NR ASZT
AU Hamaguchi,T.; Kitamoto,T.; Sato,T.; Mizusawa,H.; Nakamura,Y.; Noguchi,M.; Furukawa,Y.; Ishida,C.; Kuji,I.; Mitani,K.; Murayama,S.; Kohriyama,T.; Katayama,S.; Yamashita,M.; Yamamoto,T.; Udaka,F.; Kawakami,A.; Ihara,Y.; Nishinaka,T.; Kuroda,S.; Suzuki,N.; Shiga,Y.; Arai,H.; Maruyama,M.; Yamada,M.
TI Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease
QU Neurology 2005 Feb 22; 64(4): 643-8
PT case reports; journal article; review; review, multicase
AB BACKGROUND: No method for the clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease (sCJD) has been established except for pathologic examination. OBJECTIVE: To identify a reliable marker for the clinical diagnosis of MM2-type sCJD. METHODS: CSF, EEG, and neuroimaging studies were performed in eight patients with MM2-type sCJD confirmed by neuropathologic, genetic, and western blot analyses. RESULTS: The eight cases were pathologically classified into the cortical (n = 2), thalamic (n = 5), and combined (corticothalamic) (n = 1) forms. The cortical form was characterized by late-onset, slowly progressive dementia, cortical hyperintensity signals on diffusion-weighted imaging (DWI) of brain, and elevated levels of CSF 14-3-3 protein. The thalamic form showed various neurologic manifestations including dementia, ataxia, and pyramidal and extrapyramidal signs with onset at various ages and relatively long disease duration. Characteristic EEG and MRI abnormalities were almost absent. However, all four patients examined with cerebral blood flow (CBF) study using SPECT showed reduction of the CBF in the thalamus as well as the cerebral cortex. The combined form had features of both the cortical and the thalamic forms, showing cortical hyperintensity signals on DWI and hypometabolism of the thalamus on [18F]2-fluoro-2-deoxy-d-glucose PET. CONCLUSION: For the clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease, cortical hyperintensity signals on diffusion-weighted MRI are useful for the cortical form and thalamic hypoperfusion or hypometabolism on cerebral blood flow SPECT or [18F]2-fluoro-2-deoxy-d-glucose PET for the thalamic form.
ZR 34
MH 14-3-3 Proteins/cerebrospinal fluid; Age of Onset; Aged; Alzheimer Disease/diagnosis; Biological Markers; Blotting, Western; Cerebral Cortex/pathology/physiopathology/radionuclide imaging; Cerebrospinal Fluid Proteins/analysis; Cerebrovascular Circulation; Creutzfeldt-Jakob Syndrome/cerebrospinal; fluid/classification/*diagnosis/epidemiology/genetics/physiopathology; Diagnosis, Differential; Diffusion Magnetic Resonance Imaging; Electroencephalography; Female; Fluorodeoxyglucose F18/diagnostic use; Humans; Male; Middle Aged; Phenotype; Positron-Emission Tomography; Prions/genetics; Research Support, Non-U.S. Gov't; Supranuclear Palsy, Progressive/diagnosis; Thalamus/blood supply/pathology/radionuclide imaging; Tomography, Emission-Computed, Single-Photon
AD Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Takara-machi, Kanazawa, Japan.
SP englisch
PO USA