Lymphoma - Non-Hodgkin Flashcards
How does lymphoma differ from leukaemia
The neoplastic cells predominantly involved the lymph nodes and extra nodal sites, unlike leukaemia which mainly involves the bone marrow + blood
Epidemiology
50+
MALE
Risk Factors
Infection: HIV, EBV, H.pylori
Autoimmunity: Hashimotos, Sjorgrens
Immunodeficiency: HIV as well as hereditary immunodeficiency e.g. Wiskott-Aldrich syndrome
Pathophysiology
Non-Hodgkin’s Lymphoma can be divided by cell type: proliferation of B cells, T cells, or NK cells or grade: High or Low
- B cell is the most common type (85%)
* Low grade = follicular lymphoma, marginal zone lymphoma, hairy cell leukaemia
* High grade = diffuse large B cell lymphoma (80%)
* High grade = Burkett’s lymphoma (linked to EBV in Africa causes MASSIVE JAW LYMPHADENOMPATHY)
* Mantle cell lymphoma
Signs
Lymphadenopathy
- PAINLESS, hard, rubbery, fixed, non-contiguous spread unlike in HL - NOT AFFECTED BY ALCOHOL
Splenomegaly - more common in NHL
Extra nodal disease - bone marrow, thyroid, salivary gland, GI tract, CNS
Symptoms
B symptoms:
- Fever, weight loss, night sweats
Investigations
FIRST LINE:
- FBC = Low Hb, Platelets, High ESR, lactose dehydrogenase
GOLD STANDARD:
- Lymph node biopsy = will NOT show Reed-Sternberg cells
CT chest, abdo, pelvis
- Ann Arbour Criteria
Treatment
R-CHOP
- Rituximab
- Cyclophosphamide
- Hydroxydaunorubicin
- Vincristine (Oncovin)
- Prednisolone
CNS involvement = intrathecal methotrexate
Low grade = radiotherapy may be curative
How does rituximab work?
Monoclonal antibodies which binds to CD20 receptors on B cells to cause apoptosis.
Complications
Myelosupression + neutropenia sepsis
Tumour lysis syndrome