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?

A

TXA

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
Q

Treatment of DIC

A

Al trans retanoic acid

With daunorubicin or idarubicin

26
Q

Clinical features of ttp

A

Anaemia and thrombocytopenia (pentad)

27
Q

Triad of HUS

A
  1. Aki
  2. Microangiopathic hemolytic anaemia
  3. Thrombocytopenia
28
Q

Protein implicated in hereditary spherocytosis

A

Spectrin

29
Q

What can fludabarine cause

A

ai Haemolytic anaemia
Tx prednisolone or rituximab if no response

30
Q

Tx for raised inr with warfarin

A

Prothrombin complex concentrate

31
Q

treatment for waldestrom’s macroglobulinaemia

A

bendamustine plus rituximab

32
Q
A