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Mirizzi syndrome, although rare, is a potential complication of long-standing gallstone disease, particularly cholecystolithiasis. Due to the nonspecific nature of its symptoms, this condition often remains undiagnosed prior to surgery in most cases. While minimally invasive approaches are generally safe in expert hands, they can be challenging and entail the risk of bile duct injuries, often necessitating conversion to bail-out procedures. Delayed management of Mirizzi syndrome can lead to serious consequences, such as empyema of the gallbladder (GB), gangrene of the GB wall, perforation, and sepsis. Intraoperative indocyanine green fluorescence imaging during laparoscopic cholecystectomy can help delineate the biliary anatomy and prevent biliary tract injuries in difficult GBs like Mirizzi syndrome.
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http://dx.doi.org/10.7759/cureus.68465 | DOI Listing |
Cureus
August 2025
General and Colorectal Surgery, Mediclinic Parkview Hospital, Dubai, ARE.
While various biliary anomalies have been documented in the literature, their occurrence in clinical practice is uncommon. Common anomalies encountered in practice include variations in cystic duct insertion (such as low or medial insertion), accessory hepatic ducts, and aberrant right hepatic ducts. Less commonly, clinicians may encounter double cystic ducts, duplicated gallbladders, or rare configurations associated with conditions like Mirizzi syndrome.
View Article and Find Full Text PDFWorld J Clin Cases
October 2025
Department of Surgery, Good Samaritan Hospital, Mt Vernon, IL 62864, United States.
Background: Mirizzi syndrome is a rare complication of chronic gallstone disease in which an impacted stone causes compression or erosion of the common hepatic duct. Accurate preoperative diagnosis is crucial but often challenging. We report a case that was preoperatively diagnosed as type 1 Mirizzi syndrome but was found intraoperatively to be type 4, involving a cholecysto-biliary fistula and complete erosion of the common hepatic duct.
View Article and Find Full Text PDFJ Gastrointest Surg
August 2025
Division of Endocrine and Oncology Surgery, Department of Surgery, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA, United States. Electronic address:
Background: Mirizzi syndrome (MS) is a rare cause of biliary obstruction. Historically, malignancy was reported in a subset of MS cases, but previous studies predated modern imaging and routine endoscopic retrograde cholangiopancreatography. This study aimed to determine the prevalence of malignancy in contemporary patients with MS and assess whether modern imaging reliably distinguishes benign from malignant cases.
View Article and Find Full Text PDFInt J Surg Case Rep
September 2025
General Surgery Department, Hospital Professor Doutor Fernando da Fonseca, Lisboa, Portugal.
Introduction: Mirizzi syndrome is a rare complication of biliary lithiasis, resulting from a chronic inflammatory process caused by the compression exerted by a stone lodged in the Hartmann's pouch. Management to a Mirizzi syndrome presents a significant surgical challenge.
Case Presentation: We report a case of an 83-year-old female patient with recurrent episodes of obstructive jaundice and uncomplicated cholangitis, ultimately diagnosed with a Mirizzi Syndrome and a cholecistobiliary fistula following endoscopic retrograde cholangiopancreatography (ERCP).
Cureus
July 2025
Department of Gynecology and Obstetrics, University Clinical Centre Ljubljana, Ljubljana, SVN.
Background Acute cholecystitis (AC) is a frequent surgical emergency associated with significant variability in clinical outcomes and hospital length of stay (LOS). Early identification of patients at risk for prolonged hospitalization can improve triage and resource planning. Inflammatory markers such as C-reactive protein (CRP), white blood cell count (WBC), and total bilirubin (TBil), along with biliary complications like choledocholithiasis and Mirizzi syndrome, may have prognostic value.
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