Korean J Gastrointest Endosc.  2010 Jul;41(1):36-40.

A Case of Hamartomatous Polyp without Peutz-Jeghers Syndrome Arising from Appendix

Affiliations
  • 1Department of Internal Medicine, Bundang Jesaeng Hospital, Seongnam, Korea. parkjs@dmc.or.kr
  • 2Department of Pathology, Bundang Jesaeng Hospital, Seongnam, Korea.

Abstract

Peutz-Jeghers syndrome is a familial syndrome consisting of mucocutaneous pigmentation and gastrointestinal polyposis and appears to be inherited as a single pleiotropic autosomal dominant gene with variable and incomplete penetrance. Cases of hamartomatous polyps of the Peutz-Jeghers type without Peutz-Jeghers syndrome have only rarely been reported. Moreover, only one case of a Peutz-Jeghers polyp at the appendix has been reported; it was resected by appendectomy. We report here on a case of a 45 year old man who had a hamartomatous polyp of the Peutz-Jeghers type arising from the appendix. The polyp was successfully removed by endoscopic polypectomy. To our knowledge, this is the first case of a hamartomatous polyp of the Peutz-Jeghers type that originated from the appendix and that was resected endoscopically.

Keyword

Hamartomatous polyp; Peutz-Jeghers type; Appendix; Endoscopic polypectomy
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