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Rapunzel syndrome causing partial gastric outlet obstruction requiring emergency laparotomy
Robert Lyons1, Granit Ismaili2, Michael Devine2
1Department of General Surgery, St. Vincent's University Hospital, Dublin, Ireland robertedwardlyons@svhg.ie.
BMJ Case Reports
|January 24, 2020
Summary
A 16-year-old with trichophagia (hair eating) developed Rapunzel syndrome, a gastric bezoar causing obstruction. Surgical removal was successful, with psychiatric follow-up recommended.
Area of Science:
- Gastroenterology
- Pediatric Surgery
- Psychiatry
Background:
- Presents a rare case of trichobezoar formation in a pediatric patient with a history of trichophagia.
- Highlights the potential for trichobezoars to cause significant gastrointestinal complications.
Observation:
- A 16-year-old female presented with acute epigastric pain, anorexia, and vomiting.
- Physical examination revealed a palpable epigastric mass.
- CT scan demonstrated an intragastric trichobezoar extending into the duodenum, indicative of Rapunzel syndrome, with signs of partial gastric outlet obstruction and possible perforation.
Findings:
- Urgent laparotomy confirmed the presence of a large trichobezoar.
- Surgical extraction of the bezoar was performed successfully without intraoperative complications or evidence of perforation.
- The patient experienced an uncomplicated postoperative recovery.
Implications:
- Rapunzel syndrome, though rare, requires prompt surgical intervention to prevent life-threatening complications.
- Emphasizes the importance of psychiatric evaluation and management in patients with trichophagia and bezoar formation.
- Successful surgical outcomes are achievable with timely diagnosis and treatment.
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