2017
DOI: 10.7759/cureus.1737
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Sudden Death from Spontaneous Coronary Artery Dissection due to Polyarteritis Nodosa

Abstract: Spontaneous coronary artery dissection (SCAD) is an emerging and rare cause of acute coronary syndrome and sudden cardiac death. While it was previously reported among young females with fibromuscular dysplasia, new literature indicates that this condition could occur in older populations. Polyarteritis nodosa (PAN) causes systemic necrotizing vasculitis which typically affects small to medium-sized muscular arteries and could affect the coronary arteries. A few case reports of PAN causing acute coronary arter… Show more

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Cited by 4 publications
(7 citation statements)
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“…Coronary artery lesions are not common (7/64) in PAN [1], but they can lead to angina pectoris and myocardial infarction (MI). Spontaneous coronary artery dissection (SCAD) may occur in some severe cases, which can cause sudden cardiac death [2,3]. However, PAN is a very rare vasculitis with an annual incidence of 0-1.6 cases/million people, and a prevalence of approximately 31 cases per million people [4].…”
Section: J O U R N a L P R E -P R O O Fmentioning
confidence: 99%
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“…Coronary artery lesions are not common (7/64) in PAN [1], but they can lead to angina pectoris and myocardial infarction (MI). Spontaneous coronary artery dissection (SCAD) may occur in some severe cases, which can cause sudden cardiac death [2,3]. However, PAN is a very rare vasculitis with an annual incidence of 0-1.6 cases/million people, and a prevalence of approximately 31 cases per million people [4].…”
Section: J O U R N a L P R E -P R O O Fmentioning
confidence: 99%
“…J o u r n a l P r e -p r o o fCoronary artery lesions in PAN includ stenosis or occlusion, ectasia, aneurysms and acute coronary dissection and rupture[2]. Premature atherosclerotic coronary disease, likely secondary to coronary arteritis, has also been reported[23].…”
mentioning
confidence: 99%
“…Background: Bechet's disease (BD) is a chronic multisystemic vasculitis. Although its exact etiopathology is unknown, both autoimmune imbalances associated with genetic and abnormal immune response of effector lymphocytes promoted by infectious factors are suggested 1 . The increase of effector T cells (Teffs) and the decrease of regulatory T cells (Tregs) are possibly the involving factors in the pathogenesis of BD 2 .…”
Section: Ab0499mentioning
confidence: 99%
“…Immunoregulatory combination therapies could promote the proliferation and functional recovery of Tregs in patients with BD and might help to alleviate disease activity. References: [1]…”
Section: Ab0499mentioning
confidence: 99%
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