S5224 Case Report: Endoscopic Treatment of Bouveret Syndrome in a Nonagenarian: Overcoming Age-Related Challenges

Introduction: Bouveret syndrome is a rare type of gallstone ileus, characterized by gastric outlet obstruction caused by a gallstone lodged in the distal stomach or proximal duodenum. It results from chronic gallbladder inflammation leading to a biliary-enteric fistula. Typically, it presents with nonspecific symptoms, most commonly epigastric pain, nausea with abdominal pain and distention. The standard treatment involves a surgical procedure, though it carries a higher mortality rate. Bouveret syndrome accounts for only 1-3% of gallstone ileus cases, with just over 300 cases reported as of 2022. We report the first case in Puerto Rico of this pathology in a nonagenarian patient with classic symptomatology, further complicated by pre-existing conditions. Case Description: A 91-year-old woman with a history of Alzheimer’s disease, type 2 diabetes, hypertension, and cholecystitis presented to the emergency department with persistent diarrhea, nausea, and vomiting. Physical examination revealed severe malnutrition with right upper and lower quadrant pain. Laboratories showed leukocytosis (26.74 × 109/L) with normal liver function. Diagnosis of duodenal obstruction and gastroenteritis was established by imaging, revealing obstruction secondary to large gallstone formation, consistent with Bouveret syndrome. Given the patient's age and comorbidities, an endoscopic retrograde cholangiopancreatography (ERCP) was performed. During the exploratory part of the procedure, an impacted large gallstone (4.7 cm) was identified at the third portion of the duodenum. Removal of the gallstone with the use of endoscopic tools was unsuccessful. Laser lithotripsy was subsequently employed, fragmenting the stone into multiple large pieces. A significant amount of the gallstone fragments could not be removed. An abdominopelvic computed tomography was scheduled to revise their anatomical position. Imaging showed 2 significant gallstone fragments, located proximally and distally at the jejunum. Post-procedure course was uneventful. Discussion: Bouveret syndrome’s rarity highlights the importance of its awareness and early recognition, as a delayed treatment could lead to increased morbidity and mortality. Treatment strategies should be individualized to the patient’s clinical condition and comorbidities. In elderly patients, where surgery may pose significant risks, non-surgical options such as laser lithotripsy, a minimally invasive technique that fragments the gallstone with minimal risks to adjacent tissues, should be considered.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001148356.10237.71
Primary Topic
Biliary and Gastrointestinal Fistulas
Type
article
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article

S5224 Case Report: Endoscopic Treatment of Bouveret Syndrome in a Nonagenarian: Overcoming Age-Related Challenges

S. Rivera, Christopher G. Ortiz-Morales
The American Journal of Gastroenterology
Biliary and Gastrointestinal Fistulas
article

S5224 Case Report: Endoscopic Treatment of Bouveret Syndrome in a Nonagenarian: Overcoming Age-Related Challenges

S. Rivera, Christopher G. Ortiz-Morales
article en

Abstract

Introduction: Bouveret syndrome is a rare type of gallstone ileus, characterized by gastric outlet obstruction caused by a gallstone lodged in the distal stomach or proximal duodenum. It results from chronic gallbladder inflammation leading to a biliary-enteric fistula. Typically, it presents with nonspecific symptoms, most commonly epigastric pain, nausea with abdominal pain and distention. The standard treatment involves a surgical procedure, though it carries a higher mortality rate. Bouveret syndrome accounts for only 1-3% of gallstone ileus cases, with just over 300 cases reported as of 2022. We report the first case in Puerto Rico of this pathology in a nonagenarian patient with classic symptomatology, further complicated by pre-existing conditions. Case Description: A 91-year-old woman with a history of Alzheimer’s disease, type 2 diabetes, hypertension, and cholecystitis presented to the emergency department with persistent diarrhea, nausea, and vomiting. Physical examination revealed severe malnutrition with right upper and lower quadrant pain. Laboratories showed leukocytosis (26.74 × 109/L) with normal liver function. Diagnosis of duodenal obstruction and gastroenteritis was established by imaging, revealing obstruction secondary to large gallstone formation, consistent with Bouveret syndrome. Given the patient's age and comorbidities, an endoscopic retrograde cholangiopancreatography (ERCP) was performed. During the exploratory part of the procedure, an impacted large gallstone (4.7 cm) was identified at the third portion of the duodenum. Removal of the gallstone with the use of endoscopic tools was unsuccessful. Laser lithotripsy was subsequently employed, fragmenting the stone into multiple large pieces. A significant amount of the gallstone fragments could not be removed. An abdominopelvic computed tomography was scheduled to revise their anatomical position. Imaging showed 2 significant gallstone fragments, located proximally and distally at the jejunum. Post-procedure course was uneventful. Discussion: Bouveret syndrome’s rarity highlights the importance of its awareness and early recognition, as a delayed treatment could lead to increased morbidity and mortality. Treatment strategies should be individualized to the patient’s clinical condition and comorbidities. In elderly patients, where surgery may pose significant risks, non-surgical options such as laser lithotripsy, a minimally invasive technique that fragments the gallstone with minimal risks to adjacent tissues, should be considered.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 42%
Biliary and Gastrointestinal Fistulas
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