Anemias Flashcards

(26 cards)

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.

24
Q

howell jolly bodies

A

autosplenectomy

due to sickle cell disease

25
causes of megaloblastic anemia due to Vitamin B12 deficiency
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
clinically how does a Vit B12 deficiency anemia present
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