Assistance Publique des Hôpitaux de Paris, Paris, France.
Cephalalgia. 2010 Oct;30(10):1271-5. doi: 10.1177/0333102410365107. Epub 2010 Apr 7.
We report two patients with reversible cerebral vasoconstriction syndrome (RCVS) and carotid glomus tumour. The first patient presented with multiple thunderclap headaches. Cervical and cerebral magnetic resonance imaging showed diffuse cerebral vasoconstriction on magnetic resonance angiogram (MRA) and a carotid glomus tumour. The second patient presented with a cervical mass and was diagnosed with a non-secreting paraganglioma of the carotid body. Surgery with pre-operative angiography was followed by thunderclap headaches and MRA showed segmental cerebral vasoconstriction. Both patients were treated with nimodipine and headaches stopped. Both had normal cerebral arteries on the control MRA at 3 months. These two cases suggest that a paraganglioma may increase the susceptibility to develop RCVS. As a consequence, patients with RCVS should be investigated for a carotid glomus tumour, and patients with paraganglioma reporting severe headaches should have a cerebral MRA in order to rule out cerebral vasoconstriction.
我们报告了两例可逆性脑血管收缩综合征(RCVS)合并颈动脉球瘤的患者。第一例患者表现为多发霹雳性头痛。颈椎和脑部磁共振成像显示磁共振血管造影(MRA)上弥漫性脑血管收缩和颈动脉球瘤。第二例患者表现为颈部肿块,诊断为颈动脉体无分泌性副神经节瘤。术前血管造影后行手术治疗,随后出现霹雳性头痛,MRA 显示节段性脑血管收缩。两例患者均接受尼莫地平治疗,头痛停止。3 个月时,MRA 复查均显示正常脑动脉。这两例病例提示,副神经节瘤可能增加 RCVS 的易感性。因此,RCVS 患者应行颈动脉球瘤检查,而报告严重头痛的副神经节瘤患者应行脑部 MRA 以排除脑血管收缩。