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[Rendu-Osler disease and recurrent thromboembolic venous disease]
R Ben Salah1, F Frikha1, D Chebbi1
1Service de médecine interne, CHU Hédi Chaker, Sfax, Tunisie.
Abstract:
Rendu-Osler-Weber syndrome is a rare systemic fibrovascular dysplasia, recognized by mucocutaneous telangiectasias, arteriovenous malformations, epistaxis and family history. Venous thromboembolic disease is a poor prognostic factor in this disease given the risk of increased bleeding caused by anticoagulant therapy. We report a new case of a 56-year-old patient with Osler disease who developed recurrent thromboembolic venous disease when anticoagulants were discontinued. According to a review of the literature, this association does not appear to be fortuitous and is a factor of disease severity.
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