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一名患者同时存在三种罕见先天性心脏缺陷:一个具有重要胚胎学意义的独特病例。

Coexistence of three rare congenital heart defects in a single patient: a unique case with important embryologic implications.

作者信息

Rhodes Jonathan, Bacha Emile A, Geggel Robet L

机构信息

Departments of Cardiology and Cardiovascular Surgery, Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA.

出版信息

Pediatr Cardiol. 2006 Jul-Aug;27(4):503-7. doi: 10.1007/s00246-006-1275-6. Epub 2006 Jul 6.

Abstract

The unique anatomy, physiology, and surgical repair of a patient with features of three rare congenital heart defects (total anomalous pulmonary venous return to the coronary sinus, cor triatriatum, and unroofed coronary sinus with persistent left superior vena cava to the left atrium) is described. Analysis of this case suggests that these three conditions are linked in that they all may result as a consequence of a defect in the same embryologic process (i.e., incorporation of the pulmonary venous confluence into the left atrium).

摘要

描述了一名具有三种罕见先天性心脏缺陷特征(完全性肺静脉异位引流至冠状窦、三房心、冠状窦未闭合并永存左上腔静脉至左心房)患者的独特解剖结构、生理功能及手术修复情况。该病例分析表明,这三种情况相互关联,因为它们都可能是同一胚胎学过程(即肺静脉汇合处并入左心房)缺陷的结果。

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