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CASE REPORT
Year : 2015  |  Volume : 3  |  Issue : 2  |  Page : 53-56

Congenital cystic adenomatoid malformation of lung in fetus: Report of two cases with brief review of literature


Department of Pathology, Mahadevappa Rampure Medical College, Gulbarga, Karnataka, India

Correspondence Address:
Anuradha G Patil
Department of Pathology, Mahadevappa Rampure Medical College, Gulbarga - 585 105, Karnataka
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2320-8775.158854

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Congenital cystic adenomatoid malformations (CCAMs), also known as congenital pulmonary airway malformation is a developmental, non-hereditary, hamartomatous abnormality of lung with unknown etiology. It is a rare disease with an incidence of 1 in 25,000 to 1 in 35,000. It is a disease of infancy with most of the cases diagnosed within first 2 years of life. We report autopsy findings of two fetuses with CCAM (Stocker Type I and IV) with brief review of literature.


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