S3619 Bouveret Syndrome in a Patient Without a History of Biliary Disease

Introduction: Bouveret syndrome is a rare form of gallstone ileus characterized by gastric outlet obstruction caused gallstone migration through a cholecystoduodenal/gastric fistula and becoming impacted in the duodenum or pylorus. Gallstone ileus accounts for 1%-4% of mechanical bowel obstructions and only around 10% present as Bouveret syndrome. Case Description/Methods: A 77-year-old White woman with a past medical history of hypertension presented with emesis and 2 months of sharp, episodic back pain radiating to the left shoulder. Computed tomography showed inflammation at the gallbladder fossa with a large 2.8 cm stone eroding into the adjacent duodenum. Due to concerns of a cholecystoduodenal fistula the patient underwent endoscopic retrograde cholangiopancreatography (ERCP). On esophagogastroduodenoscopy (EGD), a large stone and 20 mm fistula from the gallbladder to the second portion of the duodenum were seen. The stone was fragmented and cleared using electrohydraulic lithotripsy (EHL) in 2 successive procedures. The distal duodenum was observed to be patent and the patient was discharged. Four days later the patient presented again with emesis. Computed tomography showed a gallstone in the distal ileum, a high-grade small bowel obstruction, and pneumobilia consistent with gallstone ileus. Exploratory laparotomy was performed and a 3 × 5 cm stone was found to have spontaneously passed into the rectosigmoid junction. No further interventions were indicated and the patient was discharged in a stable condition. Discussion: This case highlights the challenge the initial diagnosis of Bouveret syndrome and complications after treatment. Females over 60 years and a history of biliary disease are at highest risk. Symptoms lack specificity and can mimic more common causes of gastric outlet obstruction thus leading to diagnostic and management delays resulting in a high morbidity and mortality rate that is estimated to be 12-30%. Labs are non-specific and computed tomography remains the most reliable diagnostic modality. Bowel obstruction, aberrant gallstone, and pneumobilia seen on radiography (Rigler’s triad) strongly suggests Bouveret Syndrome. Recommended management with minimally invasive techniques via endoscopy has a lower mortality and morbidity rate compared to surgery but a comparatively reduced rate of success. As endoscopic treatment techniques and tools continue to improve, this disparity may be reduced. A high index of clinical suspicion is essential for timely diagnosis and intervention, thereby improving outcomes.

Authors

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001141936.56263.72
Primary Topic
Biliary and Gastrointestinal Fistulas
Type
article
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article

S3619 Bouveret Syndrome in a Patient Without a History of Biliary Disease

Anuj Vyas, Amar Thosani, Y. Fong, Shradha Gupta
The American Journal of Gastroenterology
Biliary and Gastrointestinal Fistulas
article

S3619 Bouveret Syndrome in a Patient Without a History of Biliary Disease

Anuj Vyas, Amar Thosani, Y. Fong, Shradha Gupta
article en

Abstract

Introduction: Bouveret syndrome is a rare form of gallstone ileus characterized by gastric outlet obstruction caused gallstone migration through a cholecystoduodenal/gastric fistula and becoming impacted in the duodenum or pylorus. Gallstone ileus accounts for 1%-4% of mechanical bowel obstructions and only around 10% present as Bouveret syndrome. Case Description/Methods: A 77-year-old White woman with a past medical history of hypertension presented with emesis and 2 months of sharp, episodic back pain radiating to the left shoulder. Computed tomography showed inflammation at the gallbladder fossa with a large 2.8 cm stone eroding into the adjacent duodenum. Due to concerns of a cholecystoduodenal fistula the patient underwent endoscopic retrograde cholangiopancreatography (ERCP). On esophagogastroduodenoscopy (EGD), a large stone and 20 mm fistula from the gallbladder to the second portion of the duodenum were seen. The stone was fragmented and cleared using electrohydraulic lithotripsy (EHL) in 2 successive procedures. The distal duodenum was observed to be patent and the patient was discharged. Four days later the patient presented again with emesis. Computed tomography showed a gallstone in the distal ileum, a high-grade small bowel obstruction, and pneumobilia consistent with gallstone ileus. Exploratory laparotomy was performed and a 3 × 5 cm stone was found to have spontaneously passed into the rectosigmoid junction. No further interventions were indicated and the patient was discharged in a stable condition. Discussion: This case highlights the challenge the initial diagnosis of Bouveret syndrome and complications after treatment. Females over 60 years and a history of biliary disease are at highest risk. Symptoms lack specificity and can mimic more common causes of gastric outlet obstruction thus leading to diagnostic and management delays resulting in a high morbidity and mortality rate that is estimated to be 12-30%. Labs are non-specific and computed tomography remains the most reliable diagnostic modality. Bowel obstruction, aberrant gallstone, and pneumobilia seen on radiography (Rigler’s triad) strongly suggests Bouveret Syndrome. Recommended management with minimally invasive techniques via endoscopy has a lower mortality and morbidity rate compared to surgery but a comparatively reduced rate of success. As endoscopic treatment techniques and tools continue to improve, this disparity may be reduced. A high index of clinical suspicion is essential for timely diagnosis and intervention, thereby improving outcomes.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 56%
Biliary and Gastrointestinal Fistulas
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