Hem Pathology Flashcards

(37 cards)

1
Q

What are the two main causes of Vit B12 anemia

A

Inadequate intake & Impaired Absorption

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2
Q

What is pernicious anemia

A

Type of Impaired Absoprtion Vit B12 anemia, due to intrinsic factor deficiency

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3
Q

What are lab values found with vit B12 anemia

A

low B12, high MCV, low Hgb

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4
Q

What are two MACROphagic anemias?

A

Vit B12, Folate

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5
Q

What is another name for Anemia of Chronic Disease (ACD)

A

Anemia of inflammation (AI)

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6
Q

What is the cause of ACD?

A

decreased erythropoiesis and impaired iron utilizations as a result of chronic disease

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7
Q

What is the cause of sickle cell anemia

A

decreased life span of sickle cells (10-20 days instead of 90-120)

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8
Q

What are the causes of IDA

A

dietary deficiency, impaired absorption, increased requirement, chronic blood loss

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9
Q

what lab values are expected with IDA

A

Low Fe, microcytic-hypochromic RBCs on blood smear

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10
Q

How does anemia affect the cardiac system

A

1.decreased RBCs = decreased viscosity and volume of blood so interstitial fluid moves into intravascular space to expand plasma volume further decreasing viscosity, creating a hyperdynamic circulatory state as thin blood flows faster = INCREASED STROKE VOLUME AND HR
2.hypoxia leads to dilation of arterioles/capillaries, further contributes to hyperdynamic circulatory state and increased sv&hr - leads to heart failure

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11
Q

how does anemia affect the respiratory system

A

tissue hypoxia increases rate and depth of breathing - dyspnia, palpitations, fatigue

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12
Q

What is the intrinsic pathway in the coagulation cascade?

A

XII –> XI –> IX –> VIII (12,11,9,8)
then common pathway

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13
Q

What lab test is used to measure intrinsic pathway?

A

aPTT

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14
Q

What is the extrinsic pathway in the coagulation cascade

A

TF(tissue factor/F3) and VII (7) lead to common pathway

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15
Q

What lab test is used to measure the extrinsic pathway

A

PT

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16
Q

What is the common pathway?

A

1.Factor X interacts with FV, Ca & lipids to convert prothrombin (F2) to thrombin (F2a)
2.thrombin turns soluble fibrinogen (F1) into insoluble fibrin by linking particles together into chains
3.Factor XIII then takes insoluble fibrin and cross-links it to stabilize it into fibrin mesh which holds platelet plug in place

17
Q

What is factor 2?

A

inactive = prothrombin
active = thrombin

18
Q

What are the two ways coagulation is inhibited

A

inhibition of thrombin formation & fibrinolysis

19
Q

How is thrombin formation inhibited

A
  1. thrombin activates protein c (APC)
  2. APC combines with Protein S to slow down F5a and 8a
  3. Thrombin becomes inactive
  4. antithrombin inhibits further thrombin
20
Q

How does fibrinolysis occur

A

Tissue plasminogen activatory (T-PA) converts plasminogen to plasmin, which breaks down fibrin
(shows up as Ddimer)

21
Q

what is antithrombin

A

glycoprotein synthesized in the liver that inhibits factor 2a (thrombin), factor Xa, and to a lesser extent F11a adn 9a.
(half life 2-3 days)

22
Q

what is d-dimer and what does it indicate?

A

d-dimer is a biproduct of fibrinolysis - high levels indicative there may be a blood clotting condition

23
Q

what is C-reactive protein (CRP) and what does it indicate

A

CRP becomes active when contacts thrombin, helps to slow down coagulatin process
HIGH LEVEL = INFLAMMATION

24
Q

what percentage do erythrocytes/plasma/buffy layer make up in blood

A

RBC=45%
plasma = 55
BL=<1%

25
What makes up the buffy layer of blood (2 things)
leukocytes (WBC), platelets (thrombocytes)
26
What plasma proteins are present in blood (5 things)
albumin (most common), globulins, fibrinogen, additional immune mediators, clotting factors
27
What are the functions of blood (6 things)
1. respiratory gas exchange
28
What are the functions of blood (6 things)
1. respiratory gas exchange 2.transport of nutrients 3.thermoregulation 4.hemostasis 5.immunity 6.regulate cell function, osmotic pressure & pH
29
what makes up plasma
water (90%), elecrolytes, gases, plasma proteins
30
What cells results from the myloid stem cell?
RBC (from erythroblasts), platelets (from megakaryocytes), myoblasts--> granulocytes: neutrophils, eosinophils, basophils & monocytes (turn into macrophage)
31
What cells result from the lymphoid stem cell
agranular B&T lymphocytes & NK cells
32
What does an eosinophil look like?
two piece nucleus, red granules
33
what does a basophil look like
bright blue granules
34
what does a neutrophil look like
multilobed nucleous
35
what does a monocyte look like
kidney bean shaped nucleous, no granules
36
what occurs in coagulation initiation
TF&F7 activate 9, 10, 11 and small amount of thrombin
37
what occurs in coagulation amplification
thrombin activates F5, F8, platelets, and F11