Axt R, Quijano F, Boos R, Hendrik H J, Jessberger H J, Schwaiger C, Schmidt W
Department of Obstetrics and Gynecology, University of Homburg/Saar, Germany.
Eur J Obstet Gynecol Reprod Biol. 1999 Nov;87(1):47-54. doi: 10.1016/s0301-2115(99)00078-0.
The article presents a retrospective analysis (1989-1997) of the prenatal diagnosis, the course and completion of pregnancy of 26 fetuses with omphalocele and 18 fetuses with gastroschisis.
44 pregnancies with anterior fetal wall defect diagnosed by prenatal ultrasound, clinical or patho-anatomic examination between 1989 and 1997 at the Department of Obstetrics and Gynecology, University of Homburg/Saar.
In 40 of 44 pregnancies (91%) the fetal ventral abdominal wall defect could be detected antenatally with ultrasound. Associated malformations in fetuses with omphalocele were seen in 18 cases (69%), whereas only five fetuses with gastroschisis (28%) had an associated malformation. Nineteen of 26 fetuses (73%) with omphalocele had a normal karyotype. Seven of 26 fetuses (27%) with omphalocele had an abnormal karyotype. Eleven fetuses with omphalocele were live born, three of them with minor anomalies. Ten babies with omphalocele survived. No chromosomal anomalies were detected in fetuses with gastroschisis. There were four gastrointestinal malformations and one lethal associated malformation in fetuses with gastroschisis. There were 15 live born babies with gastroschisis, all of whom have survived. In 20 of 44 cases (45%) with ventral abdominal wall defect oligohydramnios could be detected by ultrasound. In 28 of 44 cases (64%) we found fetal growth retardation <10th percentile for gestational age.
In case of a fetal ventral abdominal wall defect, the detection and appropriate classification of associated fetal anomalies is of great importance for the further course of pregnancy. Fetal karyotyping should be offered in case of a fetal abdominal wall defect. Early and close prenatal consultation of the neonatologist and the pediatric surgeon will favorably influence the perinatal outcome.
本文对1989年至1997年间26例腹裂胎儿和18例脐膨出胎儿的产前诊断、妊娠过程及结局进行回顾性分析。
1989年至1997年间在洪堡/萨尔大学妇产科经产前超声、临床或病理解剖检查诊断为胎儿前腹壁缺损的44例妊娠。
44例妊娠中有40例(91%)可通过超声产前检测出胎儿腹前壁缺损。脐膨出胎儿中有18例(69%)伴有其他畸形,而腹裂胎儿中只有5例(28%)伴有其他畸形。26例脐膨出胎儿中有19例(73%)核型正常。26例脐膨出胎儿中有7例(27%)核型异常。11例脐膨出胎儿存活出生,其中3例有轻微异常。10例脐膨出婴儿存活。腹裂胎儿未检测到染色体异常。腹裂胎儿中有4例胃肠道畸形和1例致死性相关畸形。15例腹裂婴儿存活出生,均存活。44例腹前壁缺损病例中有20例(45%)可通过超声检测出羊水过少。44例病例中有28例(64%)发现胎儿生长受限,低于孕周的第10百分位数。
对于胎儿腹前壁缺损,检测并正确分类相关胎儿异常对妊娠的进一步发展至关重要。胎儿腹壁缺损时应进行胎儿核型分析。新生儿科医生和小儿外科医生尽早并密切的产前会诊将对围产期结局产生有利影响。