“…For example, BRAF-activating mutations are less common in mucosal melanoma than in cutaneous melanoma, while other mutations, such as KRAS and cKIT, appear to be more common, making the latter two important in the pathogenesis and targeted treatment of MAM [ 13 , 14 ]. Therefore, it is necessary to develop a separate staging system, which is complicated by the rarity of cases [ 11 ]. Despite this, staging systems have been proposed for mucosal melanoma, but without distinction with respect to the location of the primary tumour [ 4 , 11 , 15 ].…”