Haematology/ Oncology Flashcards

0
Q

What are poikilocytes and fragmented res blood cells indicative of?

A

Iron deficiency anaemia

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1
Q

What is the most likely cause of iron deficiency anaemia in children?

A

Poor dietary intake combined with excessive cows mild consumption

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2
Q

What populations is thallasaemia more common in?

A

Asian and Mediterranean

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3
Q

Thallasaemia and iron deficiency anaemia both present with microcytic hypochromic RBC’s how can you differentiate?

A

In iron def. anaemia there is low ferritin, in thalasaemia there is normal ferritin

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4
Q

What are the two types of thalasaemia?

A

Alpha and beta

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5
Q

How can you differentiate between alpha and beta thalassaemia?

A

In beta there is in increase in HbF (fetal haemaglobin) and HbA2 (a normal variant of haemaglobin A)

These are normal or low in alpha thalasaemia

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6
Q

What can precipitate a sickle cell crisis?

A

Dehydration
Infection
Hypoxia
Acidosis

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7
Q

If a blood film shows target cells, poikilocytes what might this suggest?

A

Sickle cell anaemia

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8
Q

How is sickle cell diagnosed, what test?

A

Haemaglobin electrophoresis

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9
Q

What is the commonest haemaglobinopathy?

A

Sickle cell

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10
Q

What race is sickle cell more common in?

A

West Africans, Afro Caribbeans

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11
Q

How does sickle cell crisis present?

A

Painful swelling of hands and feet

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12
Q

What malignancies is Epstein Barr virus involved in the pathogenosis?

A

Burkitts lymphoma
Lymphoproliferative disease
Nasopharyngeal carcinoma

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13
Q

Describe the change in Hb conc in neonates..

A

It is high at birth (particularly after delayed cord clamping) and lowest at age 2-3 months

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14
Q

How long after birth does a baby have adequate stores of iron?

A

4 months

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15
Q

What iron supplements are given to children?

A

Sytron (sodium iron edetate)
Niferex ( polysaccharide iron complex)

Ferrous sulphate tastes too bad!

16
Q

How long should iron supplementation be continued for?

A

At least 3 months to replenish stores

17
Q

On iron treatment how quickly should iron levels rise?

A

1 g/dl per week

18
Q

What does G6PD enzyme deficiency cause?

A

Episodes of haemolysis..

Causing neonatal jaundice

19
Q

In children with G6PD deficiency what can precipitate haemolysis?

A

Infection

And maybe drugs

20
Q

In haemophilia A what clotting factor is decreased?

A

Factor 8

21
Q

In haemophilia B what clotting factor is decreased?

A

Factor 9

22
Q

Henoch Schonlein purpurin are related to what other conditions?

A
Joints 
Kidneys (protein and haematuria)
GI tract (intussception)
23
Q

What kind of patten might you see on a FBC of a child with leukaemia?

A
Pancytopenia
So 
Low platelet 
Low Hb 
Low WCC (although this could be excessively raised)
24
Q

What is the other name for a nephroblastoma?

A

Wills tumour

25
Q

How might a wills tumour present?

A
Mostly assymptomatic
Can get
Abdo mass/pain
Haematuria/uti
Hypertension
26
Q

How do you decide whether an anaemia is microcytic or normocytic?

A

Use the mean cell volume

27
Q

What is Coombs test?

What conditions might this be positive in?

A

Measures the presence of IgG on RBCs
Immune related haemolytic anaemia
Haemolytic disease of the newborn

28
Q

In DKA is potassium high or low?

A

High

29
Q

What signs might hyperkalaemia show on an ECG?

A

Widened QRS and peaked T waves

30
Q

What is the inheritance pattern for haemophilia A?

A

X linked recessive

31
Q

Which is more common haemophilia A or B

A

A is more common

32
Q

Which clotting cascade is affected by a deficiency in factor 8 and 9?
How does this affect the prothrombin time?

A

Intrinsic

It doesn’t as this is a measure of the extrinsic pathway

33
Q

When do symptoms of haemophilia usually start?

A

When the child becomes mobile - bleed into joints