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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 2
1988 2
1989 1
1991 1
1994 1
1995 1
1997 1
1998 1
1999 1
2000 1
2001 1
2002 1
2003 1
2004 1
2005 1
2006 2
2007 1
2008 2
2010 2
2011 1
2012 2
2013 1
2019 1
2020 1
2023 1
2024 0

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29 results

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Page 1
Periampullary and duodenal neoplasms in neurofibromatosis type 1: two cases and an updated 20-year review of the literature yielding 76 cases.
Relles D, Baek J, Witkiewicz A, Yeo CJ. Relles D, et al. J Gastrointest Surg. 2010 Jun;14(6):1052-61. doi: 10.1007/s11605-009-1123-0. Epub 2010 Mar 19. J Gastrointest Surg. 2010. PMID: 20300877 Review.
Mean tumor size was 3.8 cm (range 0.9-27 cm). Tumor location was the duodenum (60%), ampulla (31%), pancreas (5%), or bile duct/gallbladder (4%). Tumor type was reported as somatostatinoma (40%), GIST (34%), adenocarcinoma (8%), carcinoid (6%), neurofibroma (5%), sc …
Mean tumor size was 3.8 cm (range 0.9-27 cm). Tumor location was the duodenum (60%), ampulla (31%), pancreas (5%), or bile duct/gallb …
Duodenal somatostatinoma: a case report and review.
Kim JA, Choi WH, Kim CN, Moon YS, Chang SH, Lee HR. Kim JA, et al. Korean J Intern Med. 2011 Mar;26(1):103-7. doi: 10.3904/kjim.2011.26.1.103. Epub 2011 Mar 2. Korean J Intern Med. 2011. PMID: 21437171 Free PMC article. Review.
Somatostatinomas are rare functioning carcinoid tumors that usually arise in the pancreas and duodenum. They are seldom associated with typical clinical symptoms; their diagnosis is confirmed only by histological and immunohistochemical studies and the presence of s
Somatostatinomas are rare functioning carcinoid tumors that usually arise in the pancreas and duodenum. They are seldom associ
Duodenal neuroendocrine tumors: Classification, functional syndromes, diagnosis and medical treatment.
Hoffmann KM, Furukawa M, Jensen RT. Hoffmann KM, et al. Best Pract Res Clin Gastroenterol. 2005 Oct;19(5):675-97. doi: 10.1016/j.bpg.2005.05.009. Best Pract Res Clin Gastroenterol. 2005. PMID: 16253893 Review.
Duodenal neuroendocrine tumors (NETs) comprise 2-3% of all GI endocrine tumors and are increasing in frequency. These include gastrinomas, somatostatinomas, nonfunctional NETs, gangliocytic paragangliomas, and poorly differentiated NE carcinomas. ...
Duodenal neuroendocrine tumors (NETs) comprise 2-3% of all GI endocrine tumors and are increasing in frequency. These include gastrin
Duodenal carcinoid (somatostatinoma) combined with von Recklinghausen's disease. A case report and review of the literature.
Ohtsuki Y, Sonobe H, Mizobuchi T, Takahashi K, Hayashi K, Iwata J, Tahara E. Ohtsuki Y, et al. Acta Pathol Jpn. 1989 Feb;39(2):141-6. doi: 10.1111/j.1440-1827.1989.tb01492.x. Acta Pathol Jpn. 1989. PMID: 2541598 Review.
We report the immunohistochemical and ultrastructural features of a case of duodenal carcinoid (somatostatinoma) combined with cutaneous-type von Recklinghausen's disease in a 65-year-old woman. ...This is the tenth case of duodenal carcinoid associated with …
We report the immunohistochemical and ultrastructural features of a case of duodenal carcinoid (somatostatinoma) combined with …
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.
Thavaraputta S, Graham S, Rivas Mejia AM, Lado-Abeal J. Thavaraputta S, et al. BMJ Case Rep. 2019 Jan 10;12(1):bcr-2018-226702. doi: 10.1136/bcr-2018-226702. BMJ Case Rep. 2019. PMID: 30635305 Free PMC article. Review.
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
Somatostatinomas are rare neuroendocrine tumours, mostly located in the pancreas or duodenum, with an estimated incidence of 1
Duodenal somatostatinoma: a case report and review of 31 cases with special reference to the relationship between tumor size and metastasis.
Tanaka S, Yamasaki S, Matsushita H, Ozawa Y, Kurosaki A, Takeuchi K, Hoshihara Y, Doi T, Watanabe G, Kawaminami K. Tanaka S, et al. Pathol Int. 2000 Feb;50(2):146-52. doi: 10.1046/j.1440-1827.2000.01016.x. Pathol Int. 2000. PMID: 10792774 Review.
Somatostatinomas are rare functioning neoplasms usually arising in the pancreas and duodenum. ...A large tumor in the descending duodenum had given rise to multiple lymph node metastases. An additional 31 duodenal somatostatinoma cases were also
Somatostatinomas are rare functioning neoplasms usually arising in the pancreas and duodenum. ...A large tumor in the descendi
Duodenal somatostatinoma presenting with complete somatostatinoma syndrome.
Green BT, Rockey DC. Green BT, et al. J Clin Gastroenterol. 2001 Nov-Dec;33(5):415-7. doi: 10.1097/00004836-200111000-00015. J Clin Gastroenterol. 2001. PMID: 11606861 Review.
Somatostatinomas are the rarest pancreatic endocrine tumors and can arise in the pancreas or duodenum. ...Although several reports have documented portions of the syndrome in patients with duodenal somatostatinomas, to our knowledge, this is the first
Somatostatinomas are the rarest pancreatic endocrine tumors and can arise in the pancreas or duodenum. ...Although several rep
Mixed endocrine somatostatinoma of the ampulla of vater associated with a neurofibromatosis type 1: a case report and review of the literature.
Deschamps L, Dokmak S, Guedj N, Ruszniewski P, Sauvanet A, Couvelard A. Deschamps L, et al. JOP. 2010 Jan 8;11(1):64-8. JOP. 2010. PMID: 20065557 Review.
CONTEXT: Mixed endocrine tumors are double neoplasms with both glandular and endocrine components; these tumors are rare, especially those arising in the ampulla of Vater. Ampullary somatostatinomas are classically associated with neurofibromatosis type 1. We herein descri …
CONTEXT: Mixed endocrine tumors are double neoplasms with both glandular and endocrine components; these tumors are rare, especially those a …
Von Recklinghausen's neurofibromatosis associated with duodenal somatostatinoma. A case report and review of the literature.
Cappelli C, Agosti B, Braga M, Cumetti D, Gandossi E, Rizzoni D, Agabiti Rosei E. Cappelli C, et al. Minerva Endocrinol. 2004 Mar;29(1):19-24. Minerva Endocrinol. 2004. PMID: 15258554 Review.
A case of a patient affected by VRNF associated with duodenal somatostatinoma with consequent obstructive jaundice is reported. ...A total of 27 patients with Von Recklinghausen's disease associated with immunohistologically proved duodenal somatostatinoma
A case of a patient affected by VRNF associated with duodenal somatostatinoma with consequent obstructive jaundice is reported …
[Inherited tumor syndromes of gastroenteropancreatic and thoracic neuroendocrine neoplasms].
Couvelard A, Scoazec JY. Couvelard A, et al. Ann Pathol. 2020 Apr;40(2):120-133. doi: 10.1016/j.annpat.2020.01.002. Epub 2020 Feb 5. Ann Pathol. 2020. PMID: 32035641 Review. French.
Two inherited syndromes have a low incidence of NENs: neurofibromatosis type 1 (NF1), associated with duodenal somatostatinomas, and tuberous sclerosis (TSC), associated with pancreatic NENs. ...
Two inherited syndromes have a low incidence of NENs: neurofibromatosis type 1 (NF1), associated with duodenal somatostatinomas
29 results