MR images showed an enhancing, enlarging mass in the tectum of the mid
brain in a child with neurofibromatosis type 1. The mass was presumed
to be a tectal glioma, which initially enlarged then regressed in size
over a 3-year period and ceased to enhance, Although a tissue diagnos
is was not available, we believe the temporal evolution of this lesion
is strong presumptive evidence of a hamartoma. This case argues for t
he conservative management of patients with neurofibromatosis type I w
hen possible.