Aneurysm of sinus of valsalva (patient information): Difference between revisions
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'''For the WikiDoc page for this topic, click [[Aneurysm of sinus of valsalva|here]]''' | '''For the WikiDoc page for this topic, click [[Aneurysm of sinus of valsalva|here]]''' | ||
{{CMG}}; '''Associate Editors-In-Chief:''' | {{CMG}}; '''Associate Editors-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, MBBS]] [mailto:psingh13579@gmail.com]; '''Assistant Editor-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]] [mailto:kfeeney@elon.edu] | ||
==Overview== | ==Overview== | ||
'''[[Aneurysm]] of the [[aortic sinus]]''', also known as the [[sinus of Valsalva]], is comparatively rare, occurring in about one person in every thousand. | |||
When present, it is usually in either the right (65-85%) or in the noncoronary (10-30%) sinus, rarely in the left (< 5%) sinus. This type of aneurysm is typically [[birth defects|congenital]] and may be associated with [[heart defects]]. | When present, it is usually in either the right (65-85%) or in the noncoronary (10-30%) sinus, rarely in the left (< 5%) sinus. This type of aneurysm is typically [[birth defects|congenital]] and may be associated with [[heart defects]]. | ||
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The determination to perform surgery is usually based upon the diameter of the aortic root and the rate of increase in its size, as determined through repeated [[echocardiography]]. | The determination to perform surgery is usually based upon the diameter of the aortic root and the rate of increase in its size, as determined through repeated [[echocardiography]]. | ||
{{Congenital malformations and deformations of circulatory system}} | |||
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[[CME Category::Cardiology]] | |||
[[Category:Pediatrics]] | [[Category:Pediatrics]] | ||
[[Category:Cardiology]] | [[Category:Cardiology]] | ||
[[Category:Cardiology patient information]] | |||
[[Category:Congenital heart disease patient information]] | [[Category:Congenital heart disease patient information]] | ||
[[Category:Pediatrics patient information]] | [[Category:Pediatrics patient information]] | ||
[[Category:Patient information]] | [[Category:Patient information]] | ||
[[Category:Mature chapter]] | [[Category:Mature chapter]] | ||
[[Category:Priority chapter]] | |||
Latest revision as of 21:00, 14 March 2016
For the WikiDoc page for this topic, click here
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editors-In-Chief: Priyamvada Singh, MBBS [2]; Assistant Editor-In-Chief: Kristin Feeney, B.S. [3]
Overview
Aneurysm of the aortic sinus, also known as the sinus of Valsalva, is comparatively rare, occurring in about one person in every thousand.
When present, it is usually in either the right (65-85%) or in the noncoronary (10-30%) sinus, rarely in the left (< 5%) sinus. This type of aneurysm is typically congenital and may be associated with heart defects.
It is sometimes associated with Marfan syndrome or Loeys-Dietz syndrome, but may also result from Ehlers-Danlos syndrome, atherosclerosis, syphilis, cystic medial necrosis, chest injury, or infective endocarditis.
If unruptured, this type aneurysm may be asymptomatic and therefore go undetected until symptoms appear or medical imaging is performed for other reasons.
Treatment
Medical therapy of aneurysm of the aortic sinus includes blood pressure control through the use of drugs, such as beta blockers. The definitive treatment is surgical repair.
The determination to perform surgery is usually based upon the diameter of the aortic root and the rate of increase in its size, as determined through repeated echocardiography.