Haematological cancers Flashcards

1
Q

Types of haematological malignancy

A
Leukaemia 
Lymphoma 
Myeloma 
Myeloproliferative neoplasms 
Myelodysplastic syndromes
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2
Q

Types of myeloid malignancies

A

Acute myeloid leukaemia

Chronic myeloproliferative neoplasms

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3
Q

Types of lymphoid malignancies

A

Acute lymphoblastic leukaemia

Chronic lymphoblastic leukaemia
Lymphoma

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4
Q

Difference between leukaemia and lymphoma

A

Bone marrow affected - leukaemia

Predominantly nodal or organ-based - lymphoma

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5
Q

Presentation of haematological malignancy

A

Anaemia - fatigue, SOBOE

Thrombocytopenia - easy bruising and bleeding - nose bleeds and gum bleeding, petechial rash

Neutropenia - recurrent infection

Lumps
Splenomegaly

FLAWS - fever, lethargy, appetite loss, weight loss, sweating at night

Hypercalcaemia - Fatigue, abdo pain, N+V, constipation, confusion, headaches, polydipsia and polyuria

Viscous blood - ischaemic event, visual disturbances

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6
Q

Where is hypercalcaemia commonly seen?

A

In myeloma or high-grade lymphoma

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7
Q

Investigations for haematological malignancies

A

Bloods - FBC, U+E, LFT, CRP, bone profile - Ca2+

Blood film
Reticulocyte count and haematinics

Special bloods - LDH, urate, B2M - tumour markers

  • IgG +/- serum free light chain assay
  • PB immunophenotyping

CT CAP - staging
PET - lymphoma/ myeloma
MRI spone/pelvis - myeloma

Tissue biopsy
BM aspirate and trephine

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8
Q

Acute vs chronic leukaemia

A

Acute - affects hematopoietic stem cells or the common myeloid/lymphoid progenitor cells(immature cells)

Chronic - affects the derivatives of the myeloid or lymphoid progenitor cells (differentiated mature cells)

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9
Q

Histological signs of malignancy

A

Big nucleolus
Hyperchromic
Mitotic bodies
Polymorphic

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10
Q

Acute lymphoblastic leukaemia pathophysiology

A

Proliferation of lymphoid blasts - B or T cells

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11
Q

Acute lymphoblastic leukaemia presentation

A

Pancytopenia symptoms - visual disturbances, headaches, ischaemic events

Bone pain

+/- lymphadenopathy

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12
Q

Why does bone pain occur

A

Increase in the generation of blood cells but the bone marrow cannot expand therefore there is increased pressure

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13
Q

Treatment of acute lymphoblastic leukaemia

A

Multi-drug chemotherapy

Does not cross the blood brain or blood testicular barrier therefore given prophylactic injections to scrotum and CSF

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14
Q

Acute myeloid leukaemia presentation

A

Pancytopenia

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15
Q

Treatment of acute myeloid leukaemia

A

Intensive or non-intensive treatments available

Allogenic stem cell transplant if young

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16
Q

Chronic myeloid leukaemia pathophysiology

A

Caused by cytogenic translocation t9:22 Philadelphia
Due to BCR- ABL

Increase in all myeloid cells including basophils

17
Q

Progression of chronic myeloid leukaemia

A

Chronic phase - accelerated - blast crisis

18
Q

Presentation of chronic myeloid leukaemia

A

High white cell count

Splenomegaly

19
Q

Treatment of chronic myeloid leukaemia

A

Tyrosine kinase inhibitors - imatinib

- normal life expectancy and long remission

20
Q

Chronic lymphocytic leukaemia pathophysiology

A

Causes a high no. of mature B lymphocytes

21
Q

Presentation of chronic lymphocytic leukaemia

A

Relapsing and remitting

Can have nodal or splenic disease

Causes immune dysregulation:

  • autoimmune haemolytic anaemia
  • immune thrombocytopenic purpura

Recurrent infection due to immunoglobulins being used up

22
Q

Treatment of chronic lymphocytic leukaemia

A

Watch and wait - start treatment if symptomatic or high WCC

Chemotherapy or targetted immunobiologics

23
Q

Staging of chronic lymphocytic leukaemia

A

Rai/Binet staging

24
Q

Plasmacytomas

A

Solid tumours made of an accumulation of plasma cells

25
Q

MGUS

A

Monoclonal gammopathy of undetermined significance:

  • Paraprotein < 30g/l
  • Clonal bone marrow plasma cells < 10%
  • Absence of CRAB or amyloidosis
  • May not progress to myeloma but requires monitoring
  • Does not require a routine screen as very common
26
Q

Amyloidosis

A

Extracellular tissue deposition of fibrils (beta pleated sheets)

Can affect kidneys, liver, heart, Gi tract or peripheral nervous system

27
Q

Staining for amyloidosis

A

Congo red

28
Q

Acute myeloid leukaemia histology

A

Lots of blast cells >20%

29
Q

TdT +ve

A

Lymphoblast therefore ALL

30
Q

Findings for AML

A

Myeloperoxidase +ve

Auer rods

31
Q

Complication of acute myeloid luekaemia

A

DIC - medical emergency

32
Q

Myelodysplastic syndrome pathophysiology

A

Abnormal accumulation of blasts in bone marrow

< 20% therefore not AML

33
Q

Myelodysplastic syndrome features

A

Pancytopenia as cells not developing properly

34
Q

Myelodysplastic syndrome presentation

A

Anaemia - fatigue

Low WCC - recurrent infection

Low platelets - increased bleeding and bruising

35
Q

Complications of myelodysplastic syndrome

A

Progression to AML