Searchable abstracts of presentations at key conferences in endocrinology

ea0093p9 | Guided Poster Tour 1: Adrenal and Neuroendocrine tumors | EYES2023

A rare case of bilateral micronodular adrenal cortical disease

Ozer Ozge , Yorulmaz Goknur , Kebapci Medine Nur

Background: Bilateral micronodular adrenal cortical disease (miBACD) is a rare and difficult-to-manage disease. miBACD is one of the causes of Cushing’s syndrome. miBACD is divided into primary pigmented nodular adrenocortical disease (PPNAD) and isolated micronodular adrenocortical disease. Its more common presentation is familial PPNAD, as part of Carney syndrome. We also presented a rare case of miBACD.Case presentation: A 20-year-old female pati...

ea0081ep166 | Calcium and Bone | ECE2022

Endocrinopaties in thalassemia patients

Ozer Ozge , Yorulmaz Goknur , Ozgeyik Mufide Okay , Teke Hava Uskudar , Gunduz Eren

Objectives: Disorders concerning the endocrine system may be seen in patients with transfusion-dependent thalassemia major. It is thought that iron accumulated in the organs, especially with transfusion, causes this. In our study, we tried to reveal a relationship by comparing the iron parameters of these patients with various endocrine parameters.Methods: Our study is a retrospective study.The data of 18 thalassemia major patients who applied to Osmanga...

ea0081ep720 | Pituitary and Neuroendocrinology | ECE2022

Clinical and laboratory features and management of pituitary apoplexy: Case series

Ozer Ozge , Kebapci Medine Nur , Akalın Aysen , Efe Belgin , Yorulmaz Goknur

Introduction: Pituitary apoplexy (PA) is a clinical emergency resulting from acute ischemia or bleeding of the pituitary gland. Complaints of patients are usuallay headache and vision problems. We tried to discuss the reasons for presentation, pituitary imaging and hormones of patients.Patients and Methods: 10 patients (5 men and 5 women), median age 53 years at diagnosis were retrospectively reviewed. FSH, LH, estradiol/testosterone, GH, IGF1, TSH, FT4,...

ea0090p810 | Late-Breaking | ECE2023

Evaluation with Dynamic Contrast Enhancement (DCE)-MRI in Patients with Acromegaly

Toygar Kalkan Ahmet , Ozer Ozge , Toprak Ugur , Efe Belgin , Akalin Aysen , Nur Kebapci Medine , Yorulmaz Goknur

Acromegaly is a rare disease with high morbidity and mortality associated with excessive secretion of growth hormone due to adenoma of somatotroph cells in the pituitary gland. In patients with acromegaly, residue may remain after surgical treatment, and disease control is attempted with surgery, medical treatment or radiotherapy for these patients. Pituitary imaging, IGF-1 and GH measurement are used in the follow-ups. Dynamic Contrast Enhancement perfusion MRI provides infor...

ea0090p540 | Late-Breaking | ECE2023

Systemic inflammation in paragangliomas and pheochromocytomas

Ozer Ozge , Apaydin Kayer Merve , Yilmaz Evrim , Nur Kebapci Medine , Akalin Aysen , Efe Belgin , Fuat Acikalin Mustafa , Yorulmaz Goknur

Background: Paragangliomas (PGLs) and pheochromocytomas (PCCs) arise from chromaffin cells. We evaluated the inflammatory markers. The pan-immune-inflammation value (PIV) has recently been used as a new marker. Therefore, we evaluated the PIV association in patients with PGLs/PCCs.Methods: In the study, the data of 82 patients with PGLs/PCCs who applied between 2005 and 2020 were collected retrospectively from the records. NLR (neutrophil/lymphocyte rati...