Clinics and Practice (Apr 2011)

Association of aortic and main left coronary aneurysms with severe aortic insufficiency in Takayasu’s arteritis

  • Marcelo Ferraz de Freitas,
  • Marcelo Valladão de Carvalho,
  • Marcelo Derbli Schafranski

DOI
https://doi.org/10.4081/cp.2011.e26
Journal volume & issue
Vol. 1, no. 2

Abstract

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Takayasu’s arteritis is a granulomatous vasculitis of unknown etiology that affects mainly the aorta and its branches. As a result of intimal fibroproliferation, segmental stenosis, occlusion, dilatation, and aneurysmal formation of the involved vessels may develop. It is an uncommon disease and usually affects young Asian female patients during the second and third decades of life. Coronary arteries are exceptionally affected and coronary aneurysm formation is a very rare finding. We describe a case of a previously healthy 26-year-old Caucasian female whose Takayasu’s arteritis presented as a previously undescribed association of aortic and main left coronary aneurysms with severe aortic insufficiency.

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