Blood Disorders Flashcards

1
Q

What is polycythemia?

A
  • also known as erythrocytosis
  • too many RBCs
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2
Q

What is anaemia?

A

Too little RBCs

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3
Q

What is Leukocytosis?

A
  • too many WBCs
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4
Q

What is Leukopenia?

A
  • too few WBCs
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5
Q

What is thrombocytosis?

A
  • too many platelets
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6
Q

What is Thrombocytopenia?

A
  • too few platelets
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7
Q

What is Pancytopenia?

A
  • too few RBCs, WBCs and platelets
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8
Q

What are the possible causes of Polycythaemia?

A

Primary:
1. polycythaemia rubra vera (myoproliferative disorder)

Secondary:
2. hypoxia (e.g. living at high altitudes, chronic lung disease)
3. erythropoietin-producing tumours

Relative:
4. dehydration => apparent rise in RBC due to drop in blood plasma

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9
Q

What are the effects of Polycythaemia?

A
  • tiredness
    -CNS disturbances: headache, disturbed vision
  • bruising
  • clotting, sludging (RBC massed along vessel walls => decrease in lumen size & blood flow rate)
  • gout
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10
Q

Name the causes of Anaemia?

A

1. Decreased RBC production
- deficiency in
1. Iron => hypochromic (less Hb), microcytic (smaller RBC)
2. vit B12 => megaloblastic (bigger RBC), RBC cannot exit bone marrow

2. Loss of RBC
- due to bleeding

3. Increased destruction of RBC
- haemolysis (RBC lysis)
-> due to membrane defects (e.g. spherocytosis)
-> Hb defects (e.g. sickle cell disease, thalassaemia)
-> enzyme defects (e.g. G6PD deficiency)
- hypersplenism: splenomegaly, splenic sequestration of RBC

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11
Q

What causes decreased RBC pdn?

A
  1. Iron => hypochromic (less Hb), microcytic (smaller RBC)
  2. vit B12 => megaloblastic (bigger RBC), RBC cannot exit bone marrow
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12
Q

What can cause the increased destruction of RBCs?

A

Haemolysis (RBC lysis) due to:
1. Membrane defects (e.g. spherocytosis)
2. Hb defects (e.g. sickle cell disease, thalassaemia)
3. Enzyme defects (e.g. G6PD deficiency)

Hypersplenism (overactive spleen) due to:
Splenomegaly => causes splenic sequestration of RBC

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13
Q

What are the effects of Anaemia?

A
  • Weakness, lethargy
  • Dizziness, syncope (fainting)
  • Shortness of breath
  • Palpitations, chest pain, heart failure
  • Pallor (unhealthy pale appearance)
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14
Q

How is leukemia clinically classified?

A

Acute vs Chronic

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15
Q

Where do Leukaemias originate from?

A

Bone marrow
- malignancy of haemopoietic system
- usually large no. of tumour cells circulating in peripheral blood
- does not form masses (unlike lymphomas which arise as discrete tumour masses)

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16
Q

The 2 types of leukaemia are? (Based on cells affected)

A
  1. Lymphoid:
    - lymphoid cells give rise to B & T lymphocytes & NK
  2. Myeloid: all cells (RBC, granulocytes, monocytes & platelets + lymphocytes)