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Cerebral venous sinus thrombosis: a diagnostic challenge
1Stroke Division, Beth Israel Deaconess Medical Center, Boston, Massachusetts 02215, USA. jfink@caregroup.harvard.edu
Insights
Cerebral venous sinus thrombosis (CVT) is often underdiagnosed but treatable. Early recognition of symptoms like headache, neurological deficits, and seizures, especially during pregnancy or with intracerebral hemorrhage, is crucial for timely treatment with anticoagulation.
Area of Science:
- Neurology
- Vascular Medicine
- Diagnostic Imaging
Background:
- Cerebral venous sinus thrombosis (CVT) is a serious condition that has historically been underdiagnosed.
- Delayed diagnosis and treatment of CVT can lead to adverse outcomes, including mortality.
Purpose of the Study:
- To review local experiences with CVT to improve future diagnosis and treatment.
- Identify factors aiding in earlier and more accurate CVT diagnosis and management decisions.
Main Methods:
- Retrospective review of all CVT cases diagnosed or treated at Auckland Hospital from 1990 to 1999.
- Analysis of clinical presentations, diagnostic delays, and treatment outcomes.
Main Results:
- Twenty-five CVT cases were identified, with a notable increase in diagnoses in 1999.
- Common symptoms included headache (96%), focal neurological deficits (60%), seizures (40%), and papilloedema (43%).
- Delayed diagnoses occurred in specific patient groups, including pregnant/postpartum women and those with intracerebral hemorrhage; 20 patients improved with anticoagulant therapy.
Conclusions:
- Consider CVT in women with neurological symptoms during pregnancy/puerperium and in unexplained intracerebral hemorrhage.
- Suspect CVT in cases of progressive headache with focal neurological signs, seizures, or papilloedema.
- MRI with MR venography is the preferred diagnostic tool; anticoagulation is the primary treatment, even with hemorrhage.
Background:
Cerebral venous sinus thrombosis (CVT) is a potentially serious but treatable disorder that has been underdiagnosed in the past. Delay in diagnosis and treatment of this disorder has resulted in the death of one of our patients.
Aim:
To review the local experience with CVT in order to identify factors that may allow diagnosis and appropriate treatment decisions to be made more readily in the future.
Methods:
A retrospective review of all cases of CVT diagnosed or treated at Auckland Hospital between 1990 and 1999.
Results:
Twenty-five cases of CVT were identified. The number of cases diagnosed increased from less than one per year in 1990-94 to eight in 1999. Clinical signs at presentation included headache (96%), focal neurological deficits (60%), seizures (40%) and papilloedema (43%). Delayed diagnosis after admission to hospital occurred in two young women presenting with neurological symptoms during pregnancy or puerperium, in two cases in whom focal symptoms were not explained by negative computed tomography and in five cases presenting with intracerebral haemorrhage. Twenty patients received anticoagulant therapy and their condition remained stable or improved after treatment.
Conclusions:
The diagnosis of CVT should be considered in women with any neurological symptoms during pregnancy or puerperium and in all cases of unexplained intracerebral haemorrhage. CVT should also be considered in cases of recent onset and progressive headache, particularly when associated with focal neurological symptoms or signs, seizures or papilloedema. Magnetic resonance imaging with magnetic resonance venography is the investigation of choice. Anticoagulation with heparin remains the mainstay of treatment, even in the presence of intracerebral haemorrhage.
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