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Case Reports
. 1993 Jul;84(1):56-9.

[Peutz-Jeghers syndrome with malignization of hamartomatous polyp]

[Article in Spanish]
Affiliations
  • PMID: 8357648
Case Reports

[Peutz-Jeghers syndrome with malignization of hamartomatous polyp]

[Article in Spanish]
J M Rodríguez et al. Rev Esp Enferm Dig. 1993 Jul.

Abstract

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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