Silent neuroendocrine tumor of biliary confluence

Supreet Kumar, Rigved Gupta, Neerav Goyal, A. Pandey, Vivek Tandon
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Abstract

Neuroendocrine tumors (NETs) of the extrahepatic bile ducts are extremely rare. They are heterogeneous entities of varied histopathological features. The pathological types vary greatly with regards to biological behavior and prognosis. We presented such a case of silent tumor of the biliary tract of neuroendocrine origin in a middle-aged female with nonspecific abdominal pain without any clinically obvious signs which on radiological imaging revealed a tumor of hepatic confluence with metastatic deposits in liver for which she underwent left trisectionectomy with segment 7 metastatectomy. As per the literature reviews regarding extrahepatic bile duct NET these tumors are more common in the middle age population with a female preponderance. The tumors were symptomatic in majority of patients and the symptoms are mostly related to tumor mass and its invasion of adjacent structures or metastases rather than hormone and vasoactive peptide secretions. The low incidence and uncommon modes of presentation makes the diagnosis tough and management challenging.
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胆道汇合处无声神经内分泌肿瘤
肝外胆管神经内分泌肿瘤(NET)极为罕见。它们是具有不同组织病理学特征的异质性实体。这些病理类型在生物学行为和预后方面差异很大。我们接诊了这样一例神经内分泌源性胆道沉默肿瘤患者,患者为一名中年女性,无特异性腹痛,无任何临床明显体征,放射影像学检查显示为肝汇合部肿瘤,肝内有转移性沉积物,为此她接受了左侧三段胆管切除术和第7段转移灶切除术。根据有关肝外胆管 NET 的文献综述,这些肿瘤在中年人群中更为常见,且女性居多。大多数患者无症状,症状主要与肿瘤肿块及其对邻近结构的侵犯或转移有关,而不是与激素和血管活性肽分泌有关。由于发病率低且表现方式不常见,因此诊断和治疗都很困难。
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