Hodgkin Lymphoma Flashcards

1
Q

From what cell does Hodgkin lymphoma (HL) arise?

A

B lymphocytes

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2
Q

Name and describe two cell types present in Hodgkin lymphoma (HL).

A
  • large, multi-nucleated giant cells called ‘Reed-Sternberg’ cells
  • large, mono-nucleated cells called malignant ‘Hodgkin cells’.
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3
Q

Name the 4 subtypes of Classical Hodgkin lymphoma (HL).

A

Nodular Sclerosis
Mixed Cellularity
Lymphocyte-rich
Lymphocyte-depleted

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4
Q

What type of classical Hodgkin lymphoma (HL) is most common?

A

Nodular Sclerosis

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5
Q

Name some risk factors of developing Hodgkin lymphoma (HL).

A
  • Epstein-Barr virus (EBV): it is estimated that around 40% of Hodgkin lymphoma cases in the UK are related to EBV infection. However, most people who have glandular fever will not develop cancer as a result.
  • Human immunodeficiency virus (HIV): it is estimated that the risk of developing Hodgkin lymphoma is 11 times higher than that of the general population
  • Immunosuppression: immunosuppressant drugs and certain autoimmune conditions such as rheumatoid arthritis increase the risk of developing HL
  • Previous history of non-Hodgkin lymphoma (NHL)
  • First-degree relative family history of Hodgkin lymphoma, non-Hodgkin lymphoma (NHL) or chronic lymphocytic leukaemia (CLL)
  • Cigarette smoking
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6
Q

Describe how a patient with Hodgkin lymphoma (HL) would present.

A

The most common symptom of Hodgkin lymphoma (HL) is a painless, rubbery, enlarged lymph node/nodes, typically in the cervical or supraclavicular region.

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7
Q

Name some B symptoms of Hodgkin lymphoma (HL).

A

fever >38°C, drenching night sweats and unintentional weight loss of >10% within the last 6 months.

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8
Q

What clinical findings may be present on examination of a patient with HL?

A

Lymphadenopathy
Hepatomegaly
Splenomegaly
Superior vena cava (SVC) syndrome: a mediastinal mass may cause SVC obstruction
Paraneoplastic syndromes such as cerebellar degeneration, neuropathy or Guillain-Barré syndrome

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9
Q

Describe the relevant investigations carried out in suspected HL and their inferences on the patient’s prognosis.

A

FBC: to investigate for leukaemia, infectious mononucleosis and other causes of lymphadenopathy
U&Es: to provide a baseline measurement before treatment
LFTs: reduced albumin levels are associated with a poorer prognosis
LDH: increased levels are associated with a poorer prognosis
ESR: increased levels are associated with a poorer prognosis

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10
Q

What is the gold standard for imaging in HL?

A

Positron emission tomography CT (PET-CT)

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11
Q

Using immunochemistry what antigens are positively expressed on Reed-Sternberg cells?

A

CD15 CD30

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12
Q

What is observed in stage one of HL?

A

Involvement of one lymph-node region or lymphoid structure (e.g. spleen or thymus).

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13
Q

What is observed in stage two of HL?

A

Two or more lymph node regions on the same side of the diaphragm.

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14
Q

What is observed in stage three of HL?

A

Lymph nodes on both sides of the diaphragm.

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15
Q

What is observed in stage four of HL?

A

Involvement of extranodal site(s)

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16
Q

Due to the increased risk of opportunistic infections following chemotherapy, patients with HL are also usually vaccinated with what?

A

Polyvalent pneumococcal vaccine
Influenza vaccine
Meningococcal group C conjugate vaccine
Haemophilus influenzae type b vaccine

17
Q

Describe two commonly used chemotherapy combination regimes in patients with HL.

A
  • ABVD: Doxorubicin (used to be called Adriamycin®), Bleomycin, Vinblastine and Dacarbazine
  • BEACOPP: Bleomycin, Etoposide, Doxorubicin (Adriamycin®), Cyclophosphamide, Vincristine (Oncovin®), Procarbazine, Prednisolone
18
Q

How is relapsing HL treated?

A

Regardless of stage, relapsed disease is usually treated with high dose chemotherapy (HDCT) followed by autologous stem cell transplant (ASCT).

19
Q

If a transfusion of blood products is required, patients with or treated for Hodgkin lymphoma (at any stage of the disease) must only receive what types of products?

A

Irradiated blood products are used to reduce the risk of transfusion-associated graft-versus-host disease.