Smyth R L, van Velzen D, Smyth A R, Lloyd D A, Heaf D P
Respiratory Unit, Royal Liverpool Children's Hospital, Alder Hey, UK.
Lancet. 1994 Jan 8;343(8889):85-6. doi: 10.1016/s0140-6736(94)90817-6.
We have observed five children with cystic fibrosis, who presented over 2 months, with meconium ileus equivalent that failed to respond to medical management. At surgery, four had a stricture in the ascending colon, and all had histopathological changes of post-ischaemic ulceration repair, with mucosal and submucosal fibrosis. The only common change in the management of these children was a switch from conventional enteric-coated pancreatic enzymes to high-strength products 12-15 months before presentation.
我们观察了5名患有囊性纤维化的儿童,他们在2个多月的时间里出现了类胎粪性肠梗阻,且对药物治疗无反应。手术时,4名儿童升结肠有狭窄,所有儿童均有缺血后溃疡修复的组织病理学改变,伴有黏膜和黏膜下纤维化。这些儿童治疗中唯一的共同变化是在出现症状前12 - 15个月从传统肠溶胰酶制剂改用高强度产品。