Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease
oleh: Marianne E. M. Yee, Glaivy Batsuli, Satheesh Chonat, Sunita Park
| Format: | Article |
|---|---|
| Diterbitkan: | Wiley 2021-01-01 |
Deskripsi
Abstract 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.