Patient Presenting with Hemoptysis: A Case of Hughes-Stovin Syndrome

dc.contributor.authorAlptürker, KA
dc.contributor.authorAkgül, O
dc.date.accessioned2025-04-10T10:31:47Z
dc.date.available2025-04-10T10:31:47Z
dc.description.abstractHughes-Stovin syndrome (HSS) is a very rare autoimmune clinical disorder that has been described as the presence of thrombophlebitis and multiple aneurysms in pulmonary and/or bronchial arteries. The pathogenesis is still unknown, but this syndrome is often thought of as a manifestation of Behcet disease. Herein, we describe a 59-year-old male patient who was admitted to massive hemoptysis. HSS was diagnosed on the basis of imaging pulmonary artery aneurysms and a history of lower extremity thrombosis. It differs in terms of the occurrence of this rare syndrome in an elderly patient. In this syndrome, which has a high mortality, the results are satisfactory when the treatment is started with a rapid diagnosis.
dc.identifier.issn2147-2653
dc.identifier.urihttp://hdl.handle.net/20.500.14701/38254
dc.language.isoEnglish
dc.titlePatient Presenting with Hemoptysis: A Case of Hughes-Stovin Syndrome
dc.typeArticle

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