Haematology Flashcards

1
Q

Haemophilia A

A

Causes hemarthrosis without trauma

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

VTE

A

Anticoagulate with warfarin for 3 months is provoked and 6 months if unprovoked

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

Burkitt lymphoma

A

Starry sky appearance on lymph node biopsy

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

Sequestration crisis

A

Occurs in sickle cell anaemia and causes splenomegaly with abdominal pain

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

Beta-thalassaemia trait

A
  • microcytic anaemia
  • raised HbA2
  • lethargy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

C-myc translocation

A

Genetic change in Burkitt’s lymphoma

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

Antiphospholipid syndrome

A
  • prolonged APTT
  • history of VTE, PE and miscarriage
  • elevated anticardiolipin antibody
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Antiphospholipid syndrome (pregnancy)

A

Anticoagulate with aspirin and enoxaparin

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

Irradiated blood products

A

Used to avoid transfusion-associated graft vs host disease

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

Tranaxamic acid

A

When given in major haemorrhage give IV bolus and then slow infusion

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

Blood transfusion

A

Give if haemodynamically unstable or Hb is less than 70g/L

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

Neutropenic sepsis

A

Empirical treatment with piperacillin and tazobactam

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

Blood transfusion complications

A
  • iron overload
  • ARDS
  • hyperkalaemia
  • clotting abnormalities
  • febrile reaction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Multiple myeloma

A

Rain drop skill or pepperpot skull seen on imaging

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

Disseminated intravascular dissemination

A

Give fresh frozen plasma

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

Vitamin B12 deficiency

A

Causes macrocytic anaemia

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

G6PD

A
  • pallor
  • jaundice
  • haemolytic anaemia
  • previous URTI
  • Heinz bodies
18
Q

Multiple myeloma

A

Typically causes hypercalcaemia, pancytopenia and AKI

19
Q

Reed-Sternberg cells

A

Have mirror image nuclei and are seen in Hodgkin’s lymphoma

20
Q

Stage two Hodgkin’s lymphoma

A

Tow or more lymph nodes on the same side of the diaphragm

21
Q

Philadelphia chromosome

A

t(9;22) associated with CML

22
Q

Idarucizumab

A

Reversible agent for dabigatran

23
Q

Hereditary spherocytosis

A

-jaundice, fatigue and splenomegaly in haemolytic crisis

24
Q

Cryoprecipitate

A

Given in major haemorrhage when the fibrinogen level is low

25
Sickle cell anaemia
Normocytic anaemia with Howell-Jolly bodies
26
Autoimmune haemolytic anaemia
Can be caused by SLE
27
DVT in pregnancy
Tend to give subcutaneous low molecular weight heparin
28
Tumour lysis syndrome
Can give allopurinol or rasburicase prior to chemo to reduce the risk
29
Platelet transfusion
High risk of bacterial contamination compared to other blood products
30
Non-haemolytic febrile transfusion syndrome
Pause transfusion and assess for risk and if safe give IV paracetamol and continue
31
Coeliac disease
Can cause target cells and Howell-Jolly bodies due to hyposplenism
32
Polycythaemia rubra vera
Around 5-15% progress to myelofibrosis or AML
33
Beta thalassaemia
Microcytic, hypochromic anaemia - basophilic stippling - occasional target cells
34
Lead poisoning
- gastrointestinal and neuropsychiatric symptoms - anaemia - blue line on gum margin
35
Aplastic crisis
Seen in sickle cell disease often related to parvovirus infection
36
Haemophilia A
Factor VIII associated with 90% of all haemophilia
37
Acute haemolytic transfusion reaction
Combs test | -RBC destruction by IgM
38
Dabigatran
Direct thrombin inhibitor
39
Won willebrands disease
- prolonged bleeding time - normal platelet count - prolonged APTT
40
Factor V Leiden
Also known as activated protein C resistance and the most common inherited thrombophilia
41
Antiphospholipid syndrome
History of clotting and bleeding | -need aspirin and LMWH in pregnancy