Korean J Gastrointest Endosc > Volume 36(2); 2008 > Article
Korean Journal of Gastrointestinal Endoscopy 2008;36(2): 107-111.
직장에서 발생한 고립성 Peutz-Jeghers 용종 2예
유일영ㆍ윤세진ㆍ전원중ㆍ고병성ㆍ채희복ㆍ박선미ㆍ이호창*
충북대학교 의과대학 내과학교실, *해부병리학교실
Two Cases of a Solitary Peutz-Jeghers Polyp in the Rectum
Il Young You, M.D., Sei Jin Youn, M.D., Won Joong Jeon, M.D., Byeongseong Ko, M.D., Hee Bok Chae, M.D., Seon Mee Park, M.D. and Ho-chang Lee, M.D.*
Departments of Internal Medicine and *Anatomical Pathology, Chungbuk National University, College of Medicine, Cheongju, Korea
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. (Korean J Gastrointest Endosc 2008;36:107-111)
Key Words: Peutz-Jeghers syndrome, Solitary Peutz- Jeghers polyp
주요어: Peutz-Jeghers 증후군, 고립성 Peutz-Jeghers형 과오종성 용종
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