| Literature DB >> 28476066 |
Soundarya Selvam1, Paula James1,2.
Abstract
Severe and intractable gastrointestinal bleeding caused by angiodysplasia is a debilitating problem for up to 20% of patients with von Willebrand disease (VWD). Currently, the lack of an optimal treatment for this recurrent problem presents an ongoing challenge for many physicians in their management of affected patients. Over the past few years, studies have pointed to a regulatory role for the hemostatic protein, von Willebrand factor (VWF), in angiogenesis, providing a novel target for the modulation of vessel development. This article will review the clinical implications and molecular pathology of angiodysplasia in VWD. Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.Entities:
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Year: 2017 PMID: 28476066 PMCID: PMC5949878 DOI: 10.1055/s-0037-1599145
Source DB: PubMed Journal: Semin Thromb Hemost ISSN: 0094-6176 Impact factor: 4.180