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Reversible cerebral vasoconstriction syndrome: A review of pathogenesis, clinical presentation, and treatment

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INTERNATIONAL JOURNAL OF STROKE
卷 -, 期 -, 页码 -

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SAGE PUBLICATIONS LTD
DOI: 10.1177/17474930231181250

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Thunderclap headache; cerebral vasoconstriction; arteriopathy

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Reversible cerebral vasoconstriction syndrome (RCVS) is a condition characterized by reversible narrowing of the intracranial arteries, predominantly affecting women. The main symptoms include recurrent severe headaches and abnormal brain imaging, which may lead to complications such as hemorrhage, ischemia, and edema. The pathophysiology is not yet fully understood, and treatment mainly focuses on symptomatic management and avoiding triggers.
Reversible segmental narrowing of the intracranial arteries has been described since several decades in numerous clinical settings, using variable nosology. Twenty-one years ago, we tentatively proposed the unifying concept that these entities, based on similar clinical-imaging features, represented a single cerebrovascular syndrome. This reversible cerebral vasoconstriction syndrome or RCVS has now come of age. A new International Classification of Diseases code, (ICD-10, I67.841) has been established, enabling larger-scale studies. The RCVS2 scoring system provides high accuracy in confirming RCVS diagnosis and excluding mimics such as primary angiitis of the central nervous system. Several groups have characterized its clinical-imaging features. RCVS predominantly affects women. Recurrent worst-ever (thunderclap) headaches are typical at onset. While initial brain imaging is often normal, approximately one-third to half develop complications such as convexity subarachnoid hemorrhages, lobar hemorrhages, ischemic strokes located in arterial watershed territories and reversible edema, alone or in combination. Vasoconstriction evolves over hours to days, first affecting distal and then the more proximal arteries. An overlap between RCVS and primary thunderclap headache, posterior reversible encephalopathy syndrome, Takotsubo cardiomyopathy, transient global amnesia, and other conditions has been recognized. The pathophysiology remains largely unknown. Management is mostly symptomatic: headache relief with analgesics and oral calcium-channel blockers, removal of vasoconstrictive factors, and avoidance of glucocorticoids that can significantly worsen outcome. Intra-arterial vasodilator infusions provide variable success. Overall, 90-95% of admitted patients achieve complete or major resolution of symptoms and clinical deficits within days to weeks. Recurrence is exceptional, although 5% can later develop isolated thunderclap headaches with or without mild cerebral vasoconstriction.

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