Introduction Flashcards

(55 cards)

1
Q

components of Buffy coat

A

WBC, platelets

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2
Q

main component of plasma

A

water (92%)

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3
Q

serum

A

plasma minus clotting factors (NOT anti-coagulated)

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4
Q

characteristics of RBC

A

size of small lymphocyte, central pallor (1/3 diameter). no nuclues and biconcave

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5
Q

what originates from common myeloid progenitor?

A

megakaryocytic, RBC, myelblast, mono-blast

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6
Q

what does a megakaryocytic become after activation

A

thrombocytes

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7
Q

what does a basophil become after activation

A

mast call

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8
Q

what does a monocyte become after activation

A

macrophage

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9
Q

what originates from common lymphoid progenitor

A

natural killer cell and small lymphocyte

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10
Q

maturation of a RBC

A

stem cell..proerythroblast..early erythroblast..intermed erythro..late erythro (sheds nuclues)..reticulocyte..RBC

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11
Q

b lymphovytes

A

produced and mature in bone marrow

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12
Q

t lymphocytes

A

produced in bone marrow mature in thymus

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13
Q

when are neutrophilic band cells seen?

A

bone marrow stress

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14
Q

main component of RBC

A

hemoglobin

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15
Q

constituents of hemoglobin

A

one molecule of globin and one molecule of heme

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16
Q

how many hemoglobin molecules are in each RBC

A

270 million

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17
Q

structure of globin

A

combo of 4 polypeptide sunbunits

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18
Q

structure of heme

A

4 pyrrole rings (protoporphyrin) held toether by ferrous iron

one heme unit in each globin subunit

each heme bninds one molecule of oxygen

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19
Q

what happens when hemoglobin is degraded

A

iron and globin reused. pyrrole rings cleaved giving rise to bilirubin

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20
Q

macrocytic RBC

A

BAD HL

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21
Q

RDW

A

suggests diverend population of red cells of different sizes

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22
Q

reticulocytosis

A

bone marrow responds to stress and spits out immature RBC

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23
Q

poikilocytosis

A

variations in cell shape

24
Q

macroovalocytes

A

deficincy of vitamin b12 or folic acid

25
ovalocytes and elliptpcytes
hereditary elliptocytosis
26
spherocytes
hereditary spherocytosis and autoimmune hemolytic anemia
27
schistocytes
destruction within vascular spaces
28
tear drop cells
commonly found in extra medullary hematopoiesis which is a response to bone marrow failure
29
where does EMH occur?
spleen, liver and lymph nodes
30
hypochromic RBC
more than 1/3 is pale (iron def anemia)
31
hyperchromic RBC
lose central pallor (spherocytes)
32
anisocytosis
variation in size
33
hereditary spherocytosis
INCREASED OSMOTIC FRAGILITY - lack of spectrin
34
actue phase reactants
proteins that change their serum concentration by greater than 25% in response to inflammatory cytokines
35
what is in the cytoplasm of reticulocytes
residual ribosomal RNA
36
howell jolly bodies
inclusions of DNA remanants
37
nucleated RBC
bone marrow stress
38
basophillic stippling
ribosomes at the periphery of RBC | - heavy metal poisoning
39
heinz bodies
denatured hemoglobin seen in G6PD DEFICIENCY
40
dohle bodies
basophilic inclusions located in the peripheral cytoplasm of neutrophils RER
41
what kind of neutrophils are seen in a blood smear
bands and PMNs
42
how many lobes does a neutrophil have
3-4 (5 of more hyper-segmented)
43
what are hyper-segmented neutrophils indicative of
B12 folate deficiency
44
causes of eosinophillia
``` neoplastic asthma allergic rxn collagen (rheum) parasites ```
45
what is basophilic leukocytosis associated with
leukemia (specif. CML)
46
what controls adaptive immunity?
B and T lymphocytes
47
natural killer cells
kill tumor and virally infected cells
48
appearance of an atypical lymphocyte
larger than normal and have more cytoplasm
49
with what condition are atypical lymphocytes seen
MONO
50
what is the largest cell in the blood
monocytes
51
risk of low platelet count
bleeding
52
risk of high platelet count
clotting
53
von willebrand factor
initiates first stage of wound healing
54
steps of hemostasis
vasoconstriction platelet plus fibrin clot
55
what do platelets contain
vasoconstrictors and cytokines