Burns C D, Kuhns J G, Wieman T J
Department of Pathology and General Surgery, University of Louisville (Ky) School of Medicine.
Arch Pathol Lab Med. 1990 Dec;114(12):1287-9.
The rarity of cholangiocarcinoma occurring in von Meyenburg complexes is well appreciated. We describe the case of a 35-year-old man found to have cholangiocarcinoma in association with multiple biliary microhamartomas of the liver. Areas of ductal proliferation and atypia within the bile duct hamartomas suggest malignant transformation to cholangiocarcinoma.
胆管癌发生于梅耶堡复合体极为罕见，这一点已得到充分认识。我们报告一例35岁男性病例，该患者被发现患有胆管癌，同时伴有肝脏多发胆管微错构瘤。胆管错构瘤内的导管增生和异型性区域提示向胆管癌的恶性转化。
