Meningioangiomatosis is a rare plaque-like leptomeningeal and
perivascular proliferation of fibroblastic and meningothelial-appearing cells
which may extend along Virchow–Robin spaces. Such lesions are typically
hyperintense on FLAIR (a) and T2-weighted sequences (b), with intense contrast
enhancement on post-gadolinium T1-weighted sequences. Histologic examination of
this lesion from an NF2 patient with refractory epilepsy shows a mixed
perivascular proliferation of fibrovascular (c, d) or meningothelial-like cells
(e, f) extending from the pial surface into the cortical parenchyma. The
intervening cortex shows intact neurons with no definite evidence of focal
cortical dysplasia. The neoplastic cells are typically well differentiated with
no necrosis, atypia, or prominent nucleoli.