Juvenile Ossifying Fibroma in a 14-year-old female: A Case Report
DOI:
https://doi.org/10.48036/apims.v15i2.192Keywords:
rare, juvenile ossifying fibromaAbstract
Juvenile Ossifying Fibroma is a rare benign bone neoplasm affecting age-group of 5-15 which tends to mimic malignant lesions. This is in opposition to its conventional variant which occurs mostly in middle aged cohort and is relatively docile. It's aetiology remains unknown and it is characterized by substitution of normal bone by mineralized fibrous tissue. The rapid progression, aggressive nature and high recurrence potential are features that makes JOF of vying attention. Additionally it's prognosis being greatly dependent on time and type of intervention employed is widely documented. In this study JOF with a history of only 7 months is reported in a 14 year old female. The affected bone was maxilla with dental and palatal involvement. Partial Maxillectomy and BIPP for reconstruction were applied as treatment of choice for this patient. Yearly follow up protocol for next 5 years was devised. No post op complications were observed.
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This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.