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伴有罕见双重病理的急性阑尾炎。

Acute appendicitis with unusual dual pathology.

作者信息

Riddiough Georgina E, Bhatti Imran, Ratliff David A

机构信息

Department of Vascular Surgery, Northampton General Hospital, Cliftonville, Northampton NN1 5BD, United Kingdom.

出版信息

Int J Surg Case Rep. 2012;3(1):25-6. doi: 10.1016/j.ijscr.2011.10.008. Epub 2011 Oct 25.

Abstract

INTRODUCTION

Meckel's diverticulum is a rare congenital abnormality arising due to the persistence of the vitelline duct in 1-3% of the population. Clinical presentation is varied and includes rectal bleeding, intestinal obstruction, diverticulitis and ulceration; therefore diagnosis can be difficult.

PRESENTATION OF CASE

We report a case of acute appendicitis complicated by persistent post operative small bowel obstruction. Further surgical examination of the bowel revealed an non-inflamed, inverted Meckel's diverticulum causing intussusception.

DISCUSSION

Intestinal obstruction in patients with Meckel's diverticulum may be caused by volvulus, intussusception or incarceration of the diverticulum into a hernia. Obstruction secondary to intussusception is relatively uncommon and frequently leads to a confusing and complicated clinical picture.

CONCLUSION

Consideration of Meckel's diverticulum although a rare diagnosis is imperative and this case raises the question "should surgeons routinely examine the bowel for Meckel's diverticulum at laparoscopy?"

摘要

引言

梅克尔憩室是一种罕见的先天性异常,因卵黄管持续存在而引起,在1%至3%的人群中出现。临床表现多样,包括直肠出血、肠梗阻、憩室炎和溃疡;因此诊断可能困难。

病例介绍

我们报告一例急性阑尾炎并发术后持续性小肠梗阻的病例。对肠道进行进一步手术检查发现一个未发炎、内翻的梅克尔憩室导致肠套叠。

讨论

梅克尔憩室患者的肠梗阻可能由憩室扭转、肠套叠或憩室嵌入疝引起。肠套叠继发的梗阻相对少见,常导致复杂且令人困惑的临床情况。

结论

尽管梅克尔憩室的诊断罕见,但必须考虑到,该病例提出了一个问题:“外科医生在腹腔镜检查时是否应常规检查肠道有无梅克尔憩室?”

相似文献

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Acute appendicitis with unusual dual pathology.伴有罕见双重病理的急性阑尾炎。
Int J Surg Case Rep. 2012;3(1):25-6. doi: 10.1016/j.ijscr.2011.10.008. Epub 2011 Oct 25.
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A large incarcerated Meckel's diverticulum in an inguinal hernia.腹股沟疝内的巨大嵌顿性梅克尔憩室。
Int J Surg Case Rep. 2014;5(12):899-901. doi: 10.1016/j.ijscr.2014.09.036. Epub 2014 Oct 17.

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