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Current Concepts on Gastric Carcinoid Tumors

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Publisher Wiley
Specialty Gastroenterology
Date 2013 Jan 15
PMID 23316222
Citations 32
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Abstract

Gastric carcinoid tumors (GCs) are rare lesions representing less than 10% of carcinoid tumors and less than 1% of all stomach neoplasms. There are three distinct types of gastric carcinoids; type I includes the vast majority (70-85%) of these neoplasms that are closely linked to chronic atrophic gastritis. Type II which accounts for 5-10 %, is associated with Zollinger-Ellison syndrome and often occurs in the context of multiple endocrine neoplasia type 1. Type III, finally, represents 15-25% of gastric carcinoids and is characterized by a far more aggressive course. The optimal clinical approach to GCs remains to be elucidated, depending upon type, size, and number of carcinoids. While there is universal agreement about the surgical treatment of type III GCs, current options for type I and II include simple surveillance, endoscopic polypectomy, surgical excision associated with or without surgical antrectomy, or total gastrectomy. Moreover, the introduction of somatostatin analogues could represent another therapeutic option.

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References
1.
Gibril F, Reynolds J, Lubensky I, Roy P, Peghini P, Doppman J . Ability of somatostatin receptor scintigraphy to identify patients with gastric carcinoids: a prospective study. J Nucl Med. 2000; 41(10):1646-56. View

2.
Metz D . Diagnosis of the Zollinger–Ellison syndrome. Clin Gastroenterol Hepatol. 2011; 10(2):126-30. DOI: 10.1016/j.cgh.2011.07.012. View

3.
Lawrence B, Kidd M, Svejda B, Modlin I . A clinical perspective on gastric neuroendocrine neoplasia. Curr Gastroenterol Rep. 2010; 13(1):101-9. DOI: 10.1007/s11894-010-0158-4. View

4.
Nikou G, Toubanakis C, Moulakakis K, Pavlatos S, Kosmidis C, Mallas E . Carcinoid tumors of the duodenum and the ampulla of Vater: current diagnostic and therapeutic approach in a series of 8 patients. Case series. Int J Surg. 2011; 9(3):248-53. DOI: 10.1016/j.ijsu.2010.12.003. View

5.
Okita N, Kato K, Takahari D, Hirashima Y, Nakajima T, Matsubara J . Neuroendocrine tumors of the stomach: chemotherapy with cisplatin plus irinotecan is effective for gastric poorly-differentiated neuroendocrine carcinoma. Gastric Cancer. 2011; 14(2):161-5. DOI: 10.1007/s10120-011-0025-5. View