Introduction: Familial Midgut Carcinoid Tumors (FMCT) are a rare and poorly described entity defined by the occurrence of a midgut carcinoid tumor in at least two first-degree relatives.
Aim(s): To describe a multicentre cohort of FMCT.
Materials and methods: Patients with an FMCT were included. After eliminating hypothesis of type 1 MEN, clinical characteristics were reviewed. A central pathological review was performed.
Conference: 11th Annual ENETS Conference 2014 (2014)
Category: Clinical cases/reports
Presenting Author: Louis De Mestier
De Mestier L
, Fleury C
, Pasmant E
, Brixi H
, Murat A
, Baudin E
, Cholet F
, Lombard-Bohas C
, Hammel P
, Goichot B
, Diebold M D
, Cadiot G
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