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 report, the patient is a young man, aged misbhv tank top 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 u11-200ps 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 rapid growth.In its clinical and histological presentation, its trabecular form may mimic an osteosarcoma.