Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease
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Updated: Nov 20, 2025

Investigating von Willebrand Factor Pathophysiology Using a Flow Chamber Model of von Willebrand Factor-platelet String Formation
Published on: August 14, 2017
Marianne E M Yee1,2, Glaivy Batsuli1,2, Satheesh Chonat1,2
1Aflac Cancer and Blood Disorders Center Children's Healthcare of Atlanta Atlanta GA USA.
Thrombocytosis is common in sickle cell disease and may contribute to vaso-occlusion. Hydroxyurea treats extreme thrombocytosis. Acquired von Willebrand disease should be considered prior to aspirin therapy.
Thrombocytosis is common in sickle cell disease and may contribute to vaso-occlusion. Hydroxyurea treats extreme thrombocytosis. Acquired von Willebrand disease should be considered prior to aspirin therapy.
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