Rabie M Ezzedien, Ogunbiyi Olajide, Al Qahtani Abdullah Saad, Taha Sherif B M, El Hadad Ahmad, El Hakeem Ismail
Department of Surgery, Armed Forces Hospital, Southern Region, Khamis Mushait, Saudi Arabia.
Department of Radiology, Armed Forces Hospital, Southern Region, Khamis Mushait, Saudi Arabia.
Surg Res Pract. 2015;2015:628705. doi: 10.1155/2015/628705. Epub 2015 Aug 12.
Background. Superior mesenteric artery (SMA) syndrome is a rare condition of duodenal obstruction, caused by the overlying SMA. Aim. To report on our experience with the management of SMA syndrome, drawing the attention to its existence. Material and Methods. We reviewed our records to identify cases diagnosed with SMA syndrome, in the period from October 1995 to January 2012. Results. Seven patients were identified, one male and six females. Their mean age was 17.1 years. Vomiting and abdominal pain were the presenting complaints in all patients and history of weight loss was present in six of them. In no patient was the diagnosis suspected initially on clinical grounds. Only after radiological investigations was the diagnosis declared. Radiology took the form of gastrografin/barium meal only in four patients and both gastrografin/barium meal and computerized tomography scan in the remaining three. Four patients responded to medical treatment and surgery was performed in the remaining three, with open duodenojejunostomy in two patients and laparoscopic dissection of the ligament of Treitz in the third. Long lasting improvement was sustained in all patients except one in the surgery group who, despite initial improvement, still has infrequent attacks of abdominal pain. Conclusion. Although the clinical manifestations of SMA syndrome are shared with many other disease entities, it has unique radiological as well as endoscopic features, which enables a confident diagnosis to be made. Once diagnosed, conservative treatment with nutritional support and positioning should be tried first. In case of unresponsiveness, surgery may give a lasting cure.
背景。肠系膜上动脉(SMA)综合征是一种由肠系膜上动脉压迫导致十二指肠梗阻的罕见病症。目的。报告我们在SMA综合征治疗方面的经验,以引起对该病症的关注。材料与方法。我们回顾了1995年10月至2012年1月期间确诊为SMA综合征的病例记录。结果。共确定7例患者,1例男性,6例女性。他们的平均年龄为17.1岁。所有患者均以呕吐和腹痛为主要症状,其中6例有体重减轻史。最初没有患者基于临床症状被怀疑患有该病。仅在进行影像学检查后才确诊。4例患者仅接受了泛影葡胺/钡餐造影检查,其余3例同时接受了泛影葡胺/钡餐造影检查和计算机断层扫描。4例患者对药物治疗有反应,其余3例接受了手术治疗,2例患者行开放式十二指肠空肠吻合术,第3例患者行腹腔镜下Treitz韧带松解术。除手术组中有1例患者外,所有患者均持续获得了长期改善,该患者尽管最初有所改善,但仍偶尔发作腹痛。结论。尽管SMA综合征的临床表现与许多其他疾病有相似之处,但它具有独特的影像学和内镜特征,这使得能够做出可靠的诊断。一旦确诊,应首先尝试采用营养支持和体位调整的保守治疗。如果治疗无效,手术可能会带来持久的治愈效果。