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Second primary malignancies in patients with a gastrointestinal neuroendocrine tumour : a case report and review of the literature

Journal Volume 73 - 2010
Issue Fasc.3 - Case reports
Author(s) M. Ferrante, I. Van Boxelaer, M. De Man, A.-M. Schelfout, Y. Van Molhem, K. Hendrickx, J. Vandervoort, P. Van Der Spek, F. Sermon, L. Du Ville, L. Lepoutre
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(1) Department of Gastroenterology ; (2) Pathology and (3) Abdominal Surgery, Onze-Lieve-Vrouwziekenhuis, Aalst, Belgium ; Departments of (4) Gastroenterology and (5) Internal Medicine, University Hospital Gasthuisberg, Leuven, Belgium.

A second primary malignancy (SPM) is frequently reported in patients with a gastrointestinal neuroendocrine tumour (NET). The majority of SPM are located in the gastrointestinal tract, but malignancies at other sites are described as well. This phenome- non might just be coincidental due to high incidence rates of asymptomatic NET lesions in patients who are operated or who undergo autopsy for another primary malignancy. However, other theories have been developed since the observed incidence rates seem to be double as high as expected. Some authors suggest a common genetic predisposition, while others report tumourigenic properties of various neuroendocrine peptides, including secretin, gastrin and cholecystokinin. This review is illustrated by a case report of a patient in whom the radiological diagnosis of a diffuse liver metastasized adenocarcinoma of the rectum changed dra- matically after positron emission tomography and explorative laparoscopy to a curable adenocarcinoma of the rectum with a simultaneous well-differentiated neuroendocrine carcinoma. (Acta gastroenterol. belg., 2010, 73, 397-402).

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PMID 21086947