Evidence map›Paper›PMID 41509103›Full record

SynthesisF1000Research2025

Case Report: Creutzfeldt-Jakob disease and diagnosis challenges: case report and evidence synthesis.

Virgilio E Failoc Rojas, Yiro Yazawa-Ballena, Gustavo Alvarado-Moreno, Alba Navarro-Flores, Carlos Alva-Diaz, Kevin Pacheco-Barrios

Abstract readCase ReportsSystematic Review
In one paragraph

Synthesis in F1000Research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Virgilio E Failoc RojasUniversidad Cesar Vallejo, Piura, Piura, 20001, Peru.ORCID https://orcid.org/0000-0003-2992-9342
Yiro Yazawa-BallenaInternal medicine, Hospital Regional Lambayeque, Lambayeque, Lambayeque, 14011, Peru.
Gustavo Alvarado-MorenoInternal medicine, Hospital Regional Lambayeque, Lambayeque, Lambayeque, 14011, Peru.
Alba Navarro-FloresInternational Max Planck Research School for Translational Psychiatry (IMPRS-TP), Munich, Germany, 80804, Germany.
Carlos Alva-DiazServicio de Neurología, Departamento de Medicina y Oficina de Apoyo a la Docencia e Investigación (OADI), Hospital Daniel Alcides Carrión, Callao, Peru.
Kevin Pacheco-BarriosUniversidad San Ignacio de Loyola, Lima District, Lima Region, 150114, Peru.ORCID https://orcid.org/0000-0002-7166-2816

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Prion diseases are mortal neurodegenerative disorders, which include Creutzfeldt-Jakob disease (CJD). Due to its heterogenous clinical presentation diagnosis uncertainties are common. In this paper we explore CJD diagnostic challenges focusing on differential diagnosis and diagnostic delays. Methods: We report a case of a patient who was misclassified and evaluated by several medical specialties before the CJD suspicion. A systematic review of the literature of the CJD case reports focused on the timely and differential diagnosis was carried out in Medline and Embase until May 2023. Results: Patient with diagnosis was made due to the form of presentation and clinical evolution, neuroimaging and the presence of protein 14-3-3. In systematic review, fifteen articles were selected, who reported 31 cases of CJD with problems in the timely diagnosis and incorrect initial diagnosis, the main initial differential diagnoses were psychiatry exacerbation, myelopathy, epilepsy, stroke, parkinsonism, cerebellar ataxia and autoimmune encephalitis. The most common clinical onset was psychobehavioral disturbances (apathy, confusion and sleep disturbance), extrapyramidal signs and cognitive impairment. The diagnosis delay was from one to eighteen months. Conclusion: A discussion of the case report and the diagnostic challenges reported in the literature was made. Patients can present a wide range of symptoms. It is recommended to consider CJD for the differential diagnosis in patients with behavioral symptoms, and cognitive impairment.

Indexed as

Creutzfeldt-Jakob SyndromeDiagnosis, DifferentialHumansCreutzfeldt-Jakob syndrome; Prion diseases; differential diagnosis; behavioral symptoms; 14-3-3 Proteins; Peru

Identifiers

PMID41509103
PMCPMC12775658

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