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dc.contributor.authorGüler Özden M.
dc.contributor.authorAyyildiz T.
dc.contributor.authorŞentürk N.
dc.contributor.authorCantürk M.T.
dc.date.accessioned2020-06-21T09:04:38Z
dc.date.available2020-06-21T09:04:38Z
dc.date.issued2017
dc.identifier.issn1300-0330
dc.identifier.urihttps://doi.org/10.5336/dermato.2017-57068
dc.identifier.urihttps://hdl.handle.net/20.500.12712/2049
dc.description.abstractPrimary biliary cholangitis (PBC) is an autoimmune and cholestatic, liver disease characterized by chronic nonsuppurative destructive cholangitis, circulating antimitochondrial antibodies and interlobular bile duct destruction. Autoimmune disorders including PBC seems to have an elevated risk of lymphoma. Mycosis Fungoides, the most common type of Cutaneous T- cell lymphoma (CTCL) is also a neoplasm of the immune system. There is little information about the risk of developing lymphoma including CTCL in PBC patients. Here, we present the second case of CTCL as much as we know, reported in the literature that occurred in an adult patient with PBC. Copyright © 2017 by Türkiye Klinikleri.en_US
dc.language.isoengen_US
dc.publisherOrtadogŸu Reklam Tanitim Yayincilik Turizm Egitim Insaat Sanayi ve Ticaret A.S.en_US
dc.relation.isversionof10.5336/dermato.2017-57068en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBiliaryen_US
dc.subjectLiver cirrhosisen_US
dc.subjectMycosis fungoidesen_US
dc.titleCutaneous T cell lymphoma in a patient with primary biliary cholangitisen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume27en_US
dc.identifier.issue3en_US
dc.identifier.startpage134en_US
dc.identifier.endpage137en_US
dc.relation.journalTurkiye Klinikleri Dermatolojien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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