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Juvenile Aggressive Ossifying Fibroma of the Maxilla: A Case Report and Review of the Literature
Juvenile aggressive ossifying fibroma is a rare benign but locally aggressive tumor with high recurrent potentials. Juvenile aggressive ossifying fibroma poses diagnostic challenges because of its rapidly growing nature. A 7-years-old female child presented to the pediatric unit of our institution w...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728882/ https://www.ncbi.nlm.nih.gov/pubmed/23919209 http://dx.doi.org/10.4103/2141-9248.113685 |
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author | Osunde, OD Iyogun, CA Adebola, RA |
author_facet | Osunde, OD Iyogun, CA Adebola, RA |
author_sort | Osunde, OD |
collection | PubMed |
description | Juvenile aggressive ossifying fibroma is a rare benign but locally aggressive tumor with high recurrent potentials. Juvenile aggressive ossifying fibroma poses diagnostic challenges because of its rapidly growing nature. A 7-years-old female child presented to the pediatric unit of our institution with a 9-month history of right maxillary tumor. An initial diagnosis of Burkitt's lymphoma was made and the child has several courses of chemotherapy without adequate histologic confirmation., She was later referred to the maxillofacial unit where the appropriate diagnosis and treatment were instituted. The importance of early recognition and adequate management is highlighted. |
format | Online Article Text |
id | pubmed-3728882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37288822013-08-05 Juvenile Aggressive Ossifying Fibroma of the Maxilla: A Case Report and Review of the Literature Osunde, OD Iyogun, CA Adebola, RA Ann Med Health Sci Res Case Report Juvenile aggressive ossifying fibroma is a rare benign but locally aggressive tumor with high recurrent potentials. Juvenile aggressive ossifying fibroma poses diagnostic challenges because of its rapidly growing nature. A 7-years-old female child presented to the pediatric unit of our institution with a 9-month history of right maxillary tumor. An initial diagnosis of Burkitt's lymphoma was made and the child has several courses of chemotherapy without adequate histologic confirmation., She was later referred to the maxillofacial unit where the appropriate diagnosis and treatment were instituted. The importance of early recognition and adequate management is highlighted. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3728882/ /pubmed/23919209 http://dx.doi.org/10.4103/2141-9248.113685 Text en Copyright: © Annals of Medical and Health Sciences Research 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 Osunde, OD Iyogun, CA Adebola, RA Juvenile Aggressive Ossifying Fibroma of the Maxilla: A Case Report and Review of the Literature |
title | Juvenile Aggressive Ossifying Fibroma of the Maxilla: A Case Report and Review of the Literature |
title_full | Juvenile Aggressive Ossifying Fibroma of the Maxilla: A Case Report and Review of the Literature |
title_fullStr | Juvenile Aggressive Ossifying Fibroma of the Maxilla: A Case Report and Review of the Literature |
title_full_unstemmed | Juvenile Aggressive Ossifying Fibroma of the Maxilla: A Case Report and Review of the Literature |
title_short | Juvenile Aggressive Ossifying Fibroma of the Maxilla: A Case Report and Review of the Literature |
title_sort | juvenile aggressive ossifying fibroma of the maxilla: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728882/ https://www.ncbi.nlm.nih.gov/pubmed/23919209 http://dx.doi.org/10.4103/2141-9248.113685 |
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