| Literature DB >> 10945711 |
L Sbragia-Neto1, A A Melo-Filho, G Guerra-Júnior, S H Valente de Lemos Marini, M T Baptista, P S Sabino de Matos, A Gonçalves de Oliveira-Filho, J M Bustorff-Silva.
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.Entities:
Mesh：
Year: 2000 PMID： 10945711 DOI： 10.1053/jpsu.2000.8771
Source DB: PubMed Journal: J Pediatr Surg ISSN： 0022-3468 Impact factor: 2.545