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pubmed-article:8357648pubmed:abstractTextPeutz-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.lld:pubmed
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pubmed-article:8357648pubmed:authorpubmed-author:BalibreaJ LJLlld:pubmed
pubmed-article:8357648pubmed:authorpubmed-author:RodríguezJ...lld:pubmed
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pubmed-article:8357648pubmed:authorpubmed-author:MartínezSSlld:pubmed
pubmed-article:8357648pubmed:authorpubmed-author:TorresA JAJlld:pubmed
pubmed-article:8357648pubmed:authorpubmed-author:García...lld:pubmed
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pubmed-article:8357648pubmed:volume84lld:pubmed
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pubmed-article:8357648pubmed:pagination56-9lld:pubmed
pubmed-article:8357648pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:8357648pubmed:year1993lld:pubmed
pubmed-article:8357648pubmed:articleTitle[Peutz-Jeghers syndrome with malignization of hamartomatous polyp].lld:pubmed
pubmed-article:8357648pubmed:affiliationII Cátedra de Cirugía, Hospital Clínico Universidad Complutense, Madrid.lld:pubmed
pubmed-article:8357648pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8357648pubmed:publicationTypeEnglish Abstractlld:pubmed
pubmed-article:8357648pubmed:publicationTypeCase Reportslld:pubmed