Odontoameloblastoma: report of a case.
Identifieur interne : 00B391 ( Main/Merge ); précédent : 00B390; suivant : 00B392Odontoameloblastoma: report of a case.
Auteurs : T. Gunbay ; S. Gunbay ; F. OztopSource :
- The Journal of clinical pediatric dentistry [ 1053-4628 ] ; 1993.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Améloblastome, Tumeurs du maxillaire supérieur.
- étiologie : Mâchoire partiellement édentée.
- Améloblastome, Enfant, Humains, Mâle, Tumeurs du maxillaire supérieur.
English descriptors
- KwdEn :
- MESH :
- complications : Ameloblastoma, Maxillary Neoplasms.
- etiology : Jaw, Edentulous, Partially.
- pathology : Ameloblastoma, Maxillary Neoplasms.
- surgery : Ameloblastoma, Maxillary Neoplasms.
- Child, Humans, Male.
Abstract
Ameloblastic odontoma is a mixed odontogenic tumor, which is characterized as being extremely rare, displaying aggressive clinical behavior, resembling a mixed radiopaque and radiolucent radiographic appearance and containing both ameloblastoma and a composite odontoma. An eleven-year-old boy complaining of the edentulous area at the anterior maxilla, was seen at the Department of Oral Surgery of Ege University Dental Faculty. The lesion presented a radiopaque and radiolucent features on panoramic radiogram. Locally operated lesion was diagnosed as ameloblastic odontoma, because it contains islands of ameloblastoma with calcified dental structures as odontoma. The patient was followed-up for 7 years and no recurrence was seen. This case is presented because of its rarity, early detection in an edentulous area of a child, and the successful choice of treatment.
PubMed: 8110607
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pubmed:8110607Le document en format XML
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Gunbay</name><affiliation><nlm:affiliation>Department of Oral Surgery, Faculty of Dentistry, Ege University, Bornova, Izmir-Turkey.</nlm:affiliation><wicri:noCountry code="subField">Izmir-Turkey</wicri:noCountry></affiliation></author><author><name sortKey="Gunbay, S" sort="Gunbay, S" uniqKey="Gunbay S" first="S" last="Gunbay">S. Gunbay</name></author><author><name sortKey="Oztop, F" sort="Oztop, F" uniqKey="Oztop F" first="F" last="Oztop">F. Oztop</name></author></analytic><series><title level="j">The Journal of clinical pediatric dentistry</title><idno type="ISSN">1053-4628</idno><imprint><date when="1993" type="published">1993</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Ameloblastoma (complications)</term><term>Ameloblastoma (pathology)</term><term>Ameloblastoma (surgery)</term><term>Child</term><term>Humans</term><term>Jaw, Edentulous, Partially (etiology)</term><term>Male</term><term>Maxillary Neoplasms (complications)</term><term>Maxillary Neoplasms (pathology)</term><term>Maxillary Neoplasms (surgery)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Améloblastome ()</term><term>Améloblastome (anatomopathologie)</term><term>Enfant</term><term>Humains</term><term>Mâchoire partiellement édentée (étiologie)</term><term>Mâle</term><term>Tumeurs du maxillaire supérieur ()</term><term>Tumeurs du maxillaire supérieur (anatomopathologie)</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Améloblastome</term><term>Tumeurs du maxillaire supérieur</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Ameloblastoma</term><term>Maxillary Neoplasms</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Jaw, Edentulous, Partially</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Ameloblastoma</term><term>Maxillary Neoplasms</term></keywords><keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Ameloblastoma</term><term>Maxillary Neoplasms</term></keywords><keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Mâchoire partiellement édentée</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Child</term><term>Humans</term><term>Male</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Améloblastome</term><term>Enfant</term><term>Humains</term><term>Mâle</term><term>Tumeurs du maxillaire supérieur</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Ameloblastic odontoma is a mixed odontogenic tumor, which is characterized as being extremely rare, displaying aggressive clinical behavior, resembling a mixed radiopaque and radiolucent radiographic appearance and containing both ameloblastoma and a composite odontoma. An eleven-year-old boy complaining of the edentulous area at the anterior maxilla, was seen at the Department of Oral Surgery of Ege University Dental Faculty. The lesion presented a radiopaque and radiolucent features on panoramic radiogram. Locally operated lesion was diagnosed as ameloblastic odontoma, because it contains islands of ameloblastoma with calcified dental structures as odontoma. The patient was followed-up for 7 years and no recurrence was seen. This case is presented because of its rarity, early detection in an edentulous area of a child, and the successful choice of treatment.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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