Lymphoid Malignancy Flashcards

1
Q

What are the different ways that lymphomas can present?

A

1) Lymphadenopathy
2) Extranodal Involvement
3) Bone Marrow Involvement
4) Systemic B symptoms

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2
Q

What are the systemic (B) symptoms associated with lymphomas?

A

1 - Weight loss (>10% in 6 months)

2 - Fever

3 - Night sweats

4 - Pruritis

5 - Fatigue

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3
Q

What is the definitive way to define the type of lymphoma?

A

Biopsy (lymph node or bone marrow)

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4
Q

What information can clinical examination and imaging give us about a lymphoma?

A

Where it is

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5
Q

What are the 2 broad categories of lymphoma?

A

1) Hodgkin Lymphoma
2) Non-hodgkin Lymphoma

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6
Q

What is the difference between HL and NHL?

A

HL - specific disease

NHL: - broad term covering around 50 subtypes of lymphoma

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7
Q

What are the lymphoproliferative disorders?

A

Acute Lymphoblastic Leukaemia

Chronic Lymphocytic Leukaemia

Hodgkin Lymphoma

Non-hodgkin lymphoma

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8
Q

What are the different types of NHL?

A

High-grade

Low-grade

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9
Q

What are the characteristics of high-grade NHL?

A

Diffuse

Large B-cell lymphoma

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10
Q

What are the characteristics of low-grade NHL?

A

Follicular

Marginal zone

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11
Q

Is HL or NHL more common?

A

NHL is more common than HL

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12
Q

What is ALL and what are its features?

A

Acute Lymphoblastic Leukaemia

  • Cancer of lymphoblasts
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13
Q

How is ALL diagnosed?

A

> 20% lymphoblasts present in bone marrow

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14
Q

What is the most common age group affected by ALL?

A

Children < 6 years old

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15
Q

What is the most common presentation of ALL?

A

2-3 week history of bone/joint pain

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16
Q

What are the characteristic blood markers of ALL and what is their cause?

A

All due to bone marrow failure caused by over proliferation of lymphoblasts:

Haemoglobin - Low

WCC - High

Platelets - Low

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17
Q

Apart from joint pain, what other features are commonly seen in ALL?

A

1 - Impaired vision (retinal haemorrhages)

2 - Weight loss

3 - Infection

4 - Severe night sweats

18
Q

How is ALL treated?

A

1 - Chemotherapy cures systemic disease

2 - Stem cell transplantation if high risk

19
Q

What are some of the newer therapies available for ALL and what is their general mode of action?

A

1) BiTe molecules
2) CAR

They are both T-cell immunotherapies

20
Q

What are the common side effects of T-cell immunotherapy?

A

1) Cytokine release syndrome
2) Neurotoxicity

21
Q

What are poor prognostic factors for ALL?

A

1 - Increasing age

2 - Increased WCC

3 - Poor response to treatment

22
Q

How is CLL diagnosed?

A

Blood shows > 5x10^9/L lymphocytes

Bone marrow shows > 30% lymphocytes

B-cell markers and CD5 +VE

23
Q

Are males or females more affected by CLL?

24
Q

How does CLL present?

A

1 - Often asymptomatic at presentation

2 - Bone marrow failure (anaemia + thrombocytopenia)

3 - Lymphadenopathy

4 - Splenomegaly

5 - Fever and sweats

25
What is the staging system used for CLL?
Binet
26
What are the different stages of the Binet system and what are their clinical features?
**A** - \< 3 lymph node areas involved **B** - 3 or more lymph node areas involved **C** - Stage B + anaemia or thrombocytopenia
27
What are the indications that CLL treatment should be started?
1 - Bone marrow is failing progressively 2 - Massive lymphadenopathy 3 - Progressive splenomegaly 4 - Lymphocyte number doubles in \< 6 months
28
What is the treatment for CLL?
1 - Watch and wait 2 - Cytotoxic chemotherapy 3 - Monoclonal antibodies
29
What are poor prognostic factors for CLL?
1 - Binet stage B or C 2 - Abnormal lymphocyte morphology 3 - Rapid lymphocyte doubling time (\<12 months) 4 - Loss of p53 5 - CD 38+ expression
30
What is the classic presentation of lymphoma?
1) Lymphadenopathy 2) Extranodal disease 3) B symptoms (weight loss, night sweats, pruritis, fever) 4) Hepatic or Spleno megaly 5) Bone marrow involvement
31
How are lymphomas assessed and 'staged'?
1 - Lymph node biopsy 2 - CT scan 3 - Bone marrow aspirate
32
How are NHL's classified?
1) According to cell lineage: T-cell B-cell 2) Grade of disease (high or low) 3) Histological features
33
What cell type do most NHL's originate from?
B-cell
34
What are the features of a low-grade NHL?
1 - Asymptomatic 2 - Responds to chemo 3 - Slow growing
35
What are the features of a high-grade NHL?
1 - Aggressive + fast-growing 2 - Requires combination chemo
36
What are the 2 most common subtypes of NHL and what grade are they?
1) Diffuse large B-cell lymphoma - high grade 2) Follicular lymphoma - low grade
37
How are NHL's treated?
Monoclonal antibodies + chemotherapy
38
What is the age distribution for Hodgkin lymphomas?
**Twin peaks:** 1 - 15-35 y.o. 2 - Later in life
39
With which virus is Hodgkin lymphoma commonly associated with?
Epstein-Barr virus
40
How is Hodgkin Lymphoma treated?
1) Combination chemo 2) Monoclonal antibodies