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Unicystic ameloblastoma in an infant: a management dilemma
Ariel Israel Hirschhorn1, Marilena Vered, Amos Buchner
1Department of Oral and Maxillofacial Surgery (Head: Prof. Dr. Shlomo Taicher), The Chaim Sheba Medical Center, Tel Hashomer, Israel.
Insights
Conservative management of a rare unicystic ameloblastoma in an infant avoided surgery, prioritizing mandibular growth and tooth development. Ongoing monitoring shows no recurrence in this youngest reported patient.
Area of Science:
- Oral and Maxillofacial Surgery
- Pediatric Dentistry
- Oncology
Background:
- Unicystic ameloblastoma is a rare odontogenic tumor, with the mural subtype presenting unique management challenges, especially in pediatric patients.
- Early surgical intervention in infants can impede critical mandibular growth and dental development.
Observation:
- A 10-month-old female presented with a rare unicystic ameloblastoma (mural subtype), the youngest documented case.
- Conservative management was chosen over immediate aggressive surgery to preserve facial and dental development.
Findings:
- The patient was managed conservatively with close monitoring and a plan for delayed surgical intervention if recurrence occurred.
- At 3.5 years old, the patient shows no evidence of tumor recurrence, indicating successful conservative management.
Implications:
- Conservative, non-surgical management may be a viable option for unicystic ameloblastoma in very young children.
- Prioritizing growth and development through watchful waiting can lead to favorable outcomes, reducing the need for extensive surgical procedures in infants.
Abstract:
The authors describe the conservative management of a rare case of unicystic ameloblastoma (mural subtype) in a 10-month-old girl, the youngest patient reported thus far in the literature. Rather than subject the infant to further surgery, it was decided to monitor her closely and perform an additional operation in the event of recurrence, thus enabling uninterrupted mandibular growth and tooth development. The patient is now 3.5 years old and periodic follow-up is ongoing, with no evidence of recurrence.
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