Diagnostic approach in a patient with Creutzfeldt-Jakob disease

Author:

Tavares-Júnior José Wagner Leonel1ORCID,Carvalho Renata de Oliveira2ORCID,Feitosa Raul Raposo Pereira3ORCID,Rolim Flávia de Paiva Santos4ORCID,Rocha Felipe Araújo3ORCID,Pitombeira Milena Sales3ORCID,Malveira George Linard Silva3ORCID,Carvalho João José Freitas de3ORCID,Frota Norberto Anizio Ferreira4ORCID,Dias Daniel Aguiar1ORCID

Affiliation:

1. Universidade Federal do Ceará, Brazil

2. Hospital Monte Klinikum, Brazil

3. Hospital Geral de Fortaleza, Brazil

4. Hospital Geral de Fortaleza, Brazil; Universidade de Fortaleza, Brazil

Abstract

ABSTRACT Prion diseases are an important cause of rapidly progressive dementias. Among them, the most common is sporadic Creutzfeldt-Jakob disease (CJD). It is a rare and incurable disease, with rapid progression to death. Objective: To describe the diagnostic approach of a patient with Creutzfeldt-Jakob disease. Methods: The diagnosis is established through the clinical picture associated with characteristic changes in the brain magnetic resonance imaging, the electroencephalogram, and analysis of specific changes in the cerebrospinal fluid. Results: The present report describes the case of a 53-year-old patient in the city of Fortaleza-CE. The diagnosis was made based on the clinical condition and through diagnostic tests, including 14-3-3 protein and RT QUIC analysis. Differential diagnosis was performed with other rapidly progressive causes, such as infectious and immune-mediated diseases. Conclusions: The diagnosis of probable sporadic CJD was established.

Publisher

FapUNIFESP (SciELO)

Subject

Cognitive Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Neurology,Sensory Systems

Reference15 articles.

1. Prion diseases;Geschwind MD;Continuum (Minneap Minn),2015

2. On a particular focal disease of the central nervous system (preliminary communication), 1920;Creutzfeldt HG;Alzheimer Dis Assoc Disord,1989

3. Concerning a disorder of the central nervous system clinically resembling multiple sclerosis with remarkable anatomic findings (spastic pseudosclerosis). Report of a fourth case;Jakob A;Alzheimer Dis Assoc Disord,1989

4. Novel proteinaceous infectious particles cause scrapie;Prusiner SB;Science,1982

5. Prions;Prusiner SB;Proc Natl Acad Sci U S A,1998

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3