leukemia Flashcards
AML characteristics
most common leukemia in older adults
most idiopathic, trisomy 21, or therapy-induced, myelodysplastic syndrome
DX: bmbx w 20% blasts
symptom onset < 3 months
heme malignancy symptomatology
fatigue, anorexia, weight loss, fever, bruising/bleeding
AML labs
anemia, reduced reticulocyte count
leukocytosis/leukopenia
thrombocytopenia, odd shapes
AML exam findings
fever
splenomegaly
hepatomegaly
lymphadenopathy
general supportive care
central venous access
transfusions (hgb >7, plt >10 unless bleeding then 20)
acute infection monitoring - filgrasim 24 hr after chemo
prophylaxis - antiviral (acyclovir), anti fungal (fluconazole), PJP (bactrim)
AML treatment
induction - 7+3 regimen = cytarabine and daunorubicin
evaluate for response w BMBx (<5% blasts)
SCT for <60 yrs
continued chemotherapy to prevent relapse in select patients
ALL characteristics
greatest risk in first 5 years of life
unknown cause, some genetic risks
DX: BMBX, peripheral blood smear, LP
ALL symptomatology
B symptoms - fever, chills, night sweats, weight loss
fatigue, easy bruising
ALL labs
pancytopenia
ALL treatment
pediatric-inspired regimens
induction, consolidation, maintenance phases
intense inpatient regimen for 3 months
SCT
4+years of therapy probable
CML characteristics
mean age at diagnosis 55-65
RF: radiation
Philadelphia chromosome 90% cases
CML symptomatology
fatigue, anemia, splenomegaly
weight loss if high cell burden
hyperviscocity events - MI, CVA, visual changes, dyspnea, confusion
blast phase - fever, weight loss, bone/joint pain, bleeding and thrombotic events, infections
CML physical exam
hepatomegaly
splenomegaly
lymphadenopathy
infection?
petechiae/purpura?
CML labs
leukocytosis w left shift
thrombocytosis
thrombocytopenia (rare)
anemia
CML diagnosis
BMBx- hyper cellular with myeloid hyperplasia & high myeloid-to-erythroid ratio
blasts <5%