Anemias Flashcards

1
Q

storage form of iron

A

ferritin

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2
Q

iron transport

A

transferrin

measured by total iron binding capacity

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3
Q

what are the examples of Microcytic anemia

A
iron deficiency
thalassemia
anemia of chronic disease 
sideroblastic anemia 
lead poisoning
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4
Q

what are some causes of iron deficiency

A

dietary
decreased absorption
-gastrectomy- due to decreased acid which is needed for ferrous absorption

-chronic blood loss (menses or carcinoma, parasite)

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5
Q

why might ferritin still be elevated in a microcytic anemia

A

b/c it is an acute phase reactant so it could be elevated if the anemia is microcytic due to anemia of inflammation
whereas it would be lower in a pure iron deficiency

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6
Q

what lab findings are present with iron deficiency anemia

A

microcytic

decreased ferritin
decreased serum iron
increased TIBC
decreased MCV (microcytic)
decreased MCHC (hypochromic) 
high RDW - b/c with each round of new blood cells, they are smaller and smaller so there will be variation
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7
Q

hepcidin

A

produced by the liver–> prevents the release of iron stores, trapping it in bone marrow macrophages

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8
Q

anemia of chronic disease lab findings

A

microcytic anemia
decreased serum iron
decreased TIBC

iron is trapped in bone marrow macrophages

increased serum ferritin

hepcidin is most likely elevated in chronic inflammatory process–> prevents release of iron

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9
Q

alpha thalassemia

A

decreased alpha globin chains

excess in beta chains

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10
Q

beta thalassemia

A

excess in alpha chains

decreased beta chains

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11
Q

alpha thalassemia –> silent carrier state

A

one deletion in alpha

asymptomatic

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12
Q

alpha thalassemia trait

A

2 deletions of alpha

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13
Q

hemoglobin H disease

A

3 deletions of alpha (alpha thalassemia)

increased HbH which forms heinz bodies

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14
Q

hydrops fetalis

A

has 4 alpha deletions (alpha thalassemia)

lethal in utero

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15
Q

HbA

A

2 alpha

2 gamma

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16
Q

Hb A2

A

2 alpha

2 delta

17
Q

HbF

A

2 alpha

2 gamma

18
Q

b thalassemia minor

A

one beta chain is damaged

asymptomatic

increased hemoglobin A2 and increased hemoglobin F

19
Q

B thalassemia major

A

normal at birth

symptoms develop at about 6 months as HbF starts to decling

severe hemolytic anemia results from decreased erythrocyte life span

intramedullary destruction –> ineffective erythropoiesis

hemolysis–> jaundice

“Chipmunk face”
Hair on end skull

microcytic/hypochromic anemia

Target cells

increased retic count

20
Q

sideroblastic anemia

A

adequate iron stores but cant incoporate the iron into hemoglobin

ring sideroblasts (accumulated iron in mitochondria of erythroblasts) in bone marrow

increased serum iron
increased serum ferritin

decreased TIBC

21
Q

what are some normocytic anemias

A
acute blood loss
hemolytic anemias
sickle cell
bone marrow aplasia/hypoplasia
renal insufficiency
myelofibrosis
myelodysplasia
anemia of inflammation
22
Q

what are some macrocytic anemias

A

Vit B12 deficiency
Folate deficiency
Treatment with drugs that interfere with DNA synthesis and cell division

Cancer chemo
Mylodysplasia
Hypothyroidism
Liver disease - alcoholism

23
Q

a protein present in blood serum that binds to and removes free hemoglobin from the bloodstream.

A

haptoglobin

24
Q

howell jolly bodies

A

autosplenectomy

due to sickle cell disease

25
Q

causes of megaloblastic anemia due to Vitamin B12 deficiency

A

usually seen in vegans
decreased absorption due to decreased intrinsic factor associated with gastrectomy or pernicious anemia
pancreatic insufficiency
intestinal malabsorption due to parasites

Crohn’s

26
Q

clinically how does a Vit B12 deficiency anemia present

A

weakness
beefy tongue
increased homocysteine

CNS effects–> (Diff than folate deficiency) –> demyelination of the posterior and lateral portion of the spinal cord

loss of vibration and position
spastic paralysis
arm and leg dystaxia