[Rendu-Osler disease and recurrent thromboembolic venous disease]

J Med Vasc. 2019 Feb;44(1):76-78. doi: 10.1016/j.jdmv.2018.11.003. Epub 2018 Dec 12.
[Article in French]

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.

Keywords: Maladie de Rendu-Osler; Maladie veineuse thromboembolique; Rendu-Osler-Weber syndrome; Venous thromboembolic disease.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Humans
  • Male
  • Middle Aged
  • Recurrence
  • Telangiectasia, Hereditary Hemorrhagic / complications*
  • Telangiectasia, Hereditary Hemorrhagic / diagnostic imaging
  • Venous Thromboembolism / diagnosis
  • Venous Thromboembolism / etiology*