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Two Cases of a Solitary Peutz-Jeghers Polyp in the Rectum / 대한소화기내시경학회지
Korean Journal of Gastrointestinal Endoscopy ; : 107-111, 2008.
Article in Korean | WPRIM | ID: wpr-186040
ABSTRACT
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.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Polyps / Rectum / Pigmentation / Peutz-Jeghers Syndrome / Gastrointestinal Tract Limits: Humans Language: Korean Journal: Korean Journal of Gastrointestinal Endoscopy Year: 2008 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Polyps / Rectum / Pigmentation / Peutz-Jeghers Syndrome / Gastrointestinal Tract Limits: Humans Language: Korean Journal: Korean Journal of Gastrointestinal Endoscopy Year: 2008 Type: Article