Dement Neurocogn Disord.  2019 Dec;18(4):152-156. 10.12779/dnd.2019.18.4.152.

A Case of Creutzfeldt-Jakob Disease Presented as Rapid Progressive Parkinsonism

Affiliations
  • 1Department of Neurology, Kosin University College of Medicine, Busan, Korea.
  • 2Department of Neurology, Korea University Medical Center, Seoul, Korea. lcn001@naver.com

Abstract

No abstract available.


MeSH Terms

Creutzfeldt-Jakob Syndrome*
Parkinsonian Disorders*

Figure

  • Fig. 1 Diffusion-weighted imaging and 18F-FP-CIT of the patient. (A) Diffusion-weighted imaging (B-1000) showing abnormally high signal intensities in both parietal and temporal lobes. (B) 18F-FP-CIT positron emission tomography did not show postsynaptic dopaminergic deficits.

  • Fig. 2 Electroencephalography did not demonstrate typical rhythmic activity of Creutzfeldt-Jakob disease, revealing theta and delta slow activities.


Reference

1. Will RG. Epidemiology of Creutzfeldt-Jakob disease. Br Med Bull. 1993; 49:960–970.
Article
2. Rabinovici GD, Wang PN, Levin J, Cook L, Pravdin M, Davis J, et al. First symptom in sporadic Creutzfeldt-Jakob disease. Neurology. 2006; 66:286–287.
Article
3. Zeidler M, Stewart GE, Barraclough CR, Bateman DE, Bates D, Burn DJ, et al. New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests. Lancet. 1997; 350:903–907.
Article
4. Heath CA, Cooper SA, Murray K, Lowman A, Henry C, MacLeod MA, et al. Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK. J Neurol Neurosurg Psychiatry. 2011; 82:646–651.
Article
5. Zeidler M, Johnstone EC, Bamber RW, Dickens CM, Fisher CJ, Francis AF, et al. New variant Creutzfeldt-Jakob disease: psychiatric features. Lancet. 1997; 350:908–910.
Article
6. Spencer MD, Knight RS, Will RG. First hundred cases of variant Creutzfeldt-Jakob disease: retrospective case note review of early psychiatric and neurological features. BMJ. 2002; 324:1479–1482.
Article
7. Brandel JP, Delasnerie-Lauprêtre N, Laplanche JL, Hauw JJ, Alpérovitch A. Diagnosis of Creutzfeldt-Jakob disease: effect of clinical criteria on incidence estimates. Neurology. 2000; 54:1095–1099.
Article
8. Iida T, Doh-ura K, Kawashima T, Abe H, Iwaki T. An atypical case of sporadic Creutzfeldt-Jakob disease with Parkinson's disease. Neuropathology. 2001; 21:294–297.
Article
9. Tan AH, Toh TH, Low SC, Fong SL, Chong KK, Lee KW, et al. Chorea in sporadic Creutzfeldt-Jakob disease. J Mov Disord. 2018; 11:149–151.
Article
10. Ragno M, Scarcella MG, Cacchiò G, Capellari S, Di Marzio F, Parchi P, et al. Striatal [123I]FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease. Acta Neurol Scand. 2009; 119:131–134.
Article
11. McGuire LI, Poleggi A, Poggiolini I, Suardi S, Grznarova K, Shi S, et al. Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic Creutzfeldt-Jakob disease: an international study. Ann Neurol. 2016; 80:160–165.
Article
12. Sano K, Satoh K, Atarashi R, Takashima H, Iwasaki Y, Yoshida M, et al. Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay. PLoS One. 2013; 8:e54915.
Article
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