1. SUCCESSFUL DETECTION OF CRITICAL COARCTATION OF AORTA IN A YOUNG ADULT - CASE REPORT.
- Author
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Lupu, G., Dragulescu, Luciana, Gheorghe, A. T., Popescu, D., Stroică, Laura, and Ispas, Al. T.
- Subjects
HEART diseases ,HYPERTENSION - Abstract
Heart diseases caused by congenital malformations are an unwanted and sometimes relentless diagnostic that most patients should be aware of. Coarctation of the aorta (CoA) is a relatively common defect that represents 4-6% of the congenital heart defects and whose exact underlying mechanism is not completely known. It is defined as a narrowing of the aorta, usually just distal to the origin of the left subclavian artery, close to the ductus arteriosus, resulting in hypertension in the upper body and hypoperfusion of the lower body. A severe coarctation should be diagnosed shortly after birth and repaired by surgery immediately. To properly diagnose the aortic coarcation, chest X-ray, echocardiography, computed tomography (CT)/magnetic resonance imaging (MRI) or angiography is needed. In adults with untreated coarctation, blood often reaches the lower body through collaterals which can be easily identified on CT, as well as focal area of narrowing and constriction with dilatation of the aorta proximal and distal to the affected segment. Also on a standard radiography the post-stenotic dilatation of the aorta results in a classic "figure 3 sign". Unfortunately, coarctations are a long-life disease that cannot be prevented because their etiology is mostly congenital. The best solution for these patients is an early detection. That's why CT imaging can provide accurate information of the coarcation anatomy as well as other associated cardiac abnormalities. [ABSTRACT FROM AUTHOR]
- Published
- 2018