Haematology Flashcards

1
Q

Haemarthrosis without trauma is typically a feature of

A

Haemophilia

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2
Q

Normal/increased/reduced for the following if the patient has haemophilia
APTT
PT
bleeding time

A

APTT - increased
PT - normal
Bleeding time - normal

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3
Q

Normal/increased/reduced for the following if the patient has von wilebrand disease
APTT
PT
bleeding time

A

APTT - increased
PT - normal
Bleeding time - increased

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4
Q

‘starry sky appearance’ think

A

Burkitt’s lymphoma

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5
Q

myeloproliferative disorders can progress into

A

Acute myeloid leukaemia

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6
Q

Which mutation is commonly associated with myeloproliferative disorders?

A

JAK2 mutation

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7
Q

Main FBC finding in polycythaemia

A

Raised Hb

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8
Q

Tear dropped shaped RBCs (poikilocytes) are seen in

A

Myelofibrosis

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9
Q

First line treatment of polycythaemia

A

Venesection

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10
Q

Inheritance pattern for von wilebrands disease

A

Autosomal dominant

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11
Q

Haemophilia A - deficiency in

A

Factor XIII

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12
Q

Haemophilia B - deficiency in

A

Factor IX

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13
Q

Inheritance pattern for Haemophilia A and B

A

X linked recessive

- afects males

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14
Q

Recognised treatment for haemophilia A

A

Dedmopressin

Factor VIII supplementation

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15
Q

Philadelphia chromosome is associated with

A

Chronic myeloid leukaemia

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16
Q

Massive splenomegaly occurs in chronic myeloid leukaemia. True or false?

A

True

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17
Q

Howel jolly bodies - think

A

Splenectomy

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18
Q

What inheritance pattern does sickle cell disease carry

A

Autosomal recessive

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19
Q

Urinary bence jones proteins - think

A

Myeloma

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20
Q

Protein C deficiency, antithrombin III deficiency and factor V leiden are all causes of

A

thrombophilia

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21
Q

What has a SHORTER duration of action

  • LMWH
  • unfractioned heparin
A

Unfractioned heparin

22
Q

Which has better prognosis:

  • low grade non-hodgkins lymphoma
  • high grade non-hodgkins lymphoma
A

High grade non-hodgkins lymphoma

23
Q

Burkitts lymphoma is associated with which infection

24
Q

Pruritis developing after a hot bath makes you think of which condition

A

Polycythaemia rubra vera

25
If someone has microcytic anaemia with profound microcytosis, what do you think?
Thalassaemia
26
``` Newborn baby with prolonged jaundice and anaemia of unknown cause. Blood film shows reticulocytosis with round red cells. Direct coomb's test -ve. What is most likely - hereditary spherocytosis - haemolytic disease of the newborn ```
Hereditary spherocytosis
27
Patients with G6PD deficiency are highly susceptible to developing haemolysis when given which drug?
Nitrofurantoin
28
The characteristic triad of - splenomegaly - neutropenia - rheumatoid arthritis
Felty's syndrome
29
Sudden onset of bleeding in a young child after trivial viral illness suggests
Idiopathic thrombocytopenic purpura
30
Which of the following combinations of blood results are most likely to be seen in sickle cell patients Haemoglobin: increased/normal/reduced Reticulocyte count: increased/normal/reduced MCV: increased/normal/reduced
Haemoglobin: reduced Reticulocyte count: increased MCV: normal AKA normocytic anaemia with raised reticulocyte count
31
Subacute degeneration of the spinal cord with which anaemia
Vitamin B12 deficiency - proprioception gone - can't balance properly
32
If iron deficiency anaemia present, and you give the patient iron supplement, what is the first thing that should change on the bloods?
Reticulocytes | - an appropriate response would be a high reticulocyte count
33
WHat is the test that measures different types of Hb. Indicated in ?thalassaemia?
Hb electrophoresis
34
A 7-year-old girl has a history of intermittent jaundice and fatigue, usually occurring just after she has had a cold.  Her Dad had a splenectomy as a child. Her laboratory results are as follows: Hb                                           90 g/L MCV                                       85 fl WBC                                       6 x 109/l Platelets                                 550 x 109/l Bilirubin                                 50 µmol/l What condition might this suggest?
Haemolysis | Probs autoimmune haemolysis
35
Microcytic anaemia. Defect in - cytoplasm - nucleus
Cytoplasm | - ie problem with haemoglobinisation
36
- Serum ferritin = normal or increased - % transferrin saturation = reduced - MCV = normal (can be reduced) What pitcture does this suggest?
Anaemia of chronic disease
37
Which antiplatelet inhibits COX
Aspirin
38
What is the antidote for heparin?
Protamine sulphate
39
What are the 4 Vitamin K dependent factors?
II, VII, IX, X
40
DIC is caused by (examples)
Massive blood loss RTA Obstetric emergencies
41
Mild transfusion reaction. Is it safe to continue with the transfusion?
Yes - but slow it down
42
Best place to take bone marrow biopsy in a child
Tibia
43
Best place to take bone marrow biopsy in a young adult
Femur
44
Best place to take bone marrow biopsy in an adult
PSIS | Sternum
45
Patient with recurrent nose bleeds and infections after chemotherapy. Which type of anaemia?
Aplastic anaemia
46
What do burr cells indicate
Uraemia
47
Howel jolly bodies - hypersplenism - hyposplenism
Hyposplenism
48
Philadelphia chromosome with which leukaemia
CML
49
severe itch after hot bath think
Polycythaeia rubra vera
50
First line pain relief for bony mets
Ibuprofen