Type 1 Congenital Pulmonary Airway Malformation (CPAM): A Case Report
Journal Title: Indian Journal of Neonatal Medicine and Research - Year 2019, Vol 7, Issue 1
Abstract
Congenital Pulmonary Airway Malformation (CPAM) is a lower respiratory tract developmental malformation. It is due to overgrowth of terminal bronchiole causing a dysplastic lesion. Affected areas consist of mass of cysts lined by bronchial or cuboidal epithelium, which may contain cystic and adenomatoid portions with intervening normal lung tissue. We present a rare case of full term female baby with type 1 CPAM, antenatally diagnosed and successfully managed with left lung lower lobe complete lobectomy with maximum cyst size measuring about 5.3x2.3 cm. Histologically cyst resembling bronchioles.
Authors and Affiliations
RR Pradheep, Sahana Devadas
Keywords
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- EP ID EP610125
- DOI 10.7860/IJNMR/2019/41293.2242
- Views 128
- Downloads 0
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