Congenital Cystic Adenomatoid Malformation of the Lung
نویسنده
چکیده
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 appropriate identifi cation and ongoing surveillance are required because of the unpredictability of growth patterns for CCAM masses.
منابع مشابه
Congenital Cystic Adenomatoid Malformation (CCAM) of Lung in an Infant: A Case Report from Jammu & Kashmir, Northern India
Congenital cystic Adenomatoid malformation is a rare developmental abnormality of the lung occuring in 1-4/100000 live births.In most cases the outcome with CCAM in fetus is very good,while in some cases the outcome is very bad and can be life threatning for the fetus.we report here a case of 40 day old female infant who presented with worsening respiratory distress since birth and x ray and CT...
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 کاملFetal MRI as Complementary Study of Congenital Cystic Adenomatoid Malformation During Pregnancy: A Single Case Report
Fetal lung masses are rare findings in prenatal ultrasound scanning in general population, of which congenital cystic adenomatoid malformation is the most commonly diagnosed type. This paper reports a single case of congenital cystic adenomatoid malformation detected at our hospital and the subsequent clinical follow-up using ultrasound scanning and fetal magnetic resonance imaging.
متن کاملClinical, radiographic and lung function features of diffuse congenital cystic adenomatoid malformation of the lung in an adult.
Congenital cystic adenomatoid malformation of the bronchi with bilateral lung involvement has only previously been reported in one possible adult case. This report describes a young man with bilateral diffuse lung involvement, characteristic histological features, and a mixed restrictive/obstructive lung function pattern.
متن کاملCongenital Cystic Adenomatoid Malformation (CCAM) with Two Cases Introduction
CCAM is a rare conolition in the neonatal Period. Two babies were admitted to Mofid hospital with cyanosis and respiratory distress. Pneumectomy was done for both of them for space occupaying lesion. Pathology examination of first case showed area of cuboidal epithelium lined tubes and spaces resembling fetal bronchioles, which are torn in folds. In second case, pathologic examination revealed...
متن کاملCongenital Cystic Adenomatoid Malformation: Case Report Authors
Congenital Cystic Adenomatoid Malformation (CCAM) is a rare development abnormality of the lung occurring in 14 / 100,000 live birth.it is often confused with pneumatocoele or pneumothorax which are common in developing countries. We report here a case of 5 months old baby with features of respiratory distress since birth and CECT thorax suggestive of large cystic lesion of left lung i.e., CCAM.
متن کامل