Evidence map›Paper›PMID 40416102›Full record

ArticleCureus2025

Anterior Maxillary Ameloblastic Fibroma in a Pediatric Patient: A Case Report.

Selma Daoudi, Elmehdi Hariri, Hind Ramdi

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Selma DaoudiPediatric Dentistry, Mohammed V University in Rabat, Rabat, MAR.
Elmehdi HaririDentistry, Mohammed V University in Rabat, Rabat, MAR.
Hind RamdiPediatric Dentistry, Mohammed V University in Rabat, Rabat, MAR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ameloblastic fibroma (AF) is a rare benign mixed odontogenic tumor, more frequently observed in children and adolescents. It typically develops in the posterior region of the mandible. Radiographically, it appears as a well-defined radiolucent lesion, requiring histological confirmation to differentiate it from other odontogenic tumors. We report the case of an eight-year-old male patient in good general health who presented following an anterior trauma. The extraoral examination was normal, while the intraoral examination revealed the avulsion of tooth 11, a complicated enamel-dentin fracture of tooth 21, and a firm palatal swelling. Radiographic evaluation showed a unilocular radiolucent lesion containing radiopaque structures, initially suggesting a diagnosis of compound odontoma. Complete enucleation of the lesion revealed calcified components and soft tissue. Histopathological analysis confirmed the diagnosis of AF. A conservative enucleation was performed due to the well-defined margins of the lesion, along with apexification of the adjacent permanent tooth 21. A six-month postoperative follow-up showed satisfactory bone healing with no signs of recurrence. Given that this fibroma presents a potential for recurrence and malignant transformation, rigorous long-term follow-up is essential. This case highlights the importance of thorough clinical, radiographic, and histological evaluation of jaw lesions in pediatric patients, as well as the necessity of long-term follow-up to ensure early detection of any complications.

Indexed as

ameloblastic fibromaanterior maxillaryincidental findingoral tumorpediatric patient

Identifiers

PMID40416102
PMCPMC12103704

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.