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Literature DB >> 1403024

Magnetic resonance imaging follow-up in Creutzfeldt-Jakob disease.

J Röther¹, A Schwartz, M Härle, K U Wentz, P Berlit, M Hennerici.

Abstract

The history of a 67-year-old woman with histologically proven Creutzfeldt-Jakob disease (CJD) is presented. Before typical clinical and neurophysiological signs of CJD developed, magnetic resonance imaging (MRI) showed slightly enhanced signal intensity of the caudate nuclei and putamina in T2-weighted and proton density images, corresponding to spongiform degeneration in neuropathological examination. Five weeks later characteristical progressive cortical atrophy was demonstrated by follow-up MRI.

Entities: Disease Species

Mesh：

Year: 1992 PMID： 1403024 DOI： 10.1007/bf00812160

Source DB: PubMed Journal: J Neurol ISSN： 0340-5354 Impact factor: 4.849

17 in total

1. Creutzfeld-Jacob like syndrome due to lithium toxicity.

Authors: C J Kemperman; S L Notermans
Journal: J Neurol Neurosurg Psychiatry Date: 1989-02 Impact factor: 10.154

2. Magnetic resonance imaging of Creutzfeldt-Jacob disease.

Authors: W J Milton; S W Atlas; E Lavi; J E Mollman
Journal: Ann Neurol Date: 1991-04 Impact factor: 10.422

3. [A case of hypoglycemic coma associated with myoclonus, periodic synchronous discharges and progressive cerebral atrophy resembling Creutzfeld-Jakob disease].

Authors: Y Kida; T Sawada; H Naritomi; Y Kuriyama; J Ogata; A Kashiwagi; Y Shigeta
Journal: Nihon Naika Gakkai Zasshi Date: 1988-03

Magnetic resonance imaging follow-up in Creutzfeldt-Jakob disease.

1. Creutzfeld-Jacob like syndrome due to lithium toxicity.

2. Magnetic resonance imaging of Creutzfeldt-Jacob disease.

3. [A case of hypoglycemic coma associated with myoclonus, periodic synchronous discharges and progressive cerebral atrophy resembling Creutzfeld-Jakob disease].

4. Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease). The nature and progression of spongiform change.

5. High neuron-specific enolase level of cerebrospinal fluid in the early stage of Creutzfeldt-Jakob disease.

6. Panencephalopathic type of Creutzfeldt-Jakob disease: primary involvement of the cerebral white matter.

7. Positron emission tomography in Creutzfeldt-Jakob disease.

8. Panencephalopathic type of Creutzfeldt-Jakob disease with primary extensive involvement of white matter.

9. Serial MR imaging in Creutzfeldt-Jakob disease.

10. Cerebral MR and CT imaging in Creutzfeldt-Jakob disease.

Review 1. Radiological assessment of Creutzfeldt-Jakob disease.

2. Serial MRI in early Creutzfeldt-Jacob disease with a point mutation of prion protein at codon 180.