2017
DOI: 10.1111/echo.13423
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Multiple unruptured aortic sinus of Valsalva aneurysms: A rare presentation

Abstract: Aneurysms of sinus of Valsalva, usually a rare presentation, account for 0.1%-3.5% of congenital heart defects. They rarely present unless rupture occurs. There are very few cases of unruptured sinus of Valsalva aneurysms that presented with myocardial ischemia, symptomatic cardiac dysfunction, and conduction abnormalities. We present a case of multiple unruptured sinus of Valsalva aneurysms with particular emphasis on the transesophageal echocardiography.

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Cited by 7 publications
(7 citation statements)
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“…Real-time 3D TEE imaging also plays an important role in guiding transcatheter repair of SVAs and assessment of adequacy of the surgical repair. 12 Data on tomographic assessment using imaging modalities such as MDCT and CMR for the diagnosis of SVAs are limited. Undoubtedly, MDCT and CMR provide accurate delineation of SVA and measurement of the sinus and vascular dimensions.…”
mentioning
confidence: 99%
“…Real-time 3D TEE imaging also plays an important role in guiding transcatheter repair of SVAs and assessment of adequacy of the surgical repair. 12 Data on tomographic assessment using imaging modalities such as MDCT and CMR for the diagnosis of SVAs are limited. Undoubtedly, MDCT and CMR provide accurate delineation of SVA and measurement of the sinus and vascular dimensions.…”
mentioning
confidence: 99%
“…B. shows the aneurysm of noncoronary cusp protruded into the right atrium as a round cyst-like structure in systole. 4 Ventricular septal defect (VSD) occurs in about 50% of patients and is the most commonly associated congenital heart disease. RA = right atrium; LA = left atrium; A = aneurysm of noncoronary sinus of Valsalva The congenital form is more common.…”
Section: Discussionmentioning
confidence: 99%
“…Aortic insufficiency has been reported in 30%-50% of cases. 4 Ventricular septal defect (VSD) occurs in about 50% of patients and is the most commonly associated congenital heart disease. 5 Ascending aortic aneurysm (AAA) is reported in association with SOVA in Marfan syndrome and connective tissue disorders.…”
Section: Discussionmentioning
confidence: 99%
“…The true prevalence of SVAs is unknown; the estimated rate is approximately 0.09% of the general population and 0.1% to 3.5% of all congenital cardiac defects (2). Multiple SVAs are even rarer with very few cases reported in the literature (3)(4)(5). SVAs most often affect one of the SVs, and originate predominantly from the right SV (RSV) (2,(6)(7)(8)(9).…”
Section: Introductionmentioning
confidence: 99%
“…SVAs most often affect one of the SVs, and originate predominantly from the right SV (RSV) (2,(6)(7)(8)(9). Patients with unruptured SVAs could be asymptomatic or present with non-specific symptoms such as dyspnea, chest pain, palpitation and syncope (5,(10)(11)(12)(13)(14)(15)(16)(17)(18)(19). Unruptured SVAs may cause valvular regurgitation, annular dilation or deformity, as well as compression of the coronary arteries, cardiac chambers Review Article Surgical management for unruptured sinus of Valsalva aneurysms: a narrative review of the literature…”
Section: Introductionmentioning
confidence: 99%