Dentinogenic ghost cell tumor
Identifieur interne : 006725 ( Ncbi/Curation ); précédent : 006724; suivant : 006726Dentinogenic ghost cell tumor
Auteurs : Sweety Sagarmal Bafna ; Tabita Joy ; Jagdish Vishnu Tupkari ; Jayant Shivaji LandgeSource :
- Journal of Oral and Maxillofacial Pathology : JOMFP [ 0973-029X ] ; 2016.
Abstract
Dentinogenic ghost cell tumor (DGCT) is a rare, odontogenic neoplasm which is considered to be a solid variant of calcifying odontogenic cyst (COC) with locally aggressive behavior. It accounts for only 2–14% of all COCs. To the best of our knowledge, only 88 cases of DGCT have been reported in the literature from 1968 to 2014. Herewith, we report a case of DGCT in a 68-year-old male patient with clinical presentation as a soft tissue growth over alveolar ridge and histopathologically characterized by ameloblastomatous epithelium, abundance of eosinophilic material and ghost cells.
Url:
DOI: 10.4103/0973-029X.180985
PubMed: 27194885
PubMed Central: 4860925
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<front><div type="abstract" xml:lang="en"><p>Dentinogenic ghost cell tumor (DGCT) is a rare, odontogenic neoplasm which is considered to be a solid variant of calcifying odontogenic cyst (COC) with locally aggressive behavior. It accounts for only 2–14% of all COCs. To the best of our knowledge, only 88 cases of DGCT have been reported in the literature from 1968 to 2014. Herewith, we report a case of DGCT in a 68-year-old male patient with clinical presentation as a soft tissue growth over alveolar ridge and histopathologically characterized by ameloblastomatous epithelium, abundance of eosinophilic material and ghost cells.</p>
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