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Pentalogy of Cantrell with Sternum Agenesis—A Case Report

机译:坎特雷尔五角畸形与胸骨发育不全的病例报告

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Introduction: Pentalogy of Cantrell is a rare disorder described by Cantrell in 1958 and characterized by heart anomalies, involving defects of the diaphragm, abdominal wall, supraumbilical region and pericardium. Methods: We report a case of the disease that presented with agenesis of the sternum and partial absence of costal cartilage, treated by a multi-disciplinary team. Results: The patient underwent median sternotomy. An enlarged heart, compromising the pulmonary trunk and the right ventricle, and a left superior vena cava were identified. The right atrium was opened and an interventricular communication of around 10 mm in diameter was seen through the tricuspid valve. Following the repair of the heart defects, chondroplasty and placement of biological mesh (Bioway of Gore) were performed. Conclusion: A Successful surgical treatment for Cantrell Syndrome includes correction of the cardiac malformation, a good repair of thoracoabdominal wall.
机译:简介:坎特尔的药物是1958年坎特雷尔描述的罕见疾病,其特征在于心脏异常,涉及隔膜,腹壁,超牙科和心包的缺陷。方法:我们举报了一种患有胸骨损伤和部分缺乏肋骨软骨的病例,由多学科团队治疗。结果:病人接受了胸骨切开术中位数。鉴定了损害肺动脉干燥和右心室的放大的心脏和左上腔静脉。通过三尖瓣观察到右节庭,通过三尖瓣观察到直径约10mm的间隔通信。在修复心脏缺陷后,进行细胞成形术和生物网格的放置(血管)。结论:坎特雷尔综合征的成功外科治疗包括矫正心脏畸形,胸腔腹壁的良好修复。

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