“…It has been suggested RCC and GBM may occur in the same patient as part of genetic syndromes, although there is no clear evidence as to which genes, alleles, or mutations are responsible. [10,11] Simanjuntak et al implicate genetic syndromes, such as Li-Fraumeni syndrome, neurofibromatosis, and VHL, as possibly being involved. [10] Notably, VHL is an established predisposition to developing RCC, although it does not seem to play a role in GBM.…”