Division of Pediatric General and Thoracic Surgery, Seattle Children's Hospital and University of Washington, USA.
J Pediatr Surg. 2012 Nov;47(11):2137-9. doi: 10.1016/j.jpedsurg.2012.09.044.
We report the case of a 14-year-old boy with pectus excavatum and mild scoliosis. The patient underwent a minimally invasive Nuss repair with excellent cosmetic result. He returned 3 weeks post-operatively with bilious emesis and a 3.6-kg weight loss (5.5% of total body weight). Radiographic evaluation was consistent with the diagnosis of superior mesenteric artery syndrome and the child ultimately required nasojejunal feedings. Following return to his baseline weight, he was transitioned to oral feedings and has done well in follow-up. This is the first report of SMA syndrome following minimally invasive pectus excavatum repair.
我们报告了一例 14 岁男孩,患有漏斗胸和轻度脊柱侧凸。患者接受了微创 Nuss 修复术,效果极佳。术后 3 周,他出现胆汁性呕吐和 3.6 公斤体重减轻(占总体重的 5.5%)。放射学评估符合肠系膜上动脉综合征的诊断,患儿最终需要进行空肠喂养。体重恢复后,他转为口服喂养,随访情况良好。这是首例微创漏斗胸修复术后肠系膜上动脉综合征的报告。