Congenital Cardiopulmonary Anomalies in Infants with Recurrent Stridor and/or Respiratory Distress: Report of 3 Cases / 소아알레르기및호흡기학회지
Pediatric Allergy and Respiratory Disease
; : 183-190, 2009.
Article
en Ko
| WPRIM
| ID: wpr-80369
Biblioteca responsable:
WPRO
ABSTRACT
Although laryngomalacia is the most common cause of congenital stridor in infancy, it is a benign, self-limited disease which usually resolves by the age of 18 months with no long- term sequelae. Nevertheless, infants who suffered from recurrent stridor and respiratory distress should be evaluated for other causes of stridor such as cardiopulmonary anomalies. We report 3 cases of infants who had recurrent stridor and respiratory distress from their early infancy. Case 1 had a double aortic arch and a tracheomalacia, case 2 had a hypoplasia of the right lung, and case 3 had a horseshoe lung as well as scimitar syndrome. Physicians should be alert for the possibility of the congenital cardiopulmonary abnormalities in infants with recurrent stridor and/or respiratory distress.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Aorta Torácica
/
Síndrome de Cimitarra
/
Ruidos Respiratorios
/
Disnea
/
Laringomalacia
/
Traqueomalacia
/
Pulmón
Límite:
Humans
/
Infant
Idioma:
Ko
Revista:
Pediatric Allergy and Respiratory Disease
Año:
2009
Tipo del documento:
Article