Meconium peritonitis in utero

被引:50
作者
Kamata, S [1 ]
Nose, K [1 ]
Ishikawa, S [1 ]
Usui, N [1 ]
Sawai, T [1 ]
Kitayama, Y [1 ]
Okuyama, H [1 ]
Imura, K [1 ]
Okada, A [1 ]
机构
[1] Osaka Univ, Sch Med, Dept Pediat Surg, Osaka 5650871, Japan
关键词
prenatal diagnosis; meconium peritonitis; meconium ascites; intestinal atresia; fetal ultrasound;
D O I
10.1007/s003830000354
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
To clarify the relationship between clinical features in utero and postnatal prognosis, 20 fetuses who underwent ultrasonic (US) evaluation for meconium peritonitis (MP) over a 17-year period were reviewed. According to final US findings in utero, patients were classified into three types. Type I (massive meconium ascites) was noted is 5 cases, type II (giant pseudocyst) in 4, and the other 11 were classified as type III (calcification and/or small pseudocyst). Abdominal calcifications were identified in only 5 cases (2 type I, 1 type II, 2 type III). Seven fetuses who had associated polyhydramnios (1 Type I, 1 Type II, 2 Type III) and fetal hydrops (3 Type II) were delivered before 36 weeks' gestation. Cardiopulmonary resuscitation at birth was required in 9 cases (5 type I, 4 type II) who underwent abdominal drainage before delivery and/or immediately after birth. Although dilatation of the intestine was identified in 10 fetuses (2 type II, 8 Type III), is had intestinal atresia and 2 had fecal obstruction of the distal ileum. Four infants (2 type I, 1 type II, 1 type III) died of respiratory failure and postoperative complications. These results indicated that careful fetal US may be useful for perinatal management of MP.
引用
收藏
页码:377 / 379
页数:3
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