Sasikumar K, Noonavath Ravinder Naik, Sreenath G S, Maroju Nanda Kishore
Department of Surgery, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
J Surg Tech Case Rep. 2013 Jul;5(2):103-5. doi: 10.4103/2006-8808.128752.
Meckel's diverticulum (MD) is a commonly encountered congenital anomaly of the small intestine. We report an extremely unusual case of an axially torted, gangrenous MD presenting as acute intestinal obstruction. A 26-year-old male patient presented to our emergency department with 3 days history of abdominal pain, distention and bilious vomiting. On laparotomy, there was minimal hemorrhagic fluid localized in right iliac fossa and small bowel loops were dilated. A MD was seen attached to the mesentery of nonadjacent small bowel by a peritoneal band. The diverticulum was axially torted and gangrenous. In addition, there was compression of ileum by the peritoneal band resulting in intestinal obstruction, which was relieved on dividing the band. Resection and anastomosis of the small bowel including the MD was performed. We hereby report a rare and unusual complication of a MD. Although treatment outcome is generally good, pre-operative diagnosis is often difficult.
梅克尔憩室(MD)是小肠常见的先天性异常。我们报告了一例极为罕见的病例,即轴向扭转、坏疽性梅克尔憩室表现为急性肠梗阻。一名26岁男性患者因腹痛、腹胀和胆汁性呕吐3天就诊于我院急诊科。剖腹探查时,右髂窝仅有少量出血性液体,小肠袢扩张。可见一个梅克尔憩室通过腹膜带附着于非相邻小肠的系膜上。憩室轴向扭转且已坏疽。此外,腹膜带压迫回肠导致肠梗阻,切断腹膜带后梗阻缓解。对包括梅克尔憩室在内的小肠进行了切除和吻合。我们在此报告梅克尔憩室一种罕见且不寻常的并发症。尽管治疗效果通常良好,但术前诊断往往困难。