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dc.contributor.authorKara, Sibel
dc.contributor.authorSen, Nazan
dc.contributor.authorOzkan, Ugur
dc.contributor.authorAkcay, M.Sule
dc.date.accessioned2019-09-30T11:18:26Z
dc.date.available2019-09-30T11:18:26Z
dc.date.issued2015
dc.identifier.issn2602-3032
dc.identifier.urihttps://dergipark.org.tr/tr/pub/cumj/issue/4206/55526
dc.identifier.urihttp://hdl.handle.net/11727/4015
dc.description.abstractPrimary vascular malformations such as connection between bronchial artery and pulmonary artery or pulmonary vein are quite rare. A 18-year-old male patient with the first episode of massive hemoptysis was found to have bronchial artery-pulmonary artery fistula, a rare vascular anomaly, on selective bronchial angiography. Since medical history revealed no acquired cause, it is considered congenital. He underwent bronchial artery embolization and hemoptysis was completely resolved after endovascular treatment. The presence of such vascular anomalies should be suspected in patients with massive hemoptysis. Bronchial artery embolization is a safe and effective nonsurgical treatment option for such patients.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectHemoptysisen_US
dc.subjectvascular malformationen_US
dc.subjectbronchial artery-pulmonary artery fistulaen_US
dc.subjectbronchial artery embolizationen_US
dc.titleCongenital Bronchial Artery - Pulmonary Artery Fistula in a Young Adulten_US
dc.typearticleen_US
dc.relation.journalCUKUROVA MEDICAL JOURNALen_US
dc.identifier.volume40en_US
dc.identifier.issue4en_US
dc.identifier.startpage830en_US
dc.identifier.endpage835en_US
dc.identifier.wos000363969000027


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