ArticleClinical neurology and neurosurgery2011
Glioblastoma multiforme in the Muir-Torre syndrome.
Article in Clinical neurology and neurosurgery, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed, 4 citations in OpenAlex.
- [Hereditary tumor syndromes in neuropathology].Der Pathologe · 2017Review
- Glioblastoma multiforme as initial internal malignancy in Muir-Torre syndrome (MTS).JAAD case reports · 2015Article
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Authors and funding
8 authors at 2 institutions in 1 country.
Funding
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).
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