“…A diagnosis of AMECA is made when a malignant OT presents as a combination of histological features of AME and anaplasia. 1,12,20,21 Various types of anaplasia have been described in AMECA, such as hypercellularity, basaloid and/or pseudosarcomatous differentiation of the stellate reticulum, loss of ameloblastic differentiation, cell and nuclear pleomorphism, an increased [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][20][21][22][23][24] Moreover, an infiltrative growth pattern, neural and vascular/lymphatic invasion and necrosis have also been utilized to identify the AMECA malignant phenotype. [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][20][21][22][23][24] However, as many of these features are not observed in the same tumour, and no single pathological feature ca...…”