Renal cell carcinoma in a patient with Beckwith-Wiedemann syndrome
โ Scribed by T. Yamaguchi; T. Fukuda; M. Uetani; K. Hayashi; N. Kurosaki; H. Maeda; T. Matsumoto; H. Miyake
- Publisher
- Springer-Verlag
- Year
- 1996
- Tongue
- English
- Weight
- 272 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0301-0449
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Abstract BeckwithโWiedemann 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,
## Abstract We report on a patient with WiedemannโBeckwith 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