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Rapidly progressive neurologic decline and morbilliform rash presenting in a patient with lymphoma

机译:淋巴瘤患者出现快速进行性神经功能下降和麻疹样皮疹

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摘要

A 67-year-old male with past medical history of mantle cell lymphoma and atrial fibrillation presented with a truncal rash, bilateral lower extremity weakness, and confusion. Within three days of presentation, his condition rapidly deteriorated with the onset of diffuse flaccid paralysis, aphasia, and severe alteration in mental status. Initial results from serum studies, lumbar puncture, magnetic resonance imaging, and electroencephalogram were not diagnostic. However, on the ninth day after initial presentation, the West Nile Virus (WNV) immunoglobulin M antibody returned positive from the cerebrospinal fluid. West Nile Virus encephalitis is endemic worldwide, and is the most common viral encephalitis in the United States. WNV presents in a variety of ways, and the recognition by physicians is crucial due to the estimated 2-12% mortality rate and significant longterm morbidity of neuroinvasive disease. The initial management and long term prognosis are points of ongoing research. This case represents a particularly profound example of neuroinvasive WNV. Our patient made a significant recovery after his initial presentation with aggressive supportive care, however still suffers from bilateral lower extremity weakness more than a year later.
机译:一位67岁的男性,曾有套细胞淋巴瘤和房颤的病史,出现了皮疹,双侧下肢无力和精神错乱。在陈述的三天之内,他的病情随着弥漫性松弛性麻痹,失语和精神状态的严重改变而迅速恶化。血清研究,腰穿,磁共振成像和脑电图的初步结果不能诊断。然而,在首次出现后的第9天,西尼罗河病毒(WNV)免疫球蛋白M抗体从脑脊液中恢复阳性。西尼罗河病毒性脑炎是世界范围内的流行病,是美国最常见的病毒性脑炎。 WNV的呈现方式多种多样,由于估计2-12%的死亡率和严重的神经浸润性疾病的长期发病率,医生的认可至关重要。初始治疗和长期预后是正在进行的研究的重点。这种情况代表了神经侵入性WNV的一个特别深刻的例子。我们的患者在最初接受积极的支持治疗后恢复了明显的能力,但是一年多后仍然患有双侧下肢无力。

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