Is Mode of Presentation of B3 Breast Core Biopsies (Screen-Detected or Symptomatic) a Distinguishing Factor in the Final Histopathologic Result or Risk of Diagnosis of Malignancy?

Background The relation between histopathologic subclassification and mode of patient presentation (with a screen-detected vs. symptomatic lesion) with an abnormality in the breast core biopsy classified as having uncertain malignant potential (B3) has not been previously examined. We compared the h...

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Veröffentlicht in:World journal of surgery 2013-11, Vol.37 (11), p.2607-2612
Hauptverfasser: MacLean, Gael M., Courtney, Stephen P., Umeh, Hilary, Sanjeev, Siriathan, McCormick, Colin, Smith, Brendan M.
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container_end_page 2612
container_issue 11
container_start_page 2607
container_title World journal of surgery
container_volume 37
creator MacLean, Gael M.
Courtney, Stephen P.
Umeh, Hilary
Sanjeev, Siriathan
McCormick, Colin
Smith, Brendan M.
description Background The relation between histopathologic subclassification and mode of patient presentation (with a screen-detected vs. symptomatic lesion) with an abnormality in the breast core biopsy classified as having uncertain malignant potential (B3) has not been previously examined. We compared the histopathologic subclassification of these lesions and the frequency of malignancy in screen-detected and symptomatic patient groups. Methods All B3 core biopsies from one breast unit at the Royal Berkshire Hospital over a 5-year period (2006–2010) were analyzed ( n  = 131). After dividing the B3 biopsies into screen-detected and symptomatic groups, the National Health Service Breast Screening Programme histopathologic subclassification was used to further divide the groups into six subtypes. After surgery, a final diagnosis of invasive or in situ carcinoma was also noted. Results B3 classification comprised 3.8 % (131/3,440) of all core biopsies during that time period. There were 78 specimens from symptomatic (59 %) and 53 from screen-detected (41 %) patients. There was no statistically significant difference between papillary and fibroepithelial diagnoses between the two groups (47 vs. 42 %, p  = 0.59, NS). There was no difference between the groups for atypia, lobular neoplasia, or sclerosing lesions (49 vs. 51 %, p  = 0.8, NS). Cancer was found in 20 % of the symptomatic patients and in 17 % of the screen-detected group ( p  = 0.65, NS). Conclusions Mode of patient presentation (with a screen-detected or symptomatic lesion) was not a distinguishing factor for breast histopathologic subclassification or for the final cancer diagnosis in patients whose breast core biopsy was classified as B3.
doi_str_mv 10.1007/s00268-013-2191-6
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We compared the histopathologic subclassification of these lesions and the frequency of malignancy in screen-detected and symptomatic patient groups. Methods All B3 core biopsies from one breast unit at the Royal Berkshire Hospital over a 5-year period (2006–2010) were analyzed ( n  = 131). After dividing the B3 biopsies into screen-detected and symptomatic groups, the National Health Service Breast Screening Programme histopathologic subclassification was used to further divide the groups into six subtypes. After surgery, a final diagnosis of invasive or in situ carcinoma was also noted. Results B3 classification comprised 3.8 % (131/3,440) of all core biopsies during that time period. There were 78 specimens from symptomatic (59 %) and 53 from screen-detected (41 %) patients. There was no statistically significant difference between papillary and fibroepithelial diagnoses between the two groups (47 vs. 42 %, p  = 0.59, NS). There was no difference between the groups for atypia, lobular neoplasia, or sclerosing lesions (49 vs. 51 %, p  = 0.8, NS). Cancer was found in 20 % of the symptomatic patients and in 17 % of the screen-detected group ( p  = 0.65, NS). Conclusions Mode of patient presentation (with a screen-detected or symptomatic lesion) was not a distinguishing factor for breast histopathologic subclassification or for the final cancer diagnosis in patients whose breast core biopsy was classified as B3.</description><identifier>ISSN: 0364-2313</identifier><identifier>EISSN: 1432-2323</identifier><identifier>DOI: 10.1007/s00268-013-2191-6</identifier><identifier>PMID: 23963348</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Abdominal Surgery ; Adult ; Aged ; Aged, 80 and over ; Biopsy, Large-Core Needle ; Breast Neoplasms - pathology ; Carcinoma in Situ - pathology ; Cardiac Surgery ; Diagnosis, Differential ; Female ; General Surgery ; Humans ; Incidental Findings ; Lobular Neoplasia ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; National Health Service Breast Screening Programme ; Neoplasm Invasiveness - pathology ; Papillary Lesion ; Radial Scar ; Retrospective Studies ; Surgery ; Thoracic Surgery ; Uncertain Malignant Potential ; Vascular Surgery</subject><ispartof>World journal of surgery, 2013-11, Vol.37 (11), p.2607-2612</ispartof><rights>Société Internationale de Chirurgie 2013</rights><rights>2013 The Author(s) under exclusive licence to Société Internationale de Chirurgie</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4227-700db0b1428a47eea83093c12afc7eb759bcfb0ec3ad083ce81a3c8678dfcde93</citedby><cites>FETCH-LOGICAL-c4227-700db0b1428a47eea83093c12afc7eb759bcfb0ec3ad083ce81a3c8678dfcde93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00268-013-2191-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00268-013-2191-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,41488,42557,45574,45575,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23963348$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MacLean, Gael M.</creatorcontrib><creatorcontrib>Courtney, Stephen P.</creatorcontrib><creatorcontrib>Umeh, Hilary</creatorcontrib><creatorcontrib>Sanjeev, Siriathan</creatorcontrib><creatorcontrib>McCormick, Colin</creatorcontrib><creatorcontrib>Smith, Brendan M.</creatorcontrib><title>Is Mode of Presentation of B3 Breast Core Biopsies (Screen-Detected or Symptomatic) a Distinguishing Factor in the Final Histopathologic Result or Risk of Diagnosis of Malignancy?</title><title>World journal of surgery</title><addtitle>World J Surg</addtitle><addtitle>World J Surg</addtitle><description>Background The relation between histopathologic subclassification and mode of patient presentation (with a screen-detected vs. symptomatic lesion) with an abnormality in the breast core biopsy classified as having uncertain malignant potential (B3) has not been previously examined. We compared the histopathologic subclassification of these lesions and the frequency of malignancy in screen-detected and symptomatic patient groups. Methods All B3 core biopsies from one breast unit at the Royal Berkshire Hospital over a 5-year period (2006–2010) were analyzed ( n  = 131). After dividing the B3 biopsies into screen-detected and symptomatic groups, the National Health Service Breast Screening Programme histopathologic subclassification was used to further divide the groups into six subtypes. After surgery, a final diagnosis of invasive or in situ carcinoma was also noted. Results B3 classification comprised 3.8 % (131/3,440) of all core biopsies during that time period. There were 78 specimens from symptomatic (59 %) and 53 from screen-detected (41 %) patients. There was no statistically significant difference between papillary and fibroepithelial diagnoses between the two groups (47 vs. 42 %, p  = 0.59, NS). There was no difference between the groups for atypia, lobular neoplasia, or sclerosing lesions (49 vs. 51 %, p  = 0.8, NS). Cancer was found in 20 % of the symptomatic patients and in 17 % of the screen-detected group ( p  = 0.65, NS). 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Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>World journal of surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MacLean, Gael M.</au><au>Courtney, Stephen P.</au><au>Umeh, Hilary</au><au>Sanjeev, Siriathan</au><au>McCormick, Colin</au><au>Smith, Brendan M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Is Mode of Presentation of B3 Breast Core Biopsies (Screen-Detected or Symptomatic) a Distinguishing Factor in the Final Histopathologic Result or Risk of Diagnosis of Malignancy?</atitle><jtitle>World journal of surgery</jtitle><stitle>World J Surg</stitle><addtitle>World J Surg</addtitle><date>2013-11</date><risdate>2013</risdate><volume>37</volume><issue>11</issue><spage>2607</spage><epage>2612</epage><pages>2607-2612</pages><issn>0364-2313</issn><eissn>1432-2323</eissn><abstract>Background The relation between histopathologic subclassification and mode of patient presentation (with a screen-detected vs. symptomatic lesion) with an abnormality in the breast core biopsy classified as having uncertain malignant potential (B3) has not been previously examined. We compared the histopathologic subclassification of these lesions and the frequency of malignancy in screen-detected and symptomatic patient groups. Methods All B3 core biopsies from one breast unit at the Royal Berkshire Hospital over a 5-year period (2006–2010) were analyzed ( n  = 131). After dividing the B3 biopsies into screen-detected and symptomatic groups, the National Health Service Breast Screening Programme histopathologic subclassification was used to further divide the groups into six subtypes. After surgery, a final diagnosis of invasive or in situ carcinoma was also noted. Results B3 classification comprised 3.8 % (131/3,440) of all core biopsies during that time period. There were 78 specimens from symptomatic (59 %) and 53 from screen-detected (41 %) patients. There was no statistically significant difference between papillary and fibroepithelial diagnoses between the two groups (47 vs. 42 %, p  = 0.59, NS). There was no difference between the groups for atypia, lobular neoplasia, or sclerosing lesions (49 vs. 51 %, p  = 0.8, NS). Cancer was found in 20 % of the symptomatic patients and in 17 % of the screen-detected group ( p  = 0.65, NS). Conclusions Mode of patient presentation (with a screen-detected or symptomatic lesion) was not a distinguishing factor for breast histopathologic subclassification or for the final cancer diagnosis in patients whose breast core biopsy was classified as B3.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>23963348</pmid><doi>10.1007/s00268-013-2191-6</doi><tpages>6</tpages></addata></record>
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subjects Abdominal Surgery
Adult
Aged
Aged, 80 and over
Biopsy, Large-Core Needle
Breast Neoplasms - pathology
Carcinoma in Situ - pathology
Cardiac Surgery
Diagnosis, Differential
Female
General Surgery
Humans
Incidental Findings
Lobular Neoplasia
Medicine
Medicine & Public Health
Middle Aged
National Health Service Breast Screening Programme
Neoplasm Invasiveness - pathology
Papillary Lesion
Radial Scar
Retrospective Studies
Surgery
Thoracic Surgery
Uncertain Malignant Potential
Vascular Surgery
title Is Mode of Presentation of B3 Breast Core Biopsies (Screen-Detected or Symptomatic) a Distinguishing Factor in the Final Histopathologic Result or Risk of Diagnosis of Malignancy?
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