“…These are primarily neural crest derived tumors (neuroblastoma, medulloblastoma, oligodendroglioma, meningioma, pheochromocytoma, rhabdomyosarcoma, leiomyosarcoma, seminoma, odontoma, choristoma, hepatoblastoma, and pilomatricoma). Cases of leukemia and non-Hodgkin’s lymphoma have been reported [ 75 , 76 , 77 , 78 , 79 , 80 ]. The incidence of malignancy in RSTS patients was initially estimated to be between 3% and 10% [ 10 ].…”