1.3 Hypochromic and Microcytic Anemias Flashcards

1
Q

The osmotic fragility test result in a patient with thalassemia major would most likely show:
A. Increased hemolysis
B. Decreased hemolysis
C. Normal resistance to hemolysis
D. Decreased hemolysis after incubation at 37C

A

B. Decreased hemolysis

Osmotic fragility is decreased because numerous target cells are present and have increased surface volume in patients with thalassemia major.

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2
Q

All of the following are characteristics findings in a patient with IDA except:
A. Microcytic, hypochromic RBC morphology
B. Decreased serum iron and ferritin levels
C. Decreased total iron-binding capacity (TIBC)
D. Increased RBC protoporhyrin

A

C. Decreased total iron-binding capacity (TIBC)

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3
Q

IDA may be distinguished from anemia of chronic infection by:
A. Serum iron level
B. RBC morphology
C. RBC indices
D. TIBC

A

D. TIBC

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4
Q

Which anemia has RBC morphology similar to that seen in IDA (Iron deficiency anemia)?
A. Sickle cell anemia
B. Thalassemia syndrome
C. Pernicious anemia
D. HS

A

B. Thalassemia syndrome

Thalassemia and IDA are both classified as microcytic, hypochromic anemias. IDA is caused by defective heme synthesis, whereas thalassemia is caused by decreased globin chain synthesis.

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5
Q

IDA is characterized by:
A. Decreased plasma iron, decreased % saturation, increased TIBC
B. Decreased plasma iron, decreased % plasma ferritin, normal RBC porphyrin
C. Decreased plasma iron, decreased % saturation, decreased TIBC
D. Decreased plasma iron, increased % saturation, decreased TIBC

A

A. Decreased plasma iron, decreased % saturation, increased TIBC

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6
Q

Storage iron is usually best determined by:
A. Serum transferrin levels
B. Hgb values
C. Myoglobin values
D. Serum ferritin levels

A

D. Serum ferritin levels

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7
Q

All of the following are associated with sideroblastic anemia except:
A. Increased serum iron
B. Ringed sideroblasts
C. Hypochromic anemia
D. Decreased serum ferritin

A

D. Decreased serum ferritin

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8
Q

What is the basic hematological defect seen in patients with thalassemia major?
A. DNA synthetic defect
B. Hgb structure
C. Beta-chain synthesis
D. Hgb phosphorylation

A

C. Beta-chain synthesis

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9
Q

Which of the following is the primary Hgb in patients with thalassemia major?
A. Hgb D
B. Hgb A
C. Hgb C
D. Hgb F

A

D. Hgb F

Patients with thalassemia major are unable to synthesize the Beta-chain; hence, little or no Hgb A is produced. However, y-chains continue to be synthesized and lead to variable elevations of Hgb F in these patients.

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10
Q

A patient has an Hct of 30%, an Hgb of 8 g/dL, and a RBC count of 4.0 x 10^12/L. What is the morphological classification of this anemia?
A. Normocytic, normochromic
B. Macrocytic, hypochromic
C. Microcytic, hypochromic
D. Normocytic, hyperchromic

A

C. Microcytic, hypochromic

The indices will provide a morphological classification of this anemia. MCV is 75 fL ( reference range 80-100 fL), MCH is 20 pg ( reference range 27-31 pg), and MCHC is 26.6% (reference range 32-36%). Therefore, the anemia is microcytic hypochromic.

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11
Q

In which of the following conditions is Hgb A2 elevated?
A. Hgb H
B. Hgb SC disease
C. Beta-thalassemia minor
D. Hgb S trait

A

C. Beta-thalassemia minor

In thalassemia major, there is little or no prodution of the Beta-chain, resulting in severly depressed or no synthesis of Hgb A. Severe anemia is seen, along with skeletal abnormalitites and marked splenomegaly. The patient is usually supported with transfusion therapy.

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12
Q

Which of the following parameters may be similar for the anemia of inflammation and IDA?
A. Normocytic indices
B. Decreased serum iron concentration
C. Ringed sideroblasts
D. Pappenheimer bodies

A

B. Decreased serum iron concentration

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