Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child.
J Pediatr Surg
; 35(8): 1269-71, 2000 Aug.
Article
en En
| MEDLINE
| ID: mdl-10945711
ABSTRACT
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.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Síndrome de Beckwith-Wiedemann
/
Neoplasias de la Corteza Suprarrenal
Tipo de estudio:
Diagnostic_studies
/
Etiology_studies
/
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Límite:
Child, preschool
/
Humans
/
Male
Idioma:
En
Revista:
J Pediatr Surg
Año:
2000
Tipo del documento:
Article
País de afiliación:
Brasil