Intrauterine therapy for macrocystic congenital cystic adenomatoid malformation of the lung
نویسندگان
چکیده
منابع مشابه
Intrauterine therapy for macrocystic congenital cystic adenomatoid malformation of the lung
OBJECTIVE To report on our experiences with thoracoamniotic shunting and/or the injection of a sclerosing agent (OK-432) to treat fetuses diagnosed with macrocystic congenital cystic adenomatoid malformation (CCAM) of the lung. METHODS A retrospective study was undertaken in six fetuses with macrocystic CCAM at our institute that had been confirmed by postnatal surgery between August 1999 and...
متن کاملIntrauterine therapy in macrocystic type congenital cystic adenomatoid malformation of the lung
Results Mean gestational age at the time of shunt insertion was 25 weeks of gestation. Mediastinal shift were stated in all of the cases. Polyhydramnios was noted in ten fetuses, seven of which were hydropic. In the remaining five fetuses without impaired cardiac function, four had very large lesions (CVR > 1. 6) and one had a lesion that was rapidly increasing in size. Shunt insertion was succ...
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...
متن کاملCongenital cystic adenomatoid malformation
Australasian Journal of Ultrasound in Medicine August 2009; 12 (3) Introduction Congenital cystic adenomatoid malformation (CCAM) is an uncommon fetal lung anomaly involving cystic changes to the terminal bronchioles. The condition requires close monitoring during the antenatal period with ultrasound in addition to input from the neonatal and paediatric surgical teams. This case study involves ...
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ژورنال
عنوان ژورنال: Obstetrics & Gynecology Science
سال: 2014
ISSN: 2287-8572,2287-8580
DOI: 10.5468/ogs.2014.57.2.102