Vanishing white matter disease

Case contributed by Rabah Bouguelaa
Diagnosis probable

Presentation

Cerebellar ataxia with spasticity.

Patient Data

Age: 2 years
Gender: Male
This study is a stack
Sagittal
T1
This study is a stack
Axial
T1
This study is a stack
Axial
FLAIR
This study is a stack
Axial
T2
This study is a stack
Coronal
T2
This study is a stack
Axial
T1 C+
This study is a stack
Sagittal
T1 C+
This study is a stack
Coronal
T1 C+
This study is a stack
Axial
DWI
This study is a stack
Axial
ADC
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Info

The MRI sequences demonstrate diffuse bilateral, and relatively symmetrical cystic changes of low signal on T1, and FLAIR, and high signal on T2 involving the peri-and juxtaventricular white matter which appears of low signal on T1, and high signal on T2, and FLAIR with no enhancement following IV contrast. The dentate nuclei show also an asymmetrical low signal on T1, high signal FLAIR, and T2 with no enhancement on postcontrast sequences. The corporate-splenial segment of the corpus callosum appears small in size of high signal on FLAIR, and T2 with no enhancement. No involvement of the subcortical arcuate fibres.

Case Discussion

The clinical presentation and the MRI features are suggestive of a vanishing white matter disease, also called childhood ataxia with central hypomyelination (CACH).

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