Corticobasal syndrome due to sporadic Creutzfeldt–Jakob disease: a review and neuropsychological case report

References

• Anschel, D. J., Simon, D. K., Llinas, R., & Joseph, J. T. (2002). Spongiform encephalopathy mimicking corticobasal degeneration. Movement Disorders, 17, 606–607.10.1002/(ISSN)1531-8257
   PubMed Web of Science ®Google Scholar
• Armstrong, M. J., & Litvan, I. (2015). Corticobasal degeneration. In A. I. Troster (Ed.), Clinical neuropsychology and cognitive neurology of Parkinson’s disease and other movement disorders (pp. 399–420). New York, NY: Oxford University Press.
   Google Scholar
• Armstrong, M. J., Litvan, I., Lang, A. E., Bak, T. H., Bhatia, K. P., Borroni, B., … Josephs, K. A. (2013). Criteria for the diagnosis of corticobasal degeneration. Neurology, 80, 496–503.10.1212/WNL.0b013e31827f0fd1
   PubMed Web of Science ®Google Scholar
• Arnao, V., Gangitano, M., Giacalone, F., Riolo, M., Savettieri, G., & Aridon, P. (2015). Corticobasal syndrome-like variant of Creutzfeldt–Jakob disease: clinical description of two cases. Neurological Sciences, 36, 1303–1305.10.1007/s10072-014-2043-7
   PubMed Web of Science ®Google Scholar
• Brown, P., Brandel, J. P., Sato, T., Nakamura, Y., MacKenzie, J., Will, R. G., … Schonberger, L. B. (2012). Iatrogenic Creutzfeldt–Jakob disease, final assessment. Emerging Infectious Diseases, 18, 901–907. doi:10.3201/eid1806.120116
   PubMed Web of Science ®Google Scholar
• Caine, D., Tinelli, R. J., Hyare, H., De Vita, E., Lowe, J., Lukic, A., …. Mead, S. (2015). The cognitive profile of prion disease: A prospective clinical and imaging study. Annals of Clinical and Translation Neurology, 2, 548–558. doi:10.1002/acn3.195
   PubMed Web of Science ®Google Scholar
• Carswell, C., Thompson, A., Lukic, A., Stevens, J., Rudge, P., Mead, S., … Hyare, H. (2012). MRI findings are often missed in the diagnosis of Creutzfeldt–Jakob disease. BMC Neurology, 12, 519. doi:10.1186/1471-2377-12-153
   Web of Science ®Google Scholar
• Centers for Disease Control and Prevention. (2015). Creutzfeldt–Jakob disease, classic (CJD). Retrieved from http://www.cdc.gov/prions/cjd/occurance-transmisison.html
   Google Scholar
• Coulthart, M. B., Jansen, G. H., Olsen, E., Godal, D. L., Connolly, T., Choi, B. C., … Cashman, N. R. (2011). Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt–Jakob disease in Canada: A 6-year prospective study. BMC Neurology, 11, 1–13. Retrieved from http://bmcneurol.biomedcentral.com/articles/10.1186/1471-2377-11-133
   PubMed Web of Science ®Google Scholar
• Delis, D. C., Kaplan, E., & Kramer, J. H. (2000). Delis–Kaplan executive function system. San Antonio, TX: Psychological Corporation.
   Google Scholar
• Geschwind, M. D., Josephs, K. A., Parisi, J. E., & Keegan, B. M. (2007). A 54-year-old man with slowness of movement and confusion. Neurology, 69, 1881–1887.10.1212/01.wnl.0000290370.14036.69
   PubMed Web of Science ®Google Scholar
• Graff-Radford, J., Rubin, M. N., Jones, D. T., Aksamit, A. J., Ahlskog, J. E., Knopman, D. S., … Josephs, K. A. (2013). The alien limb phenomenon. Journal of Neurology, 260, 1880–1888.10.1007/s00415-013-6898-y
   PubMed Web of Science ®Google Scholar
• van Harten, A. C., Kester, M. I., Visser, P. J., Blankenstein, M. A., Pijnenburg, Y. A., van der Flier, W. M., & Scheltens, P. (2011). Tau and p-tau as CSF biomarkers in dementia: A meta-analysis. Clinical Chemistry and Laboratory Medicine, 49, 353–366. doi:10.1515/CCLM.2011.086
   PubMed Web of Science ®Google Scholar
• Heaton, R. K., Miller, S. W., Taylor, M. J., & Grant, I. (2004). Revised comprehensive norms for an expanded Halstead-Reitan Battery: Demographically adjusted neuropsychological norms for African American and Caucasian adults. Lutz, FL: Psychological Assessment Resources.
   Google Scholar
• Herrero Valverde, A., Costa, S., Timoteo, Â., Ginestal, R., & Pimentel, J. (2011). Rapidly progressive corticobasal degeneration syndrome. Case Reports in Neurology, 3, 185–190.10.1159/000329820
   PubMedGoogle Scholar
• Hu, W. T., Rippon, G. W., Boeve, B. F., Knopman, D. S., Petersen, R. C., Parisi, J. E., & Josephs, K. A. (2009). Alzheimer’s disease and corticobasal degeneration presenting as corticobasal syndrome. Movement Disorders, 24, 1375–1379.10.1002/mds.v24:9
   PubMed Web of Science ®Google Scholar
• Jacquin, A., Deramecourt, V., Bakchine, S., Maurage, C. A., & Pasquier, F. (2014). Unusual features of Creutzfeldt–Jakob disease followed-up in a memory clinic. Journal of Neurology, 261, 696–701.10.1007/s00415-014-7246-6
   PubMed Web of Science ®Google Scholar
• Johnson, R. T., & Gibbs, C. J. (1998). Creutzfeldt–Jakob disease and related transmissible spongiform encephalopathies. New England Journal of Medicine, 339, 1994–2004.10.1056/NEJM199812313392707
   PubMed Web of Science ®Google Scholar
• Josephs, K. A., Ahlskog, J. E., Parisi, J. E., Boeve, B. F., Crum, B. A., Giannini, C., & Petersen, R. C. (2009). Rapidly progressive neurodegenerative dementias. Archives of Neurology, 66, 201–207.
   PubMedGoogle Scholar
• Keifer, E., & Haut, M. W. (2014). Neurobehavioral examination. In M. W. Parsons & T. A. Hammeke (Eds.), Clinical neuropsychology: A pocket handbook for assessment (3rd ed.). (pp. 31–52). Washington, DC: American Psychological Association.10.1037/14339-000
   Google Scholar
• Kim, M.-O., & Geschwind, M. D. (2015). Clinical update of Jakob-Creutzfeldt disease. Current Opinion in Neurology, 28, 302–310. doi:10.1097/WCO.0000000000000197
   PubMed Web of Science ®Google Scholar
• Kleiner-Fisman, G., Bergeron, C., & Lang, A. E. (2004). Presentation of Creutzfeldt–Jakob disease as acute corticobasal degeneration syndrome. Movement Disorders, 19, 948–949.10.1002/mds.v19:8
   PubMed Web of Science ®Google Scholar
• Kojima, G., Tatsuno, B. K., Inaba, M., Velligas, S., Masaki, K., & Liow, K. K. (2013). Creutzfeldt–Jakob disease: A case report and differential diagnoses. Hawaii Journal of Medicine & Public Health, 72, 136–139.
   Google Scholar
• Lee, W., Simpson, M., Ling, H., Mclean, C., Collins, S., & Williams, D. R. (2013). Characterising the uncommon corticobasal syndrome presentation of sporadic Creutzfeldt–Jakob disease. Parkinsonism & Related Disorders, 19, 81–85.10.1016/j.parkreldis.2012.07.010
   PubMed Web of Science ®Google Scholar
• Liao, Y. C., Lebo, R. V., Clawson, G. A., & Smuckler, E. A. (1986). Human prion protein cDNA: Molecular cloning, chromosomal mapping, and biological implications. Science, 18, 364–367.10.1126/science.3014653
   Web of Science ®Google Scholar
• Litvan, I., Agid, Y., Goetz, C., Jankovic, J., Wenning, G. K., Brandel, J. P., … Jellinger, K. (1997). Accuracy of the clinical diagnosis of corticobasal degeneration: A clinicopathologic study. Neurology, 48, 119–125.10.1212/WNL.48.1.119
   PubMed Web of Science ®Google Scholar
• Manix, M., Kalakoti, P., Henry, M., Thakur, J., Menger, R., Guthikonda, B., & Nanda, A. (2015). Creutzfeldt–Jakob disease: Updated diagnostic criteria, treatment algorithm, and the utility of brain biopsy. Neurosurgical Focus, 39, e2. doi:10.3171/2015.8.FOCUS15328
   PubMed Web of Science ®Google Scholar
• McGuire, L. I., Peden, A. H., Orrú, C. D., Wilham, J. M., Appleford, N. E., Mallinson, G., … Green, A. J. (2012). Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt–Jakob disease. Annals of Neurology, 72, 278–285. doi:10.1002/ana.23589
   PubMed Web of Science ®Google Scholar
• Moreaud, O., Monavon, A., Brutti-Mairesse, M. P., Grand, S., & Lebas, J. F. (2005). Creutzfeldt–Jakob disease mimicking corticobasal degeneration. Journal of Neurology, 252, 1283–1284.10.1007/s00415-005-0828-6
   PubMed Web of Science ®Google Scholar
• Muayqil, T., Gronseth, G., & Camicioli, R. (2012). Evidence-based guideline: Diagnostic accuracy of CSF 14-3-3 protein in sporadic Creutzfeldt–Jakob disease: Report of the guideline development subcommittee of the American Academy of Neurology. Neurology, 79, 1499–1506. doi:10.1212/WNL.0b013e31826d5fc3
   PubMed Web of Science ®Google Scholar
• O’Connor, M. G., & Race, E. (2014). Amnestic syndromes. In M. W. Parsons & T. A. Hammeke (Eds.), Clinical neuropsychology: A pocket handbook for assessment (3rd ed.). (pp. 385–410). Washington, DC: American Psychological Association.10.1037/14339-000
   Google Scholar
• Orrú, C. D., Bongianni, M., Tonoli, G., Ferrari, S., Hughson, A. G., Groveman, B. R., … Zanusso, G. (2014). A test for Creutzfeldt–Jakob disease using nasal brushings. New England Journal of Medicine, 371, 519–529. doi:10.1056/NEJMoa1315200
   PubMed Web of Science ®Google Scholar
• Pachana, N. A., Byrne, G. J., Siddle, H., Koloski, N., Harley, E., & Arnold, E. (2007). Development and validation of the Geriatric Anxiety Inventory. International Psychogeriatrics, 19, 103–114.10.1017/S1041610206003504
   PubMed Web of Science ®Google Scholar
• Randolph, C. (2012). Repeatable battery for the assessment of neuropsychological status (RBANS) update manual. San Antonio, TX: Pearson.
   Google Scholar
• Reitan, R. M., & Wolfson, D. (1993). The Halstead-Reitan neuropsychological test battery: Theory and clinical applications (2nd ed.). Tucson, AZ: Neuropsychology Press.
   Google Scholar
• Rutala, W. A., & Weber, D. J. (2001). Creutzfeldt–Jakob disease: Recommendations for disinfection and sterilization. Clinical Infectious Diseases, 32, 1348–1356. doi:10.1086/319997
   PubMed Web of Science ®Google Scholar
• Shiga, Y., Miyazawa, K., Sato, S., Fukushima, R., Shibuya, S., Sato, Y., … Itoyama, Y. (2004). Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt–Jakob disease. Neurology, 63, 443–449.10.1212/01.WNL.0000134555.59460.5D
   PubMed Web of Science ®Google Scholar
• Snowden, J. S., Mann, D. M., & Neary, D. (2002). Distinct neuropsychological characteristics in Creutzfeldt–Jakob disease. Journal of Neurology, Neurosurgery, and Psychiatry, 73, 686–694.10.1136/jnnp.73.6.686
   PubMed Web of Science ®Google Scholar
• Steinhoff, B. J., Zerr, I., Glatting, M., Schulz-Schaeffer, W., Poser, S., & Kretzschmar, H. A. (2004). Diagnostic value of periodic complexes in Creutzfeldt–Jakob disease. Annals of Neurology, 56, 702–708.10.1002/(ISSN)1531-8249
   PubMed Web of Science ®Google Scholar
• Stern, R., & White, T. (2009). NAB naming test: Professional manual. Lutz, FL: Psychological Assessment Resources.
   Google Scholar
• Strauss, E., Sherman, E. M., & Spreen, O. (2006). A compendium of neuropsychological tests (4th ed.). New York, NY: Oxford.
   Google Scholar
• Takada, L. T., & Geschwind, M. D. (2013). Prion diseases. Seminars in Neurology, 33, 348–356. doi:10.1055/s-0033-1359314
   PubMed Web of Science ®Google Scholar
• Tschampa, H. J., Zerr, I., & Urbach, H. (2007). Radiological assessment of Creutzfeldt–Jakob disease. European Radiology, 17, 1200–1211.10.1007/s00330-006-0456-2
   PubMed Web of Science ®Google Scholar
• Verfaellie, M., & Cermak, L. S. (1992). Neuropsychological issues in amnesia. In J. Martinez & R. Kesner (Eds.), Learning and memory: A biological view (pp. 467–497). San Diego, CA: Academic Press.
   Google Scholar
• Vitali, P., Maccagnano, E., Caverzasi, E., Henry, R. G., Haman, A., Torres-Chae, C., … Geschwind, M. D. (2011). Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias. Neurology, 76, 1711–1719. doi:10.1212/WNL.0b013e31821a4439
   PubMed Web of Science ®Google Scholar
• Wechsler, D. (2008). Wechsler adult intelligence scale-fourth edition (WAIS-IV) manual. San Antonio, TX: Pearson.
   Google Scholar
• Wechsler, D. (2009). Advanced clinical solutions for WAIS-IV and WMS-IV. San Antonio, TX: Pearson.
   Google Scholar
• Wieser, H. G., Schindler, K., & Zumsteg, D. (2006). EEG in Creutzfeldt–Jakob disease. Clinical Neurophysiology, 117, 935–951. doi:10.1016/j.clinph.2005.12.007
   PubMed Web of Science ®Google Scholar
• Wieser, H. G., Schwarz, U., Blättler, T., Bernoulli, C., Sitzler, M., Stoeck, K., & Glatzel, M. (2004). Serial EEG findings in sporadic and iatrogenic Creutzfeldt–Jakob disease. Clinical Neurophysiology, 115, 2467–2478.10.1016/j.clinph.2004.05.032
   PubMed Web of Science ®Google Scholar
• Will, R. G., Ironside, J. W., Zeidler, M., Estibeiro, K., Cousens, S. N., Smith, P. G., … Hofman, A. (1996). A new variant of Creutzfeldt–Jakob disease in the UK. The Lancet, 347, 921–925.10.1016/S0140-6736(96)91412-9
   PubMed Web of Science ®Google Scholar
• Will, R. G., Zeidler, M., Stewart, G. E., Macleod, M. A., Ironside, J. W., Cousens, S. N., … Knight, R. S. (2000). Diagnosis of new variant Creutzfeldt–Jakob disease. Annals of Neurology, 47, 575–582.10.1002/(ISSN)1531-8249
   PubMed Web of Science ®Google Scholar
• World Health Organization. (1998). Global surveillance, diagnosis and therapy of human transmissible spongiform encephalopathies: Report of a WHO consultation. Retrieved from http://www.who.int/csr/resources/publications/bse/WHO_EMC_ZDI_98_9/en/
   Google Scholar
• Young, G. S., Geschwind, M. D., Fischbein, N. J., Martindale, J. L., Henry, R. G., Liu, S., … Dillon, W. P. (2005). Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt–Jakob disease: High sensitivity and specificity for diagnosis. American Journal of Neuroradiology, 26, 1551–1562.
   PubMed Web of Science ®Google Scholar
• Zerr, I., Kallenberg, K., Summers, D. M., Romero, C., Taratuto, A., Heinemann, U., … Sanchez-Juan, P. (2009). Updated clinical diagnostic criteria for sporadic Creutzfeldt–Jakob disease. Brain, 132, 2659–2668.10.1093/brain/awp191
   PubMed Web of Science ®Google Scholar
• Zhang, Y., Minoshima, S., Vesselle, H., & Lewis, D. H. (2012). A case of Creutzfeldt–Jakob disease mimicking corticobasal degeneration: FDG PET, SPECT, and MRI findings. Clinical Nuclear Medicine, 37, e173–e175.10.1097/RLU.0b013e31824c5f0e
   PubMed Web of Science ®Google Scholar