A congenital cystic pulmonary airway malformation occurring together with both an extralobar pulmonary sequestration and an esophageal duplication cyst

A foregut duplication cyst occurring together with both a congenital cystic pulmonary airway malformation and extralobar pulmonary sequestration is an unusual combination. Prenatal ultrasound, MRI, and postnatal CT are helpful for operative planning. Surgical resection is the definitive management f...

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Detalles Bibliográficos
Autores principales: Dewberry, Lindel C., Trecartin, Andrew, Galambos, Csaba, Hilton, Sarah A., Dannull, Kimberly, Zaretsky, Michael V., Behrendt, Nicholas, Galan, Henry L., Marwan, Ahmed I., Liechty, Kenneth W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982492/
https://www.ncbi.nlm.nih.gov/pubmed/31998479
http://dx.doi.org/10.1002/ccr3.2455
Descripción
Sumario:A foregut duplication cyst occurring together with both a congenital cystic pulmonary airway malformation and extralobar pulmonary sequestration is an unusual combination. Prenatal ultrasound, MRI, and postnatal CT are helpful for operative planning. Surgical resection is the definitive management for all three anomalies.

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