Walędziak Maciej, Różańska-Walędziak Anna, Kowalewski Piotr K, Paśnik Krzysztof
Department of General, Oncological, Metabolic and Thoracic Surgery, Military Institute of Medicine, Warsaw, Poland.
2 Department of Obstetrics and Gynecology, Medical University of Warsaw, Warsaw, Poland.
Wideochir Inne Tech Maloinwazyjne. 2018 Jun;13(2):257-259. doi: 10.5114/wiitm.2018.72751. Epub 2018 Jan 16.
Intrahepatic cholangiocarcinoma is a rare type of biliary tract malignancy, seldom found resectable at diagnosis, the 5-year survival rate depending on the possibility of complete surgical excision. In most cases it is only accidentally found in the early stage. The report presents a case of a 58-year-old obese male patient qualified for laparoscopic Roux-en-Y gastric bypass. During general inspection of the abdominal cavity, a tumor of 10 mm in diameter was found in the second hepatic segment and resected. Final pathology results showed low-grade intrahepatic cholangiocarcinoma without vascular invasion, with positive margins of incision (R1), classified as stage I. The abdominal computed tomography scan showed no evidence of metastatic disease. Two months later the patient underwent a laparoscopic partial hepatectomy. Pathological investigation showed focal bile duct hamartoma with no signs of malignancy. No adjuvant therapy was administered and no recurrence has been found to date.
肝内胆管癌是一种罕见的胆道恶性肿瘤,在诊断时很少能发现可切除,其5年生存率取决于完全手术切除的可能性。在大多数情况下,它仅在早期偶然被发现。该报告介绍了一例58岁肥胖男性患者,符合腹腔镜Roux-en-Y胃旁路手术条件。在对腹腔进行常规检查时,在肝第二段发现一个直径10毫米的肿瘤并将其切除。最终病理结果显示为低级别肝内胆管癌,无血管侵犯,切缘阳性(R1),分类为I期。腹部计算机断层扫描显示无转移疾病迹象。两个月后,患者接受了腹腔镜肝部分切除术。病理检查显示为局灶性胆管错构瘤,无恶性迹象。未给予辅助治疗,迄今为止未发现复发。