Juvenile ossifying fibroma: case report and literature review. Management and differential diagnosis

Juvenile ossifying fibroma: case report and literature review. Management and differential diagnosis

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Introduction: Juvenile ossifying fibroma (JOF) is a rare neoplasm characterized by the replacement of the normal bone matrix with osteo-fibrous tissue.It has the tendency to be locally aggressive despite its benign character and to have a strong tendency for recurrence.Observation: In this case 16th sustainment brigade patch report, the patient is a young man, aged 16, with rapidly advancing maxillary swelling.We describe the diagnostic procedure, the surgical procedure and the differential diagnosis to be eliminated.Discussion: The clinical presentation of JOF, and its rapid growth, can cause fear of other pathologies such as osteosarcoma.

The radiological characteristics should reassure the practitioner and a histological examination confirmed the diagnosis.Conclusion: JOF is a benign tumor.It should be operated on at an early stage because of its turquoise iphone 14 pro max case rapid growth.In its clinical and histological presentation, its trabecular form may mimic an osteosarcoma.