Haem Flashcards

(50 cards)

1
Q

What is the best way to measure someones iron store level?

A

Serum ferritin

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

What type of cell on blood smear indicates myelofibrosis?

A

Tear drop cells (dacrocytes)

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

What conditions causes a schistocyte on blood smear?

A

Haemolytic anaemia, DIC

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

What conditions cause a spherocyte?

A

Haemolytic anaemia

Hereditary spherocytosis

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

What conditions cause a target cell?

A

Obstructive jaundice
Liver disease
Haemaglobinopathies
Hyposplenism

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

Pt post op who had 3 blood units. PC: fever, low BP, cyanosis, dry cough. Dx?

A

TRALI - tissue related lung injury

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

What is a TRALI?

A

2-6hrs after transfusion, neutrophils get sequestered in lungs and ABs form against donor WBCs. ABs then attack the pt’s lungs

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

How do you differentiate between immediate haemolytic transfusion reaction and a delayed haemolytic reaction?

A

IHTR < 24hrs post transfusion

DHR >24hr post transfusion

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

What are 2 differentials for megaloblastic anaemia?

A

B12 deficiency

Folate deficiency

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

Limb parasthesia and numbness. Hypersegmented neutrophils. Dx?

A

B12 deficiency

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

What is pernicious anaemia?

A

AI condition where ABs bind to intrinsic factor thus preventing B12 absorption

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

What condition is associated w pernicious anaemia?

A

Thyroid disease

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

What does PT vs PTT measure?

A
PT = extrinsic pathway 
PTT = intrinsic pathway
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Normal PT and platelets. Abnormal PTT and bleeding time. Dx?

A

vWF deficiency

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

Normal bleeding time and platelets. Prolonged PT and PTT. DDx?

A

Factor V deficiency
Vitamin K deficiency
Warfarin therapy

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

Fever + neutropenia. Dx?

A

Septicaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Neutropenia, anaemia, thrombocytopenia. >20% myeloblasts. Dx?

A

AML

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Neutropenia, anaemia, thrombocytopenia. >20% lymphoblasts. Dx?

A

ALL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Sx of thrombotic thrombocytopenia purpura?

A
PENTAD 
Fever
Thrombocytopenia 
Microangiopathic haemolytic anaemia 
Renal failure 
Neuro Sx
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Headaches, dizziness, severe pruritus after hot baths. Dx?

A

Polycythaemia vera

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What is myelofibrosis?

A

Fibrosis of bone marrow due to abnormal megakaryocytes which produce XS fibrosising factors.

22
Q

List 4 causes of massive splenomegaly

A

CML
Thalassaemia
Polycythaemia rubra vera
Kala-azar

23
Q

What cell type on blood film indicates haemolysis?

24
Q

What is the function of G6PD?

A

Maintaining levels of glutathione (protects against oxidative stress)

25
What happens if someone with G6PD deficiency takes anti malarias?
Denatures Hb producing HEINZ BODIES
26
What is characteristic of microangiopathic haemolytic anamiea?
Anaemia and schistocytes on blood smear
27
Which test is used for investigating potential sickle cell?
Sodium metabisulfate
28
What test is used for B12 deficiency?
Schilling's
29
What test can be used to investigate causes of haemolytic AI anaemia?
Coomb's
30
What stain is used to differentiate between AML and ALL?
Sudan black
31
What are the erythropoetin and red cell mass levels in polycythaemia rubra vera?
HIGH red cell mass | LOW erythropoetin
32
Which iron protein is raised in iron deficiency anaemia?
Transferrin - it is the iron carrying protein so increases when reduced iron
33
Malaise, SoB, parasthesia in hands. Schillings positive. Dx?
Pernicious anaemia
34
Pancytopenia, macrocytosis with bone marrow hypocellularity. Dx?
Aplastic anaemia
35
What type of Hb is raised in aplastic anaemia?
Foetal
36
Fatigue. Fevers. Bleeding gums. Blood film shows auer rods, hypogranular neutrophils. Stains with Sudan black B. Dx?
AML
37
What cells are seen on blood film in ALL?
Lymphoblasts
38
Philadelphia chromosome present. Dx?
CML
39
Tx of CML?
Imatinib (tyrosine kinase inhibitor)
40
What is the INR?
Ratio between pt's prothrombin time vs normal
41
What is a normal INR?
0.9 to 1.3
42
Pt with rheumatic mitral valve + AF. INR?
2 - 3
43
Is multiple myeloma hereditary?
NO
44
List risk of multiple myeloma
Radiation, herbicides/insecticides, herpes HHV-8, HIV
45
What test differentiates between hypersplenism and aplastic anaemia?
Reticulocyte test - reduced in AA but raised in hypersplenism
46
What AB is associated with pernicious anaemia?
Anti-intrinsic factor AB
47
How do you investigate leukaemia?
bone marrow aspirate under microscopy
48
What is the numerical definition of acute leukaemia?
>20% of bone marrow cells being blasts
49
What type/part of AB is Bence Jones protein?
Light chain
50
Why do you get bence jones proteins?
Myeloma cells produce them