Brain magnetic resonance diffusion abnormalities in Creutzfeldt-Jakob disease

被引:71
作者
Bahn, MM
Kido, DK
Lin, WL
Pearlman, AL
机构
[1] WASHINGTON UNIV,SCH MED,EDWARD MALLINCKRODT INST RADIOL,DEPT RADIOL,DIV RADIOL SCI,ST LOUIS,MO 63110
[2] WASHINGTON UNIV,SCH MED,DEPT NEUROL,ST LOUIS,MO 63110
关键词
D O I
10.1001/archneur.1997.00550230078021
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Magnetic resonance imaging of the brain has been of limited usefulness in the diagnosis of Creutzfeldt-Jakob disease. Abnormalities on T-2-weighted images have been described, but these are neither highly sensitive nor specific. Objective: To determine whether diffusion-weighted magnetic resonance images might be useful in the evaluation of Creutzfeldt-Jakob disease. Case Presentation: A 61-year-old woman with rapidly progressive dementia was referred for cranial magnetic resonance imaging. Diffusion-weighted images were obtained as part of the examination. Brain biopsy confirmed the diagnosis of Creutzfeldt-Jakob disease histologically. Findings and Conclusions: The diffusion-weighted magnetic resonance brain images demonstrated bilaterally symmetrical marked increase in signal intensity in the caudate nuclei, putamina, thalami, cingulate gyri, and right inferior frontal cortex. The apparent diffusion coefficient map showed abnormally low diffusion in these regions (as low as 40% of normal in the caudate head). This suggests that there is restricted diffusion in these regions. The T-2-weighted images demonstrated slightly increased signal bilaterally in the caudate nuclei and putamina. These findings indicate that diffusion magnetic resonance imaging might be a sensitive means of imaging the abnormalities seen in Creutzfeldt-Jakob disease.
引用
收藏
页码:1411 / 1415
页数:5
相关论文
共 27 条
  • [1] MR DIAGNOSIS OF CREUTZFELDT-JAKOB-DISEASE - SIGNIFICANCE OF HIGH SIGNAL INTENSITY OF THE BASAL GANGLIA
    BARBORIAK, DP
    PROVENZALE, JM
    BOYKO, OB
    [J]. AMERICAN JOURNAL OF ROENTGENOLOGY, 1994, 162 (01) : 137 - 140
  • [2] CREUTZFELDT-JAKOB DISEASE OF LONG DURATION - CLINICOPATHOLOGICAL CHARACTERISTICS, TRANSMISSIBILITY, AND DIFFERENTIAL-DIAGNOSIS
    BROWN, P
    RODGERSJOHNSON, P
    CATHALA, F
    GIBBS, CJ
    GAJDUSEK, DC
    [J]. ANNALS OF NEUROLOGY, 1984, 16 (03) : 295 - 304
  • [3] CREUTZFELDT-JAKOB DISEASE - CLINICAL ANALYSIS OF A CONSECUTIVE SERIES OF 230 NEUROPATHOLOGICALLY VERIFIED CASES
    BROWN, P
    CATHALA, F
    CASTAIGNE, P
    GAJDUSEK, DC
    [J]. ANNALS OF NEUROLOGY, 1986, 20 (05) : 597 - 602
  • [4] New diagnostic tests for prion diseases
    Collinge, J
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (13) : 963 - 965
  • [5] MRI ABNORMALITIES IN CREUTZFELDT-JAKOB-DISEASE
    DIROCCO, A
    MOLINARI, S
    STOLLMAN, AL
    DECKER, A
    YAHR, MD
    [J]. NEURORADIOLOGY, 1993, 35 (08) : 584 - 585
  • [6] MAGNETIC-RESONANCE-IMAGING IN CREUTZFELDT-JAKOB DISEASE
    ESMONDE, TFG
    WILL, RG
    [J]. ANNALS OF NEUROLOGY, 1992, 31 (02) : 230 - 231
  • [7] FALCONE S, 1992, AM J NEURORADIOL, V13, P403
  • [8] FALCONE S, 1994, TOP MAGN RESON IMAG, V6, P41
  • [9] MR imaging of Creutzfeldt-Jakob disease
    Finkenstaedt, M
    Szudra, A
    Zerr, I
    Poser, S
    Hise, JH
    Stoebner, JM
    Weber, T
    [J]. RADIOLOGY, 1996, 199 (03) : 793 - 798
  • [10] COMPUTED-TOMOGRAPHY FINDINGS IN 15 CASES OF CREUTZFELDT-JAKOB DISEASE WITH HISTOLOGICAL VERIFICATION
    GALVEZ, S
    CARTIER, L
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1984, 47 (11) : 1244 - 1246