Pheochromocytomas may manifest either as sporadic instances or as components of hereditary syndromes, such as Multiple Endocrine Neoplasia type‐2 (MEN‐2), Von Hippel–Lindau syndrome (VHL), and Neurofibromatosis type‐1 (NF‐1), depending on their prevalence and frequency of occurrence [31, 32, 33]. This evidence concerns the gene NF1 and multiple endocrine neoplasia type 2.