• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/17

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

17 Cards in this Set

  • Front
  • Back
Treatment of tumor lysis syndrome
forced diuresis with alkalinization to facilitate uric acid secretion

inhibit uric acid production - allopurinol

rasburicase - destroys uric acid

watch hyperkalemia, hyperphosphatemia
lab tests for acute leukemia
flow cytometry and cytogenetics are most important
ALL epidemiology
most common cancer in children and adolescence

exception: neonates (birth to 1 month) - acute myelogenous leukemia is more common
TdT
indicates immature T or B cell

lost as T or B cell mature
ALL management
platelet/RBC transfusion for bleeding anemia

antibody therapy if neutropenic

chemo - 4 phase - remission induction, consolidation, CNS prophylaxis, maintenance

watch for tumor lysis syndrome
definition of remission in ALL
<5% blasts in BM

self sustaining - no transfusion needed

no symptoms

failed remission is after 6months of therapy
consolidation/intensification phase
elimination of leukemic cells in sacturary sites - testes or meningies

cyclic chemo to prevent myelosepression, reduce leukemic cell burden further
CNS prophylaxis ALL
worried about meningeal leukmia because its hard to treat

intraethacal chemo or irradiation
prognosis of ALL
presence of t(9,22) translocation is BAD

2-9yo do better

CNS disease - bad
AML epidemiology
most common from birth to 1mo

incidence increases in teens and more rapidly after 55
M4 with eosinophilia (M4Eo)
associated with inversion of chr 16

good prognosis
AML symptoms
bleeding due to thrombocytopenia and coagulopathy

DIC (especially M3)

gingival swelling (with monocytic) - lymphadenopathy, skin nodules, splenomegaly
cytogenetics in AML
t(15,17) in APL (M3 or M3v)

t(8,21) in M2 (favorable)

inv(16) in M4Eo (favorable)

t(9,22) philly chromosome in AML - BAD PROGNOSIS
Acute promyelocytic leukemia
generally present with DIC

t(15,17) transolcation - fusion protein involving retinoic acid receptor

treat with all-trans retinoic acid - allows differentiation of pyomyelocytes
ATRA syndrome
all trans retinoic acid therapy used in treatment of M3 can cause increased ICP, pleural effusion

treat with steroids
T/F maintenance therapy is always needed in ALL
True
T/F maintenance therapy is always needed in AML
False; maintenance has limited benefit in AML EXCEPT for M3