{Reference Type}: Case Reports
{Title}: Granulomatosis With Polyangiitis Presenting as Chest Pain: A Case Report.
{Author}: Fentie K;Singanamala S;Hozayen O;Altaf L;
{Journal}: Cureus
{Volume}: 15
{Issue}: 4
{Year}: 2023 Apr
暂无{DOI}: 10.7759/cureus.38204
{Abstract}: Granulomatosis with polyangiitis (GPA) is a relatively rare systemic autoimmune disorder of small and medium size blood vessels affecting multiple organs with a wide range of clinical presentations. We present a 57-year-old Caucasian male who presented to the ER with midsternal chest pain. He was hospitalized for non-ST elevated myocardial infarction (NSTEMI) and later diagnosed with pauci-immune necrotizing crescentic glomerulonephritis confirmed with renal biopsy.