Literature DB >> 9629513

Carcinoid tumors of the pancreas. Status report based on two cases and review of the world's literature.

C Mao1, A el Attar, D R Domenico, K Kim, J M Howard.   

Abstract

CONCLUSION: The diagnosis of a pancreatic carcinoid should be based on the measurement of serotonin in serum or its demonstration in the tumor and/or by the measurement of its derivative (5-HIAA) in urine. Carcinoid of the pancreas is a rare but definite entity; usually having metastasized by the time of diagnosis. The term "serotonin-producing tumor of the pancreas" has been suggested as an alternative designation for "pancreatic carcinoid."
BACKGROUND: The literature on carcinoid tumors of the pancreas is confusing because much of it preceded the development of the more specific immunological, chemical and staining techniques currently available.
METHODS: 43 case reports were collected from the world's literature, based on a demonstrable pancreatic neuroendocrine tumor plus a positive finding of at least one of the following without another dominant hormone being demonstrated: elevation of 5-Hydroxytryptamine (5-HT) (serotonin) in the serum or detected in tumor tissue, and/or elevation of 5-Hydroxyindole acetic acid (5-HIAA) in the urine. In addition to these two hormone-specific assays, information was collected on the silver-staining properties of the tumor; properties which have traditionally been associated with carcinoid tumors. Positive silver staining in tumor cells (argyrophilic and/or argentaffin reaction) is strongly indicative of the carcinoid tumor but the findings are less specific than the hormone assays and immunohistologic stains.
RESULTS: In this review of 43 cases, including two current ones, the pancreatic carcinoid tumor has the following important features: 1. It is a rare tumor that is usually diagnosed late when the tumor is large and has metastasized. Thirty-eight (88.4%) have been malignant. They are, therefore, associated with a high incidence of the "carcinoid syndrome." 2. To date, prognosis in therapy is poor, based on delayed diagnosis, a resultant low incidence of resectability, and an uncertain duration of survival after resection. 3. Pancreatic carcinoid tumors remain difficult to differentiate from other endocrine tumors. The measurement of urinary 5-HIAA excretion or the demonstration of elevated serotonin level in the tumor or in serum is essential to its distinction. Silver staining of the tumor, although of historic importance, has been superceded by the hormone-specific studies. 4. To distinguish it from other endocrine tumors of the pancreas, the terms "pancreatic serotoninoma" or "serotonin-producing tumor of the pancreas" have been suggested as possible alternatives. Its growth characteristics may be related more to its cell of origin than to its extent of hormone secretion. Not all of the tumors result in recognizable hyperserotoninemia.

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Year:  1998        PMID: 9629513     DOI: 10.1385/IJGC:23:2:153

Source DB:  PubMed          Journal:  Int J Pancreatol        ISSN: 0169-4197


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10.  A serotonin and beta HCG-producing islet cell carcinoma associated with focal nodular hyperplasia of the liver.

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  13 in total

1.  Neuroendocrine markers in adenocarcinomas: an investigation of 356 cases.

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4.  Serotonin expression in pancreatic neuroendocrine tumors correlates with a trabecular histologic pattern and large duct involvement.

Authors:  Chad M McCall; Chanjuan Shi; Alison P Klein; Björn Konukiewitz; Barish H Edil; Trevor A Ellison; Christopher L Wolfgang; Richard D Schulick; Günter Klöppel; Ralph H Hruban
Journal:  Hum Pathol       Date:  2012-01-04       Impact factor: 3.466

5.  Primary neuroendocrine tumors of the main pancreatic duct: a rare entity.

Authors:  Thomas Walter; Valérie Hervieu; Mustapha Adham; Rodica Gincul; Gilles Poncet; Frank Pilleul; Jean-Alain Chayvialle; Christian Partensky; Catherine Lombard-Bohas; Jean-Yves Scoazec
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6.  Carcinoid syndrome from a carcinoid tumor of the pancreas without liver metastases: A case report and literature review.

Authors:  Nikolaos Zavras; Demetrios Schizas; Nikolaos Machairas; Vasileia Damaskou; Nikolaos Economopoulos; Anastasios Machairas
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7.  Pancreatic duct stenosis secondary to small endocrine neoplasms: a manifestation of serotonin production?

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Review 8.  Pancreatic neuroendocrine tumors: biology, diagnosis,and treatment.

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9.  Causes of death and prognostic factors in multiple endocrine neoplasia type 1: a prospective study: comparison of 106 MEN1/Zollinger-Ellison syndrome patients with 1613 literature MEN1 patients with or without pancreatic endocrine tumors.

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10.  Down-regulation of 5-HT1B and 5-HT1D receptors inhibits proliferation, clonogenicity and invasion of human pancreatic cancer cells.

Authors:  Nilgun Gurbuz; Ahmed A Ashour; S Neslihan Alpay; Bulent Ozpolat
Journal:  PLoS One       Date:  2014-08-29       Impact factor: 3.240

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