Weiler H, Grandel A, Frühmorgen P
Medizinische Klinik I, Schwerpunkt Gastroenterologie/Hepatologie, Klinikum Ludwigsburg.
Ultraschall Med. 2003 Jun;24(3):197-201. doi: 10.1055/s-2003-40061.
We report a case of congenital cystic dilatation of the cystic duct detected in a 40-year-old woman. She had intermittent pain in the right upper quadrant of the abdomen independent of the intake of meals for the last two years. In the ultrasound we found a cystic formation in the vicinity of the enlarged gallbladder, the common hepatic duct/common bile duct and the portal vein. The endoscopic retrograde cholangiography confirmed a cystic duct malformation, which was associated with an anomalous pancreaticobiliary ductal junction (APBDJ). A cholecystectomy with excision of the whole cystic duct and common bile duct and Roux-en-Y hepaticojejunostomy is indicated because there is an increased risk of the development of bile duct cancer and gallbladder cancer in the presence of biliary cystic duct anomalies and APBDJ.
我们报告一例在一名40岁女性中检测到的先天性胆囊管囊状扩张病例。在过去两年里,她右上腹间歇性疼痛,与进食无关。超声检查发现,在肿大的胆囊、肝总管/胆总管及门静脉附近有一囊性结构。内镜逆行胰胆管造影证实为胆囊管畸形,且伴有胰胆管合流异常(APBDJ)。鉴于存在胆管囊肿性胆囊管异常及APBDJ时胆管癌和胆囊癌发生风险增加,建议行胆囊切除术,切除整个胆囊管和胆总管,并进行Roux-en-Y肝空肠吻合术。