Affiliation:
1. Institut für Radiologie, Charité Universitätsmedizin, Berlin, Germany
2. Deutsches Herzzentrum Berlin, Germany
Abstract
The mid-aortic syndrome is an uncommon clinical condition characterized by severe narrowing of the descending aorta, usually with involvement of its renal and visceral branches, presenting with uncontrollably elevated blood pressures of the upper body, renal and cardiac failure, intestinal ischemia, encephalopathy symptoms and claudication of the lower limbs, although clinical presentation is variable. In this article we report the case of an eleven-year-old patient with the initial diagnosis of a mid-aortic syndrome and present the computed tomography angiography pictures and reconstructions before and after surgical therapy.
Subject
Cardiology and Cardiovascular Medicine
Cited by
2 articles.
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