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Superior Mesenteric Artery Syndrome After Restorative Proctocolectomy With Ileal Pouch-Anal Anastomosis: A Case Report

机译:结肠回肠切除术与回肠袋-肛门吻合术后肠系膜上动脉综合征:一例报告

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Purpose: Superior mesenteric artery syndrome (SMAS) is a rare complication following restorative proctocolectomy with only eight previous reports. We report the case of a 16-year-old girl known to have familial adenomatous polyposis who underwent a restorative proctocolectomy with an ileal pouch-anal anastomosis. Methods: The features of the case were studied followed by a review of the current literature. Results: After an uneventful first postoperative week, the patient developed SMAS, characterised by voluminous bilious vomiting. Laparotomy revealed compression of the duodenum by the overlying mesenteric root containing the superior mesenteric artery. Unexpected dense peri-mesenteric and intraperitoneal fibrosis was also encountered. Conclusion: Previous reports suggested the aetiology is directly related to the accentuated angle between the superior mesenteric artery and the aorta, which is created at the time of surgery. Our case suggests that it may actually be events in the postoperative period such as fibrosis of the mesentery that are responsible. When surgical intervention is required, we advocate duodenojejunostomy as the preferred solution. Introduction Compression of the duodenum by the superior mesenteric artery is a rare complication following restorative proctocolectomy. We report an interesting case in point, consider the possible aetiological factors, and discuss the management of the condition. Case Report A 16-year-old girl known to have familial adenomatous polyposis underwent a restorative proctocolectomy with anastomosis of a J-shaped ileal pouch to the anal canal and fashioning of a covering loop ileostomy. The small bowel mesentery was mobilised close to its root and the ileocolic artery was divided, facilitating an anastomosis free from any tension. The initial post-operative course saw a timely reinstatement of her normal diet with a satisfactory stoma function. On the eighth day, she developed significant fresh rectal bleeding, which although required a blood transfusion, was self-limiting. The anastomosis felt intact on digital rectal examination.On the tenth day, she complained of significant pain in her left iliac fossa and had voluminous bilious vomiting. The ileostomy continued to function normally and there were no other signs suggestive of bowel obstruction. Plain abdominal radiography was normal. A computed tomography scan demonstrated a distended stomach and duodenum to its third part (see figure 1). Total parenteral nutrition was started and she was managed expectantly.
机译:目的:肠系膜上动脉综合症(SMAS)是恢复性直肠结肠切除术后的一种罕见并发症,以前只有八篇报道。我们报道了一名16岁女孩,患有家族性腺瘤性息肉病,该患者接受了回肠结肠直肠吻合术。方法:研究该病例的特征,然后回顾当前文献。结果:术后第一周的情况平稳,患者出现了SMAS,其特征是大量胆汁性呕吐。剖腹手术显示,肠系膜上层含有肠系膜上动脉的压迫十二指肠。还遇到了意料之外的致密的肠系膜周围和腹膜内纤维化。结论:以前的报道表明,病因与肠系膜上动脉和主动脉之间的加重角直接相关,这是在手术时产生的。我们的病例表明,实际上可能是术后时期的事件,例如引起肠系膜纤维化的事件。当需要手术干预时,我们建议采用十二指肠空肠吻合术作为首选解决方案。引言肠系膜上动脉压迫十二指肠是术后行结肠结肠切除术的罕见并发症。我们适当地报告了一个有趣的案例,考虑了可能的病因,并讨论了病情的管理。病例报告一名患有家族性腺瘤性息肉病的16岁女孩接受了修复性直肠结肠切除术,并将J型回肠囊与肛门吻合,并形成了回肠回肠造口术。小肠系膜动员在靠近其根部的位置,回肠动脉分裂,促进了无张力的吻合。术后最初的过程是及时恢复正常饮食,造口功能令人满意。在第八天,她出现了明显的新鲜直肠出血,尽管需要输血,但仍是自限性的。在直肠指检中,吻合口完好无损。第十天,她抱怨左窝有明显疼痛,并有大量胆汁性呕吐。回肠造口术继续正常运作,没有其他迹象表明肠梗阻。腹部平片摄片正常。计算机断层扫描显示胃和十二指肠扩张至其第三部分(见图1)。开始完全胃肠外营养,并按预期进行治疗。

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