| Literature DB >> 31969411 |
Robert Lyons1, Granit Ismaili2, Michael Devine2, Haroon Malik2.
Abstract
A 16-year-old girl with a background of childhood trichophagia presented with a 2-day history of epigastric pain and associated anorexia with vomiting. An epigastric mass was palpable on examination. A CT scan revealed an intragastric trichobezoar, extending into the duodenum consistent with Rapunzel syndrome with evidence of partial gastric outlet obstruction and a possible perforation. The patient underwent an urgent laparotomy and extraction of the trichobezoar. The bezoar was removed without complication and no intraoperative evidence of perforation was detected. After an uncomplicated postoperative recovery, she was discharged home with psychiatric follow-up. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: gastrointestinal surgery; general surgery
Mesh:
Year: 2020 PMID: 31969411 PMCID: PMC7035851 DOI: 10.1136/bcr-2019-232904
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X