Cystic adenomatoid malformation of the lung: clinical evolution and management
β Scribed by P. Bagolan; A. Nahom; C. Giorlandino; A. Trucchi; E. Bilancioni; A. Inserra; G. Gambuzza; V. Spina
- Publisher
- Springer
- Year
- 1999
- Tongue
- English
- Weight
- 71 KB
- Volume
- 158
- Category
- Article
- ISSN
- 0340-6997
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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
Neonatal survival of fetuses with space-occupying thoracic lesions is dependent upon the basic underlying disease, extent of involvement, and the presence or absence of other associated prenatal findings such as fetal hydrops, polyhydramnios, or displacement of the fetal heart, all accepted poor pro