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75 Cards in this Set

  • Front
  • Back
pig-a gene
paroxysmal nocturnal hemoglobinuria (PNH)
Abnormal clones producing
PDGF / TGF-B / EGF
myelofibrosis
GPI Anchor
anchors glycoproteins to cell membrane

part of pig-a gene
[deffect in PNH]
markers to confirm AML
CD 33/11/13/15/HLA-DR
[to help memorize 11-->13-->33]
t(15:17)
RAR alpha --> APL
drug to treat APL?
ATRA
t(15:17) is considered a good prognosis
t(8:21)
AML
good prognosis
inv(16)
AML
good prognosis
t(8:14)
Burkitt-like Lymphoma

inc c-myc
gene on chrom(8)
c-myc
t(12:21)
ALL
good prognosis
gene on chrom(12)
TEL
gene on chrom(21)
AML-1
t(4:11)
ALL
poor prognosis
t(8:2)
burkitt lymphoma
t(8:22)
burkitt lymphoma
gene on chrom(14)
Ig heavy chain

Bcl-1 (inc cell proliferation)
t(11:14)
mantle cell / B cell lymphoma

caused by inc Cyclin D1
gene on chrom(11)
cyclin D
propels cell through life cycle
"cold" antibody
anti-CD20
Rituximab works on b cells
t(14:18)
follicular lymphoma

bcl-2/IgH chimeric gene
inc bcl-2 which prevents apoptosis
t(11:18)
MALT (h pylori independant)

inc API-2
t(1:14)
MALT (h pylori independant)
MIP-1
inc RANKL and osteoclast activity
CD markers for lymphocyte predominance
+20 / -30 / -15
CD markers for hodgkins
-20 / +30 / +15
treatment of hd
ABVD
adriamycin / bleomycin / vinblastine / dacarbazine
Bcl-6
diffuse large b cell lymphoma
L3 ALL
Burkitt
t(4:14)
myeloma
FLT-3
active prt kinase
No apoptosis

poor AML
NPM1
exon mutation
decr prot aggregation in nuc.

Good AML
Hb f
a2g2
Hb H
b4
Hb Barts
g4

no alpha globin loci... hydrops fetalis
Hb A2
a2d2
chrom (16)
a globin
chrom (11)
b globin
MCV
hct/rbc count (80-100)
MCH
hb/rbc count (27-31)
MCHC
hb/hct
section of GI where iron is absorbed
duodenum / proximal jejunum
glossitis
smooth waxy tounge in fe deficiency
b12 on cns
affects myelin synth
what molecule take b12 from ileum
transcobalamin 2
schilling test
radioactive b12
heinz bodies
in g6pd def because oxidative stress denatures hb.

also found in hb h and those types
elt
euglobulin lysis time
fibrynolysis
bleeding time
platelet number and function
lupus anticoag
not assoc with bleeding

atibody bind to phospholipid reagents
desmopressin
release all vwf from granules
dense granules
atp/adp
alpha granules
vwf, factor v, anti plasmin
ITP
immune thrombocytopenic purpura

Ig bound to platelet antigens
TTP
Throbotic thrombocytopenic purpura

endo damage (perturbation) causes release of large vWF molecules. no vwf processing factors.

diffuse platelet plugs
heparin Ig complex
hep + PF4 bind. Ig made against complex.

bind platelet Fc receptor --> activate platelet to release PF4.

endothelial damage
glanzmann
defective gpIIIb-IIIa

no aggregation
storage pool def
alpha granule def / dense granule def

chronic activation states

reduced activation problem
ristocen
test for vwf
V quebec
platelet alpha protein def
LAD
leukocyte adhesion def

no adhesion or rolling. no PMN at infections site
CGD
no ndph --> no puperoxide.

mpo ok
mpo syndrome
no mpo --> inc fungus
cvid
chronic variable immuno disease

affected Tcell/Ig
normal b cell counts
Di george
no thymus. immature t cells
x linked agammaglobulinemia
no bruton tyrosine kinase

only pre-b cells
hyper-igm syndrome
no cd40l (t cells can't mediate isotype switching)
scid
severe combined immune def

no b/t (no maturation)
cd 5 marker on b cells
b-cll/sll
how to treat early malt...
antibiotic for h pylori
hypersensitivity III
immune complexes
hypersensitivity II
complement
Normal mch
28-33
hypersensitivity I
IgE IL4
meth-->heme
cytochrome B5