Lecture 8 - Haematology I (Erythrocytes) Flashcards

1
Q

What does the multipotential haematopoietic stem cell first develop into in erythropoiesis?

A

Common myeloid progenitor

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2
Q

What 5 things are required for erythropoiesis?

A

Erythropoietin
Vitamin B12 + B9 (folic acid)
Iron
Amino Acids
Intrinsic Factor

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3
Q

Where in the body does erythropoiesis occur in foetus, infant and adult?

A

Foetus: initially yolk sac, then liver + spleen, then bone marrow
Infant: in all bone marrow
Adult: in only red bone marrow

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4
Q

What happens to haemoglobin in the recycling of erythrocytes?

A

It is broken down into haem and globin. Globin -> amino acids
Haem -> Iron and Bilirubin

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5
Q

What happens to iron when haem is broken down into Iron and Bilirubin?

A

Iron either goes back to bone marrow (for erythropoiesis again) or binds with its transport protein (transferrin) to be stored in the liver (as ferritin) or spleen. Eventually, always used in erythropoiesis again.

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6
Q

4 main causes of hypoxia?

A

Increase in exercise, high altitude, smoking, bleeding

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7
Q

What is the approximate average Haemoglobin level for adults?

A

15 g/dL

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8
Q

What are the 3 main forms of anaemia?

A

Iron deficiency, megaloblastic and sickle cell

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9
Q

3 main symptoms of Iron Deficiency Anaemia

A

Hypochromic Red Blood Cells (paler than usual)
Microcytic RBCs (smaller than usual)
Decreased mean cell volume

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10
Q

Main causes of Iron Deficiency Anaemia

A

Pregnancy
Bleeding from GI Tract (ulcer, malignancy)
Malabsorption
Malnutrition
Menorrhagia

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11
Q

Causes of Megaloblastic Anaemia

A

Either Vitamin B12 or Folate deficiency

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12
Q

Symptoms of Megaloblastic Anaemia

A

Macrocytic RBCs (larger than usual)
Reduced Haemoglobin Concentration
Hypersegmented Neutrophil (more lobes than usual)

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13
Q

Define ‘Pernicious Anaemia’

A

A specific type of anaemia related to Vitamin B12 deficiency

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14
Q

Define Sickle Cell Anaemia + Effect(s)

A

A hereditary disease - abnormal (sickle) haemoglobin causes sickle-shaped cells which sometimes get stuck in blood vessels

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15
Q

(All we need to know about) Thalassaemia?

A

Hereditary disease - abnormal haemoglobin production
Alpha and Beta Thalassaemia exist

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