子宫内尿路异常的保守处理。

Fetal therapy Pub Date : 1989-01-01 DOI:10.1159/000263389
R Chierici, G Riccipetitoni, L Tamisari, F Vesce, B Zanella, L Merlo, V Vigi
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引用次数: 5

摘要

在5年的时间里,我们观察了48例通过产前超声诊断为泌尿系统畸形的胎儿。产前超声检查证实48例胎儿中有44例(91%)存在尿路异常。48例中有35例(73%)产前诊断准确。9例胎儿肾脏疾病检出,但其具体性质与产前诊断不符。在我们的研究中,最常见的异常是继发于肾盂输尿管连接处阻塞的肾积水。44例患者中有31例(70.4%)出现这种情况;7例出现梗阻性的新生儿进行早期手术修复,其余24例和1个肾单元进行早期手术修复,并定期进行临床和实验室控制。12例患者自行康复;10例患者的扩张保持不变,而3例患者的病情逐渐恶化,导致手术矫正。我们的研究结果与最近的报道一致,认为早期不加区分的手术修复几乎没有支持。此外,我们的经验证实了新生儿肾积水自发恢复的可能性,并提请注意对适当选择的患者进行保守治疗的益处。
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Conservative management of urinary abnormalities detected in utero.
During a 5-year period, we observed 48 fetuses with urinary malformations diagnosed by antenatal sonography. Postnatal investigations confirmed the presence of a urinary tract anomaly in 44 of the 48 fetuses selected by prenatal ultrasound (91%). Accurate antenatal diagnosis was made in 35 of the 48 cases (73%). In 9 fetuses renal disease was detected, but its specific nature was not in accordance with the prenatal diagnosis. In our series the most common anomaly was hydronephrosis secondary to ureteropelvic junction obstruction. This condition was observed in 31 of the 44 patients (70.4%); 7 of the newborns who showed an obstructive pattern were submitted to early surgical repair, while the remaining 24 cases and 1 renal unit of the group undergoing early surgical repair were relegated to expectant observation, with periodic clinical and laboratory controls. A spontaneous recovery was observed in 12 cases; the dilatation remained unchanged in 10 cases, while 3 patients showed a progressive worsening of the condition which led to a surgical correction. Our findings agree with those in recent reports in providing little support for early, indiscriminate surgical repair. Moreover, our experience confirms the possibility of a spontaneous recovery in newborns with hydronephrosis and draws attention to the benefit of a conservative management in properly selected patients.
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