Anaemia Flashcards

1
Q

Causes of microcytic anaemia

A
Iron deficiency
Chronic disease, malignancy
Lead poisoning
Congenital sideroblastic anaemia
Thalassaemia in South Asians
Polycythaemia rubra vera in non-South Asians
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2
Q

Types of thalassaemia

A

Beta trait, beta major and alpha

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3
Q

Beta trait thalassaemia

A

Common, causes mild hypochromic microcytic anaemia. Often asymptomatic. Hba2 raised.

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4
Q

Beta major thalassaemia

A

No beta chains. Presents in first year as failure to thrive and hepatosplenomegaly. Hba and HbF raised. Hba absent.
Treat with repeated transfusion and s/c deferoxamine.

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5
Q

Alpha thalassaemia

A

Deficiency in alpha chains. 2 separate chains on each chromosome 16. Have from 1-4 effected.
1/2 effected- hypochromic microcytic anaemia but Hb normal.
3 effected- hypochromic microcytic anaemia and splenomegaly.
4 effected- in-utero death.

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6
Q

Causes of macrocytic anaemia

A

Megaloblastic (reticulocytes big):
B12 deficiency, folate deficiency

Normoblastic:
Alcohol, liver disease, pregnancy, myelodysplasia, hypothyroid, cytotoxic drugs

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7
Q

What is pernicious anaemia?

A

Cause of macrocytic anaemia due to B12 deficiency due to antibodies to intrinsic factor.
Ab attack intrinsic factor and gastric parietal cells.

Symptoms: enlarged sore tongue, jaundice, poor concentration, confusion, depression, weakness, paraesthesia, pins and needles.

FBC: macrocytic anaemia, hypersegmented polymorphs

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8
Q

Other causes of B12 deficiency

A

Erosive gastritis, H pylori, gastrectomy, malnourishment, alcoholism

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9
Q

Management of pernicious anaemia

A

If no neurological features- 3 injections of B12 per week for 2 weeks, then every 3 months.
More often is neurological symptoms.

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10
Q

What is sickle cell disease?

A

Autosomal recessive condition, abnormal haemoglobin chain, more common in Africans.
Causes sickle shaped RBCs which haemolyse and block small vessels.

Diagnose with Hb electrophoresis.

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11
Q

Types of sickle cell crisis

A
Thrombotic crisis
Sequestration crisis
Acute chest syndrome
Aplastic crisis
Haemolytic crisis
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12
Q

Sickle cell thrombotic crisis

A

Lots of tiny blockages. AKA painful crisis.

Infarcts in various organs can cause necrosis of hip, hand, foot, lungs and spleen.

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13
Q

Sickle cell sequestration crisis

A

Pooling of blood within organs e.g. spleen and lungs.

Worsening anaemia- tiredness and lethargy.

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14
Q

Sickle cell acute chest syndrome

A

Chest pain and pulmonary infiltrates. Hypoxia. Most common cause of sickle cell death.

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15
Q

Aplastic crisis

A

Caused by infection with parvovirus

See sudden fall in Hb.

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16
Q

Haemolytic crisis

A

Rare, fall in Hb due to increased haemolysis

17
Q

Causes of haemolytic anaemias

A

Hereditary or acquired e.g. warm/cold AI haemolytic, transfusion reaction, haemolytic disease of new-born, cardiac valves, malaria, malignancy.

18
Q

Warm AIHA

A

IgG causes haemolysis at body temperature in extravascular sites eg. spleen.
Caused by lupus, lymphoma, CLL, methyldopa
Give steroids, immunosuppressive and splenectomy.

19
Q

Cold AIHA

A

IgM causes haemolysis at 4C. Usually intravascular - Reynaud’s and acrocyanosis.
Causes: EBV, lymphoma
Don’t respond as well to steroids.