Why the study?
Spontaneous coronary artery dissection is rare, typically affecting young female patients without risk factors, prompting discussion of treatment and prognosis in a male patient with systemic lupus erythematosus.
Cardiovascular complications, including SCAD and accelerated atherosclerosis, should be considered and managed appropriately in patients with systemic lupus erythematosus.
Answers are grounded in this paper and cite their sources.
SCAD can occur in young males with SLE and STEMI; extends recognized demographics but remains hypothesis-generating.
Background: Spontaneous coronary artery dissection (SCAD) is a rare coronary artery disease that frequently occurs in young, female patients without risk factors, and conservative treatment is often recommended for its management. The patient reported here is a male patient with systemic lupus erythematosus (SLE). Case summary: We described a 28-year-old man with SLE who presented with acute ST-segment elevation myocardial infarction (STEMI), and was diagnosed with SCAD through a long dissection of the left anterior descending branch (LAD) by coronary angiography. The patient was treated with percutaneous coronary intervention (PCI) with stent implantation. Ten years later, he developed in-stent stenosis and other coronary atherosclerosis and was retreated with PCIs. Based on this case and according to the literature review, the existing treatment and prognosis of SLE with spontaneous coronary artery dissection and atherosclerosis are discussed. Conclusion: Cardiovascular complications should be considered in patients with systemic lupus erythematosus, although they may not initially be atherosclerotic diseases. Attention should be paid to distinguish spontaneous coronary dissection in order to minimize missed or delayed diagnoses and take appropriate managements, as well as the development of atherosclerosis in SLE patients, and timely intervention has a better prognosis.
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Huang et al. (2022) studied this question.
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