Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease
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.
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| Format: | Article |
| Language: | English |
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Wiley
2021-01-01
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| Series: | Clinical Case Reports |
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| Online Access: | https://doi.org/10.1002/ccr3.3556 |
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doaj-32f99e8b39c14174a1aa971f91ed327f2021-05-21T11:05:45ZengWileyClinical Case Reports2050-09042021-01-019145746010.1002/ccr3.3556Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell diseaseMarianne E. M. Yee0Glaivy Batsuli1Satheesh Chonat2Sunita Park3Aflac Cancer and Blood Disorders Center Children's Healthcare of Atlanta Atlanta GA USAAflac Cancer and Blood Disorders Center Children's Healthcare of Atlanta Atlanta GA USAAflac Cancer and Blood Disorders Center Children's Healthcare of Atlanta Atlanta GA USADepartment of Pathology and Laboratory Medicine Children's Healthcare of Atlanta Atlanta GA USAAbstract 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.https://doi.org/10.1002/ccr3.3556acquired Von Willebrand diseasepriapismsickle cell diseasethrombocytosis |
| collection |
DOAJ |
| language |
English |
| format |
Article |
| sources |
DOAJ |
| author |
Marianne E. M. Yee Glaivy Batsuli Satheesh Chonat Sunita Park |
| spellingShingle |
Marianne E. M. Yee Glaivy Batsuli Satheesh Chonat Sunita Park Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease Clinical Case Reports acquired Von Willebrand disease priapism sickle cell disease thrombocytosis |
| author_facet |
Marianne E. M. Yee Glaivy Batsuli Satheesh Chonat Sunita Park |
| author_sort |
Marianne E. M. Yee |
| title |
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_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_sort |
thrombocytosis with acquired von willebrand disease in an adolescent with sickle cell disease |
| publisher |
Wiley |
| series |
Clinical Case Reports |
| issn |
2050-0904 |
| publishDate |
2021-01-01 |
| description |
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. |
| topic |
acquired Von Willebrand disease priapism sickle cell disease thrombocytosis |
| url |
https://doi.org/10.1002/ccr3.3556 |
| work_keys_str_mv |
AT marianneemyee thrombocytosiswithacquiredvonwillebranddiseaseinanadolescentwithsicklecelldisease AT glaivybatsuli thrombocytosiswithacquiredvonwillebranddiseaseinanadolescentwithsicklecelldisease AT satheeshchonat thrombocytosiswithacquiredvonwillebranddiseaseinanadolescentwithsicklecelldisease AT sunitapark thrombocytosiswithacquiredvonwillebranddiseaseinanadolescentwithsicklecelldisease |
| _version_ |
1721432178142740480 |