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

Author

Pal, Mallika, Das, Indranil, Hazra, Rathin, Mukhopadhyay, Susmita, and Bandyopadhyay, Soumyee

Subjects
CONGENITAL cystic adenomatoid malformation of lungs, POLYHYDRAMNIOS, HISTOPATHOLOGY, RADIOTHERAPY treatment planning, LOBECTOMY (Lung surgery), DIAGNOSIS
Abstract

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. [ABSTRACT FROM AUTHOR]

Published
2016
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