Microcytic anaemia Flashcards

1
Q

What are the microcytic anaemias

A

Anaemia of chronic disease
Iron deficiency anaemia
Sideroblastic anaemia
Haemoglobinopathies - thalassaemia

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3
Q

Causes of anaemia of chronic disease

A

Chronic inflammation e.g RA
Neoplasia
Renal failure

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4
Q

Blood test abnormalities in anaemia of chronic disease

A

Low EPO
Low iron
High/normal ferritin
Low/normal soluble transferrin receptor number

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5
Q

Appearance of erythrocytes in anaemia of chronic disease

A

Microcytic

Hypochromic

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6
Q

Causes of iron deficiency anaemia

A

Blood loss
Poor dietary intake
Malabsorption in duodenum - chron’s, coeliac’s

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7
Q

Clinical features of iron deficiency anaemia

A

Koilonychia
Angular stomatitis
Brittle hair and nails (hair thinning/loss)
Atrophic glossitis

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8
Q

Blood test abnormalities in iron deficiency anaemia

A

Low iron
Low ferritin
High soluble transferrin receptor number

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9
Q

Erythrocytes appearance in iron deficiency anaemia

A

Microcytic

Hypochromic

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10
Q

Investigations for iron deficiency anaemia

A

Colonoscopy

Gastroscopy

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11
Q

Treatment for iron deficiency anaemia

A

Ferrous sulphate tablets TDS

If malabsorption underlying cause, give iron injections

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12
Q

Causes of sideroblastic anaemia

A
Congenital
Isoniazid
Myelodysplasia
Alcohol
Lead
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13
Q

Pathophysiology of sideroblastic anaemia

A

Dyserythropoeisis (ineffective erythropoeisis)

Haemosiderosis

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14
Q

Blood test abnormalities in sideroblastic anaemia

A

High serum iron

High ferritin

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15
Q

Treatment for sideroblastic anaemia

A

Treat underlying cause
Can give pyridoxine (vitamin B6)
Blood transfusion in severe haemosiderosis

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16
Q

Treatment of anaemia of chronic disease

A

Not responsive to oral iron

Need to treat underlying cause e.g give EPO

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17
Q

Appearance of bone marrow in sideroblastic anaemia

A

BM contains ringed sideroblasts

Cytoplasm contains iron granules

18
Q

Where is dietary iron absorbed

A

Duodenum

19
Q

How to diagnose haemoglobinopathies

A

Hb electrophoresis

20
Q

Beta thalassaemia trait/minor vs intermedia vs major

A

Trait/minor: usually asymptomatic, well tolerated anaemia

Intermedia: moderate anaemia not requiring transfusions, there may be splenomegaly

Major: presents at <1 year with severe anaemia and failure to thrive, need life long blood transfusion

21
Q

Features of beta thalassaemia major

A

Extramedullary haemotopoeisis - hepatosplenomegaly and skull bossing
Increased marrow activity - osteopenia and ‘hair on end’ sign on skull X-ray

22
Q

What is beta thalassaemia major

A

Abnormalities in both beta globin chains leads to absent HbA (alpha2-beta2)

23
Q

Describe the 4 types of alpha thalassaemia

A

1 gene deleted: clinically normal
2 genes deleted: asymptomatic carrier
3 genes deleted: HbH disease, beta chain tetramers, moderate anaemia, symptoms of haemolysis (jaundice, hepatosplenomegaly, leg ulcers)
4 genes deleted: death in uterine