Lymphadenopathy Flashcards

1
Q

What is lymphadenopathy

A

Lymphadenopathy refers to enlarged lymph nodes

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2
Q

When is lymphadenopathy usually painful

A

Usually seen in lymph nodes that are draining a region of acute infection (acute lymphadenitis)

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3
Q

In what condition can painless LAD be seen

A

Chronic inflammation (chronic lymphadenitis)
Metastatic carcinoma
Lymphoma

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4
Q

In inflammation, lymph node enlargement is due to

A

In inflammation, lymph node enlargement is due to hyperplasia of particular regions ofthe lymph node
1. Follicular hyperplasia (B-cell region) is seen with rheumatoid arthritis and early stages of HIV infection, for example.
2. Paracortex hyperplasia (T-cell region) is seen with viral infections (e.g., infectious mononucleosis).
3. Hyperplasia of sinus histiocytes is seen in lymph nodes that are draining a tissue with cancer.

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5
Q

Neoplastic proliferation of lymphoid cells that forms a mass
May arise in a lymph node or in extranodal tissue
Divided into non-Hodgkin lymphoma (NHL, 60%) and Hodgkin lymphoma (HL, 40%)
NHL is further classified based on cell type (e.g., B versus T), cell size, pattern of cell growth, expression of surface markers, and cytogenetic translocations
1. Small B cells - follicular lymphoma, mantle cell lymphoma, marginal zone
lymphoma, and small lymphocytic lymphoma (i.e., CLL cells that involve tissue)
2. Intermediate-sized B cells-Burkitt lmphoma
3. Large B cells - diffuse large B-cell lymphoma
What condition could this be

A

Lymphoma

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6
Q

Non-Hodgkin lymphoma can be further classified based on

A

NHL is further classified based on
Cell type (e.g., B versus T)
Cell size
Pattern of cell growth
Expression of surface markers
Cytogenetic translocations.

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7
Q

Neoplastic proliferation of small B cells (CD20+) that form follicle-like nodules
Presents in late adulthood with painless lymphadenopathy
Driven by t(14;18)
1. BCL2 on chromosome 18 translocates to the Ig heavy chain locus on chromosome 14.
2. Results in overexpression of Bcl2, which inhibits apoptosis
Treatment is reserved for patients who are symptomatic and involves low-dose chemotherapy or rituximab (anti-CD20 antibody).
Progression to diffuse large B-cell lymphoma is an important complication; presents as an enlarging lymph node
What condition could this be

A

Follicular lymphoma

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8
Q

How is follicular lymphoma distinguished from reactive follicular hyperplasia

A

Disruption of normal lymph node architecture (maintained in follicular hyperplasia)
Lack of tingible body macrophages in germinal centers (tingible body macrophages are present in follicular hyperplasia)
Bcl2 expression in follicles (not expressed in follicular hyperplasia)
Monoclonality (follicular hyperplasia is polyclonal)

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9
Q

Presents in late adulthood with painless lymphadenopathy
Driven by t(11;14)
1. Cyclin D1 gene on chromosome 11 translocates to Ig heavy chain locus on chromosome 14.
2. Overexpression ofcyclin D1 promotes G1/S transition in the cell cycle, facilitating neoplastic proliferation
Neoplastic proliferation of small B cells (CD20+) that expands the mantle zone
What condition could this be

A

Mantle cell lymphoma

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10
Q

Associated with chronic inflammatory states such as Hashimoto thyroiditis, Sjögren syndrome, and H pylori gastritis
Neoplastic proliferation of small B cells (CD20+) that expands the marginal zone
What condition could this be

A

Marginal zone lymphoma

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11
Q

Neoplastic proliferation of intermediate-sized B cells (CD20+); associated with EBY
Classically presents as an extranodal mass in a child or young adult
1. African form usually involves the jaw
2. Sporadic form usually involves the abdomen
Driven by translocations of c-myc (chromosome 8)
1. t(8;14) is most common, resulting in translocation of c-myc to the Ig heavy chain locus on chromosome 14
2. Overexpression o f c-myc oncogene promotes cell growth.
Characterized by high mitotic index and ‘starry-sky’ appearance on microscopy
What condition could this be

A

Burkitt lymphoma

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12
Q

What is a diffuse large B-cell lymphoma

A

Neoplastic proliferation of large B cells (CD20+) that grow diffusely in sheets
1. Most common form of NHL
2. Clinically aggressive (high-grade)
Arises sporadically or from transformation of a low-grade lymphoma (e.g. follicular lymphoma)
1. Presents in late adulthood as an enlarging lymph node or an extranodal mass

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13
Q

What is the effect of cytokine production by RS cells

A
  1. Occasionally results in ‘B’ symptoms (fever, chills, weight loss, and night sweats)
  2. Attract reactive lymphocytes, plasma cells, macrophages, and eosinophils
  3. May lead to fibrosis
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14
Q

Neoplastic proliferation of Reed-Sternberg (RS) cells, which are large B cells with multilobed nuclei and prominent nucleoli (‘owl-eyed nuclei); classically positive for CD15 and CD30
What condition could this be

A

Hodgkin lymphoma

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15
Q

What are the subtypes of HL

A

Reactive inflammatory cells make up a bulk of the tumor and form the basis for classification of HL. Subtypes include
1. Nodular sclerosis
2. Lymphocyte-rich
3. Mixed cellularity
4. Lymphocyte-depleted

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16
Q

What is the most common subtype of HL (70% of all cases)

A

Nodular sclerosis

17
Q

Classic presentation is an enlarging cervical or mediastinal lymph node in a young adult, usually female.
Lymph node is divided by bands of sclerosis; RS cells are present in
lake-like spaces
What condition could this be

A

Nodular sclerosis subtype of HL

18
Q

Which subtype of HL has the best prognosis of all types

A

Lymphocyte-rich

19
Q

Which subtype of HL is often associated with abundant eosinophils (RS cells produce IL-5)

A

Mixed cellularity

20
Q

Which subtype of HL is the most aggressive type of all types (usually seen in the elderly and HIV-positive individuals)

A

Lymphocyte-depleted is the most aggressive of all types

21
Q

Overall frequency is 60%
Malignant cells are lymphoid cells
Composition of mass are lymphoid cells
Shows painless lymphadenopathy, usually arises in late adulthood
Mode of spread is diffuse and often extranodal
Staging is of limited importance
Leukemic phase occurs
What condition could this be

A

Non-Hodgkin lymphoma

22
Q

Malignant cells are Reed-Sternberg cells
Mass is predominantly composed of reactive cells (inflammatory cells and fibrosis)
Painless lymphadenopathy occasionally with ‘B’ symptoms, usually arises in young adults
Mode of spread is contiguous and rarely extranodal
Guides therapy; radiation is the mainstay of treatment.
Leukemic phase does not occur
What condition could this be

A

Hodgkin lymphoma

23
Q

What cells form the marginal zone

A

Post-germinal center B cells

24
Q

What type of lymphoma is a MALToma (in mucosal sites)

A

Marginal zone lymphoma

25
Q

Gastric MALToma may regress with treatment of H. pylori
True or false

A

True

26
Q

Which CD (cluster of differentiation) is found in Hodgkin’s lymphoma

A

CD15
CD30

27
Q

What are the various subtypes of Hodgkin lymphoma

A

Nodular sclerosis
Lymphocyte-rich
Mixed cellularity
Lymphocyte-depleted

28
Q

What translocation drives follicular lymphoma

A

t(14;18)
BCL2 on chromosome 18 translocates to the Ig heavy chain locus on chromosome 14.
Results in overexpression of Bcl2, which inhibits apoptosis

29
Q

What lymphoma is driven by t(11;14)

A

Mantle cell lymphoma

30
Q

How is follicular lymphoma treated

A

Treatment is reserved for patients who are symptomatic and involves low-dose chemotherapy or rituximab (anti-CD20 antibody)

31
Q

Progression to diffuse large B-cell lymphoma is an important complication; presents as an enlarging lymph node
What condition is this

A

Follicular lymphoma

32
Q

What is the most common c-myc translocation of Burkitt lymphoma

A

t(8;14)

33
Q

Heavy chain Ig is on what chromosome and c-MYC oncogenes are on what chromosome

A

14 and 8 respectively

34
Q

What is the most common form of non-Hodgkin lymphoma

A

Diffuse B-cell lymphoma

35
Q

What are Reed-Sternberg (RS) cells

A

Reed-Sternberg (RS) cells, which are large B cells with multilobed nuclei and prominent nucleoli (‘owl-eyed nuclei)