Acute myeloid leukemia with recurrent genetic abnormalities |
AML with t(8;21)(q22;q22); RUNX1-RUNX1T1 |
AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11 |
APL with t(15;17)(q22;q12); PML-RARA |
AML with t(9;11)(p22;q23); MLLT3-MLL |
AML with t(6;9)(p23;q34); DEK-NUP214 |
AML with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1 |
AML (megakaryoblastic) with t(91;22)(p13;q13); RBM15-MKL1 |
Provisional entity: AML with mutated NPM1 |
Provisional entity: AML with mutated CEBPA |
Acute myeloid leukemia with myelodysplasia-related changes |
Therapy-related myeloid neoplasms |
Acute myeloid leukemia, not otherwise specified |
AML with minimal differentiation |
AML without maturation |
AML with maturation |
Acute myelomonocytic leukemia |
Acute monoblastic/monocytic leukemia |
Acute erythroid leukemia |
Pure erythroid leukemia |
Erythroleukemia, erythroid/myeloid |
Acute megakaryoblastic leukemia |
Acute basophilic leukemia |
Acute panmyelosis with myelofibrosis |
Myeloid sarcoma |
Myeloid proliferations related to Down syndrome |
Transient abnormal myelopoiesis |
Myeloid leukemia associated with Down syndrome |
Blastic plasmacytoid dendritic cell neoplasms |