Adenocarcinoma in situ of the uterine cervix. Screening and diagnostic errors in Papanicolaou smears

Little attention has been given to the reasons for failure to detect adenocarcinoma in situ (AIS) of the uterine cervix in Papanicolaou (Pap) smears. In the current study, the authors examined a series of screening or diagnostic errors in cases in which the final histologic diagnosis was either AIS...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancer 2004-10, Vol.102 (5), p.280-287
Hauptverfasser: RUBA, Sukeerat, SCHOOLLAND, Meike, ALLPRESS, Stephen, STERRETT, Gregory
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 287
container_issue 5
container_start_page 280
container_title Cancer
container_volume 102
creator RUBA, Sukeerat
SCHOOLLAND, Meike
ALLPRESS, Stephen
STERRETT, Gregory
description Little attention has been given to the reasons for failure to detect adenocarcinoma in situ (AIS) of the uterine cervix in Papanicolaou (Pap) smears. In the current study, the authors examined a series of screening or diagnostic errors in cases in which the final histologic diagnosis was either AIS or AIS combined with a high-grade squamous intraepithelial lesion (AIS + HSIL). Smears obtained in the 3 years before histologically proven AIS or AIS + HSIL was diagnosed and within a specified 6-year period (1993-1998) were reviewed and reclassified. All were conventional Pap smears. The smears studied were those with a review diagnosis of possible or definite high-grade epithelial abnormality that initially were reported by a cytotechnologist to be negative (screening error) or that were reported by a pathologist to be negative, unsatisfactory, or indicative of a low-grade epithelial abnormality (diagnostic error). A semiquantitative, blinded assessment of the frequency of cytologic criteria for the diagnosis of AIS was made for smears with erroneous diagnoses compared with a series of smears that yielded true-positive findings. Sampling errors, which were defined as cases in which smears did not have sufficient evidence for a diagnosis of possible or definite AIS or HSIL on review, accounted for 35.1% and 36% of all smears from patients with a biopsy diagnosis of AIS and patients with a biopsy diagnosis of AIS + HSIL, respectively. With regard to AIS, there were 3 screening errors and 5 diagnostic errors, accounting for 10.4% of 77 smears. Minimal, poorly preserved material was evident in four smears, including three smears with only one sheet of abnormal glandular cells. In four other smears, there was a moderate amount of adequately preserved glandular material, mainly in large sheets, with varying degrees of crowding and hyperchromasia. With regard to AIS + HSIL, there were 6 screening errors and 6 diagnostic errors, accounting for 13.5% of 89 smears. In those smears, there generally was a moderate amount of abnormal material in the form of crowded groups of suboptimally preserved, hyperchromatic squamous cells. Only two of those smears yielded findings of possible abnormal glandular cells. Only 3 of 20 errors occurred in smears that were examined during the last 3 years of the study. In the semiquantitative assessment, smears with erroneous findings were shown to contain far less abnormal material than true-positive smears and to exhibit a corresponding
doi_str_mv 10.1002/cncr.20600
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67075847</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67075847</sourcerecordid><originalsourceid>FETCH-LOGICAL-c204t-3c117274358e08db6fd4e6da2be245c0db65433c47c9db52b115497fa509aba33</originalsourceid><addsrcrecordid>eNpFkE1r3DAQhkVJabZJL_kBQZf0UPBm9GXZxxCatBBooS30ZsbSOFWxpY1kh_bfx5ss5DTM8LwvzMPYmYCtAJCXLrq8lVADvGEbAa2tQGh5xDYA0FRGq9_H7H0pf9fVSqPesWNhlK1F22yYv_IUk8PsQkwT8hB5CfPC08DnP8SXmXKIxB3lx_Bvy3-4TBRDvOcYPfcB72Mqc3Ccck657OPfcYcxuDRiWniZCHM5ZW8HHAt9OMwT9uvm88_rL9Xdt9uv11d3lZOg50o5Iay0WpmGoPF9PXhNtUfZk9TGwXpZn1FOW9f63sheCKNbO6CBFntU6oR9fOnd5fSwUJm7KRRH44iR0lK62oI1jbYr-OkFdDmVkmnodjlMmP93Arq9027vtHt2usLnh9aln8i_ogeJK3BxALA4HIeM0YXyytWiaWVr1BOQdIAV</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67075847</pqid></control><display><type>article</type><title>Adenocarcinoma in situ of the uterine cervix. Screening and diagnostic errors in Papanicolaou smears</title><source>MEDLINE</source><source>Wiley Free Content</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Wiley Online Library All Journals</source><source>Alma/SFX Local Collection</source><creator>RUBA, Sukeerat ; SCHOOLLAND, Meike ; ALLPRESS, Stephen ; STERRETT, Gregory</creator><creatorcontrib>RUBA, Sukeerat ; SCHOOLLAND, Meike ; ALLPRESS, Stephen ; STERRETT, Gregory</creatorcontrib><description>Little attention has been given to the reasons for failure to detect adenocarcinoma in situ (AIS) of the uterine cervix in Papanicolaou (Pap) smears. In the current study, the authors examined a series of screening or diagnostic errors in cases in which the final histologic diagnosis was either AIS or AIS combined with a high-grade squamous intraepithelial lesion (AIS + HSIL). Smears obtained in the 3 years before histologically proven AIS or AIS + HSIL was diagnosed and within a specified 6-year period (1993-1998) were reviewed and reclassified. All were conventional Pap smears. The smears studied were those with a review diagnosis of possible or definite high-grade epithelial abnormality that initially were reported by a cytotechnologist to be negative (screening error) or that were reported by a pathologist to be negative, unsatisfactory, or indicative of a low-grade epithelial abnormality (diagnostic error). A semiquantitative, blinded assessment of the frequency of cytologic criteria for the diagnosis of AIS was made for smears with erroneous diagnoses compared with a series of smears that yielded true-positive findings. Sampling errors, which were defined as cases in which smears did not have sufficient evidence for a diagnosis of possible or definite AIS or HSIL on review, accounted for 35.1% and 36% of all smears from patients with a biopsy diagnosis of AIS and patients with a biopsy diagnosis of AIS + HSIL, respectively. With regard to AIS, there were 3 screening errors and 5 diagnostic errors, accounting for 10.4% of 77 smears. Minimal, poorly preserved material was evident in four smears, including three smears with only one sheet of abnormal glandular cells. In four other smears, there was a moderate amount of adequately preserved glandular material, mainly in large sheets, with varying degrees of crowding and hyperchromasia. With regard to AIS + HSIL, there were 6 screening errors and 6 diagnostic errors, accounting for 13.5% of 89 smears. In those smears, there generally was a moderate amount of abnormal material in the form of crowded groups of suboptimally preserved, hyperchromatic squamous cells. Only two of those smears yielded findings of possible abnormal glandular cells. Only 3 of 20 errors occurred in smears that were examined during the last 3 years of the study. In the semiquantitative assessment, smears with erroneous findings were shown to contain far less abnormal material than true-positive smears and to exhibit a corresponding paucity of diagnostic criteria. Sampling errors were the main cause of false-negative reports in cases of AIS and AIS + HSIL. The primary factors that contributed to screening or diagnostic errors in AIS were minimal, poorly preserved abnormal material and an overly conservative approach to the assessment of unusual large sheets or aggregates of glandular cells. With regard to AIS + HSIL, most laboratory errors were related to the presence of crowded groups of squamous epithelial cells. There were fewer errors in the last 3 years of the study, raising the possibility of improvement over time.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.20600</identifier><identifier>PMID: 15376198</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York, NY: Wiley-Liss</publisher><subject>Adenocarcinoma - diagnosis ; Adenocarcinoma - prevention &amp; control ; Biological and medical sciences ; Cervical Intraepithelial Neoplasia - diagnosis ; Cervical Intraepithelial Neoplasia - prevention &amp; control ; Cervix Uteri - pathology ; Diagnostic Errors ; False Negative Reactions ; Female ; Humans ; Medical sciences ; Papanicolaou Test ; Tissue Preservation ; Tumors ; Uterine Neoplasms - diagnosis ; Uterine Neoplasms - prevention &amp; control ; Vaginal Smears</subject><ispartof>Cancer, 2004-10, Vol.102 (5), p.280-287</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c204t-3c117274358e08db6fd4e6da2be245c0db65433c47c9db52b115497fa509aba33</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=16189295$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15376198$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RUBA, Sukeerat</creatorcontrib><creatorcontrib>SCHOOLLAND, Meike</creatorcontrib><creatorcontrib>ALLPRESS, Stephen</creatorcontrib><creatorcontrib>STERRETT, Gregory</creatorcontrib><title>Adenocarcinoma in situ of the uterine cervix. Screening and diagnostic errors in Papanicolaou smears</title><title>Cancer</title><addtitle>Cancer</addtitle><description>Little attention has been given to the reasons for failure to detect adenocarcinoma in situ (AIS) of the uterine cervix in Papanicolaou (Pap) smears. In the current study, the authors examined a series of screening or diagnostic errors in cases in which the final histologic diagnosis was either AIS or AIS combined with a high-grade squamous intraepithelial lesion (AIS + HSIL). Smears obtained in the 3 years before histologically proven AIS or AIS + HSIL was diagnosed and within a specified 6-year period (1993-1998) were reviewed and reclassified. All were conventional Pap smears. The smears studied were those with a review diagnosis of possible or definite high-grade epithelial abnormality that initially were reported by a cytotechnologist to be negative (screening error) or that were reported by a pathologist to be negative, unsatisfactory, or indicative of a low-grade epithelial abnormality (diagnostic error). A semiquantitative, blinded assessment of the frequency of cytologic criteria for the diagnosis of AIS was made for smears with erroneous diagnoses compared with a series of smears that yielded true-positive findings. Sampling errors, which were defined as cases in which smears did not have sufficient evidence for a diagnosis of possible or definite AIS or HSIL on review, accounted for 35.1% and 36% of all smears from patients with a biopsy diagnosis of AIS and patients with a biopsy diagnosis of AIS + HSIL, respectively. With regard to AIS, there were 3 screening errors and 5 diagnostic errors, accounting for 10.4% of 77 smears. Minimal, poorly preserved material was evident in four smears, including three smears with only one sheet of abnormal glandular cells. In four other smears, there was a moderate amount of adequately preserved glandular material, mainly in large sheets, with varying degrees of crowding and hyperchromasia. With regard to AIS + HSIL, there were 6 screening errors and 6 diagnostic errors, accounting for 13.5% of 89 smears. In those smears, there generally was a moderate amount of abnormal material in the form of crowded groups of suboptimally preserved, hyperchromatic squamous cells. Only two of those smears yielded findings of possible abnormal glandular cells. Only 3 of 20 errors occurred in smears that were examined during the last 3 years of the study. In the semiquantitative assessment, smears with erroneous findings were shown to contain far less abnormal material than true-positive smears and to exhibit a corresponding paucity of diagnostic criteria. Sampling errors were the main cause of false-negative reports in cases of AIS and AIS + HSIL. The primary factors that contributed to screening or diagnostic errors in AIS were minimal, poorly preserved abnormal material and an overly conservative approach to the assessment of unusual large sheets or aggregates of glandular cells. With regard to AIS + HSIL, most laboratory errors were related to the presence of crowded groups of squamous epithelial cells. There were fewer errors in the last 3 years of the study, raising the possibility of improvement over time.</description><subject>Adenocarcinoma - diagnosis</subject><subject>Adenocarcinoma - prevention &amp; control</subject><subject>Biological and medical sciences</subject><subject>Cervical Intraepithelial Neoplasia - diagnosis</subject><subject>Cervical Intraepithelial Neoplasia - prevention &amp; control</subject><subject>Cervix Uteri - pathology</subject><subject>Diagnostic Errors</subject><subject>False Negative Reactions</subject><subject>Female</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Papanicolaou Test</subject><subject>Tissue Preservation</subject><subject>Tumors</subject><subject>Uterine Neoplasms - diagnosis</subject><subject>Uterine Neoplasms - prevention &amp; control</subject><subject>Vaginal Smears</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1r3DAQhkVJabZJL_kBQZf0UPBm9GXZxxCatBBooS30ZsbSOFWxpY1kh_bfx5ss5DTM8LwvzMPYmYCtAJCXLrq8lVADvGEbAa2tQGh5xDYA0FRGq9_H7H0pf9fVSqPesWNhlK1F22yYv_IUk8PsQkwT8hB5CfPC08DnP8SXmXKIxB3lx_Bvy3-4TBRDvOcYPfcB72Mqc3Ccck657OPfcYcxuDRiWniZCHM5ZW8HHAt9OMwT9uvm88_rL9Xdt9uv11d3lZOg50o5Iay0WpmGoPF9PXhNtUfZk9TGwXpZn1FOW9f63sheCKNbO6CBFntU6oR9fOnd5fSwUJm7KRRH44iR0lK62oI1jbYr-OkFdDmVkmnodjlMmP93Arq9027vtHt2usLnh9aln8i_ogeJK3BxALA4HIeM0YXyytWiaWVr1BOQdIAV</recordid><startdate>20041025</startdate><enddate>20041025</enddate><creator>RUBA, Sukeerat</creator><creator>SCHOOLLAND, Meike</creator><creator>ALLPRESS, Stephen</creator><creator>STERRETT, Gregory</creator><general>Wiley-Liss</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>20041025</creationdate><title>Adenocarcinoma in situ of the uterine cervix. Screening and diagnostic errors in Papanicolaou smears</title><author>RUBA, Sukeerat ; SCHOOLLAND, Meike ; ALLPRESS, Stephen ; STERRETT, Gregory</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c204t-3c117274358e08db6fd4e6da2be245c0db65433c47c9db52b115497fa509aba33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adenocarcinoma - diagnosis</topic><topic>Adenocarcinoma - prevention &amp; control</topic><topic>Biological and medical sciences</topic><topic>Cervical Intraepithelial Neoplasia - diagnosis</topic><topic>Cervical Intraepithelial Neoplasia - prevention &amp; control</topic><topic>Cervix Uteri - pathology</topic><topic>Diagnostic Errors</topic><topic>False Negative Reactions</topic><topic>Female</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Papanicolaou Test</topic><topic>Tissue Preservation</topic><topic>Tumors</topic><topic>Uterine Neoplasms - diagnosis</topic><topic>Uterine Neoplasms - prevention &amp; control</topic><topic>Vaginal Smears</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RUBA, Sukeerat</creatorcontrib><creatorcontrib>SCHOOLLAND, Meike</creatorcontrib><creatorcontrib>ALLPRESS, Stephen</creatorcontrib><creatorcontrib>STERRETT, Gregory</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>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>RUBA, Sukeerat</au><au>SCHOOLLAND, Meike</au><au>ALLPRESS, Stephen</au><au>STERRETT, Gregory</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adenocarcinoma in situ of the uterine cervix. Screening and diagnostic errors in Papanicolaou smears</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2004-10-25</date><risdate>2004</risdate><volume>102</volume><issue>5</issue><spage>280</spage><epage>287</epage><pages>280-287</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>Little attention has been given to the reasons for failure to detect adenocarcinoma in situ (AIS) of the uterine cervix in Papanicolaou (Pap) smears. In the current study, the authors examined a series of screening or diagnostic errors in cases in which the final histologic diagnosis was either AIS or AIS combined with a high-grade squamous intraepithelial lesion (AIS + HSIL). Smears obtained in the 3 years before histologically proven AIS or AIS + HSIL was diagnosed and within a specified 6-year period (1993-1998) were reviewed and reclassified. All were conventional Pap smears. The smears studied were those with a review diagnosis of possible or definite high-grade epithelial abnormality that initially were reported by a cytotechnologist to be negative (screening error) or that were reported by a pathologist to be negative, unsatisfactory, or indicative of a low-grade epithelial abnormality (diagnostic error). A semiquantitative, blinded assessment of the frequency of cytologic criteria for the diagnosis of AIS was made for smears with erroneous diagnoses compared with a series of smears that yielded true-positive findings. Sampling errors, which were defined as cases in which smears did not have sufficient evidence for a diagnosis of possible or definite AIS or HSIL on review, accounted for 35.1% and 36% of all smears from patients with a biopsy diagnosis of AIS and patients with a biopsy diagnosis of AIS + HSIL, respectively. With regard to AIS, there were 3 screening errors and 5 diagnostic errors, accounting for 10.4% of 77 smears. Minimal, poorly preserved material was evident in four smears, including three smears with only one sheet of abnormal glandular cells. In four other smears, there was a moderate amount of adequately preserved glandular material, mainly in large sheets, with varying degrees of crowding and hyperchromasia. With regard to AIS + HSIL, there were 6 screening errors and 6 diagnostic errors, accounting for 13.5% of 89 smears. In those smears, there generally was a moderate amount of abnormal material in the form of crowded groups of suboptimally preserved, hyperchromatic squamous cells. Only two of those smears yielded findings of possible abnormal glandular cells. Only 3 of 20 errors occurred in smears that were examined during the last 3 years of the study. In the semiquantitative assessment, smears with erroneous findings were shown to contain far less abnormal material than true-positive smears and to exhibit a corresponding paucity of diagnostic criteria. Sampling errors were the main cause of false-negative reports in cases of AIS and AIS + HSIL. The primary factors that contributed to screening or diagnostic errors in AIS were minimal, poorly preserved abnormal material and an overly conservative approach to the assessment of unusual large sheets or aggregates of glandular cells. With regard to AIS + HSIL, most laboratory errors were related to the presence of crowded groups of squamous epithelial cells. There were fewer errors in the last 3 years of the study, raising the possibility of improvement over time.</abstract><cop>New York, NY</cop><pub>Wiley-Liss</pub><pmid>15376198</pmid><doi>10.1002/cncr.20600</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0008-543X
ispartof Cancer, 2004-10, Vol.102 (5), p.280-287
issn 0008-543X
1097-0142
language eng
recordid cdi_proquest_miscellaneous_67075847
source MEDLINE; Wiley Free Content; EZB-FREE-00999 freely available EZB journals; Wiley Online Library All Journals; Alma/SFX Local Collection
subjects Adenocarcinoma - diagnosis
Adenocarcinoma - prevention & control
Biological and medical sciences
Cervical Intraepithelial Neoplasia - diagnosis
Cervical Intraepithelial Neoplasia - prevention & control
Cervix Uteri - pathology
Diagnostic Errors
False Negative Reactions
Female
Humans
Medical sciences
Papanicolaou Test
Tissue Preservation
Tumors
Uterine Neoplasms - diagnosis
Uterine Neoplasms - prevention & control
Vaginal Smears
title Adenocarcinoma in situ of the uterine cervix. Screening and diagnostic errors in Papanicolaou smears
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T12%3A34%3A20IST&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=Adenocarcinoma%20in%20situ%20of%20the%20uterine%20cervix.%20Screening%20and%20diagnostic%20errors%20in%20Papanicolaou%20smears&rft.jtitle=Cancer&rft.au=RUBA,%20Sukeerat&rft.date=2004-10-25&rft.volume=102&rft.issue=5&rft.spage=280&rft.epage=287&rft.pages=280-287&rft.issn=0008-543X&rft.eissn=1097-0142&rft.coden=CANCAR&rft_id=info:doi/10.1002/cncr.20600&rft_dat=%3Cproquest_cross%3E67075847%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=67075847&rft_id=info:pmid/15376198&rfr_iscdi=true