Haemolytic anaemia Flashcards

1
Q

what are the clinical features of haemolytic anaemias?

A
  • pallor of mucous membranes
  • mild fluctuating jaundice
  • splenomegaly
  • urine may turn dark on standing
  • pigment gallstones may occur
  • aplastic crises may occur
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2
Q

aplastic crises are characterised by what?

A

a sudden increase in anaemia and drop in reticulocyte count

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3
Q

what are the lab findings of haemolytic anaemia?

A
  • serum bilirubin increased
  • urine urobilinogens increased
  • serum haptoglobin absent
  • reticulocytosis
  • bone marrow erythroid hyperplasia
  • damaged red cells
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4
Q

what are the causes of intravascular hemolysis?

A
  • mismatched blood transfusion
  • G6PD deficiency with oxidant stress
  • red cell fragmentation syndromes
  • Some severe autoimmune haemolytic anaemias
  • Some drug- and infection-induced haemolytic anaemias
  • Paroxysmal nocturnal haemoglobinuria
  • March haemoglobinuria
  • Unstable haemoglobin
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5
Q

what are the main lab findings of intravascular haemolysis?

A
  • haemoglobinaemia and haemoglobinuria
  • haemosiderinuria
  • methaemalbuminaemia
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6
Q

what are examples of hereditary haemolytic anaemia?

A
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7
Q

what is the pathogenesis of hereditary spherocytosis?

A
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8
Q

what are the clinical features of hereditary spherocytosis?

A
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9
Q

what are the haematological findings of hereditary spherocytosis?

A
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10
Q

what is the investigation for HS?

A
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11
Q

what is the treatment for HS?

A
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12
Q

what is the G6PD deficiency?

A
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13
Q

what is the pattern of inheritance for G6PD?

A

X-linked (affecting males)

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14
Q

What is the is the pattern of inheritance HS?

A

autosomal dominant

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15
Q

what are the clinical features of G6PD?

A
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16
Q

how is G6PD diagnosed?

A
17
Q

how is G6PD treated?

A
18
Q

what pattern of inheritance is in pyruvate kinase deficiency?

A

autosomal recessive

19
Q

what is warm AIHA?

A
20
Q

what are the clinical features of warm AIHA?

A
21
Q

what are the lab findings in warm AIHA?

A
22
Q

how is warm AIHA treated?

A
23
Q

what are the clinical features of beta thalasaemmia major?

A
24
Q
A