2006
DOI: 10.1016/j.ejso.2005.11.017
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Liver resection for primary hepatic neuroendocrine tumours: Report of three cases and review of the literature

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Cited by 33 publications
(36 citation statements)
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“…Neuroendocrine neoplasms are a relatively rare tumor of the gastrointestinal system, accounting for less than 2% of all GI neoplasms [6]. PHNETs are exceedingly rare, with less than 300 cases reported in the literature to date [3].…”
Section: Discussionmentioning
confidence: 99%
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“…Neuroendocrine neoplasms are a relatively rare tumor of the gastrointestinal system, accounting for less than 2% of all GI neoplasms [6]. PHNETs are exceedingly rare, with less than 300 cases reported in the literature to date [3].…”
Section: Discussionmentioning
confidence: 99%
“…While the origin of PHNETs remains unclear, three hypotheses have been proposed: (1) they arise from neuroendocrine cells scattered in the epithelium of the intrahepatic biliary tract; (2) they originate from heterotopic pancreatic or adrenal tissue located in the liver; and (3) they arise from the neuroendocrine differentiation of a single malignant stem cell that is the precursor of other hepatic tumors [6]. …”
Section: Discussionmentioning
confidence: 99%
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“…In patients with PHNET, the tumor may be found incidentally during routine screening. While abdominal pain and palpable mass in the right upper quadrant are the most frequent symptoms, the symptoms of carcinoid syndrome may be exhibited, even if it is rare (8). This syndrome is found in less than 10% of the gastrointestinal NETs; however, when it is found, it is always associated with hepatic metastasis.…”
Section: Tumor-like Lesionsmentioning
confidence: 99%