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Silent growth of multiple giant coronary artery aneurysms in eosinophilic granulomatosis with polyangiitis
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DOI：10.1093/eurheartj/ehag531.png)
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Abstract
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A 75-year-old woman with eosinophilic granulomatosis with polyangiitis (EGPA) underwent routine annual chest radiography. EGPA had been diagnosed 11 years earlier and was apparently controlled with immunosuppressive therapy, including mepolizumab. She had no chest pain, dyspnoea, elevated inflammatory markers, or new electrocardiographic changes.
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