“…Schwannoma, also known as neurilemmoma, is an uncommon, slow growing, solitary, benign nerve sheath tumor that originates from peripheral, cranial or autonomic nerves containing schwann cells [ 9 ] Histologically, there are seven variants of schwannoma described in the literature which includes classical (Verocay), plexiform, cellular, cranial nerve, melanotic, degenerated (ancient), and granular cell schwannoma [ 2 , 10 ] Verocay, in 1910 was the first to describe schwannoma microscopically and called it “Neurinoma,” while Arthur Stout, in 1935, coined the term neurilemmoma [ 7 , 10 ]. Between 25%–45% of schwannomas are located in the head and neck region, with the eighth cranial nerve being most commonly affected.…”