Mooney D P, Steinthorsson G, Shorter N A
Department of Surgery, Children's Hospital at Dartmouth, Lebanon, NH, USA.
J Pediatr Surg. 1996 May;31(5):695-7. doi: 10.1016/s0022-3468(96)90676-4.
Intussusception is common in infants aged 5 to 18 months, but there have been only 12 reports of its occurrence among premature infants. Nine of these previously reported cases with adequate data and one new case are reviewed. Many of the infants were believed to have necrotizing enterocolitis, leading to an average 12-day interval between the onset of signs and the operation. Bilious emesis or nasogastric contents, bloody stool, and intestinal dilation without pneumatosis intestinalis were common. A contrast enema showed the intussusception in only 1 of 7 cases. Most cases were diagnosed in the operating room and underwent successful primary anastomosis, with no recurrences. A pathological lead point was identified in 2 of the 10 cases. The overall mortality rate was 23%; the one death since 1970 was secondary to attempted hydrostatic reduction. These cases may represent what, in the absence of premature delivery, would have been the intrauterine development of intussusception likely leading to small bowel atresia.
肠套叠在5至18个月大的婴儿中很常见,但早产儿发生肠套叠的报告仅有12例。本文回顾了其中9例既往报告且资料充分的病例以及1例新病例。许多婴儿被认为患有坏死性小肠结肠炎,导致从症状出现到手术的平均间隔时间为12天。胆汁性呕吐或鼻胃管引流物、血便以及无肠壁积气的肠扩张很常见。在7例病例中,仅1例经对比灌肠显示为肠套叠。大多数病例在手术室确诊并成功进行了一期吻合,无复发。10例病例中有2例发现了病理性起始点。总死亡率为23%;自1970年以来的1例死亡是由于尝试水压复位所致。这些病例可能代表了在没有早产的情况下,肠套叠可能在子宫内发展,进而可能导致小肠闭锁。