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dc.contributor.authorDemirkan S.
dc.contributor.authorGültekin Y.
dc.date.accessioned2020-06-25T15:17:59Z
dc.date.available2020-06-25T15:17:59Z
dc.date.issued2018
dc.identifier.issn2233601X
dc.identifier.urihttps://doi.org/10.5090/kjtcs.2018.51.1.64
dc.identifier.urihttps://hdl.handle.net/20.500.12587/2587
dc.description.abstractHughes-Stovin syndrome is a rare disorder of unknown etiology. Although the association between multiple pulmonary artery aneurysms and venous thrombosis of the lower limbs was reported by Beattie and Hall in 1911, it was not until 1962 that the eponym "Hughes-Stovin syndrome" was formally introduced in the medical literature. We describe 2 patients with Hughes-Stovin syndrome who presented with pulmonary artery aneurysm, thrombophlebitis, hemoptysis, and oral ulcers, review the manifestations of the disease, and compare its similarities with and differences from Behçet disease. © The Korean Society for Thoracic and Cardiovascular Surgery. 2018.en_US
dc.language.isoengen_US
dc.publisherKorean Society for Thoracic and Cardiovascular Surgeryen_US
dc.relation.isversionof10.5090/kjtcs.2018.51.1.64en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectHughes-Stovin syndrome Behçet diseaseen_US
dc.subjectOral ulceren_US
dc.subjectPulmonary artery aneurysms Thrombosisen_US
dc.titleHughes-Stovin syndrome as an outcome of Behçet disease or as a different entityen_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume51en_US
dc.identifier.issue1en_US
dc.identifier.startpage64en_US
dc.identifier.endpage68en_US
dc.relation.journalKorean Journal of Thoracic and Cardiovascular Surgeryen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US


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