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Research Article Open access CC BY 4.0

Double Localization Trichobezoar Causing Small Bowel Obstruction in an Adolescent: A Case Report

Mohamed Ballouch, Walid Chair, Imade El Azzaoui, Mehdi Karami, Mohamed Bouzroud, Hakim EL Kaoui, Mountassir Moujahid, Sidi Mohamed Bouchentouf

Asian Journal of Research in Surgery · pp. 777–783 · Published 14 Aug 2026

10.9734/ajrs/2026/v9i2420

Abstract

Aims: Trichobezoars are rare, compacted hair masses that most often form in the stomach of young females with trichophagia associated with obsessive-compulsive disorder (OCD). Double localisation—simultaneous gastric and intestinal trichobezoars—is exceedingly rare and poses distinct diagnostic and therapeutic challenges. We report a rare case of a double-localisation trichobezoar causing mechanical small bowel obstruction (SBO), with spontaneous ileal passage followed by elective surgical extraction of the gastric component. Presentation of Case: A 17-year-old female with known OCD and trichophagia and a background of Helicobacter pylori gastritis with iron-deficiency anaemia presented with a one-week history of postprandial vomiting, progressing to a sub-occlusive syndrome with cessation of stools but preserved flatus. Contrast-enhanced CT demonstrated mechanical SBO with calibre disparity at the terminal ileum, consistent with an ileal trichobezoar, and a separate large gastric trichobezoar. Four days after admission, the patient experienced spontaneous passage of the ileal trichobezoar, confirmed by resolution of air-fluid levels on a plain radiograph. The gastric trichobezoar was subsequently treated by elective laparotomy with anterior gastrotomy and en bloc extraction. The postoperative course was uneventful, and psychiatric follow-up for OCD and trichophagia was initiated. Discussion: Trichobezoars almost invariably require surgical intervention; spontaneous intestinal passage is exceptionally rare and has been documented in only a handful of cases worldwide. The coexistence of a gastric trichobezoar mandates vigilance for Rapunzel syndrome and dual-site pathology. CT imaging is the cornerstone of diagnosis and surgical planning in such cases. Conclusion: This case underscores the importance of CT-guided management of double-localisation trichobezoars, highlights the possibility—albeit rare—of spontaneous ileal passage, and reinforces the need for multidisciplinary management, including psychiatric care, to prevent recurrence.

Trichobezoar bezoar small bowel obstruction trichophagia Rapunzel syndrome adolescent gastrotomy

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