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Introduction: Pluriglandolar endocrine disease in patients without familial inherited disease (non-MEN 1) are very rare. Primary Pancreatic Neuroendocrine Tumors (pNET) and ileal carcinoid tumors have different embryologic origin (foregut and midgut respectively).
Conference: 12th Annual ENETSConcerence (2015)
Presenting Author:
Authors: Lico V, Milanetto A, Moletta L, Scaroni C, Alaggio R,
Keywords: acromegaly, carcinoid, pNET,
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