Localization of the most severely dysplastic/invasive lesions and mucin phenotypes in intraductal papillary mucinous neoplasm of the pancreas
The aim of this study was to define the relevance of mural nodules (MNs) as a "direct" indicator of malignancy of intraductal papillary mucinous neoplasm (IPMN) of the pancreas. Thirty-nine surgically resected IPMNs excluding obviously invasive carcinomas were examined. The distribution of...
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Veröffentlicht in: | Pancreas 2011-05, Vol.40 (4), p.588-594 |
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creator | Karasaki, Hidenori Mizukami, Yusuke Tokusashi, Yoshihiko Koizumi, Kazuya Ishizaki, Akira Imai, Kouji Yoshikawa, Daitaro Kino, Shuichi Sasajima, Junpei Tanno, Satoshi Matsumoto, Kakuya Miyokawa, Naoyuki Kono, Toru Kohgo, Yutaka Furukawa, Hiroyuki |
description | The aim of this study was to define the relevance of mural nodules (MNs) as a "direct" indicator of malignancy of intraductal papillary mucinous neoplasm (IPMN) of the pancreas.
Thirty-nine surgically resected IPMNs excluding obviously invasive carcinomas were examined. The distribution of the most severely dysplastic lesions was mapped on specimens. Immunohistochemical analysis for MUC1 and MUC2 was performed on sections containing the histologically predominant lesions and the most severely dysplastic areas.
The presence of MNs correlated well with the histological grade of IPMN (P < 0.01); however, the most severely dysplastic lesions were associated with a flat/nonelevated area rather than MNs (78.9%). In the MUC1-positive subgroup, minimally invasive carcinoma was colocalized to MNs, whereas most severely dysplastic foci including minimally invasive carcinoma with components of mucinous and tubular adenocarcinoma were observed in the areas apart from MNs in the MUC2-positive and MUC1/2-negative subgroups, respectively.
Although our data support the concept that MNs represent areas of higher-grade dysplasia within IPMN, development of invasive lesions from MNs may be limited to cases that are MUC1-positive. Careful attention should be paid to the emergence of invasive IPMN from flat foci in MUC2-positive and MUC1/2-negative cases. |
doi_str_mv | 10.1097/MPA.0b013e31820d1a03 |
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Thirty-nine surgically resected IPMNs excluding obviously invasive carcinomas were examined. The distribution of the most severely dysplastic lesions was mapped on specimens. Immunohistochemical analysis for MUC1 and MUC2 was performed on sections containing the histologically predominant lesions and the most severely dysplastic areas.
The presence of MNs correlated well with the histological grade of IPMN (P < 0.01); however, the most severely dysplastic lesions were associated with a flat/nonelevated area rather than MNs (78.9%). In the MUC1-positive subgroup, minimally invasive carcinoma was colocalized to MNs, whereas most severely dysplastic foci including minimally invasive carcinoma with components of mucinous and tubular adenocarcinoma were observed in the areas apart from MNs in the MUC2-positive and MUC1/2-negative subgroups, respectively.
Although our data support the concept that MNs represent areas of higher-grade dysplasia within IPMN, development of invasive lesions from MNs may be limited to cases that are MUC1-positive. Careful attention should be paid to the emergence of invasive IPMN from flat foci in MUC2-positive and MUC1/2-negative cases.</description><identifier>ISSN: 0885-3177</identifier><identifier>EISSN: 1536-4828</identifier><identifier>DOI: 10.1097/MPA.0b013e31820d1a03</identifier><identifier>PMID: 21441843</identifier><language>eng</language><publisher>United States</publisher><subject>Adenocarcinoma, Mucinous - metabolism ; Adenocarcinoma, Mucinous - pathology ; Aged ; Carcinoma, Pancreatic Ductal - metabolism ; Carcinoma, Pancreatic Ductal - pathology ; Female ; Humans ; Immunohistochemistry ; Male ; Middle Aged ; Mucin-1 - metabolism ; Mucin-2 - metabolism ; Mucins - metabolism ; Neoplasm Invasiveness ; Pancreas - metabolism ; Pancreas - pathology ; Pancreatic Neoplasms - metabolism ; Pancreatic Neoplasms - pathology</subject><ispartof>Pancreas, 2011-05, Vol.40 (4), p.588-594</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-bf084c3b52555d8f1f9f4ecb81129e53f62b6045226311f41a77dd8a516bda333</citedby><cites>FETCH-LOGICAL-c462t-bf084c3b52555d8f1f9f4ecb81129e53f62b6045226311f41a77dd8a516bda333</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21441843$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karasaki, Hidenori</creatorcontrib><creatorcontrib>Mizukami, Yusuke</creatorcontrib><creatorcontrib>Tokusashi, Yoshihiko</creatorcontrib><creatorcontrib>Koizumi, Kazuya</creatorcontrib><creatorcontrib>Ishizaki, Akira</creatorcontrib><creatorcontrib>Imai, Kouji</creatorcontrib><creatorcontrib>Yoshikawa, Daitaro</creatorcontrib><creatorcontrib>Kino, Shuichi</creatorcontrib><creatorcontrib>Sasajima, Junpei</creatorcontrib><creatorcontrib>Tanno, Satoshi</creatorcontrib><creatorcontrib>Matsumoto, Kakuya</creatorcontrib><creatorcontrib>Miyokawa, Naoyuki</creatorcontrib><creatorcontrib>Kono, Toru</creatorcontrib><creatorcontrib>Kohgo, Yutaka</creatorcontrib><creatorcontrib>Furukawa, Hiroyuki</creatorcontrib><title>Localization of the most severely dysplastic/invasive lesions and mucin phenotypes in intraductal papillary mucinous neoplasm of the pancreas</title><title>Pancreas</title><addtitle>Pancreas</addtitle><description>The aim of this study was to define the relevance of mural nodules (MNs) as a "direct" indicator of malignancy of intraductal papillary mucinous neoplasm (IPMN) of the pancreas.
Thirty-nine surgically resected IPMNs excluding obviously invasive carcinomas were examined. The distribution of the most severely dysplastic lesions was mapped on specimens. Immunohistochemical analysis for MUC1 and MUC2 was performed on sections containing the histologically predominant lesions and the most severely dysplastic areas.
The presence of MNs correlated well with the histological grade of IPMN (P < 0.01); however, the most severely dysplastic lesions were associated with a flat/nonelevated area rather than MNs (78.9%). In the MUC1-positive subgroup, minimally invasive carcinoma was colocalized to MNs, whereas most severely dysplastic foci including minimally invasive carcinoma with components of mucinous and tubular adenocarcinoma were observed in the areas apart from MNs in the MUC2-positive and MUC1/2-negative subgroups, respectively.
Although our data support the concept that MNs represent areas of higher-grade dysplasia within IPMN, development of invasive lesions from MNs may be limited to cases that are MUC1-positive. Careful attention should be paid to the emergence of invasive IPMN from flat foci in MUC2-positive and MUC1/2-negative cases.</description><subject>Adenocarcinoma, Mucinous - metabolism</subject><subject>Adenocarcinoma, Mucinous - pathology</subject><subject>Aged</subject><subject>Carcinoma, Pancreatic Ductal - metabolism</subject><subject>Carcinoma, Pancreatic Ductal - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mucin-1 - metabolism</subject><subject>Mucin-2 - metabolism</subject><subject>Mucins - metabolism</subject><subject>Neoplasm Invasiveness</subject><subject>Pancreas - metabolism</subject><subject>Pancreas - pathology</subject><subject>Pancreatic Neoplasms - metabolism</subject><subject>Pancreatic Neoplasms - pathology</subject><issn>0885-3177</issn><issn>1536-4828</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdUc1u1DAQthAVXQpvgJBvnNJ6_JM4x6qigLSIHtpz5Nhj1SiJQ8ZZaXkH3plU23LgNBrp-5v5GPsA4hJE21x9v7u-FL0AhQqsFAGcUK_YDoyqK22lfc12wlpTKWiac_aW6KcQ0CjTvmHnErQGq9WO_dln74b025WUJ54jL4_Ix0yFEx5wweHIw5HmwVFJ_ipNB0fpgHxA2vDE3RT4uPo08fkRp1yOMxLftjSVxYXVFzfw2c1pGNxyPCHzSnzC_CQ5vhjObvILOnrHzqIbCN8_zwv2cPv5_uZrtf_x5dvN9b7yupal6qOw2qveSGNMsBFiGzX63gLIFo2KtexroY2UtQKIGlzThGCdgboPTil1wT6ddOcl_1qRSjcm8ril3JKt1NkamlbpVm5IfUL6JRMtGLt5SeN2TAeie-qh23ro_u9ho318Nlj7EcM_0svj1V92zIh_</recordid><startdate>201105</startdate><enddate>201105</enddate><creator>Karasaki, Hidenori</creator><creator>Mizukami, Yusuke</creator><creator>Tokusashi, Yoshihiko</creator><creator>Koizumi, Kazuya</creator><creator>Ishizaki, Akira</creator><creator>Imai, Kouji</creator><creator>Yoshikawa, Daitaro</creator><creator>Kino, Shuichi</creator><creator>Sasajima, Junpei</creator><creator>Tanno, Satoshi</creator><creator>Matsumoto, Kakuya</creator><creator>Miyokawa, Naoyuki</creator><creator>Kono, Toru</creator><creator>Kohgo, Yutaka</creator><creator>Furukawa, Hiroyuki</creator><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>201105</creationdate><title>Localization of the most severely dysplastic/invasive lesions and mucin phenotypes in intraductal papillary mucinous neoplasm of the pancreas</title><author>Karasaki, Hidenori ; Mizukami, Yusuke ; Tokusashi, Yoshihiko ; Koizumi, Kazuya ; Ishizaki, Akira ; Imai, Kouji ; Yoshikawa, Daitaro ; Kino, Shuichi ; Sasajima, Junpei ; Tanno, Satoshi ; Matsumoto, Kakuya ; Miyokawa, Naoyuki ; Kono, Toru ; Kohgo, Yutaka ; Furukawa, Hiroyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-bf084c3b52555d8f1f9f4ecb81129e53f62b6045226311f41a77dd8a516bda333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adenocarcinoma, Mucinous - metabolism</topic><topic>Adenocarcinoma, Mucinous - pathology</topic><topic>Aged</topic><topic>Carcinoma, Pancreatic Ductal - metabolism</topic><topic>Carcinoma, Pancreatic Ductal - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mucin-1 - metabolism</topic><topic>Mucin-2 - metabolism</topic><topic>Mucins - metabolism</topic><topic>Neoplasm Invasiveness</topic><topic>Pancreas - metabolism</topic><topic>Pancreas - pathology</topic><topic>Pancreatic Neoplasms - metabolism</topic><topic>Pancreatic Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karasaki, Hidenori</creatorcontrib><creatorcontrib>Mizukami, Yusuke</creatorcontrib><creatorcontrib>Tokusashi, Yoshihiko</creatorcontrib><creatorcontrib>Koizumi, Kazuya</creatorcontrib><creatorcontrib>Ishizaki, Akira</creatorcontrib><creatorcontrib>Imai, Kouji</creatorcontrib><creatorcontrib>Yoshikawa, Daitaro</creatorcontrib><creatorcontrib>Kino, Shuichi</creatorcontrib><creatorcontrib>Sasajima, Junpei</creatorcontrib><creatorcontrib>Tanno, Satoshi</creatorcontrib><creatorcontrib>Matsumoto, Kakuya</creatorcontrib><creatorcontrib>Miyokawa, Naoyuki</creatorcontrib><creatorcontrib>Kono, Toru</creatorcontrib><creatorcontrib>Kohgo, Yutaka</creatorcontrib><creatorcontrib>Furukawa, Hiroyuki</creatorcontrib><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>Pancreas</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karasaki, Hidenori</au><au>Mizukami, Yusuke</au><au>Tokusashi, Yoshihiko</au><au>Koizumi, Kazuya</au><au>Ishizaki, Akira</au><au>Imai, Kouji</au><au>Yoshikawa, Daitaro</au><au>Kino, Shuichi</au><au>Sasajima, Junpei</au><au>Tanno, Satoshi</au><au>Matsumoto, Kakuya</au><au>Miyokawa, Naoyuki</au><au>Kono, Toru</au><au>Kohgo, Yutaka</au><au>Furukawa, Hiroyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Localization of the most severely dysplastic/invasive lesions and mucin phenotypes in intraductal papillary mucinous neoplasm of the pancreas</atitle><jtitle>Pancreas</jtitle><addtitle>Pancreas</addtitle><date>2011-05</date><risdate>2011</risdate><volume>40</volume><issue>4</issue><spage>588</spage><epage>594</epage><pages>588-594</pages><issn>0885-3177</issn><eissn>1536-4828</eissn><abstract>The aim of this study was to define the relevance of mural nodules (MNs) as a "direct" indicator of malignancy of intraductal papillary mucinous neoplasm (IPMN) of the pancreas.
Thirty-nine surgically resected IPMNs excluding obviously invasive carcinomas were examined. The distribution of the most severely dysplastic lesions was mapped on specimens. Immunohistochemical analysis for MUC1 and MUC2 was performed on sections containing the histologically predominant lesions and the most severely dysplastic areas.
The presence of MNs correlated well with the histological grade of IPMN (P < 0.01); however, the most severely dysplastic lesions were associated with a flat/nonelevated area rather than MNs (78.9%). In the MUC1-positive subgroup, minimally invasive carcinoma was colocalized to MNs, whereas most severely dysplastic foci including minimally invasive carcinoma with components of mucinous and tubular adenocarcinoma were observed in the areas apart from MNs in the MUC2-positive and MUC1/2-negative subgroups, respectively.
Although our data support the concept that MNs represent areas of higher-grade dysplasia within IPMN, development of invasive lesions from MNs may be limited to cases that are MUC1-positive. Careful attention should be paid to the emergence of invasive IPMN from flat foci in MUC2-positive and MUC1/2-negative cases.</abstract><cop>United States</cop><pmid>21441843</pmid><doi>10.1097/MPA.0b013e31820d1a03</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma, Mucinous - metabolism Adenocarcinoma, Mucinous - pathology Aged Carcinoma, Pancreatic Ductal - metabolism Carcinoma, Pancreatic Ductal - pathology Female Humans Immunohistochemistry Male Middle Aged Mucin-1 - metabolism Mucin-2 - metabolism Mucins - metabolism Neoplasm Invasiveness Pancreas - metabolism Pancreas - pathology Pancreatic Neoplasms - metabolism Pancreatic Neoplasms - pathology |
title | Localization of the most severely dysplastic/invasive lesions and mucin phenotypes in intraductal papillary mucinous neoplasm of the pancreas |
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