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  • Title: Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child.
    Author: Sbragia-Neto L, Melo-Filho AA, Guerra-Júnior G, Valente de Lemos Marini SH, Baptista MT, Sabino de Matos PS, Gonçalves de Oliveira-Filho A, Bustorff-Silva JM.
    Journal: J Pediatr Surg; 2000 Aug; 35(8):1269-71. PubMed ID: 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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