AML and ALL Flashcards
causes of leukemia
genetic, occupational, environmental
FAB classifications
morphology
cytochemical stains
clinical findings
WHO classifications
morphology cytochemical stains clinical findings flow cytometry molecular genetic abnormalities cytogenetics
AML is characterized by two fundamental features
ability to proliferate continuously
arrested development
When AML is suspected, the following lab evaluation must include
PB testing
BM testing
cytogenetic studies
immunophenotyping
AML with t(8;21)(q22;q22) RUNXI-RUNXIT1
abnormal protein causes irregulation of hematopoiesis
favorable outcome
AML with inv(16)(p13.1q22)
dysplastic eosinophils in bone marrow
AML with t(15;17)(qLeukemia (F22;q12) PML RARA
Acute Promyelocytic Leukemia M3 young adults Differentiation block of promyelocyte stage hypergranular, butterfly nucleus can have a microgranular variant causes DIC treat with vitamin A (ATRA) favorable outcome
AML (megakaryoblastic) with t(1;22)(p13,q13) RBM15-MKL1
associated with down syndrome
dry tap due to fibrosis
causes DIC
t(9;22)(q34:q11) BCR-ABL
B-ALL
poor prognosis
older adolescents
t(v;11)(v:23)
B-ALL
infants, older adults
poor prognosis
t(12;21)(p13;q22)
most common
good prognosis
three stages of chemotherapy for ALL
Induction therapy phase
CNS prophylaxis phase
Maintenance therapy phase
four ways to differentiate AML from ALL
morphology and cytochemistry
immunophenotyping
cytogenetic analysis
molecular analysis