| Literature DB >> 25374499 |
Do Hyun Lee1, Hyun Deok Shin1, Woo Hee Cho1, Kyoung Hwang Shin1, Sora Lee1, Jeong Eun Shin1, Hwan Namgung2, Ji Eun Gwon3.
Abstract
Peutz-Jeghers syndrome is an autosomal dominant inherited disease that manifests as a combination of mucocutaneous pigmentation and gastrointestinal hamartomatous polyps that usually cause intussusception and intestinal hemorrhage. We report the case of a 40-year-old male patient who was diagnosed 20 years ago and had previously undergone 3 intestinal resection surgeries. This time, with the use of combined operative and endoscopic polypectomy, more than 100 polyps were removed. This technique is useful for providing a "clean" small intestine that allows the patient a long interval between laparotomies and reduces the complications associated with multiple laparotomies and resections.Entities:
Keywords: Endoscopy; Intussusception; Peutz-Jeghers syndrome; Polypectomy
Year: 2014 PMID: 25374499 PMCID: PMC4214960 DOI: 10.5217/ir.2014.12.4.320
Source DB: PubMed Journal: Intest Res ISSN: 1598-9100