“…Atypical and malignant meningiomas (only 1.7–4.2% of all meningiomas) differ from benign lesions according to several histological features, such as increased mitotic activity (>4 mitotic figures in atypical and >20 mitoses in malignant, per 10 hpf), increased cell density, presence of nuclear pleomorphism, loss of architectural cell disposition, existence of tumoral necrosis and brain invasion, papillary transformation and carcinoma, melanoma, or sarcomatous appearance ( Table 1 ). Type II (atypical, clear cell, and choroid variants) and III (rhabdoid, papillary, and anaplastic variants), and the presence of brain invasion in either benign or malignant meningiomas, seem to favor metastatic spread ( 8 , 9 ). Immunohistochemical analyses of a nuclear protein related to cell proliferation, Ki-67 proliferative index, or of molecular markers such as CDKN2A deletion, along with a 9p21 deletion, are also useful in evaluating the potential of meningioma recurrence and/or metastases ( 4 ).…”