Churg-Strauss syndrome is a rare condition characterised by asthma and blood eosinophilia together with an eosinophilic vasculitis
Also known as Eosinophilic granulomatosis with polyangiitis (EGPA)
- an annual incidence of 3.1 cases per million (1)
The initial phase of the disorder is one of asthma and allergic rhinitis, often followed by peripheral blood eosinophilia with eosinophilic tissue disease. The vasculitic phase that follows is life-threatening; however, it can often be treated effectively with immunosuppression.
- eosinophil-rich and necrotising granulomatous inflammation often involving the respiratory tract, and necrotising vasculitis predominantly affecting small to medium vessels, and associated with asthma and eosinophilia. ANCA is more frequent when glomerulonephritis is present
- characteristic features of EGPA are asthma (typically late-onset), peripheral blood and tissue eosinophilia, fever, and systemic vasculitis
- asthma especially distinguishes EGPA from Wegener's granulomatosis and microscopic polyangiitis (MPA)
- renal involvement is relatively uncommon.
- asthma is the cardinal feature and precedes systemic features in virtually
all cases; onset is late in life and becomes more severe until the onset of
- chest x-ray shows infiltrates in <=77%
- cardiac disease is common (<=47%) and is an important cause of mortality, due to congestive heart failure, pericardial effusion and restrictive cardiomyopathy
- mononeuritis multiplex is a common (70%) feature of EGPA, where it is much more frequent than in Wegener's and MPA
- Davies DJ. Small vessel vasculitis. Cardiovascular Pathology 2005; 14 (6): 335-346.
- ARC Autumn 2012. Topical Reviews - ANCA-associated vasculitis; 1:1-12.