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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1993-9-24
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pubmed:abstractText |
Peutz-Jeghers syndrome is characterized by hamartomatous polyps in the gastrointestinal tract associated with mucocutaneous melanin spots; the condition is inherited in an autosomic dominant fashion. Although the hamartomatous polyps are not regarded as malignant, there is an association between the Peutz-Jeghers syndrome and the development of carcinomas of the gastrointestinal tract. Similarly, there is an increasing evidence suggesting that hamartomas can give rise to adenocarcinomas. We present a patient with Peutz-Jeghers syndrome who developed an adenocarcinoma in an hamartomatous jejunal polyp.
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pubmed:language |
spa
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
|
pubmed:issn |
1130-0108
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
84
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
56-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8357648-Adenocarcinoma,
pubmed-meshheading:8357648-Female,
pubmed-meshheading:8357648-Humans,
pubmed-meshheading:8357648-Intestinal Neoplasms,
pubmed-meshheading:8357648-Middle Aged,
pubmed-meshheading:8357648-Peutz-Jeghers Syndrome,
pubmed-meshheading:8357648-Precancerous Conditions
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pubmed:year |
1993
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pubmed:articleTitle |
[Peutz-Jeghers syndrome with malignization of hamartomatous polyp].
|
pubmed:affiliation |
II Cátedra de Cirugía, Hospital Clínico Universidad Complutense, Madrid.
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|