成人先天性Gerbode缺陷1例:报告一例极为罕见的病例。

Pedro Daniel Díaz-Sarasa, Jorge Sebastián Reyes-Villanés, W Samir Cubas
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引用次数: 0

摘要

Gerbode缺损(GD)是一种罕见的先天性心脏病,主要影响隔膜上部,在左心室和右心房之间产生分流。尽管大多数病例是先天性的,但也有由于心脏手术、感染性心内膜炎、急性缺血性心脏病和侵入性经皮手术引起的获得性病例的报道。诊断检查包括临床评价和超声心动图检查。在这里,我们提出的情况下,43岁的成年患者偶然发现先天性GD的背景下急性阑尾炎。影像学在先天性疾病的诊断检查中发挥着重要作用;在这种情况下,它使我们能够确定更多的细节和我们的病人的决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Congenital Gerbode defect in an adult patient: report of an extremely rare case.

Gerbode Defect (GD) is a rare congenital heart disease that mainly affects the upper portion of the membranous septum, generating a shunt between the left ventricle and the right atrium. Even though most cases are congenital, it has also been reported acquired cases due to cardiac surgery, infective endocarditis, acute ischemic heart disease, and invasive percutaneous procedures. The diagnostic workup includes the clinical evaluation and the echocardiographic study. Here, we present the case of a 43-year-old adult patient with an incidental finding of a congenital GD in the context of acute appendicitis. Imaging plays a role in the diagnostic workup of congenital diseases; in this case, it allowed us to identify more details and the decision-making for our patient.

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0.40
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期刊最新文献
[Andersen-Tawil Syndrome, a differential of bidirectional ventricular tachycardia: a case report]. [Balloon atrioseptostomy under echocardiographic and fluoroscopic guide in patients with congenital heart diseases under 3 months in a national reference pediatric center]. [Frailty and adverse outcomes in patients over 65 years old with acute coronary syndrome in a hospital cohort in Medellin, Colombia]. [Hypertrophic cardiomyopathy with mid-ventricular phenotype and filamin C mutation, an uncommon case report]. [Neonatal screening for critical congenital heart diseases in Peru: an urgent call].
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