期刊
NEURO-ONCOLOGY
卷 8, 期 1, 页码 79-82出版社
OXFORD UNIV PRESS INC
DOI: 10.1215/S1522851705000347
关键词
atypical teratoid tumor; ganglioglioma; hSNF5/INI1; rhabdoid tumor
资金
- NCI NIH HHS [R01 CA046274, CA46274] Funding Source: Medline
- NATIONAL CANCER INSTITUTE [R01CA046274] Funding Source: NIH RePORTER
We report an atypical teratoid/rhabdoid tumor arising in a ganglioglioma from an 11-year-old male who had been treated over a nine-year period. A combined histologic, immunohistochemical, and molecular genetic analysis confirmed this diagnosis. Molecular genetic studies demonstrated a mutation in exon 9 of the INI1 gene in the tumor, which was not present in the patient's blood. This report is the first to describe progression of a ganglioglioma to atypical teratoid/rhabdoid tumor.
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