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

机译:伴神经功能减慢的伴有神经系统缺陷和脑脊液淋巴细胞增多症(HaNDL)的头痛综合征

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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 3-5Hz 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.
机译:我们描述了一个患者的脑脊液(CSF)淋巴细胞增多症的头痛和神经功能缺损的情况,该患者表现出与负面的感觉症状和吞咽困难相关的反复发作的严重头痛的3周病史。该患者无心血管危险因素,无偏头痛家族史。神经系统检查无异常。脑磁共振成像不明显。 CSF分析显示淋巴细胞增多(白细胞84×10 6 / L,100%淋巴细胞)。对脑脊液和血清的大量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。醒来的脑电图显示间歇性3-5Hz普遍减慢和额叶间歇性节律性活动,而没有癫痫样放电。重复脑脊液分析显示总白细胞计数显着减少,感染病因学仍阴性。开始使用普萘洛尔,随访中未观察到头痛或神经系统症状的复发。讨论了有关该主题的广泛文献综述。

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