Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child
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Updated: Oct 13, 2026

A Novel Method: Super-selective Adrenal Venous Sampling
Published on: September 15, 2017
L Sbragia-Neto1, A A Melo-Filho, G Guerra-Júnior
1Department of Pathology, Faculty of Medical Science, State University of Campinas, São Paulo, Brazil.
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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