Hybrid schwannoma/neurofibroma tumors, on the other hand, contain schwannoma-like Antoni A areas with nuclear palisading and Verocay bodies, alongside neurofibroma-like regions composed of fibroblasts, elongated wavy nuclei, and a collagenous or mucin-rich myxoid matrix arranged in an architecture that may be plexiform, albeit with a lack of consensus on diagnostic criteria [6]. The gene discussed is MUC5AC; the disease is neurofibroma.