Soft tissue sarcomas and central nervous system tumors in children with neurofibromatosis type 1.

Cecen E., İNCE D., Uysal K. M., ÖZER E., Cetingoz R., Ozguven A. A., ...More

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, vol.27, no.11, pp.1885-93, 2011 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 27 Issue: 11
  • Publication Date: 2011
  • Doi Number: 10.1007/s00381-011-1425-x
  • Journal Name: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.1885-93
  • Keywords: Neurofibromatosis type 1, Childhood, Cancer, Central nervous system tumors, Optic glioma, Malignant peripheral nerve sheath tumors, Sarcoma, OPTIC PATHWAY GLIOMAS, SHEATH TUMORS, SPONTANEOUS REGRESSION, FOLLOW-UP, NF1 GENE, RHABDOMYOSARCOMA, GLIOBLASTOMA, MANAGEMENT, PATIENT
  • Dokuz Eylül University Affiliated: Yes

Abstract

Objects We aim to evaluate the characteristics of pediatric patients with neurofibromatosis type 1 (NF1) who developed soft tissue sarcomas (STSs) and central nervous system(CNS) tumors that have been followed up in our center.