Journal of Chest Surgery
- Volume 17 Issue 1
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- Pages.118-124
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- 1984
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- 2765-1606(pISSN)
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- 2765-1614(eISSN)
Congenital cystic adenomatoid malformation
선천성 낭포성 선종양기형 -1례 보고-
- Sun, Kyung (Dept. of Chest Surgery, College of Medicine, Korea University) ;
- Baek, Kwang-Je (Dept. of Chest Surgery, College of Medicine, Korea University) ;
- Lee, Chol-Sei (Dept. of Chest Surgery, College of Medicine, Korea University) ;
- Chae, Sung-Soo (Dept. of Chest Surgery, College of Medicine, Korea University) ;
- Kim, Hark-Jei (Dept. of Chest Surgery, College of Medicine, Korea University) ;
- Kim, Hyung-Mook (Dept. of Chest Surgery, College of Medicine, Korea University)
- 선경 (고려대학교 의과대학 흉부외과학 교실) ;
- 백광제 (고려대학교 의과대학 흉부외과학 교실) ;
- 이철세 (고려대학교 의과대학 흉부외과학 교실) ;
- 채성수 (고려대학교 의과대학 흉부외과학 교실) ;
- 김학제 (고려대학교 의과대학 흉부외과학 교실) ;
- 김형묵 (고려대학교 의과대학 흉부외과학 교실)
- Published : 1984.03.01
Abstract
Congenital Cystic Adenomatiod Malformation (C.C.A.M.) is rare, but one of the most common congenital pulmonary anomalies that cause acute respiratory distress in the newborn infants. It is characterized and differentiated from the diffuse pulmonary cystic disease pathologically, i.e. adenomatoid appearance due to marked proliferation of the terminal respiratory components. An 2/12 year old male patient was suffered from respiratory distress and cyanosis on crying since birth, but no specific therapy was given. With progression of symptoms, he came to Korea University Hospital for further evaluation and then transfered to Dept. of Chest Surgery for operative correction under the impression of Congenital Obstructive Emphysema suggested by a pediatrician. On gestational and family history, there was nothing to be concerned such as congenital anomaly. Physical examinations showed; moderate nourishment and development (Wt. 5.5kg), cyanosis on crying, both intercostal and lower sternal retraction on inspiration, Lt. chest building with tympany, Rt. shifting of cardiac dullness, decreased breathing sound with expiratory wheezing on entire Lt. lung field, decreased breathing sound on Rt. upper lung filed, and tachycardia. The remainders were nonspecific. Laboratory findings were normal except WBC
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