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Clin Endosc. 2017 Nov;50(6):520-529. doi: 10.5946/ce.2017.181. Epub 2017 Nov 30.
2
[Analysis of primary site and pathology on 903 patients with neuroendocrine neoplasms].903例神经内分泌肿瘤患者的原发部位及病理分析
Zhonghua Wei Chang Wai Ke Za Zhi. 2017 Sep 25;20(9):993-996.
3
Clinicopathological features and surgical outcomes of neuroendocrine tumors of ampulla of Vater.壶腹神经内分泌肿瘤的临床病理特征及手术结果
BMC Gastroenterol. 2017 May 31;17(1):70. doi: 10.1186/s12876-017-0630-9.
4
Clinicopathologic study of neuroendocrine tumors of gastroenteropancreatic tract: a single institutional experience.胃肠道胰腺神经内分泌肿瘤的临床病理研究:单机构经验
J Gastrointest Oncol. 2017 Feb;8(1):139-147. doi: 10.21037/jgo.2016.12.08.
5
Report of two cases of large cell neuroendocrine carcinoma of duodenal ampulla with contrasting outcomes following pancreaticoduodenectomy according to the use of adjuvant chemotherapy.十二指肠壶腹大细胞神经内分泌癌两例报告:根据辅助化疗的使用情况,胰十二指肠切除术后预后对比。
Int J Surg Case Rep. 2017;31:132-138. doi: 10.1016/j.ijscr.2017.01.031. Epub 2017 Jan 17.
6
Prognostic factors in neuroendocrine carcinoma: biological markers are more useful than histomorphological markers.神经内分泌癌的预后因素:生物标志物比组织形态学标志物更有用。
Sci Rep. 2017 Jan 11;7:40609. doi: 10.1038/srep40609.
7
Four Neuroendocrine Tumor Types and Neuroendocrine Carcinoma of the Duodenum: Analysis of 203 Cases.十二指肠的四种神经内分泌肿瘤类型及神经内分泌癌:203例病例分析
Neuroendocrinology. 2017;104(2):112-125. doi: 10.1159/000444803. Epub 2016 Feb 25.
8
Endoscopic treatment of duodenal neuroendocrine tumors.十二指肠神经内分泌肿瘤的内镜治疗
Clin Endosc. 2013 Nov;46(6):656-61. doi: 10.5946/ce.2013.46.6.656. Epub 2013 Nov 19.
9
Neuroendocrine tumors of the small bowels are on the rise: Early aspects and management.小肠神经内分泌肿瘤的发病率呈上升趋势:早期情况与治疗
World J Gastrointest Endosc. 2010 Oct 16;2(10):325-34. doi: 10.4253/wjge.v2.i10.325.
10
Primary small-cell neuroendocrine carcinoma of the duodenum - a case report and review of literature.十二指肠原发性小细胞神经内分泌癌——一例报告并文献复习
World J Surg Oncol. 2004 Aug 15;2:28. doi: 10.1186/1477-7819-2-28.

十二指肠神经内分泌癌——一个罕见部位的罕见肿瘤

Neuroendocrine Carcinoma of Duodenum-an Uncommon Tumour at an Unusual Site.

作者信息

Dewan Palki, Bhat Shubha P, Kishan Prasad H L, Ballal Rajesh, Sajitha K

机构信息

K.S. Hegde Medical Academy, NITTE - Deemed to be University, Mangalore, Karnataka 575018 India.

出版信息

Indian J Surg Oncol. 2019 Mar;10(1):199-203. doi: 10.1007/s13193-018-0834-7. Epub 2018 Dec 7.

DOI:10.1007/s13193-018-0834-7
PMID:30948899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6414587/
Abstract

Neuroendocrine carcinoma rarely occurs in the duodenum, and most cases of neuroendocrine carcinoma in the duodenum show rapid progression of the disease. Such cases have poor prognosis even with radical surgery with or without chemotherapy with low 5-year survival rate. We present a case of a 52-year-old man who presented with abdominal pain of 1-month duration and one episode of vomiting. Upper gastrointestinal endoscopy revealed polypoidal lesions in the first and second part of the duodenum. Whipple's procedure was performed. Diagnosis of poorly differentiated neuroendocrine carcinoma was made with extension to pancreas with peripancreatic lymph node metastases. The patient expired on post operative day 17 following cardiac arrest.

摘要

神经内分泌癌很少发生于十二指肠,十二指肠神经内分泌癌的大多数病例疾病进展迅速。即使接受了根治性手术(无论是否化疗),这些病例的预后也很差,5年生存率很低。我们报告一例52岁男性患者,其出现了持续1个月的腹痛和一次呕吐。上消化道内镜检查发现十二指肠第一部和第二部有息肉样病变。施行了胰十二指肠切除术。诊断为低分化神经内分泌癌,已侵犯胰腺并伴有胰周淋巴结转移。患者在术后第17天因心脏骤停死亡。