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dc.contributor.authorOz, A.
dc.contributor.authorOguz, B.
dc.contributor.authorKarcaaltincaba, M.
dc.contributor.authorYilmaz, M.
dc.contributor.authorHaliloglu, M.
dc.date.accessioned2019-12-12T06:42:25Z
dc.date.available2019-12-12T06:42:25Z
dc.date.issued2014
dc.identifier.issn1780-2393
dc.identifier.urihttps://doi.org/10.5334/jbr-btr.5
dc.identifier.urihttp://hdl.handle.net/11655/16721
dc.description.abstractLeft atrial appendage aneurysms are usually congenital and are very infrequent anomalies of the heart. They are very rarely diagnosed during childhood, with most cases symptomatic between the 2nd and 4th decades of life. Diagnosis is vitally important due to potential life-threatening complications. Surgical excision is the treatment of choice. Surgery reduces the risks of cardiac arrest, respiratory distress, arrhythmia, heart failure, thromboembolism, or rupture. We report the case of a 3-year-old boy with incidental diagnosis of a giant aneurysm of the left atrial appendage that was confirmed with magnetic resonance imaging and treated with surgery.
dc.language.isoen
dc.publisherAssoc Royal Soc Scientifiques Medicales Belges
dc.relation.isversionof10.5334/jbr-btr.5
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectRadiology, Nuclear Medicine & Medical Imaging
dc.titleIncidentally Detected Congenital Giant Left Atrial Appendage Aneurysm In A Child: Mri Findings
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalJbr-Btr
dc.contributor.departmentKalp ve Damar Cerrahisi
dc.identifier.volume97
dc.identifier.issue1
dc.identifier.startpage30
dc.identifier.endpage32
dc.description.indexWoS
dc.description.indexScopus


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