Diagnosis of congenital von Willebrand disease during a preoperative assessment in a multiple myeloma patient without bleeding history

  • El Ouaaliti M
  • Li R
  • Gobin D
  • et al.
N/ACitations
Citations of this article
9Readers
Mendeley users who have this article in their library.

Abstract

We report a rare case of type 2M von Willebrand disease diagnosed in an elderly multiple myeloma patient who had no personal and family bleeding history. This case report emphasis the importance to not systematically exclude a congenital vWD in adult patients when coagulation screening tests indicate toward a vWD .

Cite

CITATION STYLE

APA

El Ouaaliti, M., Li, R., Gobin, D., Bron, D., & Cantinieaux, B. (2016). Diagnosis of congenital von Willebrand disease during a preoperative assessment in a multiple myeloma patient without bleeding history. Clinical Case Reports, 4(7), 703–706. https://doi.org/10.1002/ccr3.603

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free