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Year :2019
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Month :
January
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Volume :
7
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Issue :
1
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Page :
PC01 - PC03
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Type 1 Congenital Pulmonary Airway Malformation (CPAM): A Case Report
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Correspondence Address :
RR Pradheep, Sahana Devadas, Dr. RR Pradheep,
11/1-74, Pillukurichi, Morasapatti (PO), Idappadi (tk), Salem-637101, Tamil Nadu, India.
E-mail: rrpradeep66@gmail.com
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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.
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