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Acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2)

MONDO:0018435

Acute myeloid leukemia with inv(3)(q21;q26.2) or t(3;3)(q21;q26.2) is a subtype of acute myeloid leukemia with recurrent genetic abnormalities characterized by clonal proliferation of myeloid blasts in the bone marrow, blood and, rarely, other tissues. Bone marrow typically shows small, hypolobated megakaryocytes and multilineage dyslplasia. Patients typically present with leukocytosis, anemia, variable platelet counts and a variety of nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding, bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). High resistance to conventional chemotherapy is reported.

Also known as: AML with inv3(p21;q26.2) or t(3;3)(p21;q26.2), AML with inv3(q21;q26.2) or t(3;3)(q21;q26.2), acute myeloid leukaemia with inv3(q21;q26.2) or t(3;3)(q21;q26.2), acute myeloid leukemia with inv3(q21;q26.2) or t(3;3)(q21;q26.2)

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2) itself.

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