Hodgkin Lymphoma Flashcards

1
Q

what is hodgkin lymphoma (HL)?

A

a haematological malignancy that arises from B lymphocytes in the lymphatic system

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2
Q

how does hodgkin lymphoma occur?

A

when B lymphocytes, derived from the germinal centres of lymphoid tissues, mutate and lead to the presence of large, multi-nucleated giant cells called ‘reed-sternberg’ cells and large, mono-nucleated cells called malignant ‘hodgkin cells’

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3
Q

what are the two types of hodgkin lymphoma?

A
  • classical hodgkin lymphoma (95%)
  • nodular lymphocyte-predominant hodgkin lymphoma (5%)
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4
Q

classical hodgkin lymphoma (cHL) is further subclassified into which types?

A
  • nodular sclerosis
  • mixed cellularity
  • lymphocyte-rich
  • lymphocyte-depleted
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5
Q

what are the risk factors for hodgkin lymphoma?

A
  • EBV
  • HIV
  • immunosuppression
  • non-hodgkin lymphoma (NHL)
  • family history of hodgkin lymphoma (HL), non-hodgkin lymphoma (NHL) or chronic lymphocytic leukaemia (CLL)
  • smoking
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6
Q

what is the most common symptom of HL?

A

a painless, rubbery, enlarged lymph node/nodes, typically in the cervical or supraclavicular region

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7
Q

what are the other symptoms of HL?

A
  • B symptoms (e.g. fever, night sweats, weight loss)
  • chest discomfort +/- cough/dyspnoea (e.g. mediastinal mass)
  • abdominal discomfort/pain
  • alcohol-induced pain at nodal sites
  • pruritus
  • malaise
  • fatigue
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8
Q

what are the findings on examination of HL?

A
  • lymphadenopathy
  • hepatomegaly
  • splenomegaly
  • superior vena cava (SVC) syndrome (e.g. mediastinal mass)
  • paraneoplastic syndrome (e.g. cerebellar degeneration)
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9
Q

what are the investigations for HL?

A
  • FBC
  • U&Es
  • LFTs
  • LDH
  • ESR
  • CXR (e.g. intrathoracic lymphadenopathy, mediastinal expansion)
  • contrast-enhanced CT neck, chest, abdomen + pelvis
  • PET-CT
  • lymph node excision biopsy
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10
Q

what is the hallmark cell seen on light microscopy in HL?

A
  • the reed-sternberg cell, a giant malignant multi-nucleated cell often described as ‘owl-like’
  • it is typically surrounded by a collection of non-malignant immune cells
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11
Q

what are hodgkin cells?

A

giant malignant mono-nucleated cells, which tend to be present surrounding reed-sternberg cells

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12
Q

which antigens are positively expressed on reed-sternberg cells using immunocytochemistry?

A

CD15
CD30

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13
Q

what is the staging system used for HL?

A

ann arbor

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14
Q

due to the increased risk of opportunistic infections following chemotherapy, patients with HL are usually given which vaccinations?

A
  • polyvalent pneumococcal vaccine
  • influenza vaccine
  • meningococcal group C conjugate vaccine
  • haemophilus influenzae type b vaccine
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15
Q

what is the initial therapy for HL?

A
  • early-stage disease (stage IA, IB, IIA) is usually treated with one or more cycles of combination chemotherapy plus radiotherapy
  • advanced stage (stage IIB or above) is usually treated with a more intensive chemotherapy course; often without radiotherapy unless a particularly large mass is present
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16
Q

what are the most commonly used chemotherapy combination regimes in HL?

A
  • ABVD: Doxorubicin (Adriamycin®), Bleomycin, Vinblastine and Dacarbazine
  • BEACOPP: Bleomycin, Etoposide, Doxorubicin (Adriamycin®), Cyclophosphamide, Vincristine (Oncovin®), Procarbazine, Prednisolone
17
Q

how is relapse managed in HL?

A
  • high dose chemotherapy (HDCT) followed by autologous stem cell transplant (ASCT)
  • if a patient cannot tolerate intensive HDCT and ASCT, then combination chemotherapy and radiotherapy is considered
18
Q

what is the requirement for blood transfusions in patients with HL?

A
  • must only receive irradiated blood products, which is a lifelong requirement
  • irradiated blood products are used to reduce the risk of transfusion-associated graft-versus-host disease