Association of Congenital Cystic Pulmonary Airway Malformation with Schizencephaly
نویسندگان
چکیده
منابع مشابه
Congenital Pulmonary Airway Malformation (CPAM) formerly called Congenital Cystic Adenomatoid Malformation
Congenital pulmonary airway malformation (CPAM) is a rare entity. Anesthetic management for lobectomy is challenging due to sudden hemodynamic collapse which may occur during induction and ventilatory problems due to hyperinflation of cystic lesions with positive pressure ventilation. We discuss successful anesthetic management of two infants with CPAM posted for pneumonectomy with a brief ment...
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
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 ...
متن کاملPrenatal and Postnatal Management of Congenital Pulmonary Airway Malformation.
Congenital pulmonary airway malformation (CPAM) is one of the most common lung lesions detected prenatally. Despite the research efforts made in the past few years, controversy and lack of clarity in the literature still exist regarding nomenclature, classification, pathogenesis and the management of CPAM. Therefore, it is of greatest importance to delineate the natural history of CPAMs and to ...
متن کاملCongenital Pulmonary Airway Malformation (Cpam). A Diagnostic Dilemma!
Congenital pulmonary airway malformation (CPAM) of the lung is a rare lesion that typically manifests as neonatal respiratory distress, secondary to progressive expansion of the affected lung. Three distinct types have been described, based on the size of the cysts and the microscopic appearance. Type II lesions may carry a poor prognosis because of associated renal and cardiac anomalies. Malfo...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of Case Reports
سال: 2017
ISSN: 2231-6809
DOI: 10.17659/01.2017.0062