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Juvenile aggressive ossifying fibroma

Ossifying fibroma, also the cement ossifying fibroma radiographically, represents a well-demarcated mixed radiolucency/radio-opacity with smooth and often sclerotic borders. These lesions are usually solitary and most commonly seen in the mandible; cases in the maxilla have also reported. Histologic...

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Autores principales: Chandra, H. Jagadish, Krishna, Vinay, Tahir, Mohammed, Harishankar, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651245/
https://www.ncbi.nlm.nih.gov/pubmed/36393953
http://dx.doi.org/10.4103/njms.NJMS_70_18
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author Chandra, H. Jagadish
Krishna, Vinay
Tahir, Mohammed
Harishankar, S.
author_facet Chandra, H. Jagadish
Krishna, Vinay
Tahir, Mohammed
Harishankar, S.
author_sort Chandra, H. Jagadish
collection PubMed
description Ossifying fibroma, also the cement ossifying fibroma radiographically, represents a well-demarcated mixed radiolucency/radio-opacity with smooth and often sclerotic borders. These lesions are usually solitary and most commonly seen in the mandible; cases in the maxilla have also reported. Histologically, they contain a relatively avascular cellular fibrous stroma with reticular bone trabeculae and cementum-like spherules. We present a case report of an 11-year-old boy with a 2-month history of an asymptomatic swelling seen on the left side of the angle of the mandible. An initial diagnosis of ossifying fibroma was made by an incisional biopsy, and considering the age as a factor surgical resection of the tumor was done under general anesthesia following closure by a two-layer suturing under proper antibiotic and analgesic coverage. The patient has been on regular follow-ups with no adverse effects and satisfactory healing.
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spelling pubmed-96512452022-11-15 Juvenile aggressive ossifying fibroma Chandra, H. Jagadish Krishna, Vinay Tahir, Mohammed Harishankar, S. Natl J Maxillofac Surg Case Report Ossifying fibroma, also the cement ossifying fibroma radiographically, represents a well-demarcated mixed radiolucency/radio-opacity with smooth and often sclerotic borders. These lesions are usually solitary and most commonly seen in the mandible; cases in the maxilla have also reported. Histologically, they contain a relatively avascular cellular fibrous stroma with reticular bone trabeculae and cementum-like spherules. We present a case report of an 11-year-old boy with a 2-month history of an asymptomatic swelling seen on the left side of the angle of the mandible. An initial diagnosis of ossifying fibroma was made by an incisional biopsy, and considering the age as a factor surgical resection of the tumor was done under general anesthesia following closure by a two-layer suturing under proper antibiotic and analgesic coverage. The patient has been on regular follow-ups with no adverse effects and satisfactory healing. Wolters Kluwer - Medknow 2022-08 2022-08-20 /pmc/articles/PMC9651245/ /pubmed/36393953 http://dx.doi.org/10.4103/njms.NJMS_70_18 Text en Copyright: © 2022 National Journal of Maxillofacial Surgery https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Chandra, H. Jagadish
Krishna, Vinay
Tahir, Mohammed
Harishankar, S.
Juvenile aggressive ossifying fibroma
title Juvenile aggressive ossifying fibroma
title_full Juvenile aggressive ossifying fibroma
title_fullStr Juvenile aggressive ossifying fibroma
title_full_unstemmed Juvenile aggressive ossifying fibroma
title_short Juvenile aggressive ossifying fibroma
title_sort juvenile aggressive ossifying fibroma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651245/
https://www.ncbi.nlm.nih.gov/pubmed/36393953
http://dx.doi.org/10.4103/njms.NJMS_70_18
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