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首页> 外文期刊>Prenatal Diagnosis >Fetal enterolithiasis: prenatal sonographic and MRI diagnosis in two cases of urorectal septum malformation (URSM) sequence.
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Fetal enterolithiasis: prenatal sonographic and MRI diagnosis in two cases of urorectal septum malformation (URSM) sequence.

机译:胎儿肠结石:产前超声检查和MRI诊断2例尿直肠中隔畸形(URSM)序列。

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摘要

OBJECTIVES: Enterolithiasis (multiple calcifications of intraluminal meconium) is a rare, prenatal ultrasonographic finding. In this study, our aim was to evaluate the prenatal diagnostic features and discuss the management of the patients. METHODS: The data of two cases of prenatally diagnosed fetal enterolithiasis were collected from ultrasound scan, magnetic resonance imaging (MRI) and neonatal or postnatal autopsy records. The findings were evaluated in both prenatal and postnatal periods. Chromosomal analysis was performed in one case. An evaluation of primary and secondary malformations was done. Coexisting anomalies were searched for via radiology, neonatal surgery and histopathology. RESULTS: Malformations in two cases (both males) with partial and complete urorectal septum malformation (URSM) sequence were described. The absence of an anal opening and presence of a fistula between the urinary and gastrointestinal tract were common findings. These features were considered as primary malformations contributing to the formation of enterolithiasis. Secondary anomalies (urinary and gastrointestinal system malformations, pulmonary hypoplasia, genital and other coexisting anomalies) were evaluated. CONCLUSIONS: The prenatal detection of enterolithiasis carries a poor prognosis. Most of the previously reported cases were invariably associated with major fetal malformations of the urinary and gastrointestinal tract. It is a warning sign for large bowel obstruction with or without enterourinary fistula. Therefore, adequate gastrointestinal and urologic studies must be undertaken after birth for the final diagnosis. There is a high mortality rate in the reported cases, mostly attributed to associated anomalies, and all survivors required neonatal surgery. It is important to differentiate the partial from the full URSM sequence because the prognosis in the partial URSM sequence is generally good, with long-term survival being common.
机译:目的:肠结石症(腔内胎粪多钙化)是一种罕见的产前超声检查结果。在这项研究中,我们的目的是评估产前诊断特征并讨论患者的治疗。方法:从超声扫描,磁共振成像(MRI)以及新生儿或产后尸检记录中收集两例产前诊断为胎儿小石症的数据。在产前和产后均对结果进行了评估。在一例中进行了染色体分析。对原发和继发畸形进行了评估。通过放射学,新生儿手术和组织病理学检查并存的异常情况。结果:描述了两例(均为男性)的畸形,部分和完整的尿直肠隔隔膜畸形(URSM)序列。常见的发现是没有肛门开口以及在泌尿道和胃肠道之间存在瘘管。这些特征被认为是导致肠结石形成的主要畸形。评估了继发性异常(泌尿系统和胃肠系统畸形,肺发育不全,生殖器和其他并存异常)。结论:产前检测到的小石症预后较差。先前报道的大多数病例始终与胎儿的主要泌尿道和胃肠道畸形有关。对于有或没有肠瘘的大肠梗阻,这是一个警告信号。因此,出生后必须进行充分的胃肠道和泌尿科检查,以进行最终诊断。在报告的病例中,死亡率很高,主要归因于相关的异常情况,所有幸存者都需要进行新生儿手术。重要的是要区分部分URSM序列和全部URSM序列,因为部分URSM序列的预后通常很好,长期生存很普遍。

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