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头痛伴神经功能缺损和脑脊液淋巴细胞增多(HaNDL)并伴有脑电图局灶性慢波的病例。

Case of syndrome of headache with neurological deficits and cerebrospinal fluid lymphocytosis (HaNDL) with focal slowing on electroencephalogram.

机构信息

Department of Neurology, Austin Hospital, Melbourne, Victoria, Australia.

出版信息

Intern Med J. 2012 Aug;42(8):944-7. doi: 10.1111/j.1445-5994.2012.02856.x.

Abstract

We describe a case of headache and neurological deficits with cerebrospinal fluid (CSF) lymphocytosis in a patient presenting with a 3-week history of recurrent severe headaches associated with negative sensory symptoms and dysphasia. The patient had no cardiovascular risk factors and no family history of migraines. Neurological examination was unremarkable. Cerebral magnetic resonance imaging was unremarkable. CSF analysis revealed lymphocytosis (leucocytes 84 × 10(6)/L, 100% lymphocytes). Extensive laboratory investigations of CSF and serum did not reveal an infectious, autoimmune or metabolic cause. Visual evoked potentials were normal. Awake electroencephalogram revealed intermittent 3-5 Hz generalised slowing and frontal intermittent rhythmic delta activity, without epileptiform discharges. Repeat CSF analysis showed marked reduction of the total leucocyte count and remained negative for infectious aetiology. Propranolol was commenced, and no recurrence of headache or neurological symptoms was observed at follow-up. An extensive literature review on the topic is discussed.

摘要

我们描述了一例头痛和神经功能缺损病例,患者表现为复发性严重头痛,伴有阴性感觉症状和言语障碍,病史为 3 周。患者无心血管危险因素,也无偏头痛家族史。神经系统检查无明显异常。颅脑磁共振成像无明显异常。CSF 分析显示淋巴细胞增多(白细胞 84×10(6)/L,100%淋巴细胞)。对 CSF 和血清进行了广泛的实验室检查,未发现感染、自身免疫或代谢原因。视觉诱发电位正常。清醒脑电图显示间歇性 3-5 Hz 弥漫性减慢和额部间歇性节律性 δ 活动,无癫痫样放电。重复 CSF 分析显示总白细胞计数明显减少,且仍无感染性病因。开始使用普萘洛尔,随访时未再出现头痛或神经症状复发。对该主题进行了广泛的文献回顾。

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