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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
1998-8-27
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pubmed:abstractText |
Muir-Torre syndrome is a rare autosomal dominant disorder characterized by unusual sebaceous neoplasms and visceral malignancy. Excluding sebaceous hyperplasia and sebaceous nevus of Jadassohn, sebaceous neoplasms occur so rarely that the presence of a sebaceous neoplasm mandates consideration of Muir-Torre syndrome. Sebaceous neoplasms precede or are synchronous with visceral malignancies in up to 40% or more of patients with Muir-Torre syndrome, and the presence of such a lesion warrants an evaluation for visceral malignancy.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0148-7043
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
40
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
676-7
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:9641292-Adenocarcinoma,
pubmed-meshheading:9641292-Adenocarcinoma, Sebaceous,
pubmed-meshheading:9641292-Adult,
pubmed-meshheading:9641292-Back,
pubmed-meshheading:9641292-Female,
pubmed-meshheading:9641292-Humans,
pubmed-meshheading:9641292-Neoplasms, Second Primary,
pubmed-meshheading:9641292-Rectal Neoplasms,
pubmed-meshheading:9641292-Sebaceous Gland Neoplasms,
pubmed-meshheading:9641292-Syndrome
|
pubmed:year |
1998
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pubmed:articleTitle |
Muir-Torre syndrome.
|
pubmed:affiliation |
Section of Plastic and Reconstructive Surgery, University of Nebraska Medical Center, Omaha 68198-3335, USA.
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pubmed:publicationType |
Journal Article,
Case Reports
|