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- W2897524507 abstract "To evaluate agreement between prenatal and postnatal diagnosis of congenital lung malformations (CLM). We included all liveborn patients with a prenatal ultrasound diagnosis of congenital pulmonary airway malformation (CPAM), bronchopulmonary sequestration (BPS) and/or bronchogenic cysts (BC) between 2000 and 2015. The postnatal diagnosis, including congenital lobar emphysema (CLE), was made using computed tomography (CT) and/or histology. The 112 patients were prenatally diagnosed at (mean±SD) 21.6±3.4 weeks' gestation and born at 39.2±1.6 weeks. We excluded 17 patients: 10 did not receive postnatal CT imaging or histology examination and in 7 patients CT did not show any CLM. In 95 remaining patients, postnatal diagnosis was made by CT in 66 (69%) and by histology following surgical resection in 29 (31%). Correct diagnoses were made in 72/95 (76%). In 50 of these, prenatal diagnoses were completely confirmed and in 22 partially, i.e. hybrid or inconclusive diagnosis (table). The level of agreement between prenatal and postnatal diagnosis is suboptimal. Postnatal CT imaging should therefore be performed in every child with prenatally diagnosed CLM. Supporting information can be found in the online version of this abstract Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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- W2897524507 date "2018-10-01" @default.
- W2897524507 modified "2023-10-18" @default.
- W2897524507 title "P02.10: Congenital lung malformations: suboptimal agreement between prenatal and postnatal diagnosis" @default.
- W2897524507 doi "https://doi.org/10.1002/uog.19634" @default.
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