Radiological Findings in Biliary Fistula and Gallstone Ileus

1996 ◽  
Vol 37 (3P2) ◽  
pp. 917-922 ◽  
Author(s):  
H. Oikarinen ◽  
M. Päivänsalo ◽  
T. Tikkakoski ◽  
A. Saarela

Purpose: Biliary fistula and gallstone ileus are rarely found. The diagnosis is difficult and may be delayed until operation. We reviewed the radiological findings in a retrospective material. Material and Methods: The cases of 16 patients treated for biliary fistula were analyzed with respect to findings at imaging. Ten patients had a spontaneous fistula. Nine of them had an internal bilioduodenal fistula and one had an external fistula with stones passing through a subcutaneous abscess. Five patients also had gallstone ileus and one patient a rare gastric outlet obstruction caused by a gallstone (Bouveret's syndrome). Six patients had an iatrogenic fistula. One of them had internal bile ascites and 5 an external fistula, one of which was a biliocystic fistula resulting from attempted hepatic cyst sclerotherapy. Results: Various imaging modalities were used and there was often a delay in the diagnosis. Imaging did not show the fistula itself in any of the spontaneous cases. However, a nonvisualized or shrunken gallbladder seen at US often coexisted in these cases. CT yielded the diagnosis in one case of gallstone ileus, and a Gastrografin meal yielded it in the case of Bouveret's syndrome. Fistulography and cholangiography provided a correct diagnosis of fistula in all cases of iatrogenic biliocutaneous fistulas. Conclusion: Patients with biliary fistula usually undergo examinations with nonspecific results. The imaging findings could be more specific if the possibility of this diagnosis were remembered.

2021 ◽  
Vol 2021 ◽  
pp. 1-6
Author(s):  
Yuqian Tian ◽  
Neha Sarvepalli ◽  
Mustafa Nazzal

Bouveret’s syndrome refers to a gastric outlet obstruction secondary to impaction of a gallstone in the pylorus or proximal duodenum. Thus, it can be considered a very proximal form of gallstone ileus and is infrequent. We describe such a unique case that a female patient presents with Bouveret’s syndrome and concomitant common bile duct obstruction by a second gallstone. The decision over its surgical management is complicated, based on risk factors, clinical presentations, radiographic evidence, surgical risk assessment, and specific considerations tailored to individual case. Because of her stable clinical picture and low surgical risk, we proceeded with stone extractions, fistula take-down, and common bile duct exploration in a one-stage procedure. Her postoperative course was complicated by bile stained drainage through closed suction drain that resolved with conservative management.


2020 ◽  
Vol 33 (5) ◽  
pp. 347
Author(s):  
Rita Peixoto ◽  
Joana Correia ◽  
Mário Guimarães Soares ◽  
António Gouveia

Bouveret’s syndrome is a rare cause of gastric outlet obstruction. We report a case of a 68-year-old woman admitted with upper digestive obstruction. A few months later, and after several diagnostic tests and clinical surveillance, a cholecystoduodenal fistula was suspected. During exploratory laparotomy, the diagnosis of Bouveret’s syndrome was confirmed and a pyelolithotomy, pyloroplasty and a cholecystectomy were performed. The patient was asymptomatic 7 months after the operation. This syndrome represents only 1% - 3% of all cases of gallstone ileus, being more frequent in women and in the elderly. The presentation is quite nonspecific, but in most cases the symptomatology suggests an upper digestive occlusion. Treatment can be achieved by lithotripsy, but most patients require a surgical approach.


2016 ◽  
Vol 54 (201) ◽  
pp. 33-35 ◽  
Author(s):  
Mukul Bhattarai ◽  
Pardeep Bansal ◽  
Bharat Patel ◽  
Alexander Lalos

Bouveret’s syndrome is an unusual cause of gastric outlet obstruction secondary to gallstone impaction. It is so rare that it is commonly missed in clinical practice if it is not considered in differential diagnoses of intestinal obstruction more specifically in man who does not report the history of gall stone. Furthermore, there are no definitive guidelines on approach and management of this condition. We present a seventy eight year old man who developed acute abdominal symptoms due to impaction of a gallstone in the duodenum. He did not have history of gall stone. The diagnosis was supported via CT abdomen and Endoscopy. The patient was successfully managed by exploratory laparotomy followed by anterior pylorotomy to remove the stone without cholecystectomy and fistula repair. Keywords: Bouveret’s syndrome; cholelithiasis; enterolithotomy; Gallstone ileus. | PubMed


2006 ◽  
Vol 106 (4) ◽  
pp. 438-440 ◽  
Author(s):  
A. Sakarya ◽  
M.Y. Erhan ◽  
H. Aydede ◽  
E. Kara ◽  
M. Ozkol* ◽  
...  

2020 ◽  
Vol 50 (4) ◽  
pp. 383-385
Author(s):  
Rinkal B Kakadiya ◽  
Uttam Thakur ◽  
Lileshwar Kaman ◽  
Harshal S Mandavdhare

One of the rare complications of cholelithiasis is gallstone ileus which occurs in <5% of patients. Among them, <3% develop Bouveret’s syndrome: gastric outlet obstruction by a large gallstone in the pylorus or duodenum. One large review of 128 patients showed it to present at a mean age of 74.1 ± 11.1 years with a mean gallstone size of 4.6 ± 1.5 cm, with nausea or vomiting in 86%, abdominal pain in 71% and haematemesis in 15%. The diagnosis is usually clear on oesophagogastroduodenoscopy or abdominal contrast-enhanced computed tomography. We present a case with massive upper gastrointestinal bleeding, due to erosion of a cystic artery pseudoaneurysm.


2006 ◽  
Vol 4 (4) ◽  
pp. 0-0
Author(s):  
Lina Praleikienė ◽  
Marius Paškonis ◽  
Jonas Jurgaitis ◽  
Eligijus Poškus ◽  
Kęstutis Strupas

Lina Praleikienė, Marius Paškonis, Jonas Jurgaitis, Eligijus Poškus, Kęstutis StrupasVilniaus universiteto ligoninės Santariškių klinikų Pilvo chirurgijos centras,Santariškių g. 2, LT-08661 VilniusEl paštas: [email protected] Bouveret sindromas – skrandžio turinio slinkimo sutrikimas, kurio priežastis – didelis akmuo, patekęs į dvylikapirštę žarną per biliogastrinę ar bilioduodeninę fistulę. Straipsnyje aprašomas Vilniaus universiteto ligoninės Santariškių klinikose gydytas ligonis, kuriam diagnozuotas Bouveret sindromas – tulžies pūslės akmenys pragulėjo dvylikapirštės žarnos serozinį dangalą, raumeninį sluoksnį ir gleivinę, tačiau į dvylikapirštės žarnos spindį dar nebuvo patekę. Bouveret sindromas įtartas sonoskopijos ir kompiuterinės tomografijos tyrimais, patvirtintas atliekant cholecistektomiją ir piloroplastiką. Pateikiama literatūros apžvalga: diagnostikos problemos, instrumentinių tyrimų nauda ir gydymo būdai. Reikšminiai žodžiai: Bouveret sindromas, tulžies pūslės akmenligė, žarnų nepraeinamumas Bouveret’s syndrome: clinical case and review of the literature Lina Praleikienė, Marius Paškonis, Jonas Jurgaitis, Eligijus Poškus, Kęstutis Strupas.Vilnius University Hospital Santariškių Klinikos, Centre of Abdominal Surgery,Santariškių 2, LT-08661 Vilnius, LithuaniaE-mail: [email protected] Bouveret’s syndrome is described as gastric outlet obstruction caused by a large gallstone passing into duodenal bulb through a biliogastric or bilioduodenal fistula. We describe a clinical case of the forming Bouveret syndrome – the gallstones had separated serous, muscular and mucose layers of the duodenum, but did not enter the lumen of it. Bouveret’s syndrome was diagnosed by ultrasound and computed tomography and treated by cholecystectomy and pyloroplasty. Various symptoms, diagnostic and treatment approaches are discussed. Key words: Bouveret’s syndrome, cholecystitis, gallstone ileus


2012 ◽  
Vol 2012 ◽  
pp. 1-4
Author(s):  
Ayşegül Solmaz Tuncer ◽  
Safiye Gürel ◽  
Zeliha Coşgun ◽  
Ahmet Büber ◽  
Rıdvan Çakmaz ◽  
...  

The purpose of this paper is to present sonographic and CT imaging findings of xanthogranulomatous cholecystitis (XGC) presented as Bouveret’s syndrome, a very rare cause of gastric obstruction. While the patient’s physical examination, upper GI endoscopy, and radiological findings all pointed to Bouveret’s syndrome, CT differential diagnosis suggested either XGC or gallbladder carcinoma, and the final diagnosis was done histopathologically. Our paper aims to increase awareness in radiologically diagnosing XGC cases by introducing the possibility of existence of Bouveret’s syndrome.


2015 ◽  
Vol 19 (6) ◽  
pp. 1189-1191 ◽  
Author(s):  
Justin George ◽  
David D. Aufhauser ◽  
Steven E. Raper

2021 ◽  
Author(s):  
Fraser Hugh Simpson ◽  
Andrew Beatty ◽  
Michael Auld ◽  
Andrew Phillip Maurice ◽  
Manju D. Chandrasegaram

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