| Literature DB >> 31468188 |
Brent A Orr1, Michael R Clay2, Emilia M Pinto2, Chimene Kesserwan3.
Abstract
Li-Fraumeni syndrome (LFS), caused by the germline mutations in the TP53 gene, leads to significant lifetime risk to cancer in the central nervous system. Recognition of LFS, and elucidating its underlying cause has had a remarkable effect on our knowledge of the biology of brain tumors and represents a significant opportunity for cancer surveillance and screening. In this review, we discuss the historical context of the LFS with an emphasis on the clinicopathologic implications in clincal diagnosis, germline testing, and clinical management of brain tumor patients.Entities:
Keywords: Astrocytoma; Choroid plexus carcinoma; Glioblastoma; Li–Fraumeni syndrome; Medulloblastoma; TP53; p53; Germline surveillance
Mesh:
Year: 2019 PMID: 31468188 DOI: 10.1007/s00401-019-02055-3
Source DB: PubMed Journal: Acta Neuropathol ISSN: 0001-6322 Impact factor: 17.088