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dc.contributor.authorDemir, Hale
dc.contributor.authorYulek, Ozden
dc.contributor.authorOruc, Ertugrul
dc.contributor.authorGulle, Bugra Taygun
dc.contributor.authorDemir, Deniz Nur
dc.contributor.authorDemirdag, Cetin
dc.contributor.authorDurak, Haydar
dc.date.accessioned2024-03-12T19:34:46Z
dc.date.available2024-03-12T19:34:46Z
dc.date.issued2021
dc.identifier.issn2147-2270
dc.identifier.urihttps://doi.org/10.4274/uob.galenos.2020.1785
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/505066
dc.identifier.urihttps://hdl.handle.net/20.500.12450/2718
dc.description.abstractObjective: The primary aim of our study is to establish the frequency and clinicopathological features of seconder primary malignant tumours (SPMTs) in cases with renal cell carcinoma (RCC). Materials and Methods: Pathology reports of 1129 RCC cases were checked retrospectively, and 70 RCC cases with SPMTs were included in the study. One patient had two and the other had three different SPMTs, so the total number of SPMTs was 73. According to occurrence times of SPMTs, the cases were classified as the antecedent, synchronous, subsequent and unknown. The first three groups were compared according to their clinicopathological features. Results: The incidence of SPMTs with RCC in our study was 6.2% and lower than that reported by many other studies. The most common SPMTs were gastrointestinal, breast, prostate, lung, thyroid carcinomas and haematolymphoid malignancies. Sixty-two per cent of SPMTs were developed as synchronous and subsequent. There was no statistically significant difference among groups regarding age, histological subtype and RCC size. Male patients had a higher percentage in the synchronous group. In all groups, the most common RCC subtype was clear cell carcinoma. The RCC subtype in cases with multiple SPMTs was papillary. The prostatic adenocarcinoma rate was remarkable in males with papillary type RCC. Conclusion: RCC can coexist with secondary malignancies. Therefore, when a new tumour appears in a patient with RCC in clinical follow-up, it is appropriate to evaluate that tumour histopathologically or cytopathologically regarding SPMT before accepting it as a metastatic spread.en_US
dc.language.isoengen_US
dc.publisherGalenos Yayinciliken_US
dc.relation.ispartofUroonkoloji Bulteni-Bulletin Of Urooncologyen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectRenal cell carcinomaen_US
dc.subjectseconder primary malignant tumouren_US
dc.subjectsynchronous neoplasmsen_US
dc.subjectmetachronous neoplasmsen_US
dc.titleSecond Primary Malignant Tumours in Patients with Renal Cell Carcinomaen_US
dc.typearticleen_US
dc.departmentAmasya Üniversitesien_US
dc.authoridDemir, Hale/0000-0002-0773-2824
dc.authoridGulle, Bugra Taygun/0000-0003-3435-4336
dc.authoridYulek, Ozden/0000-0001-7557-0268
dc.authoridORUC, ERTUGRUL/0000-0002-6829-6528
dc.identifier.volume20en_US
dc.identifier.issue1en_US
dc.identifier.startpage49en_US
dc.identifier.endpage55en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.trdizinid505066en_US
dc.identifier.doi10.4274/uob.galenos.2020.1785
dc.department-temp[Demir, Hale] Amasya Univ, Fac Med, Dept Pathol, Amasya, Turkey; [Yulek, Ozden] Siirt State Hosp, Clin Pathol, Siirt, Turkey; [Oruc, Ertugrul] Istanbul Tuzla State Hosp, Clin Pathol, Istanbul, Turkey; [Gulle, Bugra Taygun] Istanbul Univ, Publ Hlth, Istanbul Fac Med, Istanbul, Turkey; [Demir, Deniz Nur] Istanbul Univ Cerrahpasa, Cerrahpasa Fac Med, Istanbul, Turkey; [Demirdag, Cetin] Istanbul Univ Cerrahpasa, Cerrahpasa Fac Med, Dept Urol, Istanbul, Turkey; [Durak, Haydar] Acibadem Hosp, Clin Pathol, Istanbul, Turkey; [Gurses, Iclal; Uygun, Nesrin] Istanbul Univ Cerrahpasa, Cerrahpasa Fac Med, Dept Pathol, Istanbul, Turkeyen_US
dc.identifier.wosWOS:000625432300009en_US
dc.authorwosidDemir, Hale/AAG-2277-2019
dc.authorwosidYülek, Özden/GQN-1696-2022
dc.authorwosidyulek, ozden/AAR-9680-2021


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