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- W2496074893 abstract "This paper examines a short case history of an infant born with a Congenital Cystic Adenomatoid Malformation (CCAM). CCAM is a rare congenital lung malformation representing 25% of congenital malformations and 95% of congenital lung lesions.1,2 CCAM may be diagnosed in utero by ultrasound examination, or after birth with the presentation of respiratory distress like symptoms. Differential diagnosis includes diaphragmatic hernia, pulmonary sequestration, bronchogenic cysts, and congenital lobar emphysema. Because most CCAM lesions are manageable with the proper assessment, diagnosis, and interventions, it is vital that members of the neonatal health care team be knowledgeable about this malformation. The natural history, differential diagnosis, pathophysiology and treatment of CCAM are discussed." @default.
- W2496074893 created "2016-08-23" @default.
- W2496074893 date "2003-01-01" @default.
- W2496074893 modified "2023-10-17" @default.
- W2496074893 title "Congenital Cystic Adenomatoid Malformation: A Case Study" @default.
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- W2496074893 doi "https://doi.org/10.5580/2790" @default.
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