Goodpasture syndrome is an autoimmune condition where autoantibodies against the alpha-3 subunit of type IV collagen in the basement membranes of the lungs and kidneys are produced. This leads to small vessel vasculitis in the kidneys and lungs.
The incidence peaks between 30 and 40 years. It is more common in men than in women.
- Risk factors
- Genetic predisposition
- HLA-DRB1
- Environmental exposure
- Hydrocarbons
- Tobacco smoke
- Viral respiratory infections
- Genetic predisposition
- Pathophysiology
- Production of anti-GBM antibodies → deposition of immune complexes in the glomerular and alveolar basement membrane → complement activation and inflammation → cellular damage
- Patient history
- No history of lung or renal dysfunction
- Sudden onset haemoptysis, cough, dark urine, and oliguria
- Signs and symptoms
- Haemoptysis
- Cough
- Shorness of breath
- Nausea and vomiting
- Chest pain
- Decreased urine output
- Fatigue and malaise
- Haematuria
- Fever
- Oedema
- Differentials
- Investigations
- Renal biopsy is the definitive diagnostic test
- Crescenteric glomerulonephritis
- Linear IgG staining on immunofluorescence
- Anti-GBM antibody titre to confirm the diagnosis in addition to renal biopsy
- Anti-neutrophil cytoplasmic antibodies (ANCA)
- Urea and creatinine
- Urinalysis
- Proteinuria
- Haematuria
- Casts
- Chest X-ray
- Diffuse opacities
- Chest CT scan
- Ground glass opacities in a diffuse and bilateral distribution
- Renal biopsy is the definitive diagnostic test
- Treatment
- During the acute phase:
- Plasmapheresis
- Prednisone
- Cyclophosphamide
- Long term maintenance with:
- Azathioprine
- Low dose prednisolone
- The duration of treatment may take at least 6 – 9 months
- Smoking cessation
- During the acute phase:
- Complications
- Pulmonary haemorrhage
- Plasmapheresis related bleeding
- Cyclophosphamide-related neutropaenia
- Immunosuppression-related infection
- Chronic kidney disease
- Complications of long-term immunosuppressive therapy
- Respiratory failure
- Renal failure