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梅克尔憩室系膜连同其系带形成疝囊:一例罕见的内疝病例。

Meckel's diverticulum mesentery along with its band forming a hernial sac: A rare case of internal herniation.

作者信息

Pandove Paras K, Moudgil Ashish, Pandove Megha, Sharda Divya, Sharda Vijay K

机构信息

Department of Surgery, Rajindra Hospital/Government Medical College, Patiala 147001, Punjab, India.

Department of Surgery, Rajindra Hospital/Government Medical College, Patiala 147001, Punjab, India.

出版信息

Int J Surg Case Rep. 2015;10:17-9. doi: 10.1016/j.ijscr.2015.03.005. Epub 2015 Mar 7.

Abstract

INTRODUCTION

Meckel's diverticulum is the most common congenital gastrointestinal anomaly. However, only 2% of cases are symptomatic. It can cause intestinal obstruction by various mechanisms as volvulus, adhesions, Littre's hernia, intussusception.

CASE PRESENTATION

An unusual case of internal herniation of small bowel loops into complete hernia sac formed by unusual mesentery of Meckel's diverticulum which was present upto the adhesive band, extending from tip of the Meckel's diverticulum to the adjacent mesentery of small intestine leading to small bowel obstruction (SBO). Diverticulectomy with resection of adjacent ileum with ileo-ileal anastomosis was done.

DISCUSSION

Internal herniation by MD leading to SBO is an extremely rare complication. In literature, cases of internal hernia through mesentry of Meckel's diverticulum, through mesodiverticular band, adhesion of inflamed end of MD to corresponding base of mesentry, fibrous cord extending upto umblical wall have been reported but in our case, patient had both adhesion band along with internal herniation into sac formed by unusual mesentry of the meckel's diverticulum and the adhesion band. Preoperative diagnosis is often difficult with only 6-12% of cases diagnosed correctly. Surgical intervention is indicated for patients with intestinal obstruction or high risk of incarceration.

CONCLUSION

Meckel's diverticulum causing internal hernia is rare event. It's presentation due to herniation of bowel loops into sac formed by mesentery attached to diverticulum and the adhesion is rarest, with non specific signs and symptoms. Early diagnosis and prompt treatment prevent further complications.

摘要

引言

梅克尔憩室是最常见的先天性胃肠道异常。然而,仅有2%的病例有症状。它可通过多种机制导致肠梗阻,如肠扭转、粘连、里特疝、肠套叠。

病例介绍

一例罕见病例,小肠袢内疝进入由梅克尔憩室异常系膜形成的完整疝囊,该系膜直至粘连带,从梅克尔憩室尖端延伸至相邻小肠系膜,导致小肠梗阻(SBO)。行憩室切除术,切除相邻回肠并进行回肠-回肠吻合术。

讨论

梅克尔憩室导致的内疝引起小肠梗阻是一种极其罕见的并发症。在文献中,有通过梅克尔憩室系膜、憩室中带、梅克尔憩室炎症末端与相应系膜根部粘连、延伸至脐壁的纤维索带形成内疝的病例报道,但在我们的病例中,患者既有粘连带,又有小肠袢内疝进入由梅克尔憩室异常系膜形成的疝囊及粘连带。术前诊断通常困难,仅有6% - 12%的病例能正确诊断。对于肠梗阻或有高嵌顿风险的患者,需进行手术干预。

结论

梅克尔憩室导致内疝是罕见事件。其因肠袢疝入由附着于憩室的系膜形成的囊及粘连而出现的情况最为罕见,体征和症状不具特异性。早期诊断和及时治疗可预防进一步并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4a5/4429958/9d26d40c353d/gr1.jpg

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