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[与羊水过少相关的胎儿泌尿生殖系统异常]

[Fetal genitourinary abnormalities associated with oligohydramnios].

作者信息

Shimada K, Hosokawa S, Sakaue K, Kishima Y

机构信息

Division of Urology, Osaka Medical Center and Research Institute for Maternal and Child Health.

出版信息

Nihon Hinyokika Gakkai Zasshi. 1994 Jun;85(6):990-5. doi: 10.5980/jpnjurol1989.85.990.

DOI:10.5980/jpnjurol1989.85.990
PMID:8065082
Abstract

After 16 weeks of gestation, amniotic fluid mainly consisted of fetal urine. Therefore, the association of oligohydramnios with fetal urinary tract abnormalities implies severe deterioration of renal function. The relationship of the kidney and amniotic fluid in pulmonary development has been investigated, and fetuses with oligohydramnios starting in the second trimester are considered to have uniformly fatal outcomes. We analysed underlying urological disorders, gestational age at presentation, and ultimate outcomes in 45 fetuses with severe oligohydramnios, and especially focused on clinical courses and prognosis of 7 surviving patients. Clinical and/or autopsy diagnosis included bilateral renal hypodysplasia in 20 patients, urethral atresia with/without prune belly deformity in 9, posterior urethral valve in 6, polycystic kidney disease in 4, hydrometrocolpos in 2, hereditary renal dysplasia in 2, and the others. The average gestational age at detection of severe oligohydramnios was about 30 weeks, ranging from 16 weeks in patient with urethral atresia. Urological disorders of 7 surviving patients consisted of 4 posterior urethral valves, one hydrometrocolpos, one hydronephrosis of the solitary kidney, and one bilateral megaureter. In these 7 patients severe oligohydramnios striated in the third trimester. Four patients required ventilator supports together with the administration of surfactant, but they were weaned in one to 4 days. There was no evidence of pulmonary hypoplasia on chest X-ray films. Urological emergency drainage was necessary in all patients on the day of delivery to 2 days postnatally. One patient with posterior urethral valve developed ESRF 6 months after birth. Two patients have a normal serum creatinine, but another 4 have slight elevation of SCr for their age.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

妊娠16周后,羊水主要由胎儿尿液组成。因此,羊水过少与胎儿泌尿系统异常的关联意味着肾功能严重恶化。已经对肺发育过程中肾脏与羊水的关系进行了研究,妊娠中期开始出现羊水过少的胎儿被认为结局均为致命。我们分析了45例严重羊水过少胎儿的潜在泌尿系统疾病、就诊时的孕周及最终结局,尤其关注了7例存活患儿的临床病程及预后。临床和/或尸检诊断包括20例双侧肾发育不全、9例伴有或不伴有梅干腹畸形的尿道闭锁、6例后尿道瓣膜、4例多囊肾疾病、2例阴道积血、2例遗传性肾发育不全及其他情况。检测到严重羊水过少时的平均孕周约为30周,尿道闭锁患儿为16周。7例存活患儿的泌尿系统疾病包括4例后尿道瓣膜、1例阴道积血、1例孤立肾肾积水及1例双侧巨输尿管。这7例患儿在妊娠晚期出现严重羊水过少。4例患儿需要呼吸机支持并使用表面活性剂,1至4天后脱机。胸部X线片未显示肺发育不全的证据。所有患儿在分娩当天至出生后2天均需要进行泌尿系统紧急引流。1例后尿道瓣膜患儿出生6个月后出现终末期肾衰竭。2例患儿血清肌酐正常,但另外4例患儿的血清肌酐随年龄增长略有升高。(摘要截选至250字)

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