| Literature DB >> 21288634 |
Zev A Binder1, Michael W Johnson, Avadhut Joshi, Christine L Hann, Constance A Griffin, Alessandro Olivi, Gregory J Riggins, Gary L Gallia.
Abstract
Muir-Torre syndrome (MTS) is an autosomal dominant subtype of nonpolyposis colorectal carcinoma (HNPCC) characterized by the development of sebaceous gland tumors and visceral malignancies. The most common subtype of MTS is characterized by germline mutations in mismatch repair (MMR) genes leading to microsatellite instability (MSI). Central nervous system tumors have only rarely been associated with MTS. In this report, we describe the development of a glioblastoma multiforme (GBM) in a patient with MTS. Immunohistochemical analysis of the patient's colon carcinoma and his GBM both revealed loss of the mismatch repair proteins mutS homolog 2 (MSH2) and mutS homolog 6 (MSH6).Entities:
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Year: 2011 PMID: 21288634 PMCID: PMC4612635 DOI: 10.1016/j.clineuro.2010.12.011
Source DB: PubMed Journal: Clin Neurol Neurosurg ISSN: 0303-8467 Impact factor: 1.876