ea0049ep861 | Clinical case reports - Pituitary/Adrenal | ECE2017
Pappa Dimitra
, Thoda Pinelopi
, Rizoulis Andreas
, Gountios Ioannis
, Kapsalaki Eftihia
, Bargiota Alexandra
Introduction: Acromegaly is a systematic disease with charecteristic clinical features, which is due to GH hypersecretion mainly from pituitary adenomas and in rare cases it can be due to ectopic GHRH and GH hypersecretion. Sometimes localizing the source of hypersecretion is difficult. Here we present a case of a woman with acromegalic phenotype and empty sella.Presentation: A 47 years old woman referred to our department after recent onset of high bloo...