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Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease

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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Detalhes bibliográficos
Publicado no:Clin Case Rep
Main Authors: Yee, Marianne E. M., Batsuli, Glaivy, Chonat, Satheesh, Park, Sunita
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7813102/
https://ncbi.nlm.nih.gov/pubmed/33489197
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.3556
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