20. Chronic Lymphocytic Leukemia and Related Lymphoproliferative Disorders Flashcards

1
Q
  1. The cells of CLL are morphologically identical to those of:
    a.ALL
    b. Small lymphocytic lymphoma
    c.Infectious mononucleosis
    d. Sézary syndrome
A

b. Small lymphocytic lymphoma

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2
Q
  1. Surface immunoglobulin is the most reliable surface marker for:
    a. T lymphocytes
    b. Plasma cells
    c.B lymphocytes
    d.Histiocytes
A

c.B lymphocytes

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3
Q
  1. Cells that demonstrate a positive reaction with the tar-trate-resistant acid phosphatase (TRAP) stain are most likely:
    a.T lymphoblasts of ALL
    b. Atypical lymphocytes of a viral infection
    c. Large granular lymphocytes of T-gamma lymphopro-liferative disorder
    d. Hairy cells of hairy-cell leukemia
A

d. Hairy cells of hairy-cell leukemia

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4
Q
  1. A mutated tumor suppressor gene found in a variety of human cancers, including CLL is:
    a.p53
    b.MDM2
    c.HLA-DR
    d.CD4
A

a.p53

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5
Q
  1. The immunophenotype that best describes mantle cell lymphoma is:
    a.CD5+,CD19+,CD23+,FMC7+,cyclin D1+
    b.CD5+,CD19+ CD23+,FMC7+,cyclin D1-
    c. CD5+,CD19+ CD23+,FMC7-,cyclin D1+
    d. CD5+,CD19+ CD23- ,FMC7+,cyclin D1+
    e. CD5- ,CD19+ CD23+,FMC7+,cyclin D1+
A

d. CD5+,CD19+ CD23- ,FMC7+,cyclin D1+

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6
Q
  1. In chronic lymphocytic leukemia:

a. The absolute lymphocyte count is usually equal to or exceeds 5000x109 cells/L.
b.Hemoglobin level,platelet count, and absolute number of neutrophils may be normal or elevated.
c.The neoplastic lymphocytes in the blood or bone mar-row are large with fine chromatin and prominent nucleoli.

A

a. The absolute lymphocyte count is usually equal to or exceeds 5000x109 cells/L.

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7
Q

Directions: Each item below contains one or more correct answers.Use the following letters to answer questions 7 through 9.
a. If 1,2,and 3 are correct
b.If 1 and 3 are correct
c.If 2 and 4 are correct
d.If 4 is correct
e.If 1,2,3,and 4 are correct

7.Which of the following findings would point to a diag-nosis of CLL?
1. Clonal proliferations of B lymphocytes
2. CD19+/CD51+,CD23-
3.CD19+/CD51+,CD23+
4.Ph chromosome-positive

A

b.If 1 and 3 are correct

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8
Q

Directions: Each item below contains one or more correct answers.Use the following letters to answer questions 7 through 9.
a. If 1,2,and 3 are correct
b.If 1 and 3 are correct
c.If 2 and 4 are correct
d.If 4 is correct
e.If 1,2,3,and 4 are correct

8.Which of the following clinical and laboratory manifesta-tions would point to a diagnosis of hairy-cell leukemia?
1.Pancytopenia
2.Splenomegaly
3.CD20+,CD103+,CD25+
4.Prominent generalized lymphadenopathy

A

a. If 1,2,and 3 are correct

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9
Q

Directions: Each item below contains one or more correct answers.Use the following letters to answer questions 7 through 9.
a. If 1,2,and 3 are correct
b.If 1 and 3 are correct
c.If 2 and 4 are correct
d.If 4 is correct
e.If 1,2,3,and 4 are correct

9.The poorest prognosis for patients with CLL is associ-ated with which of the following features?
1.Anemia
2.Splenomegaly
3.Thrombocytopenia
4.White cell count greater than 15,000 cells/μL

A

b.If 1 and 3 are correct

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10
Q
  1. The workup step(s) include:
    a.Cytochemical staining, including myeloperoxidase a nonspecific esterase, and TdT
    b. Immunohistochemical study of trephine biopsy sectio
    c. Immunophenotypic study by flow cytometry
    d.Cytogenetic studies
    e.All of the above
A

e.All of the above

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11
Q

11.Immunophenotypic study using flow cytometry shows negative T-cell markers.However,neoplastic cells express bright CD19,CD20,and weak CD5 and show monotypic k light-chain restriction.Cyclin D1 immunohistochemical stain is negative. These cells will also express:
a.CD103
b.Strong FMC7
c.CD23
d. Dim surface immunoglobulin
e. CD38

A

b.Strong FMC7

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12
Q

12.Cytochemical sains (myeloperoxidase, nonspecific esterase) and TdT performed on samples of bone mar-row aspirate smear were negative.The most likely diagnosis is:
a.Chronic myelocytic leukemia,accelerated phase
b.Typical chronic lymphocytic leukemia
c. Acute lymphoblastic leukemia
d. Chronic lymphocytic leukemia/prolymphocytic leukemia
e. B-cell prolymphocytic leukemia

A

e. B-cell prolymphocytic leukemia

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