Double-Chambered Left Ventricle Diagnosed in Fetus and Follow-up During the First Year of Life: A Case Report.

IF 1.1 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2024-01-01 Epub Date: 2023-09-05 DOI:10.1177/21501351231189272
Kaouthar Hakim, Rihab Benothmen, Hela Msaad, Wassim Frikha, Habiba Mizouni, Fatma Ouarda
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Abstract

Double-chambered left ventricle (DCLV) is a rare congenital cardiac lesion. It is usually an incidental finding in children and young adults. Diagnosis during fetal life is exceedingly rare. We report a case of DCLV diagnosed in the prenatal period associated with a ventricular septal defect (VSD). Transthoracic echocardiographic and magnetic resonance imaging confirmed the prenatal findings. At seven-month follow-up, the baby was asymptomatic. Transthoracic echocardiographic check-up revealed spontaneous closure of the VSD and stable aspect of the main left ventricle and the accessory chamber.

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胎儿期诊断出双腔左心室并在出生后第一年进行随访:病例报告。
双腔左心室(DCLV)是一种罕见的先天性心脏病变。它通常是儿童和年轻人的偶然发现。在胎儿期确诊则极为罕见。我们报告了一例在产前诊断为伴有室间隔缺损(VSD)的 DCLV 病例。经胸超声心动图和磁共振成像证实了产前发现。在七个月的随访中,婴儿没有任何症状。经胸超声心动图检查显示,室间隔缺损自发闭合,左心室主腔和附属腔稳定。
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CiteScore
1.80
自引率
11.10%
发文量
128
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