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Introduction: Multiple endocrine neoplasia type 1 (MEN1) is an inherited syndrome, affecting multiple endocrine glands. Duodeno-pancreatic neuroendocrine tumors (DP-NET) represent the most frequent type of NET in MEN1. Their prognosis and treatment strategy is debated.
Conference: 15th Annual ENETSConcerence (2018)
Presenting Author: Modica R
Authors: Modica R, Lo Calzo F, De Cicco F, Bottiglieri F, Sciammarella C,
Keywords: neuroendocrine tumor, MEN1 syndrome, duodeno pancreatic tumor.,
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