Hodgkin Lymphoma Flashcards
From what cell does Hodgkin lymphoma (HL) arise?
B lymphocytes
Name and describe two cell types present in Hodgkin lymphoma (HL).
- large, multi-nucleated giant cells called ‘Reed-Sternberg’ cells
- large, mono-nucleated cells called malignant ‘Hodgkin cells’.
Name the 4 subtypes of Classical Hodgkin lymphoma (HL).
Nodular Sclerosis
Mixed Cellularity
Lymphocyte-rich
Lymphocyte-depleted
What type of classical Hodgkin lymphoma (HL) is most common?
Nodular Sclerosis
Name some risk factors of developing Hodgkin lymphoma (HL).
- 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
Describe how a patient with Hodgkin lymphoma (HL) would present.
The most common symptom of Hodgkin lymphoma (HL) is a painless, rubbery, enlarged lymph node/nodes, typically in the cervical or supraclavicular region.
Name some B symptoms of Hodgkin lymphoma (HL).
fever >38°C, drenching night sweats and unintentional weight loss of >10% within the last 6 months.
What clinical findings may be present on examination of a patient with HL?
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
Describe the relevant investigations carried out in suspected HL and their inferences on the patient’s prognosis.
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
What is the gold standard for imaging in HL?
Positron emission tomography CT (PET-CT)
Using immunochemistry what antigens are positively expressed on Reed-Sternberg cells?
CD15 CD30
What is observed in stage one of HL?
Involvement of one lymph-node region or lymphoid structure (e.g. spleen or thymus).
What is observed in stage two of HL?
Two or more lymph node regions on the same side of the diaphragm.
What is observed in stage three of HL?
Lymph nodes on both sides of the diaphragm.
What is observed in stage four of HL?
Involvement of extranodal site(s)