“…AMM is recently often diagnosed at the initial presentation by anaplastic morphology, unfavorable cytogenetics, and an aggressive clinical course with a high incidence of increased serum LDH levels and refractoriness to conventional chemotherapies in case series. Large-sized plasmablastic cells with pleomorphic nuclei, such as multilobation or multinucleation, were diagnostic morphologies, [3][4][5][6][7][8] and cytogenetic abnormalities of del(17p), t(4; 14) and 1q21 gain were detected with high frequencies in AMM. 9 The present patient exhibited positive FISH for del(17p), but additional analyses of cytogenetic abnormalities, such as FISH for 1q21 gain and MAFB translocation, SKY, or RT-PCR, were unable to be performed.…”