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

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 NF2 treated with multivariate ch...

Descripción completa

Detalles Bibliográficos
Autores principales: Stachowicz-Stencel, Teresa, Synakiewicz, Anna, Bien, Ewa, Adamkiewicz-Drozynska, Elzbieta, Wybieralska-Dubaniewicz, Miroslawa, Balcerska, Anna
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3015198/
https://www.ncbi.nlm.nih.gov/pubmed/20661577
http://dx.doi.org/10.1007/s00381-010-1238-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3015198/
https://www.ncbi.nlm.nih.gov/pubmed/20661577
http://dx.doi.org/10.1007/s00381-010-1238-3

Ejemplares similares