Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/33550
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dc.date.accessioned2023-08-21T12:07:54Z-
dc.date.available2023-08-21T12:07:54Z-
dc.date.issued2017-
dc.identifier.citationUğraş, N. vd. (2017). ''Immunohistochemical expression of CDX2, CK7, HER2 and HER4 in periampullary adenocarcinoma: Implications for clinicopathology and patient outcomes''. Acta Gastro-Enterologica Belgica, 80(1), 31-37.en_US
dc.identifier.uri1784-3227-
dc.identifier.urihttp://hdl.handle.net/11452/33550-
dc.description.abstractBackground : Periampullary carcinomas originate from the pancreatic head, the ampulla, the distal bile duct, or the duodenum. The expression of CK7 and CDX2 has been used in the classification of periampullary carcinomas. There is prognostic value of human epidermal growth factor receptor (HER) 2 and HER 4, which have been linked to poor prognosis in several types of tumors, such as breast and gastric carcinomas. We aimed to evaluate the expression and prognostic value of CDX2, CK7, HER 2, and HER 4 in periampullary adenocarcinoma. Patients and Methods : We retrospectively selected 98 patients who had undergone pancreatoduodenectomy for periampullary adenocarcinoma at our pathology department. The tumor location, pathological subtype, involvement of vessels and lymph nodes, perineural invasion, clinical follow-up, and tumorstage were noted. Immunohistochemistry was performed for CK7, CDX2, HER2, and HER4. Results : CDX2 staining was predictive of perineural invasion. Additionally, there was a significant association between the overexpression of HER2 and HER4 and the presence of perineural invasion. HER4 was significantly positive in patients with the pancreatobiliary subtype compared with patients with the intestinal subtype. Patients with the pancreatobiliary subtype, lymph node involvement, and advanced pT and UICC stages had significantly lower median survival. Conclusion : Our findings suggest that only pancreatobiliary subtype, lymph node involvement and advanced pT and UICC stages were independent predictors of short survival, but the ampulla tumor location predicted a significantly better survival time. The immunohistochemical expression of CDX2, CK7, HER4, and HER2, vessel involvement, and perineural invasion were not associated with the survival of patients with periampullary adenocarcinoma.en_US
dc.language.isoenen_US
dc.publisherUniv Catholique Louvaınen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGastroenterology & hepatologyen_US
dc.subjectCDX2en_US
dc.subjectCK7en_US
dc.subjectHER2en_US
dc.subjectImmunohistochemistryen_US
dc.subjectPeriampullary adenocarcinomaen_US
dc.subjectHER4en_US
dc.subjectAmpullary canceren_US
dc.subjectOverexpressionen_US
dc.subjectCarcinomaen_US
dc.subjectPancreaticobiliaryen_US
dc.subjectPrognosisen_US
dc.subjectPapillaen_US
dc.subjectDifferentiationen_US
dc.subjectDifferentiationen_US
dc.subjectOncogeneen_US
dc.subjectDiagnosisen_US
dc.subjectVateren_US
dc.titleImmunohistochemical expression of CDX2, CK7, HER2 and HER4 in periampullary adenocarcinoma: Implications for clinicopathology and patient outcomesen_US
dc.typeArticleen_US
dc.identifier.wos000403607000006tr_TR
dc.identifier.scopus2-s2.0-85014317564tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Cerrahi Patoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Onkoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-7346-7440tr_TR
dc.identifier.startpage31tr_TR
dc.identifier.endpage37tr_TR
dc.identifier.volume80tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalActa Gastro-Enterologica Belgicaen_US
dc.contributor.buuauthorUğraş, Nesrin-
dc.contributor.buuauthorYerci, Ömer-
dc.contributor.buuauthorÖzgün, Gonca-
dc.contributor.buuauthorDeligönül, Adem-
dc.contributor.buuauthorDündar, Halit Ziya-
dc.contributor.buuauthorSarkut, Pınar-
dc.contributor.buuauthorUludağ, Özkan Kanat-
dc.contributor.researcheridAAH-2716-2021tr_TR
dc.identifier.pubmed29364095tr_TR
dc.subject.wosGastroenterology & hepatologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid55386535600tr_TR
dc.contributor.scopusid6603810549tr_TR
dc.contributor.scopusid35520074800tr_TR
dc.contributor.scopusid37088030300tr_TR
dc.contributor.scopusid55453773300tr_TR
dc.contributor.scopusid55806454400tr_TR
dc.contributor.scopusid57193505535tr_TR
dc.subject.scopusAmpulla of Vater; Duodenal Neoplasms; Adenomaen_US
dc.subject.emtreeCytokeratin 7en_US
dc.subject.emtreeEpidermal growth factor receptor 2en_US
dc.subject.emtreeEpidermal growth factor receptor 4en_US
dc.subject.emtreeTranscription factor Cdx2en_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAmpulla of vateren_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBile duct carcinomaen_US
dc.subject.emtreeBlood vesselen_US
dc.subject.emtreeCancer prognosisen_US
dc.subject.emtreeCancer stagingen_US
dc.subject.emtreeCancer survivalen_US
dc.subject.emtreeClinical evaluationen_US
dc.subject.emtreeComparative studyen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFollow upen_US
dc.subject.emtreeGene overexpressionen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman tissueen_US
dc.subject.emtreeImmunohistochemistryen_US
dc.subject.emtreeLymph node metastasisen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreePancreas adenocarcinomaen_US
dc.subject.emtreePancreaticoduodenectomyen_US
dc.subject.emtreePeriampullary adenocarcinomaen_US
dc.subject.emtreePerineural invasionen_US
dc.subject.emtreePredictive valueen_US
dc.subject.emtreeProtein expressionen_US
dc.subject.emtreeRetrospective studyen_US
dc.subject.emtreeTreatment outcomeen_US
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