Eosinophilic granulomatosis with polyangiitis

Eosinophilic granulomatosis with polyangiitis, formerly known as Churg-Strauss syndrome, is a rare systemic necrotizing vasculitis classified among the antineutrophil cytoplasmic antibody-associated vasculitides

Eosinophilic granulomatosis with polyangiitis, formerly known as Churg-Strauss syndrome, is a rare systemic necrotizing vasculitis classified among the antineutrophil cytoplasmic antibody-associated vasculitides

It predominantly targets small- to medium-sized blood vessels and most frequently affects the respiratory tract, peripheral nerves, skin, cardiovascular system, and gastrointestinal tract Systemic vasculitic complications commonly manifest as mononeuritis multiplex, pulmonary infiltrates, or eosinophilic myocarditis

It predominantly targets small- to medium-sized blood vessels and most frequently affects the respiratory tract, peripheral nerves, skin, cardiovascular system, and gastrointestinal tract Hallmark pathophysiologic and clinical features include severe adult-onset asthma, chronic rhinosinusitis, marked peripheral blood and tissue hypereosinophilia, and extravascular necrotizing granulomas

Hallmark pathophysiologic and clinical features include severe adult-onset asthma, chronic rhinosinusitis, marked peripheral blood and tissue hypereosinophilia, and extravascular necrotizing granulomas

Systemic vasculitic complications commonly manifest as mononeuritis multiplex, pulmonary infiltrates, or eosinophilic myocarditis