Mucinous Cells in Type 1 Pulmonary Congenital Cystic Adenomatoid Malformation as Mucinous Bronchioloalveolar Carcinoma Precursors

2007 ◽  
Vol 31 (6) ◽  
pp. 961-969 ◽  
Author(s):  
Sylvie Lantuejoul ◽  
Andrew G. Nicholson ◽  
Giuliana Sartori ◽  
Christian Piolat ◽  
Claire Danel ◽  
...  
Keyword(s):  
Bronchioloalveolar Carcinoma ◽  
Congenital Cystic Adenomatoid Malformation ◽  
Cystic Adenomatoid Malformation

Pulmonary Congenital Cystic Adenomatoid Malformation Stocker Class Type 1 in a 26 Year-Old Female

CHEST Journal ◽  
2015 ◽  
Vol 148 (4) ◽  
pp. 624A
Author(s):  
Beatrice Tan ◽  
Jose Paolo Panuda ◽  
Consuelo Tan ◽  
Albert Rafanan
Keyword(s):  
Congenital Cystic Adenomatoid Malformation ◽  
Cystic Adenomatoid Malformation

Bronchioloalveolar carcinoma and congenital cystic adenomatoid malformation

1995 ◽  
Vol 60 (4) ◽  
pp. 1126-1128 ◽  
Author(s):  
Michel E. Ribet ◽  
Marie-Christine Copin ◽  
Jacques G. Soots ◽  
Bernard H. Gosselin
Keyword(s):  
Bronchioloalveolar Carcinoma ◽  
Congenital Cystic Adenomatoid Malformation ◽  
Cystic Adenomatoid Malformation

scholarly journals Congenital cystic adenomatoid malformation: a rare serial case report

2021 ◽  
Vol 9 (1) ◽  
pp. 190
Author(s):  
Dedy C. Haryono ◽  
Muhammad Kartika ◽  
Prima K. Hayuningrat ◽  
Darmawan Ismail
Keyword(s):  
Respiratory Distress ◽  
Lung Resection ◽  
Left Lung ◽  
Chest Ct ◽  
Congenital Cystic Adenomatoid Malformation ◽  
Congenital Lung Malformation ◽  
Cystic Adenomatoid Malformation ◽  
The Right ◽  
Multiple Cysts

Congenital cystic adenomatoid malformation (CCAM) is a rare congenital lung malformation which a part of the lung becomes polycystic. CCAM accounts for 25% of congenital lung malformations and 95% of lung lesions. Case 1 was a 5-month-old female infant who was diagnosed with pneumothorax, with multiple cysts in the right lung, using chest computed tomography (CT). Thoracotomy lung resection was performed. Case 2 was one-day-old newborn infant who had respiratory distress with Downe score 3. Multiple cystic lesions with septations in left lung was observed on chest CT. Lobectomy inferior lobes of left lung was performed. Both patients were diagnosed as CCAM type 1 pathologically. CCAM can be detected in the gestation by ultrasonography or after delivery through the appearance of respiratory distress signs.

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