Polyorchism: a Case Report
dc.authorscopusid | 8855691800 | |
dc.authorscopusid | 56363775800 | |
dc.authorscopusid | 8855691600 | |
dc.contributor.author | Polat, F.R. | |
dc.contributor.author | Özer, A. | |
dc.contributor.author | Polat, S. | |
dc.date.accessioned | 2025-05-10T17:06:15Z | |
dc.date.available | 2025-05-10T17:06:15Z | |
dc.date.issued | 2003 | |
dc.department | T.C. Van Yüzüncü Yıl Üniversitesi | en_US |
dc.department-temp | Polat F.R., Department of Surgery, State Hospital, Van, Turkey, Arastirma Hastnesi Arkasi, Van, Kardelen sitesi, C-Blok no. 5, Turkey; Özer A., Department of Surgery, State Hospital, Van, Turkey; Polat S., Department of Pathology, Medicine Faculty, 100 Year University, Van, Turkey | en_US |
dc.description.abstract | Background: Polyorchism is a rare anomaly whose genesis is unclarified, although several theories have been proposed. It is generally associated with other disorders but seldom with malignancy. Conclusions: When a supernumerary testicle is encountered intraoperatively, it should be removed. © 2004 Kluwer Academic Publishers. | en_US |
dc.identifier.doi | 10.1023/B:UROL.0000020266.94430.15 | |
dc.identifier.endpage | 254 | en_US |
dc.identifier.issn | 0301-1623 | |
dc.identifier.issue | 2 | en_US |
dc.identifier.pmid | 15072505 | |
dc.identifier.scopus | 2-s2.0-12144285701 | |
dc.identifier.scopusquality | Q2 | |
dc.identifier.startpage | 253 | en_US |
dc.identifier.uri | https://doi.org/10.1023/B:UROL.0000020266.94430.15 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14720/6370 | |
dc.identifier.volume | 35 | en_US |
dc.identifier.wosquality | Q3 | |
dc.language.iso | en | en_US |
dc.relation.ispartof | International Urology and Nephrology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Inguinal Hernia | en_US |
dc.subject | Polyorchism | en_US |
dc.title | Polyorchism: a Case Report | en_US |
dc.type | Article | en_US |