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小儿空肠血管发育不良 1 例报告并文献复习。

Paediatric angiodysplasia of the jejunum: a case report and review of the literature.

机构信息

Department of Paediatric Surgery, Royal Manchester Children's Hospital, Manchester, England, UK.

出版信息

Scott Med J. 2012 Nov;57(4):247. doi: 10.1258/smj.2012.012082. Epub 2012 Sep 18.

Abstract

Gastrointestinal angiodysplasia (GIAD) of the jejunum is a rare cause of acute upper and lower gastrointestinal bleeding in the paediatric population. This is the case of a previously well 10-year-old girl who presented with acute rectal haemorrhage, haematemesis and syncope. Despite an exploratory laparotomy, the cause of bleeding remained unknown. A computerized tomography angiogram was performed once she was haemodynamically stable. It indicated bleeding in the jejunum. Repeat laparotomy was performed including enterotomy, copious small bowel washout and visualization of the whole small bowel. The lesion was identified at approximately 100 cm from the duodenojejunal flexure and confirmed by isolating the lesion and testing for bleeding. A 30 cm length of jejunum was resected and primary anastomosis performed. She recovered well and was discharged three days postoperatively. She remained well at six-month follow-up. This case highlights the importance of considering upper GIAD in an acute paediatric gastrointestinal bleed and the way in which surgical management can prevent a potentially fatal outcome.

摘要

空肠胃肠道血管发育不良(GIAD)是儿科人群急性上消化道和下消化道出血的罕见原因。这是一个既往健康的 10 岁女孩的病例,她出现急性直肠出血、呕血和晕厥。尽管进行了剖腹探查术,但出血原因仍不清楚。她的血流动力学稳定后,进行了计算机断层血管造影。结果显示空肠出血。再次进行剖腹手术,包括肠切开术、大量小肠冲洗和全小肠可视化。在十二指肠空肠曲附近约 100 厘米处发现病变,并通过隔离病变和出血测试进行了确认。切除 30 厘米长的空肠并进行一期吻合。她恢复良好,术后 3 天出院。她在 6 个月的随访中情况良好。这个病例强调了在小儿急性胃肠道出血时考虑上消化道 GIAD 的重要性,以及手术治疗可以预防潜在致命结局的方式。

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