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Protocol and Guidelines for Point-of-Care Lung Ultrasound in Diagnosing Neonatal Pulmonary Diseases Based on International Expert Consensus
Published on: March 6, 2019
First Trimester Echogenic Lung Lesions: A Diagnostic Challenge and Review of Differential Diagnoses
Chameli Subbaraj1, Mustafa Guma2
1Obstetrics and Gynaecology, Basildon University Hospital, Basildon, GBR.
Foetal echogenic lungs are characterised by the appearance of small bright spots within the foetal lungs observed via antenatal ultrasound, which may indicate underlying developmental abnormalities. The presence of echogenic lungs is a rare sonographic finding identified during the first trimester of pregnancy. In this report, we present the case of a healthy 25-year-old primigravida who was found to have multiple foetal abnormalities in her routine first-trimester scan, following which she was scanned by the foetal medicine team, who confirmed the finding of foetal echogenic lungs along with cystic hygroma and hydrops foetalis. Turner's syndrome was confirmed with successive invasive tests, and the pregnancy was terminated at 14 weeks. Our findings not only contribute to the limited data on this rare sonographic occurrence but also highlight the importance of vigilant foetal monitoring in cases of echogenic lungs, allowing for timely intervention and management strategies. This case strongly supports the need for further research into the implications of echogenic lung findings and their association with chromosomal abnormalities.
Foetal echogenic lungs are characterised by the appearance of small bright spots within the foetal lungs observed via antenatal ultrasound, which may indicate underlying developmental abnormalities. The presence of echogenic lungs is a rare sonographic finding identified during the first trimester of pregnancy. In this report, we present the case of a healthy 25-year-old primigravida who was found to have multiple foetal abnormalities in her routine first-trimester scan, following which she was scanned by the foetal medicine team, who confirmed the finding of foetal echogenic lungs along with cystic hygroma and hydrops foetalis. Turner's syndrome was confirmed with successive invasive tests, and the pregnancy was terminated at 14 weeks. Our findings not only contribute to the limited data on this rare sonographic occurrence but also highlight the importance of vigilant foetal monitoring in cases of echogenic lungs, allowing for timely intervention and management strategies. This case strongly supports the need for further research into the implications of echogenic lung findings and their association with chromosomal abnormalities.
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