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首页> 外文期刊>BMC Neurology >Cerebral neurocysticercosis mimicking or comorbid with episodic migraine?
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Cerebral neurocysticercosis mimicking or comorbid with episodic migraine?

机译:模仿或与发作性偏头痛并发脑神经囊尾ice病?

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Background Neurocysticercosis is a major cause of neurological symptoms in developing countries. We report a case of cerebral neurocysticercosis presenting as episodic migraine without aura, with clinico-radiological correlations and discuss the possible causal influence of neurocysticercosis on the pathomechanisms of migraine. Case presentation We report a 24?year-old male consulting for a one year history of recurrent headaches. He described bilateral frontal and/or temporal attacks of throbbing headache, moderate to severe in intensity, worsened by head movements and accompanied by nausea, photophobia and phonophobia. Attacks lasted between 12 and 60?hours if untreated. He never had symptoms suggestive of a migraine aura or an epileptic seizure. Headache attacks progressively increased in frequency to up to 5 to 7 severe attacks per month. On taking history, the patient reported having consumed undercooked porcine meat. Physical examination was unremarkable. A brain CT scan showed two contiguous occipital cystic lesions with ring enhancement and surrounding edema suggestive of cerebral neurocysticercosis. On laboratory work-up, blood serology for cysticercal antibodies was positive. Full blood count, erythrocyte sedimentation rate, c - reactive protein level, human immunodeficiency virus serology, liver and hepatic function were all normal. Albendazole (1000?mg/day) and prednisolone (60?mg/day) were prescribed for seven days. The patient was examined again two and six months after the end of his treatment and there was a significant reduction in headache severity and frequency. Conclusion We propose that in our patient the occipital neurocysticercosis lesions cause migraine without aura-like attacks via inflammation in the surrounding brain parenchyma leading to sensitization of the trigemino-vascular system. We cannot rule out, however, the possibility that our patient has a genetic predisposition for migraine without aura and that the fortuitous association of neurocysticercosis is simply an aggravating factor of his migraine.
机译:背景技术神经囊尾osis病是发展中国家神经系统症状的主要原因。我们报告一例脑神经性囊尾epi病,表现为无先兆的发作性偏头痛,与临床放射学相关,并讨论了神经性囊尾on病对偏头痛发病机制的可能因果影响。案例介绍我们报告了一位24岁男性咨询患者一年复发性头痛的病史。他描述了搏动性头痛的双边额叶和/或颞部发作,强度为中度到重度,头部运动加重,并伴有恶心,畏光和恐惧心理。如果不及时治疗,发作会持续12至60小时。他从未出现过暗示偏头痛先兆或癫痫发作的症状。头痛发作的频率逐渐增加,每月多达5至7次严重发作。根据病史,患者报告食用了未煮熟的猪肉。体格检查无异常。脑部CT扫描显示两个连续的枕部囊性病变,环增强,周围水肿提示脑神经囊尾osis病。在实验室检查中,囊性抗体的血液血清学检查呈阳性。全血细胞计数,红细胞沉降率,c-反应蛋白水平,人免疫缺陷病毒血清学,肝和肝功能均正常。处方阿苯达唑(1000?mg /天)和泼尼松龙(60?mg /天)服用7天。治疗结束后两个月和六个月再次对患者进行检查,头痛的严重程度和频率明显降低。结论我们建议对患者的枕神经囊尾neuro病病变引起偏头痛,而不会通过周围脑实质内的炎症引起先兆样发作,从而导致三叉神经-血管系统敏化。但是,我们不能排除这种可能性,即我们的患者具有无先兆的偏头痛的遗传易感性,而神经囊尾rc病的偶然关联只是其偏头痛的加重因素。

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