Congenital Lung Anomalies in Adults
Marcos Mestas Nuñez1, Gonzalo Dulcich1, Carlos S Restrepo1
1From San Lucas Diagnóstico, 25 de Mayo 1941, 3300, Posadas, Argentina (M.M.N.); Department of Radiology, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina (G.D.); Department of Radiology, University of Texas Health Science Center, San Antonio, TX (C.S.R.); Departments of Radiology (R.K., N.R., D.V.) and Pathology (N.S.), University of Colorado Anschutz Medical Campus, Aurora, CO; and Department of Radiology, Hospital San Juan de Dios, HT Médica, Córdoba, Spain (J.B.).
Abstract:
Congenital lung anomaly (CLA) refers to a rare group of malformations that are typically identified prenatally or in early childhood. However, a significant proportion of cases evade detection until adulthood and either are incidentally discovered or manifest with symptoms of recurrent respiratory infection or pulmonary hemorrhage. While most CLAs have characteristic imaging findings at CT and MRI, they remain a diagnostic challenge due to the infrequency with which they are encountered in adults. Radiologists frequently play a pivotal role in suggesting the diagnosis and guiding appropriate management strategies, and recognition of characteristic imaging patterns is crucial for accurate diagnosis. The authors examine the imaging appearances and clinical manifestations in adult patients with CLA, with a focus on patients who have bronchopulmonary involvement and those with combined bronchopulmonary and vascular anomalies. Entities discussed include bronchogenic cyst, bronchial atresia, congenital lobar overinflation, congenital pulmonary airway malformation, proximal interruption of the pulmonary artery, bronchopulmonary sequestration, hypogenetic lung syndrome, placental transmogrification of the lung, and hybrid lesions. Common complications that may arise in these patients are discussed and illustrated. ©RSNA, 2024 Supplemental material is available for this article.
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