Abstract
We report the radiologic findings in two children with Griscelli syndrome who presented
mainly with neurologic findings. Both children were born to consanguineous parents,
had normal birth and developmental histories; both had silvery gray hair from the
time of birth. The first child presented with symptoms of increased intracranial pressure
and cerebellar ataxia; the second child with cerebellar ataxia alone. Microscopic
examination of the hair in both the children demonstrated the characteristic melanin
clumps suggestive of Griscelli syndrome. Magnetic resonance imaging of the brain in
the first child demonstrated multifocal white matter hyperintensities in the cerebrum
and diffuse white matter hyperintensities in the cerebellum, with intense contrast
enhancement. In the second child, signal changes were confined to the cerebellum and
spinal cord. The first child succumbed to rapidly progressive increased intra-cranial
pressure; partial autopsy revealed necrotizing lesions involving the cerebellar hemispheres
bilaterally which corresponded to the neuroimaging abnormalities. Histology revealed
diffuse histiocytic infiltration of the parenchyma. Griscelli syndrome type 2 should
be a diagnostic consideration in a child with silvery hair, neurological deterioration
and enhancing multifocal white matter signal intensity changes
Keywords
Griscelli syndrome - silvery hair - cerebellar leukoencephalopathy - melanin clumps