Three cases from the current series presented histopathological (diffuse growth pattern, oligodendroglioma‐like morphology, calcifications for two of them, and CD34 immunoreactivity for two of them) and genetic (presence of a FGFR3::TACC3 fusion in two of them) features reminiscent of a diagnosis of PLNTY [26]. This evidence concerns the gene FGFR3 and oligodendroglioma.