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

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.

Congenital cystic adenomatoid malformation in adults, presenting as a single cyst

2018 ◽  
Vol 26 (5) ◽  
pp. 407-409 ◽  
Author(s):  
Adriana Scamporlino ◽  
Andrea Ambrosini ◽  
Ercole Turrini ◽  
Uliano Morandi ◽  
Alessandro Stefani
Keyword(s):  
Clinical Diagnosis ◽  
Preoperative Diagnosis ◽  
Congenital Cystic Adenomatoid Malformation ◽  
Large Cyst ◽  
Single Cyst ◽  
Cystic Adenomatoid Malformation ◽  
Congenital Cystic Adenomatoid Malformations

Congenital cystic adenomatoid malformations are lung anomalies usually detected prenatally or in newborns and infants. Type 1 congenital cystic adenomatoid malformations appears as a multicystic lesion, with cysts up to 2 cm in diameter, or as a single large cyst. In the latter case, when detected in adults, the preoperative diagnosis is challenging because congenital cystic adenomatoid malformations can be confused with other more common lesions. We describe two cases of uniloculated type 1 congenital cystic adenomatoid malformation in adults. In both cases, the preoperative clinical diagnosis was missed and the patients were surgically treated with lung-sparing cyst resections.

Congenital cystic adenomatoid malformation of lung type 1

2010 ◽  
Vol 45 (2) ◽  
pp. e25-e28 ◽  
Author(s):  
Alka Mary Mathai ◽  
Hema Kini ◽  
Muktha R. Pai ◽  
Ashok B. Shetty ◽  
Nirupama Murali
Keyword(s):  
Congenital Cystic Adenomatoid Malformation ◽  
Cystic Adenomatoid Malformation
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