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12 Cards in this Set

  • Front
  • Back
Myeloid failed hematopoisis
AML
Myeloid under-production
Myelodysplasias
Excess myeloid production
Myeloproliferative disorders
Myeloproliferative neoplasms (MPN)
CML
Polycythemia vera (PV)
Essential thrombocytosis (ET)
Primary Myelofibrosis (PMF)
General Features of CMPD
afebrile, splenomegaly
WBC variable may be >100
circulating blasts, inc basos
hypercellular BM
clonal
CML
t(9;22) - CC, FISH, PCR
BCR/ABL
Non-receptor tyrosine kinase activation
Tyrosine Kinase blocker (Imatinib)
PV
Erythropoietin independent erythropoiesis
Mutation of JAK2 kinase
Increased Hb and hematocrit
Exclude other MPN
Supress marrow; hydroxyurea
ET
MPD emphasizing thrombocytosis
TPO independent platelet production
Platelets >450
JAK2+; t(9;22)-
PMF
BM fibrosis with extramedullary hematopoiesis
Splenomegaly
JAK2
What is MDS
Ineffective hematopoiesis
Ineffective and disordered maturation
Abnormal cells stay in BM -->cytopenia
Symptoms due to pancytopenia
Subtypes of of MDS
primary - idiopathic
secondary to previous drug or radiation therapy (t-MDS)
t-MDS
appears 2-8 yrs after exposure
highest frequency and most rapidly transforms to AML