Non-Oncological Neuroradiological Manifestations in NF1 and Their Clinical Implications
Camilla Russo, Camilla Russo, Carmela Russo, Carmela Russo, Daniele Cascone, Federica Mazio, Claudia Santoro, Eugenio Maria Covelli, Giuseppe Cinalli
Abstract
Neurofibromatosis type 1 (NF1), the most frequent phakomatosis and one of the most common inherited tumor predisposition syndromes, is characterized by several manifestations that pervasively involve central and peripheral nervous system structures. The disorder is due to mutations in the NF1 gene, which encodes for the ubiquitous tumor suppressor protein neurofibromin; neurofibromin is highly expressed in neural crest derived tissues, where it plays a crucial role in regulating cell proliferation, differentiation, and structural organization. This review article aims to provide an overview on NF1 non-neoplastic manifestations of neuroradiological interest, involving both the central nervous system and spine. We also briefly review the most recent MRI functional findings in NF1.