Cor triatriatum overview: Difference between revisions
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{{Cor triatriatum}} | {{Cor triatriatum}} | ||
{{CMG}}; '''Associate Editors-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, | {{CMG}}; '''Associate Editors-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto:psingh13579@gmail.com]; {{CZ}}; [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu]; '''Assistant Editor(s)-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]] [mailto:kfeeney@elon.edu] | ||
==Overview== | ==Overview== | ||
'''Cor triatriatum''' is a rare [[congenital heart defect]] where a fibromuscular septum subdivides the [[left atrium]] into two chambers. Associated cardiovascular malformations are common and include [[atrial septal defect]] | '''Cor triatriatum''' is a rare [[congenital heart defect]] where a fibromuscular septum subdivides the [[left atrium]] into two chambers. Associated cardiovascular malformations are common and include [[atrial septal defect]],[[patent ductus arteriosus]] and [[common atrioventricular canal]]. The proximal or accessory chamber lies posteriorly, and usually receives blood from each of the [[pulmonary vein]]s. The distal or true [[left atrial]] chamber lies anterior, connects to the left atrial appendage,empties into the [[left ventricle]] through the [[mitral valve]], and lodges true atrial septum containing [[fossa ovalis]] . The two atrial chambers communicate through an opening in the membrane which divides the two chambers. This opening may be single and stenotic, fenestrated, and either small or large. <ref>[http://radiographics.rsnajnls.org/cgi/reprint/8/6/1227 Jolles H, A case report Volume 8, Number 6 November, 1988 RadioGraphics]</ref> | ||
==References== | ==References== | ||
{{reflist}} | {{reflist|2}} | ||
[[Category:Congenital heart disease]] | [[Category:Congenital heart disease]] | ||
Latest revision as of 13:45, 2 November 2012
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Cor triatriatum Microchapters |
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Treatment |
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Cor triatriatum overview On the Web |
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Risk calculators and risk factors for Cor triatriatum overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editors-In-Chief: Priyamvada Singh, M.B.B.S. [2]; Cafer Zorkun, M.D., Ph.D. [3]; Keri Shafer, M.D. [4]; Assistant Editor(s)-In-Chief: Kristin Feeney, B.S. [5]
Overview
Cor triatriatum is a rare congenital heart defect where a fibromuscular septum subdivides the left atrium into two chambers. Associated cardiovascular malformations are common and include atrial septal defect,patent ductus arteriosus and common atrioventricular canal. The proximal or accessory chamber lies posteriorly, and usually receives blood from each of the pulmonary veins. The distal or true left atrial chamber lies anterior, connects to the left atrial appendage,empties into the left ventricle through the mitral valve, and lodges true atrial septum containing fossa ovalis . The two atrial chambers communicate through an opening in the membrane which divides the two chambers. This opening may be single and stenotic, fenestrated, and either small or large. [1]