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  • Hughes–Stovin syndrome - Wikipedia
    Hughes–Stovin syndrome (HSS) is a rare autoimmune disorder often described as inflammation in relation to blood vessels, a form of vasculitis It is not associated with any known cause and is typically characterized by multiple aneurysms in pulmonary arteries and deep vein thromboses
  • “Hughes‐Stovin Syndrome: A Comprehensive Narrative Review . . .
    There is currently no standardized treatment protocol for Hughes–Stovin Syndrome (HSS) Therapeutic strategies are largely derived from the management of Behçet's disease and other systemic vasculitides
  • Hughes-Stovin Syndrome - PMC
    Hughes-Stovin Syndrome (HSS) is a very rare clinical disorder characterized by thrombophlebitis and multiple pulmonary and or bronchial aneurysms Less than 40 published cases of HSS have been described in English medical literature so far
  • The Down Low | House Wiki | Fandom
    He has Hughes-Stovin syndrome, an autoimmune disease As it's in its advanced stages, there is nothing they can do to treat it He has less than a day to live Thirteen informs him that even if he had been up front at the beginning, they probably could not have saved him The patient asks to call his wife
  • Hughes–Stovin syndrome without peripheral venous thrombosis: Early . . .
    Hughes–Stovin syndrome is a rare vasculitis with pulmonary artery aneurysms Venous thrombosis may be absent, adding to the diagnostic challenge Early diagnosis and aggressive immunosuppression can prevent fatal rupture This case showed marked radiologic improvement with steroids and mycophenolate
  • Hughes-Stovin Syndrome: A Case Report on a Rare, Life-Threatening . . .
    Hughes-Stovin Syndrome (HSS) is a rare vasculitic disorder characterised by widespread pulmonary artery aneurysms It shares some features with Behçet disease Currently, the diagnosis is based on clinical suspicion Our case describes a young male
  • Hughes‐Stovin syndrome (HSS): current status and future perspectives
    In both clinical conditions, thrombosis dominates the clinical presentation, and thus anticoagula-tion is an essential line of treatment
  • Hughes-Stovin syndrome - National Organization for Rare Disorders
    Hughes-Stovin syndrome (HSS) is a life-threatening disorder, believed to be a cardiovascular clinical variant manifestation of Behcet’s disease (BD) It is characterized by the association of multiple pulmonary artery aneurysms (PAAs) and peripheral venous thrombosis
  • “Hughes‐Stovin Syndrome: A Comprehensive Narrative Review . . .
    HSS presents significant diagnostic and therapeutic challenges due to its rarity and clinical overlap with other vasculitides
  • Hughes-Stovin syndrome (HSS): current status and future perspectives
    In 1959, John Patterson Hughes and Peter George Ingle Stovin, two British physicians, described two male patients presenting with an undefined systemic illness characterized by severe recurrent hemoptysis due to deep venous thrombosis (DVT) and segmental pulmonary artery aneurysms (PAA) [1]





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