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A Case of Congenital Cystic Adenomatoid Malformation (Type1) of the Lung.

Journal of the Korean Pediatric Society 1990;33(6):830-834.
Published online June 30, 1990.
A Case of Congenital Cystic Adenomatoid Malformation (Type1) of the Lung.
Dong Sik Kim1, Hwang Min Kim1, Jae Seung Yang1, Baek Keun Kim1, Jong Soo Kim1, Dong Hwan Shin2
1Department of Pediatrics, Yonsei University, Wonju College of Medicine
2Department of Pathology, Yonsei University, Wonju College of Medicine
폐의 선천성 낭포성 유선종 기형 (Type 1) 1례
김동식1, 김황민1, 양재승1, 임백근1, 김종수1, 신동환2
1연세대학교 원주의과대학 소아과학교실
2연세대학교 원주의과대학 병리학교실
Dong Hwan Shin, 
Received: 15 January 1990   • Accepted: 23 March 1990
A rare form of congenital cystic lung disease, characterized by the presence of one or usually multiple interconnecting cyst, is called congenital cystic adenomatoid malformation of the lung. This disease almost invariably presents either in live premature or stillborn infants, and death in those infants bom alive usually occurs within a few hours of birth. Infants with congenital cystic adenomatoid malformation usually have tachypnea, cyanosis, and other forms of respiratory distress at or shortly after birth. These manifestations are related to expansion of the cysts with resultant compression of the remaining normal lung. We have experienced a case of cystic adenomatoid malformation (Type I) of the lung in 10 months old female infant who had frequent upper respiratory tract infection and respiratory distress. A brief review of the related literature is presented.
Key Words: Congenital Cystic Adenomatoid Malformation, Congenital Cystic Lung Disease

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