Keratoameloblastoma of the mandible
Abstract Introduction Keratoameloblastoma is an extremely rare odontogenic tumor, as only 18 cases have been reported in the literature. Case report The authors report a case of keratoameloblastoma in a 32-year-old woman and review the literature concerning the clinical features, radiological appear...
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Veröffentlicht in: | European annals of otorhinolaryngology, head and neck diseases head and neck diseases, 2017-05, Vol.134 (3), p.205-206 |
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description | Abstract Introduction Keratoameloblastoma is an extremely rare odontogenic tumor, as only 18 cases have been reported in the literature. Case report The authors report a case of keratoameloblastoma in a 32-year-old woman and review the literature concerning the clinical features, radiological appearance, histopathological findings and treatment options. Discussion Keratoameloblastoma is a rare tumor observed more frequently in males (sex ratio: 3:1) characterized by extensive keratin production in odontogenic islets and fibrous stroma. |
doi_str_mv | 10.1016/j.anorl.2016.12.002 |
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Case report The authors report a case of keratoameloblastoma in a 32-year-old woman and review the literature concerning the clinical features, radiological appearance, histopathological findings and treatment options. Discussion Keratoameloblastoma is a rare tumor observed more frequently in males (sex ratio: 3:1) characterized by extensive keratin production in odontogenic islets and fibrous stroma.</description><identifier>ISSN: 1879-7296</identifier><identifier>EISSN: 1879-730X</identifier><identifier>DOI: 10.1016/j.anorl.2016.12.002</identifier><identifier>PMID: 28007509</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Adult ; Ameloblastoma ; Ameloblastoma - diagnosis ; Ameloblastoma - surgery ; Diagnosis, Differential ; Female ; Humans ; Keratin ; Keratins ; Mandible ; Mandibular Neoplasms - diagnosis ; Mandibular Neoplasms - surgery ; Odontogenic tumor ; Otolaryngology ; Radiography, Panoramic ; Reconstructive Surgical Procedures ; Treatment Outcome</subject><ispartof>European annals of otorhinolaryngology, head and neck diseases, 2017-05, Vol.134 (3), p.205-206</ispartof><rights>2016 Elsevier Masson SAS</rights><rights>Copyright © 2016 Elsevier Masson SAS. 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Case report The authors report a case of keratoameloblastoma in a 32-year-old woman and review the literature concerning the clinical features, radiological appearance, histopathological findings and treatment options. Discussion Keratoameloblastoma is a rare tumor observed more frequently in males (sex ratio: 3:1) characterized by extensive keratin production in odontogenic islets and fibrous stroma.</description><subject>Adult</subject><subject>Ameloblastoma</subject><subject>Ameloblastoma - diagnosis</subject><subject>Ameloblastoma - surgery</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>Humans</subject><subject>Keratin</subject><subject>Keratins</subject><subject>Mandible</subject><subject>Mandibular Neoplasms - diagnosis</subject><subject>Mandibular Neoplasms - surgery</subject><subject>Odontogenic tumor</subject><subject>Otolaryngology</subject><subject>Radiography, Panoramic</subject><subject>Reconstructive Surgical Procedures</subject><subject>Treatment Outcome</subject><issn>1879-7296</issn><issn>1879-730X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFLHTEQxkNpqWL9CwR54KWXt80kbzfJwUIRrVKhB1vwFmaTWcwzu9Fkn-B_b16f9tBLc5hk4PvmI79h7Ah4Axy6L-sGp5RjI2rTgGg4F-_YPmhllkry2_dvb2G6PXZYyprXI7U23Hxke0Jzrlpu9tnJD8o4Jxwppj5imdOIizQs5jtajDj50Ef6xD4MGAsdvt4H7PfF-a-zy-X1z-9XZ9-ul27VmnkpFUA7EHamk6qVRgvecQ-DAtd6XIEBhU71HkWHKLwWalBIPUjUZoW-lQfs827uQ06PGyqzHUNxFCNOlDbFgm6F0tC1UKVyJ3U5lZJpsA85jJifLXC7BWTX9g8guwVkQdgKqLqOXwM2_Uj-r-cNRxWc7gRUv_kUKNviAk2OfMjkZutT-E_A13_8LoYpOIz39ExlnTZ5qgQt2FIN9ma7o-2KoJNciFpfAGqcirA</recordid><startdate>20170501</startdate><enddate>20170501</enddate><creator>Anajar, S</creator><creator>Lakhbal, A</creator><creator>Abada, R</creator><creator>Mahtar, M</creator><general>Elsevier Masson SAS</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20170501</creationdate><title>Keratoameloblastoma of the mandible</title><author>Anajar, S ; Lakhbal, A ; Abada, R ; Mahtar, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-37115fea6963753982060d1f71c5da41917ac7bda26aa2d827f7aeb13a894ad53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Ameloblastoma</topic><topic>Ameloblastoma - diagnosis</topic><topic>Ameloblastoma - surgery</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>Humans</topic><topic>Keratin</topic><topic>Keratins</topic><topic>Mandible</topic><topic>Mandibular Neoplasms - diagnosis</topic><topic>Mandibular Neoplasms - surgery</topic><topic>Odontogenic tumor</topic><topic>Otolaryngology</topic><topic>Radiography, Panoramic</topic><topic>Reconstructive Surgical Procedures</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anajar, S</creatorcontrib><creatorcontrib>Lakhbal, A</creatorcontrib><creatorcontrib>Abada, R</creatorcontrib><creatorcontrib>Mahtar, M</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European annals of otorhinolaryngology, head and neck diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anajar, S</au><au>Lakhbal, A</au><au>Abada, R</au><au>Mahtar, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Keratoameloblastoma of the mandible</atitle><jtitle>European annals of otorhinolaryngology, head and neck diseases</jtitle><addtitle>Eur Ann Otorhinolaryngol Head Neck Dis</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>134</volume><issue>3</issue><spage>205</spage><epage>206</epage><pages>205-206</pages><issn>1879-7296</issn><eissn>1879-730X</eissn><abstract>Abstract Introduction Keratoameloblastoma is an extremely rare odontogenic tumor, as only 18 cases have been reported in the literature. 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subjects | Adult Ameloblastoma Ameloblastoma - diagnosis Ameloblastoma - surgery Diagnosis, Differential Female Humans Keratin Keratins Mandible Mandibular Neoplasms - diagnosis Mandibular Neoplasms - surgery Odontogenic tumor Otolaryngology Radiography, Panoramic Reconstructive Surgical Procedures Treatment Outcome |
title | Keratoameloblastoma of the mandible |
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