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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1989-3-29
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pubmed:abstractText |
The Muir-Torre syndrome of sebaceous neoplasms of the skin, with or without keratoacanthomas, and multiple low-grade visceral malignancies with prolonged survival is a rare disorder. Colonic polyps are frequently present, and the syndrome appears to be familial. We report 2 unrelated patients with the Muir-Torre syndrome. Each case exhibited sebaceous adenomas. Gastrointestinal findings included colonic adenocarcinomas and a tubulovillous adenoma. Although an unusual disease, the Muir-Torre syndrome requires recognition because these patients are at risk for multiple primary malignancies and may have family members also at risk.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0011-9075
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
178
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
23-8
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:2917677-Adenocarcinoma,
pubmed-meshheading:2917677-Adenoma,
pubmed-meshheading:2917677-Adult,
pubmed-meshheading:2917677-Chromosome Aberrations,
pubmed-meshheading:2917677-Chromosome Disorders,
pubmed-meshheading:2917677-Colorectal Neoplasms, Hereditary Nonpolyposis,
pubmed-meshheading:2917677-Facial Neoplasms,
pubmed-meshheading:2917677-Genes, Dominant,
pubmed-meshheading:2917677-Humans,
pubmed-meshheading:2917677-Male,
pubmed-meshheading:2917677-Middle Aged,
pubmed-meshheading:2917677-Neoplasms, Multiple Primary,
pubmed-meshheading:2917677-Sebaceous Gland Neoplasms,
pubmed-meshheading:2917677-Sebaceous Glands,
pubmed-meshheading:2917677-Syndrome
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pubmed:year |
1989
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pubmed:articleTitle |
The Muir-Torre syndrome: a disease of sebaceous and colonic neoplasms.
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pubmed:affiliation |
Department of Dermatology, New Jersey Medical School, Newark.
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pubmed:publicationType |
Journal Article,
Case Reports
|