RESUMEN

Cantrell syndrome is characterized by defects that involve the diaphragm, abdominal wall, pericardium, heart, and lower region of the sternum. It is a rare entity, usually diagnosed at birth and accompanied by high mortality due to the complexity and gravity of the anomalies. In this report, we present a 32-year-old male patient, who was diagnosed in infancy but who reached adult age asymptomatic.

Asunto(s)

Anomalías Múltiples/diagnóstico , Cardiopatías Congénitas/diagnóstico , Músculos Abdominales/anomalías , Adulto , Diafragma/anomalías , Humanos , Masculino , Pericardio/anomalías , Esternón/anomalías , Síndrome