Peripheral dentinogenic ghost cell tumor: report of a case and literature review.
Identifieur interne : 000C95 ( PubMed/Checkpoint ); précédent : 000C94; suivant : 000C96Peripheral dentinogenic ghost cell tumor: report of a case and literature review.
Auteurs : Ibrahim O. Bello [Arabie saoudite] ; Ahmed Qannam ; Ahmed Al-Zahrani ; Abdullah AldosariSource :
- International journal of surgical pathology [ 1940-2465 ] ; 2012.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Améloblastome, Dentine, Dysplasie de la dentine, Tumeurs de la mandibule.
- Améloblastome, Bouche édentée, Femelle, Humains, Sujet âgé, Tumeurs de la mandibule.
English descriptors
- KwdEn :
- MESH :
- complications : Ameloblastoma, Mandibular Neoplasms.
- pathology : Ameloblastoma, Dentin, Dentin Dysplasia, Mandibular Neoplasms.
- surgery : Ameloblastoma, Mandibular Neoplasms.
- Aged, Female, Humans, Mouth, Edentulous.
Abstract
Peripheral dentinogenic ghost cell tumor is a rare tumor with only 24 cases previously described in the English literature. The majority of cases have been reported to occur in the anterior part of the jaws. A case occurring in posterior (molar region) of the mandible in a 75-year-old edentulous woman is reported. The patient presented with a nodular swelling in the left mandible that showed erosion (saucerization) of the underlying bone radiographically. On microscopy, the tumor showed mainly solid epithelial islands resembling ameloblastoma in fibrous connective tissue. The islands were associated with ghost cells and dysplastic dentin. This report includes the clinical, radiographic, and microscopic features of the patient, in addition to the review of the English literature on the tumor.
DOI: 10.1177/1066896911429299
PubMed: 22134631
Affiliations:
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pubmed:22134631Le document en format XML
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<author><name sortKey="Bello, Ibrahim O" sort="Bello, Ibrahim O" uniqKey="Bello I" first="Ibrahim O" last="Bello">Ibrahim O. Bello</name>
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<author><name sortKey="Qannam, Ahmed" sort="Qannam, Ahmed" uniqKey="Qannam A" first="Ahmed" last="Qannam">Ahmed Qannam</name>
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<author><name sortKey="Al Zahrani, Ahmed" sort="Al Zahrani, Ahmed" uniqKey="Al Zahrani A" first="Ahmed" last="Al-Zahrani">Ahmed Al-Zahrani</name>
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<term>Ameloblastoma (surgery)</term>
<term>Dentin (pathology)</term>
<term>Dentin Dysplasia (pathology)</term>
<term>Female</term>
<term>Humans</term>
<term>Mandibular Neoplasms (complications)</term>
<term>Mandibular Neoplasms (pathology)</term>
<term>Mandibular Neoplasms (surgery)</term>
<term>Mouth, Edentulous</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Améloblastome ()</term>
<term>Améloblastome (anatomopathologie)</term>
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<term>Dentine (anatomopathologie)</term>
<term>Dysplasie de la dentine (anatomopathologie)</term>
<term>Femelle</term>
<term>Humains</term>
<term>Sujet âgé</term>
<term>Tumeurs de la mandibule ()</term>
<term>Tumeurs de la mandibule (anatomopathologie)</term>
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<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Améloblastome</term>
<term>Dentine</term>
<term>Dysplasie de la dentine</term>
<term>Tumeurs de la mandibule</term>
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<term>Mandibular Neoplasms</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Ameloblastoma</term>
<term>Dentin</term>
<term>Dentin Dysplasia</term>
<term>Mandibular Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Ameloblastoma</term>
<term>Mandibular Neoplasms</term>
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<term>Mouth, Edentulous</term>
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<term>Bouche édentée</term>
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<term>Humains</term>
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<front><div type="abstract" xml:lang="en">Peripheral dentinogenic ghost cell tumor is a rare tumor with only 24 cases previously described in the English literature. The majority of cases have been reported to occur in the anterior part of the jaws. A case occurring in posterior (molar region) of the mandible in a 75-year-old edentulous woman is reported. The patient presented with a nodular swelling in the left mandible that showed erosion (saucerization) of the underlying bone radiographically. On microscopy, the tumor showed mainly solid epithelial islands resembling ameloblastoma in fibrous connective tissue. The islands were associated with ghost cells and dysplastic dentin. This report includes the clinical, radiographic, and microscopic features of the patient, in addition to the review of the English literature on the tumor.</div>
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<Title>International journal of surgical pathology</Title>
<ISOAbbreviation>Int. J. Surg. Pathol.</ISOAbbreviation>
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<Abstract><AbstractText>Peripheral dentinogenic ghost cell tumor is a rare tumor with only 24 cases previously described in the English literature. The majority of cases have been reported to occur in the anterior part of the jaws. A case occurring in posterior (molar region) of the mandible in a 75-year-old edentulous woman is reported. The patient presented with a nodular swelling in the left mandible that showed erosion (saucerization) of the underlying bone radiographically. On microscopy, the tumor showed mainly solid epithelial islands resembling ameloblastoma in fibrous connective tissue. The islands were associated with ghost cells and dysplastic dentin. This report includes the clinical, radiographic, and microscopic features of the patient, in addition to the review of the English literature on the tumor.</AbstractText>
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