Abstract
Essential thrombocythemia (ET) is a risk factor for ischemic stroke and, far more rarely, hemorrhage. We report the case of an untreated 32-year-old woman with a history of JAK2 V617F-positive ET with cerebellar and subarachnoid hemorrhages without evidence of sinus vein thrombosis. She was commenced on oral cytotoxic and antiplatelet therapy. This case report discusses the underlying mechanism of hemorrhagic thrombocythemia and the management dilemma presented by the recommended treatment implications.
Keywords:
Hemorrhagic stroke; acquired von Willebrand disease; antiplatelet; essential thrombocythaemia; myeloproliferative disorder; young stroke.
Crown Copyright © 2014. Published by Elsevier Inc. All rights reserved.
MeSH terms
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Adult
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Aspirin / therapeutic use
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Cerebral Angiography / methods
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Female
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Genetic Predisposition to Disease
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Humans
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Hydroxyurea / therapeutic use
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Intracranial Hemorrhages / diagnosis
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Intracranial Hemorrhages / drug therapy
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Intracranial Hemorrhages / etiology*
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Janus Kinase 2 / genetics
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Magnetic Resonance Imaging
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Mutation
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Platelet Aggregation Inhibitors / therapeutic use
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Risk Factors
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Subarachnoid Hemorrhage / diagnosis
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Subarachnoid Hemorrhage / drug therapy
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Subarachnoid Hemorrhage / etiology
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Thrombocythemia, Essential / complications*
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Thrombocythemia, Essential / diagnosis
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Thrombocythemia, Essential / drug therapy
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Thrombocythemia, Essential / genetics
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Tomography, X-Ray Computed
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Treatment Outcome
Substances
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Platelet Aggregation Inhibitors
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JAK2 protein, human
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Janus Kinase 2
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Aspirin
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Hydroxyurea