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本文引用的文献

1
Duodenal and Ampullary Carcinoid Tumors: Size Predicts Necessity for Lymphadenectomy.十二指肠和壶腹类癌肿瘤:大小预示着淋巴结清扫的必要性。
J Gastrointest Surg. 2017 Aug;21(8):1262-1269. doi: 10.1007/s11605-017-3448-4. Epub 2017 May 17.
2
Combined presence of multiple gastrointestinal stromal tumors along with duodenal submucosal somatostatinoma in a patient with neurofibromatosis type 1.1型神经纤维瘤病患者合并存在多个胃肠道间质瘤及十二指肠黏膜下生长抑素瘤。
Indian J Pathol Microbiol. 2016 Jul-Sep;59(3):359-61. doi: 10.4103/0377-4929.188123.
3
The Coexistence of Somatostatinoma and Gastrointestinal Stromal Tumor in the Duodenum of a Patient with Von Recklinghausen's Disease.一名患有冯·雷克林豪森病患者的十二指肠中生长抑素瘤与胃肠道间质瘤并存
Intern Med. 2016;55(6):617-22. doi: 10.2169/internalmedicine.55.5761. Epub 2016 Mar 15.
4
ENETS Consensus Guidelines Update for Gastroduodenal Neuroendocrine Neoplasms.ENETS胃十二指肠神经内分泌肿瘤共识指南更新
Neuroendocrinology. 2016;103(2):119-24. doi: 10.1159/000443168. Epub 2016 Jan 19.
5
Neurofibromatosis type 1 and GIST: is there a correlation?1型神经纤维瘤病与胃肠道间质瘤:存在关联吗?
Anticancer Res. 2014 Oct;34(10):5609-12.
6
Gastrointestinal stromal tumours: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.胃肠道间质瘤:欧洲肿瘤内科学会诊断、治疗及随访临床实践指南
Ann Oncol. 2014 Sep;25 Suppl 3:iii21-6. doi: 10.1093/annonc/mdu255.
7
An esophageal gastrointestinal stromal tumor in a patient with MEN1-related pancreatic gastrinoma: an unusual association and review of the literature.一名患有MEN1相关胰腺胃泌素瘤患者的食管胃肠道间质瘤:一种不寻常的关联及文献综述
J Cancer Res Ther. 2014 Apr-Jun;10(2):443-5. doi: 10.4103/0973-1482.136685.
8
Neurofibromatosis type 1 gene mutation analysis using sequence capture and high-throughput sequencing.利用序列捕获和高通量测序进行1型神经纤维瘤病基因突变分析。
Acta Derm Venereol. 2014 Nov;94(6):663-6. doi: 10.2340/00015555-1843.
9
Education and imaging. Gastrointestinal: neurofibromatosis type 1, duodenal somatostatinoma and gastrointestinal stromal tumors; a triad worth remembering.教育与影像学。胃肠道:1型神经纤维瘤病、十二指肠生长抑素瘤和胃肠道间质瘤;一个值得记住的三联征。
J Gastroenterol Hepatol. 2014 Apr;29(4):663. doi: 10.1111/jgh.12531.
10
Duodenal somatostatinoma: a case report and review of the literature.十二指肠生长抑素瘤:一例病例报告及文献综述
J Med Case Rep. 2013 Apr 25;7:115. doi: 10.1186/1752-1947-7-115.

十二指肠生长抑素瘤表现为梗阻性黄疸并合并1型神经纤维瘤病中的胃肠道间质瘤:1例病例及文献复习

Duodenal somatostatinoma presenting as obstructive jaundice with the coexistence of a gastrointestinal stromal tumour in neurofibromatosis type 1: a case with review of the literature.

作者信息

Thavaraputta Subhanudh, Graham Suzanne, Rivas Mejia Ana M, Lado-Abeal Joaquin

机构信息

Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.

Department of Pathology, Texas Tech Univeristy Health Sciences Center, Lubbock, Texas, USA.

出版信息

BMJ Case Rep. 2019 Jan 10;12(1):bcr-2018-226702. doi: 10.1136/bcr-2018-226702.

DOI:10.1136/bcr-2018-226702
PMID:30635305
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6340528/
Abstract

Somatostatinomas are rare neuroendocrine tumours, mostly located in the pancreas or duodenum, with an estimated incidence of 1 in 40 million. Duodenal somatostatinomas (DSs) are usually found in association with neurofibromatosis type 1 (NF1), tuberous sclerosis and Von Hippel-Lindau syndrome. Gastrointestinal stromal tumours (GIST) have also been described in NF1, but the association with somatostatinoma is very uncommon. We report the case of a patient with NF1 who presented with obstructive jaundice due to multiple firm nodules around the ampulla of Vater. A pancreaticoduodenectomy was performed and revealed a 1 cm duodenal/ampullary mass which stained positive for somatostatin, together with a GIST also found on the duodenal wall. Despite its rarity, ampullary somatostatinomas should be considered in the differential diagnosis of biliary tract dilation in patients with NF1.

摘要

生长抑素瘤是一种罕见的神经内分泌肿瘤,大多位于胰腺或十二指肠,估计发病率为四千分之一。十二指肠生长抑素瘤(DSs)通常与1型神经纤维瘤病(NF1)、结节性硬化症和冯·希佩尔-林道综合征相关。胃肠道间质瘤(GIST)也在NF1中有所描述,但与生长抑素瘤的关联非常罕见。我们报告了一例NF1患者,该患者因 Vater壶腹周围多个实性结节出现梗阻性黄疸。行胰十二指肠切除术,发现一个1厘米的十二指肠/壶腹肿块,生长抑素染色呈阳性,同时在十二指肠壁上也发现了一个GIST。尽管罕见,但在NF1患者胆道扩张的鉴别诊断中应考虑壶腹生长抑素瘤。