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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.
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813102/ https://www.ncbi.nlm.nih.gov/pubmed/33489197 http://dx.doi.org/10.1002/ccr3.3556 |
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author | Yee, Marianne E. M. Batsuli, Glaivy Chonat, Satheesh Park, Sunita |
author_facet | Yee, Marianne E. M. Batsuli, Glaivy Chonat, Satheesh Park, Sunita |
author_sort | Yee, Marianne E. M. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7813102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78131022021-01-22 Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease Yee, Marianne E. M. Batsuli, Glaivy Chonat, Satheesh Park, Sunita Clin Case Rep Case Reports 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. John Wiley and Sons Inc. 2020-11-20 /pmc/articles/PMC7813102/ /pubmed/33489197 http://dx.doi.org/10.1002/ccr3.3556 Text en © 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Yee, Marianne E. M. Batsuli, Glaivy Chonat, Satheesh Park, Sunita Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease |
title | Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease |
title_full | Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease |
title_fullStr | Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease |
title_full_unstemmed | Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease |
title_short | Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease |
title_sort | thrombocytosis with acquired von willebrand disease in an adolescent with sickle cell disease |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813102/ https://www.ncbi.nlm.nih.gov/pubmed/33489197 http://dx.doi.org/10.1002/ccr3.3556 |
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