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 |
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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 |
format | Article |
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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><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 & 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 & 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 & 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 & 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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