MRI in sporadic Creutzfeldt-Jakob disease: Correlation with clinical and neuropathological data

Abstract To ascertain whether increased grey matter signal intensity on T2-weighted images in patients with sporadic Creutzfeldt-Jakob disease (CJD) corresponds to the stage and severity of this disease, we correlated MRI findings in four of our own and previously reported patients with sporadic CJD with the clinical variants, neuropathological changes at autopsy, duration of the disease and survival time after MRI examination. Of 15 patients with the extrapyramidal type of CJD, 10 showed increased signal in the basal ganglia on T2-weighted images. One of seven patients with the Heidenhain variant had increased signal in the occipital cortex. Patients without increased grey matter signal intensity had a longer overall duration of CJD (P = 0.035). Although the interval between onset of neurological symptoms and MRI was not different, patients without increased grey matter signal also survived longer after MRI examination (P = 0.022).

[1]  T. L. Bunina,et al.  [Creutzfeldt-Jakob disease]. , 1972, Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova.

[2]  J. Provenzale,et al.  MR diagnosis of Creutzfeldt-Jakob disease: significance of high signal intensity of the basal ganglia. , 1994, AJR. American journal of roentgenology.

[3]  C. Masters,et al.  The Nosology of Creutzfeldt‐Jakob Disease and Conditions Related to the Accumulation of PrPCJD in the Nervous System , 1995, Brain pathology.

[4]  P. Castaigne,et al.  Creutzfeldt‐Jakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases , 1986, Annals of neurology.

[5]  A. Hofman,et al.  A new variant of Creutzfeldt-Jakob disease in the UK , 1996, The Lancet.

[6]  H. Tsukagoshi,et al.  [An autopsy case of panencephalopathic type of Creutzfeldt-Jakob disease: an early clinical sign documented by magnetic resonance imaging]. , 1989, Rinshō shinkeigaku Clinical neurology.

[7]  S. Chin,et al.  MRI of Creutzfeldt-Jakob disease , 1995, Neurology.

[8]  R. Peatfield,et al.  Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease) with amyloid angiopathy. , 1985, Journal of neurology, neurosurgery, and psychiatry.

[9]  A. Kirk,et al.  Unilateral Creutzfeldt-Jakob Disease Presenting as Rapidly Progressive Aphasia , 1994, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[10]  M. Onofrj,et al.  MRI alterations as an early finding in Creutzfeld-Jakob disease. , 1993, European journal of radiology.

[11]  R. Anderson,et al.  Creutzfeldt-Jakob disease: high caudate signal on magnetic resonance imaging. , 1989, Southern medical journal.

[12]  H. Gertz,et al.  Creutzfeldt-Jakob disease: correlation of MRI and neuropathologic findings. , 1988, Neurology.

[13]  T. Naidich,et al.  Creutzfeldt-Jakob disease: focal symmetrical cortical involvement demonstrated by MR imaging. , 1992, AJNR. American journal of neuroradiology.

[14]  T. Erkinjuntti,et al.  Cerebral MR and CT Imaging in Creutzfeldt‐Jakob Disease , 1985, Journal of computer assisted tomography.

[15]  R. Will New variant Creutzfeldt-Jakob disease. , 1999, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[16]  T. Mizutani,et al.  Panencephalopathic type of Creutzfeldt-Jakob disease: primary involvement of the cerebral white matter , 1981, Journal of neurology, neurosurgery, and psychiatry.

[17]  K. Ikeda,et al.  Magnetic resonance imaging and neuropathological findings in two patients with Creutzfeldt-Jakob disease , 1994, Journal of the Neurological Sciences.

[18]  S W Atlas,et al.  Magnetic resonance imaging of Creutzfeldt‐Jacob disease , 1991, Annals of neurology.