Primary Neuroendocrine Tumor of Peripancreatic Lymph Node - A Rare Case Report

IF 0.1 Q4 GASTROENTEROLOGY & HEPATOLOGY Journal of the Pancreas Pub Date : 2021-01-01 DOI:10.36648/1590-8577.22.1.29-30
V. Hosdurg
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Abstract

Neuroendocrine tumors are a heterogenous group of tumors arising most commonly in the gastrointestinal tract and in the bronchus pulmonary tree. Other rare sites include parathyroid and adrenal glands. Peripancreatic lymph-node as a primary site for neuroendocrine tumor is extremely rare and no reports could be seen in literature. A thorough search of literature found a case report of a primary neuroendocrine tumor of the inguinal lymph-node. Reporting the case report of a 48year old man who presented with complains of epigastric pain and on evaluation found to have an exophytic tumor from the superior border of the body of pancreas. At surgery the tumor was found to be separate from the pancreas and was easily enucleated off the superior border of pancreas. Histopathology of the excised tumor showed features of an NET within a lymph-node. He was followed up closely and at 1year post operatively patient is asymptomatic and in good health.
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原发性胰周淋巴结神经内分泌肿瘤1例报告
神经内分泌肿瘤是一种异质性肿瘤,最常见于胃肠道和支气管肺。其他罕见的部位包括甲状旁腺和肾上腺。胰周淋巴结作为神经内分泌肿瘤的原发部位极为罕见,文献中未见报道。经过深入的文献检索,发现一例腹股沟淋巴结原发性神经内分泌肿瘤的报告。报告一例病例报告的48岁男子谁提出抱怨胃脘痛和评估发现有一个外生性肿瘤从胰腺体的上边界。手术时发现肿瘤与胰腺分离,很容易从胰腺上缘切除。切除肿瘤的组织病理学表现为淋巴结内网状瘤的特征。术后1年患者无症状,健康状况良好。
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来源期刊
Journal of the Pancreas
Journal of the Pancreas GASTROENTEROLOGY & HEPATOLOGY-
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