OC180: Pregnancy neonatal outcome of antenatally diagnosed cystic adenomatoid malformation of the lung
نویسندگان
چکیده
منابع مشابه
Management and outcome of antenatally diagnosed congenital cystic adenomatoid malformation of the lung.
OBJECTIVE To review the management and outcome of babies with antenatally diagnosed congenital cystic adenomatoid malformation. DESIGN Retrospective cohort review. SETTING Tertiary neonatal care unit at Queen Mary Hospital and antenatal diagnostic centre at Tsan Yuk Hospital. PATIENTS Consecutive patients with antenatally suspected congenital cystic adenomatoid malformation in their conce...
متن کاملOutcome of antenatally suspected congenital cystic adenomatoid malformation of the lung: 10 years' experience 1991-2001.
OBJECTIVE To determine the outcome of antenatally suspected congenital cystic adenomatoid malformation of the lung (CCAM) over a 10 year period. METHODS This is a retrospective study of all babies diagnosed antenatally in the Prenatal Diagnosis Unit and delivered in Oxford between 1991 and 2001. Data were obtained from the Oxford Congenital Anomaly Register, theatre records, and histopatholog...
متن کاملManagement of antenatally diagnosed pulmonary sequestration associated with congenital cystic adenomatoid malformation.
BACKGROUND Sequestration with associated cystic adenomatoid malformation is rare. A study was undertaken to determine whether pulmonary sequestration associated with congenital cystic adenomatoid malformation has a more favourable natural history than that of sequestration without associated cystic adenomatoid malformation. METHODS An outline of the postnatal work up leading to the management...
متن کاملCongenital Cystic Adenomatoid Malformation of the Lung
Congenital cystic adenomatous malformations (CCAMs) of the lung represent the most common lung defect diagnosed prenatally. CCAMs are intrapulmonary lesions with a typical hyperechoic appearance on ultrasound (US), with or without cystic components. Both sides of the lung, both sexes, and all races are equally affected. Most fetuses with CCAM are detected prenatally and have a good outcome, but...
متن کاملCongenital cystic adenomatoid malformation of the lung.
Ultrastructural study of a congenital cystic adenomatoid malformation of the lung revealed a persistence of type 2 pneumocytes lining the alveolar and gland-like spaces. The larger cystic areas were lined by normal bronchiolar-type epithelium and were surrounded by a few smooth muscle cells. The interstitium contained undifferentiated mesenchymal cells. No cartilage or bronchial glands were pre...
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ژورنال
عنوان ژورنال: Ultrasound in Obstetrics and Gynecology
سال: 2004
ISSN: 0960-7692,1469-0705
DOI: 10.1002/uog.1296