Evidence map›Paper›PMID 39462411›Full record

ArticleBMC oral health2024

Central odontogenic fibroma: retrospective study of six cases with variable histopathologic features using 2022 WHO classification.

Sopee Poomsawat, Sirada Choakdeewanitthumrong, Jira Kitisubkanchana, Theerachai Kosanwat

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Article in BMC oral health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sopee PoomsawatDepartment of Oral and Maxillofacial Pathology, Faculty of Dentistry, Mahidol University, Yothi Street, Bangkok, 10400, Thailand. spoomsawat@gmail.com.ORCID http://orcid.org/0000-0002-1709-5953
Sirada ChoakdeewanitthumrongDepartment of Oral and Maxillofacial Pathology, Faculty of Dentistry, Mahidol University, Yothi Street, Bangkok, 10400, Thailand.ORCID http://orcid.org/0009-0008-3110-7966
Jira KitisubkanchanaDepartment of Oral and Maxillofacial Radiology, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.ORCID http://orcid.org/0000-0003-0020-863X
Theerachai KosanwatDepartment of Oral and Maxillofacial Pathology, Faculty of Dentistry, Mahidol University, Yothi Street, Bangkok, 10400, Thailand.ORCID http://orcid.org/0000-0001-7487-2483

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCentral odontogenic fibroma (COF) is a rare benign odontogenic tumor with a wide range of histopathologic features. We evaluated COF diagnosed in our institute with 16 years' experience using 2022 WHO classification.

methodsOur archives were reviewed and cases diagnosed as COF were selected. Clinical, radiographic and microscopic features were tabulated and analyzed.

resultsOf 13,736 specimens, six cases (0.04%) of COF were discovered. Patients ranged in age from 14 to 44 years. There were two males and four females. Maxilla and mandible were affected equally. Five cases showed radiolucent appearance (4 unilocular, 1 multilocular) and one case showed a mixed radiolucent-radiopaque pattern. Histopathologically, three cases were conventional type (2 epithelium-rich, 1 epithelium-poor). Two cases were the hybrid COF with central giant cell granuloma (CGCG) and one of which was also associated with secondary aneurysmal bone cyst (ABC). The last case with a mixed radiolucent-radiopaque pattern was the ossifying subtype.

conclusionOur results demonstrated that COF is a rare odontogenic tumor and exhibits diverse radiographic and microscopic appearances. The triphasic tumor consisting of the COF, CGCG and ABC, is reported here for the first time, while the ossifying subtype is considered the tenth case reported in the English-language literature. Oral and maxillofacial pathologists and other healthcare personnel must be aware of this rare odontogenic tumor and its variants to achieve the definite diagnosis. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Odontogenic TumorsAdolescentAdultFemaleFibromaHumansMaleRetrospective StudiesWorld Health OrganizationYoung AdultAneurysmal bone cystCentral giant cell granulomaCentral odontogenic fibromaHybrid odontogenic lesionsOssifying subtype

Identifiers

PMID39462411
PMCPMC11514888

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