2014
DOI: 10.1007/s00330-014-3444-y
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The contribution of fetal MR imaging to the assessment of oesophageal atresia

Abstract: • Challenges are to improve the prenatal diagnosis of EA and associated malformations. • fMRI is able to diagnose EA through demonstration of the pouch sign. • Tracheal bowing is a promising indirect sign of EA. • Tracheoesophageal fistula can also be suspected thanks to fMRI. • Obstetrical US, fMRI and fetal CT are complementary for assessing associated malformations.

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Cited by 38 publications
(18 citation statements)
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“…More recently, the role of fetal magnetic resonance imaging (MRI) and amniotic fluid (AF) analysis in the diagnosis of EA has been investigated as a potential tool to increase prenatal detection. Gamma‐glutamyl transpeptidase (GGTP) is an AF digestive enzyme, secreted by microvilli.…”
Section: Introductionmentioning
confidence: 99%
“…More recently, the role of fetal magnetic resonance imaging (MRI) and amniotic fluid (AF) analysis in the diagnosis of EA has been investigated as a potential tool to increase prenatal detection. Gamma‐glutamyl transpeptidase (GGTP) is an AF digestive enzyme, secreted by microvilli.…”
Section: Introductionmentioning
confidence: 99%
“…The value of ultrasound, MRI, and biochemistry of the amniotic fluid in the prenatal diagnosis of EA has already been evaluated in prenatal series, which are usually in selected population, but rarely from postnatal series . In this pragmatic study, we investigated the performance of prenatal diagnosis of EA from a postnatal cohort of infants managed in the pediatric/neonatal intensive care unit.…”
Section: Introductionmentioning
confidence: 99%
“…12,14,15 The value of ultrasound, MRI, and biochemistry of the amniotic fluid in the prenatal diagnosis of EA has already been evaluated in prenatal series, which are usually in selected population, but rarely from postnatal series. 14,16,17 In this pragmatic study, we investigated the performance of prenatal diagnosis of EA from a postnatal cohort of infants managed in the pediatric/neonatal intensive care unit. We evaluated the relevance of ultrasound in the prenatal detection of EA and of associated anomalies, and we also evaluated the performance of second-line tools such as MRI and biochemistry of the amniotic fluid.…”
Section: Introductionmentioning
confidence: 99%
“…Polyhydramnios and empty or small stomach can help to make the diagnosis of EA, but they occur only between a third and half of cases [13]. Visualisation of dilated, blind-ending, fluid filled proximal oesophagus (oesophageal pouch) is crucial [14][15][16]. Nevertheless, prenatal diagnosis of EA remains a challenge [13,17].…”
Section: Abdominal and Pelvic Abnormalitiesmentioning
confidence: 99%