Lymphoma Flashcards

1
Q

What are the two classes of lymphoma

A

Hodgkin’s and non-Hodgkin’s

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2
Q

What chemotherapy is used for DLBCL-NHL?

A

R-CHOP

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3
Q

Describe how high calcium leads to pre-renal AKI?

A

High calcium causes water to move out of the cells, causing dehydration, PTH is low, polyuria and polydipsia

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4
Q

What is rituximab?

A
Targets B cells 
Chimeric human-murine monoclonal antibody 
Directed to CD20
Cell mediated toxicity/complement
Induction of apoptosis
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5
Q

How does the material from the tumour exit the body when rituximab is given?

A

Broken down into proteins and amino acids - turns into uric acid
Through the kidney

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6
Q

What is a complication of rituximab treating lymphoma

A

Can develop gout and intrinsic renal failure

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7
Q

What is tumour lysis syndrome?

A

Breakdown of products of cancer affecting the kidney

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8
Q

What is the management of tumour lysis syndrome

A

Anticipate
Hydrate and allopurinol for low/medium risk
Rasburicase (recombinant urate oxidase)
Dialysis

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9
Q

What are the causes of NHL?

A

Immunodeficiency - primary and secondary
Age
Infection - HTLV-1, EBV, H.pylori

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10
Q

What happens to the electrolytes in tumour lysis syndrome

A

Increased uric acid, potassium and phosphorous

Lower calcium due to phosphorous soaking this up

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11
Q

Describe the staging of lymphoma

A

Ann Arbor
1 - single lymph node
2 - >2 sites, same side of diaphragm
3 - both sides of diaphragm
4 - Diffuse/disseminated involvement of >1 extra lymphatic organ
Stage A - no systemic symptoms other than pruitis
Stage B - B symptoms present
Stage E - localised extra-nodal extension - does not advance the stage and denoted by subscript

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12
Q

Describe follicular NHL

A

30-40%
Majority disseminated disease at diagnosis
Median survival 15-20yrs
Not curable

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13
Q

When do you start treatment for NHL?

A

When patient becomes symptomatic

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14
Q

Describe the treatment of high-grade lymphoma

A

Chemo/radiotherapy - potentially curable

R-CHOP - short/long course

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15
Q

What are the two main types of NHL?

A

Follicular - slow growing

Diffuse large B cell - aggressive

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16
Q

Which virus is HL associated with?

A

EBV

17
Q

Which age group does Hodgkin’s most commonly affect

A

Younger people (15-24yo) but also can affect the elderly - two peaks

18
Q

What are lymphomas?

A

Disorders caused by malignant proliferations of lymphocytes. These accumulate in the lymph nodes, peripheral blood or infiltrate organs

19
Q

What characteristic cells are found in Hodgkin’s lymphoma

A

Reed Sternberg cells - Mirror nuclei

20
Q

What are the RF for HL

A

An affected sibling
EBV
SLE
Post-transplantation

21
Q

List the symptoms of HL

A

Enlarged, non tender, rubbery superficial lymph node (mostly cervical, but can be axillary or inguinal) - node size may fluctuate and become matted
Constitutional upset - fever, weight loss, night sweats, Pruitus, lethargy
Alcohol induced lymph node pain
Mediastinal lymph node involvement may cause mass effect - bronchial or SVC obstruction or direct extension (pleural effusion)

22
Q

List the signs of HL

A

Lymphadenopathy
Cachexia
Anaemia
Spleno or hepatomegaly

23
Q

What tests would you do if suspecting lymphoma

A

Lymph node excision biopsy if possible, image-guided needle biopsy, laparotomy or mediastinoscopy
Bloods - FBC, film, ESR, LFT, LDH, urate, Ca2+
Imaging - CXR, CT/PET CAP

24
Q

What are the B symptoms

A

Weight loss >10% in last 6 months
Unexplained fever >38%
Night sweats - needing to change clothes

25
Q

Describe the treatment of HL

A

Chemoradiotherapy - radiotherapy and short course of chemo for stages I-A and II-A (<3 areas of involvement). Longer courses of chemo for II-A with >3 areas of involvement through to IV-B
ABVD - Adriamycin (doxorubicin), bleomycin, vinblastine, dacarbazine cures 80%
More intensive regimes if poor prognosis/advanced disease
In relapsed disease, high dose chemo followed by autologous stem cell transplant

26
Q

What are the complications of radiotherapy?

A

Increased risk of some solid tumours
IHD
Lung fibrosis
Hypothyroidism

27
Q

What is the 5 year survival for HL?

A

I-A lymphocyte predominant >95%

IV-B lymphocyte depleted <40%

28
Q

Name the different subtypes of HL and state the percentage of cases and prognosis

A
Nodular sclerosis (70%) - good prognosis
Mixed cellularity (20-25% - good prognosis
Lymphocyte rich (5%) - good prognosis
Lymphocyte depleted (1%) - poor prognosis
29
Q

Which two subtypes of HL have a worse prognosis in a HIV positive patient

A

Mixed cellularity

Lymphocyte depleted

30
Q

What is NHL?

A

Group of lymphomas without reed-sternberg cells

Mostly derived from B cell lines

31
Q

What is the most common NHL

A

Diffuse large B cell lymphoma

32
Q

What causes NHL

A
Immunodeficiency - drugs and HIV
HTLV-1
H.Pylori
Toxins
Congenital
33
Q

Give some signs and symptoms of NHL

A

Superficial lymphadenopathy
Extranodal disease - gut (gastric and non-gastric MALT , small bowel lymphoma - diarrhoea, vomiting, abdo pain and weight loss), skin (clonal T cells in mycosis fungiodes), oropharynx (waldeyers ring lymphoma causes sore throat and obstructed breathing), bone, CNS, lung
Fever, night sweats, weight loss
Pancytopenia - anaemia, infection and bleeding (thrombocytopenia)

34
Q

What tests would you request when suspecting NHL?

A
Blood - FBC,U&Es, LFT, LDH
Marrow and node biopsy - classification 
Staging - Ann Arbor system - CT and PET CAP
Cytology of any effusion
LP for CSF cytology if CNS signs
35
Q

Describe the treatment of high grade NHL

A

R-CHOP - Rituximab, cyclophosphamide, hydroxydaunorubicin, vincristine and prednisolone

36
Q

Describe how rituximab works

A

Kills CD20 positive cells by antibody-directed cytotoxicity and apoptosis induction
Also sensitises cells to CHOP