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Reversible Cerebral Vasoconstriction Syndrome: Recognition and Treatment
Cecilia Cappelen-Smith1,2,3, Zeljka Calic4,5,6, Dennis Cordato4,5,6
1Department of Neurology and Neurophysiology, Liverpool Hospital, Clinical Building, Elizabeth St, Liverpool, New South Wales, Australia. Cecilia.Cappelen-Smith@sswahs.nsw.gov.au.
Reversible cerebral vasoconstriction syndrome (RCVS) causes severe headaches and artery narrowing. Early recognition and supportive care are key for favorable outcomes, though complications can occur.
Area of Science:
- Neurology
- Vascular Neurology
Background:
- Reversible cerebral vasoconstriction syndrome (RCVS) is a rare neurological disorder.
- It presents with thunderclap headaches and reversible cerebral artery narrowing.
- RCVS is linked to various triggers like medications, drugs, and postpartum state.
Purpose of the Study:
- To review the clinical features, pathophysiology, differential diagnoses, and management of RCVS.
- To emphasize the importance of early recognition and current treatment recommendations for RCVS.
Main Methods:
- Literature review of over 500 published RCVS cases.
- Analysis of associated conditions, complications, and treatment outcomes.
Main Results:
- RCVS is associated with hemorrhagic or ischemic brain lesions in 33-50% of cases.
- Posterior reversible encephalopathy syndrome (PRES) often co-occurs with RCVS.
- Calcium channel blockers may reduce headache intensity but not vasoconstriction; glucocorticoids are contraindicated.
Conclusions:
- RCVS is typically benign and self-limited, but can lead to permanent deficits or death.
- Supportive management, including removal of triggers, is the cornerstone of RCVS treatment.
- Early diagnosis and appropriate management are crucial for improving patient outcomes in RCVS.
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