ea0050ep062 | Neoplasia, Cancer and Late Effects | SFEBES2017
Arefin Aamer Rashad
, Hay Cathy
Background: Multiple Endocrine Neoplasia Type 1 (MEN1) is a rare autosomal dominant syndrome that predisposes individuals to multiple endocrine tumours, predominantly affecting the parathyroid, anterior pituitary and pancreatic islet cells. This unusual case shows features of three of the main MEN1 tumour types, yet genetic testing was negative for the MEN1 mutation.Case esentation: A 56-year-old lady first presen...