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Prenatal diagnosis of congenital cystic adenomatoid malformation using three‐dimensional inversion rendering: A case report
Author(s) -
SanzCortés Magdalena,
Raga Francisco,
BonillaMusoles Fernando
Publication year - 2008
Publication title -
journal of obstetrics and gynaecology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.597
H-Index - 50
eISSN - 1447-0756
pISSN - 1341-8076
DOI - 10.1111/j.1447-0756.2008.00897.x
Subject(s) - medicine , hydrothorax , amniocentesis , congenital cystic adenomatoid malformation , radiology , prenatal diagnosis , echogenicity , lung , polyhydramnios , ultrasound , fetus , pregnancy , obstetrics , surgery , biology , genetics , ascites
Abstract We report a case of a congenital cystic adenomatoid malformation of the lung (CCAM). At 12 weeks of gestation, an echogenic lung associated to a hydrothorax was detected. Despite the results of the combined test that informed of a high risk of chromosomopathy, normal karyotype was confirmed after an amniocentesis. The three‐dimensional ultrasound inversion mode depicted all the cysts within the fetal lungs as opaque areas that were seen concurrently together, which was compatible with CCAM. After parental counseling, the patient opted to terminate the pregnancy at 18 weeks. Pathological analysis of the lungs confirmed the diagnosis of a CCAM type II. The recent advent of the three‐dimensional ultrasound inversion mode opens many diagnostic options until now unavailable or difficult to attain sonographically and therefore it may help us to increase the sonographic detection rates of congenital cystic adenomatoid malformation.