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Differences in germinal centre and non-germinal center phenotype in gastric and intestinal diffuse large B-cell lymphomas
The gastrointestinal tract is the most common extranodal site of lymphoma, and the most common gastrointestinal lymphoma is diffuse large B-cell type (DLBCL). DLBCL can be separated into germinal centre (GCP) and non-germinal centre phenotypes (non-GCP) using CD10, BCL-6 and MUM1 immunohistochemistr...
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Published in: | Leukemia & lymphoma 2008-01, Vol.49 (9), p.1717-1723 |
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container_title | Leukemia & lymphoma |
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creator | Mitchell, Kisha A. Finn, William G. Owens, Scott R. |
description | The gastrointestinal tract is the most common extranodal site of lymphoma, and the most common gastrointestinal lymphoma is diffuse large B-cell type (DLBCL). DLBCL can be separated into germinal centre (GCP) and non-germinal centre phenotypes (non-GCP) using CD10, BCL-6 and MUM1 immunohistochemistry, but primary gastrointestinal DLBCL has not been extensively studied. We investigated 48 cases of primary gastrointestinal DLBCL (33% involving the small intestine, 50% the stomach, 13% the large intestine and 4% the ileocecal junction) and found that most (88%) DLBCL in the intestines were of GCP, while only 58% of gastric DLBCL were of GCP. This difference in GCP and non-GCP in gastric vs. intestinal DLBCL may be due to variations in lymphomagenesis reflecting acquired vs. native mucosa-associated lymphoid tissue. There was no significant difference in either overall survival or disease-free survival between the germinal centre and non-germinal centre groups. The distribution of Helicobacter pylori in different gastric DLBCL phenotypes raises interesting questions about the pathogenesis of H. pylori-associated lymphomas. |
doi_str_mv | 10.1080/10428190802238552 |
format | article |
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DLBCL can be separated into germinal centre (GCP) and non-germinal centre phenotypes (non-GCP) using CD10, BCL-6 and MUM1 immunohistochemistry, but primary gastrointestinal DLBCL has not been extensively studied. We investigated 48 cases of primary gastrointestinal DLBCL (33% involving the small intestine, 50% the stomach, 13% the large intestine and 4% the ileocecal junction) and found that most (88%) DLBCL in the intestines were of GCP, while only 58% of gastric DLBCL were of GCP. This difference in GCP and non-GCP in gastric vs. intestinal DLBCL may be due to variations in lymphomagenesis reflecting acquired vs. native mucosa-associated lymphoid tissue. There was no significant difference in either overall survival or disease-free survival between the germinal centre and non-germinal centre groups. The distribution of Helicobacter pylori in different gastric DLBCL phenotypes raises interesting questions about the pathogenesis of H. pylori-associated lymphomas.</description><identifier>ISSN: 1042-8194</identifier><identifier>EISSN: 1029-2403</identifier><identifier>DOI: 10.1080/10428190802238552</identifier><identifier>PMID: 18798105</identifier><language>eng</language><publisher>United States: Informa UK Ltd</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Diffuse large B-cell lymphoma ; Disease-Free Survival ; Female ; gastrointestinal lymphoma ; Germinal Center - pathology ; germinal centre cell ; Helicobacter pylori ; Humans ; Intestinal Neoplasms - mortality ; Intestinal Neoplasms - pathology ; Lymphoma, Large B-Cell, Diffuse - mortality ; Lymphoma, Large B-Cell, Diffuse - pathology ; Male ; Middle Aged ; Phenotype ; Stomach Neoplasms - mortality ; Stomach Neoplasms - pathology ; Survival Rate</subject><ispartof>Leukemia & lymphoma, 2008-01, Vol.49 (9), p.1717-1723</ispartof><rights>2008 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-30cd183fbc4736cd2752740cf6a77c351d435d2b8b43fc039dfdec9a45cb9ea13</citedby><cites>FETCH-LOGICAL-c404t-30cd183fbc4736cd2752740cf6a77c351d435d2b8b43fc039dfdec9a45cb9ea13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18798105$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mitchell, Kisha A.</creatorcontrib><creatorcontrib>Finn, William G.</creatorcontrib><creatorcontrib>Owens, Scott R.</creatorcontrib><title>Differences in germinal centre and non-germinal center phenotype in gastric and intestinal diffuse large B-cell lymphomas</title><title>Leukemia & lymphoma</title><addtitle>Leuk Lymphoma</addtitle><description>The gastrointestinal tract is the most common extranodal site of lymphoma, and the most common gastrointestinal lymphoma is diffuse large B-cell type (DLBCL). DLBCL can be separated into germinal centre (GCP) and non-germinal centre phenotypes (non-GCP) using CD10, BCL-6 and MUM1 immunohistochemistry, but primary gastrointestinal DLBCL has not been extensively studied. We investigated 48 cases of primary gastrointestinal DLBCL (33% involving the small intestine, 50% the stomach, 13% the large intestine and 4% the ileocecal junction) and found that most (88%) DLBCL in the intestines were of GCP, while only 58% of gastric DLBCL were of GCP. This difference in GCP and non-GCP in gastric vs. intestinal DLBCL may be due to variations in lymphomagenesis reflecting acquired vs. native mucosa-associated lymphoid tissue. There was no significant difference in either overall survival or disease-free survival between the germinal centre and non-germinal centre groups. The distribution of Helicobacter pylori in different gastric DLBCL phenotypes raises interesting questions about the pathogenesis of H. pylori-associated lymphomas.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Diffuse large B-cell lymphoma</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>gastrointestinal lymphoma</subject><subject>Germinal Center - pathology</subject><subject>germinal centre cell</subject><subject>Helicobacter pylori</subject><subject>Humans</subject><subject>Intestinal Neoplasms - mortality</subject><subject>Intestinal Neoplasms - pathology</subject><subject>Lymphoma, Large B-Cell, Diffuse - mortality</subject><subject>Lymphoma, Large B-Cell, Diffuse - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Phenotype</subject><subject>Stomach Neoplasms - mortality</subject><subject>Stomach Neoplasms - pathology</subject><subject>Survival Rate</subject><issn>1042-8194</issn><issn>1029-2403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp9kEtrFzEUxYMotlY_gBvJyt1onvNAN1ofLRTctOuQSW76T8kkYzKDzLc3_wdIEbq6l3t_53A4CL2l5AMlPflIiWA9HerKGO-lZM_QOSVsaJgg_Pl-F6ypgDhDr0p5IITIoWUv0Rntu6GnRJ6j7Zt3DjJEAwX7iO8hTz7qgA3EJQPW0eKYYvPoDhnPO4hp2WY4iHRZsjcH2Nd3WQ6ordZrARx0vgf8tTEQAg7bNO_SpMtr9MLpUODNaV6gux_fby-vmptfP68vv9w0RhCxNJwYS3vuRiM63hrLOsk6QYxrddcZLqkVXFo29qPgzhA-WGfBDFpIMw6gKb9A74--c06_15pNTb7so-gIaS2qHWTLpBQVpEfQ5FRKBqfm7CedN0WJ2vet_uu7at6dzNdxAvtPcSq4Ap-PgI8u5Un_STlYtegtpOyyjsYXxZ_y__RIvgMdlp3RGdRDWnNtuTyR7i8I36Jb</recordid><startdate>20080101</startdate><enddate>20080101</enddate><creator>Mitchell, Kisha A.</creator><creator>Finn, William G.</creator><creator>Owens, Scott R.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</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>7X8</scope></search><sort><creationdate>20080101</creationdate><title>Differences in germinal centre and non-germinal center phenotype in gastric and intestinal diffuse large B-cell lymphomas</title><author>Mitchell, Kisha A. ; Finn, William G. ; Owens, Scott R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-30cd183fbc4736cd2752740cf6a77c351d435d2b8b43fc039dfdec9a45cb9ea13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Diffuse large B-cell lymphoma</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>gastrointestinal lymphoma</topic><topic>Germinal Center - pathology</topic><topic>germinal centre cell</topic><topic>Helicobacter pylori</topic><topic>Humans</topic><topic>Intestinal Neoplasms - mortality</topic><topic>Intestinal Neoplasms - pathology</topic><topic>Lymphoma, Large B-Cell, Diffuse - mortality</topic><topic>Lymphoma, Large B-Cell, Diffuse - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Phenotype</topic><topic>Stomach Neoplasms - mortality</topic><topic>Stomach Neoplasms - pathology</topic><topic>Survival Rate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mitchell, Kisha A.</creatorcontrib><creatorcontrib>Finn, William G.</creatorcontrib><creatorcontrib>Owens, Scott R.</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>Leukemia & lymphoma</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mitchell, Kisha A.</au><au>Finn, William G.</au><au>Owens, Scott R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differences in germinal centre and non-germinal center phenotype in gastric and intestinal diffuse large B-cell lymphomas</atitle><jtitle>Leukemia & lymphoma</jtitle><addtitle>Leuk Lymphoma</addtitle><date>2008-01-01</date><risdate>2008</risdate><volume>49</volume><issue>9</issue><spage>1717</spage><epage>1723</epage><pages>1717-1723</pages><issn>1042-8194</issn><eissn>1029-2403</eissn><abstract>The gastrointestinal tract is the most common extranodal site of lymphoma, and the most common gastrointestinal lymphoma is diffuse large B-cell type (DLBCL). DLBCL can be separated into germinal centre (GCP) and non-germinal centre phenotypes (non-GCP) using CD10, BCL-6 and MUM1 immunohistochemistry, but primary gastrointestinal DLBCL has not been extensively studied. We investigated 48 cases of primary gastrointestinal DLBCL (33% involving the small intestine, 50% the stomach, 13% the large intestine and 4% the ileocecal junction) and found that most (88%) DLBCL in the intestines were of GCP, while only 58% of gastric DLBCL were of GCP. This difference in GCP and non-GCP in gastric vs. intestinal DLBCL may be due to variations in lymphomagenesis reflecting acquired vs. native mucosa-associated lymphoid tissue. There was no significant difference in either overall survival or disease-free survival between the germinal centre and non-germinal centre groups. The distribution of Helicobacter pylori in different gastric DLBCL phenotypes raises interesting questions about the pathogenesis of H. pylori-associated lymphomas.</abstract><cop>United States</cop><pub>Informa UK Ltd</pub><pmid>18798105</pmid><doi>10.1080/10428190802238552</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Diffuse large B-cell lymphoma Disease-Free Survival Female gastrointestinal lymphoma Germinal Center - pathology germinal centre cell Helicobacter pylori Humans Intestinal Neoplasms - mortality Intestinal Neoplasms - pathology Lymphoma, Large B-Cell, Diffuse - mortality Lymphoma, Large B-Cell, Diffuse - pathology Male Middle Aged Phenotype Stomach Neoplasms - mortality Stomach Neoplasms - pathology Survival Rate |
title | Differences in germinal centre and non-germinal center phenotype in gastric and intestinal diffuse large B-cell lymphomas |
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