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Case Report: Focal neurological presentation in Hashimoto's encephalopathy mimicking a vascular occlusion of the middle cerebral artery

机译:病例报告:桥本脑病的局灶神经系统表现,模仿大脑中动脉的血管闭塞

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摘要

Hashimoto’s encephalopathy is a rare form of autoimmune encephalopathy. It is likely an underdiagnosed entity especially in the setting of focal neurological defects. We report a case of a 49-year-old man who presented with “strange behavior”of a day’s duration. Examination was significant only for lethargy, poor attention span and agitation. Routine labs revealed leucocytosis. Head CT scan was unremarkable. Lumbar puncture showed high white blood cells with lymphocytosis and elevated protein level. The patient was empirically treated for meningitis without improvement. His symptoms progressed to sudden right-sided weakness, ataxia and right facial droop. The MRI and magnetic resonance angiogram (MRA)were normal. The patient’s focal neurological signs improved spontaneously. Encephalopathy work-up was negative except for positive anti-Thyroid Peroxidaseand antithyroglobulin. The patient was treated as Hashimoto encephalopathy with steroids and azathioprine with marked improvement. Our case highlights how focal neurological findings can potentially mislead the provider to consider vascular aetiologies in Hashimoto’s encephalopathy.
机译:桥本脑病是一种罕见的自身免疫性脑病。这可能是诊断不足的实体,尤其是在局灶性神经系统缺损的情况下。我们报告了一例49岁的男子,该男子一天之内表现出“奇怪的行为”。检查仅对嗜睡,注意力不集中和躁动有意义。常规实验室发现白细胞增多。头部CT扫描无异常。腰椎穿刺显示白细胞增多,有淋巴细胞增多和蛋白质水平升高。根据经验对患者进行脑膜炎治疗,但无改善。他的症状发展为突然的右侧无力,共济失调和右侧面部下垂。 MRI和磁共振血管造影(MRA)正常。患者的局灶性神经系统症状自发改善。除抗甲状腺过氧化物酶和抗甲状腺球蛋白阳性外,脑病检查结果均为阴性。该患者以类固醇和硫唑嘌呤治疗桥本脑病,病情明显好转。我们的案例凸显了局灶性神经系统发现如何可能会误导提供者考虑桥本脑病的血管病因。

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