Hem Onc Flashcards

1
Q

fetal erythropoeisis sites

A

yolk sac (3 to 8 wks)
Liver (6 wks to birth)
spleen (10 to 28 wks)
bone marrow (18 wks to adult)

Young Liver Synthesizes Blood

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2
Q

Fetal hemoglobin

A

HbF
A2G2

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3
Q

Adult hemoglobin

A

A2B2
HbA

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4
Q

HbA2

A

adult hemoglobin present in small amounts
A2D2

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5
Q

hemoglobin electrophoresis results

A

A Fat Santa Claus cant go far
(descending order of farthest) (farthest meaning closer to anode)
HbA
HbF
HbS
HbC

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6
Q

coombs test use

A

detect Ab against RBCs

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7
Q

Direct Coombs test done for

A

AIHA

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8
Q

direct coombs test mech

A

patient blood + anti human globins (coombs reagent)

agglutinatn present- AIHA
agglutinatn abs- AIHA no

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9
Q

indirect coombs test done for

A

pretransfusion testing

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10
Q

indirect coombs test mech

A

patient blood + coombs reagent + donor blood

agglutinatn- reaction present
no agglutinatn- rxn absent

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11
Q

hemoglobin made up of

A

heme + globin

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12
Q

heme made up of

A

iron + protoporphyrin

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13
Q

Etiologies of microcytic anemia

A

iron def
thalassemia
chronic ds
sideroblastic anemia

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14
Q

tibc measures

A

transferrin levels

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15
Q

ferritin tibc trend

A

inversely prop

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16
Q

treatment of IDA

A

FeSO4
rule out risk factors

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17
Q

m/c anemia in hosp pt

A

anemia of chronic ds

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18
Q

pathophysio of anemia of chronic ds

A

acute phase prot formed
hepcidin formed
hepcidin functns-

  1. dec erythropeitin prodcutn
  2. inc sequestering of Fe to macrophages (as Fe is reqd by bacteria)
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19
Q

sideroblastic anemia cause

A

low synth of protoporphyrin

20
Q

ringed sideroblast cause

A

as there is low protoporphyrin
Fe is trapped in mitochondria, which forms a ring around nucleus

21
Q

lead poisoning denatures which enzymes

A

ALA-D and ferrochelatase

22
Q

vit b6 def affects which enzyme

23
Q

which drug causes vit B6 def

24
Q

rx for sideroblastic anemia

A

pyridoxine (vit B6)

25
Q

dohle bodies

A

found in neutrophils
they are peripheral inclusions

26
Q

neutrophil chemotactic agents

A

c5a, il-8, ltb4, 5-hete, kallikiren, platelet activating factor, n-formylmethionine (bacterial proteins)

27
Q

tear drop cells seen in

A

myelofibrosis

28
Q

bite cells seen in

A

g6pd def due to removal of heinz bodies

29
Q

target cells found in

A

HALT
hbc ds
asplenia
liver ds
thalassemia

30
Q

howell jolly bodies what are they and where are they seen

A

sickle cell ds
basophilic nuclear remnants

31
Q

basophilic stippling seen in

A

sideroblastic anemia

32
Q

fanconi anemia

A

dna repair defect leading to bone marrow failure

33
Q

acute intermittent porphyria affected enzyme

A

porphobillinogen deaminase

34
Q

porphyria cutanea tarda affected enzyme

A

uroporphyrinogen decarboxylase

35
Q

adult t cell lymphoma cause

36
Q

treatment for heparin induced thrombocytopenia

A

stop heparin
use alt anticoagulant (argatroban)

37
Q

if pt has renal insufficiency, what kind of heparin is used

A

unfractioned heparin

38
Q

warfarin reversal

A

vitamin k
give ffp or pcc for rapid reversal

39
Q

factor 2 inhibitors

A

bivalirudin
argatroban
dabigatran

40
Q

factor 2 inhibitors reversor

A

ida-ruci-zumab

41
Q

factor 10a inhibitors

A

apixaban, rivaroxaban, edoxaban

42
Q

factor 10a inh reversor

A

andexanet alfa

43
Q

eptifibatide, tirofiban moa, use

A

block FIB-rinogen receptor (gp2b/3a), unstable angina

44
Q

cilostazol, dipyridamole moa, use

A

block phosphodiesterase, used in stroke prevention

45
Q

thrombolytics names

A

alteplase, reteplase, tenecteplase

46
Q

thrombolytics moa

A

aid onversion to plasminogen to plasmin which inhibits cleaves thrombin and fibrin