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Congenital cystic adenomatoid malformation of the lung with prolonged marked lung compression and neonatal survival

โœ Scribed by David M. Sherer; Jerome N. Kopelman; James S. Rawlings; Jerome E. Degnan; Robert T. Schaller

Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
521 KB
Volume
22
Category
Article
ISSN
0091-2751

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โœฆ Synopsis

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 prognostic We present a case in which despite the presence of prolonged, marked, bilateral lung compression due to congenital cystic malformation of the left lung and displacement of the heart throughout gestation,

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Antenatal ultrasound diagnosis of congen
Antenatal ultrasound diagnosis of congenital cystic adenomatoid malformation of the lung: Spontaneous resolution in utero
โœ Reuven Mashiach; Moshe Hod; Shmuel Friedman; Alex Schoenfeld; Jardena Ovadia; Pa ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 506 KB

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