Hereditary nonpolyposis colorectal cancer classification: Difference between revisions
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==Overview== | ==Overview== | ||
Hereditary nonpolyposis colorectal cancer may be classified according to MSI-H into 3 subtypes: right-sided poorly differentiated cancers, right-sided mucinous cancers, and [[adenocarcinomas]] in any location showing any measurable level of [[intraepithelial lymphocyte]] (TIL). In addition, HNPCC can be divided into ''Lynch syndrome I'' (familial colon cancer) and ''Lynch syndrome II'' (HNPCC associated with other cancers of the gastrointestinal tract or [[reproductive system]]).<ref>[http://emedicine.medscape.com/article/188613-overview Hereditary Colorectal Cancer > Background]. From Medscape. By Juan Carlos Munoz and Louis R Lambiase. Updated: Oct 31, 2011</ref> | |||
==Classification== | ==Classification== | ||
==References== | ==References== |
Revision as of 19:06, 1 December 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]
Overview
Hereditary nonpolyposis colorectal cancer may be classified according to MSI-H into 3 subtypes: right-sided poorly differentiated cancers, right-sided mucinous cancers, and adenocarcinomas in any location showing any measurable level of intraepithelial lymphocyte (TIL). In addition, HNPCC can be divided into Lynch syndrome I (familial colon cancer) and Lynch syndrome II (HNPCC associated with other cancers of the gastrointestinal tract or reproductive system).[1]
Classification
References
- ↑ Hereditary Colorectal Cancer > Background. From Medscape. By Juan Carlos Munoz and Louis R Lambiase. Updated: Oct 31, 2011