Aouraghe, H. and Filali, I. and Chtouki, L. and Bentahila, A. (2023) Congenital Cystic Adenomatoid Malformation: A Case Report. Asian Journal of Pediatric Research, 13 (2). pp. 16-20. ISSN 2582-2950
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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.
Item Type: | Article |
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Subjects: | Eprints STM archive > Medical Science |
Depositing User: | Unnamed user with email admin@eprints.stmarchive |
Date Deposited: | 12 Jul 2023 10:39 |
Last Modified: | 16 Sep 2023 05:45 |
URI: | http://public.paper4promo.com/id/eprint/887 |