Haematology Flashcards

1
Q

Thrombotic thombocytopaenic purpura

?signs

A

Fever, neuro signs, thrombocytopaenia, haemolytic anaemia, renal failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Factor V Leiden

A

Most common inherited Thrombophilia

Activated protein C resistance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Anti-phospholipid syndrome

A

Arterial and venous thrombosis
Foetal loss
Thrombocytopaenia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Basophilic stippling (conditions)

A

Heavy metal poisoning e.g. lead
Myelodysplastic syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Heinz bodies

A

G6PD deficiency
Removed by spleen resulting in bite cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Howell-Jolly bodies

A

Hyposplenism e.g coeliac disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Target cells

A

Hyposplenism e.g coeliac disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Acanthocytes

A

Hyposplenism e.g coeliac disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Immune thrombocytopenia (ITP)

Antibodies against…
Signs/symptoms
Treatment

A

Antibodies against glycoprotein IIa/IIIb or Ib-V-IX complex

Purpura, petechiea, bleeding (eg epistaxis)

Oral prednisolone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Low haemoglobin 2/52 post-transfusion
Positive direct antiglobulin test
Raised unconjugated bilirubin
Reticulocytosis
High LDH

A

Delayed transfusion reaction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Factor V Leiden prevalence

A

5%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

TTP - cells seen on film

A

Fragmented cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

central cyanosis (blue lips, nails, body)
Steel-grey complexion
Elevated/normal pO2 but low saturations

A

Methaemoglobinaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Left shift of oxygen dissociation curve

A

Increased binding affinity with decreased release into the tissues

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Hypersegmented neutrophils

A

Vitamin B12 deficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Microangiopathic haemolytic anaemia = non-immune haemolytic anaemia (Coombs negative)

Causes

A

DIC
TTP
HUS
Atypical HUS

17
Q

Haemolytic uraemic syndrome

Features

A

Abdominal pain, bloody diarrhoea -> Shiga toxin
AKI
Haemolytic anaemia
Coombs test negative

18
Q

Atypical uraemic syndrome

Features

A

Diarrhoea/abdo symptoms not present
AKI
Haemolytic anaemia
Coombs test negative

19
Q

TTP

A

Haemolytic anaemia
Coombs test negative
Neurological symptoms
GI symptoms
AKI can occur but is rare

20
Q

Paroxysmal nocturnal haemoglobinuria

diagnostic test

A

flow cytometry of blood to detect low levels of CD59 and CD55

21
Q

TTP treatment

A

Plasma exchange

22
Q

Medication used in prevention of sickle cells crises

A

Hydroxycarbamide

23
Q

Immune thrombocytopaenia (ITP)

Features
Treatment

A

Thrombocytopaenia

Platelet >30, nil effects - observation
Platelet <30 or effects on daily life - Oral prednisolone

Life threatening/organ threatening bleeding - platelet transfusion, IV methylpred, IV Immunoglobulin

24
Q

Most common haemophilia

A

Haemophilia A

25
Q

Haemophilia A

Affects what test and clotting factor?

A

APTT - intrinsic
Factor VIII

26
Q

smudge cells

A

CLL

27
Q

Basophilic stippling

A

Lead poisoning
Beta-thalassaemia

28
Q

Leukemoid reaction vs CML

A

Leukemoid reaction
- high leucocyte alkaline phosphatase
- toxic granulation (dohle bodies) in WC
- ‘left shift’ of neutrophils

CML
- cytogenics = presence of Philadelphia chromosome

29
Q

Hereditary spherocytosis

Investigation of choice

A

EMA binding test

30
Q

G6PD deficiency haemolysis

Investigation of choice

A

Beutler fluorescent spot test

31
Q

low ADAMTS13

diagnosis

A

TTP