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Year : 2016  |  Volume : 5  |  Issue : 5  |  Page : 466-469

Congenital cystic adenomatoid malformation of lung: Report of three cases and review of this rare entity

Department of Pathology, Nilratan Sircar Medical College and Hospital, Kolkata, West Bengal, India

Correspondence Address:
Indranil Das
28/11 A. K. Mukherjee Road, Noapara, Baranagar, Kolkata - 700 090, West Bengal
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/2278-0513.197868

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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.

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