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Korean Journal of Gastrointestinal Endoscopy ; : 107-111, 2008.
Artículo en Coreano | WPRIM | ID: wpr-186040

RESUMEN

Peutz-Jeghers syndrome is a rare autosomal dominant disorder in which multiple hamartomatous polyps are present in the gastrointestinal tract in association with distinctive mucocutaneous pigmentation. A single hamartomatous polyp arising in a patient without pigmentation or familial history of Peutz-Jeghers syndrome is termed a solitary Peutz-Jeghers polyp; such a case is rare and would result in a case report being presented even in other countries. We experienced two cases of a solitary Peutz-Jeghers polyp that developed in the rectum, and report the cases with a review of the literature.


Asunto(s)
Humanos , Tracto Gastrointestinal , Síndrome de Peutz-Jeghers , Pigmentación , Pólipos , Recto
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