# Gallstone Ileus Causing Mechanical Bowel Obstruction in a Patient With Caroli's Disease: A Case Report

**Authors:** Inês Soares, Ana Sofia Silva, Mariana Batista, Tiago Fernandes

PMC · DOI: 10.7759/cureus.93125 · 2025-09-24

## TL;DR

A 65-year-old woman with Caroli's disease developed gallstone ileus, a rare cause of bowel obstruction, requiring surgical intervention.

## Contribution

This case report highlights gallstone ileus as a rare complication in patients with Caroli's disease.

## Key findings

- Gallstone ileus was diagnosed in a patient with Caroli's disease via CT scan.
- Surgical removal of the obstructive gallstone was required.
- The case emphasizes the need for high clinical suspicion in diagnosing rare causes of bowel obstruction.

## Abstract

Gallstone ileus is a rare but significant cause of abdominal pain and mechanical bowel obstruction. Its management usually involves minimally invasive surgical intervention.

This case report describes a 65-year-old woman with a history of Caroli disease and prior abdominal surgery, who presented with a one-month history of progressive, cramp-like abdominal pain, accompanied by nausea and intermittent vomiting. Due to these persistent symptoms, she underwent a CT scan, which confirmed gallstone ileus with obstruction of a jejunal loop, necessitating surgical removal of the gallstone.

This case underscores the importance of integrating a patient’s medical history with their presenting symptoms and maintaining a high level of clinical suspicion for rare but serious causes of mechanical bowel obstruction that may otherwise be overlooked.

## Linked entities

- **Diseases:** bowel obstruction (MONDO:0004565)

## Full-text entities

- **Diseases:** cramp (MESH:D009120), Gallstone Ileus (MESH:D045823), gallstone (MESH:D042882), Mechanical Bowel Obstruction (MESH:D041781), nausea (MESH:D009325), Caroli disease (MESH:D016767), abdominal pain (MESH:D015746), vomiting (MESH:D014839)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12551798/full.md

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Source: https://tomesphere.com/paper/PMC12551798