Japanese encephalitis MRI: Difference between revisions
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==Overview== | ==Overview== | ||
[[Magnetic resonance imaging]] ([[MRI]]) of the brain is better than [[computed tomography]] ([[CT]]) for detecting Japanese encephalitis virus-associated abnormalities such as changes in the [[thalamus]], [[basal ganglia]], [[midbrain]], [[pons]], and [[medulla]]. Thalamic [[lesions]] are the most commonly described abnormality; although these can be highly [[specificity|specific]] for JE in the appropriate clinical context, they are not a very [[sensitivity (test)|sensitive]] marker of JE. | [[Magnetic resonance imaging]] ([[MRI]]) of the brain is better than [[computed tomography]] ([[CT]]) for detecting Japanese encephalitis virus-associated abnormalities such as changes in the [[thalamus]], [[basal ganglia]], [[midbrain]], [[pons]], and [[medulla]]. Thalamic [[lesions]] are the most commonly described abnormality; although these can be highly [[specificity|specific]] for JE in the appropriate clinical context, they are not a very [[sensitivity (test)|sensitive]] marker of JE. | ||
parenchymal oedema in affected regions | |||
DWI: variable restricted diffusion | |||
T1: low signal | |||
T2/FLAIR: high signal | |||
if haemorrhage is present: | |||
GRE: patchy blooming | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} |
Revision as of 15:59, 14 April 2016
Japanese encephalitis Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Japanese encephalitis MRI On the Web |
American Roentgen Ray Society Images of Japanese encephalitis MRI |
Risk calculators and risk factors for Japanese encephalitis MRI |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
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Overview
Magnetic resonance imaging (MRI) of the brain is better than computed tomography (CT) for detecting Japanese encephalitis virus-associated abnormalities such as changes in the thalamus, basal ganglia, midbrain, pons, and medulla. Thalamic lesions are the most commonly described abnormality; although these can be highly specific for JE in the appropriate clinical context, they are not a very sensitive marker of JE.
parenchymal oedema in affected regions DWI: variable restricted diffusion T1: low signal T2/FLAIR: high signal if haemorrhage is present: GRE: patchy blooming