Searchable abstracts of presentations at key conferences in endocrinology

ea0073aep852 | Late Breaking | ECE2021

Rare hypophysis tumor arising in a case with diabetes incipidus: Granular cell tumor

Ince Nurcan , Serdar Deniz Muzaffer , Keskin Muge , Dirikoc Ahmet , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

IntroductionPituitary gland tumors constitute approximately 10–15% of primary brain tumors, and posterior pituitary tumors are extremely rare. Granular cell tumor (GCT) is a low grade non-neuroendocrine neoplasm. Here, we will present our case who was found to have GCT during follow-up of diabetes insipidus (DI).CaseA 23-year-old male patient applied to our outpatient clinic for routine control. 12 years...

ea0070ep350 | Pituitary and Neuroendocrinology | ECE2020

Case report: the combination of acromegaly, primary hyperparathyroidism and colon cancer

Akdoğan Leyla , Serdar Deniz Muzaffer , Saçikara Muhammed , Nasiroğlu Narin , Ali Tam Abbas , Çuhaci Seyrek Neslihan

Introduction: Acromegaly is a chronic disease caused by excess growth hormone (GH) release from an adenoma caused by somatotroph cells of pituitary gland.In acromegaly, it is known that the risk of thyroid and colon cancer is increased 8 and 4 times, respectively, compared to the normal population.Moderate hypercalcemia, due to vitaminD activation, is seen in acromegaly, but overt hypercalcemia, generally secondary to primary hyperparathyroidism, is rare.Combination of acromeg...