RESUMO

The authors report a case of a virilizing adrenal tumor that developed in a 2-year-old child with Beckwith-Wiedemann syndrome (BWS). He had a fetal diagnosis of omphalocele and a history of neonatal adrenal cysts. The importance of prenatal diagnosis of BWS and postnatal follow-up of tumors is discussed. The differential diagnosis of adrenal pathologies occurring in BWS also is reviewed.

Assuntos

Neoplasias do Córtex Suprarrenal/complicações , Síndrome de Beckwith-Wiedemann/complicações , Neoplasias do Córtex Suprarrenal/diagnóstico , Síndrome de Beckwith-Wiedemann/diagnóstico , Pré-Escolar , Seguimentos , Humanos , Masculino , Diagnóstico Pré-Natal , Fatores de Tempo , Virilismo/etiologia