Primary intraosseous mucoepidermoid carcinoma of the jaw: Reappraisal of The MD Anderson Cancer Center experience

Background Mucoepidermoid carcinoma arises from major or minor salivary glands, making up 10% of salivary gland tumors. Intraosseous mucoepidermoid carcinomas are rare, and make up only 2% to 3% of all mucoepidermoid carcinomas. The t(11;19) and its CRTC1‐MAML2 fusion gene transcript have been ident...

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Veröffentlicht in:Head & neck 2016-04, Vol.38 (S1), p.E1312-E1317
Hauptverfasser: Bell, Diana, Lewis, Carol, El-Naggar, Adel K., Weber, Randal S.
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creator Bell, Diana
Lewis, Carol
El-Naggar, Adel K.
Weber, Randal S.
description Background Mucoepidermoid carcinoma arises from major or minor salivary glands, making up 10% of salivary gland tumors. Intraosseous mucoepidermoid carcinomas are rare, and make up only 2% to 3% of all mucoepidermoid carcinomas. The t(11;19) and its CRTC1‐MAML2 fusion gene transcript have been identified in mucoepidermoid carcinoma and are associated with a subset of mucoepidermoid carcinomas. The extent to which the transcript influences disease features and patient survival is unclear. Methods We conducted a retrospective analysis of records for clinical features, surgical interventions, and prognoses. Reverse transcriptase‐polymerase chain reaction (RT‐PCR) and fluorescence in situ hybridization (FISH) used to assess the t(11;19) fusion gene in intraosseous mucoepidermoid carcinoma. Results Twenty‐five patients with intraosseous mucoepidermoid carcinoma treated between 1998 and 2013 were identified. The t(11;19) fusion gene transcript CRTC1‐MAML2 manifested in 9 intraosseous mucoepidermoid carcinomas, whereas is was not detected in another 9 intraosseous carcinomas. Although the incidence of this fusion in mucoepidermoid carcinoma varies, it is generally accepted that more than 50% of this entity manifest the CRTC1‐MAML2. Conclusion Intraosseous mucoepidermoid carcinoma diagnosis should be based on clinical and pathologic manifestations and complete resection is the first choice for patient treatment. The need for neck dissection and adjuvant treatment are debatable. Radiotherapy may improve prognosis and may be recommended in the postoperative period. Primary intraosseous mucoepidermoid carcinoma can manifest the fusion transcript in a subset of tumors. © 2015 Wiley Periodicals, Inc. Head Neck 38: E1312–E1317, 2016
doi_str_mv 10.1002/hed.24219
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Intraosseous mucoepidermoid carcinomas are rare, and make up only 2% to 3% of all mucoepidermoid carcinomas. The t(11;19) and its CRTC1‐MAML2 fusion gene transcript have been identified in mucoepidermoid carcinoma and are associated with a subset of mucoepidermoid carcinomas. The extent to which the transcript influences disease features and patient survival is unclear. Methods We conducted a retrospective analysis of records for clinical features, surgical interventions, and prognoses. Reverse transcriptase‐polymerase chain reaction (RT‐PCR) and fluorescence in situ hybridization (FISH) used to assess the t(11;19) fusion gene in intraosseous mucoepidermoid carcinoma. Results Twenty‐five patients with intraosseous mucoepidermoid carcinoma treated between 1998 and 2013 were identified. The t(11;19) fusion gene transcript CRTC1‐MAML2 manifested in 9 intraosseous mucoepidermoid carcinomas, whereas is was not detected in another 9 intraosseous carcinomas. Although the incidence of this fusion in mucoepidermoid carcinoma varies, it is generally accepted that more than 50% of this entity manifest the CRTC1‐MAML2. Conclusion Intraosseous mucoepidermoid carcinoma diagnosis should be based on clinical and pathologic manifestations and complete resection is the first choice for patient treatment. The need for neck dissection and adjuvant treatment are debatable. Radiotherapy may improve prognosis and may be recommended in the postoperative period. Primary intraosseous mucoepidermoid carcinoma can manifest the fusion transcript in a subset of tumors. © 2015 Wiley Periodicals, Inc. Head Neck 38: E1312–E1317, 2016</description><identifier>ISSN: 1043-3074</identifier><identifier>EISSN: 1097-0347</identifier><identifier>DOI: 10.1002/hed.24219</identifier><identifier>PMID: 26316332</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Bone Neoplasms - pathology ; Bone Neoplasms - surgery ; Carcinoma, Mucoepidermoid - pathology ; Carcinoma, Mucoepidermoid - surgery ; Child ; DNA-Binding Proteins - genetics ; Female ; fusion transcript ; histogenesis ; Humans ; In Situ Hybridization, Fluorescence ; intraosseous ; Male ; Middle Aged ; mucoepidermoid carcinoma ; Nuclear Proteins - genetics ; Oncogene Proteins, Fusion - genetics ; Retrospective Studies ; Salivary Gland Neoplasms - pathology ; Salivary Gland Neoplasms - surgery ; Transcription Factors - genetics ; translocation</subject><ispartof>Head &amp; neck, 2016-04, Vol.38 (S1), p.E1312-E1317</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4299-ded779258aecb1a75eebd77f7aa601218cafa899ab390c36031496464bd6301c3</citedby><cites>FETCH-LOGICAL-c4299-ded779258aecb1a75eebd77f7aa601218cafa899ab390c36031496464bd6301c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhed.24219$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhed.24219$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26316332$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bell, Diana</creatorcontrib><creatorcontrib>Lewis, Carol</creatorcontrib><creatorcontrib>El-Naggar, Adel K.</creatorcontrib><creatorcontrib>Weber, Randal S.</creatorcontrib><title>Primary intraosseous mucoepidermoid carcinoma of the jaw: Reappraisal of The MD Anderson Cancer Center experience</title><title>Head &amp; neck</title><addtitle>Head Neck</addtitle><description>Background Mucoepidermoid carcinoma arises from major or minor salivary glands, making up 10% of salivary gland tumors. Intraosseous mucoepidermoid carcinomas are rare, and make up only 2% to 3% of all mucoepidermoid carcinomas. The t(11;19) and its CRTC1‐MAML2 fusion gene transcript have been identified in mucoepidermoid carcinoma and are associated with a subset of mucoepidermoid carcinomas. The extent to which the transcript influences disease features and patient survival is unclear. Methods We conducted a retrospective analysis of records for clinical features, surgical interventions, and prognoses. Reverse transcriptase‐polymerase chain reaction (RT‐PCR) and fluorescence in situ hybridization (FISH) used to assess the t(11;19) fusion gene in intraosseous mucoepidermoid carcinoma. Results Twenty‐five patients with intraosseous mucoepidermoid carcinoma treated between 1998 and 2013 were identified. The t(11;19) fusion gene transcript CRTC1‐MAML2 manifested in 9 intraosseous mucoepidermoid carcinomas, whereas is was not detected in another 9 intraosseous carcinomas. Although the incidence of this fusion in mucoepidermoid carcinoma varies, it is generally accepted that more than 50% of this entity manifest the CRTC1‐MAML2. Conclusion Intraosseous mucoepidermoid carcinoma diagnosis should be based on clinical and pathologic manifestations and complete resection is the first choice for patient treatment. The need for neck dissection and adjuvant treatment are debatable. Radiotherapy may improve prognosis and may be recommended in the postoperative period. Primary intraosseous mucoepidermoid carcinoma can manifest the fusion transcript in a subset of tumors. © 2015 Wiley Periodicals, Inc. Head Neck 38: E1312–E1317, 2016</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Bone Neoplasms - pathology</subject><subject>Bone Neoplasms - surgery</subject><subject>Carcinoma, Mucoepidermoid - pathology</subject><subject>Carcinoma, Mucoepidermoid - surgery</subject><subject>Child</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Female</subject><subject>fusion transcript</subject><subject>histogenesis</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>intraosseous</subject><subject>Male</subject><subject>Middle Aged</subject><subject>mucoepidermoid carcinoma</subject><subject>Nuclear Proteins - genetics</subject><subject>Oncogene Proteins, Fusion - genetics</subject><subject>Retrospective Studies</subject><subject>Salivary Gland Neoplasms - pathology</subject><subject>Salivary Gland Neoplasms - surgery</subject><subject>Transcription Factors - genetics</subject><subject>translocation</subject><issn>1043-3074</issn><issn>1097-0347</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1PFTEUhhsjEQQW_gHTpS4G-jXtrTtyQTCg3gDGxE1zpnMmFOeLdm6Af2-vw3Xn6jRvnvdN-hDyjrMjzpg4vsP6SCjB7Suyx5k1BZPKvN68lSwkM2qXvE3pnjEmtRJvyK7QkmspxR55WMXQQXymoZ8iDCnhsE60W_sBx1Bj7IZQUw_Rh37ogA4Nne6Q3sPjJ3qNMI4RQoJ2k9_m_OspPelzKw09XULvMdIl9lM--DRiDJijA7LTQJvw8OXukx-fz26XF8XV9_Mvy5OrwithbVFjbYwV5QLQVxxMiVjlpDEAmnHBFx4aWFgLlbTMS80kV1YrrapaS8a93Ccf5t0xDg9rTJPrQvLYttBv_ui4WSijylKWGf04oz5mAxEbN85WHGduY9hlw-6v4cy-f5ldV11Ot-RWaQaOZ-AxtPj8_yV3cXa6nSzmRkgTPv1rQPzttJGmdD-_nbuVuSx_6RV3N_IPU56U5Q</recordid><startdate>201604</startdate><enddate>201604</enddate><creator>Bell, Diana</creator><creator>Lewis, Carol</creator><creator>El-Naggar, Adel K.</creator><creator>Weber, Randal S.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>201604</creationdate><title>Primary intraosseous mucoepidermoid carcinoma of the jaw: Reappraisal of The MD Anderson Cancer Center experience</title><author>Bell, Diana ; Lewis, Carol ; El-Naggar, Adel K. ; Weber, Randal S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4299-ded779258aecb1a75eebd77f7aa601218cafa899ab390c36031496464bd6301c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Bone Neoplasms - pathology</topic><topic>Bone Neoplasms - surgery</topic><topic>Carcinoma, Mucoepidermoid - pathology</topic><topic>Carcinoma, Mucoepidermoid - surgery</topic><topic>Child</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Female</topic><topic>fusion transcript</topic><topic>histogenesis</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>intraosseous</topic><topic>Male</topic><topic>Middle Aged</topic><topic>mucoepidermoid carcinoma</topic><topic>Nuclear Proteins - genetics</topic><topic>Oncogene Proteins, Fusion - genetics</topic><topic>Retrospective Studies</topic><topic>Salivary Gland Neoplasms - pathology</topic><topic>Salivary Gland Neoplasms - surgery</topic><topic>Transcription Factors - genetics</topic><topic>translocation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bell, Diana</creatorcontrib><creatorcontrib>Lewis, Carol</creatorcontrib><creatorcontrib>El-Naggar, Adel K.</creatorcontrib><creatorcontrib>Weber, Randal S.</creatorcontrib><collection>Istex</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>Head &amp; neck</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bell, Diana</au><au>Lewis, Carol</au><au>El-Naggar, Adel K.</au><au>Weber, Randal S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary intraosseous mucoepidermoid carcinoma of the jaw: Reappraisal of The MD Anderson Cancer Center experience</atitle><jtitle>Head &amp; neck</jtitle><addtitle>Head Neck</addtitle><date>2016-04</date><risdate>2016</risdate><volume>38</volume><issue>S1</issue><spage>E1312</spage><epage>E1317</epage><pages>E1312-E1317</pages><issn>1043-3074</issn><eissn>1097-0347</eissn><abstract>Background Mucoepidermoid carcinoma arises from major or minor salivary glands, making up 10% of salivary gland tumors. Intraosseous mucoepidermoid carcinomas are rare, and make up only 2% to 3% of all mucoepidermoid carcinomas. The t(11;19) and its CRTC1‐MAML2 fusion gene transcript have been identified in mucoepidermoid carcinoma and are associated with a subset of mucoepidermoid carcinomas. The extent to which the transcript influences disease features and patient survival is unclear. Methods We conducted a retrospective analysis of records for clinical features, surgical interventions, and prognoses. Reverse transcriptase‐polymerase chain reaction (RT‐PCR) and fluorescence in situ hybridization (FISH) used to assess the t(11;19) fusion gene in intraosseous mucoepidermoid carcinoma. Results Twenty‐five patients with intraosseous mucoepidermoid carcinoma treated between 1998 and 2013 were identified. The t(11;19) fusion gene transcript CRTC1‐MAML2 manifested in 9 intraosseous mucoepidermoid carcinomas, whereas is was not detected in another 9 intraosseous carcinomas. Although the incidence of this fusion in mucoepidermoid carcinoma varies, it is generally accepted that more than 50% of this entity manifest the CRTC1‐MAML2. Conclusion Intraosseous mucoepidermoid carcinoma diagnosis should be based on clinical and pathologic manifestations and complete resection is the first choice for patient treatment. The need for neck dissection and adjuvant treatment are debatable. Radiotherapy may improve prognosis and may be recommended in the postoperative period. Primary intraosseous mucoepidermoid carcinoma can manifest the fusion transcript in a subset of tumors. © 2015 Wiley Periodicals, Inc. Head Neck 38: E1312–E1317, 2016</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>26316332</pmid><doi>10.1002/hed.24219</doi><tpages>6</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Bone Neoplasms - pathology
Bone Neoplasms - surgery
Carcinoma, Mucoepidermoid - pathology
Carcinoma, Mucoepidermoid - surgery
Child
DNA-Binding Proteins - genetics
Female
fusion transcript
histogenesis
Humans
In Situ Hybridization, Fluorescence
intraosseous
Male
Middle Aged
mucoepidermoid carcinoma
Nuclear Proteins - genetics
Oncogene Proteins, Fusion - genetics
Retrospective Studies
Salivary Gland Neoplasms - pathology
Salivary Gland Neoplasms - surgery
Transcription Factors - genetics
translocation
title Primary intraosseous mucoepidermoid carcinoma of the jaw: Reappraisal of The MD Anderson Cancer Center experience
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