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Heme/Onc by Minnie: AH Update > 245/246: Congenital and Acquired Hemolytic Anemias > Flashcards

245/246: Congenital and Acquired Hemolytic Anemias Flashcards

1
Q

How long do red blood cells usually live?

A

90-120 days

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2
Q

What is the difference between extracorpuscular and intracorpuscular hemolysis?

A
  • Extracorpuscular = something is attacking the RBC
    • Immunologic (warm or cold antibodies)
    • Mechanical
    • Infectious (malaria or babesiosis)
    • Hypersplenism
  • Intracorpuscular = Something is wrong with the RBC
    • Hemoglobinopathies
    • Enzyme defects
    • Membrane abnormalities (spur cell anemia or PNH)
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3
Q

What hemolytic anemia will demonstrate absent CD55 and CD59 expression on flow cytometry?

A

Paroxysmal nocturnal hemoglobinuria

Acquired disorder of stem cells. Lose PIG-A → normally anchors proteins to the lipid bilayer→ lose membrane associated proteins→ RBCs are destroyed by complement-mediated lysis

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4
Q

Which protein is deficient in Southeast Asian Ovalocytosis?

A

Band 3

Rigidity of of the RBC membrane.

No real clinical symptoms

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5
Q

What is the only FDA-approved, commonly used drug to treat sickle cell disease?

What is its effect?

A

Hydroxyurea

Results in increased fetal Hb

Fetal Hb does not sickle

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6
Q

What is the treatment for spur cell anemia?

A

Liver transplant

  • Spur cell anemia is caused by liver disease
    • -> Membrane defect results in excess cholesterol
    • -> Fragility
    • Achanthocytosis
    • Severe anemia and splenomegaly
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7
Q

List 3 mechanisms by which drugs can induce hemolytic anemia

A
  • Haptan-induced
    • Antibody binds to the drug, that is bound to the RBC
    • Penicillin, cephalosporin, tetracyclinc
  • Immune-complex
    • Antibody binds to the drug-RBC complex
    • Quinine, quinidine, sulfonamides
  • Autoimmune
    • Drug induces formation of antibodies against RBCs
    • Drug does NOT need to be bound to RBC
    • Stopping the drug will not stop the hemolysis immediately

These are all warm hemolytic anemias

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8
Q

Which inherited hemolytic anemia is most common?

Which protein is most commonly mutated in this disorder?

A

Hereditary spherocytosis

  • Deficiency in membrane proteins
    • Ankyrin >> spectrin > band 3
    • -> mechanical instability, membrane loss
    • Spheroid, fragile RBCs
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9
Q

What is the most common cause of death in children with sickle cell disease worldwide?

A

Infection

  • People with SCD are more susceptible to infection by encapsulated bacteria (due to functional asplenia)
  • Viral infections (parvovirus) may trigger an aplastic crisis
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10
Q

What is the mechanism of hemolysis in hereditary spherocytosis?

A

Fragile RBCs are trapped in the spleen

-> Hemolysis

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11
Q

Where in the body is vaso-occlusion due to RBC sickling most likely to occur?

A

Post-capillary venules

  • This is where RBCs have the least oxygen => most prone to sickling
  • Also, these vessels are small
    • Sickling -> log jam -> more sickling -> :(((
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12
Q

List two medical complications associated with sickle cell trait

(one mutated copy, one normal copy)

A

Increased risk of:

  • Chronic kidney disease
  • Venous Thromboembolism

Previously thought that sickle cell trait did not cause any problems and was protective against malaria, but looks like it may confer an increased risk of these conditions in adults. Not clinically significant for kids?

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13
Q

What kind of immunoglobulin (IgM or IgG) is responsible for warm and cold hemolytic anemia?

A
  • Warm: IgG (or complement)
  • Cold: IgM
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14
Q

List 3 important proteins found in the red blood cell membrane

A
  • Band 3
    • Transfers
    • Binds cytoplasmic components of the RBC membrane
    • South Asian Ovalocytosis
  • Spectrin
    • Peripheral
    • Supports the lipid bilayer
    • Hereditary Elliptocytosis
  • Ankyrin
    • Peripheral
    • Links spectrin and Band 3
    • Most common form of Hereditary Spherocytosis
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15
Q

Which virus may lead to an aplastic crisis in patients with sickle cell disease?

A

Parvovirus

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16
Q

What would you suspect if a patient has warm autoimmune hemolytic anemia with low reticulocytes?

A

Suspect secondary process, like iron deficiency

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17
Q

How is G6PD deficiency inherited?

A

X-linked recessive mutation in G6PD gene

Heterozygous 46,XX individuals may have variable expression

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18
Q

List 4 possible genotypes that can result in sickle cell disease

A
  • Hb S/S (most severe clinical disease)
  • Hb S/Beta null
  • Hb S/C
  • Hb S/Beta (+) (least severe)

Wild type is Hb A/A

Basically, any combination of 2 non-A alleles can result in sickled red blood cells

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19
Q

What kind of antibodies are responsible for Rh hemolytic disease of the fetus/newborn?

A

IgG (the Ig that can cross the placenta)

  • Note: ABO antibodies are IgG or IgM, but Rh hemolytic disease more serious (but less common)*
  • Fetus does not produce much ABO antigen as Rh (D) antigen*
20
Q

What mutation causes paroxysmal nocturnal hemoglobinuria?

A

Mutation in phosphatidyl-iositol-glycan A

  • Results in GPI-anchored protein deficiencies
    • Proteins that protect RBC from complement destruction cannot bind (CD55, CD59)
  • Results in complement-mediated lysis or RBCs
21
Q

Which protein is deficient in hereditary eliptocytosis?

A

Alpha or beta spectrin

May result in carrier state or severe condition (hereditary pyropoikilocytosis)

22
Q

List the most common acute complications of sickle cell disease

A
  • Acute pain episodes
  • Acute chest syndrome
  • Functional asplenia
    • -> increased risk of infections w/encapsulated bacteria
  • Splenic sequestration
  • Stroke
  • Aplastic crisis (triggered by parvovirus infection)

End organ damage = later complication

23
Q

What RBC morphology will you see in warm antibody hemolytic anemia?

How are the RBCs destroyed?

A

Spherocytes

Parts of the membrane are chomped off due to antibody binding -> spherocytes

24
Q

List the two hemoglobin “switches” that occur during development

Which globins are present in each type of hemoglobin?

A
  • Embryonic Hb (δ2ε2) -> Fetal Hb (α2γ2)
    • Occurs at 10 weeks gestational age
  • Fetal Hb (α2γ2) -> Adult Hb (α2β2)
    • Occurs after birth, around 6 months fetal Hb will be gone
25
Q

What molecules mediate:

  • Warm antibody autoimmune hemolysis:
  • Cold antibody autoimmune hemolysis:
A
  • Warm antibody autoimmune hemolysis: Antibodies
  • Cold antibody autoimmune hemolysis: Complement
26
Q

List the 2 metabolic pathways that RBCs use to produce energy

What is the major product of each pathway?

A
  • Pentose phosphate pathway: generate NADPH
    • Protection from oxidative stress
  • Glycolysis (anaerobic): ATP
    • Energy!

RBCs cannot produce energy through the Kreb’s cycle because they don’t have mitochondria!

27
Q

What conditions are associated with cold antibody hemolytic anemia? (2 acute, 2 chronic)

A
  • Acute:
    • Mycoplasma
    • EBV
  • Chronic
    • Lymphoproliferative disorders
    • Idiopathic
28
Q

In a patient with sickle cell disease, what is the most common reason for presenting to the ED?

A

Pain crisis

  • Caused by vaso-occlusive episode
29
Q

On which chromosome is each genetic loci found?

  • Beta-globin:
  • Alpha-globin:
A
  • Beta-globin: Chromosome 11
  • Alpha-globin: Chromosome 16

Regulatory components are upstream (toward the 5’) of each locus

30
Q

After RBC sickling, what is the next step in the pathogenesis that eventually leads to pain, disability, and end organ damage?

A

Vaso-occlusion

Most likely to occur in post-capillary venules

(lowest O2 concentration -> RBCs most prone to sickling)

31
Q

What is the treatment for paroxysmal nocturnal hemoglobinuria?

A

Goal is to prevent complement from destroying RBCs

  • Eculizumab
    • Antibody against C5
  • Anticoagulation to prevent thrombosis
  • Stem cell transplant is curative
32
Q

List 6 major pathophysiologic processes that contribute to vaso-occlusion in sickle cell disease

A
  • Inflammation
  • Leukocyte / platelet activation
  • Nitric oxide dysregulation
  • Endothelial dysfunction
  • Hypercoagulability
  • Oxidative stress from reperfusion injury
33
Q

What is the difference in the management of Rh hemolytic disease and ABO hemolytic disease of the newborn?

A
  • Rh hemolytic disease
    • Give anti-D immune globulin to Rh negative pregnant women during all pregnancies, in 3rd trimester, and any time there may be maternal-fetal blood exchange (goal is to prevent mom from developing antibodies; if she has them, goal is to prevent antibodies from killing the baby)
  • ABO hemolytic disease
    • Transfusions in utero before delivery, if there is evidence of hemolysis
    • ABO hemolytic disease is more common, but less serious than Rh hemolytic disease
34
Q

Describe the pathophysiology of hereditary spherocytosis (spherocyte formation)

A

2 possible pathways, depending on which protein is mutated

  • Spectrin or ankyrin deficiency -> Unsupported membrane
  • Band 3 deficiency -> Clustered lipids
  • Both result in budding off of membrane parts -> spherocyte
35
Q

List the 2 primary structural components that make up the RBC membrane

A
  • Lipid bilayer
  • Network of skeletal and transmembrane proteins
36
Q

What defines acute chest syndrome in a patient with sickle cell disease? (3)

A

Fever + Abnormal chest X-ray + Any respiratory sign/sx

  • Etiology is multifactorial
    • Infection, pulmonary infarction, fat emboli
    • Often preceded by pain episode
37
Q

What is actually happening in a red blood cell when it sickles?

What is the major trigger for sickling?

A

Polymerization -> sickling

Occurs during deoxygenation

Sickling may be exacerbated by:

  • Increased HbS concentration
  • More acidic pH
  • Cation homeostasis: activation of the KCl cotransporter
  • Dehydration
38
Q

What is the major complication that results from Paroxysmal nocturnal hemoglobinuria?

A

Thrombis, especially in unusual sites

  • Portal vein
  • Cerebral vessels
  • Cutaneous veins

Results from complemented-mediated destruction of RBCs -> membranes in the circulation -> clots

39
Q

What does the Direct Coombs Test detect?

How does it work?

A

Detects auto-antibody or complement directly bound to patient’s RBCs

  • Take pt’s RBCs, add standard antiglobulin (ex: anti-IgG, anti-IgM, anti-complement, or a mix)
  • Look to see if these antiglobulins bind to the pt’s RBCs (clumping)
    • If so, they are bound to IgG, IgM, complement (depending on the antiglobulin use
  • Usually do all anti-globulins together, and then if positive do them individually*
  • Indirect Coombs takes normal RBCs and mixes with pt plasma, detects both autoantibodies and alloantibodies*
40
Q

Describe the mutation and resulting amino acid substitution that causes sickle hemoglobin

A

A -> T in the 6th codon of the beta-globin gene

Results in glutamic acid -> valine substitution

41
Q

How will the following change in hemolytic anemia?

  • Reticulocytes:
  • Haptoglobin:
  • BIlirubin:
  • LDH:
A

Hemolytic anemia

  • Reticulocytes: Increased
  • Haptoglobin: Decreased
  • BIlirubin: Increased indirect
  • LDH: Increased

Differences in amt of change in extravascular vs. intravascular

42
Q

What red blood cell morphology will result from pyruvate kinase deficiency?

A

Echinocytes (Burr cells)

43
Q

Describe the pathophysiology of cold antibody hemolytic anemia

A

Cold agglutinin antibodies (usually IgM) interact with polysaccharides on the RBC surface

44
Q

List 2 scenarios in which 46,XX individuals who are heterozygous for G6PD deficiency will be symptomatic

A
  • X chromosome inactivation
  • Skewed lyonization
45
Q

What does the Indirect Coombs Test detect?

How does it work?

A

Can find both autoantibodies and alloantibodies in the patient’s plasma

Pts may have developed antibodies to previously transfused blood

  • Mix normal RBCs with patient’s plasma
  • If binding occurs, implies that there are antibodies in the plasma

vs. Direct coombs measures antibodies that are bound to RBCs, can only detect autoantibodies

46
Q

What is the mechanism of action of hemolysis in G6PD deficiency?

A

No G6PD -> cannot make NADPH -> cannot reduce glutathione

-> cannot deal with oxidative stress

Oxidative stress -> hemoglobin denatures -> hemolysis

Will see Heinz bodies and Bite Cells in RBCs

Heme/Onc by Minnie: AH Update (36 decks)

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