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Neurofibromatosis 1-associated optic pathway gliomas.

Authors :
Shofty B
Ben Sira L
Constantini S
Source :
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery [Childs Nerv Syst] 2020 Oct; Vol. 36 (10), pp. 2351-2361. Date of Electronic Publication: 2020 Jun 11.
Publication Year :
2020

Abstract

Background: Optic Pathway Gliomas (OPG) are the most common brain tumor in Neurofibromatosis 1 patients (NF1). They are found along the optic pathway and may involve the optic nerves, chiasm, retro-chiasmatic structures, and the optic radiations. NF1 associate OPG (NF1-OPG) have variable presentation, disease course and response to treatment. The optimal management is patient-specific and should be tailored by a multidisciplinary team. Age, sex, histology, and molecular markers may be important factors in the individualized decision-making process. Chemotherapy is the first-line treatment in cases of progressive tumors, and visual preservation is the main goal of treatment.<br />Purpose: In this paper we will review the disease, practical management, and recent advances of NF1-OPG.

Details

Language :
English
ISSN :
1433-0350
Volume :
36
Issue :
10
Database :
MEDLINE
Journal :
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Publication Type :
Academic Journal
Accession number :
32524182
Full Text :
https://doi.org/10.1007/s00381-020-04697-1