Eastern Journal of Medicine, cilt.15, sa.3, ss.111-113, 2010 (Scopus)
Interrupted aortic arch (IAA) is a rare and usually lethal congenital malformation. Without previous surgical intervention to reach adult age is very rare in patients with complete IAA. The present report describes a 70-year-old hyptertensive women who was incidentally diagnosed to have IAA and aortic stenosis. Aortography showed a complete IAA below the origin of left subclavian artery and gadolinium contrast-enhanced magnetic resonance angiogram (1.5 T scanners) clearly reaffirmed a complete interruption of the arcus aorta, with markedly developed collateral circulation.