Published May 2007 | Version v1
Journal article

Radiological assessment of Creutzfeldt-Jakob disease

  • 1. University of Bonn, Department of Radiology, Bonn (Germany)
  • 2. University of Goettingen, National Reference Center for TSE Surveillance at the Department of Neurology, Goettingen (Germany)

Description

Creutzfeldt-Jakob disease is a rare fatal neurodegenerative disorder, characterized by rapidly progressive dementia and neurological signs. There is a need for early and accurate clinical diagnosis in order to exclude any treatable disorder. Additionally, it is of public interest to differentiate the sporadic form of the disease from the variant CJD type (vCJD), which is probably transmitted from cattle infected with bovine spongiform encephalopathy (BSE). High signal in the striatum on T2-weighted, FLAIR and diffusion weighted (DW) MRI as well as cortical high signal in FLAIR and DW MRI are the classical findings in sCJD. The ''pulvinar sign'', defined as high signal in the pulvinar thalami that is brighter than potential additional high signal in the basal ganglia, is considered pathognomonic for vCJD. (orig.)

Availability note (English)

Available from: http://dx.doi.org/10.1007/s00330-006-0456-2

Additional details

Identifiers

Publishing Information

Journal Title
European Radiology
Journal Volume
17
Journal Issue
5
Journal Page Range
p. 1200-1211
ISSN
0938-7994
CODEN
EURAE3

INIS

Country of Publication
Germany
Country of Input or Organization
Germany
INIS RN
38064007
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
BRAIN; DIAGNOSIS; GENETICS; NERVOUS SYSTEM DISEASES; NMR IMAGING
Descriptors DEC
BIOLOGY; BODY; CENTRAL NERVOUS SYSTEM; DIAGNOSTIC TECHNIQUES; DISEASES; NERVOUS SYSTEM; ORGANS