Department of Pediatric Surgery, Graduate School of Comprehensive Human Sciences and University Hospital, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Eur J Cardiothorac Surg. 2011 Mar;39(3):412-3. doi: 10.1016/j.ejcts.2010.08.012. Epub 2010 Sep 16.
We reviewed six cases demonstrating acquired tracheomalacia due to innominate artery compression of the trachea and investigated the benefit and effectiveness of a technique for correcting tracheomalacia. All the patients developed scoliosis and the innominate artery run over the trachea. Four cases had permanent neurologic impairment, whereas two patients developed acquired neurologic impairment. The surgical strategy for acquired tracheomalacia due to innominate artery compression of the trachea involved superior mediastinal exposure, external reinforcement with autologous cartilage graft, anterior sling of the innominate artery with a muscle sling, and tracheopexy. Our surgical procedure has been effective in maintaining the patency of the tracheal lumen in all cases but one. This patient suffered from straight back syndrome and developed recurrence of tracheomalacia owing to mucosal infolding secondary to the deformed spine in a supine position. The authors believe our surgical procedure is effective to relieve the symptoms of tracheomalacia, but it is important to select surgical interventions in accordance with the specific patient's condition.
我们回顾了 6 例因无名动脉压迫气管引起的获得性气管软化症,并研究了一种纠正气管软化症的技术的益处和效果。所有患者均出现脊柱侧凸,无名动脉位于气管上方。4 例患者出现永久性神经功能障碍,2 例患者出现获得性神经功能障碍。由于无名动脉压迫气管引起的获得性气管软化症的手术策略包括上纵隔显露、自体软骨移植物外部加固、无名动脉前吊带和肌肉吊带以及气管固定术。我们的手术程序在所有病例中都有效,除了 1 例。该患者患有直背综合征,由于脊柱畸形导致仰卧位时黏膜内陷,再次出现气管软化症。作者认为,我们的手术程序可以有效缓解气管软化症的症状,但重要的是要根据特定患者的情况选择手术干预措施。