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Trabeculae type of juvenile aggressive ossifying fibroma of the maxilla: Report of two cases
Juvenile ossifying fibroma (JOF) is a rare controversial fibroosseous lesion affecting the craniofacial skeleton and occurring commonly in children and young adults. It is highly aggressive and has a high tendency to recur. It is distinguished from the adult variant of ossifying fibroma on the basis...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354804/ https://www.ncbi.nlm.nih.gov/pubmed/22629066 http://dx.doi.org/10.4103/0976-237X.95104 |
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author | Rai, Shalu Kaur, Mandeep Goel, Sumit Prabhat, Mukul |
author_facet | Rai, Shalu Kaur, Mandeep Goel, Sumit Prabhat, Mukul |
author_sort | Rai, Shalu |
collection | PubMed |
description | Juvenile ossifying fibroma (JOF) is a rare controversial fibroosseous lesion affecting the craniofacial skeleton and occurring commonly in children and young adults. It is highly aggressive and has a high tendency to recur. It is distinguished from the adult variant of ossifying fibroma on the basis of age, site, clinical behavior and microscopic appearance. Because of its high recurrence rate, which is 30–58%, complete excision is essential. Early diagnosis will circumvent the necessity of radical treatment. We report a rare case of trabecular JOF of maxilla where a computed tomography scan was taken to further support the characteristic feature of the lesion. |
format | Online Article Text |
id | pubmed-3354804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33548042012-05-24 Trabeculae type of juvenile aggressive ossifying fibroma of the maxilla: Report of two cases Rai, Shalu Kaur, Mandeep Goel, Sumit Prabhat, Mukul Contemp Clin Dent Case Report Juvenile ossifying fibroma (JOF) is a rare controversial fibroosseous lesion affecting the craniofacial skeleton and occurring commonly in children and young adults. It is highly aggressive and has a high tendency to recur. It is distinguished from the adult variant of ossifying fibroma on the basis of age, site, clinical behavior and microscopic appearance. Because of its high recurrence rate, which is 30–58%, complete excision is essential. Early diagnosis will circumvent the necessity of radical treatment. We report a rare case of trabecular JOF of maxilla where a computed tomography scan was taken to further support the characteristic feature of the lesion. Medknow Publications & Media Pvt Ltd 2012-04 /pmc/articles/PMC3354804/ /pubmed/22629066 http://dx.doi.org/10.4103/0976-237X.95104 Text en Copyright: © Contemporary Clinical Dentistry 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 Rai, Shalu Kaur, Mandeep Goel, Sumit Prabhat, Mukul Trabeculae type of juvenile aggressive ossifying fibroma of the maxilla: Report of two cases |
title | Trabeculae type of juvenile aggressive ossifying fibroma of the maxilla: Report of two cases |
title_full | Trabeculae type of juvenile aggressive ossifying fibroma of the maxilla: Report of two cases |
title_fullStr | Trabeculae type of juvenile aggressive ossifying fibroma of the maxilla: Report of two cases |
title_full_unstemmed | Trabeculae type of juvenile aggressive ossifying fibroma of the maxilla: Report of two cases |
title_short | Trabeculae type of juvenile aggressive ossifying fibroma of the maxilla: Report of two cases |
title_sort | trabeculae type of juvenile aggressive ossifying fibroma of the maxilla: report of two cases |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354804/ https://www.ncbi.nlm.nih.gov/pubmed/22629066 http://dx.doi.org/10.4103/0976-237X.95104 |
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