Yger M, Zavanone C, Abdennour L, Koubaa W, Clarençon F, Dupont S, Samson Y
Unité Neurovasculaire, Hôpital de la Pitie-Salpetrière, APHP, 75013 Paris, France ; Université Pierre et Marie Curie, 75006 Paris, France.
Unité Neurovasculaire, Hôpital de la Pitie-Salpetrière, APHP, 75013 Paris, France ; Service de Rééducation Neurologique, Hôpital de la Pitie-Salpetrière, APHP, 75013 Paris, France.
Case Rep Emerg Med. 2015;2015:503871. doi: 10.1155/2015/503871. Epub 2015 Feb 10.
Introduction. Reversible cerebral vasoconstriction syndrome is becoming widely accepted as a rare cause of both ischemic and haemorrhagic stroke and should be evocated in case of thunderclap headaches associated with stroke. We present the case of a patient with ischemic stroke associated with cortical subarachnoid haemorrhage (cSAH) and reversible diffuse arteries narrowing, leading to the diagnosis of reversible vasoconstriction syndrome. Case Report. A 48-year-old woman came to the emergency department because of an unusual thunderclap headache. The computed tomography of the brain completed by CT-angiography was unremarkable. Eleven days later, she was readmitted because of a left hemianopsia. One day after her admission, she developed a sudden left hemiparesis. The brain MRI showed ischemic lesions in the right frontal and occipital lobe and diffuse cSAH. The angiography showed vasoconstriction of the right anterior cerebral artery and stenosis of both middle cerebral arteries. Nimodipine treatment was initiated and vasoconstriction completely regressed on day 16 after the first headache. Conclusion. Our case shows a severe reversible cerebral vasoconstriction syndrome where both haemorrhagic and ischemic complications were present at the same time. The history we reported shows that reversible cerebral vasoconstriction syndrome is still underrecognized, in particular in general emergency departments.
引言。可逆性脑血管收缩综合征作为缺血性和出血性卒中的一种罕见病因正被广泛认可,对于伴有卒中的霹雳样头痛患者应考虑该诊断。我们报告一例伴有皮质下蛛网膜下腔出血(cSAH)和可逆性弥漫性动脉狭窄的缺血性卒中患者,最终诊断为可逆性血管收缩综合征。病例报告。一名48岁女性因异常的霹雳样头痛前来急诊科就诊。头颅计算机断层扫描及CT血管造影未见明显异常。11天后,她因左侧偏盲再次入院。入院一天后,她突然出现左侧偏瘫。脑部磁共振成像显示右侧额叶和枕叶有缺血性病变以及弥漫性cSAH。血管造影显示右侧大脑前动脉血管收缩以及双侧大脑中动脉狭窄。开始使用尼莫地平治疗,首次头痛后第16天血管收缩完全消退。结论。我们的病例显示了一种严重的可逆性脑血管收缩综合征,同时存在出血性和缺血性并发症。我们报告的病例情况表明,可逆性脑血管收缩综合征仍未得到充分认识,尤其是在普通急诊科。