Hereditary Creutzfeldt-Jakob Disease: A Case Presentation of a Rare Stroke Mimic

Acute ischemic cerebrovascular accident (CVA) is a time-sensitive emergent diagnosis, requiring rapid diagnosis and consideration of thrombolytic administration. However, a myriad of cerebrovascular mimics creates a diagnostic challenge. A rare CVA mimic is Creutzfeldt-Jakob disease (CJD), a rapidly...

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Veröffentlicht in:Curēus (Palo Alto, CA) CA), 2024-03, Vol.16 (3), p.e55559
Hauptverfasser: Bridwell, Rachel E, Barlow, Jessica A, Jacobson, Andrew R, Curell, Angela, Long, Brit
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Barlow, Jessica A
Jacobson, Andrew R
Curell, Angela
Long, Brit
description Acute ischemic cerebrovascular accident (CVA) is a time-sensitive emergent diagnosis, requiring rapid diagnosis and consideration of thrombolytic administration. However, a myriad of cerebrovascular mimics creates a diagnostic challenge. A rare CVA mimic is Creutzfeldt-Jakob disease (CJD), a rapidly progressive fatal dementia due to protein misfolding. Magnetic resonance imaging (MRI) and neurology consultation for electroencephalogram (EEG) and specialized cerebrospinal fluid (CSF) studies are diagnostic while the patient is alive. All forms are fatal within months, and diagnosis can be confirmed on postmortem brain testing. While incredibly uncommon, emergency clinicians should consider this diagnosis in the proper patient to advocate for specialized CSF testing and potential palliative care consultation.
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subjects Ataxia
Cerebrospinal fluid
Creutzfeldt-Jakob disease
Dementia
Diagnostic tests
Diplopia
Electroencephalography
Emergency medical care
Emergency Medicine
Etiology
Family medical history
Hospitals
Iatrogenesis
Infectious Disease
Ischemia
Magnetic resonance imaging
Mutation
Neurology
Neurosurgery
Patients
Proteins
Tomography
Transplants & implants
Trauma
Visual acuity
title Hereditary Creutzfeldt-Jakob Disease: A Case Presentation of a Rare Stroke Mimic
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