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首页> 外文期刊>World journal for pediatric & congenital heart surgery >A Rare Case of Pulmonary Artery Sling and Complete Atrioventrlcular Canal Defect in an Infant With Trisomy 21
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A Rare Case of Pulmonary Artery Sling and Complete Atrioventrlcular Canal Defect in an Infant With Trisomy 21

机译:婴幼儿三体性21例肺动脉吊带和完全房室管缺损病例

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摘要

Pulmonary artery sling is a very rare congenital vascular anomaly. Patients usually present in infancy with symptoms of airway compression. Patients with trisomy 21 often have upper airway obstruction, most commonly related to pharyngeal causes or subglottic stenosis. Although the incidence of congenital heart defects in patients with trisomy 21 is very high, a review of the literature showed only one previously reported case of pulmonary artery sling in an infant with trisomy 21. We report a case of pulmonary artery sling and complete atrioventricular canal defect in a one-month-old female with trisomy 21. Echocardiography is an important diagnostic method for pulmonary artery sling, but this anomaly may be easily overlooked in the presence of more commonly anticipated defects in this population.
机译:肺动脉吊带是非常罕见的先天性血管异常。患者通常在婴儿期出现气道受压症状。 21三体症患者常有上呼吸道阻塞,最常与咽部原因或声门下狭窄相关。尽管21三体综合征患者先天性心脏缺陷的发生率很高,但文献回顾显示,在21三体综合征的婴儿中只有一例先前报道的肺动脉悬吊病例。我们报道了一例肺动脉悬吊和完整的房室管腔病例患有21三体性疾病的1个月大女性的心脏缺损。超声心动图是肺动脉悬带的重要诊断方法,但是在该人群中存在更普遍预期的缺损时,这种异常现象很容易被忽略。

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