Two Cases of a Solitary Peutz-Jeghers Polyp in the Rectum / 대한소화기내시경학회지
Korean Journal of Gastrointestinal Endoscopy
; : 107-111, 2008.
Article
in Ko
| WPRIM
| ID: wpr-186040
Responsible library:
WPRO
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.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Polyps
/
Rectum
/
Pigmentation
/
Peutz-Jeghers Syndrome
/
Gastrointestinal Tract
Limits:
Humans
Language:
Ko
Journal:
Korean Journal of Gastrointestinal Endoscopy
Year:
2008
Type:
Article