Türk Osteoporoz Dergisi (Aug 2023)

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

  • Kezban Armağan Alptürker,
  • Özgür Akgül

DOI
https://doi.org/10.4274/tod.galenos.2022.59023
Journal volume & issue
Vol. 29, no. 2
pp. 127 – 129

Abstract

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Hughes-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.

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