Deck 10: Abnormalities of White Blood Cells: Quantitative, Qualitative, and the Lipid Storage Diseases

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Question
Opsonization of foreign bodies is defined as:

A) Preparing a foreign body for phagocytosis
B) Degranulation of neutrophils
C) Fusion of cytoplasmic granules
D) Bacteriocidal activity
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Question
A 17-year-old boy is admitted to the hospital with a fever of unknown origin.His WBC count is 20.0 109/L.All of the following can be seen on his peripheral smear except:

A) Toxic granulation
B) Reactive monocytes
C) Increased band neutrophils
D) Dohle bodies
Question
All of the following are lipid storage syndromes/diseases except:

A) Gaucher's disease
B) Tay-Sachs disease
C) Chediak-Higashi syndrome
D) Niemann-Pick disease
Question
A patient who presents with a low white cell count, thrombocytopenia, elevated liver enzymes, and mulberry-like inclusions in the granulocytes is most likely suffering from:

A) May-Hegglin anomaly
B) Chediak-Higashi anomaly
C) Human ehrlichiosis
D) Alder's anomaly
Question
Infectious mononucleosis is caused by the EBV virus, which infects B lymphocytes.
Question
All of the following are mechanisms by which neutropenia is usually produced except:

A) Decreased production by the bone marrow
B) Impaired release from the bone marrow to the blood
C) Increased destruction
D) Bacterial infection
Question
Dohle bodies consist of:

A) DNA
B) Primary granules
C) Ribosomes RNA
D) Lipid deposits
Question
Toxic vacuolization occurs most frequently in:

A) Neutrophils
B) Monocytes
C) Lymphocytes
D) Erythrocytes
Question
Pelger-Huët anomaly is characterized mainly by:

A) Neutrophils with gray-green granules
B) Lipid depositions in the cytoplasm
C) Giant platelets
D) Hyposegmentation of the nucleus in the neutrophils
Question
In which white cell disorder will you see gray-green cytoplasmic granules in the neutrophils?

A) May-Hegglin anomaly
B) Alder's anomaly
C) Pelger-Huët anomaly
D) Chediak-Higashi syndrome
Question
A patient who has a persist leukocytosis, Dohle bodies, and an elevated LAP score most likely has a (an):

A) Leukemoid reaction
B) Pelger-Huët anomaly
C) Parasitic infection
D) HIV infection
Question
Toxic granulation in neutrophils is a direct result of:

A) Cytokine production
B) Enhanced lysosome enzyme production
C) Toxic granulation
D) Ehrlichia infection
Question
The normal ratio of CD4 to CD8 lymphocytes is:

A) 1:2
B) 1:1
C) 2:1
D) 4:1
Question
<strong>  Name the cell at the tip of the pointer (Wright stain).</strong> A) Spherocyte B) Target cell C) Platelet D) Acanthocyte <div style=padding-top: 35px>
Name the cell at the tip of the pointer (Wright stain).

A) Spherocyte
B) Target cell
C) Platelet
D) Acanthocyte
Question
In which white cell disorder will you see prominent deposition of granules in every cell line?

A) May-Hegglin anomaly
B) Alder's anomaly
C) Pelger-Huët anomaly
D) Chediak-Higashi syndrome
Question
A typical blood picture in infectious mononucleosis is an absolute:

A) Lymphocytosis and anemia with many reactive lymphocytes
B) Lymphocytosis without anemia and many reactive lymphocytes
C) Monocytosis and anemia with many atypical monocytes
D) Monocytosis without anemia and many atypical monocytes
Question
The best corrective action for a patient who exhibits platelet satellitism on peripheral blood smear is to:

A) Make a duplicate slide and see if this phenomenon disappears
B) Warm the tube of blood
C) Redraw the sample in sodium citrate
D) Vortex the sample of blood
Question
Which of the following statements is common to most lipid storage diseases?

A) They are caused by an amino acid substitution.
B) They are caused by a DNA synthetic defect.
C) They are caused by a missing metabolic enzyme.
D) They are caused by the invasion of a rickettsial organism.
Question
Which of the following is an unusual complication that may occur in infectious mononucleosis?

A) Splenic infarctions
B) Dactylitis
C) Hemolytic anemia
D) Giant platelets
Question
An autosomal disorder that manifests itself with large lysosomal inclusions, recurring infections, and albinism is:

A) Chediak-Higashi
B) Pelger-Huët
C) May-Hegglin
D) Alder-Reilly
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Deck 10: Abnormalities of White Blood Cells: Quantitative, Qualitative, and the Lipid Storage Diseases
1
Opsonization of foreign bodies is defined as:

A) Preparing a foreign body for phagocytosis
B) Degranulation of neutrophils
C) Fusion of cytoplasmic granules
D) Bacteriocidal activity
A
2
A 17-year-old boy is admitted to the hospital with a fever of unknown origin.His WBC count is 20.0 109/L.All of the following can be seen on his peripheral smear except:

A) Toxic granulation
B) Reactive monocytes
C) Increased band neutrophils
D) Dohle bodies
B
3
All of the following are lipid storage syndromes/diseases except:

A) Gaucher's disease
B) Tay-Sachs disease
C) Chediak-Higashi syndrome
D) Niemann-Pick disease
C
4
A patient who presents with a low white cell count, thrombocytopenia, elevated liver enzymes, and mulberry-like inclusions in the granulocytes is most likely suffering from:

A) May-Hegglin anomaly
B) Chediak-Higashi anomaly
C) Human ehrlichiosis
D) Alder's anomaly
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k this deck
5
Infectious mononucleosis is caused by the EBV virus, which infects B lymphocytes.
Unlock Deck
Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
6
All of the following are mechanisms by which neutropenia is usually produced except:

A) Decreased production by the bone marrow
B) Impaired release from the bone marrow to the blood
C) Increased destruction
D) Bacterial infection
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Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
7
Dohle bodies consist of:

A) DNA
B) Primary granules
C) Ribosomes RNA
D) Lipid deposits
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Unlock Deck
k this deck
8
Toxic vacuolization occurs most frequently in:

A) Neutrophils
B) Monocytes
C) Lymphocytes
D) Erythrocytes
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Unlock Deck
k this deck
9
Pelger-Huët anomaly is characterized mainly by:

A) Neutrophils with gray-green granules
B) Lipid depositions in the cytoplasm
C) Giant platelets
D) Hyposegmentation of the nucleus in the neutrophils
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Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
10
In which white cell disorder will you see gray-green cytoplasmic granules in the neutrophils?

A) May-Hegglin anomaly
B) Alder's anomaly
C) Pelger-Huët anomaly
D) Chediak-Higashi syndrome
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Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
11
A patient who has a persist leukocytosis, Dohle bodies, and an elevated LAP score most likely has a (an):

A) Leukemoid reaction
B) Pelger-Huët anomaly
C) Parasitic infection
D) HIV infection
Unlock Deck
Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
12
Toxic granulation in neutrophils is a direct result of:

A) Cytokine production
B) Enhanced lysosome enzyme production
C) Toxic granulation
D) Ehrlichia infection
Unlock Deck
Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
13
The normal ratio of CD4 to CD8 lymphocytes is:

A) 1:2
B) 1:1
C) 2:1
D) 4:1
Unlock Deck
Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
14
<strong>  Name the cell at the tip of the pointer (Wright stain).</strong> A) Spherocyte B) Target cell C) Platelet D) Acanthocyte
Name the cell at the tip of the pointer (Wright stain).

A) Spherocyte
B) Target cell
C) Platelet
D) Acanthocyte
Unlock Deck
Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
15
In which white cell disorder will you see prominent deposition of granules in every cell line?

A) May-Hegglin anomaly
B) Alder's anomaly
C) Pelger-Huët anomaly
D) Chediak-Higashi syndrome
Unlock Deck
Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
16
A typical blood picture in infectious mononucleosis is an absolute:

A) Lymphocytosis and anemia with many reactive lymphocytes
B) Lymphocytosis without anemia and many reactive lymphocytes
C) Monocytosis and anemia with many atypical monocytes
D) Monocytosis without anemia and many atypical monocytes
Unlock Deck
Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
17
The best corrective action for a patient who exhibits platelet satellitism on peripheral blood smear is to:

A) Make a duplicate slide and see if this phenomenon disappears
B) Warm the tube of blood
C) Redraw the sample in sodium citrate
D) Vortex the sample of blood
Unlock Deck
Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
18
Which of the following statements is common to most lipid storage diseases?

A) They are caused by an amino acid substitution.
B) They are caused by a DNA synthetic defect.
C) They are caused by a missing metabolic enzyme.
D) They are caused by the invasion of a rickettsial organism.
Unlock Deck
Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
19
Which of the following is an unusual complication that may occur in infectious mononucleosis?

A) Splenic infarctions
B) Dactylitis
C) Hemolytic anemia
D) Giant platelets
Unlock Deck
Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
20
An autosomal disorder that manifests itself with large lysosomal inclusions, recurring infections, and albinism is:

A) Chediak-Higashi
B) Pelger-Huët
C) May-Hegglin
D) Alder-Reilly
Unlock Deck
Unlock for access to all 20 flashcards in this deck.
Unlock Deck
k this deck
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Unlock for access to all 20 flashcards in this deck.