Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)

Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) is a rare subtype of acute myeloid leukemia with recurrent cytogenetic abnormalities characterized by clonal proliferation of myeloid blasts with predominantly megakaryoblastic differentiation in the bone marrow and blood, often with extensive infiltration of the abdominal organs. It occurs typically in infants and usually presents with hepatosplenomegaly, anemia, thrombocytopenia and nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections). Myelofibrosis and fibrosis of other infiltrated organs is also characteristic of this disease.

Also known as: megakaryoblastic AML with t(1;22)(p13;q13)

3080 clinical trials for this condition and its sub-types, 0 tagged with Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) itself.