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经食管对比超声心动图诊断先天性右心房增大——病例报告

Contrast transesophageal echocardiography in diagnosing congenital enlargement of the right atrium--a case report.

作者信息

Yukiiri Kazushi, Mizushige Katsufumi, Ohmori Koji, Wada Yoshihiro, Tanimoto Kojiro, Ueda Takashi, Takagi Yuichiro, Kohno Masakazu

机构信息

Second Department of Internal Medicine, Kagawa Medical University, 1750-1, Miki, Kita, Kagawa 761-0793, Japan.

出版信息

Angiology. 2003 Sep-Oct;54(5):619-23. doi: 10.1177/000331970305400514.

Abstract

Congenital malformation of the right atrium or the coronary sinus is rare, and cases are classified into 1 of the following 4 categories: (1) congenital enlargement of right atrium, (2) single diverticulum, (3) multiple diverticula of the right atrium, and (4) diverticulum of the coronary sinus. This report presents a 63-year-old man with cardiomegaly and no chest symptoms. A chest radiograph revealed an enlarged cardiac silhouette with a prominent right heart border. Although a transesophageal echocardiography revealed marked enlargement of the right atrium, neither further anomaly nor massive regurgitation was observed. The systolic pulmonary artery pressure derived from the peak velocity of mild tricuspid regurgitation was 38 mm Hg. Secondary enlargement of the right atrium due to atrial septal defect or pulmonary venous connection anomaly was deemed negligible by use of transesophageal contrast echocardiography, and primary enlargement of the right atrium was confirmed. Transesophageal echocardiography using ultrasound contrast was determined to be feasible for diagnosing congenital malformation of the right atrium.

摘要

右心房或冠状静脉窦的先天性畸形较为罕见,病例可分为以下4类中的1种:(1)右心房先天性扩大,(2)单个憩室,(3)右心房多个憩室,以及(4)冠状静脉窦憩室。本报告介绍了一名63岁的男性,有心脏扩大但无胸部症状。胸部X线片显示心脏轮廓增大,右心缘突出。尽管经食管超声心动图显示右心房明显扩大,但未观察到进一步的异常或大量反流。由轻度三尖瓣反流的峰值速度得出的收缩期肺动脉压为38 mmHg。经食管对比超声心动图显示,因房间隔缺损或肺静脉连接异常导致的右心房继发性扩大可忽略不计,从而证实了右心房的原发性扩大。经确定,使用超声对比剂的经食管超声心动图对于诊断右心房先天性畸形是可行的。

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