Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child |
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| Authors: | Sbragia-Neto L Melo-Filho A A Guerra-Júnior G Valente de Lemos Marini S H Baptista M T Sabino de Matos P S Gonçalves de Oliveira-Filho A Bustorff-Silva J M |
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| Affiliation: | Department of Pathology, Faculty of Medical Science, State University of Campinas, S?o Paulo, Brazil. |
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| 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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