pom-rbc disorders Flashcards

(50 cards)

1
Q

polycythemia-

A

myeloproliferative disorder leading to overproduction of rbc- polycythemia vera

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2
Q

primary cause of polycethemia

A

ideopathic- 10M/mm

cyanosis secondary to decreaesed blood flow/stasis

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3
Q

secondary cause

A

drugs, high altitude, chronic smoker

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4
Q

anemia-

A

reduction in o2 carrying capcity of blood resulting from a decreased amount of hemoglobin

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5
Q

labs to look at that include rbc

A

hematocrit, hemoglobin, rbc count

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6
Q

reticulocyte

A

immature rbc

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7
Q

narrowing down diagnosis of anemia- reduce the diag by these lab result

A

low eticulocyte count (hypoproliferative anemia), speriopheral blood smear shows sickel cells, spherocytes, schistocytes

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8
Q

elevated reticulocyte count in pt with anemia indicates

A

acute blood loss, peripheral rbc destruction

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9
Q

types of hypoprolierative anemia

A

macrocytic, microcytic-hypochromic,normochromic-chormocytic

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10
Q

macrocytic hypoprolierative anemia cuased by

A

vit b12, folar def

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11
Q

microcytic - hypochromic hypoprolif anemia caused by

A

iron def, thalassemia

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12
Q

normochromic/normocytic hypoproliferative anemia caused by

A

secondary anemia, marrow aplasia

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13
Q

hemolytic anemai- 4 types

A

immune hemolysis, mechanical hemolysis, sickel cell anemia, g6pd deficiency

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14
Q

b12 def- what is b12 for?

A

dna synth

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15
Q

poikilocytes

A

seen in b12 def, - large cells with small immature nuclei

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16
Q

cuases of b12 def- 4

A

pernicious anemia, gi bac overgrowth, loss of ideal fxn, vegetraian diet

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17
Q

what tests to do do diag b12 def

A

meausre serum b12, peripheral blood film, elevated ldh, plasma bilirubin, iron, schilling test

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18
Q

schilling test-

A

test dose of b12 is administern, then intestinal absoprtion is measured

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19
Q

b12 deficiency can lead to this nerve problem

A

demylination of peripheral nerves- leads to megaloblasitic madness, glossodynia

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20
Q

pernicious anemia is assoc with

A

atrophic gastritis

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21
Q

poor vit b12 in pernicous anemia bc of loss of

A

intrinsic factor

22
Q

what do you see in the labs for pernicious anemia

A
macrocytic  or normocytic cells on smear
elevated mcv and mch while normal mchc
large platelets, hypersegmented pmns
serum levels
schilling test
23
Q

folate deficiency

A

just take supplement, no big deal

24
Q

iron deficiency is a ? type anemia

25
clinical features of iron def
parasthesia, glositis, angular chelitis, pallor
26
iron def diag
microcytiic hypochromic anemia on blood film, rbc incices- mcv, mch, mchc iron and ferrin conc
27
how to tx iron def
give iron- can give orally but tast e bad but do first
28
thalessemia
decreased sytn of globin chains
29
major thalassemia
homozynous
30
minor thalassemia
heterozygous
31
rbc count in minor thal
>5.5 million/ml
32
are iron stores normal in mild thalassemia
yes
33
what is normochromic-normocytic anemia usually from?
secondary anemia to chronic inflamm state or uremia- renal failure, or marrow aplasia,
34
aplastic anemia
bone marrow failure- mno blood cells
35
fanconi's anemia
aplastic anemia, childhood, rare auo recessive, can cause oral cancer, risk of infection
36
in hemolytic anemia you see
decreased hemoglobin- bone marrow can't keep up with what is being lysed
37
immune hemolysis
warm igg reacting anti rbc ag- detect with coombs test
38
mechanical hemolysis
lysis is caused by prosth heart valvue, malignatnt hypertension, disseminated intravstular coag, thrombotic thromccytopenia purpura
39
blood film in mechanical hemolysis shows:
schistocytes, and other rbc fragments
40
sickel cell anemia
altered hbg, auto recessive, betwa chain hemoglobin
41
problems in pt with sickel anemia
consequnces of tissue infaction, recurrent sickel crisis
42
g6pd deficiency
x-linked, most common metab disorder of rbcs
43
2 forms of g6pd def
a form, mediterranean type (acute and fatal)
44
action of g6pd
protect rbc from oxidative damage by main intracellular nadpa
45
clinical signs of hemolytic anemia
pallor of oral tissue, jaundice, koilonychia, atrophy of tongue, esophageal stricture, dyspaha, increased trabeculation
46
sickel cell anemia- clinical signs
hair on end lateral ceph, ladder like appears of alveolar bone, increased trabeculation, hypoplasia of dentision, dense lamina dura, area of scleroisis, thickend diploe on skull films shows hari on end
47
clinical signs of thalessemia
chipmunk face, hair on end, nerve palsies, discoloration of teeth
48
clinical signs of b12 and pernicious anemia
neuro manif, skin pigmentation, systolic murmur, tonue atrophy and glossodynia, dyspha and taste alteration
49
folic acid signs
neural tube defect, pharyntis, uclertive stomatistis, angular chelitis
50
aplastic anemia signs
bornw skin, mental and sexual retard, oral petichia, gingival hypertrophy, spontaneous gingival hemorrhage, increased herpetic leasions