%0 Journal Article
%T Congenital cystic adenomatoid malformation of lung: Report of three cases and review of this rare entity
%A Mallika Pal
%A Indranil Das
%A Rathin Hazra
%A Susmita Mukhopadhyay
%A Soumyee Bandyopadhyay
%J Clinical Cancer Investigation Journal
%@ 2278-0513
%D 2016
%V 5
%N 5
%R 10.4103/2278-0513.197868
%P 466-469
%X Congenital cystic adenomatoid malformations (CCAMs) are rare congenital, developmental, nonhereditary, hamartomatous pulmonary airway malformations. Etiology is unknown. It is a rare disease with an incidence of 1 in 11,000 to 1 in 35,000. It is a disease of infancy with most of the cases diagnosed within the first 2 years of life. We report cases of three infants with CCAM (Stocker Type II and I) with brief review of literature.
%U https://ccij-online.org/article/congenital-cystic-adenomatoid-malformation-of-lung:-report-of-three-cases-and-review-of-this-rare-entity-638