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可逆性脑血管收缩综合征:识别与治疗

Reversible Cerebral Vasoconstriction Syndrome: Recognition and Treatment.

作者信息

Cappelen-Smith Cecilia, Calic Zeljka, Cordato Dennis

机构信息

Department of Neurology and Neurophysiology, Liverpool Hospital, Clinical Building, Elizabeth St, Liverpool, New South Wales, Australia.

South Western Clinical School, University of New South Wales, Sydney, New South Wales, Australia.

出版信息

Curr Treat Options Neurol. 2017 Jun;19(6):21. doi: 10.1007/s11940-017-0460-7.

Abstract

Reversible cerebral vasoconstriction syndrome (RCVS) is a rare but increasingly recognized disorder with over 500 cases published in the literature. The condition is characterized by recurrent severe thunderclap headaches with or without other neurological symptoms and diffuse segmental narrowing of the cerebral arteries which is reversible within 3 months. RCVS may occur spontaneously but in over 50% of cases, it is associated with various other conditions, including vasoactive medications or illicit drugs and the post-partum state. One third to a half of cases develop hemorrhagic or ischemic brain lesions or a combination of both. Posterior reversible encephalopathy syndrome (PRES) often occurs in association with RCVS and the conditions are likely to share a common pathophysiology. The pathogenesis of RCVS remains uncertain but autonomic dysregulation, oxidative stress, and genetic predisposition are postulated. Significant differential diagnoses include subarachnoid hemorrhage (SAH) due to aneurysmal rupture, cervical artery dissection, and primary angiitis of the central nervous system (PACNS). Although there is no proven treatment, calcium channel antagonists including nimodipine and verapamil have been administered with reported reduction of headache intensity but without effect on the time course of cerebral vasoconstriction. Glucocorticoids have been reported as an independent predictor of worse outcome and should be avoided. The cornerstone of RCVS management remains largely supportive with bed rest and analgesics and removal of precipitating factors. Invasive neurointerventional techniques should be reserved for severe deteriorating cases. The condition is usually benign and self-limited and the majority of patients have a favorable outcome but around 5-10% are left with permanent neurological deficits and rare cases may die. This review details the importance of the early recognition of this increasingly described condition and current treatment recommendations.

摘要

可逆性脑血管收缩综合征(RCVS)是一种罕见但越来越受到认可的疾病,文献中已发表了500多例病例。该疾病的特征是反复出现严重的霹雳样头痛,伴有或不伴有其他神经症状,以及脑动脉弥漫性节段性狭窄,这种狭窄在3个月内可逆转。RCVS可能自发发生,但在超过50%的病例中,它与各种其他情况有关,包括血管活性药物或非法药物以及产后状态。三分之一到一半的病例会出现出血性或缺血性脑损伤或两者兼而有之。后部可逆性脑病综合征(PRES)常与RCVS相关,且这两种情况可能具有共同的病理生理学。RCVS的发病机制仍不确定,但推测与自主神经调节异常、氧化应激和遗传易感性有关。重要的鉴别诊断包括动脉瘤破裂引起的蛛网膜下腔出血(SAH)、颈动脉夹层和中枢神经系统原发性血管炎(PACNS)。虽然没有经过证实的治疗方法,但已使用包括尼莫地平和维拉帕米在内的钙通道拮抗剂,据报道可减轻头痛强度,但对脑血管收缩的病程没有影响。据报道,糖皮质激素是预后较差的独立预测因素,应避免使用。RCVS管理的基石在很大程度上仍然是支持性的,包括卧床休息、止痛以及消除诱发因素。侵入性神经介入技术应仅用于病情严重恶化的病例。这种疾病通常是良性的且具有自限性,大多数患者预后良好,但约5-10%的患者会留下永久性神经功能缺损,极少数病例可能死亡。本综述详细阐述了早期识别这种越来越多地被描述的疾病的重要性以及当前的治疗建议。

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