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镜像右位心伴孤立性心房反位:一种罕见的解剖结构。

Isolated atrial inversion in situs inversus: a rare anatomic arrangement.

作者信息

Santoro G, Masiello P, Farina R, Baldi C, Di Leo L, Di Benedetto G

机构信息

Division of Cardiac Surgery, Ospedale S. Leonardo, Salerno, Italy.

出版信息

Ann Thorac Surg. 1995 Apr;59(4):1019-21. doi: 10.1016/0003-4975(94)00745-s.

Abstract

Isolated atrial inversion in situs inversus is a rare congenital cardiac malformation. Its physiology resembles transposition of great vessels, and the best option for its surgical treatment is the atrial switch operation. In this article, we present a case of isolated atrial inversion in concordance with visceral situs inversus diagnosed at birth by echocardiography and cardiac catheterization, which was successfully treated at 8 months of age by a Senning procedure.

摘要

镜像右位心合并孤立性心房反位是一种罕见的先天性心脏畸形。其生理机制类似于大动脉转位,手术治疗的最佳选择是心房调转术。在本文中,我们报告一例出生时经超声心动图和心导管检查诊断为镜像右位心合并孤立性心房反位的病例,该患儿在8个月大时通过森宁手术成功治愈。

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