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Dentinogenic ghost cell tumor.
Sweety Sagarmal Bafna1, Tabita Joy1, Jagdish Vishnu Tupkari1
1Department of Oral Pathology and Microbiology, Government Dental College and Hospital, Mumbai, Maharashtra, India.
Journal of Oral and Maxillofacial Pathology : JOMFP
|May 20, 2016
Summary
Dentinogenic ghost cell tumor (DGCT) is a rare odontogenic neoplasm. This case report details a DGCT presentation in a 68-year-old male, highlighting its characteristic histopathology.
Area of Science:
- Oral Pathology
- Odontogenic Neoplasms
Background:
- Dentinogenic ghost cell tumor (DGCT) is a rare odontogenic neoplasm, considered a solid variant of calcifying odontogenic cyst (COC).
- DGCT exhibits locally aggressive behavior and accounts for a small percentage (2-14%) of all COCs.
- Limited case reports (88 cases from 1968-2014) highlight the rarity of DGCT.
Observation:
- This report presents a case of DGCT in a 68-year-old male patient.
- Clinical presentation included a soft tissue growth over the alveolar ridge.
- Histopathological examination revealed characteristic features of DGCT.
Findings:
- The tumor displayed ameloblastomatous epithelium, a hallmark of odontogenic tumors.
- Abundant eosinophilic material was observed, consistent with DGCT.
- Presence of ghost cells, a defining feature, was confirmed on histopathology.
Implications:
- This case contributes to the limited literature on Dentinogenic Ghost Cell Tumors.
- Understanding DGCT's clinical and histopathological features is crucial for accurate diagnosis.
- Further research may elucidate the specific behavior and optimal management of DGCT.
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