Primary neuroendocrine tumour of the extrahepatic biliary duct.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Sarah Fennelly, Basilie Teoh, Jyothirmayi Velaga, Nezor Houli
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引用次数: 0

Abstract

Neuroendocrine tumours of the extrahepatic bile ducts are extremely rare, accounting for only 0.2-2% of gastrointestinal tract neuroendocrine neoplasms. Here, we present an incidental finding of this rare tumour, identified during staging scans post-resection of a malignant rectosigmoid polyp and treated with resection and biliary reconstruction. A suspicious, arterially enhancing porta hepatis lymph node was identified on CT and further investigated with liver MRI and 68Ga DOTATATE PET. These revealed a lobulated lesion of the hilum which showed marked avidity without metastases. The patient underwent a successful radical resection of the extrahepatic biliary ducts (including the left, right and common hepatic ducts), the common bile duct and hepaticojejunostomy formation. Histology revealed a 20-mm well-differentiated NET, WHO Grade 2. Two years later, the patient is alive and well without recurrence. This fascinating case illustrates the importance of thorough preoperative planning of surgical resection for tumours at an unusual primary site.

肝外胆管原发性神经内分泌肿瘤。
肝外胆管神经内分泌肿瘤极为罕见,仅占胃肠道神经内分泌肿瘤的 0.2-2%。在这里,我们介绍一个偶然发现的罕见肿瘤,该肿瘤是在切除恶性直肠乙状结肠息肉后进行分期扫描时发现的,并通过切除和胆道重建进行了治疗。CT 发现了一个可疑的、动脉增强的肝门淋巴结,并进一步进行了肝脏 MRI 和 68Ga DOTATATE PET 检查。检查结果显示,肝门淋巴结呈分叶状病变,淋巴结明显增大,但无转移。患者成功接受了肝外胆管(包括左、右和肝总管)、胆总管根治性切除术,并形成了肝空肠吻合术。组织学检查发现了一个 20 毫米的分化良好的 NET,WHO 2 级。两年后,患者仍健在,没有复发。这个精彩的病例说明,对原发部位不常见的肿瘤进行手术切除时,必须进行周密的术前规划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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