Searchable abstracts of presentations at key conferences in endocrinology

ea0049ep854 | Clinical case reports - Pituitary/Adrenal | ECE2017

A case of cystic prolactinoma responsed to medical treatment

Omma Tulay , Gulcelik Nese Ersoz , Karaca Anara , Taskaldiran Isilay

Introduction: Cystic prolactinomas are considered resistant to volume depletion by dopamine agonists (DAs). Because of the effectiveness and tolerability, dopamine agonists (DAs) are the first line therapies in prolactinoma and reduce tumor mass as well as prolactin levels in most of all patients. Rathke’s cleft cysts, craniopharyngiomas and arachnoid cysts are differential diagnoses to keep in mind. DAs resistance or intolerance, psychiatric disorders associated with dop...

ea0049ep384 | Clinical case reports - Pituitary/Adrenal | ECE2017

Prediction of type 1 diabetes in autoimmune polyglandular syndrome type 2

Karaca Anara , Gulcelik Nese Ersoz , Omma Tulay , Taskaldiran Isilay , Firat Sevde Nur , Bozkurt Nujen

Introduction: Autoimmune Polyglandular Syndrome (APS) is a very rare endocrinopaty, characterized by the coexistence of at least two glandular autoimmune mediated diseases. In this case a patient presented with hyperpigmentation of the whole body, significant weight loss for last 6 months.Case: A-49 year old male were refered to our deparment with loss of appetite, fatigue, nausea, weight loss and with marked buccal pigmentation. Blood pressure was 80/50...

ea0049ep1175 | Male Reproduction | ECE2017

A case with taurodontism and Klinefelter syndrome

Taskaldiran Isilay , Omma Tulay , Karaca Anara , Taskaldiran Alper , Ersoz Gulcelik Nese

: In this paper we present an 18-year-old patient with Klinefelter syndrome who has taurodontism. Klinefelter syndrome is the most common abnormality of sex chromosomes. It is characterized by hypogonadism, gynaecomastia, azoospermia or oligospermia, and increased levels of gonadotropins. Associated medical disorders can be categorized as follows; cancer, autoimmune disorders, intellectuel and psychiatric disorder, osteoporosis, endocrine disorders, venous disease and taurodon...

ea0032p279 | Clinical case reports - Thyroid / Others | ECE2013

Giant cell granuloma as initial presentation of primary hyperparathyroidism: a case report

Polat Sefika Burcak , Taskaldiran Isilay , Evranos Berna , Kilicaslan Aydan , Kaya Elif , Ersoy Reyhan , Cakir Bekir

Giant cell granuloma is a skeletal manifestation seen now rarely in hyperparathyroidism due to early recognition of the disease. Lesions usually occur in the areas of intense bone resorption. They can affect mandible, maxilla, clavicle, ribs and pelvic bones. Most of the patients who have primary hyperparathyroidism are asymptomatic and are discovered incidentally during laboratory examinations. Here, we represent a female patient who was referred to endocrinology clinics beca...

ea0056p1089 | Thyroid (non-cancer) | ECE2018

Riedel’s Thyroiditis with Hypothyroidism and Hypoparathyroidism

Taskaldiran Isilay , Firat Sevde Nur , Koc Gonul , Demirturk Pelin , Culha Cavit , Erdogan Murat Faik

Riedel thyroiditis (RT) is a rarest form of thyroiditis, and characterized by dense fibrosis of the throid gland and infiltration into surrounding tissues. RT generally presents with local symptoms association with compression and also fibrotic process can impact thyroid and parathyroid functions. We report a case with RT which presents with compression findings and also hypoparathyroidism and hypothyroidism. 30 year old women visited our outpatient clinic with a complaint of ...

ea0056ep6 | Adrenal and Neuroendocrine Tumours | ECE2018

Co-existence of malign insulinoma and diabetes mellitus

Taskaldiran Isilay , Kuskonmaz Serife Mehlika , Ozenmis Tahsin , Koc Gonul , Kucuk Nuriye Ozlem , Culha Cavit

Insulinomas are rare neuroendocrine tumors (NETs) of the pancreas with an incidence of four per 1 million persons per year. The co-existence of diabetes mellitus (DM) and insulinoma is very rare. We report a case of 73 year old women with malignant insulinoma and type 2 DM. A 73 year old woman with type 2 diabetes was referred to our clinic for recurrent and severe hypoglycemia especially in the early morning hours. The patient had a history of type 2 DM for 10 years. Although...

ea0056ep9 | Adrenal and Neuroendocrine Tumours | ECE2018

Case report: management of a patient with malignant insulinoma

Topaloglu Oya , Sendur Mehmet Ali , Dumlu Gurkan , Yildirim Fatma , Taskaldiran Isilay , Soydal Cigdem , Ersoy Reyhan , Cakir Bekir

Introduction: Malignant insulinoma is a rare functional endocrine tumor of the pancreas. Therefore, there are few data regarding their optimal therapy and long term prognosis. Malignancy is defined by the presence of metastases, mostly in lymph nodes or the liver. Generally these patients present with severe hypoglycemia and require multiple therapies. Here, we described the management of a patient with malignant insulinoma.Case: A 41-year-old woman with...

ea0070aep182 | Bone and Calcium | ECE2020

Clinical characteristics of subjects with very high serum 25 OH vitamin D levels in turkey: DeVIT-TOX survey

Pekkolay Zafer , Gogas Yavuz Dilek , Sedar Saygili Emre , Topaloğlu Ömercan , Emir Önder Çağatay , Soylu Hikmet , Taskaldiran Isilay , Esen Pazır Ayșe , Ugur Kader , Tanrikulu Seher , Nur Firat Sevde , Meryem Atak Burcu , Batman Adnan , Omma Tülay , Cagiltay Eylem , Ozdemir Kutbay Nilufer , Çetinkaya Altuntaș Seher , Nasiroglu Imga Narin , Karakilic Ersen , Hekimsoy Zeliha , Kılınç Faruk , Yay Adnan , Eroğlu Mustafa , Kemal Tuzcu Alpaslan

Background: Treatment of vitamin D deficiency orinappropriate vitamin D supplementation may cause side effects associated with hypercalcemia. We observed a tendency to use very high single dose cholecalciferol for treatment of vitamin D deficiency.Aim: The primary aim of this study was to examine the clinical characteristics of patientswith very high serum 25OHD levels of vitamin D toxicity in Turkey.Materials and methods: An invit...