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

摘要

IntroductionNeurofibromatosis 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 NF2 treated with multivariate chemotherapy.