Creutzfeldt-Jakob disease presented with dizziness, weakness and neuropsychiatric symptoms: 2 Case Reports

Baş dönmesi, halsizlik ve nöropsikiyatrik semptomlar ile prezente olan Creutzfeldt-Jakob hastalığı: 2 olgu sunumu


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Authors

  • Yusuf İnanç Başkent University School of Medicine, Department of Neurology
  • Zülfikar Arlıer Başkent University School of Medicine, Department of Neurology
  • Yılmaz İnanç Hayat Hospital, Neurology Clinics
  • Sırma Geyik Gaziantep University School of Medicine, Department of Neurology
  • Semih Giray Başkent University School of Medicine, Department of Neurology
  • Özcan Kocatürk Harran University School of Medicine, Department of Neurology

DOI:

https://doi.org/10.5455/GMJ-30-173253

Keywords:

Creutzfeldt-Jakob disease, dementia, myoclonus

Abstract

Creutzfeldt-Jakob disease (CJD) is among very rare, progressive, untreatable, neurodegenerative prion diseases. While the incidence is reported as 1/1000000 years in European countries, sporadic cases are rarely presented in Turkey. Clinical findings are in the form of rapid progressive dementia, myoclonus, cerebellar, pyramidal and extra pyramidal symptoms. Definitive diagnosis is established by histopathological examination. Our case is a 64-year-old male and 70-year-old female patients admitted with dizziness emerged as sub-acute weakness, nausea, vomiting, insomnia, imbalance and additional neuropsychiatric complaints. Focal activity slowness and common periodic sharp wave activities were observed in EEG. CJD was considered because bilateral symmetrical diffusion limitation was observed at both sides in the basal ganglia level in cranial diffusion MRI’s and 14-3-3 protein was resulted as positive in CSF examinations. CJD, which is a very rare disease in patients presenting with progressive neuropsychiatric symptoms and seizure, is one of the diagnosis to be considered and we wanted to emphasize that there is no treatment for it and preventive measures should be taken

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References

Glatzel M, Stoeck K, Seeger H, Lührs T, Aguzzi A. Human prion diseases molecular and clinical aspects. Arch Neurol. 2005;62(4):545-52.

MT, Will RG, Manson JC. Defining sporadic CreutzfeldtJakob disease strains and their transmission properties. Proc Natl Acad Sci U S A. 2010; 107(26): 12005–10.

Fujita K, Harada M, Sasaki M, Yuasa T, Sakai K, Hamaguchi T et al. Multicentre multiobserver study of diffusion weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt–Jakob disease: a reliability and agreement study. BMJ Open. 2012; 2(1): e000649.

Thompson A, MacKay A, Rudge P, Lukic A, Porter MC, Lowe J et al. Behavioral and psychiatric symptoms in prion disease. Am J Psychiatry. 2014 Mar;171(3):265-74.

Jubelt B, Miller JR. Viral infections. In: Rowland LP,ed. Merrit's Textbook of Neurology. 9th Ed. Philadelphia Williams and Wilkins 1995; 142-179.

Jonathan D. F. Wadsworth, John Collinge. Molecular pathology of human prion disease. Acta Neuropathol. 2011; 121(1): 69–77.

Maltete D, Guyant Marechal L, Mihout B. Movement disorders and Creutzfeldt-Jakob disease: A review. Parkinsonism and Related Disorders 2006; 12(2): 65-71.

Wieser HG, Schindler K, Zumsteg D. EEG in Creutzfeldt-Jakob disease. Clin. Neurophysiol. 2006;117(5):935-51.

Cambier DM, Kantarci K, Worrell GA et all. Lateralized and focal clinical, EEG, and FLAIR MRI abnormalities in Creutzfeldt-Jakob disease. Clin Neurophysiol. 2003;114(9):1724-28.

Green AJ, Thompson EJ, Stewart GE, Zeidler M, McKenzie JM, MacLeod MA et al. Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt Jakob disease. J Neurol Neurosurg Psychiatry. 2001 Jun;70(6):744-8.

Van Everbroeck B, Boons J, Cras P. Cerebrospinal fluid biomarkers in Creutzfeldt-Jakob disease. Clin Neurol Neurosurg 2005; 107(5):355-60.

Caobelli F, Cobelli M, Pizzocaro C, Pavia M, Magnaldi S, Guerra UP. The Role of Neuroimaging in Evaluating Patients Affected by Creutzfeldt-Jakob Disease: A Systematic Review of the Literature. J Neuroimaging. 2014; 5. doi: 10.1111.

Bergui M, Bradac GB, Rossi G, Orsi L. Extensive cortical damage in a case of Creutzfeldt-Jakob disease: Clinicoradiological correlations. Neuroradiology. 2003;45(5):304-7

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Published

2023-05-06

How to Cite

İnanç, Y., Arlıer, Z., İnanç, Y., Geyik, S., Giray, S., & Kocatürk, Özcan. (2023). Creutzfeldt-Jakob disease presented with dizziness, weakness and neuropsychiatric symptoms: 2 Case Reports: Baş dönmesi, halsizlik ve nöropsikiyatrik semptomlar ile prezente olan Creutzfeldt-Jakob hastalığı: 2 olgu sunumu. European Journal of Therapeutics, 21(2), 142–146. https://doi.org/10.5455/GMJ-30-173253

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Case Reports