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Outcome and treatment in an antenatally diagnosed congenital cystic adenomatoid malformation of the lung

โœ Scribed by Kouji Nagata; Kouji Masumoto; Risa Tesiba; Genshirou Esumi; Kiyomi Tsukimori; Wake Norio; Tomoaki Taguchi

Publisher
Springer-Verlag
Year
2009
Tongue
English
Weight
218 KB
Volume
25
Category
Article
ISSN
0179-0358

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Antenatal ultrasound diagnosis of congen
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Congenital cystic adenomatoid malformation (CCAM) of the lung is a rare pulmonary lesion, characterized by an excessive overgrowth of the terminal respiratory bronchioles.',' About 200 cases have been reported in the literature to date. The lesion is almost always unilateral3 and may occur in any lo

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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