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dc.contributor.authorBoyan, Neslihan
dc.contributor.authorKubat, Huseyin
dc.contributor.authorUzum, Ayşe Kubat
dc.date.accessioned2021-03-03T13:49:11Z
dc.date.available2021-03-03T13:49:11Z
dc.date.issued2007
dc.identifier.citationBoyan N., Kubat H., Uzum A. K. , "Crossed renal ectopia with fusion: Report of two patients", CLINICAL ANATOMY, cilt.20, sa.6, ss.699-702, 2007
dc.identifier.issn0897-3806
dc.identifier.othervv_1032021
dc.identifier.otherav_36319959-3952-453a-857d-47d7e8f08671
dc.identifier.urihttp://hdl.handle.net/20.500.12627/40606
dc.identifier.urihttps://doi.org/10.1002/ca.20464
dc.description.abstractCrossed renal ectopia is one of the rarest urinary system anomalies. It is more often seen at autopsy than in clinical practice. Most cases of renal ectopia remain asymptomatic during life and are diagnosed incidentally. Renal ultrasonography, intravenous pyelography, computerized tomography, and renal scintigraphy (technetium-based tests) are the imaging methods used for diagnosis. Demonstration of crossed renal ectopia is important because it is a predisposing factor for obstruction, infection, and neoplasia of the urinary system. We report two male patients who had Unremarkable clinical findings. Both had left-to-right inferior crossed renal ectopia with fusion. Additionally, the first patient had a history of surgery for a recurrent inguinal hernia, whereas the second had crossed fused renal ectopia associated with nephroptosis. Surgeons should be aware of ectopic and fused kidneys to minimize perioperative complications because of the uncertain anatomy.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectANATOMİ VE MORFOLOJİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectTemel Tıp Bilimleri
dc.subjectAnatomi
dc.subjectBiyokimya
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.titleCrossed renal ectopia with fusion: Report of two patients
dc.typeMakale
dc.relation.journalCLINICAL ANATOMY
dc.contributor.department, ,
dc.identifier.volume20
dc.identifier.issue6
dc.identifier.startpage699
dc.identifier.endpage702
dc.contributor.firstauthorID183879


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