An Intraabdominal Pulmonary Sequestration Containing Congenital Cystic Adenomatoid Malformation
Journal of the Korean Association of Pediatric Surgeons
; : 138-142, 1996.
Article
en Ko
| WPRIM
| ID: wpr-740653
Biblioteca responsable:
WPRO
ABSTRACT
Pulmonary sequestration is a complex anomaly involving the pulmonary parenchymal tissue and its vasculature. It presents as a cystic mass of nonfunctional lung tissue without communication with the tracheobronchial system. Usually, it receives blood supply from anomalous systemic vessels. Therefore, preoperative diagnosis of the pulmonary sequestration is difficult, especially when it is located in the abdomen and combined with congenital cystic adenomatoid malformation (CCAM). We encountered such a mass(CCAM type 2) detected prenatally by ultrasonography. It was a kidney bean shaped, pinkish mass straddling the thorax and abdomen on the right side. Because of the sonographic appearance, neuroblastoma was diagnosed preoperatively. The mass was completely extirpated without difficulty.
Palabras clave
Texto completo:
1
Base de datos:
WPRIM
Asunto principal:
Tórax
/
Malformación Adenomatoide Quística Congénita del Pulmón
/
Secuestro Broncopulmonar
/
Ultrasonografía
/
Phaseolus
/
Diagnóstico
/
Abdomen
/
Pulmón
/
Neuroblastoma
Tipo de estudio:
Diagnostic_studies
Idioma:
Ko
Revista:
Journal of the Korean Association of Pediatric Surgeons
Año:
1996
Tipo del documento:
Article