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  • Title: A critical analysis of 57 cases of Hughes-Stovin syndrome (HSS). A report by the HSS International Study Group (HSSISG).
    Author: Emad Y, Ragab Y, Kechida M, Guffroy A, Kindermann M, Robinson C, Erkan D, Frikha F, Ibrahim O, Al-Jahdali H, Silva RS, Tornes L, Margolesky J, Bennji S, Kim JT, Abdelbary M, Fabi M, Hassan M, Cruz V, El-Shaarawy N, Jaramillo N, Khalil A, Demirkan S, Tekavec-Trkanjec J, Elyaski A, de FreitasRibeiro BN, Kably I, Al-Zeedy K, Jayakrishnan B, Ghirardo S, Barman B, Farber HW, Pankl S, Abou-Zeid A, Young P, Amezyane T, Agarwala MK, Bawaskar P, Hawass M, Saad A, Rasker JJ.
    Journal: Int J Cardiol; 2021 May 15; 331():221-229. PubMed ID: 33529654.
    Abstract:
    BACKGROUND: Hughes-Stovin syndrome (HSS) is a systemic disease characterized by widespread vascular thrombosis and pulmonary vasculitis with serious morbidity and mortality. The HSS International Study Group is a multidisciplinary taskforce aiming to study HSS, in order to generate consensus recommendations regarding diagnosis and treatment. METHODS: We included 57 published cases of HSS (43 males) and collected data regarding: clinical presentation, associated complications, hemoptysis severity, laboratory and computed tomography pulmonary angiography (CTPA) findings, treatment modalities and cause of death. RESULTS: At initial presentation, DVT was observed in 29(33.3 %), thrombophlebitis in 3(5.3%), hemoptysis in 24(42.1%), and diplopia and seizures in 1 patient each. During the course of disease, DVT occurred in 48(84.2%) patients, and superficial thrombophlebitis was observed in 29(50.9%). Hemoptysis occurred in 53(93.0%) patients and was fatal in 12(21.1%). Pulmonary artery (PA) aneurysms (PAAs) were bilateral in 53(93%) patients. PAA were located within the main PA in 11(19.3%), lobar in 50(87.7%), interlobar in 13(22.8%) and segmental in 42(73.7%). Fatal outcomes were more common in patients with inferior vena cava thrombosis (p = 0.039) and ruptured PAAs (p < 0.001). Death was less common in patients treated with corticosteroids (p < 0.001), cyclophosphamide (p < 0.008), azathioprine (p < 0.008), combined immune modulators (p < 0.001). No patients had uveitis; 6(10.5%) had genital ulcers and 11(19.3%) had oral ulcers. CONCLUSIONS: HSS may lead to serious morbidity and mortality if left untreated. PAAs, adherent in-situ thrombosis and aneurysmal wall enhancement are characteristic CTPA signs of HSS pulmonary vasculitis. Combined immune modulators contribute to favorable outcomes.
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