Peripheral dentinogenic ghost cell tumor: a case report and review of the literature.
Identifieur interne : 001C45 ( PubMed/Corpus ); précédent : 001C44; suivant : 001C46Peripheral dentinogenic ghost cell tumor: a case report and review of the literature.
Auteurs : Germano Angarani Candido ; Karolline Alves Viana ; Satiro Watanabe ; Eneida Franco VencioSource :
- Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics [ 1528-395X ] ; 2009.
English descriptors
- KwdEn :
- Dental Arch (pathology), Dentin (pathology), Dentin Dysplasia (pathology), Humans, Jaw, Edentulous (pathology), Keratin-14 (analysis), Keratins (analysis), Langerhans Cells (pathology), Male, Mandibular Neoplasms (pathology), Melanocytes (pathology), Middle Aged, Odontogenic Tumors (pathology), S100 Proteins (analysis).
- MESH :
- chemical , analysis : Keratin-14, Keratins, S100 Proteins.
- pathology : Dental Arch, Dentin, Dentin Dysplasia, Jaw, Edentulous, Langerhans Cells, Mandibular Neoplasms, Melanocytes, Odontogenic Tumors.
- Humans, Male, Middle Aged.
Abstract
Dentinogenic ghost cell tumor (DGCT) is a rare neoplasm, representing 1.9% to 2.1% of all odontogenic tumors. Few cases of DGCT have been reported and only 11 show no bone involvement. A rare case of peripheral DGCT is reported, located in the anterior mandible of a 45-year-old man. The patient presented a slow painless growth in the canine region of an edentulous mandible. Radiographically, no bone involvement was registered. The lesion was enucleated and microscopically characterized by islands of epithelial cells showing ameloblastomalike features in fibrous tissue. Dysplasic dentin and ghost cells were frequently observed. Areas showing a connection between tumor cells and the overlying mucosa were also identified. Immunohistochemical analysis demonstrated positivity for pan-cytokeratin, cytokeratin-14, and 2 neural markers. Denditric cells (Langerhans cells and melanocytes) were identified inside tumoral islands. A rare case of peripheral DGCT is reported, with immunohistochemical analysis and a review of the English literature.
DOI: 10.1016/j.tripleo.2009.04.033
PubMed: 19716497
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pubmed:19716497Le document en format XML
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<author><name sortKey="Candido, Germano Angarani" sort="Candido, Germano Angarani" uniqKey="Candido G" first="Germano Angarani" last="Candido">Germano Angarani Candido</name>
<affiliation><nlm:affiliation>Department of Oral Pathology, School of Dentistry, Federal University of Goias, Goiania, Brazil.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Viana, Karolline Alves" sort="Viana, Karolline Alves" uniqKey="Viana K" first="Karolline Alves" last="Viana">Karolline Alves Viana</name>
</author>
<author><name sortKey="Watanabe, Satiro" sort="Watanabe, Satiro" uniqKey="Watanabe S" first="Satiro" last="Watanabe">Satiro Watanabe</name>
</author>
<author><name sortKey="Vencio, Eneida Franco" sort="Vencio, Eneida Franco" uniqKey="Vencio E" first="Eneida Franco" last="Vencio">Eneida Franco Vencio</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Peripheral dentinogenic ghost cell tumor: a case report and review of the literature.</title>
<author><name sortKey="Candido, Germano Angarani" sort="Candido, Germano Angarani" uniqKey="Candido G" first="Germano Angarani" last="Candido">Germano Angarani Candido</name>
<affiliation><nlm:affiliation>Department of Oral Pathology, School of Dentistry, Federal University of Goias, Goiania, Brazil.</nlm:affiliation>
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<author><name sortKey="Viana, Karolline Alves" sort="Viana, Karolline Alves" uniqKey="Viana K" first="Karolline Alves" last="Viana">Karolline Alves Viana</name>
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<author><name sortKey="Watanabe, Satiro" sort="Watanabe, Satiro" uniqKey="Watanabe S" first="Satiro" last="Watanabe">Satiro Watanabe</name>
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<author><name sortKey="Vencio, Eneida Franco" sort="Vencio, Eneida Franco" uniqKey="Vencio E" first="Eneida Franco" last="Vencio">Eneida Franco Vencio</name>
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<series><title level="j">Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Dental Arch (pathology)</term>
<term>Dentin (pathology)</term>
<term>Dentin Dysplasia (pathology)</term>
<term>Humans</term>
<term>Jaw, Edentulous (pathology)</term>
<term>Keratin-14 (analysis)</term>
<term>Keratins (analysis)</term>
<term>Langerhans Cells (pathology)</term>
<term>Male</term>
<term>Mandibular Neoplasms (pathology)</term>
<term>Melanocytes (pathology)</term>
<term>Middle Aged</term>
<term>Odontogenic Tumors (pathology)</term>
<term>S100 Proteins (analysis)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Keratin-14</term>
<term>Keratins</term>
<term>S100 Proteins</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Dental Arch</term>
<term>Dentin</term>
<term>Dentin Dysplasia</term>
<term>Jaw, Edentulous</term>
<term>Langerhans Cells</term>
<term>Mandibular Neoplasms</term>
<term>Melanocytes</term>
<term>Odontogenic Tumors</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
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<front><div type="abstract" xml:lang="en">Dentinogenic ghost cell tumor (DGCT) is a rare neoplasm, representing 1.9% to 2.1% of all odontogenic tumors. Few cases of DGCT have been reported and only 11 show no bone involvement. A rare case of peripheral DGCT is reported, located in the anterior mandible of a 45-year-old man. The patient presented a slow painless growth in the canine region of an edentulous mandible. Radiographically, no bone involvement was registered. The lesion was enucleated and microscopically characterized by islands of epithelial cells showing ameloblastomalike features in fibrous tissue. Dysplasic dentin and ghost cells were frequently observed. Areas showing a connection between tumor cells and the overlying mucosa were also identified. Immunohistochemical analysis demonstrated positivity for pan-cytokeratin, cytokeratin-14, and 2 neural markers. Denditric cells (Langerhans cells and melanocytes) were identified inside tumoral islands. A rare case of peripheral DGCT is reported, with immunohistochemical analysis and a review of the English literature.</div>
</front>
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<Month>12</Month>
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<Issue>3</Issue>
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<Title>Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics</Title>
<ISOAbbreviation>Oral Surg Oral Med Oral Pathol Oral Radiol Endod</ISOAbbreviation>
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<ArticleTitle>Peripheral dentinogenic ghost cell tumor: a case report and review of the literature.</ArticleTitle>
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<Abstract><AbstractText>Dentinogenic ghost cell tumor (DGCT) is a rare neoplasm, representing 1.9% to 2.1% of all odontogenic tumors. Few cases of DGCT have been reported and only 11 show no bone involvement. A rare case of peripheral DGCT is reported, located in the anterior mandible of a 45-year-old man. The patient presented a slow painless growth in the canine region of an edentulous mandible. Radiographically, no bone involvement was registered. The lesion was enucleated and microscopically characterized by islands of epithelial cells showing ameloblastomalike features in fibrous tissue. Dysplasic dentin and ghost cells were frequently observed. Areas showing a connection between tumor cells and the overlying mucosa were also identified. Immunohistochemical analysis demonstrated positivity for pan-cytokeratin, cytokeratin-14, and 2 neural markers. Denditric cells (Langerhans cells and melanocytes) were identified inside tumoral islands. A rare case of peripheral DGCT is reported, with immunohistochemical analysis and a review of the English literature.</AbstractText>
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<ForeName>Germano Angarani</ForeName>
<Initials>GA</Initials>
<AffiliationInfo><Affiliation>Department of Oral Pathology, School of Dentistry, Federal University of Goias, Goiania, Brazil.</Affiliation>
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<NumberOfReferences>20</NumberOfReferences>
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