Development of bile duct bezoars following cholecystectomy caused by choledochoduodenal fistula formation: a case report
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The formation of bile duct bezoars is a rare event. Its occurrence when there is no history of choledochoenteric anastomosis or duodenal diverticulum constitutes an extremely scarce finding.
We present a case of obstructive jaundice, caused by the concretion of enteric material (bezoars) in the common bile duct following choledochoduodenal fistula development. Six years after cholecystectomy, a 60-year-old female presented with abdominal pain and jaundice. Endoscopic retrograde cholangiopancreatography demonstrated multiple filling defects in her biliary tract. The size of the obstructing objects necessitated surgical retrieval of the stones. A histological assessment of the objects revealed fibrinoid materials with some cellular debris. Post-operative T-tube cholangiography (9 days after the operation) illustrated an open bile duct without any filling defects. Surprisingly, a relatively long choledochoduodenal fistula was detected. The fistula formation was assumed to have led to the development of the bile duct bezoar.
Bezoar formation within the bile duct should be taken into consideration as a differential diagnosis, which can alter treatment modalities from surgery to less invasive methods such as more intra-ERCP efforts. Suspicions of the presence of bezoars are strengthened by the detection of a biliary enteric fistula through endoscopic retrograde cholangiopancreatography. Furthermore, patients at a higher risk of fistula formation should undergo a thorough ERCP in case there is a biliodigestive fistula having developed spontaneously.
KeywordsBile Duct Common Bile Duct Obstructive Jaundice Extrahepatic Bile Duct Ascariasis
The recurrence of obstructive jaundice after cholecystectomy is estimated to occur in one to seven per cent of all cholecystectomy cases [1, 2, 3, 4]. Symptoms may be due to retained stones which were unrecognized at the time of the initial operation, the development of a bile duct stricture or the presence of a long cystic duct remnant. Furthermore, parasitic infections of the hepatobiliary system, such as fascioliasis and ascariasis, account for other rare causes of recurrent bile duct obstructions, which may mimic the choledocholithiasis picture [5, 6, 7, 8, 9].
We present another cause of cholestatic jaundice, not commonly considered in differential diagnoses: the obstruction of the extrahepatic bile ducts by the concretions of fibrinoid materials (biliary bezoars), attributed to the existence of a fistula between the duodenum and the bile duct.
The patient is a 60-year-old Iranian female referred to our hospital with several-weeks history of abdominal pain, severe pruritus, yellow sclera, light-colored stool, and nausea and vomiting. In addition to fever and chills, she reported intermittent episodes of sustained abdominal pain in the past two months, which worsened by meals and radiating to the right-scapular area. Six years previously, she had undergone cholecystectomy without choledochoenteric anastomosis for symptomatic cholelithiasis.
The patient was a known case of rheumatoid arthritis and diabetes mellitus, her medications consisting of insulin, prednisolone, chloroquine and methotroxate.
On admission, the patient had a temperature of 38.5 C and was noted to have icteric sclera. A right upper quadrant scar was seen on her abdomen. The patient's abdomen was soft and non-distended with normal bowel sounds, albeit tender to deep palpation in the epigastrium and the right upper quadrant. There was no evidence of rebound tenderness or peritoneal signs.
Laboratory data on admission were notable for an elevated total bilirubin of 7.1 mg/dl (nl 0.2–1.1); direct bilirubin of 4.7 mg/dl (nl up to 0.5); alkaline phosphatase of 1217 IU/L (nl 64–306); SGOT of 78 U/L (nl 5–40); and SGPT of 185 U/L (nl 5–40). The total white blood cell count was 10,800 /cmm; prothrombin time was 13 second (nl 10–13) and the c-reactive protein was 2+.
A histological assessment of the objects removed revealed fibrinoid materials with some cellular debris. The patient remained well during the one-year follow-up.
This report describes a case of cholestatic jaundice caused by concretions of fibrinoid materials obstructing the extrahepatic bile ducts (biliary bezoars). It is noteworthy that there is a paucity of information regarding the formation of the biliary tract bezoar.
The first case report of bezoar-induced obstructive jaundice dates back to 1989, in which Seyrig JA et al. reported a case of cholestasis caused by an intradiverticular bezoar . The second case report (1993) is about a brown pigment gallstone, having formed around a phytobezoar without spontaneous biliary enteric fistula . Lamotte M et al. (1995) described the development of a biliary phytobezoar 15 years after surgical cholecystogastrostomy . In another study, gallstones containing surgical suturing material were found in a number of patients who had undergone a previous cholecystectomy .
The formation of the fistula, detected accidentally through post-operative cholangiography, is believed to be the cause of bezoar development in the present study.
Induced by intra-enteric materials transmitted through long fistulae, bezoar formation should be considered as an extremely rare differential diagnosis for obstructive jaundice since it is not normally associated with such relatively common predisposing factors as choledochoenteric anastomosis or duodenal diverticulum The ability of ERCP in detecting fistulae in a case of obstructive jaundice helps less invasive measures (more intra-ERCP views and efforts) outweigh surgery. The detection of biliodigestive fistulae in obstructive jaundice patients requires a thorough ERCP. Moreover, when the macroscopic characteristics of the stones resemble those of bezoar material, it is expedient that surgeons allocate more time and effort to detecting and ligating the possible fistula. We hope that this case report of fistula formation with subsequent bezoar production and obstructive jaundice will raise the awareness of gastroenterologists and surgeons about such an interesting phenomenon.
Thanks are due to our patient for having granted us written consent for publishing her clinical details, cholangiography and bezoar material photographs.
The authors would also like to thank Dr. Ali A. Kashani and Dr. Pedram Amouzadeh for their assistance in grammatical revision of our manuscript.
We would like to extend particular thanks to Dr. Hosein Ghofrani and Dr. Mehdi Rashighi Firoozabadi for their invaluable advice.
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-230X/6/1/prepub
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