Retrocaval ureter: Two case reports.

dc.contributor.authorKyei, M.Y.
dc.contributor.authorYeboah, E.D.
dc.contributor.authorKlufio, G.O.
dc.contributor.authorMensah, J.E.
dc.contributor.authorGepi-Atee, S.
dc.contributor.authorZakpaa, L.
dc.contributor.authorMorton, B.
dc.contributor.authorAdusei, B.
dc.date.accessioned2013-06-18T11:36:09Z
dc.date.accessioned2017-10-19T13:10:58Z
dc.date.available2013-06-18T11:36:09Z
dc.date.available2017-10-19T13:10:58Z
dc.date.issued2011-12
dc.description.abstractRetrocaval ureter also referred to as pre-ureteral vena cava is a rare congenital anomaly with the ureter passing posterior to the inferior vena cava. Though it is a congenital anomaly, patients do not normally present with symptoms until the 3rd and 4th decades of life from a resulting hydronephrosis. We present the first two cases to be reported in Ghana; a 36-year-old male and a 40-year-old female both with right flank pains and associated right hydronephrosis. Diagnoses were confirmed with retrograde ureteropyelogram and both had an open surgical repair of the anomaly.en_US
dc.identifier.citationKyei, M. Y., Yeboah, E. D., Klufio, G. O., Mensah, J. E., Gepi-Atee, S., Zakpaa, L., . . . Adusei, B. (2011). Retrocaval ureter: Two case reports. Ghana Medical Journal, 45(4), 177-180.en_US
dc.identifier.issn00169560
dc.identifier.urihttp://197.255.68.203/handle/123456789/3464
dc.language.isoenen_US
dc.subjectEMTREE medical terms: adult; article; case report; congenital malformation; female; human; hydronephrosis; male; radiography; ureteren_US
dc.subjectMeSH: Adult; Female; Humans; Hydronephrosis; Male; Ureteren_US
dc.titleRetrocaval ureter: Two case reports.en_US
dc.typeArticleen_US

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