## Abstract We report on a patient with Wiedemann‐Beckwith syndrome (WBS) who developed abdominal neuroblastoma. Although WBS patients are known to have a higher incidence of embryonal tumors, this is only the 4th known case of neuroblastoma associated with this syndrome. Chromosomes on peripheral
✦ LIBER ✦
Focal nodular hyperplasia in a child with Beckwith–Wiedemann syndrome
✍ Scribed by Liliana Bordeianou; Daniel P. Ryan; Allan M. Goldstein
- Publisher
- Springer-Verlag
- Year
- 2005
- Tongue
- English
- Weight
- 247 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0179-0358
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## Abstract Beckwith–Wiedemann syndrome (BWS) is a genetic disorder associated with an increased risk of childhood tumors. Here we describe a patient with BWS who developed a central nervous system atypical teratoid/rhabdoid tumor (AT/RT). To our knowledge, despite the known cancer predisposition,