Rare tumours of the testis: twelve years of experience

Basit Öğe Kaydı
dc.authorid0000-0002-7931-2941en_US
dc.authorid0000000308820524en_US
dc.contributor.authorOruç, Zeynep
dc.contributor.authorEbinç, Senar
dc.contributor.authorKaplan, Muhammet Ali
dc.date.accessioned2021-08-05T13:21:03Z
dc.date.available2021-08-05T13:21:03Z
dc.date.issued2020en_US
dc.departmentDicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, İç Hastalıklar Ana Bilim Dalıen_US
dc.description.abstractRare tumours of the testis includes a wide variety of tumours. We aim to present clinical and histological characteristics of our patients with rare tumours of the testis. The medical records of 33 patients who were treated and followed-up for testicular rare tumours in our center between 2007 and 2020 were retrospectively reviewed. Of all the 243 testicular tumours, 222 cases (91.4%) were germ cell tumours and 21 cases (8.6%) were non-germ cell tumours. Thirty-three rare tumours of the testis including rare germ cell tumours and non-germ cell tumours were detected. The mean age of the patients at diagnosis was 34 years (range 18-68 years). The histological types of rare testicular tumours were as follows: teratoma 4.5% (n=11), sex-cord stromal tumours 4.5% (n=11), paratesticular tumours 3.2% (n=8), and the others [lymphoma 0.4% (n=1), mesothelioma 0.4% (n=1) and choriocarcinoma 0.4% (n=1)]. The median duration of follow-up was 32 months (range 1 to 256 months). None of the patients with non-metastatic disease stage developed recurrence after having received appropriate therapy. Metastatic disease was documented in 9 cases at the time of diagnosis (five patients with teratomas, two patients with Leydig cell tumour, one patient with choriocarcinoma and rhabdomyosarcoma). The most common subtypes of testicular rare tumours in our center was teratoma and sex-cord stromal tumours. Because of testicular rare tumours have different biological features and different clinical outcomes, the management of each tumour requires a different approach.en_US
dc.identifier.citationOruç, Z., Ebinç, S. ve Kaplan, M. A. (2020). Rare Tumours of the Testis: Twelve Years of Experience. Prague Medical Report, 121(3), 181-193.en_US
dc.identifier.doi10.14712/23362936.2020.17
dc.identifier.endpage193en_US
dc.identifier.issn1214-6994
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-85092683410
dc.identifier.scopusqualityQ3
dc.identifier.startpage181en_US
dc.identifier.urihttps://pmr.lf1.cuni.cz/121/3/0181/
dc.identifier.urihttps://hdl.handle.net/11468/7262
dc.identifier.volume121en_US
dc.indekslendigikaynakScopus
dc.institutionauthorOruç, Zeynep
dc.institutionauthorEbinç, Senar
dc.institutionauthorKaplan, Muhammet Ali
dc.language.isoenen_US
dc.publisherUniversitas Carolina Pragensisen_US
dc.relation.ispartofPrague Medical Report
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectGonadal tumoursen_US
dc.subjectRare tumoursen_US
dc.subjectTestis tumoursen_US
dc.titleRare tumours of the testis: twelve years of experienceen_US
dc.titleRare tumours of the testis: twelve years of experience
dc.typeArticleen_US

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