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16 岁患者胆汁性呕吐合并肠系膜上动脉综合征。

Superior mesenteric artery syndrome in a 16-year-old with bilious emesis.

机构信息

Department of Digestive Health, University of Colorado Denver School of Medicine, The Children's Hospital, Aurora, CO 80045, USA.

出版信息

Curr Opin Pediatr. 2010 Oct;22(5):664-7. doi: 10.1097/MOP.0b013e32833c4947.

Abstract

Superior mesenteric artery (SMA) syndrome describes vascular compression of the third portion of the duodenum and presents with nausea, postprandial vomiting, and epigastric abdominal pain. The syndrome is rare and may be missed if appropriate radiologic studies are not performed or the clinical presentation is atypical. The clinical contexts in which SMA syndrome develops usually involve rapid weight loss, alterations in spine anatomy, or external increases in abdominal pressure. Diagnostic methods for identifying duodenal obstruction by the SMA include upper gastrointestinal barium contrast studies, computed tomography scans, or angiography of the aorta with either contrast or magnetic resonance angiography. Medical therapy relies upon nutritional rehabilitation with either jejunal tube feedings or parenteral nutrition until weight gain results in relief of the obstruction. In instances where this approach fails, surgical correction is necessary, most often with laparoscopic duodenojejunostomy.

摘要

肠系膜上动脉(SMA)综合征描述了十二指肠第三部分的血管受压,并表现为恶心、餐后呕吐和上腹痛。该综合征较为罕见,如果未进行适当的影像学研究或临床表现不典型,可能会被漏诊。SMA 综合征发展的临床情况通常涉及体重迅速下降、脊柱解剖结构改变或腹部压力增加。通过 SMA 识别十二指肠梗阻的诊断方法包括上消化道钡剂造影、计算机断层扫描或主动脉造影(对比剂或磁共振血管造影)。医疗治疗依赖于营养康复,包括空肠管喂养或肠外营养,直到体重增加缓解梗阻。在这种方法失败的情况下,通常需要手术矫正,最常见的方法是腹腔镜十二指肠空肠吻合术。

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