Lymphomas Flashcards
1
Q
What is lymphoma?
A
- malignant tumours of lymphoid origin which can arise anywhere lymphoid tissue is present
2
Q
What are the two classifications of lymphomas?
A
- Hodgkin’s lymphoma
- Non-Hodgkin’s lymphoma
3
Q
What is the epidemiology of lymphomas?
A
- more common in males
- age-dependent which varies with type
4
Q
What is the lymphatic system?
A
- systemic network of various tissues, glands, organs and ducts
e. g. lymph nodes, bone marrow, spleen, liver - produces, stores and transports lymph
5
Q
What is lymph?
A
- a portion of blood plasma separated from interstitial fluid
- contains waste from cell
- travels one-way toward the subclavian veins to be returned to the venous system
- lymph nodes treat and filter harmful entities
6
Q
What are the similarities between HL and NHL?
A
- lymphocyte origin
- painless swelling of LNs
- can occur anywhere in the body but most frequently occur in LNs
- General symptoms of weight loss, fevers, night sweats
7
Q
What is the orgin of HL?
A
- arise mostly from b-cells
- reed-sternberg cells
- distinct under light micro (enlarged, multi or bi-loaded nucleus)
8
Q
What characterises HL?
A
- reed-sternberg cells
- two age groups (15-40; 55+)
- more often in upper body
- usually contiguous nodes
- rarely extra-nodal
- distinct type
9
Q
What characterises NHL?
A
- risk increases with age (60+)
- no site predominance
- widely disseminated node groups
- common extra-nodal involvement (90% stage 3 or 4 include bone marrow involvement)
- more then 30 types
10
Q
What is the aetiology of HL?
A
- genetic
- familial (siblings especially identical twins)
- socioeconomic status-higher
- environmental
- infections EBV, glandular fever, HIV
11
Q
What are the histological subtypes of HL?
A
- lymphocyte predominant
- nodular sclerosis
- mixed cellularity
- lymphocyte depleted
12
Q
What are the signs and symptoms of HL?
A
- lymphadenopathy (cervical and sup’clav, mediastinal)
- splenomegaly/abdo mass
- spread to contiguous nodes
- alcohol induced pain
- chest pain
- bronchial obstruction
- SVC obstrucion
SYSTEMIC - pruritus
- fatigue
- bone pain
13
Q
Where does HL metasesis extranodally to?
A
- liver (20%)
- bone marrow (10%)
- bone (7%)
- lung (5%)
14
Q
What is used to diagnose HL and NHL?
A
- biopsy
- physical exam
- full medical history
- chest x-ray/CT
- CT abdomen, pelvis
- FBC
- bone marrow biopsy
15
Q
What is the staging of HL and NHL?
A
- stage 1: single lymph node group
- stage 2: multiple LNs on same side of diaphragm
- stage 3: multiple LNs on both sides of diaphragm
- stage 4: mutliple extranodal sites of Lns and extranodal disease
- stage 5: bulk>10cm
A/B - B symptoms: weight loss>10%, fever, drenching night sweats