[Acquired von Willebrand syndrome: a hemostatic disorder frequently encountered in the fields of cardiology and gastroenterology].

Rinsho Ketsueki

Department of Molecular and Cellular Biology, Institute of Development, Aging and Cancer, Tohoku University.

Published: August 2020

AI Article Synopsis

  • von Willebrand disease is a genetic disorder affecting blood clotting due to issues with von Willebrand factor (VWF), which plays a key role in hemostasis.
  • Acquired von Willebrand syndrome (AVWS) can occur without genetic mutations and is linked to conditions like cancer and thyroid problems, as well as high-stress cardiovascular diseases.
  • The treatment for AVWS requires careful attention, as the condition stems from the rapid breakdown of VWF, leading to increased bleeding risk.

Article Abstract

von Willebrand disease is a genetic hemostatic disorder that is caused by the qualitative or quantitative dysfunction of the von Willebrand factor (VWF), which is involved in hemostasis. A similar dysfunction sometimes develops without mutations, known as acquired von Willebrand syndrome (AVWS) , which has been associated with lymphoproliferative diseases, myeloproliferative diseases, malignant tumors, and hypothyroidism. Recently, it was remarkably noted that cardiovascular diseases with high intravascular shear stress could cause AVWS . The incidence of cardiovascular disease-associated AVWS is exceptionally high, and we may encounter such patients in daily clinical settings. Further, special consideration is necessary for the treatment of bleeding since the cause of AVWS is based on the accelerated degradation of VWF.

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Source
http://dx.doi.org/10.11406/rinketsu.61.542DOI Listing

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