Deck 20: Chronic Lymphocytic Leukemia and Related Lymphoproliferative Disorders
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Unlock Deck
Sign up to unlock the cards in this deck!
Unlock Deck
Unlock Deck
1/29
Play
Full screen (f)
Deck 20: Chronic Lymphocytic Leukemia and Related Lymphoproliferative Disorders
1
All of the following are features of CLL except:
A) Monoclonality
B) Polyclonality
C) Hypogammaglobulinemia
D) Autoimmune disease
E) None of the above
A) Monoclonality
B) Polyclonality
C) Hypogammaglobulinemia
D) Autoimmune disease
E) None of the above
Polyclonality
2
The final diagnosis of any lymphoproliferative disorder encompasses clinical data obtained from __________ analysis.
A) Morphologic
B) Histologic
C) Immunologic
D) All of the above
E) None of the above
A) Morphologic
B) Histologic
C) Immunologic
D) All of the above
E) None of the above
All of the above
3
What age group does CLL primarily affect?
A) 4-20 years
B) 20-40 years
C) >50 years
D) 1-5 years
E) None of the above
A) 4-20 years
B) 20-40 years
C) >50 years
D) 1-5 years
E) None of the above
>50 years
4
Diagnosis of CLL can be confirmed immunologically by the use of monoclonal antibodies that detect __________ antigens.
A) Cluster differentiation (CD)
B) Chromosome designation
C) Cytoplasmic differentiation
D) Leukocyte differentiation
E) None of the above
A) Cluster differentiation (CD)
B) Chromosome designation
C) Cytoplasmic differentiation
D) Leukocyte differentiation
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
5
Clinical features of CLL include all of the following except:
A) Absolute lymphocytosis
B) Splenomegaly
C) Axial lymphadenopathy
D) Thrombocytosis
E) None of the above
A) Absolute lymphocytosis
B) Splenomegaly
C) Axial lymphadenopathy
D) Thrombocytosis
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
6
What is the classification of anemia in CLL?
A) Macrocytic/hyperchromic
B) Normocytic/normochromic
C) Microcytic/hypochromic
D) Microcytic/normochromic
E) None of the above
A) Macrocytic/hyperchromic
B) Normocytic/normochromic
C) Microcytic/hypochromic
D) Microcytic/normochromic
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
7
A cell that could suggest that lymphocytes in CLL are not normal is a:
A) Smudge cell
B) Lymphoblast
C) Monoblast
D) All of the above
E) None of the above
A) Smudge cell
B) Lymphoblast
C) Monoblast
D) All of the above
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
8
CLL has been known to occur simultaneously with what hematologic disorder?
A) Acute myeloblastic leukemia (AML)
B) Acute lymphocytic leukemia (ALL)
C) Non-Hodgkin's lymphoma
D) Hairy cell leukemia
E) None of the above
A) Acute myeloblastic leukemia (AML)
B) Acute lymphocytic leukemia (ALL)
C) Non-Hodgkin's lymphoma
D) Hairy cell leukemia
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
9
The laboratory test for detecting minimal residual disease in patients who have previously been treated for CLL but currently lack histopathologic evidence of relapse is the:
A) Polymerase chain reaction (PCR)
B) Complete blood count (CBC) and differential
C) Electrophoresis
D) All of the above
E) None of the above
A) Polymerase chain reaction (PCR)
B) Complete blood count (CBC) and differential
C) Electrophoresis
D) All of the above
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
10
In CLL, all of the following might result from the autoimmune phenomenon except:
A) Thalassemia
B) Autoimmune hemolytic anemia
C) Idiopathic thrombocytopenic purpura (ITP)
D) Immune neutropenia
E) None of the above
A) Thalassemia
B) Autoimmune hemolytic anemia
C) Idiopathic thrombocytopenic purpura (ITP)
D) Immune neutropenia
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
11
What is meant by monoclonality?
A) Presence of kappa and lambda chains
B) Presence of either kappa or lambda light chains
C) Absence of kappa and lambda light chains
D) Presence of epsilon chain
E) None of the above
A) Presence of kappa and lambda chains
B) Presence of either kappa or lambda light chains
C) Absence of kappa and lambda light chains
D) Presence of epsilon chain
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
12
Which morphologic factors distinguish the lymphocytes of CLL from normal mature lymphocytes?
A) Nucleoli
B) N/C ratio
C) Exaggerated nuclear chromatin
D) Secondary granules
E) None of the above
A) Nucleoli
B) N/C ratio
C) Exaggerated nuclear chromatin
D) Secondary granules
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
13
Required hematologic findings for a diagnosis of CLL include:
A) 5000/µL lymphocytes in the peripheral blood
B) 30% lymphocytosis in bone marrow
C) Normocytic/hypochromic anemia
D) A and B
E) A and C
A) 5000/µL lymphocytes in the peripheral blood
B) 30% lymphocytosis in bone marrow
C) Normocytic/hypochromic anemia
D) A and B
E) A and C
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
14
What are the consequences of the accumulation of the lymphocytes in the peripheral blood and bone marrow in a patient with CLL?
A) Neutropenia
B) Anemia
C) Thrombocytopenia
D) All of the above
E) None of the above
A) Neutropenia
B) Anemia
C) Thrombocytopenia
D) All of the above
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
15
Autoimmune hemolytic anemia in CLL is characterized by the following:
A) A positive direct Coombs' test
B) An increased indirect serum bilirubin
C) Reticulocytosis
D) All of the above
E) None of the above
A) A positive direct Coombs' test
B) An increased indirect serum bilirubin
C) Reticulocytosis
D) All of the above
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
16
In CLL there is a malignant proliferation of which cell?
A) B lymphocytes
B) T lymphocytes
C) Natural killer (NK) lymphocytes
D) Null lymphocytes
E) None of the above
A) B lymphocytes
B) T lymphocytes
C) Natural killer (NK) lymphocytes
D) Null lymphocytes
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
17
Immune dysfunction within proliferating B cells of CLL is indicated by:
A) Monoclonal gammopathy
B) Hypogammaglobulinemia
C) Hypergammaglobulinemia
D) All of the above
E) None of the above
A) Monoclonal gammopathy
B) Hypogammaglobulinemia
C) Hypergammaglobulinemia
D) All of the above
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
18
Which immunologic technique is helpful in detecting very small numbers of malignant cells or amplifying gene rearrangements in malignant clones?
A) Monoclonal antibodies
B) Polyclonal antibodies
C) PCR technology
D) DNA probe
E) None of the above
A) Monoclonal antibodies
B) Polyclonal antibodies
C) PCR technology
D) DNA probe
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
19
Suppression of all classes of immunoglobulin is evident in CLL, resulting in:
A) Hypergammaglobulinemia
B) Decreased susceptibility to infections
C) Autoimmune disease
D) Hypothyroidism
E) None of the above
A) Hypergammaglobulinemia
B) Decreased susceptibility to infections
C) Autoimmune disease
D) Hypothyroidism
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
20
The demonstration of SIg (surface immunoglobulin) is the classic marker for __________.
A) T cells
B) B cells
C) Null cells
D) NK cells
E) None of the above
A) T cells
B) B cells
C) Null cells
D) NK cells
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
21
The following is true regarding hairy cell leukemia:
A) Pancytopenia is a common finding
B) Lymphocytes appear as hair-like cytoplasmic projections
C) Alkaline phosphatase is not inhibited by tartrate-resistant acid phosphatase (TRAP) reaction
D) A and B
E) A, B, and C
A) Pancytopenia is a common finding
B) Lymphocytes appear as hair-like cytoplasmic projections
C) Alkaline phosphatase is not inhibited by tartrate-resistant acid phosphatase (TRAP) reaction
D) A and B
E) A, B, and C
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
22
The most common chromosomal abnormality in B-CLL (B lymphocytes) is an extra chromosome called __________.
A) Inversion 12
B) Trisomy 12
C) Trisomy 7
D) Inversion 7
E) None of the above
A) Inversion 12
B) Trisomy 12
C) Trisomy 7
D) Inversion 7
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
23
What is characteristic morphology for Sézary cells?
A) Dark-staining hyperchromatic nuclear chromatin with numerous folds
B) Light-staining hyperchromatic nuclear chromatin with numerous folds
C) Dark-staining hypochromatic nuclear chromatin with many clumps
D) Light-staining hypochromatic nuclear chromatin with numerous grooves
E) None of the above
A) Dark-staining hyperchromatic nuclear chromatin with numerous folds
B) Light-staining hyperchromatic nuclear chromatin with numerous folds
C) Dark-staining hypochromatic nuclear chromatin with many clumps
D) Light-staining hypochromatic nuclear chromatin with numerous grooves
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
24
Atypical lymphocytes in reactive lymphocytosis are a proliferation of which type of cell?
A) T cell
B) B cell
C) NK cell
D) Null cell
E) None of the above
A) T cell
B) B cell
C) NK cell
D) Null cell
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
25
What definitive factor differentiates prolymphocytic leukemia (PL) from CLL?
A) Extreme leukocytosis (>100 10/L)
B) Splenomegaly without lymphadenopathy
C) Presence of prolymphocytes
D) A and B
E) B and C
A) Extreme leukocytosis (>100 10/L)
B) Splenomegaly without lymphadenopathy
C) Presence of prolymphocytes
D) A and B
E) B and C
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
26
The most common etiologic agent for reactive lymphocytosis is:
A) Viral
B) Bacterial
C) Fungal
D) Unknown
E) None of the above
A) Viral
B) Bacterial
C) Fungal
D) Unknown
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
27
The leukemia phase of cutaneous T-cell lymphoma, mycosis fungoides, is called __________.
A) Hunter's syndrome
B) Hairy cell leukemia
C) Sézary syndrome
D) Idiopathic myelofibrosis
E) None of the above
A) Hunter's syndrome
B) Hairy cell leukemia
C) Sézary syndrome
D) Idiopathic myelofibrosis
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
28
Well-differentiated lymphocytic leukemia is a diffuse non-Hodgkin's lymphoma that is characterized by neoplastic transformation of __________.
A) T lymphocytes
B) B lymphocytes
C) NK cells
D) Null cells
E) None of the above
A) T lymphocytes
B) B lymphocytes
C) NK cells
D) Null cells
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck
29
Which may be used to differentiate CLL from ALL?
A) Age of patient
B) Nuclear chromatin pattern
C) Presence of nucleoli
D) All of the above
E) None of the above
A) Age of patient
B) Nuclear chromatin pattern
C) Presence of nucleoli
D) All of the above
E) None of the above
Unlock Deck
Unlock for access to all 29 flashcards in this deck.
Unlock Deck
k this deck