Shankar Kikkeri Nidhi, Nagarajan Elanagan, Premkumar Keerthivas, Nattanamai Premkumar
Neurology, University of Missouri, Columbia, USA.
Cureus. 2019 Mar 20;11(3):e4285. doi: 10.7759/cureus.4285.
Reversible cerebral vasoconstriction syndrome (RCVS) is a rare neurological condition that typically presents with a sudden-onset thunderclap headache associated with or without focal neurological deficits. The diagnosis is established by the presence of reversible segmental or diffuse cerebral vasoconstriction on diagnostic cerebral angiogram. Autonomic dysreflexia is a known complication resulting from spinal cord injury. It manifests as episodes of flushing, headache, and fluctuations in blood pressure. Midodrine is an alpha-1 agonist that causes vasoconstriction and is commonly used in patients with autonomic dysreflexia. Here, we report the case of a young woman with a history of autonomic dysreflexia, who presented with a thunderclap headache and was subsequently diagnosed with reversible cerebral vasoconstriction syndrome.
可逆性脑血管收缩综合征(RCVS)是一种罕见的神经系统疾病,通常表现为突发的霹雳样头痛,可伴有或不伴有局灶性神经功能缺损。通过诊断性脑血管造影显示可逆性节段性或弥漫性脑血管收缩来确诊。自主神经反射异常是脊髓损伤已知的并发症。它表现为潮红、头痛发作以及血压波动。米多君是一种α-1激动剂,可引起血管收缩,常用于自主神经反射异常的患者。在此,我们报告一例有自主神经反射异常病史的年轻女性病例,该患者出现霹雳样头痛,随后被诊断为可逆性脑血管收缩综合征。