Backer C L, Hillman N, Mavroudis C, Holinger L D
Department of Surgery, Northwestern University Medical School, Chicago, IL, USA.
Eur J Cardiothorac Surg. 2002 Jul;22(1):64-9. doi: 10.1016/s1010-7940(02)00213-0.
A Kommerell's diverticulum in patients with a right aortic arch may become aneurysmal and be an independent cause of tracheoesophageal compression, even after ligation and division of a left ligamentum. We review the indications for and results of Kommerell's diverticulum resection and left subclavian artery transfer in children with a right aortic arch who previously underwent vascular ring (ligamentum) division.
From 1998 through 2001, eight children have been referred with recurrent respiratory symptoms (n=8) and/or recurrent dysphagia (n=4) after vascular ring division. Each child had a right aortic arch with a left ligamentum and had undergone division of the ligamentum elsewhere. All had a Kommerell's diverticulum that was not addressed at the initial operation. All patients had a repeat left thoracotomy with resection of the diverticulum. Five patients had division and reimplantation of the left subclavian artery into the left carotid artery to relieve the sling-like effect of the retroesophageal left subclavian artery on the right aortic arch. One other patient had primary Kommerell's diverticulum resection and transfer of the left subclavian artery to the left carotid artery.
The mean age at the initial operation was 1.7+/-0.9 years, and the mean age at reoperation was 8.0+/-3.7 years. In all patients postoperative bronchoscopy confirmed relief of the tracheal compression. There were no complications related to the subclavian artery transfer. Two patients developed postoperative chylothorax, one requiring thoracic duct ligation. The median hospital stay was 5 days. All patients had dramatic resolution of their preoperative symptoms.
Kommerell's diverticulum is an important anatomic structure that can cause recurrent symptoms in patients with a right aortic arch after ligamentum division. In selected patients, reoperation with resection of the Kommerell's diverticulum and transfer of a retroesophageal left subclavian artery results in relief of symptoms. This technique has become our procedure of choice as a primary operation for children with a right aortic arch and a significant Kommerell's diverticulum.
右主动脉弓患者的Kommerell憩室可能会形成动脉瘤,并且即使在结扎并切断左韧带后,它也可能是气管食管受压的独立原因。我们回顾了右主动脉弓儿童患者Kommerell憩室切除术及左锁骨下动脉移位术的适应证及手术结果,这些患儿之前均接受过血管环(韧带)切断术。
1998年至2001年,8例患儿因血管环切断术后出现反复呼吸道症状(n = 8)和/或反复吞咽困难(n = 4)前来就诊。每个患儿均为右主动脉弓伴左韧带,且已在其他地方接受过韧带切断术。所有患儿均有Kommerell憩室,初次手术时未处理。所有患者均再次行左胸切开术切除憩室。5例患者切断左锁骨下动脉并将其重新植入左颈动脉,以解除食管后左锁骨下动脉对右主动脉弓的吊带样作用。另有1例患者行原发性Kommerell憩室切除术,并将左锁骨下动脉移位至左颈动脉。
初次手术时的平均年龄为1.7±0.9岁,再次手术时的平均年龄为8.0±3.7岁。所有患者术后支气管镜检查均证实气管压迫得到缓解。未发生与锁骨下动脉移位相关的并发症。2例患者术后发生乳糜胸,1例需要行胸导管结扎术。中位住院时间为5天。所有患者术前症状均显著缓解。
Kommerell憩室是一个重要的解剖结构,可导致右主动脉弓患者在韧带切断术后出现反复症状。对于选定的患者,再次手术切除Kommerell憩室并移位食管后左锁骨下动脉可缓解症状。该技术已成为我们对有明显Kommerell憩室的右主动脉弓患儿首选的主要手术方法。