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与复杂先天性心脏病相关的肺动脉异常起源和位置异常(交叉肺动脉)

Anomalous origin and malposition of the pulmonary arteries (crisscross pulmonary arteries) associated with complex congenital heart disease.

作者信息

Wolf W J, Casta A, Nichols M

出版信息

Pediatr Cardiol. 1986;6(5):287-91.

PMID:3725636
Abstract

Anomalous origin and malposition of the branch pulmonary arteries is an uncommon malformation that has previously been noted only at the time of pathologic examination. Two infants with complex congenital cardiac disease had malposition of the branch pulmonary arteries (crisscross pulmonary arteries) detected by angiography and confirmed during surgery and in one case, at autopsy. The presence of this clinically unsuspected lesion complicated the accurate interpretation of both the two-dimensional echocardiographic appearance of the great vessels, and the catheter course and location during cardiac catheterization. Angiography clearly defined the crisscrossing pattern of the branch pulmonary arteries. The recognition of this malformation was important in planning and executing the surgical palliation or repair for these infants.

摘要

肺分支动脉的异常起源和位置异常是一种罕见的畸形,以前仅在病理检查时才被发现。两名患有复杂先天性心脏病的婴儿通过血管造影检测到肺分支动脉位置异常(交叉肺动 脉),并在手术中得到证实,其中一例在尸检时得到证实。这种临床未被怀疑的病变的存在使对大血管二维超声心动图表现以及心导管检查期间导管的走行和位置的准确解读变得复杂。血管造影清楚地显示了肺分支动脉的交叉模式。认识到这种畸形对于为这些婴儿制定和实施手术姑息治疗或修复手术非常重要。

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