2015
DOI: 10.1186/s13019-015-0277-y
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Surgical repair of a giant congenital right atrial aneurysm: a case report

Abstract: Giant congenital right atrial aneurysms are rare defects of the heart. Though usually asymptomatic, they can be potentially life-threatening. Major risks include heart failure, supraventricular arrhythmias, rupture of the wall of the aneurysm. This defect is usually diagnosed incidentally. It is commonly found when transthoracic echocardiography or chest X-ray is performed. In some cases computed tomography or cardiac magnetic resonance imaging is needed to establish the diagnosis. Potential therapeutic option… Show more

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Cited by 23 publications
(30 citation statements)
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References 14 publications
(35 reference statements)
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“…[2] found 60 reported cases of right atrial aneurysm from which only 17 (28%) had been submitted to surgical treatment. Subsequently, sporadic cases have been described, including one of our experience [3-6] . In this article, we not only present another case, but probably more relevant, we describe the late results (17 years) of the surgery in the previously reported child.…”
Section: Introductionmentioning
confidence: 99%
“…[2] found 60 reported cases of right atrial aneurysm from which only 17 (28%) had been submitted to surgical treatment. Subsequently, sporadic cases have been described, including one of our experience [3-6] . In this article, we not only present another case, but probably more relevant, we describe the late results (17 years) of the surgery in the previously reported child.…”
Section: Introductionmentioning
confidence: 99%
“…6 Having opted for surgical intervention, and taking into account the very large aneurysm, we preferred to use cardiopulmonary bypass, combined with normothermia and a beating heart, in order to decompress the heart and prevent any sudden rupture. Another consideration in favor of this form of surgical treatment was the previously reported finding 7 of huge dilatation of the right coronary artery, possibly separated from the right atrioventricular groove as proved to be the case in our patient. We can only speculate that the right coronary artery dilatation follows the huge dilatation of the right atrium.…”
Section: Discussionmentioning
confidence: 67%
“…Phình tiểu nhĩ bẩm sinh là bệnh lý tim mạch hiếm gặp và có thể bên trái hoặc bên phải, hoặc cả hai bên [1,7]. Đến nay, có khoảng 50 trường hợp bệnh được báo cáo trong y văn.…”
Section: Bàn Luậnunclassified