Pyopneumothorax with Stocker type III congenital cystic adenomatoid malformation in a 5-month-old infant
Sujeet M Chilkar1, Venkat Leelakumar2, Chakravarthy P Ranjani3
1Department of Pediatric Intensive Care Unit, Ankura Hospital for Women and Children, Hyderabad, Telangana, India.
Abstract:
Congenital cystic adenomatoid malformation (CCAM) is a rare, developmental, hamartomatous abnormality of the lung characterized by a cessation of normal bronchiolar maturation, resulting in cystic overgrowth of the terminal bronchioles. We report one such case of CCAM in a 5-month-old female infant who was in perfect health until she suffered from spontaneous pyopneumothorax with type III CCAM of the lung and recovered after lobectomy.
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