TY - JOUR
T1 - Congenital cystic adenomatoid malformation of the lung
T2 - Prenatal management and prognosis
AU - Revillon, Y.
AU - Jan, D.
AU - Plattner, V.
AU - Sonigo, P.
AU - Dommergues, M.
AU - Mandelbrot, L.
AU - Dumez, Y.
AU - Nihoul-Fékété, C.
PY - 1993/8
Y1 - 1993/8
N2 - Thirty-two cases of congenital cystic adenomatoid malformation of the lung diagnosed antenatally are reported. Antenatal diagnosis has made it possible to document the progress of the condition in utero and the postnatal prognosis. It has been possible to advise on termination and intrauterine intervention, to counsel the parents, and to plan arrangements for delivery and postnatal care among obstetricians, neonatologists, and pediatric surgeons. According to Stocker's classification there were 12 cases of type I, 15 of type II, and 5 of type III. Five pregnancies were terminated. Antenatal drainage of a cyst was performed in four patients with two survivors. Thirteen babies showed relative regression of the cyst as pregnancy progressed. After delivery the extent of the cystic malformation was assessed by chest x-rays and computed tomography scanning in 25 and angiography in 6. Treatment consisted of observation in 4, embolization in 2, operation as an emergency in 3, and electively around 4 months in 15.
AB - Thirty-two cases of congenital cystic adenomatoid malformation of the lung diagnosed antenatally are reported. Antenatal diagnosis has made it possible to document the progress of the condition in utero and the postnatal prognosis. It has been possible to advise on termination and intrauterine intervention, to counsel the parents, and to plan arrangements for delivery and postnatal care among obstetricians, neonatologists, and pediatric surgeons. According to Stocker's classification there were 12 cases of type I, 15 of type II, and 5 of type III. Five pregnancies were terminated. Antenatal drainage of a cyst was performed in four patients with two survivors. Thirteen babies showed relative regression of the cyst as pregnancy progressed. After delivery the extent of the cystic malformation was assessed by chest x-rays and computed tomography scanning in 25 and angiography in 6. Treatment consisted of observation in 4, embolization in 2, operation as an emergency in 3, and electively around 4 months in 15.
KW - Congenital cystic adenomatoid malformation
KW - antenatal diagnosis
KW - lung
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U2 - 10.1016/0022-3468(93)90504-E
DO - 10.1016/0022-3468(93)90504-E
M3 - Article
C2 - 8229585
AN - SCOPUS:0027259481
SN - 0022-3468
VL - 28
SP - 1009
EP - 1011
JO - Journal of Pediatric Surgery
JF - Journal of Pediatric Surgery
IS - 8
ER -