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家族性先天幽门闭锁是罕见的胎儿胃肠道畸形,由于患病胎儿不能消化吸收吞下的羊水,超声检查常见到母体羊水过多和胎儿胃扩张,近来文献报告近150例。作者对-29岁孕妇进行观察,此次是第3次妊娠,孕33周时超声扫描观察到羊水过多。该孕妇第一次妊娠在34周时早产,娩出一男婴,生后第一天诊断为幽门闭锁,紧急剖腹实施胃十二指肠吻合术。第二次妊娠在42周时娩出一健康女婴。本次妊娠33周时,物理检查表明子宫底在耻骨联合上38
Familial congenital pyloric atresia is a rare fetal gastrointestinal deformity, due to diseased fetus can not digest and absorb swallowing amniotic fluid, ultrasound is common to the mother of polyhydramnios and fetal stomach expansion, the recent reports of nearly 150 cases. The author of -29-year-old pregnant women were observed, this is the third pregnancy, 33 weeks pregnant ultrasound scans observed when polyhydramnios. The first pregnancy of pregnant women at 34 weeks of preterm delivery, delivered a baby boy, the first day after birth diagnosis of pyloric atresia, emergency laparotomy gastroduodenal anastomosis. The second pregnancy delivered a healthy baby girl at 42 weeks. At 33 weeks of gestation, a physical examination showed the end of the uterus in the pubic symphysis