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dc.contributor.authorAyanoglu, O. H.
dc.contributor.authorTokat, Y.
dc.contributor.authorKurt, Z.
dc.contributor.authorKilli, R.
dc.contributor.authorYuzer, Y.
dc.contributor.authorUraz, S.
dc.contributor.authorDuran, C.
dc.contributor.authorBalci, D.
dc.contributor.authorAkin, B.
dc.contributor.authorDayangac, M.
dc.date.accessioned2021-03-03T09:49:12Z
dc.date.available2021-03-03T09:49:12Z
dc.date.issued2007
dc.identifier.citationUraz S., Duran C., Balci D., Akin B., Dayangac M., Kurt Z., Ayanoglu O. H. , Killi R., Yuzer Y., Tokat Y., "A very rare venous anomaly in a living liver donor: Left hepatic venous connection to the right atrium", TRANSPLANTATION PROCEEDINGS, cilt.39, sa.5, ss.1714-1715, 2007
dc.identifier.issn0041-1345
dc.identifier.othervv_1032021
dc.identifier.otherav_1f06ebf2-6d28-44bf-a539-6118477ef175
dc.identifier.urihttp://hdl.handle.net/20.500.12627/26003
dc.identifier.urihttps://doi.org/10.1016/j.transproceed.2006.11.009
dc.description.abstractIn humans, three main hepatic veins drain the liver into the inferior vena cava below the diaphragm. This report represents the first living donor liver that had a rare anatomic variation of the left hepatic vein draining directly to the right atrium, which was detected preoperatively by routine investigations of the living donor transplantation. This type of anomaly may present potentially fatal challanges to a donor operation if not detected preoperatively, especially when the left lobe is the choice for explantation.
dc.language.isoeng
dc.subjectCerrahi Tıp Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectTRANSPLANTASYON
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectCERRAHİ
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectİmmünoloji
dc.titleA very rare venous anomaly in a living liver donor: Left hepatic venous connection to the right atrium
dc.typeMakale
dc.relation.journalTRANSPLANTATION PROCEEDINGS
dc.contributor.department, ,
dc.identifier.volume39
dc.identifier.issue5
dc.identifier.startpage1714
dc.identifier.endpage1715
dc.contributor.firstauthorID182836


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