| Literature DB >> 25726075 |
Abstract
Congenital diseases of the aorta tend to be obstructive when they present early in life, and aneurysmal when they present later in life. The latter group also tends to be associated with connective tissue disorders and with repaired conotruncal lesions. The indications for intervention in the aneurysm group are still in evolution but are clearly age- and lesion-dependant. Disorders such as Loeys-Dietz syndrome and Turner syndrome may deserve aggressive prophylactic surgery, as well as Marfan syndrome to a lesser extent. The natural history of the dilated aorta after repair of congenital heart lesions is probably more benign than de novo aneurysms and therefore should be treated conservatively.Entities:
Mesh:
Year: 2014 PMID: 25726075 DOI: 10.1016/j.jtcvs.2014.10.084
Source DB: PubMed Journal: J Thorac Cardiovasc Surg ISSN: 0022-5223 Impact factor: 5.209