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Abstract
Coronary artery disease (CAD) due to Takayasu arteritis (TA) is rare. This article reports a case of severe involvement of multiple coronary arteries in a young woman. She was treated with coronary artery bypass grafting and had an early venous graft stenosis despite immunosuppressants. She became asymptomatic one year after a drug-eluting stent placement. This report shows the complexity of the diagnostic and therapeutic approach to TA with complex CAD.
- ischaemic heart disease
- vasculitis
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Footnotes
Contributors LMM: conception of the work, data analysis and interpretation, drafting the article, critical revision of the article and final approval of the version to be published. NdAL: conception of the work, data analysis and interpretation, drafting the article, critical revision of the article and final approval of the version to be published. RLdC Jr: data collection, critical revision of the article and final approval of the version to be published. SFB: drafting the article, critical revision of the article and final approval of the version to be published.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
Patient consent for publication Obtained.
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