Formative assessment Flashcards

1
Q

A blood film contains macrovalocytes and hypersegmented neutrophils.

Which type of anaemia is these buzzwords referring to?

What is the cause?

A

Megaloblastic anaemia (a type of macrocytic anaemia)

Vitamin B12 / Folate deficiency

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2
Q

Which autoimmune disease can cause B12 / Folate malabsorption?

A

Pernicious anaemia

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3
Q

What are two blood film buzzwords for B12 / Folate deficiency?

A

Macrovalocytes

Hypersegmented neutrophils

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4
Q

What is a blood film finding specific to acute myeloid leukaemia?

A

Auer rods

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5
Q

A patient’s blood film contains Auer rods.

Which haematological malignancy is this referring to?

A

Acute myeloid leukaemia (AML)

Remember CML has its own buzzwords: Philadelphia chromosome (22) mutation, BCR-ABL1 positive, treated with imatinib

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6
Q

What does a monocyte look like under the microscope?

A

Horseshoe nucleus

White vacuoles

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7
Q

In which situations would you give a patient

a) iron tablets

b) iron injections?

A

a) Mild iron deficiency anaemia

b) Severe iron deficiency anaemia

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8
Q

How do you treat autoimmune haemolytic anaemia?

A

Steroids

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9
Q

How do you treat Waldenstrom’s (IgM) disease?

A

Cytotoxic drugs

Plasma electropharesis

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10
Q

Which anticoagulant drugs target Factor Xa?

A

Rivaroxaban

Apixaban

Edoxaban

i.e all the novel anticoagulants with -xa- in their name

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11
Q

Which type of blood cells express CD20 antigens?

A

B cells

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12
Q

Which type of blood cells express CD30 antigens?

A

T cells

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13
Q

Which drug targets CD20 and can therefore be used to target B cell lymphomas?

A

Rituximab

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14
Q

Which drug targets BCR-ABL1 tyrosine kinase?

Which haematological malignancy is this enzyme associated with?

A

Imatinib

CML

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15
Q

Which drug targets Factors II, VII, IX and X?

A

Warfarin

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16
Q

Which disease is JAK2 mutation associated with?

A

Polycythaemia rubra vera

17
Q

Which drug potentiates the action of antithrombin?

Which types of this drug potentiate antithrombin’s action against

a) thrombin
b) factor Xa?

A

Heparin

a) Unfractionated heparin

b) LMWH e.g dalteparin

18
Q

Which drug inhibits platelet activation by inactivating cycloxygenase enzymes?

A

Aspirin

19
Q

Which drug inhibits primary haemostasis by antagonising ADP?

A

Clopidogrel

Ticagrelor

20
Q

Which NOAC directly inhibits thrombin?

A

Dabigatran

21
Q

Bence Jones proteins (light chains found in a urine sample) indicates which haematological malignancy?

A

Multiple myeloma

22
Q

Which drugs tend to cause a prolonged

a) PT / INR

b) APTT?

A

a) Warfarin

b) Heparin

23
Q

Which disease causes a drop in platelets and fibrinogen, plus prolonged clotting times?

A

Disseminated intravascular coagulation (DIC)

Treat with platelet transfusions and fresh frozen plasma

Treat underlying cause

24
Q

Which disease are you testing for with a JAK2 gene analysis?

A

Polycythaemia rubra vera

i.e primary polycythaemia

25
Q

What is the purpose of a Coombs test?

A

To differentiate between an autoimmune and non-autoimmune cause of haemolytic anaemia

(Autoimmune HA is Coombs positive, other causes e.g Sickle cell are Coombs negative)

26
Q

What disease is associated with a raised serum caeruloplasmin?

A

Wilson’s disease

27
Q

Immunophenotyping is used to differentiate between different kinds of ___.

A

lymphoma

28
Q

What is a Kleihauer test used to detect?

A

Antepartum haemorrhage

29
Q

Name two tests which can be used to detect thalassaemia.

A

Osmotic fragility analysis

Haemoglobin analysis

because this is a disease affecting globin chains

30
Q

Name a cause of single factor deficiency.

A

Haemophilia A/B

31
Q

Name some causes of multiple factor deficiency.

A

DIC

Liver failure

32
Q

If an investigation references the red cell membrane, which disease does it likely involve?

A

Hereditary spherocytosis

but you’d see this on a blood film???

33
Q

What is the (really simple) pathophysiology of sickle cell anaemia?

A

Point mutation in globin gene producing HbS instead of HbA

34
Q

Transfusions can acutely injure which organs?

A

Lungs

35
Q

Loss of central pallor is a buzzword for which disease?

A

Spherocytosis

36
Q

What is a sickle crisis?

A

Episodes of ischaemia (pain) caused by blockage of capillaries by sickle cells

37
Q

Antiphospholipid syndrome is an (inherited / acquired) cause of thrombophilia.

A

acquired

others, like Factor V Leiden & antithrombin, protein C & S deficiencies are usually INHERITED