Lymphadenopathy Study Guide Flashcards

1
Q

Lymph nodes may become enlarged, termed lymphadenopathy, in two kinds of processes. What are they?

A

reactive and neoplastic

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2
Q

What causes reactive lymphadenopathy and what does does the histology look like?

A

Causes:

  1. Infectious: Infectious mononucleosis, Cat scratch, Others
  2. Autoimmune

Histology:

  1. Follicular hyperplasia: B cell expansions
  2. Paracortical hyperplasia: T cell expansions
  3. Sinus histiocytosis
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3
Q

What are the two major sub-classes of lymphoma?

A

Non-Hodgkin lymphomas and Hodgkin lymphomas

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4
Q

What are the two sub-classes of Non-Hodgkin lymphomas?

A

Mature B cell vs mature T cell

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5
Q

What are the mature B cell lymphomas?

A

a. Follicular lymphoma
b. Mantle cell lymphoma
c. Diffuse large B cell lymphoma (DLBCL)
d. Burkitt lymphoma
e. Extranodal marginal zone lymphoma

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6
Q

What are the mature T cll lymphomas?

A

a. Peripheral T-cell lymphoma
b. Extranodal NK/T-cell lymphoma
c. Anaplastic large cell lymphoma

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7
Q

What causes Burkitt lymphoma?

A

Translocations involving c-MYC and immunoglobulin loci, usually t(8; 14) but may be t(2;8) or t(8;22)

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8
Q

Who gets Burkitt lymphoma?

A

Adolescents or young adults withrapidly growing extranodal masses (ileocecum)

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9
Q

What course does Burkitt’s take?

A

Aggressive.

uncommonly presents as “leukemia”; 3 variants: endemic (EBV associated),
sporatic, and
immunosuppression-related (EBVassociated

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10
Q

What are the CD markers for Burkitts?

A

CD10(+)
CD19(+)
CD20(+)

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11
Q

What causes Diffuse large B-cell lymphoma?

A

Diverse chromosomal rearrangements

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12
Q

Who gets Diffuse large B-cell lymphoma?

A

All ages, but most common in adults

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13
Q

What is the course of Diffuse large B-cell lymphoma?

A

Aggressive.

often appears as a rapidly growing mass/lymphadenopathy

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14
Q

What are the CD markers for Diffuse large B-cell lymphoma?

A

CD19(+)

CD20(+)

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15
Q

What causes Extranodal

marginal zone lymphoma (MALToma)?

A

t(11;18) is the most common abnormality observed in gastric MALTomas, creating MALT1-IAP2 fusion genes

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16
Q

Who gets MALToma?

A

Arises in the lymphoid tissue of mucosal/epithelial-based sites in adults

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17
Q

What the clinical course of MALToma?

A

Indolent.

tend to be localized; most frequent sites of involvement include:
gastric, orbital, thyroid, lung; may be observed in association with chronic infections or inflammatory diseases

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18
Q

What are the CD markers for MALToma?

A

CD5(-)
CD10(-)
CD19(+)
CD20(+)

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19
Q

What causes follicular lymphoma?

A

t(14;18) creating BCL2-IgH fusion gene or less commonly BCL6 rearrangements

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20
Q

Who gets follicular lymphoma?

A

Adults with generalized lymphadenopathy, frequent retroperitoneal involvement

21
Q

What is the clinical course of follicular lymphoma?

A

usually slow growth however 40% transform to a more aggressive lymphoma

22
Q

What are the CD markers for follicular lymphoma?

A

CD5(-)
CD10(+)
CD19(+)
CD20(+)

23
Q

What causes mantel cell lymphoma?

A

t(11;14) creating cyclinD1-IgH fusion gene

24
Q

Who gets mantle cell lymphoma?

A

Older males with disseminated disease;

frequent GI involvement

25
What is the course of mantle cell lymphoma?
moderately aggressive
26
What are the CD markers for mantle cell lymphoma?
CD5(+) CD10(-) CD19(+) CD20(+)
27
What are the Mature T/NK cell lymphomas?
a. Peripheral T-cell lymphoma b. Extranodal NK/T-cell lymphoma c. Anaplastic large cell lymphoma
28
What is the cell of origin in Peripheral T-cell | lymphoma?
helper T cell
29
What mutation causes Peripheral T-cell | lymphoma?
No specific chromosomal abnormality
30
What are the clinical features of peripheral t cell lymphoma?
Aggressive. Mainly older adults; usually presents with lymphadenopathy
31
What is the cell of origin for Anaplastic large-cell lymphoma?
cytotoxic t cell
32
What is the mutation that causes Anaplastic large-cell lymphoma?
Rearrangements of ALK gene
33
What are the clinical features of Anaplastic large-cell lymphoma?
Aggressive. Children and young adults, usually with lymph node and soft-tissue disease
34
What is the cell of origin in Extranodal NK/T-cell lymphoma?
NK-cell (common) or cytotoxic T cell (rare)
35
What is the mutation that leads to Extranodal NK/T-cell lymphoma?
EBV-associated; no specific chromosomal abnormality
36
What is the clinical course of Extranodal NK/T-cell lymphoma?
Aggressive. Adults with destructive extranodal masses, most commonly sinonasa
37
What are the two types of hodgkin lymphoma?
Classical Hodgkin lymphoma and Nodular lymphocyte predominate Hodgkin lymphoma (NLPHL)
38
Who gets classical hodgkins?
Adolescents/younger adults
39
What sites are involved in classical hodgkins?
Mediastinum, cervical
40
What do the cells look like in classical hodgkins?
Reed Sternberg cells in the background of reactive inflammatory cells (eosinophils, neutrophils), “lacunar” cells, nodules and sclerosis in a subset
41
What are the CD markers of classical hodgkins?
CD15(+) CD30(+) CD20(-) CD45(-)
42
What is the cell of origin for classical hodgkins?
B cell
43
What is the clinical course of classical hodgkins?
moderately aggressive. Contiguous, predictable spread
44
Who gets Nodular lymphocyte predominate Hodgkin lymphoma (NLPHL)?
Middle-age adults
45
What sites are involved in Nodular lymphocyte predominate Hodgkin lymphoma (NLPHL)?
Cervical, axillary
46
What do the cells look like in Nodular lymphocyte predominate Hodgkin lymphoma (NLPHL)?
Nodular collections of “popcorn” cells admixed with lymphocytes
47
What are the CD markers in Nodular lymphocyte predominate Hodgkin lymphoma (NLPHL)?
CD15(-) CD30(-) CD20(+) CD45(+)
48
What is the cell of origin in Nodular lymphocyte predominate Hodgkin lymphoma (NLPHL)?
B cell
49
What are the clinical course of Nodular lymphocyte predominate Hodgkin lymphoma (NLPHL)?
Indolent. Frequent relapses