## 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,
Brown tumor with atypical localization in a normocalcemic patient
โ Scribed by Oguz Cebesoy; Metin Karakok; Omer Arpacioglu; Enver Taner Baltaci
- Publisher
- Springer
- Year
- 2007
- Tongue
- English
- Weight
- 298 KB
- Volume
- 127
- Category
- Article
- ISSN
- 1434-3916
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
We describe a four-month-old child who presented with an atypical teratoid/rhabdoid tumor of the brain and subsequently developed a renal rhabdoid tumor. Distinct histologic features, immunophenotypic profiles, and deletions of chromosome 22 were supportive of two primary tumors. An identical mutati
The case of a 7-year-old boy presenting at diagnosis with a localized (stage 111) Wilms' tumor of favorable histology is presented. lmmunocytologic analysis of bone marrow aspirates revealed cells positive for neural cell adhesion molecule (NCAM) and negative for class I major histocompatibility com