ArticleClinical case reports2026
Maxillofacial Cemento-Ossifying Fibroma: A Rare Case Report.
Article in Clinical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cemento-ossifying fibroma is a relatively rare lesion affecting the jaws, especially the anterior mandible. The most common clinical presentation is swelling. Diagnosis based on clinical observation only is challenging. Radiological images and histological findings can be misleading due to similitudes with other osteo-fibrous lesions. We report a rare case of a 22-year-old female patient who presented with a painless mass in the upper right maxillary region that has been developing for 10 years. On examination, this tumor was bulky, ulcerated, disfiguring, hard to the touch, and occupying the whole of nasal, malar and maxillary regions. CT scan showed a well-circumscribed mass spanning from the right palatal and maxillary bones with mixed density content of soft tissue and diffuse calcified foci. The mass harbored dense bundles of fibrocollagenous connective tissue in a cellular stroma on histopathological examination. After a provisional diagnosis of osteoblastoma based on clinical and computed tomography features, the final diagnosis was based upon correlation of histopathological characteristics with both clinical and radiographic findings. A one-time surgical resection was performed to enucleate the tumor. This was followed by curettage. The lateral maxillary location of this tumor makes it unusual. Henceforth, a proper conclusive diagnosis of cemento-ossifying fibroma should be obtained from a histopathological study, in conjunction with clinical and radiological findings, and particular traits that the patient may present.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.