Peutz-Jehger’s Syndrome presenting as adult intussusception

Authors

  • Z. Athar Department of Surgery, Tribhuvan University Teaching Hospital, Institute of Medicine
  • A. Rajbhandari Department of Surgery, Tribhuvan University Teaching Hospital, Institute of Medicine
  • P. Kansakar Department of Surgery, Tribhuvan University Teaching Hospital, Institute of Medicine
  • Y.P. Singh Department of Surgery, Tribhuvan University Teaching Hospital, Institute of Medicine
  • P. Vaidya Department of Surgery, Tribhuvan University Teaching Hospital, Institute of Medicine

DOI:

https://doi.org/10.59779/jiomnepal.374

Keywords:

Cutaneous melanin, Hamartomatous polyp, Intussusception, Peutz Jegher’s syndrome

Abstract

Abstract: Peutz- Jehger’s syndrome is an autosomal dominant disorder. It is the second most common hamartomatous syndrome with hamartomatous polyp of gastrointestinal tract and cutaneous melanin deposit. Majority of patients remain relatively asymptomatic. Some present with abdominal pain secondary to obstruction or impending obstruction owing to an intussuscepted polyp with GI bleeding. We report a case of 21 year male who presented with upper central abdominal pain, distension, vomiting and blood mixed stool. He also had black colored spots on perioral region and fingers. Ultrasound revealed mass lesion with echogenic centre suggestive of intussusception. Emergency laparotomy revealed jejunojejunal intususception with gangreneous intussusceptum and two other large polyps. Resection anastomosis of jejunum and excision of polyps was done. Peutz – Jehger’s syndrome is a rare but important cause of intussusception in adults presenting with cutaneous manifestations and features of intestinal obstruction

Downloads

Published

2009-04-30

Most read articles by the same author(s)

Similar Articles

1-10 of 69

You may also start an advanced similarity search for this article.