| Literature DB >> 34790621 |
Nedia Moussa1, Tasnim Znegui1, Mouna Snoussi2, Rahma Gargouri1, Zouhaier Bahloul2, Sourour Abid1, Samy Kammoun1.
Abstract
Hughes-Stovin syndrome is a very rare condition with no defined diagnostic criteria. We present the case of a 26-year-old man who had haemoptysis revealing Hughes-Stovin syndrome. We will consider the aetiology, therapeutic and evolutionary aspects of this disease. LEARNING POINTS: Hughes-Stovin syndrome is a very rare disorder of unknown aetiology which can be fatal.It is considered a variant of Behcet's disease.Early diagnosis and treatment improve prognosis. © EFIM 2021.Entities:
Keywords: Hughes-Stovin syndrome; aneurysms; thrombosis
Year: 2021 PMID: 34790621 PMCID: PMC8592656 DOI: 10.12890/2021_002810
Source DB: PubMed Journal: Eur J Case Rep Intern Med ISSN: 2284-2594