Hostname: page-component-76fb5796d-vvkck Total loading time: 0 Render date: 2024-04-30T02:10:17.049Z Has data issue: false hasContentIssue false

Sporadic Creutzfeldt-Jakob Disease with Worsening Depression and Cognition

Published online by Cambridge University Press:  02 December 2014

Mark Hudon
Affiliation:
Division of Neurology, Department of Medicine, Walter C. Mackenzie Health Sciences Center, University of Alberta, Edmonton, Alberta, Canada
Richard Farb
Affiliation:
Division of Neurology, Department of Medicine, Walter C. Mackenzie Health Sciences Center, University of Alberta, Edmonton, Alberta, Canada
Taim Muayqil
Affiliation:
Division of Neurology, Department of Medicine, Walter C. Mackenzie Health Sciences Center, University of Alberta, Edmonton, Alberta, Canada
Zaeem A. Siddiqi
Affiliation:
Division of Neurology, Department of Medicine, Walter C. Mackenzie Health Sciences Center, University of Alberta, Edmonton, Alberta, Canada
Rights & Permissions [Opens in a new window]

Extract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

A 58-year-old male presented with a one-year history of low mood, early morning awakening from sleep, apathy, difficulty with memory, concentration and organization. This had been associated with intrusive concerns of a recent social stressor. He was no longer able to work and was on medical disability. Except for a 20kg weight loss there were no other constitutional or neurological symptoms. He had hypertension and hypercholesterolemia and was on atorvastatin and aspirin. He scored 28/30 on mini-mental status examination (MMSE) with errors on object recall; however he could recall forgotten items after cueing. He had difficulty with concentration, was apathic andhad a negative outlook to the future. His neurological examination and a detailed hematological work up including chemistry, cell counts, vitamin B12, folate, and renal, hepatic and thyroid function tests were normal. A brain magnetic resonance image (MRI) showed mild cerebral atrophy. Based on a formal neuropsychological assessment he was diagnosed with depression and started on Venlafaxine.

Type
Neuroimaging Highlight
Copyright
Copyright © The Canadian Journal of Neurological 2007

References

1. Elsaadany, S, Semenciw, R, Ricketts, M, Mao, Y, Giulivi, A. Epidemiological study of Creutzfeldt-Jakob disease death certificates in Canada, 1979-2001. Neuroepidemiology. 2005;24(1-2):1521.CrossRefGoogle ScholarPubMed
2. Meissner, B, Kortner, K, Bartl, M, Jastrow, U, Mollenhauer, B, Schroter, A, et al. Sporadic Creutzfeldt-Jakob disease: magnetic resonance imaging and clinical findings. Neurology. 2004 Aug 10;63(3):4506.Google Scholar
3. Wall, CA, Rummans, TA, Aksamit, AJ, Krahn, LE, Pankratz, VS. Psychiatric manifestations of Creutzfeldt-Jakob disease: a 25-year analysis. J Neuropsychiatry Clin Neurosci. 2005 Fall; 17(4):48995.Google Scholar
4. Young, GS, Geschwind, MD, Fischbein, NJ, Martindale, JL, Henry, RG, Liu, S, et al. Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosis. AJNR Am J Neuroradiol. 2005 Jun-Jul;26(6):155162.Google Scholar
5. Murata, T, Shiga, Y, Higano, S, Takahashi, S, Mugikura, S. Conspicuity and evolution of lesions in Creutzfeldt-Jakob disease at diffusion-weighted imaging. AJNR Am J Neuroradiol. 2002 Aug;23(7):116472.Google ScholarPubMed
6. Tschampa, HJ, Zerr, I, Urbach, H. Radiological assessment of Creutzfeldt-Jakob disease. Eur Radiol. 2007 May;17(5):120011.Google Scholar
7. EUROCJD, Group. Genetic epidemiology of Creutzfeldt-Jakob disease in europe. Rev Neurol (Paris). 2001 Jul;157(6-7):6337.Google Scholar
8. Urbach, H, Klisch, J, Wolf, HK, Brechtelsbauer, D, Gass, S, Solymosi, L. MRI in sporadic Creutzfeldt-Jakob disease: correlation with clinical and neuropathological data. Neuroradiology. 1998 Feb;40(2):6570.CrossRefGoogle Scholar
9. Gains, M, LeBlanc, A. Prion protein and prion diseases: the good and the bad. Can J Neurol Sci. 2007;34:12645.Google Scholar
10. Collins, SJ, Sanchez-Juan, P, Masters, CL, Klug, GM, van Duijn, C, Poleggi, A, et al. Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease. Brain. 2006 Sep;129(Pt 9):227887.CrossRefGoogle ScholarPubMed
11. Zerr, I, Pocchiari, M, Collins, S, Brandel, JP, de Pedro Cuesta, J, Knight, RS, et al. Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease. Neurology. 2000 Sep 26;55(6):8115.Google Scholar
12. Zochodne, DW, Young, GB, McLachlan, RS, Gilbert, JJ, Vinters, HV, Kaufmann, JC. Creutzfeldt-Jakob disease without periodic sharp wave complexes: a clinical, electroencephalographic, and pathologic study. Neurology. 1988 Jul;38(7):105660.Google Scholar