heme-onc Flashcards

1
Q

poikilocytosis

A

RBCs of differing shapes

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2
Q

life span of platelets

A

8-10 days

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3
Q

leads to petechiae

A

thrombocytopenia

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4
Q

vWF receptor

A

GpIb on platelets

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5
Q

fibrinogen receptor

A

GpIIb/IIIa on platelets

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6
Q

neutrophils with more than 4 lobes indicate

A

b12/folate decieciency

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7
Q

increase in band cells can indicate

A

increased myeloid production (bacterial infection, CML)

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8
Q

neutrophil granules contain

A

alkaline phosphatase, collagenase, lysozyme, lactoferrin

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9
Q

activates macrophages

A

g-interferon

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10
Q

cell surface marker for macrophages

A

CD-14

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11
Q

bilobate nucleus with lots of granules

A

eosinphils

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12
Q

so many granules you can’t see the nucleus

A

basophils

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13
Q

basophil granules contain

A

heparin, histamine, leukotriene

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14
Q

eosinphil granules contain

A

histamine, arylsulfatase

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15
Q

how mast cells cause allergic reaction

A

binds Fc portion of IgE to membrane. IgE cross-links upon antigen binding, causing degranulation - releasing histamine

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16
Q

prevents mast cell degranulation

A

cromolyn

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17
Q

dendritic cells express

A

MHC-II and c receptor

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18
Q

what B cells do when encountering an antigen

A

differentiate into plasma cells that produce antibodies and memory cells

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19
Q

cancer of plasma cells

A

multiple myeloma

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20
Q

off center nucleus, clock-face chromatin distribution, abundant RER and golgi

A

plasma cell

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21
Q

universal recipient of RBCs

22
Q

universal donor of plasma

23
Q

universal donor of RBCs

24
Q

universal recpient of plasma

25
tx for mom who gives birth to the oposite Rh- baby (first birth)
give Rho(D) immune globulin to mom to prevent immune sensititation to subsequent babies
26
begins extrinsic coag path
factor VII
27
activates factor VII
thromoplastin
28
VIIa activates
X (joins intrinsic coag pathway)
29
begins intrinsic coag pathway
XII activated to XIIa by collagen, BM and activated platelets
30
hemophilia A a lack of
factor VIII
31
hemophila B a lack of
factor IX (christmas disease)
32
effect of bradykinin
increase of vasodilation, permeability, and pain
33
turns prothrombin into thrombin
Va
34
cleaves fibrinogen into fibrin
IIa (thrombin)
35
creates fibrin mesh out of fibrin monomers
XIIIa (and Ca++)
36
turns plasminogen into plasmin
kallikrein (tPA)
37
actvates bradykinin
kallikrein
38
degrades fibrin mesh
plasmin
39
Vit K needed to mature
II, VII, IX, X, C, S
40
reduces Vit K for use
epoxide reductase
41
MOA of warfarin
inhibits epoxide reductase
42
carries/protects VIII
vWF
43
cleaves and inactivates Va, VIIIa
activated protein C
44
activates protein C
thrombomudulin from endothelial cells
45
cofactor for activated protein C
protein S
46
MOA of heparin
activates antithrombin
47
factor V leiden mutation effect
produces a factor V resistant to inhibition by activated protein C
48
path of platelet plug formation
1) injury - vWF binds to exposed collegen upon endothelial damage 2) adhesion - platlets bind vWF at site of injury --> release ADP (helps platelet adhere to endothelium) and Ca (for coag cascade) 3) activation - > ADP binding to receptor induces GpIIb/IIIa expression at platelet surface 4) fibrinogen binds GpIIb/IIIa receptors and binds links platelets
49
MOA of asprin
inhibits cyclooxxygenase preventing TXA2 synth
50
MOA of ticlopidine and clopidogrel
inhibit ADP indiced expression of GpIIb/IIIa
51
MOA of abciximab
inhibits GpIIb/IIIa directly