Abstract
Polyarteritis nodosa (PAN) is a multisystem disease with necrotizing vasculitis of middle and small sized arteries. Takayasu arteritis (TA) is a rare nonspecific inflammatory disease with unknown cause, predominantly affecting the aorta and its main branches. There has not yet been a consensus on graft choice for patients with vasculitis syndromes. Here, we report one case with PAN and the other with TA undergoing coronary revascularization surgery.
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