Deck 9: Introduction to Hemolytic Anemias: Intracorpuscular Defects: I Hereditary Defects of the Red Cell Membrane

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Question
Which of the following is the major type of hemolysis characteristic of the majority of cases of HS?

A) Extravascular hemolysis
B) Intravascular hemolysis
C) No hemolysis
D) Both A and B
E) None of the above
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Question
Once a hemolytic anemia is determined, which of the following tests would rule out an immune hemolytic anemia if negative?

A) Coombs' test (direct antiglobulin test [DAT])
B) Osmotic fragility
C) Autohemolysis test
D) Red cell indices
E) None of the above
Question
The majority of hereditary RBC membrane defects are inherited by what pattern?

A) Autosomal dominant
B) Autosomal recessive
C) Sex-linked
D) Codominant
E) None of the above
Question
The reticulocyte production index (RPI) corrects the hematocrit to a normal value of which percentage, and takes into account the maturation time of the reticulocyte at a particular hematocrit?

A) 35%
B) 25%
C) 55%
D) 45%
E) None of the above
Question
Which RBC membrane skeletal protein represents a dimer of two highly flexible alpha and beta chains that forms tetramers in the membrane?

A) Actin
B) Ankyrin
C) Glycophorin
D) Protein 4.1
E) Spectrin
Question
Staining the urine sediment for iron with Prussian blue will detect which of the following during a hemolytic anemia?

A) Hemoglobin
B) Hemosiderin
C) Methemalbumin
D) Haptoglobin
E) None of the above
Question
An RPI of greater than __________ is generally regarded as indicative of a hemolytic state.

A) 2.5-3.0
B) 1-1.5
C) 0-1
D) 4-5
E) 5-6
Question
Which of the following are classic clinical manifestations of hereditary spherocytosis (HS)?

A) Jaundice
B) Anemia
C) Enlarged spleen
D) Mild uncompensated hemolytic anemia
E) All of the above
Question
The normal bone marrow is able to increase its output how many times to compensate for anemia?

A) 6-8 times
B) 1-2 times
C) 2-4 times
D) 15-18 times
E) 10-12 times
Question
Which of the following represents a normal reticulocyte count in an adult?

A) 4-6%
B) 8-10%
C) 0.5-2.0%
D) 10-12%
E) None of the above
Question
The major components of the red cell membrane skeleton are:

A) Spectrin
B) Actin
C) Protein 4.1
D) All of the above
E) None of the above
Question
Which of the following characterizes hereditary spherocytosis (HS)?

A) Decreased surface-to-volume ratio
B) Increased MCHC
C) Hemolytic anemia
D) Spherocytes on the peripheral smear
E) All of the above
Question
Which of the following membrane defects is the most common hereditary hemolytic anemia in Caucasians?

A) Hereditary elliptocytosis
B) Hereditary spherocytosis
C) Thalassemia
D) Hereditary pyropoikilocytosis
E) None of the above
Question
The morphologic hallmark of HS hereditary spherocytosis on the peripheral blood smear is:

A) Polychromasia
B) Ovalocytes
C) Spherocytes
D) Poikilocytes
E) Sickle cells
Question
Which of the following RPI results will suggest an inadequate response of erythropoiesis by bone marrow in response to anemia?

A) >3.0
B) 2.0-3.0
C) <2.0
D) 2.5
E) None of the above
Question
Which of the following represents hereditary intracorpuscular defects?

A) Red blood cell (RBC) membrane defects
B) Enzyme deficiencies
C) Hemoglobinopathies
D) Thalassemia
E) All of the above
Question
What does (HE) (4.1) denote?

A) Hereditary spherocytosis with the absence of spectrin
B) Hereditary elliptocytosis with the absence of protein 4.1
C) Hereditary elliptocytosis with the absence of spectrin
D) Hereditary elliptocytosis with a partial deficiency of protein 4.1
E) None of the above
Question
Which of the following tests reflect an increase in red cell destruction?

A) Bilirubinemia
B) Hemoglobinemia
C) Hemoglobinuria
D) Hemosiderinuria
E) All of the above
Question
Which of the following represent extracorpuscular defects?

A) Immune hemolytic anemias
B) Infections
C) Microangiopathic hemolytic anemia
D) Hypersplenism
E) All of the above
Question
In a hemolytic anemia, the first normal compensatory bone marrow response will be reflected in which of the following?

A) Decrease in reticulocyte count
B) Increase in RBC count
C) Increase in reticulocyte count
D) Increase in MCHC (mean corpuscular hemoglobin concentration)
E) None of the above
Question
Which of the following laboratory results is not characteristic of HPP?

A) Low MCV
B) Increase in osmotic fragility
C) Increase in autohemolysis test
D) RBC thermal instability at 45°C leading to fragmentation
E) Normal MCV
Question
Which of the following is the most common treatment for most patients with HS?

A) Exchange transfusion
B) Chemotherapy
C) Splenectomy
D) No treatment
E) None of the above
Question
Which of the following represent the major clinical and morphologic syndromes of HE?

A) Common HE (minimal or no hemolysis)
B) Spherocytic HE (hybrid of mild HE and HS)
C) Stomatocytic HE (common only in Melanesians)
D) All of the above
E) None of the above
Question
Which of the following is characteristic of HE?

A) Elliptocytes in the peripheral blood (>30%)
B) Demonstrates variable linkage to the Rh gene
C) Most often inherited autosomal dominant
D) Demonstrates a biochemical and genetic relationship to HPP
E) All of the above
Question
Which of the following is characteristic of HPP?

A) Microspherocytosis
B) Partial deficiency of spectrin
C) RBC fragmentation and micropoikilocytosis
D) Thermal instability of red cells when heated to 45°C in vitro
E) All of the above
Question
Which of the following is not characteristic of hereditary xerocytosis?

A) Presence of red cells with hemoglobin concentration in one part of the cell
B) Increase in MCV and increase in MCHC
C) Decrease in osmotic fragility test
D) Altered permeability of RBC membrane showing increased influx of potassium
E) Decreased MCV and decreased MCHC
Question
What does the autohemolysis test measure?

A) Surface-to-volume ratio of the RBC
B) Structural and metabolic integrity of RBC membrane
C) Amount of RBC membrane spectrin
D) RBC metabolic pathways
E) None of the above
Question
Which of the following laboratory results is characteristic of the common type of HE?

A) Normal RBC indices (MCV, MCH, MCHC)
B) Normal osmotic fragility
C) Normal autohemolysis test
D) Greater then 75% elliptocytes on the peripheral smear of many patients
E) All of the above
Question
Which of the following laboratory results are characteristic of HS?

A) Increased MCHC
B) Abnormal osmotic fragility test
C) Abnormal autohemolysis test
D) Normal MCV (mean corpuscular volume) and MCH (mean corpuscular hemoglobin)
E) All of the above
Question
Which of the following may be found on the peripheral smear of a patient with HS (hereditary spherocytosis) prior to splenectomy?

A) Spherocytes
B) Polychromasia
C) Poikilocytes
D) Anisocytosis
E) All of the above
Question
A 40-year-old patient was admitted to the hospital with acute cholecystitis and a palpable spleen. A CBC was performed: Hemoglobin, 13.0 g/dL; MCV, 80 fL; Hct, 38%; MCH, 28 pg; Retic, 7%; MCHC, 36%; RPI, 3.9; Coombs' test negative; spherocytes, 2+; anisocytosis, 2+; poikilocytosis, 2+. Which of the following disorders is consistent with the laboratory profile?

A) Autoimmune hemolytic anemia
B) Thalassemia
C) Hereditary elliptocytosis (HE)
D) Hereditary spherocytosis (HS)
E) Hereditary pyropoikilocytosis (HPP)
Question
Which of the following laboratory results would be found in a patient with spherocytosis associated with autoimmune hemolytic anemia?

A) No correction of the autohemolysis test with glucose
B) Some correction of the autohemolysis test with the addition of glucose
C) Normal incubated osmotic fragility test
D) Abnormal radioimmunoassay for spectrin
E) All of the above
Question
Which of the following represents the pattern of inheritance of hereditary pyropoikilocytosis (HPP)?

A) Autosomal recessive
B) Autosomal dominant
C) X-linked
D) Any of the above
E) Acquired, not inherited
Question
What does the osmotic fragility test measure?

A) Surface-to-volume ratio of the RBC
B) Structural and metabolic integrity of RBC membrane
C) Amount of RBC membrane spectrin
D) RBC metabolic pathways
E) None of the above
Question
Which of the following is not characteristic of hereditary hydrocytosis (stomatocytosis)?

A) Inherited autosomal dominant
B) Presence of stomatocytes on the peripheral smear
C) Increased passive permeability of sodium into red cell and potassium out of red cell
D) Increased MCV and decreased MCHC
E) Decreased MCV and increased MCHC
Question
Which of the following describes the procedure of the autohemolysis test?

A) Incubation of patient RBCs with a series of graded hypotonic salt solutions
B) Sterile incubation of patient RBCs in their own plasma for 48 hours at 37°C
C) Sterile incubation of patient RBCs in their own plasma for 24 hours at 25°C
D) Sterile incubation of patient RBCs in their own plasma for 72 hours at 56°C
E) None of the above
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Deck 9: Introduction to Hemolytic Anemias: Intracorpuscular Defects: I Hereditary Defects of the Red Cell Membrane
1
Which of the following is the major type of hemolysis characteristic of the majority of cases of HS?

A) Extravascular hemolysis
B) Intravascular hemolysis
C) No hemolysis
D) Both A and B
E) None of the above
Extravascular hemolysis
2
Once a hemolytic anemia is determined, which of the following tests would rule out an immune hemolytic anemia if negative?

A) Coombs' test (direct antiglobulin test [DAT])
B) Osmotic fragility
C) Autohemolysis test
D) Red cell indices
E) None of the above
Coombs' test (direct antiglobulin test [DAT])
3
The majority of hereditary RBC membrane defects are inherited by what pattern?

A) Autosomal dominant
B) Autosomal recessive
C) Sex-linked
D) Codominant
E) None of the above
Autosomal dominant
4
The reticulocyte production index (RPI) corrects the hematocrit to a normal value of which percentage, and takes into account the maturation time of the reticulocyte at a particular hematocrit?

A) 35%
B) 25%
C) 55%
D) 45%
E) None of the above
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Unlock Deck
k this deck
5
Which RBC membrane skeletal protein represents a dimer of two highly flexible alpha and beta chains that forms tetramers in the membrane?

A) Actin
B) Ankyrin
C) Glycophorin
D) Protein 4.1
E) Spectrin
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
6
Staining the urine sediment for iron with Prussian blue will detect which of the following during a hemolytic anemia?

A) Hemoglobin
B) Hemosiderin
C) Methemalbumin
D) Haptoglobin
E) None of the above
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
7
An RPI of greater than __________ is generally regarded as indicative of a hemolytic state.

A) 2.5-3.0
B) 1-1.5
C) 0-1
D) 4-5
E) 5-6
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8
Which of the following are classic clinical manifestations of hereditary spherocytosis (HS)?

A) Jaundice
B) Anemia
C) Enlarged spleen
D) Mild uncompensated hemolytic anemia
E) All of the above
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
9
The normal bone marrow is able to increase its output how many times to compensate for anemia?

A) 6-8 times
B) 1-2 times
C) 2-4 times
D) 15-18 times
E) 10-12 times
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
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10
Which of the following represents a normal reticulocyte count in an adult?

A) 4-6%
B) 8-10%
C) 0.5-2.0%
D) 10-12%
E) None of the above
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Unlock for access to all 36 flashcards in this deck.
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11
The major components of the red cell membrane skeleton are:

A) Spectrin
B) Actin
C) Protein 4.1
D) All of the above
E) None of the above
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
12
Which of the following characterizes hereditary spherocytosis (HS)?

A) Decreased surface-to-volume ratio
B) Increased MCHC
C) Hemolytic anemia
D) Spherocytes on the peripheral smear
E) All of the above
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Unlock for access to all 36 flashcards in this deck.
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k this deck
13
Which of the following membrane defects is the most common hereditary hemolytic anemia in Caucasians?

A) Hereditary elliptocytosis
B) Hereditary spherocytosis
C) Thalassemia
D) Hereditary pyropoikilocytosis
E) None of the above
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14
The morphologic hallmark of HS hereditary spherocytosis on the peripheral blood smear is:

A) Polychromasia
B) Ovalocytes
C) Spherocytes
D) Poikilocytes
E) Sickle cells
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
15
Which of the following RPI results will suggest an inadequate response of erythropoiesis by bone marrow in response to anemia?

A) >3.0
B) 2.0-3.0
C) <2.0
D) 2.5
E) None of the above
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
16
Which of the following represents hereditary intracorpuscular defects?

A) Red blood cell (RBC) membrane defects
B) Enzyme deficiencies
C) Hemoglobinopathies
D) Thalassemia
E) All of the above
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
17
What does (HE) (4.1) denote?

A) Hereditary spherocytosis with the absence of spectrin
B) Hereditary elliptocytosis with the absence of protein 4.1
C) Hereditary elliptocytosis with the absence of spectrin
D) Hereditary elliptocytosis with a partial deficiency of protein 4.1
E) None of the above
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
18
Which of the following tests reflect an increase in red cell destruction?

A) Bilirubinemia
B) Hemoglobinemia
C) Hemoglobinuria
D) Hemosiderinuria
E) All of the above
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
19
Which of the following represent extracorpuscular defects?

A) Immune hemolytic anemias
B) Infections
C) Microangiopathic hemolytic anemia
D) Hypersplenism
E) All of the above
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
20
In a hemolytic anemia, the first normal compensatory bone marrow response will be reflected in which of the following?

A) Decrease in reticulocyte count
B) Increase in RBC count
C) Increase in reticulocyte count
D) Increase in MCHC (mean corpuscular hemoglobin concentration)
E) None of the above
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
21
Which of the following laboratory results is not characteristic of HPP?

A) Low MCV
B) Increase in osmotic fragility
C) Increase in autohemolysis test
D) RBC thermal instability at 45°C leading to fragmentation
E) Normal MCV
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Unlock Deck
k this deck
22
Which of the following is the most common treatment for most patients with HS?

A) Exchange transfusion
B) Chemotherapy
C) Splenectomy
D) No treatment
E) None of the above
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
23
Which of the following represent the major clinical and morphologic syndromes of HE?

A) Common HE (minimal or no hemolysis)
B) Spherocytic HE (hybrid of mild HE and HS)
C) Stomatocytic HE (common only in Melanesians)
D) All of the above
E) None of the above
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
24
Which of the following is characteristic of HE?

A) Elliptocytes in the peripheral blood (>30%)
B) Demonstrates variable linkage to the Rh gene
C) Most often inherited autosomal dominant
D) Demonstrates a biochemical and genetic relationship to HPP
E) All of the above
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
25
Which of the following is characteristic of HPP?

A) Microspherocytosis
B) Partial deficiency of spectrin
C) RBC fragmentation and micropoikilocytosis
D) Thermal instability of red cells when heated to 45°C in vitro
E) All of the above
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
26
Which of the following is not characteristic of hereditary xerocytosis?

A) Presence of red cells with hemoglobin concentration in one part of the cell
B) Increase in MCV and increase in MCHC
C) Decrease in osmotic fragility test
D) Altered permeability of RBC membrane showing increased influx of potassium
E) Decreased MCV and decreased MCHC
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
27
What does the autohemolysis test measure?

A) Surface-to-volume ratio of the RBC
B) Structural and metabolic integrity of RBC membrane
C) Amount of RBC membrane spectrin
D) RBC metabolic pathways
E) None of the above
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
28
Which of the following laboratory results is characteristic of the common type of HE?

A) Normal RBC indices (MCV, MCH, MCHC)
B) Normal osmotic fragility
C) Normal autohemolysis test
D) Greater then 75% elliptocytes on the peripheral smear of many patients
E) All of the above
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Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
29
Which of the following laboratory results are characteristic of HS?

A) Increased MCHC
B) Abnormal osmotic fragility test
C) Abnormal autohemolysis test
D) Normal MCV (mean corpuscular volume) and MCH (mean corpuscular hemoglobin)
E) All of the above
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k this deck
30
Which of the following may be found on the peripheral smear of a patient with HS (hereditary spherocytosis) prior to splenectomy?

A) Spherocytes
B) Polychromasia
C) Poikilocytes
D) Anisocytosis
E) All of the above
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
31
A 40-year-old patient was admitted to the hospital with acute cholecystitis and a palpable spleen. A CBC was performed: Hemoglobin, 13.0 g/dL; MCV, 80 fL; Hct, 38%; MCH, 28 pg; Retic, 7%; MCHC, 36%; RPI, 3.9; Coombs' test negative; spherocytes, 2+; anisocytosis, 2+; poikilocytosis, 2+. Which of the following disorders is consistent with the laboratory profile?

A) Autoimmune hemolytic anemia
B) Thalassemia
C) Hereditary elliptocytosis (HE)
D) Hereditary spherocytosis (HS)
E) Hereditary pyropoikilocytosis (HPP)
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
32
Which of the following laboratory results would be found in a patient with spherocytosis associated with autoimmune hemolytic anemia?

A) No correction of the autohemolysis test with glucose
B) Some correction of the autohemolysis test with the addition of glucose
C) Normal incubated osmotic fragility test
D) Abnormal radioimmunoassay for spectrin
E) All of the above
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
33
Which of the following represents the pattern of inheritance of hereditary pyropoikilocytosis (HPP)?

A) Autosomal recessive
B) Autosomal dominant
C) X-linked
D) Any of the above
E) Acquired, not inherited
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
34
What does the osmotic fragility test measure?

A) Surface-to-volume ratio of the RBC
B) Structural and metabolic integrity of RBC membrane
C) Amount of RBC membrane spectrin
D) RBC metabolic pathways
E) None of the above
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
35
Which of the following is not characteristic of hereditary hydrocytosis (stomatocytosis)?

A) Inherited autosomal dominant
B) Presence of stomatocytes on the peripheral smear
C) Increased passive permeability of sodium into red cell and potassium out of red cell
D) Increased MCV and decreased MCHC
E) Decreased MCV and increased MCHC
Unlock Deck
Unlock for access to all 36 flashcards in this deck.
Unlock Deck
k this deck
36
Which of the following describes the procedure of the autohemolysis test?

A) Incubation of patient RBCs with a series of graded hypotonic salt solutions
B) Sterile incubation of patient RBCs in their own plasma for 48 hours at 37°C
C) Sterile incubation of patient RBCs in their own plasma for 24 hours at 25°C
D) Sterile incubation of patient RBCs in their own plasma for 72 hours at 56°C
E) None of the above
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Unlock Deck
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