Malformación adenomatoide quística. Diagnóstico diferido de una anomalía congénita
- S. Rupérez Peña
- M.aY. Ruiz del Prado
- N. Arostegi Kareaga
- N. García de Andoin Barandiarán
- A. Iturrioz Mata
- L. Alonso Tomás
ISSN: 1695-4033, 1696-4608
Datum der Publikation: 2003
Ausgabe: 59
Nummer: 4
Seiten: 396-399
Art: Artikel
Andere Publikationen in: Anales de Pediatría: Publicación Oficial de la Asociación Española de Pediatría ( AEP )
Zusammenfassung
Cystic adenomatoid malformation (CAM) is a congenital lung malformation characterized by adenomatoid proliferation of alveoli and terminal bronchioli. It is usually diagnosed perinatally, but some silent cases are discovered during childhood or adulthood. We present the case of a 9-year-old girl who presented with chest pain. Chest X-ray showed a cystic image in the upper lobe of the left lung, which was confirmed by computed tomography and magnetic resonance angiography. Lobectomy of the affected segment was performed and histological examination confirmed the diagnosis of CAM type I