Haemotological malignancy Flashcards

1
Q

What is the epidemiology of haematological malignancy?

A

○ Haematological Malignancies account for approximately 10% of all human cancers
○ They occur in all age groups, including children
○ Adult males are more commonly affected than females

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2
Q

What is the epidemiology of Hodgkin disease?

A
  • Has a peak incidence at 18-35 years

- One of the main causes is the Epstein Barr virus

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3
Q

When is the peak incidence of non-hodgkins disease and AML?

A

70-80

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4
Q

What is the pathogenesis of haematological malignancy?

A

○ Multi step process
○ Acquired genetic alterations to a long lived cell
○ Proliferative/survival advantage to that mutated cell
○ This produces the malignant clone
○ The malignant clone grows to dominate the tissue
- (e.g. bone marrow or lymph nodes)

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5
Q

What type of cells cause myeloid malignancies?

A
  • red cells
  • Platalets
  • Gram cells
  • Monocytes
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6
Q

What type of cells cause lymphoid malignancies?

A

> B-cell

> T-cell

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7
Q

What is acute myeloid leukaemia?

A

Ongoing proliferation of myeloid cells with no end cells

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8
Q

What is chronic myeloid leukaemia?

A

An increase in myeloid end cells in the blood

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9
Q

What is acute lymphoid leukaemia?

A

Too much lymphoid progenitor and not enough end cells

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10
Q

What is the difference between a leukaemia and a lymphoma?

A

○ Disease in the blood and bone marrow is called leukaemia
○ Disease in the lymphoid is called lymphoma
○ Some diseases can present in the blood and the lymphoid

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11
Q

What are the major groups of haematological malignancies?

A
○ Acute Leukaemias
- Acute lymphoblastic leukaemia (ALL)
- Acute Myeloid Leukaemia (AML)
○ Chronic Leukaemias
- Chronic myeloid leukaemia (CML)
- Chronic lymphocytic leukaemia (CLL)
○ The malignant lymphomas
- Non-Hodgkin lymphoma (NHL)
- Hodgkin lymphoma (HL)
○ Multiple myeloma
○ Myelodysplastic syndromes (MDS)
○ The chronic myeloproliferative neoplasm (biologically malignant)
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12
Q

Explain acute leukaemia?

A
  • Leukemic cells do not differentiate
  • Bone marrow failure
  • Rapidly fatal if untreated
  • Potentially curable
    □ E.g. childhood acute lymphoblastic leukaemia
    □ Good prognosis acute myeloid leukaemia treated with chemotherapy
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13
Q

What are the clinical features of acute leukaemia?

A

□ Anaemia
□ Thrombocytopenic bleeding (Purpura and mucosal membrane bleeding)
□ Infection because of neutropenia (predominantly bacterial and fungal)

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14
Q

Explain chronic leukaemia?

A
  • Leukemic cells retain ability to differentiate
  • Proliferation without bone marrow failure
  • Survival for a few years
  • Potentially curable with modern therapy
    □ E.g. Tyrosine Kinase inhibitors in CML
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15
Q

What percentages of lymphomas present with nodal disease?

A

□ > 90% HL present with nodal disease

□ ~ 60% NHL present with purely nodal disease

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16
Q

What are the different types of lymphadenopathies?

A

> Localised and painful
Localised and painless
Generalised and painful/ tender
Generalised and painless

17
Q

what causes loactlised and painful lymphadenopathy?

A

Bacterial infection in draining site

18
Q

what are the causes loaclised and painless lymphadenopathy

A

◊ Rare infections, catch scratch fever, TB
◊ Metastatic carcinoma from draining site- hard
◊ Lymphoma-rubbery
◊ Reactive, no cause identified

19
Q

What causes generalised painful lymphadenopathies?

A

Viral infections, EBV, CMV, hepatitis, HIV

20
Q

What are the causes of generalised painless lymphadenopathy?

A
◊ Lymphoma
◊ Leukaemia
◊ Connective tissue diseases, sarcoidosis
◊ Reactive, no cause identified
◊ Drugs
21
Q

What percentages of lymphomas present with extranodal disease?

A

~ 40% NHL present with an extranodal component, with or without nodal involvement

22
Q

What are the systemic features of lymphomas?

A
□ Fever
□ Drenching sweats
□ Loss of weight
□ Pruritis
□ Fatigue