Abstract
Myeloproliferative neoplasms (MPN) are defined by clonal expansion of hematopoietic progenitor cells and often associated with systemic thrombosis. Arterial thrombi due to MPN have a multifactorial etiology and are typically managed with antiplatelet agents. However, recent mechanistic studies on patients with JAK2V617F mutations have demonstrated alterations in cellular heparanase activity that results in a hypercoagulable state. We report a patient with MPN presenting with acute ischemic stroke caused by a basilar artery thrombus due to JAK2V617F mutation related hypercoagulability. Newer direct oral anticoagulants may be appropriate for secondary stroke prevention in such cases.
Original language | English (US) |
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Pages (from-to) | 85-87 |
Number of pages | 3 |
Journal | Neurology and Clinical Neuroscience |
Volume | 7 |
Issue number | 2 |
DOIs | |
State | Published - Mar 2019 |
Externally published | Yes |
Keywords
- direct oral anticoagulants
- hypercoagulable state
- JAK2V617F mutation
- myeloproliferative neoplasm
- stroke
ASJC Scopus subject areas
- Neurology
- Clinical Neurology