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Apport du scanner multi-coupe dans les anomalies des arcs et de larche aortique chez lenfant

机译:多节段扫描器对儿童弓和主动脉弓畸形的贡献

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摘要

Congenital malformations of the aortic arches are a heterogeneous group of diseases associated with developmental disorders of the primitive branchial arches during fetal life. The coarctation of the aorta is a common congenital vascular malformation which is a congenital narrowing of the aortic isthmus, a segment of the aorta between the left subclavian artery and the ductus arteriosus. The interruption of the aortic arch is considered by some authors as an extreme coarctation of the aorta, characterized by discontinuity between ascending and descending aorta. These abnormalities are integrated, in most cases, in the context of cardiac malformations from which they are indivisible. CT angiogram plays an essential role in the examination of these abnormalities, their preoperative assessment and their follow-up in the long term. We conducted a retrospective study of 42 patients undergoing CT angiogram following the detection of heart disease on echocardiography. CT angiogram was performed in 6 cases. The average age of patients was 2 years, ranging from 6 days to 14 years; a male predominance was reported with a sex ratio of 1,6. The main diseases were: coarctation of the aorta: 18 cases; hypoplasies of the aortic arch: 8 cases; interruptions of the aortic arch: 7 cases; abnormalities of the aortic arches: 9 cases. Some of these abnormalities were associated. Extracardiac abnormalities associated with congenital heart diseases are relatively frequent; multislice scanner allows for good analysis of the cardiac afferent and efferent pathways. CT complements echocardiogram for pre-treatment assessment of the main malformative diseases, especially for the detection of the associated extra-cardiac vascular abnormalities, thanks to its satisfactory tridimensional multiplanar exploration. It tends to supplant angiography in many pathological malformations for several reasons: it is less invasive; it provides high-resolution 3D images useful to surgeons; it established the anatomical diagnosis, assesses tracheal compression and any associated malformation; it guides surgical treatment.
机译:主动脉弓的先天畸形是与胎儿生命期间原始分支弓的发育障碍相关的异质性疾病。主动脉缩窄是一种常见的先天性血管畸形,是先天性主动脉峡部狭窄,主动脉峡部位于左锁骨下动脉和动脉导管之间。一些作者认为主动脉弓的中断是主动脉的极度缩窄,其特征是升主动脉和降主动脉之间不连续。在大多数情况下,这些异常是在无法识别的心脏畸形的背景下整合在一起的。 CT血管造影在这些异常检查,术前评估以及长期随访中起着至关重要的作用。在超声心动图检查中发现心脏病后,我们对42例接受CT血管造影的患者进行了回顾性研究。 6例行CT血管造影。患者的平均年龄为2岁,从6天到14岁不等;据报道,男性占主导地位,性别比为1.6。主要疾病为:主动脉缩窄18例。主动脉弓发育不全8例;主动脉弓中断:7例;主动脉弓异常:9例。其中一些异常是相关的。与先天性心脏病相关的心外异常相对频繁。多层扫描仪可以很好地分析心脏的传入和传出路径。由于其令人满意的三维多平面探索,CT补充了超声心动图,可对主要畸形疾病进行治疗前评估,尤其是用于检测相关的心脏外血管异常。由于多种原因,它倾向于取代许多病理畸形的血管造影:侵入性较小;它提供了对外科医生有用的高分辨率3D图像;它建立了解剖学诊断,评估气管压迫和任何相关的畸形;它指导外科治疗。

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