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- W2055141017 abstract "The aim of this study was to describe the natural history and outcomes of fetal congenital cystic adenomatoid malformation (CCAM) of the lung in three antenatally diagnosed cases. Five women whose fetuses had CCAM of the lung between 2006 and 2010 chose to continue their pregnancies. We followed up these fetuses and observed whether there were CCAM-related complications, such as polyhydramnios, mediastinal shifting, and even hydrops fetalis. We also used three-dimensional ultrasound to calculate CCAM volume serially until delivery. At presentation, the five cases of fetal CCAM were all unilateral and were not accompanied by any complications. One of Five cases was lost in follow up. Serial ultrasound of the other four cases demonstrated a trend toward a decreasing CCAM size. Complete resolution was noted in two cases by antenatal sonography. But, persistent lung lesions were found by postnatal computed tomography scans. In one of four cases, postnatal chest radiography showed no abnormality and computed tomography scan was not performed. In the other three cases, postnatal computed tomography scans confirmed persistent lung lesions. The outcomes of the prenatally detected CCAMs were good in our cases. If the CCAM is not accompanied by complications, maintaining the pregnancy with continuing management seems to be a reasonable recommendation. Despite antenatal resolution of CCAM on ultrasound, postnatal examination with chest radiography and computed tomography scan is necessary." @default.
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- W2055141017 date "2011-09-14" @default.
- W2055141017 modified "2023-10-14" @default.
- W2055141017 title "P14.14: Prenatal diagnosis of congenital cystic adenomatoid malformations: evolution and outcome, 5 case reports" @default.
- W2055141017 doi "https://doi.org/10.1002/uog.9792" @default.
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