Narang Raghav, Kumar Shishir, Radhakrishnan Aravindh, Giri Prakriti, Sarin Yogesh Kumar
Department of Pediatric Surgery and Pediatric Urology, BLK-MAX Superspeciality Hospital, New Delhi, India.
Oman Med J. 2024 May 30;39(3):e637. doi: 10.5001/omj.2024.19. eCollection 2024 May.
An 11-year-old girl presented with an extremely rare complication of Meckel's diverticulum. The patient presented with complaints of abdominal distension, abdominal pain, decreased appetite, and non-bilious vomiting for 20 days with a history of mass protruding per rectum. Examination revealed a distended abdomen and prolapsing bowel loops during rectal examination, resembling intussusception. Radiological findings indicated intestinal obstruction. Surgical exploration revealed Meckel's diverticulum invading the rectum, accompanied by dense inter-bowel adhesions. The patient underwent resection of Meckel's diverticulum and repair of the rectal rent. This case highlights the rarity of Meckel's diverticulum fistulating into the rectum.
一名11岁女孩出现了梅克尔憩室极其罕见的并发症。该患者主诉腹胀、腹痛、食欲减退及非胆汁性呕吐20天,有经直肠肿物脱出史。检查发现腹部膨隆,直肠指检时可触及脱垂的肠袢,类似肠套叠。影像学检查结果提示肠梗阻。手术探查发现梅克尔憩室侵犯直肠,并伴有肠管间致密粘连。患者接受了梅克尔憩室切除术及直肠裂口修补术。本病例凸显了梅克尔憩室瘘入直肠的罕见性。