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妊娠前半期合并巨大膀胱胎儿的围产期结局

Perinatal outcome in fetuses with megacystis in the first half of pregnancy.

作者信息

Jouannic Jean-Marie, Hyett Jon A, Pandya Pranav P, Gulbis Béatrice, Rodeck Charles H, Jauniaux Eric

机构信息

Academic Department of Obstetrics and Gynaecology, University College London, London, UK.

出版信息

Prenat Diagn. 2003 Apr;23(4):340-4. doi: 10.1002/pd.593.

Abstract

OBJECTIVE

To present the outcome of a consecutive series of 19 fetuses referred to our center for megacystis in the first half of the pregnancy.

STUDY DESIGN

Retrospective analysis.

METHODS

19 cases of early fetal megacystis were reviewed. Inclusion criteria were the visualization of an enlarged bladder with a maximum longitudinal diameter >10 mm and a gestational age of no more than 19 weeks.

RESULTS

The median gestational age at diagnosis was 16 weeks (range 12-19 weeks). The median maximum longitudinal diameter of the fetal bladder at the time of diagnosis was 21 mm (range 11-35 mm). The fetal megacystis was associated with another extra renal anomaly in six cases (30%). There was no fetus with abnormal karyotype. Termination of pregnancy was performed in 11 cases because of the severity of the renal disease. One spontaneous intrauterine death occurred. A vesicoamniotic shunt was inserted in three cases, two of which died in utero. The surviving fetus that was shunted died in the neonatal period from acute renal failure. In the remaining four fetuses, resolution of the megacystis occurred spontaneously (n = 2) or following serial single-needle aspiration (n = 2). One of these had renal insufficiency requiring kidney transplantation.

CONCLUSION

The outcome of fetuses with early obstructive uropathy is poor, with or without in utero therapy. Pathophysiology, clinical presentation and outcome of fetuses with early uropathy may differ from those previously described in the latter part of pregnancy.

摘要

目的

介绍妊娠前半期因巨大膀胱转诊至本中心的连续19例胎儿的结局。

研究设计

回顾性分析。

方法

回顾19例早期胎儿巨大膀胱病例。纳入标准为超声显示膀胱增大,最大前后径>10 mm且孕周不超过19周。

结果

诊断时的中位孕周为16周(范围12 - 19周)。诊断时胎儿膀胱的中位最大前后径为21 mm(范围11 - 35 mm)。6例(30%)胎儿巨大膀胱合并其他肾外异常。无胎儿染色体核型异常。11例因肾病严重行引产。1例发生自然宫内死亡。3例行羊膜腔分流术,其中2例宫内死亡。分流术后存活的胎儿新生儿期死于急性肾衰竭。其余4例胎儿中,2例巨大膀胱自发消退,2例经系列单针穿刺后消退。其中1例有肾功能不全需肾移植。

结论

早期梗阻性肾病胎儿的结局不佳,无论是否接受宫内治疗。早期肾病胎儿的病理生理、临床表现和结局可能与先前报道的妊娠后半期不同。

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