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先天性肺动脉异常的横断面成像

Cross-sectional imaging of congenital pulmonary artery anomalies.

作者信息

Zucker Evan J

机构信息

Department of Radiology, Stanford University School of Medicine, 725 Welch Road, Stanford, CA, 94305, USA.

出版信息

Int J Cardiovasc Imaging. 2019 Aug;35(8):1535-1548. doi: 10.1007/s10554-019-01643-4. Epub 2019 Jun 7.

Abstract

Congenital pulmonary artery (PA) anomalies comprise a rare and heterogeneous spectrum of disease, ranging from abnormal origins to complete atresia. They may present in early infancy or more insidiously in adulthood, often in association with congenital heart disease such as tetralogy of Fallot or other syndromes. In recent years, cross-sectional imaging, including computed tomography (CT) and magnetic resonance imaging (MRI), has become widely utilized for the noninvasive assessment of congenital PA diseases, supplementing echocardiography and at times supplanting invasive angiography. In this article, modern CT and MRI techniques for imaging congenital PA disorders are summarized. The key clinical features, cross-sectional imaging findings, and treatment options for the most commonly encountered entities are then reviewed. Emphasis is placed on the ever-growing role of cross-sectional imaging options in facilitating early and accurate diagnosis and tailored treatment.

摘要

先天性肺动脉(PA)异常是一类罕见且异质性的疾病谱,范围从起源异常到完全闭锁。它们可能在婴儿早期出现,或在成年期更隐匿地出现,常与诸如法洛四联症等先天性心脏病或其他综合征相关。近年来,包括计算机断层扫描(CT)和磁共振成像(MRI)在内的横断面成像已广泛用于先天性PA疾病的无创评估,补充了超声心动图,有时还取代了有创血管造影。本文总结了用于先天性PA疾病成像的现代CT和MRI技术。然后回顾了最常见实体的关键临床特征、横断面成像表现及治疗选择。重点在于横断面成像方法在促进早期准确诊断和个体化治疗方面日益重要的作用。

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