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Correlating routine cytology, quantitative nuclear morphometry by digital image analysis, and genetic alterations by fluorescence in situ hybridization to assess the sensitivity of cytology for detecting pancreatobiliary tract malignancy
Routine cytologic (RC), fluorescence in situ hybridization (FISH), digital image analysis (DIA), and quantifiable morphometric results from 284 pancreatobiliary stricture brushings were compared. We chose specific DIA nuclear features assessed by pathologists in evaluating RC specimens, such as area...
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Published in: | American journal of clinical pathology 2007-08, Vol.128 (2), p.272-279 |
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creator | BARR FRITCHER, Emily G KIPP, Benjamin R SLEZAK, Jeffrey M MORENO-LUNA, Laura E GORES, Gregory J LEVY, Michael J ROBERTS, Lewis R HALLING, Kevin C SEBO, Thomas J |
description | Routine cytologic (RC), fluorescence in situ hybridization (FISH), digital image analysis (DIA), and quantifiable morphometric results from 284 pancreatobiliary stricture brushings were compared. We chose specific DIA nuclear features assessed by pathologists in evaluating RC specimens, such as area and shape. A visual nuclear morphometric score (VNMS) was calculated. There was a difference (P < .001) in the mean VNMS when RC results were classified as negative (11.5), atypical (12.5), suspicious (13.8), and positive (16.5). The mean VNMS of specimens diagnosed as disomy (11.3), trisomy 7 (12.1), and polysomy (14.7) by FISH was also different (P < .001). There was no difference in the VNMS of false-negative and true-negative cytologic specimens (P = .225). Our findings substantiate the relationship between cell nuclear visual alterations and genetic FISH abnormalities. The low sensitivity of cytologic examination for pancreatobiliary carcinoma is due to an absence of tumor cells or the presence of well-differentiated tumor lacking recognizable nuclear atypia. |
doi_str_mv | 10.1309/BC6DY755Q3T5W9EE |
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We chose specific DIA nuclear features assessed by pathologists in evaluating RC specimens, such as area and shape. A visual nuclear morphometric score (VNMS) was calculated. There was a difference (P < .001) in the mean VNMS when RC results were classified as negative (11.5), atypical (12.5), suspicious (13.8), and positive (16.5). The mean VNMS of specimens diagnosed as disomy (11.3), trisomy 7 (12.1), and polysomy (14.7) by FISH was also different (P < .001). There was no difference in the VNMS of false-negative and true-negative cytologic specimens (P = .225). Our findings substantiate the relationship between cell nuclear visual alterations and genetic FISH abnormalities. The low sensitivity of cytologic examination for pancreatobiliary carcinoma is due to an absence of tumor cells or the presence of well-differentiated tumor lacking recognizable nuclear atypia.</description><identifier>ISSN: 0002-9173</identifier><identifier>EISSN: 1943-7722</identifier><identifier>DOI: 10.1309/BC6DY755Q3T5W9EE</identifier><identifier>PMID: 17638662</identifier><identifier>CODEN: AJCPAI</identifier><language>eng</language><publisher>Chicago, IL: American Society of Clinical Pathologists</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Bile Duct Neoplasms - genetics ; Bile Duct Neoplasms - pathology ; Biological and medical sciences ; Cell Nucleus - pathology ; Child ; Chromosome Aberrations ; Female ; Humans ; Image Processing, Computer-Assisted - methods ; In Situ Hybridization, Fluorescence - methods ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Middle Aged ; Pancreatic Neoplasms - genetics ; Pancreatic Neoplasms - pathology ; Pathology. Cytology. Biochemistry. Spectrometry. 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We chose specific DIA nuclear features assessed by pathologists in evaluating RC specimens, such as area and shape. A visual nuclear morphometric score (VNMS) was calculated. There was a difference (P < .001) in the mean VNMS when RC results were classified as negative (11.5), atypical (12.5), suspicious (13.8), and positive (16.5). The mean VNMS of specimens diagnosed as disomy (11.3), trisomy 7 (12.1), and polysomy (14.7) by FISH was also different (P < .001). There was no difference in the VNMS of false-negative and true-negative cytologic specimens (P = .225). Our findings substantiate the relationship between cell nuclear visual alterations and genetic FISH abnormalities. The low sensitivity of cytologic examination for pancreatobiliary carcinoma is due to an absence of tumor cells or the presence of well-differentiated tumor lacking recognizable nuclear atypia.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Bile Duct Neoplasms - genetics</subject><subject>Bile Duct Neoplasms - pathology</subject><subject>Biological and medical sciences</subject><subject>Cell Nucleus - pathology</subject><subject>Child</subject><subject>Chromosome Aberrations</subject><subject>Female</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>In Situ Hybridization, Fluorescence - methods</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pancreatic Neoplasms - genetics</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Sensitivity and Specificity</subject><subject>Trisomy</subject><issn>0002-9173</issn><issn>1943-7722</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNpdkkFv1DAQhSMEotvCnROaC5wacOxNvDnSZQtIlRBSEeIUTZxx1sixt7ZTKfxn_gNuu6ISp7E033t6M-OieFWxd5Vg7fuLbfPxp6zrb-K6_tHudk-KVdWuRSkl50-LFWOMl20lxUlxGuMvxiq-YevnxUklG7FpGr4q_mx9CGQxGTdC8HOuBGpJ3vpxOYebGV0yKbdvCdysLGGAyYfD3k-UwgL9AoMZM2HBTDgSoEO7RBPP82uAkRwlowBtopBdvIt3Em1nHygqcorAOIgmzbBf-mAG8_seg-QBY6QYIe0JIrnMmFuTFvD6X0DQPsBAidR9_gM6FQiT7401mNOlgCrBhNaMLveWF8UzjTbSy2M9K75f7q63n8urr5--bD9clUpwmcpacKzaTct7OQgpqRHIZVuTqIVGmRnVkGqUZqpdS11r3Whd8_Wm73uJFevFWfH2wfcQ_M1MMXWTydNai478HDvJJBeMrTPIHkAVfIyBdHcIeY9h6SrW3Z24-__EWfL66D33Ew2PguNNM_DmCGBUaHXIk5v4yG3yD-G8FX8B61G5CQ</recordid><startdate>20070801</startdate><enddate>20070801</enddate><creator>BARR FRITCHER, Emily G</creator><creator>KIPP, Benjamin R</creator><creator>SLEZAK, Jeffrey M</creator><creator>MORENO-LUNA, Laura E</creator><creator>GORES, Gregory J</creator><creator>LEVY, Michael J</creator><creator>ROBERTS, Lewis R</creator><creator>HALLING, Kevin C</creator><creator>SEBO, Thomas J</creator><general>American Society of Clinical Pathologists</general><scope>IQODW</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>20070801</creationdate><title>Correlating routine cytology, quantitative nuclear morphometry by digital image analysis, and genetic alterations by fluorescence in situ hybridization to assess the sensitivity of cytology for detecting pancreatobiliary tract malignancy</title><author>BARR FRITCHER, Emily G ; KIPP, Benjamin R ; SLEZAK, Jeffrey M ; MORENO-LUNA, Laura E ; GORES, Gregory J ; LEVY, Michael J ; ROBERTS, Lewis R ; HALLING, Kevin C ; SEBO, Thomas J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-532a19892b7d377e63a2795e353fa7c32c6ec6cf0c947f5ff6ff5248bbb7a10b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Bile Duct Neoplasms - genetics</topic><topic>Bile Duct Neoplasms - pathology</topic><topic>Biological and medical sciences</topic><topic>Cell Nucleus - pathology</topic><topic>Child</topic><topic>Chromosome Aberrations</topic><topic>Female</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>In Situ Hybridization, Fluorescence - methods</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pancreatic Neoplasms - genetics</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Sensitivity and Specificity</topic><topic>Trisomy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BARR FRITCHER, Emily G</creatorcontrib><creatorcontrib>KIPP, Benjamin R</creatorcontrib><creatorcontrib>SLEZAK, Jeffrey M</creatorcontrib><creatorcontrib>MORENO-LUNA, Laura E</creatorcontrib><creatorcontrib>GORES, Gregory J</creatorcontrib><creatorcontrib>LEVY, Michael J</creatorcontrib><creatorcontrib>ROBERTS, Lewis R</creatorcontrib><creatorcontrib>HALLING, Kevin C</creatorcontrib><creatorcontrib>SEBO, Thomas J</creatorcontrib><collection>Pascal-Francis</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>American journal of clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BARR FRITCHER, Emily G</au><au>KIPP, Benjamin R</au><au>SLEZAK, Jeffrey M</au><au>MORENO-LUNA, Laura E</au><au>GORES, Gregory J</au><au>LEVY, Michael J</au><au>ROBERTS, Lewis R</au><au>HALLING, Kevin C</au><au>SEBO, Thomas J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlating routine cytology, quantitative nuclear morphometry by digital image analysis, and genetic alterations by fluorescence in situ hybridization to assess the sensitivity of cytology for detecting pancreatobiliary tract malignancy</atitle><jtitle>American journal of clinical pathology</jtitle><addtitle>Am J Clin Pathol</addtitle><date>2007-08-01</date><risdate>2007</risdate><volume>128</volume><issue>2</issue><spage>272</spage><epage>279</epage><pages>272-279</pages><issn>0002-9173</issn><eissn>1943-7722</eissn><coden>AJCPAI</coden><abstract>Routine cytologic (RC), fluorescence in situ hybridization (FISH), digital image analysis (DIA), and quantifiable morphometric results from 284 pancreatobiliary stricture brushings were compared. We chose specific DIA nuclear features assessed by pathologists in evaluating RC specimens, such as area and shape. A visual nuclear morphometric score (VNMS) was calculated. There was a difference (P < .001) in the mean VNMS when RC results were classified as negative (11.5), atypical (12.5), suspicious (13.8), and positive (16.5). The mean VNMS of specimens diagnosed as disomy (11.3), trisomy 7 (12.1), and polysomy (14.7) by FISH was also different (P < .001). There was no difference in the VNMS of false-negative and true-negative cytologic specimens (P = .225). Our findings substantiate the relationship between cell nuclear visual alterations and genetic FISH abnormalities. The low sensitivity of cytologic examination for pancreatobiliary carcinoma is due to an absence of tumor cells or the presence of well-differentiated tumor lacking recognizable nuclear atypia.</abstract><cop>Chicago, IL</cop><pub>American Society of Clinical Pathologists</pub><pmid>17638662</pmid><doi>10.1309/BC6DY755Q3T5W9EE</doi><tpages>8</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Bile Duct Neoplasms - genetics Bile Duct Neoplasms - pathology Biological and medical sciences Cell Nucleus - pathology Child Chromosome Aberrations Female Humans Image Processing, Computer-Assisted - methods In Situ Hybridization, Fluorescence - methods Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Middle Aged Pancreatic Neoplasms - genetics Pancreatic Neoplasms - pathology Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Sensitivity and Specificity Trisomy |
title | Correlating routine cytology, quantitative nuclear morphometry by digital image analysis, and genetic alterations by fluorescence in situ hybridization to assess the sensitivity of cytology for detecting pancreatobiliary tract malignancy |
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