In the thick of it: cerebral venous sinus thrombosis precipitated by iron-deficiency anaemia and sickle cell trait

CVST is a form of venous thrombosis within the intracranial venous sinuses. 1 The incidence is 3-4 cases per million individuals with an 8% mortality rate. 2 CVST is predisposed to by prothrombotic disorders, anaemia and is associated with a number of clinical conditions. 1 2 Sickle cell disease con...

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Published in:BMJ case reports Vol. 2016; p. bcr2016215399
Main Authors: Boon, Ian S, Starkey, Kerry Jo, Samsonova, Oksana, Johnston, Andrew McDonald
Format: Journal Article
Language:English
Published: England BMJ Publishing Group LTD 17-05-2016
BMJ Publishing Group
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Summary:CVST is a form of venous thrombosis within the intracranial venous sinuses. 1 The incidence is 3-4 cases per million individuals with an 8% mortality rate. 2 CVST is predisposed to by prothrombotic disorders, anaemia and is associated with a number of clinical conditions. 1 2 Sickle cell disease contributes to a hypercoagulable state by distortion of the phospholipid membrane of red blood cells and inappropriate activation of tissue factors on endothelial cells. 3 Learning points Cerebral venous sinus thrombosis (CVST) is a rare entity which usually presents subacutely over several days or weeks. 1 2 Patients present with wide-ranging symptoms, commonly headache, neurologic deficit, altered consciousness and seizures reflecting the underlying brain damage and raised intracranial pressure due to venous thrombosis. 1 2 CVST may be provoked by prothrombotic factors associated with anaemia and a myriad of other clinical conditions, including sickle cell disease, protein C and protein S deficiency, anticardiolipin antibodies, systemic lupus erythematous, dehydration, infection, sepsis and malignancy. 1 2 These medical conditions should be investigated and excluded. Low-molecular-weight heparin should be followed by treatment with warfarin. 1 2 Direct oral anticoagulants are not yet licensed for treatment of CVST.
Bibliography:ObjectType-Case Study-2
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ISSN:1757-790X
1757-790X
DOI:10.1136/bcr-2016-215399