Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:American journal of clinical pathology 2007-08, Vol.128 (2), p.272-279
Main Authors: 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
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c327t-532a19892b7d377e63a2795e353fa7c32c6ec6cf0c947f5ff6ff5248bbb7a10b3
cites cdi_FETCH-LOGICAL-c327t-532a19892b7d377e63a2795e353fa7c32c6ec6cf0c947f5ff6ff5248bbb7a10b3
container_end_page 279
container_issue 2
container_start_page 272
container_title American journal of clinical pathology
container_volume 128
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70723004</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70723004</sourcerecordid><originalsourceid>FETCH-LOGICAL-c327t-532a19892b7d377e63a2795e353fa7c32c6ec6cf0c947f5ff6ff5248bbb7a10b3</originalsourceid><addsrcrecordid>eNpdkkFv1DAQhSMEotvCnROaC5wacOxNvDnSZQtIlRBSEeIUTZxx1sixt7ZTKfxn_gNuu6ISp7E033t6M-OieFWxd5Vg7fuLbfPxp6zrb-K6_tHudk-KVdWuRSkl50-LFWOMl20lxUlxGuMvxiq-YevnxUklG7FpGr4q_mx9CGQxGTdC8HOuBGpJ3vpxOYebGV0yKbdvCdysLGGAyYfD3k-UwgL9AoMZM2HBTDgSoEO7RBPP82uAkRwlowBtopBdvIt3Em1nHygqcorAOIgmzbBf-mAG8_seg-QBY6QYIe0JIrnMmFuTFvD6X0DQPsBAidR9_gM6FQiT7401mNOlgCrBhNaMLveWF8UzjTbSy2M9K75f7q63n8urr5--bD9clUpwmcpacKzaTct7OQgpqRHIZVuTqIVGmRnVkGqUZqpdS11r3Whd8_Wm73uJFevFWfH2wfcQ_M1MMXWTydNai478HDvJJBeMrTPIHkAVfIyBdHcIeY9h6SrW3Z24-__EWfL66D33Ew2PguNNM_DmCGBUaHXIk5v4yG3yD-G8FX8B61G5CQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70723004</pqid></control><display><type>article</type><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><source>Oxford Journals Online</source><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</creator><creatorcontrib>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</creatorcontrib><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 &lt; .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 &lt; .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. Miscellaneous investigative techniques ; Sensitivity and Specificity ; Trisomy</subject><ispartof>American journal of clinical pathology, 2007-08, Vol.128 (2), p.272-279</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c327t-532a19892b7d377e63a2795e353fa7c32c6ec6cf0c947f5ff6ff5248bbb7a10b3</citedby><cites>FETCH-LOGICAL-c327t-532a19892b7d377e63a2795e353fa7c32c6ec6cf0c947f5ff6ff5248bbb7a10b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18943229$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17638662$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><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><title>American journal of clinical pathology</title><addtitle>Am J Clin Pathol</addtitle><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 &lt; .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 &lt; .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 &lt; .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 &lt; .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>
fulltext fulltext
identifier ISSN: 0002-9173
ispartof American journal of clinical pathology, 2007-08, Vol.128 (2), p.272-279
issn 0002-9173
1943-7722
language eng
recordid cdi_proquest_miscellaneous_70723004
source Oxford Journals Online
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T01%3A05%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Correlating%20routine%20cytology,%20quantitative%20nuclear%20morphometry%20by%20digital%20image%20analysis,%20and%20genetic%20alterations%20by%20fluorescence%20in%20situ%20hybridization%20to%20assess%20the%20sensitivity%20of%20cytology%20for%20detecting%20pancreatobiliary%20tract%20malignancy&rft.jtitle=American%20journal%20of%20clinical%20pathology&rft.au=BARR%20FRITCHER,%20Emily%20G&rft.date=2007-08-01&rft.volume=128&rft.issue=2&rft.spage=272&rft.epage=279&rft.pages=272-279&rft.issn=0002-9173&rft.eissn=1943-7722&rft.coden=AJCPAI&rft_id=info:doi/10.1309/BC6DY755Q3T5W9EE&rft_dat=%3Cproquest_cross%3E70723004%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c327t-532a19892b7d377e63a2795e353fa7c32c6ec6cf0c947f5ff6ff5248bbb7a10b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=70723004&rft_id=info:pmid/17638662&rfr_iscdi=true