Anemia- Krafts Flashcards

(56 cards)

1
Q

Symptoms of Anemia

A
Pale skin/mucous membranes
Jaundice
Tachycardia
Breathlessness 
Dizziness
Fatigue
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2
Q

Koilonychia

A

Spoon shaped nails

in IDA

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3
Q

3 ways to get anemic

A
  1. Lose blood
  2. Destroy too much blood (intracorpusular or extracorpuscular reasons)
  3. Make too little blood
    • too few building blocks
    • Too few erythroblasts (aplastic anemia)
    • Not enough room
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4
Q

3 Morphologic Groups of Anemia

A
  1. Weird Size
  2. Weird Shape
  3. Normal size and shape
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5
Q

Weird Size

A

Iron- deficiency anemia
Thalassemia
Megaloblastic anemia

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6
Q

Iron Deficiency Anemia

A
  • Most important cause–> GI bleeding
  • Microcytic, hypochromic anemia
  • increased anisocytosis (varying cell sizes) & poikilocytosis (abnormal shape)
  • Abnormal iron studies
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7
Q

Iron:
Absorption?
Circulation?

A

Absorbed in duodenum

Carried in circulation by transferrin

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8
Q

Iron:
Absorption?
Circulation?

A

Absorbed in duodenum

Carried in circulation by transferrin

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9
Q

Hemoglobin

A

4 globin chains (2 alpha, 2 beta)

4 heme molecules
-iron only binds O2 in ferrous (Fe2+) state

Fe3+/ferric state=methemoglobin

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10
Q

Ferritin vs hemosiderin?

A

Ferritin is quick iron storage

Hemosiderin is long term

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11
Q

Causes of iron deficiency

A

Decreased iron intake (bad diet/absorption)

Increased Iron loss( GI bleed, menses, hemorrhage)

Increased iron requirement (prego)

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12
Q

IDA in premenopausal women?

IDA in everyone else?

A

premen women–> MENORRHAGIA

everyone else–> GI BLOOD LOSS

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13
Q

Signs/symptoms of IDA:

A

Asymptomatic
Fatigue, dizziness
Signs: pale, spoon nails, smooth tonue
Pica

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14
Q

First sign of ID?

A

Poikilocytosis: see elliptocytes –cigar shaped cells

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15
Q

Blood smear in IDA?

A
  • hypochromic, microcytic anemia
  • anisocytosis
  • poikilocytosis
  • decreased reticulocytes
  • increased platelets
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16
Q

Bone marrow biopsy findings in IDA?

A
  • erythroid hypoplasia (not as many RBC as you would expect)
  • dyserythropoiesis (funny looking RBCs)
  • decreased iron stores
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17
Q

Labs in IDA? **

A
  • decreased serum iron
  • increased TIBD
  • decreased ferritin
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18
Q

Labs in IDA? **

A
  • decreased serum iron
  • increased Total iron binding capacity
  • decreased ferritin *** only ID will make this low
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19
Q

Do look at what lab test first for diagnosis of IDA?

A

Ferritin

DECREASED in IDA!

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20
Q

Tx of IDA?

A

Figure out why they are iron deficient

-give oral iron

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21
Q

Megaloblastic anemia

THINGS TO KNOW

A
  • Defective DNA synthesis
  • Nuclear/cytoplasmic asynchrony (nuc lags behind in maturity)
  • decreased B12/folate
  • Macocytic anemia with oval macrocytes and hypersegmented neutrophils
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22
Q

Megaloblastic anemia

Retarded DNA syn & unimpaired RNA syn —–>

A

BIG BIG Cells

Immature nucleus
Mature cytoplasm

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23
Q

B12 sources & absorption

A

Meat, dairy, cereal. (NOT veggies, dude!)

Need IF secreted by parietal cells to get absorbed in distal ileum

24
Q

Causes of B12 Deficiency

A
diet
lack of IF (pernicious anemia)
pancreatic damage
Ileal damage
Tapeworm
25
Megoloblastic symptoms?
Atrophic glossitis --beefy tongue, lack of papilli
26
Long term B12 def
Subacute combined degeneration -sensory & motor probs Need B12 to convert homocysteine --> methionine
27
Folate: sources & absorption
Green leafy veggies | -Absorbed in jejunum
28
Causes of folate def
diet alcohol abuse jejunal damage drugs
29
What will you see in a blood smear with megalobastic anemia?
- macrocytic anemia - oval macrocytes - Hypersegmented neutrophils (*only happens with this)
30
What will you see in a blood smear with megaloblastic anemia? Labs?
- macrocytic anemia - oval macrocytes - Hypersegmented neutrophils (*only happens with this) MCV >100
31
What do you see in BM biopsy with megaloblastic anemia?
- megaloblastic erythroblasts | - megaloblastic neutrophils
32
Weird Shaped Anemias? Hemolytic anemias!
- HS - AIHA - Sickle cell anemia - G6PD deficiency - MAHA
33
Weird Shaped Anemias? Hemolytic anemias!
- HS - AIHA - Sickle cell anemia - G6PD deficiency - MAHA
34
Symptoms of acute hemolytic anemia
back, abdominal, limb pain headache malaise, fever jaundice, pallow, tachycardia
35
Types of hemolytic Anemia
1. Chronic (hereditary) -well compensated 2. Acute (acquired) 3. Inherited- defects in RBCs 4. Acquired -infection or drug related
36
Bottom line of hemolytic anemia, you'll see signs of both:
increased RBC destruction --------> Increased RBC production
37
Signs of Increased RBC Destruction
- increased serum bilirubin - increased LDH - Decreased haptoglobin
38
Signs of Increased RBC PRODCUTION:
- Reticulocytosis | - Nucleated RBCs in blood
39
Signs of Increased RBC PRODCUTION:
- Reticulocytosis | - Nucleated RBCs in blood
40
Labs test in hemolytic anemia
1. direct antiglobulin test (DAT)- look for Abs on RBC surface by using a anti-human globulin (+ = immune process) 2. Osmotic fragility test: +=spherocytes present
41
Morphology of hemolytic anemia
- Normochromic, normocytic anemia - Spherocytes - Poikilocytes: targets, sickles, fragmented
42
How to diagnose Hemolytic anemia
Look for signs of destruction & production | Determine cause with DAT (immune vs non immune)
43
Tx of hemolytic anemia
Depends on cause Acute: tx shock Splenectomy if needed
44
Hereditary Spherocytosis (HS)
- Tons of spherocytes - Defect in RBC cytoskeleton (spectrin) - Splenectomy is curative
45
Triad of Hereditary Spherocytosis
1. anemia 2. jaundice 3. spenomegaly
46
Pathogeneisis of HS:
- abnormal RBC cytoskeleton - loss of surface area - spleen removes spheres (macrophages)
47
HS Morphology
- mild normochromic, normocytic anemia | - numerous spherocytes
48
HS tx:
Splenectomy
49
Autoimmune Hemolytic Anemia (AIHA) Warm and cold types THINGS TO KNOW
- IgG bind to RBCs - destruction happens in spleen - Spherocytes
50
Pathogenesis of WAHA
IgG coats RBCs --->Macs eat whole cell OR nibble and cell becomes spherocytes Get Splenomegaly
51
WAHA dx and tx
Dx: DAT (direct antiglobulin test) Tx: steroids and maybe splenectomy
52
WAHA dx and tx
Dx: DAT (direct antiglobulin test) Tx: steroids and maybe splenectomy
53
Cold AIHA | THINGS TO KNOW:
-IgM, complement bind at colder temp areas, hands ears feet. falls off in warm body parts - some intravasulcar hemolysis (b/c of complement) - mostly spleen - Agglutination: IgM forms petamers and clumps RBCs up (bridges RBCs)
54
Clinical signs of Cold AIHA
chronic hemolysis aggravated by cold. Pallor, cyanosis in cold body parts
55
Morphology of Cold AIHA
Red cell agglutinates (from IgM) | Rare spherocytes
56
Cold AIHA dx and tx
Dx: DAT positive for complement (doesn't pick up IgM) tx: keep patient warm, treat underlying cause