Artículos de revistas
Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child
Registro en:
Journal Of Pediatric Surgery. W B Saunders Co, v. 35, n. 8, n. 1269, n. 1271, 2000.
0022-3468
WOS:000089146500028
10.1053/jpsu.2000.8771
Autor
Sbragia-Neto, L
Melo, AA
Guerra, G
Marini, SHVD
Baptista, MTM
de Matos, PS
de Oliveira, AG
Bustorff-Silva, JM
Institución
Resumen
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. J Pediatr Surg 35:1269-1277. Copyright (C) 2000 by W.B. Saunders Company. 35 8 1269 1271