Multiple primary cranio-spinal tumours in a 13-year-old female with neurofibromatosis type 2 management strategy

# The Author(s) 2010. This article is published with open access at Springerlink.com Introduction Neurofibromatosis type 2 (NF2) is an inherited, rare autosomal dominant syndrome characterised by the development of multiple benign cranial and spinal tumours, peripheral neuropathy, ophthalmological and cutaneous lesions. Herein, we report one case of NF