P14.08: First trimester prenatal diagnosis of congenital cystic adenomatoid malformation of the lung
β Scribed by N. Jastrow; E. Antonelli; P. Extermann; O. Irion; Y. Vial
- Book ID
- 112223064
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 38 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0960-7692
- DOI
- 10.1002/uog.1608
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Congenital cystic adenomatoid malformation (CCAM) of the lung is a rare benign disorder. Three types have been distinguished: cystic, intermediate, and solid,' or types I, 11, and 111, respectively.2 Type I11 lesions are the rarest; we found only six case^^-^ in an extensive review of the English li
Bilateral cystic adenomatoid malformation of the lung (CAML), solid type (Stocker 111), is a rare malformation that we observed sonographically in two fetuses at 23 weeks. The ultrasonic image showed an echogenic mass compressing the heart and occupying the whole thoracic cavity. Massive ascites, pr