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. 2019 Dec 20;2(Suppl 1):i98–i106. doi: 10.1093/noajnl/vdz054

Table 1.

Comparison between sporadic and NF1-associated OPGs in children

NF1-associated Sporadic
Age < 6 years < 6 years (frequently <1 year)
Location Optic nerve, chiasm, and posterior optic radiations Chiasm
Relation with visual pathway Infiltration Compression
Risk of progression Around 50% Constant
Spontaneous regression Possible No
Visual Acuity Impairment More important (+++) Less important (++)
Motor impairment Less important (++) More important (+++)
Histopathology Pilocytic Astrocytoma Pilocytic Astrocytoma, Ganglioglioma
Molecular alterations NF1 loss KIAA1549-BRAF fusion+++, Other fusions or mutations, less frequently: NTRK2, FGFR1, BRAF V600E, KRAS, RAF1, PTPN11

References: 1, 15 and 18–21.