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Adenomas involving the extrahepatic biliary tree are rare but have an aggressive clinical course

机译:涉及肝外胆道树的腺瘤很少见但具有侵袭性的临床病程

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摘要

Biliary adenomas that are usually found in surgically removed gallbladders are rare, but can also occur in the extrahepatic biliary tree. We present a case series of extrahepatic bile duct adenomas at our institution, along with a review of the literature. All three patients with extrahepatic biliary adenomas (two in the common bile ducts, one in the hepatic duct) were female with a mean age of 74 years. On initial presentation, none of the patients had obstructive jaundice but two of the three patients had symptoms of biliary origin. Case 1 is an 85-year-old woman with an incidental biliary dilation seen on chest imaging; endoscopic ultrasound revealed a sessile adenomatous polyp in the distal bile duct. The patient refused surgery and presented with occlusive biliary stricture and jaundice 5 months after initial presentation, with cytology confirming malignant progression. Case 2 is a 78-year-old woman with a history of primary sclerosing cholangitis and who presented with cholangitis, and Gram-negative sepsis. A polypoid lesion was seen on imaging in the common hepatic duct and direct cholangioscopy with biopsies confirmed the presence of adenoma with high grade dysplasia. The patient underwent successful total bile duct resection and hepaticojejunostomy but represented 1 year later with diffuse metastatic disease to the bone, liver, and peritoneum. Case 3 is a 61-year-old woman who presented with symptoms suggestive of gallbladder pathology and was found to have a polypoid bile duct lesion on intraoperative cholangiogram. Endoscopic retrograde cholangioscopy showed an adenomatous polyp with high grade dysplasia involving the distal common bile duct. The patient underwent distal bile duct resection with choledochojejunostomy but presented with jaundice 4 years after surgery. She was found to have adenocarcinoma involving the small bowel in the Roux limb of jejunum and transverse colon. All three patients in our series presented with interval gastrointestinal malignancy and we therefore recommend aggressive surgical intervention and close postoperative surveillance when diagnosis of extrahepatic bile duct adenoma is made.
机译:通常在手术切除的胆囊中发现的胆道腺瘤很少见,但也可能发生在肝外胆道树中。我们在我们的机构介绍了一系列肝外胆管腺瘤病例,并对文献进行了回顾。所有三例肝外胆腺瘤患者(胆总管两例,肝管一例)均为女性,平均年龄为74岁。最初就诊时,无一例患者发生阻塞性黄疸,但三例患者中有两例出现胆源性症状。病例1是一名85岁的女性,在胸部影像学检查中发现胆管偶然性扩张;内镜超声检查发现远端胆管有无蒂腺瘤性息肉。初次就诊后5个月,患者拒绝手术并出现闭塞性胆管狭窄和黄疸,细胞学检查证实其恶性进展。病例2是一名78岁的女性,有原发性硬化性胆管炎的病史,并出现胆管炎和革兰氏阴性败血症。在肝总管成像中发现息肉样病变,活检直接胆道镜检查证实存在高度不典型增生的腺瘤。该患者成功进行了全胆管切除术和肝空肠吻合术,但一年后又出现了骨,肝和腹膜弥漫性转移病。病例3是一名61岁的女性,其症状表现为胆囊病理,并在术中胆管造影上发现息肉样胆管病变。内镜逆行胆管镜检查发现腺瘤性息肉伴远端胆总管严重增生。该患者接受了胆总管空肠吻合术的远端胆管切除术,但术后4年出现了黄疸。发现她患有空肠Roux肢和横结肠结肠小肠腺癌。我们系列中的所有三名患者均表现为间歇性胃肠道恶性肿瘤,因此,当诊断出肝外胆管腺瘤时,我们建议采取积极的外科手术干预措施并进行密切的术后监测。

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