Searchable abstracts of presentations at key conferences in endocrinology

ea0099p496 | Diabetes, Obesity, Metabolism and Nutrition | ECE2024

Assessment of overactive bladder syndrome symptoms (OABSS) score following the start of sodium-glucose co-transporter-2 inhibitors in individuals with type-2 diabetes mellitus

sema yaman kalender Derya , Cavdar Umit , Sercan Erturk Mehmet , Onder Pamuk Barış

Background: In addition to glucose-lowering effects, Sodium-Glucose Cotransporter-2 Inhibitors (SGLT2i) are the preferred treatment of choice in patients with heart failure due to their diuretic effects through glucosuria and natriuresis. However, there is limited data about urinary symptoms associated with SGLT2i use.Objectives: Low urinary tract symptoms such as increased urinary frequency, urgency, or incontinence due to SGLT2i use are not described i...

ea0063p466 | Adrenal and Neuroendocrine Tumours 2 | ECE2019

A case of metastatic pheochromocytoma diagnosed at a young age with hypertensive attack

Cankurtaran Yılmaz , Oruk Guzide Gonca , Cağlar Sevinc , Yazır Merve Gulec , Onder Pamuk Barış , Cengiz Fevzi , Etit Demet Arıkan

Introduction: Although the radiographic and histological features are the same as benign pheochromocytomas, malignant and metastatic pheochromocytoma is differentiated by invasion of the surrounding tissues and organ metastasis. Here, we present a young patient with a diagnosis of metastatic pheochromocytoma presenting with hypertension attacks, headache and flushing.Case presentation: A 22-year-old woman with a history of hypertension who had been suffe...

ea0063p847 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

A Adrenocortical carcinoma (ACC) presenting with episodes of intermittent hypertension: Sarcomatoid type adrenocortical carcinoma

Gulec Yazır Merve , Cankurtaran Yılmaz , Gonca Oruk Guzide , Onder Pamuk Barış , Arıkan Etit Demet

Introduction: Adrenocorticalcarcinoma (ACC) is a rare malignancy with an aggressive prognosis, an incidance of 1–2 cases/million/year. It is the cause of 0.2% of all cancer deaths. It is seen in the 4th and 5th decades in adults and mostly unilateral and sporadic. Herein, we present a case of sarcomatoid type ACC which is symptomatic with mass compression and hypertansive attacks.Case presentation: A-52-year-old male was referred to our endocrinolog...

ea0090p685 | Pituitary and Neuroendocrinology | ECE2023

Panhypopituitarism in an Adult Patient with William-Beuren Region Duplication Syndrome: A Rare Case Report

Sema Yaman kalender Derya , Gasımlı Roya , Subaşıoğlu Aslı , Sercan Erturk Mehmet , Cavdar Umit , Gonca Oruk Guzide , Onder Pamuk Barış

Background: William-Beuren region duplication syndrome (WBDS) is a rare multisystem disease caused by the gain on chromosome 7q and transmitted autosomal dominant, with approximately a population frequency of 1 in 13,000-20,000. The age of diagnosis is variable, but generally, it is diagnosed during childhood. It include endocrine (growth hormone deficiency) and non-endocrine (facial dysmorphology, cardiovascular problems, gastrointestinal and genitourinary problems, neurologi...