De novo development of gliomas in a child with neurofibromatosis type 1, fragile X and previously normal brain magnetic resonance imaging

Research output: Contribution to journalArticlepeer-review

Abstract

Fifteen to 20% of children with neurofibromatosis type 1 develop low-grade glial neoplasms. However, since neuroimaging is not routinely obtained until a child is clinically symptomatic, little is known about presymptomatic radiographic characteristics of gliomas in this at-risk population. Herein, we describe a child with neurofibromatosis type 1 who initially had normal brain imaging before the development of multifocal gliomas. Comparison of these serial images demonstrated that brain tumors can arise de novo in children with this cancer predisposition syndrome, further underscoring the limited prognostic value of normal baseline magnetic resonance imaging.

Original languageEnglish
Pages (from-to)33-35
Number of pages3
JournalRadiology Case Reports
Volume11
Issue number1
DOIs
StatePublished - Mar 1 2016

Keywords

  • Astrocytoma
  • Inherited cancer syndrome
  • Neuroimaging
  • T2-hyperintensities

Fingerprint

Dive into the research topics of 'De novo development of gliomas in a child with neurofibromatosis type 1, fragile X and previously normal brain magnetic resonance imaging'. Together they form a unique fingerprint.

Cite this