Searchable abstracts of presentations at key conferences in endocrinology

ea0056p813 | Pituitary - Clinical | ECE2018

The association between Ki-67 proliferation index, P53 expression, mitotic index, tumor invasion and the risk of recurrence in pituitary adenomas

Hasanov Rovshan , Aydogan Berna Imge , Gullu Sevim

Background: The 4th edition of World Health Organization (WHO) classification of pituitary tumors recommended evaluation of tumor proliferation and invasion to identify aggressiveness. We aimed to assess the relationship between Ki-67, mitotic index, P53 expression, invasion and recurrence risk in pituitary adenomas.Methods: Among 601 patients who underwent TN/TS adenomectomy between 2001 and 2016, 101 patients (16.8%) who had tumors with Ki-67 index &#8...

ea0049ep1487 | Thyroid (non-cancer) | ECE2017

Development of hypoparathyroidism due to targeted therapies

Gokcay Canpolat Asena , Aydogan Berna Imge , Canlar Sule , Gullu Sevim , Erdogan Murat Faik

Due to inhibition affect on proliferation, motility, resistance to apoptosis and growth of metastasis, the epidermal growth factor receptor (EGFR) inhibitor erlotinib and vascular endothelial growth factor receptor (VEGF) and EGFR inhibitor vandetanib are viable treatment options for treatment of advanced non-small cell lung cancer and thyroid cancer respectively. Advanced non-small cell lung carcinomas (NSCLC) or medullary and differentiated thyroid carcinomas (MTC and DTC) m...

ea0032p130 | Calcium and Vitamin D metabolism | ECE2013

Fahr’s disease with dystonia: a case report

Aydogan Berna Imge , Unluturk Ugur , Can Ferda , Sahin Mustafa , Uysal Ali Riza

Background: Fahr’s disease is a rare degenerative disorder characterized by symmetrical and bilateral intracranial calcification. Movement disorders are the most common symptoms of Fahr’s disease and dystonia is an uncommon presentation which accounts for only 8% of symptomatic patients.Case report: A 47 years old female admitted to emergency department with involuntary movements of extremities and anxiety. Neurological examination was normal e...

ea0032p391 | Diabetes | ECE2013

Atypical early onset Werner's syndrome

Aydogan Berna Imge , Yurumez Seda , Sengul Gozde , Sahin Mustafa , Baskal Nilgun

Introduction: Werner’s Syndrome (WS) is a rare autosomal recessive adult onset progeroid disorder characterized by the early onset of aged-appearance and age related metabolic disorders. Patients usually develop normally until the 3rd decades of life.Case report: We report a 27 years old female who admitted to our clinic at the age of 15 with hyperglycemia. She was diagnosed as diabetes and type 4 dyslipidemia at the age of 7 years. In her family hi...

ea0037oc3.4 | Calcium, vitamin D and bone | ECE2015

Cardiovascular risk factors in patients with medically observed and operated primary hyperparathyroidism

Colak Sevgi , Aydogan Berna Imge , Canpolat Asena Gokcay , Kaya Cansin Tulunay , Sahin Mustafa , Corapcioglu Demet , Uysal Ali Riza , Emral Rifat

Introduction: It is known that patients with primary hyperparathyroidism (PHPT) have an increased cardiovascular morbidity and mortality. In our study, we aimed to investigate the cardiovascular risk factors in medically observed and operated PHPT patients.Materials and methods: Twenty-nine medically observed (group A), 25 pre-operative (group B) and 23 post-operative (group C) patients with PHPT and 26 normocalcemic patients as control group (group D) w...

ea0037ep823 | Pituitary: clinical | ECE2015

Clinical features and treatment outcomes of resistant acromegaly patients: a single-centre study

Demir Ozgur , Canpolat Asena Gokcay , Aydogan Berna Imge , Keskin Caglar , Canlar Sule , Sahin Mustafa , Emral Rifat , Gullu Sevim , Gedik Vedia Tonyukuk , Uysal Ali Riza , Corapcioglu Demet

Introduction: Disease control in acromegaly can be achieved by surgery, medical treatment, and radiotherapy either alone or in combination. The acromegaly patients whom tumour shrinkage cannot be provided or growth hormone levels do not decrease under multiple treatment modalities are designated as resistant acromegaly. We aimed in our study to evaluate the clinical features of resistant acromegaly patients and determine their responds to different treatment modalities.<p ...

ea0032p1103 | Thyroid cancer | ECE2013

Evaluation of whole-body scan, stimulated thyroglobulin after thyroxine withdrawal vs recombinant TSH administration according to the risk groups of tumor recurrence

Sahin Mustafa , Aydogan Berna Imge , Yuksel Bagdagul , Erdogan Murat Faik , Gullu Sevim , Emral Rifat , Corapcioglu Demet , Baskal Nilgun , Uysal Ali Riza

Background: Recombinant human thyroid-stimulating hormone (rhTSH)-stimulated serum thyroglobulin (Tg) (s-Tg) and (131)I whole-body scanning (WBS) are supposed to provide equal diagnostic information with thyroxine withdrawal (THW) at follow-up thyroid cancer patients without the symptoms of hypothyroidism. We aimed to compare the WBS and s-Tg levels after thyrogen injection and thyroid hormone withdrawal for tumor recurrence/persistance according to the risk groups.<p clas...

ea0032p1086 | Thyroid cancer | ECE2013

Evaluation of treatment approaches to the sporadic and hereditary medullary thyroid carcinoma in Turkey

Yuksel Bagdagul , Aydogan Berna Imge , Gursoy Alptekin , Tuna Mazhar Muslum , Basaran Mehtap Vardar , Akkurt Aysen , Ertorer M Eda , Aydin Kadriye , Guldiken Sibel , Simsek Yasin , Karaca Zuleyha , Yilmaz Merve , Akturk Mujde , Anaforoglu Inan , Kebapci Nur , Taslipinar Abdullah , Kulaksizoglu Mustafa , Berker Dilek , Erbas Tomris , Erdogan Murat Faik

Introduction: RET mutation analysis has a critical importance for determining clinical approach to hereditary medullary thyroid carcinoma (MTC). The current guidelines recommends to determine the timing of prophylactic thyroidectomy depending on the risk stratification, mainly decided by the type of the mutation.Methods: Society of Endocrinology and Metabolism of Turkey (SEMT) sponsored ret genetic screening between July 2008 and January 2012 in 513 pati...

ea0032p1090 | Thyroid cancer | ECE2013

Distribution of ret proto-oncogene mutations among Turkish familial medullary thyroid cancer/multiple endocrine neoplasia 2 patients

Yuksel Bagdagul , Aydogan Berna Imge , Gursoy Alptekin , Tuna Mazhar Muslum , Basaran Mehtap Navdar , Akkurt Aysen , Ertorer Eda , Aydin Kadriye , Guldiken Sibel , Simsek Yasin , Karaca Zuleyha , Yilmaz Merve , Akturk Mujde , Anaforoglu Inan , Kebapci Nur , Taslipinar Abdullah , Kulaksizoglu Mustafa , Berker Dilek , Erbas Tomris , Faik Erdogan Murat

Introduction: TURK-MEN study was carried out to evaluate the mutational analysis of so called sporadic MTC patients between 1994 and 2005. Our aim was to evaluate the ret genetic screening results, distribution of mutations among so called sporadic and hereditary MTC patients in Turkey between 2008 and 2012.Methods: Society of Endocrinology and Metabolism of Turkey (SEMT) sponsored ret genetic screening between July 2008 and January 2012 in 513 patients....