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dc.contributor.author Tímár József
dc.contributor.author Hársing Judit
dc.contributor.author Somlai Beáta
dc.date.accessioned 2014-12-11T09:09:00Z
dc.date.available 2014-12-11T09:09:00Z
dc.date.issued 2013
dc.identifier.citation pagination=73-78; journalVolume=57; journalIssueNumber=2; journalTitle=MAGYAR ONKOLÓGIA;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/739
dc.description.abstract Pathological classification of malignant melanoma did not change in the past decade, it was just completed with UV-induced skin alterations. A new feature, however, is the establishment of molecular classification of melanoma indicating that beside the most frequent genetic alterations (BRAF, NRAS, CKIT mutations) there is a wide variety of rare molecular subclasses. Unfortunately, none of these genetic alterations can be used to discriminate benign lesions from malignant ones. The frequently used "melanoma" markers are mostly melanosomal markers, therefore they are not helpful for this diagnostic purpose either. More recently, novel FISH kits have been developed analyzing characteristic copy number alterations specific for malignant melanoma. Though melanosomal markers are helpful in differencial diagnostics, the presence of normal melanocytes in various tissues (lymph nodes, intestine or brain) requires application of molecular techniques when melanoma metastasis is in question.
dc.relation.ispartof urn:issn:0025-0244
dc.title A malignus melanóma molekuláris klasszifikációja és markerei [Molecular classification and markers of malignant melanoma]
dc.type Journal Article
dc.date.updated 2014-12-10T18:35:47Z
dc.language.rfc3066 hu
dc.identifier.mtmt 2362488
dc.identifier.pubmed 23795351
dc.contributor.department SE/ÁOK/K/Bőr-, Nemikórtani és Bőronkológiai Klinika
dc.contributor.department SE/ÁOK/I/II. Sz. Patológiai Intézet
dc.contributor.institution Semmelweis Egyetem


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