Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep935 | Thyroid (non-cancer) | ECE2015

Evaluation of acoustic voice analysis in patients with subclinical thyrotoxicosis

Demirci Taner , Uyar Mehmet , Catalli Emel Tatar , Caliskan Mustafa , Ucan Bekir , Demiral Dilek , Arslan Muyesser Sayki , Ozbek Mustafa , Korkmaz Mehmet Hakan , Delibasi Tuncay

Introduction: The relationship between hyperthyroidism and voice disorders has not been identified before. The aim of this study was to investigate the changes in the acoustic values in patients with subclinical thyrotoxicosis.Methods: In this study, acoustic voice analysis was evaluated in a total of 115 cases. Sixty of 115 individuals (18 men and 42 women) had subclinical thyrotoxicosis, aged between 18 and 65 years, and all had no history of laryngeal...

ea0070ep507 | Thyroid | ECE2020

What is responsible for subacute thyroiditis? Virus or immune system: A case report

Geneș Dilek , Pekkolay Zafer , Güven Mehmet , Şimșek Mehmet , Saraçoğlu Hüsna , Kemal Tuzcu Alpaslan

Background: Subacute thyroiditis (SAT) is a transient thyrotoxic state characterized by suppressed TSH and low uptake of iodine 123 on thyroid scanning. SAT is a self limiting, possibly viral and inflammatory thyroid disorder that is usually associated with thyroid pain and systemic symptoms. Many factors can cause SAT. Infections are considered the most common cause. Vaccines can also lead to SAT.Case report: A 46-year-old male with a history of type 1 ...

ea0099p516 | Pituitary and Neuroendocrinology | ECE2024

Cytokeratin 18: An early biomarker of increased liver fibrosis in newly diagnosed acromegaly

Coskun Meric , Nahit Sendur Halit , Babayeva Afruz , Nur Cerit Mahi , Turgay Cerit Ethem , Muhittin yalcin Mehmet , Eroglu Altinova Alev , Akturk Mujde , Ayhan Karakoc Mehmet , Balos Toruner Fusun

Purpose: The liver is known to be protected from steatosis under the influence of high GH/IGF-1. Cytokeratin 18 (CK18) and insulin-like growth factor binding protein 7 (IGFBP7) increase in liver steatosis and fibrosis. Whether decreasing lipid content completely protects the liver from metabolic alterations and the response of CK18 and IGFBP7 to liver changes in acromegaly is unknown.Methods: This single-center, multidisciplinary, cross-sectional study i...

ea0090p669 | Endocrine-related Cancer | ECE2023

Clinical findings, treatment modality and outcomes of adrenocortical carcinoma: a retrospective review of single tertiary center experience

Selek Alev , Koksalan Damla , Sozen Mehmet , Gezer Emre , Alkan Ozlem , Canturk Zeynep , Cetinarslan Berrin

Background & Aim: Adrenocortical carcinoma (ACC) is an extremely rare malignancy usually with poor outcomes, although the prognosis varies greatly depending on the initial tumor stage. Here we present clinical and outcome diversity of the patients in a single center.Methods: We retrospectively analyzed 16 patients with ACC diagnosed between 2000 and 2022. Demographical findings, hormonal status, radiological findings, ENSAT stage, weiss score and Ki6...

ea0090ep33 | Adrenal and Cardiovascular Endocrinology | ECE2023

A case of Merkel cell carcinoma in the CNC 1 (Carney complex 1) gene positive family with a rare component of the Carney complex

Nasrullayeva Fidan , Bayraktar Fırat , Unal Mehmet Cağrı , Semiz Gokcen Gungor

Introduction: CNC (Carney complex) is a rare inherited autosomal dominant syndrome characterized by prominent pigmented lesions on the skin and mucosal surfaces, cardiac and noncardiac myxomatous tumors, and multiple endocrine neoplasms. About 70% of cases have a family history, while the remaining 30% occur sporadically as a result of de novo mutation. Two genetic loci linked to CNC have been found: the CNC1 gene on chromosome 17q22-24, which encodes the regulatory subunit (R...

ea0069p72 | Poster Presentations | SFENCC2020

Parathyroid adenoma in a young man <35 years old

Khanam Amina , Salema Valmiki , Charles Debbie-Ann , Ibrahim Sharaf , Mehmet Sherife , Tremble Jennifer

Section 1: Case history: 23 Year old Caribbean gentleman attended A&E with several month history of non-specific headaches, changes in memory/mood and joint pains. Since the age of 5 he had been medically treated for renal stones, He had a past medical history of sickle cell trait and was not on any regular medications. There was no significant family history apart from sickle cell disease. He had initial bloods which showed serum adjusted calcium level 3.7 mmol/l and PTH ...

ea0063p1024 | Interdisciplinary Endocrinology 2 | ECE2019

Association of the Period3 clock gene polymorphism with adrenocorticotropin-stimulated cortisol levels among patients with autoimmune thyroid disease

Helvaci Nafiye , Oguz Seda , Kabacam Serkan , Karabulut Erdem , Akbiyik Filiz , Alikasifoglu Mehmet , Gurlek Alper

Background: Immune function and responses are tightly regulated by the circadian clock system and hypothalamic-pituitary-adrenal (HPA) axis. Accumulating evidence supports that there is a strong mutual relationship between these two regulatory systems at multiple levels. Recent publications suggest that the clock system may also regulate glucocorticoid release from adrenal glands by altering the sensitivity of the adrenal cortex to adrenocorticotropic hormone (ACTH).<p cla...

ea0049gp212 | Thyroid 2 | ECE2017

Association of the Period3 clock gene polymorphism with autoimmune thyroid diseases

Helvaci Nafiye , Oguz Seda , Kabacam Serkan , Karabulut Erdem , Akbiyik Filiz , Alikasifoglu Mehmet , Gurlek Alper

Background: Circadian rhythmicity is generated by a set of genes including Period3. Changes in the expression of Period3 and other clock genes have been linked with regulation of the immune system. Period3 polymorphisms have been associated with circadian disruption and so immune system dysregulation and altered secretion of several cytokines, which can lead to inflammatory and autoimmune disorders.Aim: To investigate the influence of a polymorphism in P...

ea0049ep118 | Clinical case reports - Pituitary/Adrenal | ECE2017

Case with metastatic lung cancer who developed adrenal insufficiency

Bulbul Buket Yilmaz , Celik Ece , Celik Mehmet , Ayturk Semra , Ustun Funda , Guldiken Sibel

Adrenal metastasis is common (35%) among the patients with lung cancer, while less than 3% of the patients develop bilateral adrenal metastasis. Adrenal metastases are generally small and clinically asymptomatic. Adrenal insufficiency is rare despite the presence of adrenal metastasis. Lam et al. reported this ratio as 0.7%. We aimed to present a case with lung cancer and bilateral adrenal metastasis who developed adrenal insufficiency.A 63-year old male...

ea0049ep121 | Clinical case reports - Pituitary/Adrenal | ECE2017

A rare case: adrenal lymphangioma

Durmus Yusuf , Celik Mehmet , Bulbul Buket Yilmaz , Ayturk Semra , Can Nuray , Tastekin Ebru , Guldiken Sibel

Adrenal lymphangioma is a rare benign tumors of the adrenal gland. Because of the increased use of imaging methods in recent times, the diagnosis is usually made incidentally. It is usually due to malformation between the lymphatic and the venous system. Those with small indiameters are generally asymptomatic and can be evacuated by needlea spiration. However, surgery is recommended for cysts over 6 cm in diameter due to risk of infection, bleeding, compression of neighboring ...