Alptürker K.A.Akgül Ö.2024-07-222024-07-22202321463816http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/12185Hughes-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 Behçet 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. ©2023 by the Turkish Osteoporosis Society / Turkish Journal of Osteoporosis published by Galenos Publishing House. Licensed by CC BY-NC-ND.EnglishAll Open Access; Gold Open Accesscyclophosphamidemethylprednisolonesteroidwarfarinabnormal respiratory soundadultaphthous stomatitisArticleautoimmune diseasebleedingbody weight losscase reportclinical articlecomputer assisted tomographydeep vein thrombosisdrug dose reductiondrug pulse therapydry coughdyspneaemergency wardfevergenital ulcerground glass opacityhemoptysishospital admissionHughes Stovin syndromehumanlung hemorrhagemalemiddle agedpulmonary artery aneurysmpulmonary artery thrombosisskin defectsweatingthorax painthorax radiographytuberculosisuveitisArticle10.4274/tod.galenos.2022.59023