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独特的锁骨下血管环异常:CT血管造影的见解

Unique Subclavian Vascular Ring Anomaly: Insights from CT Angiography.

作者信息

Baz Radu Octavian, Enyedi Mihaly, Scheau Cristian, Didilescu Andreea Cristiana, Baz Radu Andrei, Niscoveanu Cosmin

机构信息

Clinical Laboratory of Radiology and Medical Imaging, "Sf. Apostol Andrei" County Emergency Hospital, 900591 Constanta, Romania.

Department of Radiology and Medical Imaging, Faculty of Medicine, "Ovidius" University, 900527 Constanta, Romania.

出版信息

Life (Basel). 2025 Jan 10;15(1):77. doi: 10.3390/life15010077.

Abstract

Aortic arch anomalies represent a range of congenital vascular malformations resulting from disruptions in the typical embryological development of the aortic arch and its branches. These anomalies, which vary widely in their presentation, can lead to significant clinical symptoms depending on their structure and position. We report the case of a 75-year-old male with intermittent hypertension, palpitations, and episodic warmth in the upper body. Computed tomography (CT) angiography revealed an atypical aortic arch anatomy with a unique right subclavian artery anomaly. The aortic arch displayed a typical orientation but included an additional arterial branch arising from the medial wall of the descending aorta. This aberrant branch with a tortuous aspect coursed posteriorly around the esophagus and merged with the subclavian branch of the brachiocephalic trunk, forming a vascular ring. A possible embryological hypothesis requires the persistence of both the distal segment of the right dorsal aorta and the right seventh intersegmental artery, as well as the right fourth aortic arch; however, the imaging aspect of our patient is not that of a classic double aortic arch. This case emphasizes the importance of advanced imaging techniques, such as CT angiography, in identifying and managing rare vascular anomalies that may influence patient care and clinical outcomes.

摘要

主动脉弓异常代表了一系列先天性血管畸形,这些畸形是由主动脉弓及其分支在典型胚胎发育过程中受到干扰所致。这些异常在表现形式上差异很大,根据其结构和位置的不同,可能会导致明显的临床症状。我们报告了一例75岁男性患者,其患有间歇性高血压、心悸以及上身阵发性潮热。计算机断层扫描(CT)血管造影显示主动脉弓解剖结构不典型,伴有独特的右锁骨下动脉异常。主动脉弓呈现典型的走行方向,但有一个额外的动脉分支起自降主动脉的内侧壁。这个异常分支走行迂曲,向后绕过食管,并与头臂干的锁骨下分支汇合,形成一个血管环。一种可能的胚胎学假说是右背主动脉远端节段、右第七节间动脉以及右第四主动脉弓均持续存在;然而,我们患者的影像学表现并非典型的双主动脉弓。该病例强调了先进成像技术,如CT血管造影,在识别和处理可能影响患者治疗及临床结局的罕见血管异常方面的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfd6/11766760/6f0b93bad18d/life-15-00077-g001.jpg

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