Abstract
Infantile myofibromatosis is the most common fibrous disorder of infancy and early childhood. It can present in three forms—solitary lesion, multicentric with visceral involvement and multi-centeric without visceral involvement. Intracranial involvement is rare and when it occurs, it is generally extension of extracranial lesion into the intracranial compartment. Here we present a rare case of isolated posterior fossa involvement presenting clinically as congenital facial palsy.
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