Mammaglobin and DOG‐1 expression in polymorphous low‐grade adenocarcinoma: an appraisal of its origin and morphology
Background Polymorphous low‐grade adenocarcinoma (PLGA) remains a diagnostic challenge for most pathologists due to its large spectrum of histological patterns. In this study, the expression of two new markers recently described for salivary gland tumors was studied in PLGA. Methods The morphology o...
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Veröffentlicht in: | Journal of oral pathology & medicine 2017-03, Vol.46 (3), p.182-187 |
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creator | Montalli, Victor Angelo Martins Passador‐Santos, Fabricio Martinez, Elizabeth Ferreira Furuse, Cristiane Aguiar, Maria Cássia Soares, Fernando Augusto Soares, Andresa Borges Brown, Amy Louise Araújo, Ney Soares Araújo, Vera Cavalcanti |
description | Background
Polymorphous low‐grade adenocarcinoma (PLGA) remains a diagnostic challenge for most pathologists due to its large spectrum of histological patterns. In this study, the expression of two new markers recently described for salivary gland tumors was studied in PLGA.
Methods
The morphology of 33 cases of PLGA was carefully evaluated using hematoxylin‐and‐eosin‐stained sections and confirmed by immunohistochemistry for cytokeratin 7, vimentin, and S‐100. Periodic acid–Schiff with diastase digestion was also used. The expression of mammaglobin and DOG‐1 was carried out using the EnVision System. Mammaglobin was assessed according to the percentage of positively stained tumor cells, while DOG‐1 was evaluated according to its presence and site. For MCM‐2 and Ki‐67, markers of proliferation, the labeling index of cell nuclei positivity was evaluated using total cell number. The ETV6‐NTRK3 fusion was examined by fluorescence in situ hybridization analysis.
Results
The histological patterns of the tumor were classified as lobular or non‐lobular. For the non‐lobular pattern, tubular, cribriform, glomeruliform, trabecular, and papillary patterns were observed. Mammaglobin was present in all PLGA cases, and its expression was stronger (P = 0.01) in the lobular than in the non‐lobular pattern. The expression of DOG‐1 was present in the apical portion and cytoplasm of the cells. Proliferation markers were low for all cases independent of histological pattern.
Conclusions
Polymorphous low‐grade adenocarcinoma has been confirmed to originate from the intercalated duct and to feature high expression of mammaglobin in its lobular pattern resembling that of mammary secretory analogue carcinoma, except for the ETV6 gene rearrangement. |
doi_str_mv | 10.1111/jop.12491 |
format | Article |
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Polymorphous low‐grade adenocarcinoma (PLGA) remains a diagnostic challenge for most pathologists due to its large spectrum of histological patterns. In this study, the expression of two new markers recently described for salivary gland tumors was studied in PLGA.
Methods
The morphology of 33 cases of PLGA was carefully evaluated using hematoxylin‐and‐eosin‐stained sections and confirmed by immunohistochemistry for cytokeratin 7, vimentin, and S‐100. Periodic acid–Schiff with diastase digestion was also used. The expression of mammaglobin and DOG‐1 was carried out using the EnVision System. Mammaglobin was assessed according to the percentage of positively stained tumor cells, while DOG‐1 was evaluated according to its presence and site. For MCM‐2 and Ki‐67, markers of proliferation, the labeling index of cell nuclei positivity was evaluated using total cell number. The ETV6‐NTRK3 fusion was examined by fluorescence in situ hybridization analysis.
Results
The histological patterns of the tumor were classified as lobular or non‐lobular. For the non‐lobular pattern, tubular, cribriform, glomeruliform, trabecular, and papillary patterns were observed. Mammaglobin was present in all PLGA cases, and its expression was stronger (P = 0.01) in the lobular than in the non‐lobular pattern. The expression of DOG‐1 was present in the apical portion and cytoplasm of the cells. Proliferation markers were low for all cases independent of histological pattern.
Conclusions
Polymorphous low‐grade adenocarcinoma has been confirmed to originate from the intercalated duct and to feature high expression of mammaglobin in its lobular pattern resembling that of mammary secretory analogue carcinoma, except for the ETV6 gene rearrangement.</description><identifier>ISSN: 0904-2512</identifier><identifier>EISSN: 1600-0714</identifier><identifier>DOI: 10.1111/jop.12491</identifier><identifier>PMID: 27591391</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>Adenocarcinoma ; Adenocarcinoma - metabolism ; Adenocarcinoma - pathology ; Adult ; Aged ; Aged, 80 and over ; Anoctamin-1 - metabolism ; Biomarkers, Tumor - metabolism ; Cell fusion ; Cell number ; Cell proliferation ; Cytokeratin ; Cytoplasm ; Dentistry ; Digestion ; DOG‐1 ; Female ; Fluorescence in situ hybridization ; Gene rearrangement ; Humans ; Hybridization analysis ; Immunohistochemistry ; Male ; mammaglobin ; Mammaglobin A - metabolism ; Middle Aged ; Morphology ; Neoplasm Proteins - metabolism ; Nuclei ; Oral cancer ; origin ; Polylactide-co-glycolide ; polymorphous low‐grade adenocarcinoma ; Salivary gland ; Salivary Gland Neoplasms - metabolism ; Salivary Gland Neoplasms - pathology ; Tumor cells ; Tumors ; Vimentin</subject><ispartof>Journal of oral pathology & medicine, 2017-03, Vol.46 (3), p.182-187</ispartof><rights>2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4521-34f8110d471da486970c03a5fa20c869ab6621a33162f11e6157a212760e5d2d3</citedby><cites>FETCH-LOGICAL-c4521-34f8110d471da486970c03a5fa20c869ab6621a33162f11e6157a212760e5d2d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjop.12491$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjop.12491$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27591391$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Montalli, Victor Angelo Martins</creatorcontrib><creatorcontrib>Passador‐Santos, Fabricio</creatorcontrib><creatorcontrib>Martinez, Elizabeth Ferreira</creatorcontrib><creatorcontrib>Furuse, Cristiane</creatorcontrib><creatorcontrib>Aguiar, Maria Cássia</creatorcontrib><creatorcontrib>Soares, Fernando Augusto</creatorcontrib><creatorcontrib>Soares, Andresa Borges</creatorcontrib><creatorcontrib>Brown, Amy Louise</creatorcontrib><creatorcontrib>Araújo, Ney Soares</creatorcontrib><creatorcontrib>Araújo, Vera Cavalcanti</creatorcontrib><title>Mammaglobin and DOG‐1 expression in polymorphous low‐grade adenocarcinoma: an appraisal of its origin and morphology</title><title>Journal of oral pathology & medicine</title><addtitle>J Oral Pathol Med</addtitle><description>Background
Polymorphous low‐grade adenocarcinoma (PLGA) remains a diagnostic challenge for most pathologists due to its large spectrum of histological patterns. In this study, the expression of two new markers recently described for salivary gland tumors was studied in PLGA.
Methods
The morphology of 33 cases of PLGA was carefully evaluated using hematoxylin‐and‐eosin‐stained sections and confirmed by immunohistochemistry for cytokeratin 7, vimentin, and S‐100. Periodic acid–Schiff with diastase digestion was also used. The expression of mammaglobin and DOG‐1 was carried out using the EnVision System. Mammaglobin was assessed according to the percentage of positively stained tumor cells, while DOG‐1 was evaluated according to its presence and site. For MCM‐2 and Ki‐67, markers of proliferation, the labeling index of cell nuclei positivity was evaluated using total cell number. The ETV6‐NTRK3 fusion was examined by fluorescence in situ hybridization analysis.
Results
The histological patterns of the tumor were classified as lobular or non‐lobular. For the non‐lobular pattern, tubular, cribriform, glomeruliform, trabecular, and papillary patterns were observed. Mammaglobin was present in all PLGA cases, and its expression was stronger (P = 0.01) in the lobular than in the non‐lobular pattern. The expression of DOG‐1 was present in the apical portion and cytoplasm of the cells. Proliferation markers were low for all cases independent of histological pattern.
Conclusions
Polymorphous low‐grade adenocarcinoma has been confirmed to originate from the intercalated duct and to feature high expression of mammaglobin in its lobular pattern resembling that of mammary secretory analogue carcinoma, except for the ETV6 gene rearrangement.</description><subject>Adenocarcinoma</subject><subject>Adenocarcinoma - metabolism</subject><subject>Adenocarcinoma - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anoctamin-1 - metabolism</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cell fusion</subject><subject>Cell number</subject><subject>Cell proliferation</subject><subject>Cytokeratin</subject><subject>Cytoplasm</subject><subject>Dentistry</subject><subject>Digestion</subject><subject>DOG‐1</subject><subject>Female</subject><subject>Fluorescence in situ hybridization</subject><subject>Gene rearrangement</subject><subject>Humans</subject><subject>Hybridization analysis</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>mammaglobin</subject><subject>Mammaglobin A - metabolism</subject><subject>Middle Aged</subject><subject>Morphology</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Nuclei</subject><subject>Oral cancer</subject><subject>origin</subject><subject>Polylactide-co-glycolide</subject><subject>polymorphous low‐grade adenocarcinoma</subject><subject>Salivary gland</subject><subject>Salivary Gland Neoplasms - metabolism</subject><subject>Salivary Gland Neoplasms - pathology</subject><subject>Tumor cells</subject><subject>Tumors</subject><subject>Vimentin</subject><issn>0904-2512</issn><issn>1600-0714</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc9O3DAQh62qqGy3PfQFkKVe6CHgcew46Q3xH4G2BzhHs4mzeOXErs0K9sYj8Iw8SU2z7QEJCUsjazSfP2n8I-QbsD1IZ3_p_B5wUcEHMoGCsYwpEB_JhFVMZFwC3yafY1wyBioX8IlscyUryCuYkIcr7HtcWDc3A8WhpUez0-fHJ6D6wQcdo3EDTRPv7Lp3wd-6VaTW3SdkEbDVNNXgGgyNGVyPP5OCovcBTURLXUfNXaQumMXGPjqsW6y_kK0ObdRfN_eU3JwcXx-eZZez0_PDg8usEZJDlouuBGCtUNCiKItKsYblKDvkrEktzouCA-Y5FLwD0AVIhRy4KpiWLW_zKdkdvT643ysd7-rexEZbi4NOy9RQKlVCxUX-DlRWCqRkRUK_v0KXbhWGtEidXFUp-csHT8mPkWqCizHorvbB9BjWNbD6Jbn0ytd_k0vszsa4mve6_U_-iyoB-yNwb6xev22qL2a_RuUf6eyjBw</recordid><startdate>201703</startdate><enddate>201703</enddate><creator>Montalli, Victor Angelo Martins</creator><creator>Passador‐Santos, Fabricio</creator><creator>Martinez, Elizabeth Ferreira</creator><creator>Furuse, Cristiane</creator><creator>Aguiar, Maria Cássia</creator><creator>Soares, Fernando Augusto</creator><creator>Soares, Andresa Borges</creator><creator>Brown, Amy Louise</creator><creator>Araújo, Ney Soares</creator><creator>Araújo, Vera Cavalcanti</creator><general>Wiley Subscription Services, Inc</general><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>7QP</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201703</creationdate><title>Mammaglobin and DOG‐1 expression in polymorphous low‐grade adenocarcinoma: an appraisal of its origin and morphology</title><author>Montalli, Victor Angelo Martins ; Passador‐Santos, Fabricio ; Martinez, Elizabeth Ferreira ; Furuse, Cristiane ; Aguiar, Maria Cássia ; Soares, Fernando Augusto ; Soares, Andresa Borges ; Brown, Amy Louise ; Araújo, Ney Soares ; Araújo, Vera Cavalcanti</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4521-34f8110d471da486970c03a5fa20c869ab6621a33162f11e6157a212760e5d2d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adenocarcinoma</topic><topic>Adenocarcinoma - metabolism</topic><topic>Adenocarcinoma - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anoctamin-1 - metabolism</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Cell fusion</topic><topic>Cell number</topic><topic>Cell proliferation</topic><topic>Cytokeratin</topic><topic>Cytoplasm</topic><topic>Dentistry</topic><topic>Digestion</topic><topic>DOG‐1</topic><topic>Female</topic><topic>Fluorescence in situ hybridization</topic><topic>Gene rearrangement</topic><topic>Humans</topic><topic>Hybridization analysis</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>mammaglobin</topic><topic>Mammaglobin A - metabolism</topic><topic>Middle Aged</topic><topic>Morphology</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Nuclei</topic><topic>Oral cancer</topic><topic>origin</topic><topic>Polylactide-co-glycolide</topic><topic>polymorphous low‐grade adenocarcinoma</topic><topic>Salivary gland</topic><topic>Salivary Gland Neoplasms - metabolism</topic><topic>Salivary Gland Neoplasms - pathology</topic><topic>Tumor cells</topic><topic>Tumors</topic><topic>Vimentin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Montalli, Victor Angelo Martins</creatorcontrib><creatorcontrib>Passador‐Santos, Fabricio</creatorcontrib><creatorcontrib>Martinez, Elizabeth Ferreira</creatorcontrib><creatorcontrib>Furuse, Cristiane</creatorcontrib><creatorcontrib>Aguiar, Maria Cássia</creatorcontrib><creatorcontrib>Soares, Fernando Augusto</creatorcontrib><creatorcontrib>Soares, Andresa Borges</creatorcontrib><creatorcontrib>Brown, Amy Louise</creatorcontrib><creatorcontrib>Araújo, Ney Soares</creatorcontrib><creatorcontrib>Araújo, Vera Cavalcanti</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of oral pathology & medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Montalli, Victor Angelo Martins</au><au>Passador‐Santos, Fabricio</au><au>Martinez, Elizabeth Ferreira</au><au>Furuse, Cristiane</au><au>Aguiar, Maria Cássia</au><au>Soares, Fernando Augusto</au><au>Soares, Andresa Borges</au><au>Brown, Amy Louise</au><au>Araújo, Ney Soares</au><au>Araújo, Vera Cavalcanti</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mammaglobin and DOG‐1 expression in polymorphous low‐grade adenocarcinoma: an appraisal of its origin and morphology</atitle><jtitle>Journal of oral pathology & medicine</jtitle><addtitle>J Oral Pathol Med</addtitle><date>2017-03</date><risdate>2017</risdate><volume>46</volume><issue>3</issue><spage>182</spage><epage>187</epage><pages>182-187</pages><issn>0904-2512</issn><eissn>1600-0714</eissn><abstract>Background
Polymorphous low‐grade adenocarcinoma (PLGA) remains a diagnostic challenge for most pathologists due to its large spectrum of histological patterns. In this study, the expression of two new markers recently described for salivary gland tumors was studied in PLGA.
Methods
The morphology of 33 cases of PLGA was carefully evaluated using hematoxylin‐and‐eosin‐stained sections and confirmed by immunohistochemistry for cytokeratin 7, vimentin, and S‐100. Periodic acid–Schiff with diastase digestion was also used. The expression of mammaglobin and DOG‐1 was carried out using the EnVision System. Mammaglobin was assessed according to the percentage of positively stained tumor cells, while DOG‐1 was evaluated according to its presence and site. For MCM‐2 and Ki‐67, markers of proliferation, the labeling index of cell nuclei positivity was evaluated using total cell number. The ETV6‐NTRK3 fusion was examined by fluorescence in situ hybridization analysis.
Results
The histological patterns of the tumor were classified as lobular or non‐lobular. For the non‐lobular pattern, tubular, cribriform, glomeruliform, trabecular, and papillary patterns were observed. Mammaglobin was present in all PLGA cases, and its expression was stronger (P = 0.01) in the lobular than in the non‐lobular pattern. The expression of DOG‐1 was present in the apical portion and cytoplasm of the cells. Proliferation markers were low for all cases independent of histological pattern.
Conclusions
Polymorphous low‐grade adenocarcinoma has been confirmed to originate from the intercalated duct and to feature high expression of mammaglobin in its lobular pattern resembling that of mammary secretory analogue carcinoma, except for the ETV6 gene rearrangement.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27591391</pmid><doi>10.1111/jop.12491</doi><tpages>6</tpages></addata></record> |
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subjects | Adenocarcinoma Adenocarcinoma - metabolism Adenocarcinoma - pathology Adult Aged Aged, 80 and over Anoctamin-1 - metabolism Biomarkers, Tumor - metabolism Cell fusion Cell number Cell proliferation Cytokeratin Cytoplasm Dentistry Digestion DOG‐1 Female Fluorescence in situ hybridization Gene rearrangement Humans Hybridization analysis Immunohistochemistry Male mammaglobin Mammaglobin A - metabolism Middle Aged Morphology Neoplasm Proteins - metabolism Nuclei Oral cancer origin Polylactide-co-glycolide polymorphous low‐grade adenocarcinoma Salivary gland Salivary Gland Neoplasms - metabolism Salivary Gland Neoplasms - pathology Tumor cells Tumors Vimentin |
title | Mammaglobin and DOG‐1 expression in polymorphous low‐grade adenocarcinoma: an appraisal of its origin and morphology |
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