pom-rbc disorders Flashcards

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

A

micro

25
Q

clinical features of iron def

A

parasthesia, glositis, angular chelitis, pallor

26
Q

iron def diag

A

microcytiic hypochromic anemia on blood film, rbc incices- mcv, mch, mchc iron and ferrin conc

27
Q

how to tx iron def

A

give iron- can give orally but tast e bad but do first

28
Q

thalessemia

A

decreased sytn of globin chains

29
Q

major thalassemia

A

homozynous

30
Q

minor thalassemia

A

heterozygous

31
Q

rbc count in minor thal

A

> 5.5 million/ml

32
Q

are iron stores normal in mild thalassemia

A

yes

33
Q

what is normochromic-normocytic anemia usually from?

A

secondary anemia to chronic inflamm state or uremia- renal failure, or marrow aplasia,

34
Q

aplastic anemia

A

bone marrow failure- mno blood cells

35
Q

fanconi’s anemia

A

aplastic anemia, childhood, rare auo recessive, can cause oral cancer, risk of infection

36
Q

in hemolytic anemia you see

A

decreased hemoglobin- bone marrow can’t keep up with what is being lysed

37
Q

immune hemolysis

A

warm igg reacting anti rbc ag- detect with coombs test

38
Q

mechanical hemolysis

A

lysis is caused by prosth heart valvue, malignatnt hypertension, disseminated intravstular coag, thrombotic thromccytopenia purpura

39
Q

blood film in mechanical hemolysis shows:

A

schistocytes, and other rbc fragments

40
Q

sickel cell anemia

A

altered hbg, auto recessive, betwa chain hemoglobin

41
Q

problems in pt with sickel anemia

A

consequnces of tissue infaction, recurrent sickel crisis

42
Q

g6pd deficiency

A

x-linked, most common metab disorder of rbcs

43
Q

2 forms of g6pd def

A

a form, mediterranean type (acute and fatal)

44
Q

action of g6pd

A

protect rbc from oxidative damage by main intracellular nadpa

45
Q

clinical signs of hemolytic anemia

A

pallor of oral tissue, jaundice, koilonychia, atrophy of tongue, esophageal stricture, dyspaha, increased trabeculation

46
Q

sickel cell anemia- clinical signs

A

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
Q

clinical signs of thalessemia

A

chipmunk face, hair on end, nerve palsies, discoloration of teeth

48
Q

clinical signs of b12 and pernicious anemia

A

neuro manif, skin pigmentation, systolic murmur, tonue atrophy and glossodynia, dyspha and taste alteration

49
Q

folic acid signs

A

neural tube defect, pharyntis, uclertive stomatistis, angular chelitis

50
Q

aplastic anemia signs

A

bornw skin, mental and sexual retard, oral petichia, gingival hypertrophy, spontaneous gingival hemorrhage, increased herpetic leasions