Literature DB >> 17033730

Thoracoabdominal aorta coarctation with bilateral renal artery involvement: diagnosis with multidetector CT angiography (MDCTA).

Ahmet Turan Ilica1, Aslan Bilici, Abdullah Ilhan, Muammer Kara, Serkan Gür.   

Abstract

Atypical coarctation of the descending thoracic and abdominal aorta is a very uncommon vascular disease. Congenital, acquired, inflammatory, and infectious etiologies have been proposed. Patients typically presents with uncontrolled secondary hypertension in the upper half of the body or hypotension in the lower extremities in the first three decades of their lives. We report the case of a 20-year-old man with severe hypertension. Diffuse coarctation of thoracoabdominal aorta associated with bilateral renal artery stenosis was demonstrated clearly by multidetector CT angiography. This is the first case of atypical aortic coarctation diagnosed by MDCTA.

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Year:  2006        PMID: 17033730     DOI: 10.1007/s10554-006-9135-2

Source DB:  PubMed          Journal:  Int J Cardiovasc Imaging        ISSN: 1569-5794            Impact factor:   2.357


  16 in total

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Journal:  Int J Cardiovasc Imaging       Date:  2006-05-09       Impact factor: 2.357

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Journal:  J Vasc Surg       Date:  2005-04       Impact factor: 4.268

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  1 in total

1.  Neonatal midaortic syndrome and renal artery atresia presenting as malignant hypertension.

Authors:  Tal A Gospin; Jarrod D Knudson; Christopher J Petit
Journal:  Pediatr Cardiol       Date:  2012-03-25       Impact factor: 1.655

  1 in total

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