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#883 Primary Hepatic Neuroendocrine Tumors: Four Familial Case Series with Review of Literature

Introduction: Non-multiple endocrine neoplasia (MEN) familial neuroendocrine tumors (NET) are very rare with only six families being described to date. Primary hepatic neuroendocrine tumors (PHNETs) are rare tumors with a particular sporadic diagnosis. Herein, we report a series of four members of one Lebanese family, diagnosed with primary hepatic neuroendocrine tumors.

Conference: 11th Annual ENETSConcerence (2014)

Presenting Author: Assi R

Authors: Assi R, Haidar A, Khalife M, Temraz S, Mukherji D,

Keywords: familial primary hepatic neurendocrine tumors, genetic studies ,