Paroxysmal nocturnal haemoglobinuria (PNH) is caused by clonal defects in the RBC membrane protein (GPI), which is responsible for inactivating complement. This defect increases activation of complement and intravascular haemolysis.
- Pathophysiology
- Acquired mutation on the PIGA gene located on the X chromosome → deficiency in CD55/DAF (decay-accelerating factors) and CD59/MIRL (membrane Inhibitor of reactive lysis), which are part of the GPI anchor protein → GPI defect leads to increased activation of complement → intravascular haemolysis
- GPI defect in WBCs and Platelets → Pancytopenia
- Complement activation in platelets → activation → increased risk of thrombosis
- Complement activation is enhanced by the slightly acidotic state that happens during sleep → symptoms of hemolysis on waking up
- Signs and symptoms
- Symptoms of anaemia
- Dark “cola” or “tea-coloured urine” when waking up
- Investigations
- Flow cytometry: most accurate test
- Deficiency in CD55/59
- Acidified serum lysis “Ham” test
- Sugar-water test
- Urinalysis
- Hemoglobinuria
- Flow cytometry: most accurate test
- Treatment
- Eculizumab (first-line)
- Iron and Folate Supplementation
- Iron is supplemented since iron is lost in urine due to intravascular hemolysis
- Corticosteroids in severe cases
- Anticoagulation due to increased risk of hepatic and dermal thrombosis