Ch.13 Complete Test Bank Lympho & Plasma Disorders - Test Bank | Hematology in Practice 3e by Betty Ciesla by Betty Ciesla. DOCX document preview.

Ch.13 Complete Test Bank Lympho & Plasma Disorders

Chapter 13. Lymphoproliferative Disorders and Related Plasma Cell Disorders

Multiple Choice

1. Which of the following genetic alterations is associated with a poor prognosis in CLL?

A. Trisomy 13

B. Trisomy 12

C. t(15:17)

D. t(9:21)

L.O. 13.2

2. Hypogammaglobulinemia is a significant feature in half of patients with CLL. This complication can lead to:

A. Refractory anemia

B. Essential thrombocytosis

C. Autoimmune hemolytic anemia

D. Pernicious anemia

L.O. 13.2

3. A peripheral blood picture dominated by mature lymphocytes that resemble nucleated red blood cells would most likely be seen in:

A. Sézary syndrome

B. Burkitt’s lymphoma

C. CLL

D. Infectious mononucleosis

L.O. 13.2

4. All of the following are consistent with the clinical and pathological picture of Waldenström’s macroglobulinemia except:

A. M spike due to IgM

B. Lymphadenopathy and splenomegaly

C. Proliferation of lymphocytes and plasmacytoid lymphocytes

D. Destructive bone lesions

L.O. 13.7

5. A significant feature of hairy cell leukemia not seen is other acute leukemias is:

A. Panmyelosis

B. Pancytosis

C. Pancytopenia

D. Panhyperplasia

L.O. 13.3

6. The most characteristic change seen in the peripheral smear of a patient with multiple myeloma is the presence of:

A. Microcytic hypochromic cells

B. Intracellular inclusion bodies

C. Rouleaux

D. Agglutination

L.O. 13.5

7. An abnormal proliferation of B lymphocytes seen in lymph node biopsy with a morphology resembling an owl’s eye is commonly associated with:

A. Acute lymphocytic leukemia

B. Chronic lymphocytic leukemia

C. Infectious mononucleosis

D. Hodgkin’s disease

L.O. 13.4

8. All of the following are related to the pathophysiology of multiple myeloma except:

A. Acceleration of plasma cells in the bone marrow

B. Increased levels of tyrosine kinase activity

C. Activation of osteoclasts

D. Production of an abnormal monoclonal protein

L.O. 13.6

9. Patients with CLL:

A. Die most often of blast crisis

B. Are usually younger than 40 years

C. May develop monoclonal spikes

D. Often are immunocompromised

L.O. 13.2

10. A new treatment for multiple myeloma that was once banned from use in pregnant women is:

A. EPO

B. Thalidomide

C. Demerol

D. Interferon

L.O. 13.6

11. The CD markers associated with CLL include all of the following except:

A. CD 4

B. CD 15

C. CD 19

D. CD 20

L.O. 13.8

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12. The cells at the tip of the pointer are most frequently associated with:

A. CLL

B. Hairy cell leukemia

C. Sézary syndrome

D. Multiple myeloma

NAR: Figure 13-4

L.O. 13.3

13. Lymphoma cells in the peripheral smear are associated with:

A. Hodgkin’s lymphoma

B. CLL

C. non-Hodgkin’s lymphoma

D. Multiple myeloma

L.O. 13.4

14. The immunoglobulin responsible for secondary immunological response and a monoclonal over-production in multiple myeloma is:

A. IgA

B. IgM

C. IgD

D. IgG

L.O. 13.6

15. Russell bodies are associated with:

A. Multiple myeloma

B. Hodgkin’s lymphoma

C. Non-Hodgkin’s lymphoma

D. Waldenström’s macroglobulinemia

L.O. 13.6

16. The TRAP stain is useful in the diagnosis of:

A. CLL

B. PLL

C. Hairy cell leukemia

D. Hodgkin’s lymphoma

L.O. 13.3

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17. The protein electrophoresis pattern pictured here is most frequently associated with:

A. Hodgkin’s lymphoma

B. Multiple myeloma

C. Thalassemia major

D. Essential thrombocytopenia

NAR: Figure 13-8B

L.O. 13.6

18. All of the following describe characteristics of a plasma cell except:

A. Medium-sized cell

B. Eccentric nucleus

C. Well-defined Golgi apparatus

D. Very little, light blue cytoplasm

L.O. 13.5

19. Which of the following statements about Hodgkin’s disease is false?

A. The peak incidence for the disease is 15 to 40 years of age.

B. The disease occurs more frequently in males.

C. It is a precursor to T-cell lymphoma

D. Individuals who have been exposed to the Epstein-Barr virus may be more vulnerable to Hodgkin’s lymphoma.

L.O. 13.4

20. Which of the following statements is true about chronic lymphoproliferative disorders?

A. Complications are related to overactive immune systems.

B. They are often seen in elderly patients and progress quickly.

C. They are often seen in elderly patients and progress slowly.

D. They are a clonal proliferation of granulocytes.

L.O. 13.1

Document Information

Document Type:
DOCX
Chapter Number:
13
Created Date:
Aug 21, 2025
Chapter Name:
Chapter 13 Lympho & Plasma Disorders
Author:
Betty Ciesla

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