Intest Res.  2010 Dec;8(2):181-186. 10.5217/ir.2010.8.2.181.

A Case of Peutz-Jeghers Syndrome Diagnosed by Wireless Capsule Endoscopy

Affiliations
  • 1Department of Internal Medicine, Jeju National University School of Medicine, Jeju, Korea. songhj@jejunu.ac.kr
  • 2Department of Surgery, Jeju National University School of Medicine, Jeju, Korea.
  • 3Department of Pathology, Jeju National University School of Medicine, Jeju, Korea.

Abstract

Peutz-Jeghers syndrome (PJS), is a rare autosomal dominant hereditary disorder. Intestinal hamartomatous polyps in association with melanocytic pigmentation of the skin and mucous membranes characterize PJS. Patients with PJS often have complications associated with the polyps, such as intestinal obstruction, intussusception, acute or chronic gastrointestinal bleeding, and the development of various types of cancer. Enteroclysis, small bowel follow-through, and push enteroscopy are generally used to identify the presence and location of small bowel polyps. Wireless capsule endoscopy (CE) has been confirmed as a feasible, safe, and sensitive test for the surveillance of small bowel polyps in patients with PJS and could replace radiographic small bowel surveillance. Here, a case of PJS newly diagnosed by CE is reported. The patient, a 30-year-old man who had developed rectal polyps associated with anal extrusion 7 years previously, had six episodes of hematochezia.

Keyword

Peutz-Jeghers Syndrome; Capsule Endoscopy

MeSH Terms

Adult
Capsule Endoscopy
Gastrointestinal Hemorrhage
Hemorrhage
Humans
Intestinal Obstruction
Intussusception
Mucous Membrane
Peutz-Jeghers Syndrome
Pigmentation
Polyps
Skin
Full Text Links
  • IR
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr