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Treatment of congenital pulmonary airway malformation with rare high cystic volume ratio: A case report and literature review

RATIONALE: Congenital pulmonary airway malformation (CPAM) is a rare congenital dysplastic malformation and accounts for 25% of congenital lung lesions. Commonly, it is diagnosed prenatally in ultrasound. The CPAM volume ratio (CVR) is a well-recognized predictor of fetal prognosis, and when the CVR...

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Detalles Bibliográficos
Autores principales:	Huang,, Miao, Gong, Yun-Hui
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2023
Materias:	5600
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10681422/ https://www.ncbi.nlm.nih.gov/pubmed/38013315 http://dx.doi.org/10.1097/MD.0000000000036249

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