Department of Digestive Surgery and Transplantation, Lille University Hospital, Rue Michel Polonovski, 59037, Lille, France.
University of Lille, Lille, France.
J Gastrointest Surg. 2021 Apr;25(4):1087-1088. doi: 10.1007/s11605-020-04851-9. Epub 2020 Nov 25.
Intraductal papillary neoplasm of the bile duct (IPNB) or biliary papillomatosis is a precursor lesion of papillary cholangiocarcinoma.1 IPNB is recognized as a biliary counterpart of IPMN (pancreatic intraductal papillary mucinous neoplasm). IPNB is a rare disease involving entire (diffuse type) or one part (localized type) of biliary tree. Patients without distant metastasis are considered for surgical resection. For patients with distal bile duct papillomatosis, pancreaticoduodenectomy (PD) is recommended for patients with invasive distal bile duct IPNB. PD is a high complex procedure associated with the deterioration of endocrine and exocrine functions leading to a significant impact on quality of life.2 Some authors have reported a new surgical approach leading to a complete resection of the common bile duct without pancreatectomy.3 METHODS: We report the case of a 71-year-old female presented to our department with jaundice. At endoscopic ultrasound with cholangioscopy and CT scan, 2-cm distal bile duct mass tumor with villous component was seen. All needle biopsies were benign, and no distant disease was found. According to the risk of degeneration of this tumor, a surgical resection was decided.
Intraoperative frozen section assessed the benignity of peripancreatic lymph nodes. We performed surgical ampullectomy with resection of the common bile duct. The intrapancreatic common bile duct was completely mobilized between the ampullectomy area and the upper edge of the pancreas. Frozen sections on distal and proximal margins of common bile duct were performed to discard malignancy. Finally, reconstruction consisted on the main pancreatic duct reimplantation to the duodenum and choledochoduodenostomy. The histological analysis confirmed the diagnosis of biliary papillomatosis with low-grade dysplasia.
This procedure allows complete resection of benign tumors with endobiliary extension and preserve intestinal continuity and pancreatic parenchyma.
胆管内乳头状肿瘤(IPNB)或胆管乳头状瘤病是乳头状胆管癌的前体病变。1 IPNB 被认为是胰腺内导管乳头状黏液性肿瘤(IPMN)的胆管对应物。IPNB 是一种罕见的疾病,涉及整个(弥漫型)或胆管的一部分(局灶型)。无远处转移的患者被认为适合手术切除。对于远端胆管乳头状瘤病患者,如果存在侵袭性远端胆管 IPNB,则推荐行胰十二指肠切除术(PD)。PD 是一种高复杂度的手术,与内分泌和外分泌功能的恶化相关,导致对生活质量产生重大影响。2 一些作者报告了一种新的手术方法,可实现胆总管的完全切除而无需行胰腺切除术。3 方法:我们报告了一例 71 岁女性的病例,因黄疸就诊于我科。在超声内镜下胆管镜和 CT 扫描中,可见远端胆管 2cm 肿块肿瘤,呈绒毛状成分。所有针吸活检均为良性,未发现远处疾病。根据该肿瘤退化的风险,决定进行手术切除。
术中冷冻切片评估了胰周淋巴结的良性。我们进行了胰管壶腹切除术和胆总管切除术。胰内胆总管在壶腹切除术区域和胰腺上缘之间完全游离。对胆总管远端和近端边缘进行冷冻切片检查,以排除恶性肿瘤。最后,重建包括主胰管再植入十二指肠和胆肠吻合术。组织学分析证实了胆管乳头状瘤病伴低级别异型增生的诊断。
该手术方法可实现伴胆管内延伸的良性肿瘤的完全切除,并保留肠道连续性和胰腺实质。