Creutzfeldt-Jakob Disease: Case Discussion and Imaging Review

  • Morgan C
  • Gupta M
  • El-Feky W
  • et al.
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Abstract

65-year-old man initially experienced difficulty forming his tie and felt unsteady while driving. Days later, these symptoms were followed by periods of dizziness and vague episodes of confusion that he felt were "out of character." The patient was extremely concerned , especially given a strong family history of strokes. With an unremarkable physical examination, laboratory tests, and brain imaging, the patient's symptoms were attributed to his inadvertent ingestion of codeine-containing medication and to multiple increasing life stressors, including recent prostatectomy for prostate cancer. One week later, the patient returned complaining of significant confusion, problems opening doors, and progressive difficulty performing activities of daily living. Physical examination at this time revealed the patient to be confused with notable psychomotor retardation. Decreased left arm swing was noted on gait exam. An electroencephalogram (EEG) showed findings of right temporal slowing. Because of this finding and the patient's deteriorating mental status, he was admitted for further evaluation. Repeat EEG demonstrated bihemispheric triphasic wave complexes. Cerebrospinal fluid cytology and cultures were normal, but cerebrospinal fluid protein 14-3-3 was abnormally elevated. Magnetic resonance imaging (MRI) of the brain revealed areas of diffusion restriction in the right cerebral cortex and right basal ganglia (Figure 1). No abnormalities were found after extensive laboratory tests, including a metabolic panel and tests for syphilis, HIV, her-pes simplex virus, human herpesvirus-6, C-reactive protein, antinuclear antibodies, folate, erythrocyte sedimentation rate, and homocysteine levels. His neurologic condition continued to deteriorate rapidly. Without effective treatment options, he was referred to hospice and succumbed to his disease process approximately 2 months from the time of initial presentation. Figure 1. (a, b, c) Multiple axial images from the patient's brain MRI demonstrate abnormal signal hyperintensity (arrows) at several cortical locations and in the caudate head on the diffusion-weighted sequence. (d, e, f) Less conspicuous signal hyperintensity is present at the corresponding locations on the fluid-attenuated inversion recovery (FLAIR) sequence. a b c d e f 69 A

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Morgan, C., Gupta, M., El-Feky, W., Shamim, S., & Opatowsky, M. (2009). Creutzfeldt-Jakob Disease: Case Discussion and Imaging Review. Baylor University Medical Center Proceedings, 22(1), 69–71. https://doi.org/10.1080/08998280.2009.11928476

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