Abstract
The treatment of Bouveret syndrome lacks specific guidelines and is strictly interdisciplinary. Especially, if electrohydraulic lithotripsy is not available and endoscopic removal fails, a timely surgical approach is advised.
Keywords: bouveret syndrome, endoscopy, gastrointestinal surgery, fistula, gastric outlet obstruction
The treatment of Bouveret syndrome lacks specific guidelines and is strictly interdisciplinary. Especially, if electrohydraulic lithotripsy is not available and endoscopic removal fails, a timely surgical approach is advised.

Bouveret syndrome is a difficult clinical entity to diagnose and treat, characterized by high morbidity and mortality. This syndrome should be promptly considered in case of symptomatic cholelithiasis complicated by intestinal obstruction, in order to define the proper individualized treatment, endoscopic or surgical, without a therapeutic delay.
A 65‐year‐old woman with symptomatic cholelithiasis, waiting for elective cholecystectomy, presented with abdominal pain, fever, and vomiting. An emergent abdominal CT showed a cholecystoduodenal fistula and a 4 cm calcific gallstone in the duodenum, determining gastric ectasia due to gastric outlet obstruction (Figure 1).
FIGURE 1.

Abdominal CT showing a 4 cm gallstone in the duodenal lumen
EGDS confirmed the presence of an impacted stone in the duodenal bulb, leading to the diagnosis of Bouveret syndrome. 1 Several attempts to fragment and remove the biliary calculus were made using foreign body forceps, polypectomy snare, mechanical lithotriptor, and Fogarty catheter, all resulting unsuccessful due to the size, location, and hard consistency of the gallstone (Figure 2). Electrohydraulic lithotripsy could not be attempted, as this technique was not available in our institution. As the clinical condition determined occlusion and treatment could not be delayed, the patient underwent surgical laparoscopic duodenotomy with removal of the impacted calculus. 2 In postoperative day 3, a radiological follow‐through showed regular progression of gastrografin in the small bowel, with retrograde opacification of the biliary tree through the fistula (Figure 3). Eighteen months after surgery, the patient is fine and asymptomatic.
FIGURE 2.

A, Gallstone in the duodenal bulb, seen through the pylorus; B, endoscopic attempts with accessories to remove the gallstone
FIGURE 3.

Small‐bowel follow‐through with retrograde opacification of the biliary tree
CONFLICT OF INTEREST
The authors have no conflict of interest to declare.
AUTHOR CONTRIBUTION
PCV: conceptualized the study, wrote the original manuscript, prepared the draft, and edited the manuscript. FG: conceptualized the study and edited the manuscript. MLG: edited the manuscript. RDV: supervised the study. GLdA: supervised the study.
ETHICAL APPROVAL
Informed consent was obtained from the patient for this report.
ACKNOWLEDGMENTS
None.
Cortegoso Valdivia P, Le Grazie M, Gaiani F, Dalla Valle R, de'Angelis GL. Bouveret syndrome in a cholecysto‐duodenal fistula. Clin Case Rep. 2021;9:2485–2486. 10.1002/ccr3.3958
DATA AVAILABILITY STATEMENT
Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.
REFERENCES
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.
