Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep322 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Long-term glycaemic follow-up results of hospitalised COVID-19 patients with hyperglycemia

Gecti Sinem , Saygili Emre Sedar , Karakilic Ersen

Introduction and Aims: A higher prevalence of hyperglycemia has been reported in patients affected by coronavirus disease 2019 (COVID-19). Our study aims to retrospectively evaluate the course of hyperglycemia in patients recovering from COVID-19.Methods: All patients who were hospitalised in Çanakkale Onsekiz Mart University Hospital between March 2020 and March 2022 due to COVID-19 and whose HbA1c values were checked during hospitalisation were ex...

ea0049ep109 | Clinical case reports - Pituitary/Adrenal | ECE2017

Prolonged zona glomerulosa insuffiency with hyperkalemia in primary hyperaldosteronism after adrenalectomy

Ozturk Feyza Yener , Sen Esra Cil , Erol Rumeysa Selvinaz , Saygili Emre Sedar , Basmaz Seda Erem , Cakir Sezin Dogan , Batman Adnan , Altuntas Yuksel

Introduction: Hyperkalemia due to zona glomerulosa (ZG) insufficiency is generally transient and mild for patients with aldosterone-producing adenoma (APA) after adrenalectomy. We report here a case with prolonged ZG insuffiency requiring long-term mineralocorticoid replacement (MR) therapy.Case report: A 45-years-old female with hypertension and hypokalemia admitted to outpatient clinic with incidentally detected right adrenal adenoma (3 cm) showing sig...

ea0049ep836 | Clinical case reports - Pituitary/Adrenal | ECE2017

Successful management of macroprolactinoma with aromatase inhibitor in a patient with hypogonadotropic hypogonadism

Ozturk Feyza Yener , Sen Esra Cil , Erol R Selvinaz , Cakir Sezin Dogan , Basmaz Seda Erem , Saygili Emre Sedar , Batman Adnan , Altuntas Yuksel

Introduction: Hypogonadism persisting in man with macroprolactinoma requires exogenous testosterone replacement therapy (TRT). But TRT may cause secondary elevations of prolactin. We report here a case of macroprolactinoma and hypogonadotropic hypogonadism with persistently high prolactin level after initiating TRT.Case report: A 28 year-old male was admitted to outpatient clinic with complaints of headache, low libido and blurred vision on left eye for ...

ea0056gp191 | Pituitary / Growth Hormone ' IGF Axis | ECE2018

Ectopic Cushing’s syndrome secondary to medullary thyroid carcinoma with apparent signs of hypercortisolism: a case report

Canat M Masum , Cakir Sezin Dogan , Yildiz Duygu , Ozturk Feyza Yener , Erol Rumeysa Selvinaz , Sen Esra Cil , Saygili Emre Sedar , Basmaz Seda Erem , Batman Adnan , Altuntas Yuksel

Introduction: Ectopic ACTH syndrome (EAS) is a rare cause of Cushing’s syndrome. EAS is most frequently caused by bronchial carcinoid tumor or small cell lung cancer. Medullary thyroid carcinoma (MTC) is a rare source of EAS, as reported in this case.Case report: A 65-years-old-female with back pain and weight gain referred to our outpatient clinic with determined signs and symptoms of hypercortisolism. She had arterial hypertension, her sister had ...

ea0056p709 | Clinical case reports - Pituitary/Adrenal | ECE2018

Successful management of Cushing’s disease in pregnancy: a case report

Batman Adnan , Ozturk Feyza Yener , Sen Esra Cil , Erol Rumeysa Selvinaz , Canat Muhammed Masum , Saygili Emre Sedar , Cakir Sezin Dogan , Basmaz Seda Eren , Yildiz Duygu , Altuntas Yuksel

Introduction: Cushing’s disease (CD) frequently leads to hypogonadotropic hypogonadism by hypercortisolism and hyperandrogenemia. In the literature, there are totally 96 cases of CD and pregnancy. Only four of 11 cases, operated transsphenoidally, were cured. We aimed to present a case of CD developing pregnancy in which hypercortisolism was successfully controlled by transsphenoidal surgery (TSS) in 2nd trimester.Case report: 28 years old female wa...

ea0056ep84 | Diabetes, Obesity and Metabolism | ECE2018

A case report of MODY 2 treated as type 2 diabetes mellitus in pregnancy

Batman Adnan , Saygili Emre Sedar , Basmaz Seda Eren , Cakir Sezin Dogan , Yildiz Duygu , Ozturk Feyza Yener , Sen Esra Cil , Erol Rumeysa Selvinaz , Canat Muhammed Masum , Altuntas Yuksel

Introduction: Maturity-onset diabetes of young (MODY) type 2 is caused by mutation of the glucokinase gene. It is characterized by mild fasting hyperglicemia and absence of vascular complications. It is estimated that the incidence of gestational diabetes is 3%. We aimed to present a pregestational diabetic case with MODY-type 2 in pregnancy.Case report: A 38-year-old pregnant woman was referred to our clinic for glycemic regulation at 22th week of gesta...

ea0056ep95 | Interdisciplinary endocrinology | ECE2018

A case with autoimmune polyglanduler syndrome type 3A

Batman Adnan , Erol Rumeysa Selvinaz , Ozturk Feyza Yener , Sen Esra Cil , Canat Muhammed Masum , Saygili Emre Sedar , Cakir Sezin Dogan , Basmaz Seda Eren , Yildiz Duygu , Altuntas Yuksel

Introduction: Autoimmune polyendocrine syndromes (APS) are rare endocrinopathies characterized by the coexistence of at least two glandular autoimmune diseases. APS comprise a wide spectrum of autoimmune disorders and are divided into a very rare juvenile (APS type 1) and a more common adult type with (APS 2) or without adrenal failure (APS 3). We present a patient with polyglanduler syndrome type 3a.Case report: A 39-years-old female patient was present...

ea0056p271 | Clinical case reports - Thyroid/Others | ECE2018

Regression of multipl brown tumors after surgical removal of mediastinal ectopic parathyroid adenoma

Cakir Sezin Dogan , Erol Rumeysa Selvinaz , Saygili Emre Sedar , Basmaz Seda Erem , Batman Adnan , Ozturk Feyza Yener , Sen Esra Cil , Canat Muhammed Masum , Yildiz Duygu , Ersen Ezel , Altuntas Yuksel

Introduction: Parathyroid adenoma is the most common cause of primer hyperparathyroidism (PHPT). Mediastinal ectopic parathyroid adenomas constitute about 1–3% of the cases. Brown tumors ocur in less than 2% of the patients with PHPT. Moreover, those skeletal manifestations are even rarely demonstrated with maxillofacial bones involvement.Case presentaton: Here we report a 36-years-old woman presented with approximately 30×26 mm mass growth in ...

ea0090ep19 | Adrenal and Cardiovascular Endocrinology | ECE2023

21-hydroxylase deficient congenital adrenal hyperplasia in adult endocrinology clinics of turkey: A nationwide multicenter study

Ertorer Melek Eda , Anaforoglu İnan , Yilmaz Nusret , Akkus Gamze , Turgut Seda , Unluhizarci Kursad , Selcukbiricik Ozlem Soyluk , Merdin Fatma Avcı , Karakilic Ersen , Pehlivan Esma , Yorulmaz Goknur , Gul Ozen Oz , Emral Rifat , Kebapci Medine Nur , Acubucu Fettah , Tuzun Dilek , Gorar Suheyla , Topuz Emek , Bagir Gulay Simsek , Genc Selin , Demir Kezban , Tamer Gonca , Yaylali Guzin , Omma Tulay , Firat Sevde Nur , Koc Gonul , Saygili Emre Sedar , Yurekli Banu Sarer

Introduction: Congenital adrenal hyperplasia (CAH) is a group of autosomal recessively inherited disorders that are characterised by inactivating mutations at various steps of adrenal steroidogenic pathways causing defective cortisol biosynthesis. 21-Hydroxylase enzyme deficiency (21-OHd) constitutes more than 95% of all CAH cases.Material & Methods: Medical records of patients with all forms of CAH from 19 adult endocrinology clinics located at six ...