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Research Article Open access CC BY 4.0

Congenital Cystic Adenomatoid Malformation: A Case Report

H. Aouraghe, I. Filali, L. Chtouki, A. Bentahila

Asian Journal of Pediatric Research · pp. 16–20 · Published 10 Jul 2023

10.9734/ajpr/2023/v13i2257

Abstract

The case report is being done to increase the knowledge of Congenital Cystic Adenomatoid Malformation (CCAM) along with to better understand about the disease and its management & raise awareness. A female infant (aged 9 months and birth weight 2500 gm) was selected as participant. After physical examination, the state of the participant was good (fever:37.6ºC, heart rate: 120/min, respiratory rate: 40/min). Holding a good health certificate, a cystic image was identified at pulmonary artery in chest X-ray report. The histology findings were consistent with CPAM Type I. CPAM surgery, generally favorable, results in low postoperative morbidity and mortality. CPAM is a rare developmental malformation of lung that causes pulmonary compression and hypoplasia leading to respiratory distress but the postnatal management of asymptomatic CPAM remains controversial.

CCAM cystic image morbidity mortality congenital abnormality carcinoma

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