ArticleJournal of oral and maxillofacial pathology : JOMFP
A rare case of mandibular dentinogenic ghost cell tumor: Histopathological, clinical and surgical management.
Article in Journal of oral and maxillofacial pathology : JOMFP. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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Who cites it
5 citing papers in PubMed, 7 citations in OpenAlex.
- Ameloblastic Carcinoma: A 40-Year Scoping Review of the Literature.Current issues in molecular biology · 2025Review
- Dentinogenic Ghost Cell Tumor in an Elderly Female: A Rare Case Report.Case reports in dentistry · 2025Article
- Central dentinogenic ghost cell tumor of the maxilla: a case report with new imaging findings and review of the literature.Oral radiology · 2024Review
- Unravelling the mystery of the central dentinogenic ghost cell tumor- a rare case report and recurrent insights.Autopsy & case reports · 2024Article
- A massive dentinogenic ghost cell tumor that crossed the midline: A rare case report.Journal of oral and maxillofacial pathology : JOMFPArticle
Corrections and comments
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Dentinogenic ghost cell tumor (DGCT) is a rare benign tumorous form of calcifying odontogenic cyst (COC) characterized by the presence of ghost cells but it seems to have more aggressive behavior. It represents 11.5% of COCs. In this work, we report a case of a 60-year-old male patient with DGCT in the posterior region of the right mandible treated with surgical enucleation.
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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.