Double Intussusceptions in Peutz-Jeghers Syndrome Patient: A Case Report

Abstract

Background: Peutz-Jeghers Syndrome is one of the hereditary gastro-intestinal cancer syndrome with characteristic mucocutaneous pigmentation and histologically distinctive hamartomatous polyps in gastro-intestinal tract. Although it is characteristically benign  hamartomatous polyp, majority of affected individuals develop symptoms starting from their second decades. We reported a known  Peutz-Jeghers Syndrome case developed recurrent polyps leading to double intussusceptions required bowel resection. Multidisciplinary  management and patient compliance to surveillance regime are important in managing PJS patients with potential gastro-intestinal tract  complications and relative high risk of developing syndrome specific cancers.