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梗阻性或非梗阻性巨膀胱:产前难题。

Obstructive or non-obstructive megacystis: a prenatal dilemma.

作者信息

Mandaletti Martina, Cerchia Elisa, Ruggiero Elena, Teruzzi Elisabetta, Bastonero Simona, Pertusio Annasilvia, Della Corte Marcello, Sciarrone Andrea, Gerocarni Nappo Simona

机构信息

Pediatric Urology Unit, Department of Public Health and Pediatric Sciences, Regina Margherita Children's Hospital, Turin, Italy.

Division of Urology, Department of Oncology, School of Medicine, San Luigi Gonzaga Hospital, University of Turin, Orbassano, Italy.

出版信息

Front Pediatr. 2024 Jul 2;12:1379267. doi: 10.3389/fped.2024.1379267. eCollection 2024.

Abstract

INTRODUCTION

Diagnosis of prenatal megacystis has a significant impact on the pregnancy, as it can have severe adverse effects on fetal and neonatal survival and renal and pulmonary function. The study aims to investigate the natural history of fetal megacystis, to try to differentiate congenital lower urinary tract obstruction (LUTO) from non-obstructive megacystis, and, possibly, to predict postnatal outcome.

MATERIALS AND METHODS

A retrospective single-center observational study was conducted from July 2015 to November 2023. The inclusion criteria were a longitudinal bladder diameter (LBD) >7 mm in the first trimester or an overdistended/thickened-walled bladder failing to empty in the second and third trimesters. Close ultrasound follow-up, multidisciplinary prenatal counseling, and invasive and non-invasive genetic tests were offered. Informed consent for fetal autopsy was obtained in cases of termination of pregnancy or intrauterine fetal demise (IUFD). Following birth, neonates were followed up at the same center. Patients were stratified based on diagnosis: LUTO (G1), urogenital anomalies other than LUTO ("non-LUTO") (G2), and normal urinary tract (G3).

RESULTS

This study included 27 fetuses, of whom 26 were males. Megacystis was diagnosed during the second and third trimesters in 92% of the fetuses. Of the 27 fetuses, 3 (11.1%) underwent an abortion, and 1 had IUFD. Twenty-three newborns were live births (85%) at a mean gestational age (GA) of 34 ± 2 weeks. Two patients (neonates) died postnatally due to severe associated malformations. Several prenatal parameters were evaluated to differentiate patients with LUTO from those with non-LUTO, including the severity of upper tract dilatation, keyhole sign, oligohydramnios, LBD, and GA at diagnosis. However, none proved predictive of the postnatal diagnosis. Similarly, none of the prenatal parameters evaluated were predictive of postnatal renal function.

DISCUSSION

The diagnosis of megacystis in the second and third trimesters was associated with live births in up to 85% of cases, with LUTO identified as the main cause of fetal megacystis. This potentially more favorable outcome, compared to the majority reported in literature, should be taken into account in prenatal counseling. Megacystis is an often misinterpreted antennal sign that may hide a wide range of diagnoses with different prognoses, beyond an increased risk of adverse renal and respiratory outcomes.

摘要

引言

产前巨膀胱的诊断对妊娠有重大影响,因为它可能对胎儿和新生儿的存活以及肾脏和肺功能产生严重不利影响。本研究旨在调查胎儿巨膀胱的自然病史,试图区分先天性下尿路梗阻(LUTO)与非梗阻性巨膀胱,并可能预测出生后的结局。

材料与方法

2015年7月至2023年11月进行了一项回顾性单中心观察性研究。纳入标准为孕早期纵向膀胱直径(LBD)>7 mm,或孕中期和晚期膀胱过度扩张/壁增厚且不能排空。提供密切的超声随访、多学科产前咨询以及侵入性和非侵入性基因检测。对于终止妊娠或宫内胎儿死亡(IUFD)的病例,获得了胎儿尸检的知情同意书。出生后,在同一中心对新生儿进行随访。根据诊断对患者进行分层:LUTO(G1)、LUTO以外的泌尿生殖系统异常(“非LUTO”)(G2)和正常尿路(G3)。

结果

本研究纳入了27例胎儿,其中26例为男性。92%的胎儿在孕中期和晚期被诊断为巨膀胱。27例胎儿中,3例(11.1%)流产,1例发生IUFD。23例新生儿为活产(85%),平均胎龄(GA)为34±2周。2例患者(新生儿)因严重的相关畸形在出生后死亡。评估了几个产前参数以区分LUTO患者和非LUTO患者,包括上尿路扩张的严重程度、钥匙孔征、羊水过少、LBD以及诊断时的GA。然而,没有一个参数能预测出生后的诊断。同样,评估的产前参数中没有一个能预测出生后的肾功能。

讨论

孕中期和晚期巨膀胱的诊断与高达85%的活产相关,LUTO被确定为胎儿巨膀胱的主要原因。在产前咨询中应考虑到这一与文献中大多数报道相比可能更有利的结果。巨膀胱是一种经常被误解的产前体征,除了肾脏和呼吸不良结局风险增加外,它可能隐藏着一系列预后不同的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f09/11249744/158168fa686b/fped-12-1379267-g001.jpg

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