• 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

1/61

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;

61 Cards in this Set

  • Front
  • Back
childhood leukemia
ALL
adult leukemia
CLL
most common lymphoma in the US
diffuse large B cell lymphoma
Reed-Sternberg
Hodgkins Lymphoma
AML with Downs syndrome
M7 AML
Leukemia with more mature cells and then 5% blasts
chronic leukemia
AML that are CD13+ and CD33+
MO-M6 AML
EBV blood cancers
burkitts and hodgkins
Auer Rods
AML M2 and M3
long term celiac disease
intestinal T-Cell lymphoma
greater than 20% blasts in the marrow
acute leukemia
myelodysplastic syndromes progress to ....
AML
myeloproliferate disorders progress to
AML
AML that is CD41 and CD61 positive
M7 AML
PAS positive acute leukemia
ALL
presents with bone pain
ALL
viscous blood, headache, plethora, splenomegally, low EPO
PV
leukemia equivalent of Burketts lymphoma
L3 or B variant ALL
Lymphoma equivolent to CLL
small lymphocytic lymphoma
numerous basophils, splenomegaly, and negative for leukocyte alkaline phosphatase
CML
most common neonatal leukemia
M7 AML (megakaryocytic)
always positive philly chrom (9:22)
CML
only AML that is CD13 and CD33 negative
M7 AML (neonatal)
starry sky pattern due to phagocytosis of apoptotic tumor cells
burketts
BCR:ABL genes
CML
A/W sjogrens, hashimotos, and h pylori
marginal cell MALToma
Acute leukemia positive for peroxidase
AML
solid sheets of lymphomblasts
ALL
PAS (-) acute leakemia
AML (ALL is positive)
Hams test positive
PNH
Basophilic stippling (degeneration of RNA-denatured)
TAIL... thal, anemia of chrnic disease, iron def, LEAD!!!
positive DEB test
fanconis anemia
ristocetin positive test
vWF deficiny
Urinalysis for MM shows
nothing (need UPEP)
streptokinase.urokinase. tPa
plasmin
clopidogrel and ticlopidine
ADP receptor blocker which prevents the expression of Gp2b/3a
Abciximab and tirofiban and eptifibatide
bind directly to GP2b/3a
enoxaparin
LMW heparin increase ATIII
increased HbA2 and HbF and basophilic stippling
thalasemia (beta from mediteranian and alpha from asia)
treatment for HIT
rudin and argatroban (direct thrombin inhibitors)
platelet to platelet aggregation
GP2b/3a
lead poisening
basophilic stippling
abetalipoproteinemia
irregular spikes...acanthocytes
HbC
two alpha, two beta...glu to lysine
HbBart
severe alpha thal...4 HbF (no a)
HbH
sever alpha thal...4 HbB (no a
microcytic anemia with swollowing problems and glossitis with increaed risk of cancer
plummer vision
microcytic anemia with elevated HbA2
beta thal
megaloblastic not correctable by B12 or folate
orotic aciduria
microcytic anemia with basophilic stippling
lead poisen
microcytic anemia that reverses with B6 vitamen...
sideroblastic anemia (ALA synthase)
HIV patient with macrocytic anemia
AZT...zidovudine
normocytic anemia with red urine in the morning
PNH (55 and 59...no DAF)
normocytic anemia with elevated creatinine
chronic renal disease (waxy casts---urine stasis)
use of indirect coombs test
screen fro antibodies in forign blood... does mom have antibodies to fetus
cold aggultination causes
mycoplasms (i antigen), Mono EBV
warm aggultination causes
virsus, SLE, CLL and methydopa (drugs)
cause of ITP
antibodies against GP2b/3a...very similar to Abciximab/tirofiban/eptifibatide
heredity thrombotic diseases
factor 5 laiden, deficienies in AtII, PC and PS
inherit disease of decreased Gp1b...with decreased platelets
bernard Soulier
inherited disease of GP2b/3a
Glanzzman...platelt count normal