Searchable abstracts of presentations at key conferences in endocrinology

ea0056p491 | Diabetes therapy | ECE2018

Six months of retrospective glycemic control and anthropometric outcomes in type 2 diabetic patients with new dapagliflozin treatment; actual clinical experience data from single center

Cander Soner , Calapkulu Murat , Gul Ozen Oz , Ersoy Canan

Introduction: SGLT2 inhibitors have been an important step in the treatment of diabetes. With numerous controlled experimental studies of these antidiabetic drugs, evaluation of real-life data after entry into clinical practice is an important condition. In our study, it was aimed to evaluate short-term results on glycemic control and weight loss in a narrow group of patients in the single tertiary medical center.Methods: The study was retrospectively de...

ea0063p1176 | Thyroid 3 | ECE2019

Coexistence of primary mucosa-associated lymphoid tissue lymphoma of thyroid and papillary thyroid microcarcinoma in a background of hashimoto’s thyroiditis

Duger Hakan , Calapkulu Murat , Ucan Bekir , Cakal Erman , Ozbek Mustafa , Yılmazer Demet

Introduction: Papillary thyroid carcinoma (PTC) is the most common endocrine cancer however extranodal marginal zone lymphoma of the mucosa-associated lymphoid tissue (MALT) of the thyroid gland is quite rare. The simultaneous association of both cancers is much more rare.Case report: 65-year-old woman underwent a thyroid ultrasound examination due to palpable thyroid nodules. Thyroid ultrasound revealed thyroiditis and multiple nodules on the right and ...

ea0070ep548 | Hot topics (including COVID-19) | ECE2020

Teriparatide treatment in a patient with resistance hypoparathyroidism

Erkam Sencar Muhammed , Calapkulu Murat , Ozturk Unsal İlknur , Hepsen Sema , Ozbek Mustafa , Cakal Erman

Background: Hypoparathyroidism is an uncommon disorder of calcium metabolism characterized by hypocalcemia, hyperphosphatemia, and reduced level of parathyroid hormone (PTH). The most common cause of hypoparathyroidism is accidental damage to the parathyroid glands during thyroid surgery. There are no formal guidelines for hypoparathyroidism management. The main goal of treatment is to improve the symptoms of hypocalcemia, to keep the serum calcium within the low normal range,...

ea0056p703 | Clinical case reports - Pituitary/Adrenal | ECE2018

A rare cause of central hypothyroidism: oral isotretinoin treatment

Gul Ozen Oz , Cander Soner , Calapkulu Murat , Ersoy Canan , Erturk Erdinc

Background: Isotretinoin has been used for many years to treat moderate or severe nodulocystic acne, disorders of sebaceous gland and keratinization and in the prevention of skin cancer. Certain types of retinoids may cause abnormalities in serum thyroid function tests by suppressing thyroid stimulating hormone (TSH). However, it is uncertain whether systemic isotretinoin has any effect on thyroid functions.Case: 18 years old woman has admitted to our ho...

ea0070aep33 | Adrenal and Cardiovascular Endocrinology | ECE2020

Adrenocortical cancer mimicking lymphoma on magnetic resonance scan

Calapkulu Murat , Erkam Sencar Muhammed , Duger Hakan , Kizilgul Muhammed , Ucan Bekir , Ozturk Unsal İlknur , Akhanli Pinar , Cakal Erman

Background: Adrenocortical carcinoma (ACC) is a rare cancer that originates from the cortex of the adrenal gland. Although its exact etiology is not clear, it has been found to be associated with some hereditary cancer syndromes. Sometimes patients present with hormonal excess symptoms (virilization, Cushing’s syndrome) or local symptoms consistent with an abdominal mass. In ACC, computed tomography (CT) and magnetic resonance imaging (MRI) are preferred imaging modaliti...

ea0070aep601 | Pituitary and Neuroendocrinology | ECE2020

A case of wolfram syndrome with primary hypogonadism

Calapkulu Murat , Erkam Sencar Muhammed , Ozturk Unsal İlknur , Duger Hakan , Kizilgul Muhammed , Bostan Hayri , Cakal Erman , Ozbek Mustafa

Introduction: Wolfram syndrome, is a rare autosomal recessive genetic disorder that is characterized by diabetes mellitus (DM), diabetes insipidus (DI), optic atrophy, and sensorineural deafness as well as various other possible disorders. DM is the first manifestation, and optic atrophy also onsets in the first decade of life. The onsets of DI and sensorineural deafness are in the second decade, urinary tract abnormalities are in the third decade, and neurologic abnormalities...