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首页> 外文期刊>Pediatric Radiology >Tracheal agenesis with tracheoesophageal fistulae: fetal MRI diagnosis with confirmation by ultrasound during an ex utero intrapartum therapy (EXIT) delivery and postdelivery MRI
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Tracheal agenesis with tracheoesophageal fistulae: fetal MRI diagnosis with confirmation by ultrasound during an ex utero intrapartum therapy (EXIT) delivery and postdelivery MRI

机译:气管食管瘘的气管发育不全:胎儿MRI诊断,在分娩前子宫内治疗(EXIT)和分娩后MRI期间通过超声确认

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摘要

Tracheal agenesis is a rare and essentially lethal anomaly with divergent prenatal imaging findings depending on the presence or absence of a tracheoesophageal fistula. All prenatally diagnosed cases of tracheal agenesis reported to date have not had a tracheoesophageal fistula and presented with thoracoabdominal findings similar to congenital high airway obstruction syndrome. We present the case of a 32-week gestation fetus with rapid onset of polyhydramnios and no persistent findings of congenital high airway obstruction syndrome that was ultimately diagnosed with tracheal agenesis plus tracheoesophageal fistula by fetal MRI. Additionally, we present the novel uses of intraoperative US during a staged ex utero intrapartum therapy delivery and postdelivery MRI, facilitated by proximity within the neonatal ICU, to confirm diagnosis and direct patient management while minimizing unnecessary investigations.
机译:气管发育不全是一种罕见的,本质上致命的异常,其产前影像学表现各不相同,具体取决于是否存在气管食管瘘。迄今报道的所有产前诊断的气管发育不全病例都没有气管食管瘘,并表现出与先天性高气道阻塞综合征相似的胸腹发现。我们介绍了一个32周妊娠胎儿的案例,该病例羊水过少迅速发作,先天性高气道阻塞综合征没有持续性发现,最终被胎儿MRI诊断为气管发育不全和气管食管瘘。此外,我们介绍了分娩前分娩前宫内分娩治疗和分娩后MRI期间术中超声的新颖用途,并通过新生儿ICU内的邻近性来促进诊断,指导患者管理,同时最大程度地减少不必要的检查。

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