MR imaging of Creutzfeldt-Jakob disease.

被引：0

作者：

Gabaudan, C. ^{[1
]}

Kaphan, E. ^{[2
]}

Felician, O. ^{[2
]}

Girard, N. ^{[1
]}

机构：

[1] CHU Timone, Serv Neuroradiol Diagnost & Intervent, F-13385 Marseille 5, France

[2] CHU Timone, Serv Neurol, F-13385 Marseille 5, France

来源：

FEUILLETS DE RADIOLOGIE | 2009年 / 49卷 / 03期

关键词：

Creutzfeldt-Jakob disease; MR; DIFFUSION-WEIGHTED MRI; STROKE-LIKE LESIONS; PULVINAR SIGN; DIAGNOSIS; ABNORMALITIES; INVOLVEMENT; SENSITIVITY; PATTERNS;

D O I：

10.1016/S0181-9801(09)74608-1

中图分类号：

R8 [特种医学]; R445 [影像诊断学];

学科分类号：

1002 ; 100207 ; 1009 ;

摘要：

Creutzfeldt-Jakob disease is a fatal neurodegenerative disease characterized by an abnormal accumulation of human prion protein PrPSc. It causes a rapidly progressive dementia syndrome. The imaging work-up is based on MRI which often discloses the typical disease anomaly seen as high signal intensity in the basal ganglia and cerebral cortex on Flair sequences and/or more readily on diffusion weighted sequences. This work recalls our fundamental knowledge concerning this disease and presents MRI data from 7 cases and a review of the literature.

引用

页码：171 / 185

页数：15

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