Haematological malignancies Flashcards

1
Q

Which subtype of AML should be treated as a medical emergency?

A

Acute promyelocytic leukaemia (associated with high risk of DIC)

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2
Q

What is the appearance of AML on blood count?

A

WCC high
Anaemia
Thrombocytopenia

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3
Q

Treatment of AML

A

Chemo & stem cell transplantation

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4
Q

Which 3 agents are typically used to treat ALL?

A

Vincristine, steroid, asparaginase

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5
Q

What are the long term side effects of chemo treatment of ALL in children?

A

Endocrine problems
Secondary leukaemia
Cardiotoxicity

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6
Q

When is the peak incidence of ALL?

A

Childhood

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7
Q

What is the pathological hallmark of CML?

A

Philadelphia chromosome and the resulting chimeric BCR-ABL gene

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8
Q

Clinical features of CML

A

Anaemia
Anorexia
Weight loss
Splenomegaly

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9
Q

What is the preferred definitive drug treatment for patients with CML?

A

Imatinib

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10
Q

What is the most common form of leukaemia in the western world?

A

CLL

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11
Q

When should treatment be commenced in CLL?

A

When the patient develops significant symptoms, when the disease is progressing rapidly or when it is already at an advanced clinical stage

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12
Q

What is the most effective treatment of hairy cell leukaemia?

A

Nucleoside analogues

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13
Q

How does classical Hodgkin’s lymphoma present clinically?

A

Asymmetrical painless lymphadenopathy (cervical)

May have splenomegaly & hepatomegaly

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14
Q

How is Hodgkin’s lymphoma diagnosed?

A

Reed-Sternberg cells on lymph node biopsy

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15
Q

How are stages I & II Hodgkin’s lymphoma treated?

A

Radiotherapy (short course of chemo if unsuccessful)

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16
Q

How are stages III & IV Hodgkin’s lymphoma treated?

A

Chemo plus radio if bulky disease

STC for younger patients who fail at chemo

17
Q

What factors can trigger NHL?

A

H. Pylori in MALT lymphoma
Hep C in marginal zone lymphoma
Immunosupression

18
Q

What are the characteristics of high grade NHL?

A

Large poorly differentiated lymphoid cells

Aggressive clinical course but are often curable

19
Q

What are the characteristics of low grade NHL?

A

Smaller better differentiated cells

More indolent clinically but havea tendency to relapse

20
Q

How does NHL present?

A
Painless lymphadenopathy in cervical region 
Extranodal involvement (intestinal, CNS, bone marrow)
21
Q

What is the prognosis of follicular lymphoma?

A

Typically disseminated at presentation, initial good response to therapy but increasing relapses
Median survival 6-10 years

22
Q

What is the commonest type of ‘high grade’ NHL?

A

Diffuse large B-cell lymphoma

23
Q

What is the prognosis of diffuse large B-cell lymphoma?

A

70-80% remission

50% cured

24
Q

What is the prognosis for mantle cell lymphoma?

A

Poor (typically disseminated with marrow involvement)

25
Q

How can MALT lymphoma be treated?

A

Antibiotics can lead to regression

26
Q

What is the prognosis for peripheral T-cell lymphomas?

A

Poor due to high incidence of extra-nodal disease