Lymphoproliferative disorders Flashcards

(26 cards)

1
Q

How might lymphoma present?

A
Weight loss
Fever
Drenching night sweats
Pruritis
General fatigue
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2
Q

Where do leukaemias like ALL typically start?

A

Bone marrow

Where hematopoietic cells kept there before differentiating into progenitor cells

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3
Q

What does ALL mean?

A

Acute lymphoblastic leukaemia

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4
Q

What does CLL mean?

A

Chronic lymphocytic leukaemia

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5
Q

Which is the most common kind of lymphoma?

A

High-grade non-hodgkin lymphoma

Most common of these is Diffuse Large B-cell lymphoma

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6
Q

What is the most common low grade leukaemia?

A

Chronic lymphocytic leukaemia (CLL)

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7
Q

Which cells are affected in ALL?

A

Lymphoid progenitor cells

These are meant to be the cells from which healthy lymphocytes differentiate

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8
Q

How does ALL usually present?

A

Bilateral impaired vision loss
SOB
Bone marrow failure (Low platelets, WCC and platelets)
Wee dots of haemorrhage all over fundoscopy

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9
Q

What are some histology results in ALL?

A

Large cells

Raised CD34 and TDT indicating immature cells

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10
Q

How is ALL treated?

A

Combination chemo
Consolidation therapy for long term solution
If high risk then maybe stem cell (bone marrow) transplant

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11
Q

What are BiTe molecules?

A

Bi-specific T cell engager
Guides immune system to send T cells after cancerous cells
Blinatumumab

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12
Q

What is CAR T cell therapy?

A

Chimeric Antigen Receptor T cell
Patient’s healthy T cells harvested
Modified to express specific T cell receptors against CD-19 marker
Cultured then infused into patient

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13
Q

What are some side effects of CAR T cell therapy?

A

Cytokine release syndrome (Fever, hypotension, dyspnoea)

Neurotoxicity (confusion, seizure, headache, coma)

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14
Q

What are some risk factors for ALL?

A

Increasing age
Increased WCC
Poor treatment response
Genetic predisposition

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15
Q

How is CLL diagnosed?

A

Slow growing
Cells normal mature lymphocytes
Easier to pick up as they carry many normal B lymphocyte markers

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16
Q

How might CLL present?

A
Often asymptomatic and picked up accidentally
Bone marrow failure
Lymphadenopathy
Splenomegaly
Fever and sweats
Hepatomegaly
Infection
Weight loss
17
Q

What other conditions are associated with CLL?

A

Immune paresis

Haemolytic anaemia

18
Q

Describe a staging system for CLL.

A

Binet

Graded A-C

19
Q

How is CLL treated?

A
Often just watch and wait
Cytotoxic chemo
Monoclonal antibodies
Ibrutinab
Idelisib
Venetoclax
20
Q

What is Ibrutinib?

A

Bruton tyrosine kinase inhibitor

21
Q

What kind of cells are usually affected by non-hodgkin lymphoma?

A

B cell mostly

Sometimes T cells

22
Q

How is low grade non-hodgkins lymphoma treated?

A

Responds well to chemo

23
Q

How is high grade non-hodgkins lymphoma treated?

A

Combination chemo

Can be cured

24
Q

What are some associations of hodgkins lymphoma?

A

Epstein Barr virus

Familial and geographical clustering

25
How is hodgkins lymphoma treated?
Combination chemo Very sensitive to radiotherapy Monoclonal antibodies Immunotherapy
26
How is response of hodgkins lymphoma to treatment tracked?
PET