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Salivary gland fine‐needle aspiration cytology with the application of the Milan system for risk stratification and histological correlation: A retrospective 6‐year study

Background The Milan System for Reporting Salivary Gland Cytopathology (MSRSGC) is based on risk stratification. We presented our experience with fine‐needle aspiration cytology (FNAC) for the diagnosis of salivary glands lesions by applying the MSRSGC categorization to the cytological diagnoses, an...

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Published in:Diagnostic cytopathology 2020-11, Vol.48 (11), p.1067-1074
Main Authors: Rivera Rolon, Maria, Schnadig, Vicki J., Faiz, Sara, Nawgiri, Ranjana, Clement, Cecilia G.
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container_issue 11
container_start_page 1067
container_title Diagnostic cytopathology
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creator Rivera Rolon, Maria
Schnadig, Vicki J.
Faiz, Sara
Nawgiri, Ranjana
Clement, Cecilia G.
description Background The Milan System for Reporting Salivary Gland Cytopathology (MSRSGC) is based on risk stratification. We presented our experience with fine‐needle aspiration cytology (FNAC) for the diagnosis of salivary glands lesions by applying the MSRSGC categorization to the cytological diagnoses, and determined risk of malignancy (ROM) for each category. Methods Fine‐needle aspiration cytology of salivary gland lesions performed over a 6‐year period was retrieved. FNAC results were retrospectively categorized according to the MSRSGC criteria, and correlated with corresponding histologic follow‐up. ROM for each diagnostic category was calculated. Results A total of 208 FNAC of salivary gland lesions were reviewed and retrospectively categorized as: non‐diagnostic (ND) 23 (11%), non‐neoplastic (NN) 54 (26%), atypia of undetermined significance (AUS) 10 (4.8%), benign neoplasms (BN) 77 (37%), salivary gland of uncertain malignant potential (SUMP) 13 (6.3%), suspicious for malignancy (SM) 7 (3.4%), and malignant (M) 24 (11.5%). Histopathological follow‐up was available for 84 of 208 cases (40.4%). Overall concordance rate between FNAC and histology was 78.8%. Sensitivity, specificity, positive predictive value, and negative predictive value were calculated as 93.3%, 94.6%, 82.4%, and 98.2%, respectively. Diagnostic accuracy to distinguish benign from malignant disease was 94.4%. ROM for each category was ND 0%, NN 0%, AUS 75%, BN 2.2%, SUMP 28.6%, SM 50%, and M 100%. Conclusion Fine‐needle aspiration cytology continues to be an accurate diagnostic tool for most salivary gland neoplasms showing classical morphologic features. However, difficult cases with unusual or overlapping features will occur. In these situations, the use of MSRSGC risk‐stratification could be helpful to define appropriate management.
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We presented our experience with fine‐needle aspiration cytology (FNAC) for the diagnosis of salivary glands lesions by applying the MSRSGC categorization to the cytological diagnoses, and determined risk of malignancy (ROM) for each category. Methods Fine‐needle aspiration cytology of salivary gland lesions performed over a 6‐year period was retrieved. FNAC results were retrospectively categorized according to the MSRSGC criteria, and correlated with corresponding histologic follow‐up. ROM for each diagnostic category was calculated. Results A total of 208 FNAC of salivary gland lesions were reviewed and retrospectively categorized as: non‐diagnostic (ND) 23 (11%), non‐neoplastic (NN) 54 (26%), atypia of undetermined significance (AUS) 10 (4.8%), benign neoplasms (BN) 77 (37%), salivary gland of uncertain malignant potential (SUMP) 13 (6.3%), suspicious for malignancy (SM) 7 (3.4%), and malignant (M) 24 (11.5%). Histopathological follow‐up was available for 84 of 208 cases (40.4%). Overall concordance rate between FNAC and histology was 78.8%. Sensitivity, specificity, positive predictive value, and negative predictive value were calculated as 93.3%, 94.6%, 82.4%, and 98.2%, respectively. Diagnostic accuracy to distinguish benign from malignant disease was 94.4%. ROM for each category was ND 0%, NN 0%, AUS 75%, BN 2.2%, SUMP 28.6%, SM 50%, and M 100%. Conclusion Fine‐needle aspiration cytology continues to be an accurate diagnostic tool for most salivary gland neoplasms showing classical morphologic features. However, difficult cases with unusual or overlapping features will occur. In these situations, the use of MSRSGC risk‐stratification could be helpful to define appropriate management.</description><identifier>ISSN: 8755-1039</identifier><identifier>EISSN: 1097-0339</identifier><identifier>DOI: 10.1002/dc.24478</identifier><identifier>PMID: 32452653</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Cellular biology ; cytology‐histology correlation ; fine‐needle aspiration ; Milan system for reporting salivary gland cytopathology ; salivary gland lesions ; Tumors</subject><ispartof>Diagnostic cytopathology, 2020-11, Vol.48 (11), p.1067-1074</ispartof><rights>2020 Wiley Periodicals LLC</rights><rights>2020 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3498-74a86b1599db6debb9e82b969b1cb671ed3fd7f219d3021b0448d3a30a632a373</citedby><cites>FETCH-LOGICAL-c3498-74a86b1599db6debb9e82b969b1cb671ed3fd7f219d3021b0448d3a30a632a373</cites><orcidid>0000-0002-4423-0313</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32452653$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rivera Rolon, Maria</creatorcontrib><creatorcontrib>Schnadig, Vicki J.</creatorcontrib><creatorcontrib>Faiz, Sara</creatorcontrib><creatorcontrib>Nawgiri, Ranjana</creatorcontrib><creatorcontrib>Clement, Cecilia G.</creatorcontrib><title>Salivary gland fine‐needle aspiration cytology with the application of the Milan system for risk stratification and histological correlation: A retrospective 6‐year study</title><title>Diagnostic cytopathology</title><addtitle>Diagn Cytopathol</addtitle><description>Background The Milan System for Reporting Salivary Gland Cytopathology (MSRSGC) is based on risk stratification. We presented our experience with fine‐needle aspiration cytology (FNAC) for the diagnosis of salivary glands lesions by applying the MSRSGC categorization to the cytological diagnoses, and determined risk of malignancy (ROM) for each category. Methods Fine‐needle aspiration cytology of salivary gland lesions performed over a 6‐year period was retrieved. FNAC results were retrospectively categorized according to the MSRSGC criteria, and correlated with corresponding histologic follow‐up. ROM for each diagnostic category was calculated. Results A total of 208 FNAC of salivary gland lesions were reviewed and retrospectively categorized as: non‐diagnostic (ND) 23 (11%), non‐neoplastic (NN) 54 (26%), atypia of undetermined significance (AUS) 10 (4.8%), benign neoplasms (BN) 77 (37%), salivary gland of uncertain malignant potential (SUMP) 13 (6.3%), suspicious for malignancy (SM) 7 (3.4%), and malignant (M) 24 (11.5%). Histopathological follow‐up was available for 84 of 208 cases (40.4%). Overall concordance rate between FNAC and histology was 78.8%. Sensitivity, specificity, positive predictive value, and negative predictive value were calculated as 93.3%, 94.6%, 82.4%, and 98.2%, respectively. Diagnostic accuracy to distinguish benign from malignant disease was 94.4%. ROM for each category was ND 0%, NN 0%, AUS 75%, BN 2.2%, SUMP 28.6%, SM 50%, and M 100%. Conclusion Fine‐needle aspiration cytology continues to be an accurate diagnostic tool for most salivary gland neoplasms showing classical morphologic features. However, difficult cases with unusual or overlapping features will occur. In these situations, the use of MSRSGC risk‐stratification could be helpful to define appropriate management.</description><subject>Cellular biology</subject><subject>cytology‐histology correlation</subject><subject>fine‐needle aspiration</subject><subject>Milan system for reporting salivary gland cytopathology</subject><subject>salivary gland lesions</subject><subject>Tumors</subject><issn>8755-1039</issn><issn>1097-0339</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kc9u1DAQhy0EotuCxBMgS1y4pPhP4sTcqi0FpCIOwNly7EnXxRsH22mVG4_Ak_BQPAne3RYkJE6WZj59npkfQs8oOaWEsFfWnLK6brsHaEWJbCvCuXyIVl3bNBUlXB6h45SuCSGSUfEYHXFWN0w0fIV-ftLe3ei44CuvR4sHN8Kv7z9GAOsB6zS5qLMLIzZLDj5cLfjW5Q3Om9KcJu_MoRuGfemDKxKclpRhi4cQcXTpK0555xju2d03G5f2ulLz2IQYwe-br_EZjpBjSBOY7G4AizLNAjoWy2yXJ-jRoH2Cp3fvCfpy8ebz-l11-fHt-_XZZWV4LbuqrXUnetpIaXthoe8ldKyXQvbU9KKlYPlg24FRaTlhtCd13VmuOdGCM81bfoJeHrxTDN9mSFltXTLgy3oQ5qRYTYSsG9KQgr74B70OcxzLdGp3ZcKLm_wVmrJbijCoKbptubuiRO0yVNaofYYFfX4nnPst2D_gfWgFqA7ArfOw_FekztcH4W8z8anw</recordid><startdate>202011</startdate><enddate>202011</enddate><creator>Rivera Rolon, Maria</creator><creator>Schnadig, Vicki J.</creator><creator>Faiz, Sara</creator><creator>Nawgiri, Ranjana</creator><creator>Clement, Cecilia G.</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4423-0313</orcidid></search><sort><creationdate>202011</creationdate><title>Salivary gland fine‐needle aspiration cytology with the application of the Milan system for risk stratification and histological correlation: A retrospective 6‐year study</title><author>Rivera Rolon, Maria ; Schnadig, Vicki J. ; Faiz, Sara ; Nawgiri, Ranjana ; Clement, Cecilia G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3498-74a86b1599db6debb9e82b969b1cb671ed3fd7f219d3021b0448d3a30a632a373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cellular biology</topic><topic>cytology‐histology correlation</topic><topic>fine‐needle aspiration</topic><topic>Milan system for reporting salivary gland cytopathology</topic><topic>salivary gland lesions</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rivera Rolon, Maria</creatorcontrib><creatorcontrib>Schnadig, Vicki J.</creatorcontrib><creatorcontrib>Faiz, Sara</creatorcontrib><creatorcontrib>Nawgiri, Ranjana</creatorcontrib><creatorcontrib>Clement, Cecilia G.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Diagnostic cytopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rivera Rolon, Maria</au><au>Schnadig, Vicki J.</au><au>Faiz, Sara</au><au>Nawgiri, Ranjana</au><au>Clement, Cecilia G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Salivary gland fine‐needle aspiration cytology with the application of the Milan system for risk stratification and histological correlation: A retrospective 6‐year study</atitle><jtitle>Diagnostic cytopathology</jtitle><addtitle>Diagn Cytopathol</addtitle><date>2020-11</date><risdate>2020</risdate><volume>48</volume><issue>11</issue><spage>1067</spage><epage>1074</epage><pages>1067-1074</pages><issn>8755-1039</issn><eissn>1097-0339</eissn><abstract>Background The Milan System for Reporting Salivary Gland Cytopathology (MSRSGC) is based on risk stratification. We presented our experience with fine‐needle aspiration cytology (FNAC) for the diagnosis of salivary glands lesions by applying the MSRSGC categorization to the cytological diagnoses, and determined risk of malignancy (ROM) for each category. Methods Fine‐needle aspiration cytology of salivary gland lesions performed over a 6‐year period was retrieved. FNAC results were retrospectively categorized according to the MSRSGC criteria, and correlated with corresponding histologic follow‐up. ROM for each diagnostic category was calculated. Results A total of 208 FNAC of salivary gland lesions were reviewed and retrospectively categorized as: non‐diagnostic (ND) 23 (11%), non‐neoplastic (NN) 54 (26%), atypia of undetermined significance (AUS) 10 (4.8%), benign neoplasms (BN) 77 (37%), salivary gland of uncertain malignant potential (SUMP) 13 (6.3%), suspicious for malignancy (SM) 7 (3.4%), and malignant (M) 24 (11.5%). Histopathological follow‐up was available for 84 of 208 cases (40.4%). Overall concordance rate between FNAC and histology was 78.8%. Sensitivity, specificity, positive predictive value, and negative predictive value were calculated as 93.3%, 94.6%, 82.4%, and 98.2%, respectively. Diagnostic accuracy to distinguish benign from malignant disease was 94.4%. ROM for each category was ND 0%, NN 0%, AUS 75%, BN 2.2%, SUMP 28.6%, SM 50%, and M 100%. Conclusion Fine‐needle aspiration cytology continues to be an accurate diagnostic tool for most salivary gland neoplasms showing classical morphologic features. However, difficult cases with unusual or overlapping features will occur. In these situations, the use of MSRSGC risk‐stratification could be helpful to define appropriate management.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>32452653</pmid><doi>10.1002/dc.24478</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-4423-0313</orcidid></addata></record>
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subjects Cellular biology
cytology‐histology correlation
fine‐needle aspiration
Milan system for reporting salivary gland cytopathology
salivary gland lesions
Tumors
title Salivary gland fine‐needle aspiration cytology with the application of the Milan system for risk stratification and histological correlation: A retrospective 6‐year study
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