Haematology Flashcards

1
Q

what are the features of rhesus cross matching transfusion reaction

A

back pain, dyspnoea and cv collapse

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2
Q

what haematological disorder is associated with bcr abl gene?

A

chronic myeloid leukaemia (also ALL)

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3
Q

what is typical of paroxysmal nocturnal haemoglobinria

A

brown urine and dipstick positive for blood but then no red cells on microscopsy

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4
Q

What is the pathophysiology in methaemoglobinaemia

A

oxidation of Fe2+ to Fe3+

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5
Q

what chromosomal abnormalities is associated with a poor prognosis in AML

A

chromosome 7

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6
Q

should a lump suspicious for a lymphoma be excision biopsied or fine needle biopsied?

A

excision

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7
Q

if a blood sample is contaminated with heparin what will be rasied?

A

aptt

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8
Q

what finding is there after a splenectomy on blood film

A

howell jolly bodies

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9
Q

Where do you see heinz bodies

A

g6pd deficiency

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10
Q

where are auer rods seen

A

blast cells in aml

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11
Q

what is the worst category of hodgkin’s

A

lymphocyte deplete hodkin’s

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12
Q

what haematological conditions result in gout

A

myeloproliferative disorders eg polycythaemia vera

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13
Q

what is underlying cause of haemolysis in G6PD deficiency

A

reduced levels of NADPH

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14
Q

how is g6pd inherited

A

x linked

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15
Q

In which condition is philadelphia chromosome a poor prognosis

A

ALL (always found in CML)

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16
Q

which paraprotein is increased in waldestrom’s macroglbulinaemia

A

IgM paraprotein

17
Q

what abnormality does cyclosporin toxicity cause

A

renal dysfunction

18
Q

What is the drug for heparin reversal

A

protamine sulphate

19
Q

what is the drug for the reversal of warfarin

A

prothrombin complex concentrate (in acute), less acute is vitamin K

20
Q

what should be used to reverse systemic effects alteplase?

21
Q

When does sideroblastic anaemia occur (rings of iron around nuclei of developing erythrocytes)

A

lead poisoining, myelodysplastic syndroe

22
Q

what is mycosis fungoides

A

cutaneous t cell lymphoma

23
Q

What clotting disorder has been described in nephrotic syndrome

A

protein S deficiency

24
Q

Why do we use irradiated blood products

A

inactivates donor lymphocytes

25
Treatment of DIC
Al trans retanoic acid With daunorubicin or idarubicin
26
Clinical features of ttp
Anaemia and thrombocytopenia (pentad)
27
Triad of HUS
1. Aki 2. Microangiopathic hemolytic anaemia 3. Thrombocytopenia
28
Protein implicated in hereditary spherocytosis
Spectrin
29
What can fludabarine cause
ai Haemolytic anaemia Tx prednisolone or rituximab if no response
30
Tx for raised inr with warfarin
Prothrombin complex concentrate
31
treatment for waldestrom's macroglobulinaemia
bendamustine plus rituximab
32