Hugin Silje, Johnson Egil, Johannessen Hans-Olaf, Hofstad Bjørn, Olafsen Kjell, Mellem Harald
Departments of Gastrointestinal Surgery, Oso University Hospital, Ullevål, P. O. Box 4950 Nydalen, Oslo, Norway.
Departments of Gastrointestinal Surgery, Oso University Hospital, Ullevål, P. O. Box 4950 Nydalen, Oslo, Norway; Institute of Clinical Medicine, University of Oslo, Kirkeveien 166, 0450 Oslo, Norway.
Int J Surg Case Rep. 2015;17:31-5. doi: 10.1016/j.ijscr.2015.10.023. Epub 2015 Oct 21.
Myotonic dystrophies are inherited multisystemic diseases characterized by musculopathy, cardiac arrythmias and cognitive disorders. These patients are at increased risk for fatal post-surgical complications from pulmonary hypoventilation. We present a case with myotonic dystrophy and esophageal cancer who had a minimally invasive esophagectomy complicated with gastrobronchial fistulisation.
A 44-year-old male with myotonic dystrophy type 1 and esophageal cancer had a minimally invasive esophagectomy performed instead of open surgery in order to reduce the risk for pulmonary complications. At day 15 respiratory failure occurred from a gastrobronchial fistula between the right intermediary bronchus (defect 7-8mm) and the esophagogastric anastomosis (defect 10mm). In order to minimize large leakage of air into the gastric conduit the anastomosis was stented and ventilation maintained at low airway pressures. His general condition improved and allowed extubation at day 29 and stent removal at day 35. Bronchoscopy confirmed that the fistula was healed. The patient was discharged from hospital at day 37 without further complications.
The fistula was probably caused by bronchial necrosis from thermal injury during close dissection using the Ligasure instrument. Fistula treatment by non-surgical intervention was considered safer than surgery which could be followed by potentially life-threatening respiratory complications. Indications for stenting of gastrobronchial fistulas will be discussed.
Minimally invasive esophagectomy was performed instead of open surgery in a myotonic dystrophy patient as these patients are particularly vulnerable to respiratory complications. Gastrobronchial fistula, a major complication, was safely treated by stenting and low airway pressure ventilation.
强直性肌营养不良症是一种遗传性多系统疾病,其特征为肌肉病变、心律失常和认知障碍。这些患者因肺通气不足而发生致命术后并发症的风险增加。我们报告一例强直性肌营养不良症合并食管癌患者,该患者接受了微创食管切除术,术后并发胃支气管瘘。
一名44岁男性,患有1型强直性肌营养不良症和食管癌,为降低肺部并发症风险,接受了微创食管切除术而非开放手术。术后第15天,右中间支气管(缺损7 - 8毫米)与食管胃吻合口(缺损10毫米)之间出现胃支气管瘘,导致呼吸衰竭。为尽量减少大量空气漏入胃管道,对吻合口进行了支架置入,并维持低气道压力通气。患者一般状况改善,于术后第29天拔管,第35天取出支架。支气管镜检查证实瘘口已愈合。患者于术后第37天出院,无进一步并发症。
瘘口可能是在使用Ligasure器械进行精细解剖时,因热损伤导致支气管坏死所致。非手术干预治疗瘘口被认为比手术更安全,手术可能会引发潜在的危及生命的呼吸并发症。将讨论胃支气管瘘支架置入的指征。
在强直性肌营养不良症患者中,选择了微创食管切除术而非开放手术,因为这些患者特别容易发生呼吸并发症。胃支气管瘘这一主要并发症通过支架置入和低气道压力通气得到了安全治疗。