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Thrombocytosis with Acquired von Willebrand Disease in an Adolescent with Sickle Cell Disease
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  • Marianne Yee,
  • Glaivy Batsuli,
  • Satheesh Chonat,
  • Sunita Park
Marianne Yee
Emory University

Corresponding Author:marianne.yee@choa.org

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Glaivy Batsuli
Emory University
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Satheesh Chonat
Emory University School of Medicine
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Sunita Park
Children's Healthcare of Atlanta Inc
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Thrombocytosis is common in children with sickle cell disease (SCD). Reactive thrombocytosis must be distinguished from myeloproliferative disorder or inherited thrombocytosis syndrome. We present an adolescent with hemoglobin SS and thrombocytosis associated with increased frequency of pain, priapism, and acquired von Willebrand disease.
14 Oct 2020Submitted to Clinical Case Reports
16 Oct 2020Assigned to Editor
16 Oct 2020Submission Checks Completed
28 Oct 2020Reviewer(s) Assigned
03 Nov 2020Review(s) Completed, Editorial Evaluation Pending
03 Nov 2020Editorial Decision: Accept
Jan 2021Published in Clinical Case Reports volume 9 issue 1 on pages 457-460. 10.1002/ccr3.3556