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Diffusion-weighted MRI findings and clinical correlations in sporadic Creutzfeldt-Jakob disease. | LitMetric

AI Article Synopsis

  • The study explores the link between hyperintense lesions on diffusion-weighted MRI and clinical symptoms in patients with sporadic Creutzfeldt-Jakob disease (sCJD).
  • A total of 58 sCJD patients were analyzed, showing that those with lesions in specific brain areas (basal ganglia and occipital cortex) experienced shorter disease duration and different symptoms like myoclonus and akinetic mutism.
  • The research identifies that lower apparent diffusion coefficient (ADC) values in the basal ganglia correspond to a faster onset of severe symptoms and shorter overall disease duration.

Article Abstract

The objective of this study is to investigate the hyperintense lesions on diffusion-weighted magnetic resonance imaging (DWI) and its clinical correlation in sporadic Creutzfeldt-Jakob disease (sCJD). Patients who suffered from sCJD and followed up at the Department of Neurology at the General Hospital of the People's Liberation Army during the period of June 1, 2007 to July 1, 2014 were reviewed. The location of the hyperintense lesions on DWI, apparent diffusion coefficient (ADC) values of the hyperintense lesions were correlated with symptoms and clinical course. A total of 58 sCJD patients and ten healthy controls were included. Hyperintense lesions on DWI were observed in all the patients. The patients with basal ganglia (BG) hyperintense lesions on DWI had shorter disease duration and higher incidence of myoclonus (92 versus 44 %) than those without BG hyperintense lesions. The patients with occipital cortex hyperintense lesions on DWI had shorter disease duration between symptom onset and akinetic mutism than those without these lesions. The lower of the BG ADC value the faster presence of akinetic mutism and the shorter disease duration the patients will have. The presence of BG and occipital cortex hyperintense lesions on DWI and BG ADC values is correlated with the clinical course and clinical symptoms.

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Source
http://dx.doi.org/10.1007/s00415-015-7723-6DOI Listing

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