克雅氏病的非典型脑共振表现:病例报告

Q4 Medicine
Rodrigo Sanjinez , Rocío Márquez , Juan Pablo Rodríguez , Otto Vega , José Zuñiga , Alejandra Heriz
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引用次数: 0

摘要

克雅氏病是一种罕见的、进行性和致命性的海绵状脑病,由朊病毒引起。2010年,MRI检查结果被纳入诊断标准。我们描述了一个不典型的表现在图像的病人。临床病例:73岁快速进展性痴呆患者,脑MRI伴边缘系统高强度。患者在出现临床症状5个月后发展为动力性缄默症并死亡。结论磁共振成像是快速进展性痴呆患者诊断评价的基础支柱,特别是在克雅氏病与自身免疫性脑炎的鉴别诊断中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Presentación atípica en resonancia de cerebro de la enfermedad de Creutzfeldt-Jakob: reporte de un caso

Introduction

Creutzfeldt-Jakob disease is a rare, progressive and fatal spongiform encephalopathy that is caused by a prion. In 2010, the MRI findings were included in the criteria for diagnosing the disease. We describe a patient with an atypical presentation in images.

Clinical case

73-year-old patient with rapidly progressive dementia and brain MRI with hyperintensity in the limbic system. The patient evolves with akinetic mutism and death 5 months after the onset of the clinical picture.

Conclusions

Magnetic resonance imaging is a fundamental pillar in the diagnostic evaluation of patients with rapidly progressive dementia and, in particular, in the differential diagnosis between Creutzfeldt-Jakob disease and autoimmune encephalitis.

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来源期刊
Neurologia Argentina
Neurologia Argentina Medicine-Neurology (clinical)
CiteScore
0.50
自引率
0.00%
发文量
34
期刊介绍: Neurología Argentina es la publicación oficial de la Sociedad Neurológica Argentina. Todos los artículos, publicados en español, son sometidos a un proceso de revisión sobre ciego por pares con la finalidad de ofrecer información original, relevante y de alta calidad que abarca todos los aspectos de la Neurología y la Neurociencia.
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