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三房心罕见变异型的外科矫正术。

Surgical correction of a rare variant of cor triatriatum.

作者信息

Victor S, Santosham R, Rajaram S, Subraminiam N S, Balakrishnan P V, Chochalingam V, Lakshmikanthan C

出版信息

J Thorac Cardiovasc Surg. 1975 Aug;70(2):354-7.

PMID:1152518
Abstract

Cor triatratum is a rare congenital malformation. Problems in diagnosis and surgery arise due to associated anomalies such as atrial septal defects and anomalous pulmonary venous drainage. A 21-year-old man proved to have a rare variant of cor triatiatum in which both the upper and lower compartments of the left atrium communicated with the right atrium through two separate atrial septal defects. In addition, he had anomalous drainage of the right superior pulmonary vein into the superior vena cava. Intracardiac repair was undertaken successfully.

摘要

三房心是一种罕见的先天性畸形。由于合并房间隔缺损和肺静脉异常引流等相关异常,导致诊断和手术出现问题。一名21岁男性被证实患有三房心的罕见变异型,其中左心房的上、下腔室通过两个独立的房间隔缺损与右心房相通。此外,他还存在右上肺静脉异常引流至上腔静脉的情况。成功进行了心内修复。

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