Acute Myeloid Leukemia Flashcards
mutations in myeloproliferative disorders
- TET2 for clonal dominance
- JAK/STAT for proliferation of mature peripheral blood cells
chromosome translocation found in all CML pts
between q of chr 22 and q of chr 9 (leading to fusion gene between BCR on ch22 and ABL on chr9 (chr is called a philadelphia chr)
consequence of BCR and ABL fusion
- ABL protein is Tyr Kinase which strongly inhibits apoptosis
- DNA binding of ABL is enhanced
clinical sign of CML
leukocytosis, splenomegaly 50% of the time
Granulocytes in peripheral blood
therapy of CML
imatinibmesylate
clinical findings of AML
anemia (low reticlocyte count), fatigue, thrombocytopenia, leukopenia, splenomgaly
acute pro myelocytic leukemia chromosome issue is
t(15,17) (q22,q12)
resulting in fusion gene RARA on chr 17 with PML gene on chr 15. This blocks differentiation of granulocytes
presentation of acute pro myelocytic leukemia
Disseminated intravascular coagulation
what are schistocytes
damaged erythroid cells
mutations in AML
- FLT3-ITD
- NPM-1 (for regulation of p53 pathway)
- CEBP-alpha (regulates granulocyte differentiation)
treatment of APL
all leukemic cells are sensitive to all trans retinoic acid