvenile psammomatoid ossifying fibroma of the posterior fossa: a case report and review
title_full Juvenile psammomatoid ossifying fibroma of the posterior fossa: a case report and review
title_fullStr Juvenile psammomatoid ossifying fibroma of the posterior fossa: a case report and review
title_full_unstemmed Juvenile psammomatoid ossifying fibroma of the posterior fossa: a case report and review
title_short Juvenile psammomatoid ossifying fibroma of the posterior fossa: a case report and review
title_sort juvenile psammomatoid ossifying fibroma of the posterior fossa: a case report and review
topic Case Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947081/
https://www.ncbi.nlm.nih.gov/pubmed/27468389
http://dx.doi.org/10.1186/s40064-016-2758-4
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