ea0063gp151 | Interdisciplinary Endocrinology 1 | ECE2019
, Odou Marie-Francoise
, Demonchy Jordane
, Cardot-Bauters Catherine
, Vantyghem Marie-Christine
MEN4 is a rare disease characterized by the development of multiple endocrine tumors caused by mutations in the CDKN1b gene encoding the cyclin dependent kinase inhibitor P27Kip1. Here we report two new cases and address the potential link of MEN4 with autoimmunity. The 1st patient, a 66-year old woman, presented at 35 years high prolactin levels without evidence of pituitary adenoma, treated medically. At 51 years, she was diagnosed with mild primary hyper...