| Literature DB >> 31719287 |
E A Disu1, O A Kehinde1, A L Anga2, P O Ubuane2, A Itiola2, I J Akinola2, B Falase3.
Abstract
Congenital pulmonary airway malformation (CPAM), formerly known as congenital cystic adenomatoid malformation (CCAM), is a rare developmental dysplastic lesion of the fetal tracheobronchial tree. CPAM is a rare cause of neonatal respiratory distress; however, its presence may span fetal to adult period. In two previous case-reports from Nigeria, CPAM was present in post-neonatal infants. We report the case of a neonate, who presented with increasing respiratory distress and an abnormal chest radiograph, initially assumed as pneumonic changes. A revised diagnosis of CPAM was made after a chest computed tomography (CT) scan. The neonate subsequently had a successful excision of the affected lobe with remarkable clinical improvement. The case highlights the need to utilize superior imaging studies such as CT when plain radiographs are inconclusive.Entities:
Keywords: Case report; Nigeria; congenital cystic adenomatoid malformation; congenital pulmonary airway malformation; neonate; respiratory distress
Year: 2019 PMID: 31719287 DOI: 10.4103/njcp.njcp_20_19
Source DB: PubMed Journal: Niger J Clin Pract Impact factor: 0.968