The simultaneous appearance of congenital infiltrating lipomatosis of the face that
causes facial hemihypertrophy and ipsilateral hemimegalencephaly is extremely rare.
We report a 4-year-old boy with congenital facial asymmetry and infantile-onset epilepsy.
Magnetic resonance imaging (MRI) results led to the diagnosis of infiltrating lipomatosis
of the face; the diagnosis was confirmed on the basis of the results of pathological
examinations. Additionally, brain MRI revealed ipsilateral hemimegalencephaly, associated
with band heterotopia and the hemihypertrophy of the ipsilateral brainstem and cerebellum.
He had no nevi or other skin abnormalities suggesting neurocutaneous syndrome. His
seizures were so intractable that they necessitated functional hemispherectomy. The
lipomatous lesion was successfully resected without relapse. Psychomotor delay and
left hemiplegia were observed at the last follow-up.
congenital infiltrating lipomatosis of the face - hemimegalencephaly - band heterotopia
- epilepsy