Fetal thoracoamniotic shunting for large macrocystic congenital cystic adenomatoid malformations of the lung
نویسندگان
چکیده
منابع مشابه
Antenatal thoracoamniotic shunting in congenital cystic adenomatoid malformation.
Cullen T, et al. BMJ Case Rep 2017. doi:10.1136/bcr-2016-217940 Description This case report describes a baby who was diagnosed antenatally with a significant left-sided congenital cystic adenomatoid malformation. Following diagnosis of a fluid-filled, macrocystic structure on the left side of the chest, the mother was referred at 27 weeks’ gestation to her regional fetal medicine unit for asse...
متن کاملIntrauterine 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 کاملFetal Thoracoamniotic Shunting in a Case of Congenital Pulmonary Airway Malformations with Hydrops Fetalis
Aim We report a case of congenital pulmonary airway malformation (CPAM) with hydrops in which the fetus underwent thoracoamniotic shunting. Case Report A 40-year-old (G1P1) woman was diagnosed with a macrocystic CPAM. Thoracoamniotic shunting was performed at 19 weeks of gestation but not well drained and was successfully performed again at 23 weeks. However, the CPAM volume ratio, abdominal ...
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...
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ژورنال
عنوان ژورنال: Ultrasound in Obstetrics & Gynecology
سال: 2012
ISSN: 0960-7692
DOI: 10.1002/uog.11084