Almasaid Sharifeh, Suhail Fathima Keshia, Bensaadi Nesrine, Singh Kelita, Sapkota Bishnu
Department of Internal Medicine, State University of New York Upstate Medical University Hospital, Syracuse, NY.
Department of Internal Medicine, Division of Gastroenterology, State University of New York Upstate Medical University Hospital, Syracuse, NY.
ACG Case Rep J. 2025 Sep 15;12(9):e01829. doi: 10.14309/crj.0000000000001829. eCollection 2025 Sep.
Cholangiocarcinoma is a rare gastrointestinal malignancy with an annual incidence of 0.3 to 6 cases per 100,000, and, usually, it is reported as adenocarcinoma in about 95% of the cases. It can develop as a result of combination of genetic predispositions and various risk factors like but not limited to choledochal cysts, cholelithiasis/choledocholithiasis, yet its diagnosis is challenging due to difficulties in obtaining tissue for diagnosis. In this study, we present a challenging case in diagnosis that reveals undifferentiated carcinoma with osteoclast-like giant cells in the perihilar region of the bile duct.
胆管癌是一种罕见的胃肠道恶性肿瘤,年发病率为每10万人中有0.3至6例,通常约95%的病例报告为腺癌。它可能由遗传易感性和各种风险因素共同作用而发生,如但不限于胆总管囊肿、胆石症/胆总管结石症,然而由于难以获取用于诊断的组织,其诊断具有挑战性。在本研究中,我们展示了一例具有挑战性的诊断病例,该病例显示在胆管肝门周围区域存在具有破骨细胞样巨细胞的未分化癌。