Haematology🩸 Flashcards

1
Q

What does TAILS stand for?

A

Thalassaemia
Anaemia of chromic disease
Iron deficiency
Lead poisoning
Sideroblastic

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2
Q

HbA2 results in B thalassaemia

A

High

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3
Q

HbA2 results in alpha thalassaemia

A

Normal or low

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4
Q

Key symptoms of anaphylactic blood transfusion reaction

A

Resp distress
Wheezing
Skin - rash

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5
Q

Initial management of cold AIHA

A

Avoid cold

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6
Q

Initial management of warm AIHA

A

Prednisolone

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7
Q

Factor reduced in haemophilia B

A

IX

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8
Q

Management for severe haemophilia B

A

Prophylactic recombinant factor IX

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9
Q

What is the Philadelphia chromosome

A

Translocations between 9 and 22

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10
Q

Philadelphia chromosome is hallmark of what blood cancer

A

CML

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11
Q

Diagnostic test for ALL

A

Bone marrow biopsy and aspiration

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12
Q

“Dry tap” on bone marrow aspiration is usually due to what

A

Bone marrow fibrosis

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13
Q

First line treatment for symptomatic myelofibrosis

A

Ruxolitinib

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14
Q

Ruxolitinib MOA

A

JAK1/2 inhibitor

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15
Q

Characteristic signs of warm AIHA (5)

A

Haemolysis
Reticulocytosis
Elevated bilirubin
Raised LDH
Low haptoglobin

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16
Q

What does Coomb’s test test for

A

Direct antiglobulin - IgG and/or C3d

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17
Q

Initial CML treatment

A

Imatinib

18
Q

Imatinib MOA

A

tyrosine kinase inhibitor

19
Q

Presence of what genes confirms CML

A

BCR-ABL1 fusion
Philadelphia chromosome

20
Q

Lymphoma with alcohol induced pain

A

Hodgkin’s

21
Q

DIC is characterised by what feature

A

Simultaneous thrombosis and bleeding due to consumption of clotting factors and platelets

22
Q

Haemophilia blood test results - aPTT, PT, bleeding time

A

Prolonged aPTT
Normal PT
Normal bleeding time

23
Q

Intrinsic pathway dysfunction leads to prolonged what

A

Prolonged aPTT

24
Q

Management of TACO

A

Stop transfusion
Furosemide

25
Q

Symptoms of AML (4)

A

Fatigue
Frequent infections
Bruising
Bleeding

26
Q

Polycythemia Vera can progress to what blood cancer

A

CML

27
Q

Clopidogrel MOA

A

Irreversible inhibitor of P2Y12 receptor on platelets, preventing ADP-induced activation of GPIIb/IIIa receptors complex

28
Q

Which haemophilia is more likely

A

A

29
Q

Smudge cells suggest what

A

CLL

30
Q

AML findings on blood film

A

Auer rods

31
Q

Howell-Jolly bodies suggest what

A

Splenic dysfunction or absence

32
Q

4 features of acute haemolytic transfusion reaction

A

Fever
Hypotension
Nausea
Anxietu

33
Q

2 Symptoms which suggest haemolysis

A

Fatigue
Mild jaundice

34
Q

Reed-Sternberg cells are present in which blood cancer

A

Hodgkin’s

35
Q

EBV is a risk factor for which blood cancer

A

Hodgkin’s

36
Q

First line anti platelet for PV

A

Low-dose aspirin

37
Q

What is Richter’s transformation

A

Usually CLL, progressing to more aggressive lymphoma, usually diffuse large B cell

38
Q

2 characteristic features of aplastic anaemia

A

Pancytopenia
Hypo cellular bone marrow

39
Q

Initial treatment for mild-moderate haemophilia A

A

Desmopressin DDAVP

40
Q

Sickle cell crisis initial management

A

IV morphine