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Ameloblastic fibroma: report of two cases
The British Journal of Oral Surgery
|July 1, 1978
Summary
Ameloblastic fibroma, a rare jaw tumor, occurred in two children, impacting tooth eruption in the maxilla. Surgical removal was performed, but one case experienced a recurrence, highlighting the need for vigilant follow-up.
Area of Science:
- Oral and Maxillofacial Pathology
- Pediatric Dentistry
- Neoplastic Disease
Background:
- Ameloblastic fibroma is a rare odontogenic tumor.
- It typically occurs in the posterior jaws.
- Association with unerupted teeth is common.
Observation:
- Two pediatric cases of ameloblastic fibroma are presented.
- Tumors were located in the posterior maxilla.
- Both cases presented with impacted primary or permanent molars.
Findings:
- Local excision was the surgical approach for both patients.
- One patient experienced a recurrence of the ameloblastic fibroma ten months post-surgery.
- Histopathological analysis confirmed ameloblastic fibroma in both instances.
Implications:
- Early diagnosis and complete surgical excision are crucial for ameloblastic fibroma.
- Recurrence potential necessitates long-term monitoring.
- Understanding the clinical presentation aids in managing pediatric jaw tumors.