Helicobacter pylori infection and gastric lymphoma
Gastric lymphoma of mucosa associated lymphoid tissue (MALT) has characteristic clinicopathological features that are different from nodal-type B cell lymphomas. Before a lymphoma can arise within the stomach, MALT has to be acquired as part of a response to an immunological stimulus. In most instan...
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Veröffentlicht in: | British medical bulletin 1998, Vol.54 (1), p.79-85 |
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description | Gastric lymphoma of mucosa associated lymphoid tissue (MALT) has characteristic clinicopathological features that are different from nodal-type B cell lymphomas. Before a lymphoma can arise within the stomach, MALT has to be acquired as part of a response to an immunological stimulus. In most instances, gastric MALT is acquired in response to infection ny Helicobacter pylori. There are several features of MALT lymphoma, such as plasma cell differentiation and follicular colonisation, that suggest that these lymphomas, although demonstrated on the basis of clonality studies to be neoplastic, retain some immunological drive. In vitro studies have shown that co-culturing cells derived from low grade MALT lymphomas with H. pylori results in tumour cell proliferation in a T cell dependant manner. Clinical studies have taken this discovery further and shown that patients with early low grate gastric MALT lymphoma treated with anti-Helicobacter therapy can show regression of their tumours. It is now generally accepted that eradication of H. pylori is a central component of the management of MALT lymphoma. |
doi_str_mv | 10.1093/oxfordjournals.bmb.a011683 |
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Before a lymphoma can arise within the stomach, MALT has to be acquired as part of a response to an immunological stimulus. In most instances, gastric MALT is acquired in response to infection ny Helicobacter pylori. There are several features of MALT lymphoma, such as plasma cell differentiation and follicular colonisation, that suggest that these lymphomas, although demonstrated on the basis of clonality studies to be neoplastic, retain some immunological drive. In vitro studies have shown that co-culturing cells derived from low grade MALT lymphomas with H. pylori results in tumour cell proliferation in a T cell dependant manner. Clinical studies have taken this discovery further and shown that patients with early low grate gastric MALT lymphoma treated with anti-Helicobacter therapy can show regression of their tumours. 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Before a lymphoma can arise within the stomach, MALT has to be acquired as part of a response to an immunological stimulus. In most instances, gastric MALT is acquired in response to infection ny Helicobacter pylori. There are several features of MALT lymphoma, such as plasma cell differentiation and follicular colonisation, that suggest that these lymphomas, although demonstrated on the basis of clonality studies to be neoplastic, retain some immunological drive. In vitro studies have shown that co-culturing cells derived from low grade MALT lymphomas with H. pylori results in tumour cell proliferation in a T cell dependant manner. Clinical studies have taken this discovery further and shown that patients with early low grate gastric MALT lymphoma treated with anti-Helicobacter therapy can show regression of their tumours. It is now generally accepted that eradication of H. pylori is a central component of the management of MALT lymphoma.</description><subject>Helicobacter Infections - complications</subject><subject>Helicobacter pylori</subject><subject>Humans</subject><subject>Lymphoma, B-Cell, Marginal Zone - microbiology</subject><subject>Middle Aged</subject><subject>Stomach Neoplasms - microbiology</subject><issn>0007-1420</issn><issn>1471-8391</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkEtLw0AUhQdRaq3-BCG4cJd6JzOZhzupj1oKulAUN8MkmdHUJFNnEmj_vZGGgqu7-M65Bz6ELjBMMUhy5TbW-WLlOt_oKkyzOptqwJgJcoDGmHIcCyLxIRoDAI8xTeAYnYSwAsCEgBihkWRAKSFjlMxNVeYu03lrfLTeVs6XUdlYk7elayLdFNGnDq0v86ja1usvV-tTdGT7WXM23Al6vb97mc3j5dPD4-xmGeeUQxtbxqwQjFINCZUCjMgTQ7JUWq01TTnmTAtLqU3B0pQwA4WxBpjUkieYZGSCLnd_1979dCa0qi5DbqpKN8Z1QXEpARhP-uD1Lph7F4I3Vq19WWu_VRjUnzD1X5jqhalBWF8-H1a6rDbFvjoY6nm842VozWaPtf9WjBOeqvn7h5pJsXhbpLfqmfwCJp58TA</recordid><startdate>1998</startdate><enddate>1998</enddate><creator>Wotherspoon, A C</creator><general>Oxford University Press</general><scope>BSCLL</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>1998</creationdate><title>Helicobacter pylori infection and gastric lymphoma</title><author>Wotherspoon, A C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-f66f88644a024980e8c2e3b59faaa457176a8f44f50f4536e0defe069a97213b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Helicobacter Infections - complications</topic><topic>Helicobacter pylori</topic><topic>Humans</topic><topic>Lymphoma, B-Cell, Marginal Zone - microbiology</topic><topic>Middle Aged</topic><topic>Stomach Neoplasms - microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wotherspoon, A C</creatorcontrib><collection>Istex</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>British medical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wotherspoon, A C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Helicobacter pylori infection and gastric lymphoma</atitle><jtitle>British medical bulletin</jtitle><addtitle>Br Med Bull</addtitle><date>1998</date><risdate>1998</risdate><volume>54</volume><issue>1</issue><spage>79</spage><epage>85</epage><pages>79-85</pages><issn>0007-1420</issn><eissn>1471-8391</eissn><abstract>Gastric lymphoma of mucosa associated lymphoid tissue (MALT) has characteristic clinicopathological features that are different from nodal-type B cell lymphomas. Before a lymphoma can arise within the stomach, MALT has to be acquired as part of a response to an immunological stimulus. In most instances, gastric MALT is acquired in response to infection ny Helicobacter pylori. There are several features of MALT lymphoma, such as plasma cell differentiation and follicular colonisation, that suggest that these lymphomas, although demonstrated on the basis of clonality studies to be neoplastic, retain some immunological drive. In vitro studies have shown that co-culturing cells derived from low grade MALT lymphomas with H. pylori results in tumour cell proliferation in a T cell dependant manner. Clinical studies have taken this discovery further and shown that patients with early low grate gastric MALT lymphoma treated with anti-Helicobacter therapy can show regression of their tumours. It is now generally accepted that eradication of H. pylori is a central component of the management of MALT lymphoma.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>9604433</pmid><doi>10.1093/oxfordjournals.bmb.a011683</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals |
subjects | Helicobacter Infections - complications Helicobacter pylori Humans Lymphoma, B-Cell, Marginal Zone - microbiology Middle Aged Stomach Neoplasms - microbiology |
title | Helicobacter pylori infection and gastric lymphoma |
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