Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child

被引:9
作者
Sbragia-Neto, L
Melo, AA
Guerra, G
Marini, SHVD
Baptista, MTM
de Matos, PS
de Oliveira, AG
Bustorff-Silva, JM
机构
[1] State Univ Campinas, Fac Med Sci, Dept Pathol, Sao Paulo, Brazil
[2] State Univ Campinas, Fac Med Sci, Div Pediat Surg, Sao Paulo, Brazil
[3] State Univ Campinas, Fac Med Sci, Div Pediat Endocrinol, Sao Paulo, Brazil
关键词
Beckwith-Wiedemann syndrome; adrenal gland diseases; adrenal; omphalocele;
D O I
10.1053/jpsu.2000.8771
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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.
引用
收藏
页码:1269 / 1271
页数:3
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