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March 3, 2026Cureus0 citationsOpen Access

Rapunzel Syndrome Complicated by Cholecystoduodenal Fistula Secondary to Biliary Compression: A Case Report of a Patient With Cerebral Palsy

JSJosé Luis Serafio-GómezISIan-Arfaxad Saldaña-BadilloDMDana Karina Mauleon-Tiscareño

Key Points

  • Intestinal obstruction was caused by a gastric trichobezoar that extended into the small intestine, leading to complications.
  • A computed tomography scan revealed a mass in the stomach and intestine, necessitating urgent surgical intervention.
  • A laparotomy identified a gastric and duodenal trichobezoar alongside complications from biliary compression.
  • This case underscores the need for a multidisciplinary approach in complex surgical cases, particularly in patients with neurological conditions.

Abstract

Rapunzel syndrome is a rare form of gastric trichobezoar that extends into the small intestine, leading to intestinal obstruction. Biliary-enteric fistulas are abnormal communications between the biliary system and the gastrointestinal tract, generally occurring spontaneously. We report the case of a 26-year-old female patient with a history of cerebral palsy who presented to the emergency department with an acute abdomen. Computed tomography revealed a mass occupying the stomach and intestine. A laparotomy was performed, identifying a gastric and duodenal trichobezoar complicated by an acute perforated gastric ulcer, in addition to a vesicoduodenal fistula secondary to extrinsic compression of the gallbladder. This fistula clinically mimicked a type V Mirizzi syndrome. A Roux-en-Y hepaticojejunostomy was carried out. The patient died from nosocomial pneumonia 30 days later. This case highlights the importance of a multidisciplinary approach in patients with underlying neurological conditions and underscores the surgical feasibility of hepaticojejunostomy in complex scenarios of secondary biliary involvement.

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Cite This Study

Serafio-Gómez et al. (2026) studied this question.

synapsesocial.com/papers/69a75e53c6e9836116a28cddhttps://doi.org/10.7759/cureus.102568
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