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当代的Kommerell憩室:全面综述

Kommerell's diverticulum in the current era: a comprehensive review.

作者信息

Tanaka Akiko, Milner Ross, Ota Takeyoshi

机构信息

Department of Surgery, Section of Cardiac and Thoracic Surgery, University of Chicago, 5841 Maryland Avenue, Suite E-500/MC5040, Chicago, IL, 60637, USA.

出版信息

Gen Thorac Cardiovasc Surg. 2015 May;63(5):245-59. doi: 10.1007/s11748-015-0521-3. Epub 2015 Jan 31.

Abstract

Kommerell's diverticulum is a developmental error with a remnant of fourth dorsal aortic arch, named after Dr. Kommerell, a radiologist, who made the first diagnosis in a living individual. The diverticulum can occur in both the left and right aortic arch, from which an aberrant subclavian artery rises to the contralateral side. Pediatric patients often present with airway symptoms whereas dysphagia and chest discomfort are more common in the adult patients. Computed tomography or magnetic resonance imaging can provide details of the diverticulum, associated arch anomalies, and its relationship with surrounding organs. Recent histological studies indicated the presence of cystic medial necrosis in the diverticulum wall, which would explain the reported high rates of aortic dissection and rupture associated with the diverticulum. Accumulated knowledge on this entity and the recent advancement of imaging techniques, surgical/endovascular strategies, and perioperative management, have led to more aggressive intervention to the diverticulum in the early phase. While still under debate it is generally accepted to consider surgical intervention when the diameter of the diverticulum orifice exceeds over 30 mm, and/or the diameter of the descending aorta adjacent to the diverticulum exceeds over 50 mm. Treatment options include open surgical repair, hybrid endovascular repair, and total endovascular repair. The selection of treatment strategy for Kommerell's diverticulum should be based on the anatomy, comorbidities of the patient, and surgical expertise available. The summaries of open and endovascular repairs of over 210 cases from literature search from 2004 to 2014 are also provided in this review.

摘要

科默雷尔憩室是一种发育异常,为第四对背主动脉弓的残余部分,以放射科医生科默雷尔博士的名字命名,他首次在活体中作出诊断。憩室可发生于左、右主动脉弓,异常锁骨下动脉由此向对侧发出。儿科患者常表现为气道症状,而成人患者吞咽困难和胸部不适更为常见。计算机断层扫描或磁共振成像可提供憩室的详细情况、相关的主动脉弓异常及其与周围器官的关系。最近的组织学研究表明憩室壁存在囊性中层坏死,这可以解释报道中与憩室相关的主动脉夹层和破裂的高发生率。关于该疾病的知识积累以及成像技术、外科/血管内治疗策略和围手术期管理的最新进展,促使在早期对憩室采取更积极的干预措施。虽然仍存在争议,但一般认为当憩室口直径超过30mm,和/或与憩室相邻的降主动脉直径超过50mm时,应考虑手术干预。治疗选择包括开放手术修复、杂交血管内修复和完全血管内修复。科默雷尔憩室治疗策略的选择应基于患者的解剖结构、合并症以及现有的手术专业知识。本综述还提供了2004年至2014年文献检索中210多例开放手术和血管内修复的总结。

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