Red Blood Cell Disorders Flashcards

1
Q

Absorption of iron occurs in the

A

Duodenum

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2
Q

takes both heme and non-heme iron into erythrocyte from intestinal lumen

A

DMT1

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3
Q

transports iron across cell membrane of erythrocytes into blood

A

Ferroportin

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4
Q

transports iron in blood and delivers to bone marrow and liver MQs for storage

A

transferrin

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5
Q

stored intracellular iron is bound to

A

Ferritin (prevents Fenton reaction)

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6
Q

Fenton reaction

A

how iron forms free radicals

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7
Q

measure of transferrin molecules in the bood

A

TIBC

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8
Q

%transferrin molecules bound by iron

A

% saturation (normal is 33%)

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9
Q

Solely breast fed infant

A

Iron deficiency b/c human milk is low in iron

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10
Q

Pregnancy

A

iron deficiency because need alot of iron to grow fetus

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11
Q

PUD males

A

iron deficiency

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12
Q

Ancylostoma duodenale and Necator americanus

A

hookworms; cause of iron deficiency in developing worlds

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13
Q

gastrectomy

A

iron deficiency because acid aids iron absorption by maintaining Fe2+ state, which is more readily absorbed than Fe3+.

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14
Q

decreased ferritin, increased TIBC

A

storage iron depleted

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15
Q

stages or iron deficiency

A

depletion of stored iron->depletion of serum iron->normocytic anemia->microcytic, hypochromic anemia

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16
Q

anemia, koilonychia, pica

A

iron deficiency clinical features

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17
Q

measures the spectrum of size of RBCs

A

red cell distribution width (if all cells similar size, then would be low; normal). increased in microcytic hypochromic anemia.

18
Q

Fe+protoporphyrin

19
Q

FEP (free erythrocyte protoporphyrin)

A

increased in iron deficiency anemia

20
Q

anemia, dysphagia, beefy red tounge

A

Plummer-vinson syndrome; iron deficiency anemia with esophageal web and glossitis

21
Q

Hepcidin

A

acute phase reactant produced by liver in chronic disease

22
Q

increased ferritin, decreased TIBC, decreased serum iron, decreased %saturation, increased FEP

A

Anemia of Chronic Disease

23
Q

anemia due to defective protoporphyrin synthesis

A

sideroblastic anemia

24
Q

converts succinyl CoA to aminolevulinic acid (ALA)

A

Aminolevulinic acid synthetase (ALAS)+B6 (cofactor)

25
converts ALA to porphobilinogen
Aminolevulinic acid dehydratase (ALAD)
26
attaches protoporphyrin to iron to make heme
Ferrochelatase (final reaction; occurs in MT)
27
iron-laden mitochondria form ring around nucleus of erythroid precursors
ringed sideroblast
28
most commonly seen as a side effect of isoniazid treatment for tuberculosis; required cofactor of ALAS.
vitamin B6 (sideroblastic anemia)
29
inhibits ALAD and Ferrochelatase
Lead poisoning (sideroblastic anemia)
30
decreased synthesis of the globin chains of hemoglobin
Thalassemia
31
HbBarts
Hb formed from gamma chain tetramers (Hydrops fetalis)
32
HbH
Hb formed from beta chain tetramers
33
2 genes on chromosome 11
Beta thalassemia
34
4 genes on chromosome 16
Alpha thalassemia
35
microcytic hypochromic RBCs and target cells on blood smear
Beta thalassemia minor (nomal Beta, diminished Beta)
36
decreased HbA, increased HbA2, increased HbF
Beta thalassemia minor (Hb electrophoresis)
37
expansion of hematopoiesis into skull and facial bones
Beta thalassemia major; due to massive erythroid hyperplasia
38
risk of aplastic crisis with parvovirus b19 inf. of erythroid precursors
Beta thalassemia major
39
HbA2, HbF, no HbA (very little)
Beta thalassemia major
40
impaired division of RBC precursors and granulocyte precursors, and megaloblastic change in rapidly dividing epithelial cells
Megaloblastic anemia
41
inhibits dihydrofolate reductase
methotrexate
42
autoimmune dest. of parietal cells of stomach
pernicious anemia