Cystic adenomatoid malformation of the lung: Prenatal diagnosis, prognostic factors and fetal outcome

Citation
T. Golaszewski et al., Cystic adenomatoid malformation of the lung: Prenatal diagnosis, prognostic factors and fetal outcome, GYNECOL OBS, 46(4), 1998, pp. 241-246
Citations number
20
Categorie Soggetti
da verificare
Journal title
GYNECOLOGIC AND OBSTETRIC INVESTIGATION
ISSN journal
03787346 → ACNP
Volume
46
Issue
4
Year of publication
1998
Pages
241 - 246
Database
ISI
SICI code
0378-7346(1998)46:4<241:CAMOTL>2.0.ZU;2-R
Abstract
Aim: To evaluate 14 cases of cystic adenomatoid malformation (CAM) of the l ung with regard to antenatal management and fetal outcome. Results: Intraut erine shunts were placed in 3 fetuses to avoid pulmonary hypoplasia.-Prenat al sonography showed that the lesions had a tendency to resolve in 4 cases. Of the 9 infants who survived, 5 were treated surgically (lobectomy), Conc lusions: The antenatal evolution of these lesions is highly variable; the l esions may even resolve spontaneously, therefore the diagnosis of CAM types II and III should be followed by a period of observation. Intrauterine dra inage is recommended in cases of CAM type I if unfavorable prognostic facto rs are encountered.