梅克尔憩室(Meckel’s diverticulum)是一种先天性消化道畸形,发生率约1%~3%,男女比例约为3∶1,绝大多数终生无症状,只是在腹部手术或尸解时偶然发现,少部分可引起多种并发症。文献报道发生并发症者占15%~30%,并发症可发生于任何年龄,10岁以前占半数,合并症中以小肠梗阻(30%),急性消化道出血(40%)和急性憩室炎(20%)为主。最近我们在临床工作中遇到1例新生儿期发病且并发穿孔的患儿,现报道如下:1临床资料女孩,主因胎龄35+4周,生后1小时入院。患儿其母患妊高症,行剖宫产,生后无窒息,羊水无污染,wt2.3kg,为观察治疗转入我科。查体:,次/,次/、血氧饱和度,早产儿貌,胎脂 Meckel’s diverticulum is a congenital gastrointestinal deformity that occurs in about 1% to 3% of men and women with a ratio of about 3: 1, most of whom are lifelong asymptomatic, only occasionally in abdominal surgery or autopsy Found that a small part can cause a variety of complications. Complications reported in the literature accounted for 15% to 30%, complications can occur at any age, before the age of 10 accounted for half of the complications of small bowel obstruction (30%), acute gastrointestinal bleeding (40%) and acute diverticulitis (20%) based. Recently, we encountered in clinical work of a neonatal morbidity and complicated with perforation of the children, are reported as follows: 1 clinical data of the girls, mainly due to gestational age 35 +4 weeks after birth 1 hour admitted to hospital. Children with her mother suffering from pregnancy-induced hypertension, cesarean section, postnatal asphyxia, amniotic fluid pollution, wt2.3kg, for observation and treatment into our department. Physical examination :, times /, times /, oxygen saturation, appearance of premature children, fetal fat