Abstract
Objective
Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention.
Methods and design
Case report and literature review.
Setting
We report on the ultrasound and pathological findings of a hydropic fetus due to a CCAM Type II at 22 weeks of gestation.
Conclusions
Congenital cystic adenomatoid malformation is a rare fetal lung disease with an excellent prognosis in the absence of fetal hydrops. CCAM associated with fetal hydrops carries a grave prognosis but survival rates of 70% can be achieved by thoraco-amniotic drainage in those with macrocystic lesions.
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We thank Professor Falko Fend for critical reading of the manuscript.
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S. Schott, G. Meyberg-Solomayer, and K. O. Kagan have contributed equally to the senior authorship.
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Schott, S., Mackensen-Haen, S., Wallwiener, M. et al. Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature. Arch Gynecol Obstet 280, 293–296 (2009). https://doi.org/10.1007/s00404-008-0880-4
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DOI: https://doi.org/10.1007/s00404-008-0880-4