Abstract
Neuroendocrine gut and pancreatic tumours are considered to be rather rare neoplasms; however, due to increased awareness, improved diagnostic procedures and, not least, improved treatment, the number of cases has increased during the last two decades. The first case was described already in 1902 by Oberndorfer, who introduced the term carcinoid for a less malignant neoplasm. The incidence of patients with clinically significant carcinoid tumours is 0.5/100 000 and for endocrine pancreatic tumours 0.4/100 000. These are the two main groups of endocrine gastrointestinal tumours.
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© 1997 Springer-Verlag Berlin Heidelberg
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Öberg, K. (1997). Interferon Therapy of Neuroendocrine Tumours. In: Aul, C., Schneider, W. (eds) Interferons. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-60411-9_4
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DOI: https://doi.org/10.1007/978-3-642-60411-9_4
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