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梅克尔憩室在其自身腔内发生套叠:一种未知的并发症。

Intussusception of the Meckel's diverticulum within its own lumen: Unknown complication.

作者信息

Kassir Radwan, Debs Tark, Boutet Claire, Baccot Sylviane, Abboud Karine, Dubois Joëlle, Bourlier Alexia Boueil, Yvorel Violaine, Tiffet Olivier

机构信息

Department of General Surgery, CHU Hospital, Jean Monnet University, Saint Étienne, France.

Department of General Surgery, CHU Hospital Archet 2, Nice, France.

出版信息

Int J Surg Case Rep. 2015;10:111-4. doi: 10.1016/j.ijscr.2015.03.042. Epub 2015 Mar 25.

Abstract

INTRODUCTION

Intussusception with the Meckel's diverticulum (MD) is a rare cause of chonic abdominal pain in the adults. We wish to present this first case of intussusception of MD within its own lumen without small bowel obstruction.

PRESENTATION OF CASE

We report the case of a 27-year-old man who was admitted to the emergency room due to a diffuse abdominal pain. Abdominal CT scan showed invagination of MD. The exploratory laparoscopy revealed the presence of intussusception of MD within its own lumen. Segmental resection of the small intestine was performed. The patient was discharged on the third post-operative day.

DISCUSSION

The prevalence of MD is 1 to 4%. Diagnosis is often difficult and delayed because clinical symptoms are not specific and the diagnosis is performed mainly by imaging studies. Factors pre-disposing these patients to intussusception of MD within its own lumen include a narrow diverticulum, large diverticululm, and associated inflammation of the diverticulum. Intestinal obstruction is a more common complication in adults, whereas in children, bleeding is the more common complication. In our case, the patient had a diffuse abdominal pain without small bowel obstruction because the intussusception of MD was within its own lumen. Laparoscopy may be useful for confirming the presence of intussusception, and demonstrating the underlying organic lesion serving as the lead point.

CONCLUSION

It is important to differentiate this rare pathological feature of MD from other entities as the treatment is surgical rather than medical. Abdominal surgeons should bear in mind this rare entity.

摘要

引言

梅克尔憩室(MD)所致肠套叠是成人慢性腹痛的罕见原因。我们希望呈现首例MD在其自身肠腔内发生肠套叠且无小肠梗阻的病例。

病例介绍

我们报告一名27岁男性因弥漫性腹痛入住急诊室的病例。腹部CT扫描显示MD套叠。探查性腹腔镜检查发现MD在其自身肠腔内发生肠套叠。对小肠进行了节段性切除。患者术后第三天出院。

讨论

MD的发生率为1%至4%。由于临床症状不具特异性且诊断主要依靠影像学检查,诊断往往困难且延迟。使这些患者易发生MD在其自身肠腔内肠套叠的因素包括憩室狭窄、憩室较大以及憩室相关炎症。肠梗阻在成人中是更常见的并发症,而在儿童中,出血是更常见的并发症。在我们的病例中,患者有弥漫性腹痛但无小肠梗阻,因为MD的肠套叠发生在其自身肠腔内。腹腔镜检查可能有助于确认肠套叠的存在,并显示作为套叠起点的潜在器质性病变。

结论

将MD这种罕见的病理特征与其他疾病相鉴别很重要,因为治疗是手术治疗而非药物治疗。腹部外科医生应牢记这一罕见疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f6/4430118/b23747c28404/gr1.jpg

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