Acute myeloid leukemia with t(8;16)(p11;p13) translocation

MONDO:0018256

A distinct form of Acute myeloid leukemia (AML) in which this chromosomal anomaly is found de novo or in therapy-related AML cases, and is characterized by frequent extramedullary involvement (mainly hepatomegaly, splenomegaly, lymphadenopathies, cutaneous infiltration, but also gum, bone, central nervous system, testicles involvement), severe coagulation disorder (disseminated intravascular coagulopathy or primary fibrinolysis) and poor prognosis. Morphologically, a blast population with a myelomonocytic stage of differentiation is observed.

Also known as: AML with t(8;16)(p11;p13) translocation

3080 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia with t(8;16)(p11;p13) translocation itself.

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↑ Acute myeloid leukemia (1192)

Including sub-types (3080) Tagged with Acute myeloid leukemia with t(8;16)(p11;p13) translocation (0)

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