Case of the Week: Hemolysis Flashcards

1
Q

What are two things that might be going on if you have anemia and a HIGH RETICULOCYTE COUNT?

A

active bleeding

red cell destruction

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2
Q

What clues would favor RBC destruction instead of blood loss?

A
elevated LDH
elevated indirect bilirubin
spherocytes of peripheral smear
low haptoglobin
positive DAT
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3
Q

Two mechanisms of hemolysis?

A

intravascular: destruction of RBCs within the vasculature, releasing free Hb into circulation
extravascular: macrophages in spleen, liver, and marrow remove damaged or antibody coated red cells

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4
Q

What are some clues that make you think of increased red cell production:

in the blood?
in the bone marrow?
in the bones?

A

blood: elevated reticulocyte count or circulating nucleated RBCs

bone marrow: erythroid hyperplasia

bones: deformities in long bones

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5
Q

What’s the diagnosis?

Etiology: Mechanical destruction of red blood cells in circulation
Causes: TTP, DIC, HUS, Pre-eclampsia, malignant HTN, prosthetic values
Diagnosis – Schistocytes
Treatment of underlying disorder

A

microangiopathy

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6
Q

What’s the diagnosis?

Etiology – Malaria, babesiosis, clostridium
Diagnosis – cultures, thick and thin smears, serologies
Treatment - Antibiotics

A

Infection

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7
Q

What are 3 inherited/hereditary defects in RBCs?

A
  1. enzyme probs: G6PD deficiency
  2. membranopathies: hereditary spherocytosis
  3. hemoglobinopathies: thalassemia and sickle cell diseases
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8
Q

What are two general mechanisms you think of when you are presented with ANEMIA?

A
  1. decreased bone marrow production

2. increased destruction

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9
Q

What are some clinical clues unique to intravascular hemolysis?

A

hemoglobinuria

hemosidinuria

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10
Q

This is a feature of neutrophils in Vit B12 deficiency (also seen in folate deficiency).

A

hypersegmented neutrophils

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11
Q

When would you see spherocytes?

A
hereditary spherocytosis (look at history for clues)
immune hemolytic anemia
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12
Q

What do reticulocytes look like?

A

retics have bluish staining compared to normal RBCs

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13
Q

When would you see bite cells?

A

intravascular hemolysis (like G6PD deficiency, membrane defects, hemoglobin defects)

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14
Q

When do you get aplastic anemia?

A

parvovirus B19 infection

**infects erythroid precursors so all red cell line cells are affected

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15
Q

Immune hemolytic anemia can involve warm agglutinins or cold agglutinins. Which Ig is involved in warm agglutinins? Cold agglutinins?

A

IgG; IgM/complement

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16
Q

When would you use plasmapheresis as treatment?

A

only in intravascular hemolysis (not extravascular)

17
Q

Should you treat a patient for anemia if they are asymptomatic?

A

no!

18
Q

If LDH > 1000, think (blank) hemolysis

If LDH < 1000, think (blank) hemolysis

A

intravascular; extravascular