Prolapse-related changes are a confounding factor in misdiagnosis of sessile serrated adenomas in the rectum
Summary The differential diagnosis of rectal serrated polyps is challenging due to its unique anatomic location, the evolving concept of serrated polyps over the past several years, and to histologic changes seen in rectal mucosal prolapse. We reclassified 95 rectal polyps diagnosed originally as “s...
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Veröffentlicht in: | Human pathology 2013-04, Vol.44 (4), p.480-486 |
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description | Summary The differential diagnosis of rectal serrated polyps is challenging due to its unique anatomic location, the evolving concept of serrated polyps over the past several years, and to histologic changes seen in rectal mucosal prolapse. We reclassified 95 rectal polyps diagnosed originally as “sessile serrated adenoma” (SSA), “serrated polyp,” or “hyperplastic polyp (HP) with features of SSA” in a 5-year period based on World Health Organization classification criteria for colorectal serrated polyps. BRAF (V600E) mutation assay was performed to explore its value in the differential diagnosis for serrated polyps. Twenty-six originally diagnosed SSAs were reclassified as SSA (15/26, 57.7%), HP with mucosal prolapse (HP-P; 7/26, 26.9%), and HP (4/26, 15.4%). Fifty-two polyps originally diagnosed “HP with features of SSA” were reclassified as HP-P (24/52, 46.2%), HP (10/52, 19.2%), inflammatory-type polyp (5/52, 9.6%), and serrated polyp unclassifiable (13/52, 25.0%). Thirty-one of the 78 originally diagnosed SSA or HP with features of SSA were reclassified as HP-P, which accounted for 32.6% of the rectal polyps in this study. Mucosal prolapse along with chronic inflammation and tissue embedding artifact were the most common features that led to misdiagnosis in rectal serrated polyps. BRAF mutation was identified in 8 of 11 HP, 4 of 4 SSA, and 8 of 11 unclassifiable serrated polyp of the rectum, and was absent in control tissue. Thus, histopathologic changes suggesting prolapsed rectal mucosa should take precedence over BRAF results. |
doi_str_mv | 10.1016/j.humpath.2012.06.011 |
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We reclassified 95 rectal polyps diagnosed originally as “sessile serrated adenoma” (SSA), “serrated polyp,” or “hyperplastic polyp (HP) with features of SSA” in a 5-year period based on World Health Organization classification criteria for colorectal serrated polyps. BRAF (V600E) mutation assay was performed to explore its value in the differential diagnosis for serrated polyps. Twenty-six originally diagnosed SSAs were reclassified as SSA (15/26, 57.7%), HP with mucosal prolapse (HP-P; 7/26, 26.9%), and HP (4/26, 15.4%). Fifty-two polyps originally diagnosed “HP with features of SSA” were reclassified as HP-P (24/52, 46.2%), HP (10/52, 19.2%), inflammatory-type polyp (5/52, 9.6%), and serrated polyp unclassifiable (13/52, 25.0%). Thirty-one of the 78 originally diagnosed SSA or HP with features of SSA were reclassified as HP-P, which accounted for 32.6% of the rectal polyps in this study. Mucosal prolapse along with chronic inflammation and tissue embedding artifact were the most common features that led to misdiagnosis in rectal serrated polyps. BRAF mutation was identified in 8 of 11 HP, 4 of 4 SSA, and 8 of 11 unclassifiable serrated polyp of the rectum, and was absent in control tissue. Thus, histopathologic changes suggesting prolapsed rectal mucosa should take precedence over BRAF results.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2012.06.011</identifier><identifier>PMID: 23069257</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenoma - diagnosis ; Adenoma - epidemiology ; Adenoma - genetics ; Adult ; Aged ; Aged, 80 and over ; BRAF V600E mutation ; Colon ; Colonic Polyps - diagnosis ; Colonic Polyps - epidemiology ; Colonic Polyps - genetics ; Colorectal cancer ; Comorbidity ; Confounding Factors (Epidemiology) ; Diagnosis ; Diagnosis, Differential ; Diagnostic Errors ; DNA methylation ; DNA Mutational Analysis ; DNA, Neoplasm - analysis ; Female ; Humans ; Hyperplasia ; Male ; Middle Aged ; Mutation ; Pathology ; Proteins ; Proto-Oncogene Proteins B-raf - genetics ; Rectal Neoplasms - diagnosis ; Rectal Neoplasms - epidemiology ; Rectal Neoplasms - genetics ; Rectal Prolapse - diagnosis ; Rectal Prolapse - epidemiology ; Rectal Prolapse - genetics ; Rectum ; Serrated polyp ; World Health Organization</subject><ispartof>Human pathology, 2013-04, Vol.44 (4), p.480-486</ispartof><rights>Elsevier Inc.</rights><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Apr 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c514t-8052769ac5298a2e26de9eb2aae8c51c53ad0770708c40a8aa9d49a10c91ffba3</citedby><cites>FETCH-LOGICAL-c514t-8052769ac5298a2e26de9eb2aae8c51c53ad0770708c40a8aa9d49a10c91ffba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.humpath.2012.06.011$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23069257$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Cheng Cheng, MD, PhD</creatorcontrib><creatorcontrib>Frankel, Wendy L., MD</creatorcontrib><creatorcontrib>Doukides, Theodore, MD</creatorcontrib><creatorcontrib>Zhou, Xiao-Ping, MD, PhD</creatorcontrib><creatorcontrib>Zhao, Weiqiang, MD, PhD</creatorcontrib><creatorcontrib>Yearsley, Martha M., MD</creatorcontrib><title>Prolapse-related changes are a confounding factor in misdiagnosis of sessile serrated adenomas in the rectum</title><title>Human pathology</title><addtitle>Hum Pathol</addtitle><description>Summary The differential diagnosis of rectal serrated polyps is challenging due to its unique anatomic location, the evolving concept of serrated polyps over the past several years, and to histologic changes seen in rectal mucosal prolapse. We reclassified 95 rectal polyps diagnosed originally as “sessile serrated adenoma” (SSA), “serrated polyp,” or “hyperplastic polyp (HP) with features of SSA” in a 5-year period based on World Health Organization classification criteria for colorectal serrated polyps. BRAF (V600E) mutation assay was performed to explore its value in the differential diagnosis for serrated polyps. Twenty-six originally diagnosed SSAs were reclassified as SSA (15/26, 57.7%), HP with mucosal prolapse (HP-P; 7/26, 26.9%), and HP (4/26, 15.4%). Fifty-two polyps originally diagnosed “HP with features of SSA” were reclassified as HP-P (24/52, 46.2%), HP (10/52, 19.2%), inflammatory-type polyp (5/52, 9.6%), and serrated polyp unclassifiable (13/52, 25.0%). Thirty-one of the 78 originally diagnosed SSA or HP with features of SSA were reclassified as HP-P, which accounted for 32.6% of the rectal polyps in this study. Mucosal prolapse along with chronic inflammation and tissue embedding artifact were the most common features that led to misdiagnosis in rectal serrated polyps. BRAF mutation was identified in 8 of 11 HP, 4 of 4 SSA, and 8 of 11 unclassifiable serrated polyp of the rectum, and was absent in control tissue. Thus, histopathologic changes suggesting prolapsed rectal mucosa should take precedence over BRAF results.</description><subject>Adenoma - diagnosis</subject><subject>Adenoma - epidemiology</subject><subject>Adenoma - genetics</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>BRAF V600E mutation</subject><subject>Colon</subject><subject>Colonic Polyps - diagnosis</subject><subject>Colonic Polyps - epidemiology</subject><subject>Colonic Polyps - genetics</subject><subject>Colorectal cancer</subject><subject>Comorbidity</subject><subject>Confounding Factors (Epidemiology)</subject><subject>Diagnosis</subject><subject>Diagnosis, Differential</subject><subject>Diagnostic Errors</subject><subject>DNA methylation</subject><subject>DNA Mutational Analysis</subject><subject>DNA, Neoplasm - analysis</subject><subject>Female</subject><subject>Humans</subject><subject>Hyperplasia</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Pathology</subject><subject>Proteins</subject><subject>Proto-Oncogene Proteins B-raf - genetics</subject><subject>Rectal Neoplasms - diagnosis</subject><subject>Rectal Neoplasms - epidemiology</subject><subject>Rectal Neoplasms - genetics</subject><subject>Rectal Prolapse - diagnosis</subject><subject>Rectal Prolapse - epidemiology</subject><subject>Rectal Prolapse - genetics</subject><subject>Rectum</subject><subject>Serrated polyp</subject><subject>World Health Organization</subject><issn>0046-8177</issn><issn>1532-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk-LFDEQxYMo7rj6EZSAFy_dVtJ_c1Fk0VVYUFDPoSapnsnYnYxJt7Df3rQzq7AXT3X51auq94qx5wJKAaJ9fSj3y3TEeV9KELKEtgQhHrCNaCpZ9JWSD9kGoG6LXnTdBXuS0gEy0dTNY3YhK2iVbLoNG7_EMOIxURFpxJksN3v0O0ocI3HkJvghLN46v-MDmjlE7jyfXLIOdz4kl3gYeKKU3Ei5xvhHBC35MGFa4XlPPJKZl-kpezTgmOjZuV6y7x_ef7v6WNx8vv509e6mMI2o56KHRnatQtNI1aMk2VpStJWI1GfCNBVa6DrooDc1YI-obK1QgFFiGLZYXbJXJ91jDD8XSrPOCxsaR_QUlqRFJXpQlRIyoy_voYewRJ-3W6muBpXHZKo5USaGlCIN-hjdhPFWC9BrHPqgz3HoNQ4Nrc5m574XZ_VlO5H923XnfwbengDKdvxyFHUyjrwh61bLtA3uvyPe3FMwo_PO4PiDbin9u0an3KO_rj-xvoSQALISbfUbkHOz3Q</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Huang, Cheng Cheng, MD, PhD</creator><creator>Frankel, Wendy L., MD</creator><creator>Doukides, Theodore, MD</creator><creator>Zhou, Xiao-Ping, MD, PhD</creator><creator>Zhao, Weiqiang, MD, PhD</creator><creator>Yearsley, Martha M., MD</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><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>K9.</scope><scope>7X8</scope></search><sort><creationdate>20130401</creationdate><title>Prolapse-related changes are a confounding factor in misdiagnosis of sessile serrated adenomas in the rectum</title><author>Huang, Cheng Cheng, MD, PhD ; Frankel, Wendy L., MD ; Doukides, Theodore, MD ; Zhou, Xiao-Ping, MD, PhD ; Zhao, Weiqiang, MD, PhD ; Yearsley, Martha M., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c514t-8052769ac5298a2e26de9eb2aae8c51c53ad0770708c40a8aa9d49a10c91ffba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adenoma - diagnosis</topic><topic>Adenoma - epidemiology</topic><topic>Adenoma - genetics</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>BRAF V600E mutation</topic><topic>Colon</topic><topic>Colonic Polyps - diagnosis</topic><topic>Colonic Polyps - epidemiology</topic><topic>Colonic Polyps - genetics</topic><topic>Colorectal cancer</topic><topic>Comorbidity</topic><topic>Confounding Factors (Epidemiology)</topic><topic>Diagnosis</topic><topic>Diagnosis, Differential</topic><topic>Diagnostic Errors</topic><topic>DNA methylation</topic><topic>DNA Mutational Analysis</topic><topic>DNA, Neoplasm - analysis</topic><topic>Female</topic><topic>Humans</topic><topic>Hyperplasia</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Pathology</topic><topic>Proteins</topic><topic>Proto-Oncogene Proteins B-raf - genetics</topic><topic>Rectal Neoplasms - diagnosis</topic><topic>Rectal Neoplasms - epidemiology</topic><topic>Rectal Neoplasms - genetics</topic><topic>Rectal Prolapse - diagnosis</topic><topic>Rectal Prolapse - epidemiology</topic><topic>Rectal Prolapse - genetics</topic><topic>Rectum</topic><topic>Serrated polyp</topic><topic>World Health Organization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Cheng Cheng, MD, PhD</creatorcontrib><creatorcontrib>Frankel, Wendy L., MD</creatorcontrib><creatorcontrib>Doukides, Theodore, MD</creatorcontrib><creatorcontrib>Zhou, Xiao-Ping, MD, PhD</creatorcontrib><creatorcontrib>Zhao, Weiqiang, MD, PhD</creatorcontrib><creatorcontrib>Yearsley, Martha M., MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Human pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Cheng Cheng, MD, PhD</au><au>Frankel, Wendy L., MD</au><au>Doukides, Theodore, MD</au><au>Zhou, Xiao-Ping, MD, PhD</au><au>Zhao, Weiqiang, MD, PhD</au><au>Yearsley, Martha M., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prolapse-related changes are a confounding factor in misdiagnosis of sessile serrated adenomas in the rectum</atitle><jtitle>Human pathology</jtitle><addtitle>Hum Pathol</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>44</volume><issue>4</issue><spage>480</spage><epage>486</epage><pages>480-486</pages><issn>0046-8177</issn><eissn>1532-8392</eissn><abstract>Summary The differential diagnosis of rectal serrated polyps is challenging due to its unique anatomic location, the evolving concept of serrated polyps over the past several years, and to histologic changes seen in rectal mucosal prolapse. We reclassified 95 rectal polyps diagnosed originally as “sessile serrated adenoma” (SSA), “serrated polyp,” or “hyperplastic polyp (HP) with features of SSA” in a 5-year period based on World Health Organization classification criteria for colorectal serrated polyps. BRAF (V600E) mutation assay was performed to explore its value in the differential diagnosis for serrated polyps. Twenty-six originally diagnosed SSAs were reclassified as SSA (15/26, 57.7%), HP with mucosal prolapse (HP-P; 7/26, 26.9%), and HP (4/26, 15.4%). Fifty-two polyps originally diagnosed “HP with features of SSA” were reclassified as HP-P (24/52, 46.2%), HP (10/52, 19.2%), inflammatory-type polyp (5/52, 9.6%), and serrated polyp unclassifiable (13/52, 25.0%). Thirty-one of the 78 originally diagnosed SSA or HP with features of SSA were reclassified as HP-P, which accounted for 32.6% of the rectal polyps in this study. Mucosal prolapse along with chronic inflammation and tissue embedding artifact were the most common features that led to misdiagnosis in rectal serrated polyps. BRAF mutation was identified in 8 of 11 HP, 4 of 4 SSA, and 8 of 11 unclassifiable serrated polyp of the rectum, and was absent in control tissue. Thus, histopathologic changes suggesting prolapsed rectal mucosa should take precedence over BRAF results.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23069257</pmid><doi>10.1016/j.humpath.2012.06.011</doi><tpages>7</tpages></addata></record> |
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subjects | Adenoma - diagnosis Adenoma - epidemiology Adenoma - genetics Adult Aged Aged, 80 and over BRAF V600E mutation Colon Colonic Polyps - diagnosis Colonic Polyps - epidemiology Colonic Polyps - genetics Colorectal cancer Comorbidity Confounding Factors (Epidemiology) Diagnosis Diagnosis, Differential Diagnostic Errors DNA methylation DNA Mutational Analysis DNA, Neoplasm - analysis Female Humans Hyperplasia Male Middle Aged Mutation Pathology Proteins Proto-Oncogene Proteins B-raf - genetics Rectal Neoplasms - diagnosis Rectal Neoplasms - epidemiology Rectal Neoplasms - genetics Rectal Prolapse - diagnosis Rectal Prolapse - epidemiology Rectal Prolapse - genetics Rectum Serrated polyp World Health Organization |
title | Prolapse-related changes are a confounding factor in misdiagnosis of sessile serrated adenomas in the rectum |
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