Heme/Onco I Flashcards

(38 cards)

1
Q

anisocytosis

A

variable size

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2
Q

poikilcytosis

A

variable shape

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3
Q

RBC membrane

A

Cl/HCO3 antiport

export HCO3 and transport CO2 from periphery to lungs

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4
Q

GpIIb/IIIa

A

fibrinogen receptor

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5
Q

platelet granules

A

dense - ADP and Ca

a- vWF and fibrinogen

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6
Q

band cells

A

immature neutro

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7
Q

polysegmented neutro

A

B12/folate deficiency

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8
Q

chemotaxis of neutrophils

A
C5a
IL-8
LTB4
kallikrein
PAF
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9
Q

lipid A

A

from LPS

bind CD14 on macros - septic shock

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10
Q

macrophage activation

A

IFN-gamma

can present MHC II - antigen presentation

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11
Q

major basic protein

A

from eosinophil

defense against helminth

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12
Q

basophil content

A

heparin

histamine

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13
Q

mast cell

A

bind Fc of IgE

release histamine, heparin, eosinophil chemotactic factors

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14
Q

dendritic cell

A

APC

MHC class II

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15
Q

lymphocyte

A

B cell
T cells
NK cells

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16
Q

CD28

A

for T cell activation

17
Q

cross placenta

18
Q

universal blood donor

19
Q

universal blood recipient

20
Q

Rh incompatible

A

Rh - mother - make anti-D IgG - cross placenta

hemolytic disease of newborn (erythroblastosis fetalis)

tx - rhogam

Rh = D

21
Q

plasma Abs for A and B blood groups

22
Q

extrinsic coag

A

tissue factor to factor VII

23
Q

intrinsic pathway

A

collagen to factor XII

also - activated by HMWK - kinin cascade

24
Q

epoxide reductase

A

reduces vitamin K - to active clot factors

25
factor V leidein mutation
factor V resistant to inhibition by protein C
26
source of vWF
endothelial cell - wiebel paladie body | platelet - a-granules
27
platelet binding
release Ca and ADP, and TXA2 ADP - induces GpIIb/IIIa on platelet surface
28
aspirin
inhiit COX inhibit TXA2
29
ristocetin
vWF binding Gp1b diagnosis of vWD and BS syndrome
30
inhibit GpIIb/IIIa
abciximab eptifibatide tirofiban
31
acanthocyte
spur cell
32
ringed sideroblast
sideroblast anemia excess iron in mito
33
schistocyte
helmet cell with hemolysis mechanical CID, TTP/HUS, HHELLP, heart valve
34
sickling
with dehydration, deoxygenation, and high altitude
35
dacrocyte
teardrop shaped bone marrow infiltration
36
target disease
HbC disease asplenia liver thalassemia
37
heniz body
oxidation of Hb SH group to disulfide bond precipitate phagocytosed - bite cells with G6PD deficiency
38
howel jolly bodies
nuclear remnants in RBCs normal removed by splenic indicate hyposplenia or asplenia