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大动脉完全转位合并三房心：一种罕见的共存情况。

Complete transposition of great arteries with cor triatriatum: an unusual coexistence.

作者信息

Gupta Saurabh Kumar, Saxena Anita, Ramakrishnan S, Juneja Rajneesh, Devagourou V

机构信息

Department of Cardiology, All India Institute of Medical Sciences, New Delhi, 110029, India.

出版信息

Pediatr Cardiol. 2012 Oct;33(7):1190-5. doi: 10.1007/s00246-012-0245-4. Epub 2012 Mar 8.

DOI:10.1007/s00246-012-0245-4
PMID:22398635
Abstract

The combination of complete transposition of the great arteries and cor triatriatum is extremely rare. We report three infants with this rare combination and discuss the anatomic details apparently unique to the combined lesion.

摘要

大动脉完全转位合并三房心极为罕见。我们报告了三名患有这种罕见组合病症的婴儿，并讨论了这种合并病变明显独特的解剖学细节。

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本文引用的文献

1
Congenitally corrected transposition of the great arteries in a patient with cor triatriatum: a rare combination.先天性矫正型大动脉转位合并三房心：一种罕见的组合。
Pediatr Cardiol. 2011 Apr;32(4):515-7. doi: 10.1007/s00246-011-9912-0. Epub 2011 Feb 22.
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Surgical repair and postoperative course of an infant with infracardiac total anomalous pulmonary venous connection, cor triatriatum sinistrum and transposition of the great arteries.一名患有心内型完全性肺静脉异位连接、左房三房心和大动脉转位婴儿的手术修复及术后病程
Eur J Cardiothorac Surg. 1990;4(1):45-7. doi: 10.1016/1010-7940(90)90240-z.
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Cor triatriatum: study of 20 cases.
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