Dentinogenic ghost cell tumor—a rare case report with review of literature
Identifieur interne : 001B16 ( Pmc/Curation ); précédent : 001B15; suivant : 001B17Dentinogenic ghost cell tumor—a rare case report with review of literature
Auteurs : Yash Agrawal [Inde] ; Giridhar S. Naidu [Inde] ; Ramanpal Singh Makkad [Inde] ; Ravleen Nagi [Inde] ; Supreet Jain [Inde] ; Dilip R. Gadewar [Inde] ; Raman Kataria [Inde]Source :
- Quantitative Imaging in Medicine and Surgery [ 2223-4292 ] ; 2017.
Abstract
Dentinogenic ghost cell tumors (DGCT) are very rare tumors considered as solid variants of calcifying epithelial odontogenic cysts (CEOC). They are locally invasive neoplasms and their main characteristic features are ameloblastoma like odontogenic epithelial proliferation, an aberrant keratinization in the form of ghost cells and dysplastic dentin. DGCT occur as two forms intraosseous (central) and extra osseous (peripheral), of which more aggressive intraosseous variety requires careful monitoring and aggressive local resection to prevent recurrence. This paper discusses a case of a 14-year-old male patient with a complaint of swelling in his right mandibular premolar molar region since 4 months and missing permanent right mandibular canine and first premolar was also observed. The lesion was diagnosed with radiological, cytological and histopathological investigations which revealed it to be rarest entity.
Url:
DOI: 10.21037/qims.2017.03.06
PubMed: NONE
PubMed Central: 5682399
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<series><title level="j">Quantitative Imaging in Medicine and Surgery</title>
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<front><div type="abstract" xml:lang="en"><p>Dentinogenic ghost cell tumors (DGCT) are very rare tumors considered as solid variants of calcifying epithelial odontogenic cysts (CEOC). They are locally invasive neoplasms and their main characteristic features are ameloblastoma like odontogenic epithelial proliferation, an aberrant keratinization in the form of ghost cells and dysplastic dentin. DGCT occur as two forms intraosseous (central) and extra osseous (peripheral), of which more aggressive intraosseous variety requires careful monitoring and aggressive local resection to prevent recurrence. This paper discusses a case of a 14-year-old male patient with a complaint of swelling in his right mandibular premolar molar region since 4 months and missing permanent right mandibular canine and first premolar was also observed. The lesion was diagnosed with radiological, cytological and histopathological investigations which revealed it to be rarest entity.</p>
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<pmc article-type="case-report"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Quant Imaging Med Surg</journal-id>
<journal-id journal-id-type="iso-abbrev">Quant Imaging Med Surg</journal-id>
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<journal-title-group><journal-title>Quantitative Imaging in Medicine and Surgery</journal-title>
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<article-id pub-id-type="doi">10.21037/qims.2017.03.06</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject>
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<title-group><article-title>Dentinogenic ghost cell tumor—a rare case report with review of literature</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Agrawal</surname>
<given-names>Yash</given-names>
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<xref ref-type="aff" rid="aff1"><sup>1</sup>
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<contrib contrib-type="author"><name><surname>Naidu</surname>
<given-names>Giridhar S.</given-names>
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<xref ref-type="aff" rid="aff1"><sup>1</sup>
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<contrib contrib-type="author"><name><surname>Makkad</surname>
<given-names>Ramanpal Singh</given-names>
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<xref ref-type="aff" rid="aff1"><sup>1</sup>
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<contrib contrib-type="author"><name><surname>Nagi</surname>
<given-names>Ravleen</given-names>
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<xref ref-type="aff" rid="aff1"><sup>1</sup>
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<contrib contrib-type="author"><name><surname>Jain</surname>
<given-names>Supreet</given-names>
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<xref ref-type="aff" rid="aff1"><sup>1</sup>
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<contrib contrib-type="author"><name><surname>Gadewar</surname>
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Department of Oral Medicine and Radiology, New Horizon Dental College & Research Institute, Sakri,<addr-line>Bilaspur, Chhattisgarh</addr-line>
,<country>India</country>
;</aff>
<aff id="aff2"><label>2</label>
Jan Swasthya Sahyog, Hospital and Community Health Centre, Ganiyari,<addr-line>Bilaspur, Chhattisgarh</addr-line>
,<country>India</country>
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<author-notes><corresp id="cor1"><italic>Correspondence to:</italic>
Dr. Yash Agrawal, Post Graduate Student. Dept. of Oral Medicine and Radiology, New Horizon Dental College & Research Institute, Sakri, Bilaspur, Chhattisgarh, India. Email: <email xlink:href="yashagrawalinfo1989@gmail.com">yashagrawalinfo1989@gmail.com</email>
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<volume>7</volume>
<issue>5</issue>
<fpage>598</fpage>
<lpage>604</lpage>
<history><date date-type="received"><day>25</day>
<month>2</month>
<year>2017</year>
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<date date-type="accepted"><day>19</day>
<month>3</month>
<year>2017</year>
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<permissions><copyright-statement>2017 Quantitative Imaging in Medicine and Surgery. All rights reserved.</copyright-statement>
<copyright-year>2017</copyright-year>
<copyright-holder>Quantitative Imaging in Medicine and Surgery.</copyright-holder>
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<abstract><p>Dentinogenic ghost cell tumors (DGCT) are very rare tumors considered as solid variants of calcifying epithelial odontogenic cysts (CEOC). They are locally invasive neoplasms and their main characteristic features are ameloblastoma like odontogenic epithelial proliferation, an aberrant keratinization in the form of ghost cells and dysplastic dentin. DGCT occur as two forms intraosseous (central) and extra osseous (peripheral), of which more aggressive intraosseous variety requires careful monitoring and aggressive local resection to prevent recurrence. This paper discusses a case of a 14-year-old male patient with a complaint of swelling in his right mandibular premolar molar region since 4 months and missing permanent right mandibular canine and first premolar was also observed. The lesion was diagnosed with radiological, cytological and histopathological investigations which revealed it to be rarest entity.</p>
</abstract>
<kwd-group kwd-group-type="author"><title>Keywords: </title>
<kwd>Calcifying odontogenic cyst (COC)</kwd>
<kwd>dentinogenic ghost cell tumor (DGCT)</kwd>
<kwd>intraosseous</kwd>
<kwd>treatment</kwd>
</kwd-group>
</article-meta>
</front>
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