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Guideline for the Management of Pancreatic Neuroendocrine Tumor

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Pancreatic Cancer

Abstract

Pancreatic neuroendocrine neoplasms (PNENs) have been steadily increasing in terms of incidence and prevalence over the last two decades. As a broad variety of tumors in regard to presentation, histology, and prognosis, they represent a growing challenge for the clinicians of many specialties. Lately, surgeons are called to decide whether to offer surgery for neoplasms that may be indolent and very limited and have potentially small benefit from major operations, while in others cases can manifest at advanced stages when symptom control is the only rationale for surgical treatment.

Functioning P-NENs (F-PNENs) are encountered less often than the past more but might be easily recognizable since they cause syndromes from unregulated hormone secretion. They are treated according to the different subtype as they carry different characteristics and prognosis.

No functioning PNENs (NF-PNENS) have been detected more frequently with the refinement in imaging techniques overtime. When of small size, they carry little potential for malignant behavior; instead, the risk increases proportionally with size. According to size and grading, management options may vary from observation only to extensive resections of primary and metastatic deposits up to liver transplantation.

This chapter offers a perspective on the surgical management of the various types of PNENs.

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Spoletini, G. et al. (2017). Guideline for the Management of Pancreatic Neuroendocrine Tumor. In: Kim, SW., Yamaue, H. (eds) Pancreatic Cancer. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-47181-4_13

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