Mature Lymphoid Neoplasms

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31 Terms

1
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What is a lymphoproliferative disorder?

Any condition in which lymphocytes (B cells, T cells, or NK cells) grow and multiply excessively, ranging from benign/reactive expansions to malignant cancers like lymphomas and leukemias

2
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Let me list all the disorders in this chapter

  • Chronic Lymphocytic Leukemia

  • B cell Prolymphocytic Leukemia

  • Hairy Cell Leukemia

  • Plasma Cell Disorders

  • Lymphoma

3
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Which cell more more common in Chronic Lymphocytic Leukemia (CLL)?

B cell more than T cell

4
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What is the problem in CLL?

The lymphocytes in CLL are unable to fight infection very wel. So the lymphs increase in the blood and bm, so there is less room for healthy WBCs, RBCs, and platelets

5
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Symptoms of CLL

  • weight loss

  • lymphadenopathy

  • anemia symptoms

  • thrombocytopenia

  • splenomegaly

  • hepatomegaly

6
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What are the CBC findings of CLL?

  • Leukocytosis

  • Lymphocytosis

  • Smudge cells

7
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Why are smudge cells found in CLL?

The neoplastic lymphocytes are more fragile than normal ones

8
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The bone marrow of CLL is…

hypercellular with a predominance of lymphocytes

9
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What marker characterizes B cell CLL?

CD5

10
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What is B cell prolymphocytic leukemia?

An aggressive leukemia dominated by large promyelocytes with strong surface markers. Much higher WBC than CLL: >300 × 10^9/L

11
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What is Hairy Cell Leukemia (HCL)?

The malignancy of B cells. They do not work normally. They increase in number in the blood and bm, so less room for WBC, RBC, and platelets

12
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What are the hallmark features of HCL?

  • pancytopenia

  • dry tap aspiration

  • hairy cells

  • normocytic, normochromic anemia

13
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Why does the aspirate need to be a dry tap in HCL?

Due to the bm being so hypercellular. Need a biopsy to confirm presence of hairy lymphs

14
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What cytochemical stain differentiates hairy cell leukemia?

a positive TRAP stain

15
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What are the two plasma cell disorders in the chapter?

Multiple Myeloma and Waldenstrom’s Macroglobulinemia

16
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What cytokine is responsible for the stimulation in bone marrow resulting in excess plasma cells in Multiple Myeloma (MM)?

IL 6

17
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What is the most common antibody class that is overproduced?

IgG (with IgA also being kinda common)

18
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What characterizes MM?

XS plasma cells = XS antibodies = XS proteins

19
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Therefore in MM, there is excess protein in…

urine, serum, and body

20
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The xs antibodies/proteins in MM cause the blood to be thick. What is another name for this?

Hyperviscosity

21
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In some cases of MM, the body will try to excrete the xs antibodies in the urine. What protein will the antibodies appear as when tested?

Bence-Jones protein

22
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What arrangement are the RBCs in on the pb?

Rouleaux due to the increased viscosity

23
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There is bone pain in MM and on xrays, the bones appear to have “punched out lesions”. What causes this?

IL-6 because it is an activator of bone dissolvement

24
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What are laboratory findings of MM?

  • leukocytosis

  • anemia

  • Rouleaux

  • Increased ESR due to rouleaux

  • hypercellular bone marrow with Mott cells and Flame cells

25
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How do mott cells appear?

Plasma cells filled with globules which contain immunoglobulin

26
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What spikes from the xs antibody produced in MM on Serum protein Electrophoresis (SPE)?

the monoclonal (M) spike

27
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What is the difference between MM and Waldenstrom’s Macroglobulinemia?

The xs antibody is IgM NOT IgG. BUT OTHERWISE EVERYTHING IS THE SAME. ALSO NO BONE PAIN

28
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What is lymphoma?

A group of cancers (malignant neoplasms) that originate in the lymphatic system

29
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How is the diagnosis of lymphoma confirmed?

Lymph node biopsy

30
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What are symptoms of lymphoma?

  • painless swelling of lymph nodes

  • fatigue

  • recurrent high fever

31
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What cells found in lymph nodes characterize Hodgkin’s lymphoma?

Reed-Sternberg cells

  • extremely large abnormal lymphs that are bi-nucleus