Recurrent Intussusception Secondary to Multiple Peutz-jegher polyps: An Unusual Case with Review of Literature

Copyright © 2018 Phcog.Net. This is an openaccess article distributed under the terms of the Creative Commons Attribution 4.0 International license. Cite this article: Bhatia C, Dalal S, Singh M, Malwal JS. Recurrent Intussusception Secondary to Multiple Peutz-jegher polyps: An Unusual Case with Review of Literature. OGH Reports. 2018;7(1):43-5. ABSTRACT Peutz-Jegher polyps are hamartomas of the small bowel which occur as part of the PeutzJegher syndrome, a rare autosomal dominant condition characterized by gastrointestinal polyps and mucocutaneous melanotic pigmentation. Here we report the case of a young male suffering from this syndrome who presented with acute intestinal obstruction due to intussception. Exploratory laparotomy was done which revealed jejuno-jejunal and jejunoileal intussusceptions for which resection and anastomosis was done. There were multiple intraluminal polyps in the jejunum which on histopathological examination, showed features of Peutz-Jegher Polyp. Patient behaved well in the post-operative period and is still on follow up with us.