Cavalcanti Elisabetta, Stasi Elisa, Coletta Sergio, Lorusso Dionigi, Rinaldi Caterina Mammone, Armentano Raffaele
National Institute of Gastroenterology "S. de Bellis", Research Hospital Castellana Grotte Bari, Via Turi 27, 70013 Castellana Grotte (Ba), Bari, Italy.
World J Surg Oncol. 2020 Apr 28;18(1):80. doi: 10.1186/s12957-020-01860-5.
Gastrinoma is a rare form of neuroendocrine neoplasm. The presence of a primary lymph node localization of gastrinoma is a much debated and controversial topic in the literature, as regards whether these cases represent metastatic disease from an as yet unidentified primary tumor, or the de novo occurrence of a gastrinoma in a lymph node.
We report the case of a 24-year-old male with intense epigastric pain treated at the beginning with high dose proton pump inhibitors. Further workup with CT and subsequent laparotomy revealed a single peripancreatic lymph node. Histological examination highlighted a well-differentiated neuroendocrine tumor.
This case underlines that the primitive lymph node gastrinoma is a distinct nosological entity with a precise location in the context of rare neuroendocrine tumors that should be considered when specific symptoms are associated with the identification of isolated lymph nodes, after excluding any possible primitive locations of neoplastic localization.
胃泌素瘤是一种罕见的神经内分泌肿瘤。胃泌素瘤原发性淋巴结定位的存在在文献中是一个备受争议的话题,涉及这些病例是代表来自尚未明确的原发性肿瘤的转移性疾病,还是淋巴结中胃泌素瘤的新发。
我们报告一例24岁男性,有剧烈上腹部疼痛,最初用高剂量质子泵抑制剂治疗。进一步的CT检查及随后的剖腹手术发现一个胰腺周围淋巴结。组织学检查显示为高分化神经内分泌肿瘤。
该病例强调原发性淋巴结胃泌素瘤是一种独特的疾病实体,在罕见的神经内分泌肿瘤中具有精确的定位,当出现特定症状并发现孤立淋巴结时,在排除肿瘤定位的任何可能原发部位后应予以考虑。