ea0063p681 | Pituitary and Neuroendocrinology 2 | ECE2019
Chiloiro Sabrina
, Domenico Capolungo Ettore
, Schinzari Giovanni
, Concolino Paola
, Rossi Ernesto
, Martini Maurizio
, Cocomazzi Alessandra
, Grande Giuseppe
, Milardi Domenico
, Maiorano Brigida
, Giampietro Antonella
, Rindi Guido
, Pontecorvi Alfredo
, De Marinis Laura
, Bianchi Antonio
Introduction: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominantly inherited endocrine tumor syndrome characterized by development of cancer in various endocrine organs, particularly in pituitary, parathyroid and pancreas. Moreover, in some cases, also non-endocrine tumors can be diagnosed, developing atypical phenotypes.Case report: We report herein the clinical history of a patient affected by MEN-1 syndrome who developed atypical feat...