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Glioblastoma multiforme in the Muir-Torre syndrome.

Authors :
Binder ZA
Johnson MW
Joshi A
Hann CL
Griffin CA
Olivi A
Riggins GJ
Gallia GL
Source :
Clinical neurology and neurosurgery [Clin Neurol Neurosurg] 2011 Jun; Vol. 113 (5), pp. 411-5. Date of Electronic Publication: 2011 Feb 01.
Publication Year :
2011

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).<br /> (Copyright © 2011 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-6968
Volume :
113
Issue :
5
Database :
MEDLINE
Journal :
Clinical neurology and neurosurgery
Publication Type :
Academic Journal
Accession number :
21288634
Full Text :
https://doi.org/10.1016/j.clineuro.2010.12.011