Fibrosarcoma de arteria pulmonar simulando un síndrome de Hughes Stovin

Erlij, Daniel; Michalland, Susana; Neira, Óscar; Fernández, Cristina; Wolff, Verónica

doi:10.4067/s0034-98872014001100017

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2023

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(2 citation statements)

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“…A total of 40 patients were analyzed. 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 The comparison of surgical/medical or medical alone therapy on length of follow-up is reported in Fig 3 . No differences in survival rate were observed between the two groups.…”

Section: Discussionmentioning

confidence: 99%

See 1 more Smart Citation

A Rare but Fatal Behçet Variant: The Hughes–Stovin Syndrome—Successful Case Report and New Evidence from Literature Review

Ascoli Marchetti,

Belvivere,

Argirò

et al. 2023

Aorta (Stamford)

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Hughes–Stovin syndrome (HSS) is a rare potentially fatal vasculitis supposedly belonging to the spectrum of Behçet disease without ocular involvement. HSS tends to play by a temporal pattern, starting with thrombosis and followed by formation of pulmonary aneurysms. Since its mortality can reach 25% of cases, early recognition and appropriate therapy represent the major clinical challenges. We describe a rare case of HSS successfully treated via multidisciplinary management by an endovascular approach and immunosuppressive therapy.

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Section: Discussionmentioning

confidence: 99%

“…The advent of endovascular procedures has expanded the possibilities for treatment. At the beginning, therapeutically options were represented by pneumectomy, 16 lobectomy, 3 4 5 9 25 37 50 52 and segmentectomy. 40 Aneurysm resection with saphenous vein replacement 9 or lung transplantation 10 were also proposed.…”

Section: Discussionmentioning

confidence: 99%