Haematology Flashcards

1
Q

Criteria for starting treatment in CLL (5)

A

Thrombocytopaenia
Marrow failure
Lymphadenopathy
Splenomegaly
(both of these have to be widespread/massive)
Systemic symptoms - >10% weight loss in 6 months

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2
Q

Management of genetic methahaemaglobinaemia

A

Asorbic acid

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3
Q

2nd line agent in CLL

A

Ibrutinib

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4
Q

Burkitt’s Lymphoma
- association
- genetics

A

HIV
t8:14

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5
Q

What qualifies as progressive lymphocytosis in CLL requiring treatmetnt?

A

Doubling over 2 months

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6
Q

MDS vs AML - blood film findings

A

AML >20% blasts in peripheral blood

MDS = hypogranular, hypo lobulated neutrophils

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7
Q

ADAMST13

A

Can be low in HUS
Not as low as in TTP

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8
Q

Platelet refractoriness
- definition
- management

A

= PLT rise <10
Check anti-HLA or anti-platelet antibodies

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9
Q

Wells Score for DVT
- pathway

A

< 2 = d-dimer
>= 2 = leg US

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10
Q

Haemophilia A
vs
vWF

A

Both have low factor VIII

vWF = prolonged bleeding time, platelet aggregation impaired

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11
Q

Investigation of choice in CLL

A

Immunophenotyping
Cytogenetics used for prognostication

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12
Q

Anticoagulation in HIT

A

Bivalirudin (direct thrombin inhibitor)
Cannot use warfarin - doesn’t help with the risk of thrombus and increased risk of skin gangrene

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13
Q

Hairy cell leukaemia
- what is the associated mutation?

A

BRAF mutation

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14
Q

Blood product of use in DIC

A

Fresh frozen plasma

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15
Q

Investigation of choice in multiple myeloma

A

Whole body MRI

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16
Q

Need to raise platelets quickly in ITP

A

IV immunoglobulin