2026-05-10T08:12:18Z https://www.peertechzpublications.org/oai-pmh

oai:www.peertechzpublications.org:10.17352/2455-2968.000165 2024-10-17 PTZ.JSSR:VOL10

Rare Case Reports on Ectopic Liver Tissue: Incidence, Surgical Management, and Outcomes Mohamed Dheker Touati Ahmed Bouzid Wassim Romdhane Fahd Khefacha Med Raouf Ben Othmane Wassim Dziri Anis Belhadj Ahmed SaidaniFaouzi Chebbi<p>Introduction and importance: Ectopic liver tissue is a rare finding, often discovered incidentally during procedures like cholecystectomy. Understanding its clinical implications, including potential malignancy and complications, is crucial for effective management and improving patient outcomes.</p><p>Case presentation: A 45-year-old female presented with six months of biliary colic, worsened by fatty meals. Preoperative ultrasound revealed a gallbladder with microcalculi. During elective laparoscopic cholecystectomy, a brownish tissue fragment resembling hepatic parenchyma was found on the gallbladder fundus and removed. Histopathology confirmed ectopic liver tissue with mild steatosis and no malignancy.</p><p>Clinical discussion: Ectopic liver tissue, with a prevalence of 0.47%, typically attaches to the gallbladder but can also be found in other abdominal and thoracic locations. It may be linked to congenital malformations and has a risk of degeneration into malignancy due to its incomplete vascular and ductal system. Diagnosis is usually incidental during surgery, and en-bloc removal is advised to prevent complications and potential neoplastic transformation. Identifying its vascular supply before dissection is crucial to avoid severe bleeding.</p><p>Conclusion: Ectopic liver tissue, despite its rarity, requires careful management due to its potential for malignancy and complications. Timely detection and en-bloc removal are vital to prevent adverse outcomes and ensure optimal patient care.</p> Journal of Surgery and Surgical Research - Peertechz Publications 2024-10-17 Case Report https://doi.org/10.17352/2455-2968.000165 en Copyright © Mohamed Dheker Touati et al.