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Juvenile ossifying fibroma: Psammamatoid variant
Shivani Aggarwal1, Ashish Garg, Ashim Aggarwal
1Department of Oral and Maxillofacial Pathology, Manav Rachna Dental College, Faridabad, Haryana, India.
Juvenile ossifying fibroma is a rare, aggressive tumor. This case report details a 28-year-old female patient
Area of Science:
- Oral pathology
- Surgical oncology
Background:
- Juvenile ossifying fibroma (JO F) is a rare, aggressive fibro-osseous lesion.
- It exhibits bone or cementum-like calcified masses within a cellular stroma.
- JO F can invade adjacent structures and has a high recurrence rate.
Observation:
- A 28-year-old female presented with a growth in the upper left vestibule.
- The lesion extended from the canine to the molar region.
- Clinical, histopathological, and radiological features were evaluated.
Findings:
- The observed lesion presented characteristics consistent with juvenile ossifying fibroma.
- Surgical intervention was performed for management.
- Regular follow-up was recommended post-surgery.
Implications:
- This case highlights the aggressive nature and management of juvenile ossifying fibroma.
- Early diagnosis and surgical treatment are crucial for effective management.
- Understanding JO F behavior aids in optimizing patient care and prognosis.
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