J Korean Radiol Soc.  1987 Aug;23(4):653-657. 10.3348/jkrs.1987.23.4.653.

A case report of congenital cystic adenomatoid malformation

• Jun SA
• Cha KS
• Chi JG

• KMID: 2359436
• DOI: http://doi.org/10.3348/jkrs.1987.23.4.653

Abstract

Congenital cystic adnomatoid malformation(CCAM) is rare pulmonary cystic disease, CCAM has been detected on prematurity, stillborn and respiratory distress infant or child by chest X-ray film and CT scan. One case of CCAM diagnosed in utero at gestational age 22 weeks is reported with sonographic findings and autopsy findings. Ultrasonographic findings are large cystic lesions in fetal thorax and fetal hydrops without hydramnios. The survival of these infants is very poor despite accurate prenatal diagnosis and maximal postnatal care.

MeSH Terms

Autopsy
Child
Cystic Adenomatoid Malformation of Lung, Congenital*
Gestational Age
Humans
Hydrops Fetalis
Infant
Polyhydramnios
Postnatal Care
Prenatal Diagnosis
Thorax
Tomography, X-Ray Computed
Ultrasonography
X-Ray Film