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dc.contributor.author Ágoston, Emese
dc.contributor.author Horvath E
dc.contributor.author Győrffy, Balázs
dc.contributor.author Harsányi, László
dc.contributor.author Szász, Attila Marcell
dc.date.accessioned 2018-10-04T08:13:32Z
dc.date.available 2018-10-04T08:13:32Z
dc.date.issued 2018
dc.identifier.citation pagination=206-214; journalVolume=159; journalIssueNumber=6; journalTitle=ORVOSI HETILAP;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/5666
dc.identifier.uri doi:10.1556/650.2018.30974
dc.description.abstract Today, colorectal cancer is regarded as a heterogeneous disease. Its heterogeneity is caused by genetic alterations, molecular aberrations, different developing pathways as well as by micro- and macroenviromental agents. In the last decade, beside the classic genetic model for colorectal tumuorgenesis that follows the adenoma-carcinoma sequence, an alternative pathway has been identified. This pathway is called the serrated pathway and it is responsible for approximately one third of all colorectal lesions. Beyond their dissimilar molecular characteristics, these tumours also show different macroscopic and histologic appearance. Moreover, their malignant potency and progressive ability distinguish them from tumours of the classic genetic model. The aim of this review is to summarize the molecular and pathologic features of serrated lesions and the serrated pathway to colorectal cancer and to highlight their clinical impact.
dc.relation.ispartof urn:issn:0030-6002
dc.title Heterogén vastagbéldaganat: a fogazott útvonalon kialakuló, sporadikus laesiók jelentősége a klinikai gyakorlatban
dc.type Journal Article
dc.date.updated 2018-06-22T10:59:01Z
dc.language.rfc3066 hu
dc.identifier.mtmt 3378457
dc.identifier.wos 000425110100002
dc.identifier.pubmed 29400100
dc.contributor.department SE/AOK/K/Onkológiai Központ
dc.contributor.department SE/AOK/K/I. Sz. Sebészeti Klinika
dc.contributor.institution Semmelweis Egyetem


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