Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2398
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dc.contributor.authorAtmaca, Husnu-
dc.contributor.authorBektas, Osman-
dc.contributor.authorGunaydin, Zeki Yuksel-
dc.contributor.authorKurt, Ali Bekir-
dc.date.accessioned2022-08-17T05:47:24Z-
dc.date.available2022-08-17T05:47:24Z-
dc.date.issued2015-
dc.identifier.urihttp://doi.org/10.5543/tkda.2015.97383-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2398-
dc.description.abstractLeriche Syndrome is an uncommon variant of atherosclerotic occlusive disease, and is characterised by total occlusion in the abdominal aorta and/or both iliac arteries. Chronic abdominal aortic occlusion can extend as far as the renal arteries, causing juxtarenal aortic occlusion, also known as Leriche Syndrome. A 60-year-old female patient was admitted to the emergency department with claudication. On admission, her physical examination was unremarkable except for a decreased femoral artery pulse. Increased cardiothoracic ratio and mild calcification on the wall of the aortic arch and descending aorta were observed in the thoracic computed tomography (CT) angiogram. Calcified plaque was present in the abdominal aorta just below the renal artery, and complete thrombotic occlusion of the abdominal aorta was observed in the abdominal CT angiogram.en_US
dc.language.isoengen_US
dc.relation.isversionof10.5543/tkda.2015.97383en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectleriche syndrome, computed tomographyen_US
dc.titleJuxtarenal Leriche Syndromeen_US
dc.typearticleen_US
dc.relation.journalTURK KARDIYOLOJI DERNEGI ARSIVI-ARCHIVES OF THE TURKISH SOCIETY OF CARDIOLOGYen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.contributor.authorID0000-0001-9779-7578en_US
dc.contributor.authorID0000-0002-6616-9891en_US
dc.identifier.volume43en_US
dc.identifier.issue2en_US
dc.identifier.startpage212en_US
dc.identifier.endpage212en_US
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