Haemolytic anaemia encompasses a number of conditions that result in the premature destruction of RBCs. The causes can be divided into inheritied and acquired, it can also be due to a underlying malignancy
Features
- Anaemia - Reduction in circulating RBC
- Splenomegaly - Spleen becomes filled wtih destroyed RBC
- Jaundice - Released bilirubin during destruction of RBC
Investigations
- FBC - normocytic anaemia, increased reticulocytes
- Blood film - Schistocytes (fragments of RBC)
- Raised unconjugated bilirubin
- Haptoglobin (a plasma protein that binds free Hb in blood), Bound haptoglobin is ingested by macrophages - In haemolytic anaemia haptoglobin is low as it is being consumed
- LDH - high.
- High LDH + low haptoglobin is 90% specific for haemolytic anaemia
Inheritied haemolytic anaemias
Hereditary spherocytosis
- Hereditary Elliptocytosis - Very similar to hereditary spherocytosis except the RBC are ellipse shaped. Also autosomal dominant inheritance. PC and Management are the same.
- Hereditory stomatocytosis - red cells in which the pale central area appears slit like, excess alcohol intake is a common cause.
Sickle cell anaemia
Thalassaemia