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Ameloblastic fibroma: A case report
Abdullah Nasir1, Abhisheik Khare1, Iqbal Ali2
1Department of Oral and Maxillofacial Pathology and Oral Microbiology, Career Post Graduate Institute of Dental Sciences and Hospital, Ghaila, Lucknow, Uttar Pradesh, India.
Ameloblastic fibroma is a rare benign jaw tumor. This case highlights its diagnosis and management in a 34-year-old male patient, emphasizing its potential for recurrence.
Area of Science:
- Oral and Maxillofacial Surgery
- Oncology
- Pathology
Background:
- Ameloblastic fibroma is a rare mixed odontogenic tumor, predominantly affecting the posterior mandible in young males.
- It is characterized by neoplastic epithelial and mesenchymal tissues resembling dental papilla and enamel organ, but without hard tissue formation.
Observation:
- A 34-year-old male presented with mandibular pain and swelling, exhibiting facial asymmetry.
- Clinical and imaging findings suggested an odontogenic cyst or recurrent ameloblastoma.
- The lesion was surgically enucleated under general anesthesia.
Findings:
- Histopathological examination confirmed the diagnosis of Ameloblastic fibroma.
- This rare odontogenic tumor comprises epithelial and ectomesenchymal components.
Implications:
- Ameloblastic fibroma has an 18% recurrence rate and a 45% potential for malignant transformation into ameloblastic fibrosarcoma.
- Accurate diagnosis and complete surgical excision are crucial for managing this benign jaw neoplasm.
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