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Dentinogenic ghost cell tumor

Identifieur interne : 006725 ( Ncbi/Curation ); précédent : 006724; suivant : 006726

Dentinogenic ghost cell tumor

Auteurs : Sweety Sagarmal Bafna ; Tabita Joy ; Jagdish Vishnu Tupkari ; Jayant Shivaji Landge

Source :

RBID : PMC:4860925

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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PMC:4860925

Le document en format XML

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<name sortKey="Tupkari, Jagdish Vishnu" sort="Tupkari, Jagdish Vishnu" uniqKey="Tupkari J" first="Jagdish Vishnu" last="Tupkari">Jagdish Vishnu Tupkari</name>
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<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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