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Forschungsdatenbank PMU-SQQUID

Clinical and diagnostic findings in a patient with Creutzfeldt-Jakob disease (type Heidenhain).
Staffen, W; Trinka, E; Iglseder, B; Pilz, P; Homann, N; Ladurner, G;
J Neuroimaging. 1997; 7(1): 50-54.
Fallberichte

PMU-Autor/inn/en

Iglseder Bernhard
Staffen Wolfgang
Trinka Eugen

Abstract

A 61-year-old woman had Creutzfeldt-Jakob disease, type Heidenhain, that progressed for 4 months until death, 3 of which she spent in a hospital. The diagnosis was verified by autopsy. Consecutive brain computed tomography, magnetic resonance imaging, blood flow measurements, electroencephalography (EEG), and routine laboratory tests were performed, All imaging techniques showed nonspecific pathological changes, whereas EEG revealed alterations indicative for Creutzfeldt-Jakob disease.


Useful keywords (using NLM MeSH Indexing)

Brain/pathology

Creutzfeldt-Jakob Syndrome/diagnosis*

Creutzfeldt-Jakob Syndrome/pathology

Diagnosis, Differential

Electroencephalography

Female

Humans

Magnetic Resonance Imaging*

Middle Aged

Prions/analysis

Tomography, Emission-Computed, Single-Photon*

Tomography, X-Ray Computed*