ArticleCureus2026
Prenatal Diagnosis and Monitoring of Type III Congenital Pulmonary Airway Malformation: A Case Report.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
3 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Congenital pulmonary airway malformation (CPAM) is a rare congenital lung anomaly resulting from abnormal bronchial development and disorganized respiratory structures, producing nonfunctional pulmonary lesions. Although uncommon, CPAM is the most frequently diagnosed congenital lung malformation. Prenatal identification allows for risk stratification and anticipatory management. Here we present a case of a fetus prenatally diagnosed with a type III CPAM during routine obstetric ultrasonography. Weekly ultrasonography was performed to monitor lesion progression and evaluate for complications, including mediastinal shift and hydrops fetalis. Multidisciplinary prenatal surveillance guided management during pregnancy. The pregnancy course, delivery planning, and neonatal outcomes are presented.
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