4.6 Article

Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: Case study

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

  1. NCI NIH HHS [R01 CA046274, CA46274] Funding Source: Medline
  2. NATIONAL CANCER INSTITUTE [R01CA046274] Funding Source: NIH RePORTER

向作者/读者索取更多资源

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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