Endocrine Abstracts

Background: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal-dominant tumor syndrome associated with a wide tumor spectrum, in endocrine and nonendocrine tissues, key association being pituitary, parathyroid and enteropancreatic neuroendocrine tumors. Management of MEN1 is challenging because of its polymorphic, variable phenotypic expression.Case report: Here, we present the case of a 68 year old patient diagnosed in 2004 with an 18 mm ist...