Intro to Hematopathology + anemia Flashcards

1
Q

MCV

A

Mean Corpuscular Volume

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2
Q

RDW

A

Red cell Distribution Width:

variance in cell size

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3
Q

MCH

A

weight of Hgb

in red cell

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4
Q

MCHC

A

concentration of Hgb

in red cell

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5
Q

MPV

A

Mean platelet volume

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6
Q

10 Things to look at on a blood smear

A
  1. Red cell number
  2. Red cell size
  3. Red cell shape
  4. Red cell chromasia
  5. Reticulocytes
  6. Weird stuff
  7. White cell number
  8. White cell differential
  9. Platelet count
  10. Platelet morphology
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7
Q

Iron-Deficiency Anemia

A

Most important cause: GI bleeding
Microcytic, hypochromic anemia
Increased anisocytosis and poikilocytosis
Abnormal iron studies

Bottom line:
Premenopausal women: 
think MENORRHAGIA
Everyone else: 
think GI BLOOD LOSS
Symptoms:
asymptomatic
…or fatigue, dizziness
Signs:
pale
spoon nails
smooth tongue
Pica
craving for dirt, ice, Windex
cause or symptom?
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8
Q

Iron storage

A

ferritin: quick in, quick out
hemosiderin: more stable

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9
Q

Morphology of Iron-Deficiency Anemia

A
Blood
hypochromic, microcytic anemia
anisocytosis (RBCs of unequal size)
poikilocytosis (abnormally shaped RBCs)
decreased reticulocytes
increased platelets

Bone marrow
erythroid hypoplasia
dyserythropoiesis (defective RBC development)
decreased iron stores

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10
Q

Labs in Iron-Deficiency Anemia

A

decreased serum iron
increased total iron-binding capacity
decreased ferritin

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11
Q

Megaloblastic Anemia

A

Defective DNA synthesis
Nuclear/cytoplasmic asynchrony
decreased B12/folate
Macrocytic anemia with oval macrocytes and hypersegmented neutrophils

retarded DNA synthesis  and
unimpaired RNA synthesis
lead to...
BIG cells! 
immature nucleus
mature cytoplasm

In a patient with macrocytosis…
ALWAYS check for B12 deficiency.
(Even if folate is low!)

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12
Q

B12

A

B12 sources
Meat, dairy, cereal
Not veggies!

B12 absorption, transport
Binds to IF (from parietal cells)
Absorbed in distal ileum
Carried in blood by transcobalamin II

converts homocysteine to methothionine

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13
Q

Causes of B12 Deficiency

A
Diet (rare)
Lack of IF
Pancreatic damage
Ileal damage
Tapeworm
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14
Q

Folate

A

Folate sources
Lots!
Green leafy veggies

Folate absorption, transport
Absorbed in jejunum
Converted to methyl-FH4
Transported freely to liver, red cells

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15
Q

Causes of Folate Deficiency

A

Diet (small reserve)
Alcohol abuse
Jejunal damage
Drugs

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16
Q

Morphology of Megaloblastic Anemia

A

Blood:
Macrocytic anemia
Oval macrocytes
Hypersegmented neutrophils

Bone marrow:
Megaloblastic erythroblasts
Megaloblastic neutrophils

17
Q

Megaloblastic Anemia: Diagnosis

A

MCV>100

smear:

megaloblastic
changes:
Serum B12: if decreased do schilling, pernicious anemia
Serum folate: if decreased, due to diet
RBC folate
if folate and B12 normal, its drugs or congenital

or no megaloblastic
changes:
alcoholism
myelodysplasia

18
Q

Types of Hemolytic Anemia

A

Chronic (usually congenital)
Well-compensated
Sometimes have crises

Acute (usually acquired)
Back, abdominal, limb pain
Headache, malaise, fever
Jaundice, pallor, tachycardia

Inherited
Membrane defects
Enzyme deficiencies
Globin defects

Acquired
Autoimmune hemolytic anemia 
Microangiopathic hemolytic anemia
Infection-related
Drug-related
19
Q

Signs of Destruction and Production

A
increased RBC destruction:
increased serum bilirubin
increased LDH
decreased haptoglobin
Hemoglobinemia/-uria 

increased RBC production:
Reticulocytosis
Nucleated red cells in blood

20
Q

Osmotic fragility test

A

Measures fragility of red cells

Positive result means spherocytes present

21
Q

Morphology of Hemolytic Anemia

A
Normochromic, normocytic anemia
Spherocytes
Other poikilocytes:
targets
sickles
fragmented red cells
22
Q

How to diagnose a Hemolytic Anemia

A

Look for signs of hemolysis:
Signs of destruction
Signs of production

Determine cause:
DAT + means immune cause
DAT - means non-immune cause

23
Q

Treatment of Hemolytic Anemia

A

Treatment depends on cause
If acute:
treat shock
use transfusions with caution

Splenectomy may help

24
Q

Hereditary Spherocytosis

A

Tons of spherocytes
Spectrin defect
Splenectomy is curative

Triad: anemia, jaundice, splenomegaly
“Common” (1 in 5000)
Variable age of onset, severity
Crises (often: parvovirus)

treatment:
Splenectomy
Or RBC transfusions as needed