Hodgkin's lymphoma Flashcards

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1
Q

What investigations would you order to investigate for lymphadenopathy ?HL?

A
  • Excisional lymph node biopsy
  • Immunohistochemistry to determine different types of lymphomas
  • Flow cytometry
  • Fine needle aspirate (RS cells make up 10-15% of the total cell population)
  • Autoimmune antibodies (ANA, antiphospholipid antibodies, Anti-SM, Anti-CCP, RA)
  • Microbiology
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2
Q

What are the different types of HL (in order of most common to least common)

A
  1. Nodular sclerosing lymphoma (RS cells)
  2. Mixed cellularity (eosinophils)
  3. Lymphocyte rich
  4. Lymphocyte depletion
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3
Q

HL vs. NHL

Which lymphoma is more likely to occur in younger population?

A

Answer: HL

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4
Q

HL vs. NHL

Which lymphoma is more likely to present with constitutional B symptoms?

A

Answer: HL

RS cells secrete cytokines with polymorphonuclear inflammation and consequently more type B symptoms, (fever, weight loss, night sweats)

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5
Q

Which lymph nodes are HL more associated with?

A

Neck, supraclavicular, axilla, more axial/superficial LN

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6
Q

HL vs. NHL

Which lymphoma is more likely to be associated with metastases with extranodal involvement?

A

Answer: NHL

Increased likelihood of anaemia, CNS metastases and extranodal involvements.

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7
Q

What staging system can be used for lymphoma?

A

Ann-Arbor staging system can be used.

  • Stage 1 and 2: on the same side of the the diaphragm (single vs. many)
  • Stage 3 and 4: LN involved on both sides of the diaphragm
A: no type B symptoms 
B: presence of B symptoms from overproduction of cytokines from RS cells 
X: largest deposit diameter
E: extra-nodal involvement 
S: splenic involvement
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8
Q

What is the importance of staging HL and NHL?

A

HL is contiguous spread and a more predictable spread, meaning staging has a prognostic value and guide treatment options.

NHL has disseminated pattern of spread. Prognosis can be determined by grade, bone marrow involvement, B symptoms.

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9
Q

How is NHL staged?

A

NHL is more difficult to stage due to non-contiguous spread (Ann-Arbor staging system will be stage 3 and 4). Histopathology can be used to determine the tumour margins of spread, determine subtype of NHL and determine prognosis.

It will show cell phenotype, morphology and location, cytogenetics.

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10
Q

What is the treatment of HL? (divide into stage 1, 2 and stage 3, 4)

A

HL stage 1 and 2: only radiotherapy
HL stage 3 and 4: chemotherapy regime due to widespread nature of the disease ABVD therapy (adriamycin, bleomycin, vinblastine, darcarbazine) for 28 days

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11
Q

What is treatment of NHL?

A

6-8 cycles of R-CHOP chemotherapy (rituximab, cyclophosphamide, hydroxydoxirubicin, vincristine, prednisone)

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12
Q

What is prognosis like for HL?

A

Good prognosis; 90% 5-year survival rate.

Best prognosis in lymphocyte-rich subtype;
worst prognosis in lymphocyte-depleted subtype.

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13
Q

What is prognosis for NHL?

A

Poorest prognosis with aggressive NHLs like diffused large B-cell, having 5-year survival rate of 50%.

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14
Q

Describe the anatomy of lymph node.

A

It is divided into medulla, cortex, primary and secondary lymphoid follicles containing germinal centres. Lymph nodes are contained within a capsule.

It has afferent and efferent lymphatic vessels, with artery and vein to supply the lymphoid follicles.

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15
Q

In terms of lymph node anatomy, where do B cells reside?

A

B cells originate & mature in the bone marrow and spleen. Active B cells reside in the germinal centres of the primary lymphoid follicles, inactive cells remain in the marginal areas.

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16
Q

In terms of lymph node anatomy, where do T cells reside?

A

T cells mature in the thymus and they migrate to paracortex.

17
Q

What is HL? What cells does it affect?

A

HL arises from the germinal centre or post-germinal centre B cells.

In developed countries, it affects young adults and older age adults.

In developing countries, there is more prevalence in young boys and older adults.

18
Q

What are the risk factors of HL?

A
  • Young age
  • Female
  • Low SES and environment
  • Immunosuppression
  • Autoimmune disorders
  • Family history