Searchable abstracts of presentations at key conferences in endocrinology

ea0041ep947 | Pituitary - Clinical | ECE2016

A case of acromegaly presenting with lacrimal gland hypertrophy

Cakir Mehtap

Introduction: Acromegaly is a chronic endocrine disorder caused by excess growth hormone (GH) secretion. Hypersecretion of GH causes increased IGF-1 secretion from the liver which in turn leads to a series of multisystemic complications including somatic overgrowth and multiple comorbidities.Case report: Thirty-nine-year-old female patient was seen in ophthalmology outpatient clinic with the complaint of a mass inside the right upper eyelid. On ophthalmo...

ea0020s12.2 | Growth factors and signaling networks in pituitary tumours | ECE2009

MAPK and PI3K/AKT pathways in pituitary tumorigenesis

Cakir Mehtap

Mitogen-activated protein kinases (MAPK) are a family of serine/threonine kinases and are key signaling pathways involved in the regulation of normal cell proliferation, survival and differentiation. In mammals, there are more than a dozen MAPK genes. The best known are the extracellular signal-regulated protein kinases (ERK1 and 2); c-Jun N-terminal kinases (JNK1-3); p38s (α, β, γ, δ) and ERK5. Aberrant regulation of MAPK cascades contribute to cancer and ...

ea0015p112 | Diabetes, metabolism and cardiovascular | SFEBES2008

Significant hyperkalemia and hyponatremia with telmisartan/hydrochlorotiazide combination

Cakir Mehtap

A 71-year-old hypertensive and diabetic male patient was seen in the outpatient clinic for routine control. On laboratory examination his serum potassium level was 5.76 mmol/l and serum sodium level was 135 mmol/l. Control serum potassium level was 5.7 mmol/l. In past medical history he was prescribed telmisartan/hydrochlorothiazide combination (80 mg/12.5 mg) 1 month ago for treatment of hypertension. His other medications included nifedipine, fluvastatin sodium, aspirin, pio...

ea0035p842 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

Clinical evaluation of follow-up of 62 patients: do treatment methods in acromegaly affect the rates of cure and hypophyseal insufficiency?

Evran Mehtap , Sert Murat , Tetiker Tamer

Background: Transsphenoidal surgery of pituitary adenoma is often first-line therapy for patients with acromegaly. Pharmacotherapy and/or radiotherapy are applied when surgery fails to achieve good disease control, or when surgery is impossible or contraindicated. In this study, we report the results of therapies, rates of cure and hypophyseal insufficiency in our acromegalic patients.Methods and results: Medical files of the 62 patients who were followe...

ea0049ep1241 | Thyroid (non-cancer) | ECE2017

Two pseudomalabsorbtion cases successfully treated with parenteral levothyroxine

Altuntaş Seher Cetinkaya , Evran Mehtap , Sert Murat , Tetiker Tamer

Hypothyroidism is a common endocrine disorder which is easily treatable by an appropriate thyroid hormone replacement therapy in the majority of patients. In some patients, hypothyroidism is refractory to oral levothyroxine substitution. Common causes of lack of response to levothyroxine replacement comprise non-compliance and impaired absorption. We report a case of pseudomalabsorption of levothyroxine. Here, we report two female patients with hypothyroidism who had multinod&...

ea0041ep18 | Adrenal cortex (to include Cushing's) | ECE2016

Carotid intima-media thickness as the cardiometabolic risk indicator in patients with nonfunctional adrenal mass and metabolic syndrome screening

Akkus Gamze , Tetiker Tamer , Deniz Ali , Evran Mehtap , Sert Murat

Objective: Nonfunctional adrenal masses are a risk indicator of increased cardiometabolic risk. Especially; increased thrombogenic ambient, insulin resistance, hepatosteatosis and abdominal obesity are determined in these patients with nonfunctional adrenal masses. Our purpose was to show the association of adrenal incidentalome and metabolic syndrome in consideration of the studies and to detect the increase in the carotid intima-media thickness which is regarded as the prece...

ea0037ep31 | Adrenal cortex | ECE2015

A case of aldosterone-secreting giant adrenal carcinoma: a case report

Evran Mehtap , Akkus Gamze , Sert Murat , Tetiker Tamer

Introduction: Primary aldosteronism is presented with signs of hypertension and hypokalaemia classically, however, primary adrenal carcinoma is very rare condition. We aimed to present a patient with a metastatic adrenal carcinoma after the primary diagnosis of hyperaldosteronism.Case report: A 46 years old male patient was referred to our hospital with weakness, dry mouth and weight loss. He had lost weight as 31 pounds during last 3 months. Physical ex...

ea0037ep1183 | Clinical Cases–Pituitary/Adrenal | ECE2015

Laryngeal carcinoma in acromegalic patients: a rare case

Akkus Gamze , Evran Mehtap , Sert Murat , Tetiker Tamer

Introduction: Acromegaly is a very rare disease with persistent GH secretion due to excessive release of liver IGF1. The risk of malignancy, particularly colon cancer, is increased in acromegalic patients. But no evidence is found in the literature associated increasing of laryngeal carcinoma in acromegalic patients. We aimed to present this case that laryngeal carcinoma should be considered in acromegaly by the clinicians.Case report: A 51-year-old male...

ea0035p118 | Calcium and Vitamin D metabolism | ECE2014

The relationship with plasma calcium levels, metabolic syndrome, and risk parameters in overweight and obese Turkish women

Ipek Emel , Ucer Mehtap , Cikim Ayse , Tanyolac Sinan

Introduction: Obesity prevalance is rapidly increasing all over the world and become a serious health problem. There is a significant correlation between serum calcium levels and body fat mass. It was indicated that when plasma calcium levels increase, BMI decrease however, insulin, total cholesterol, and triglycerides levels increase. In this study, it was investigated the relationship between plasma calcium levels and cardiovascular risk factors and metabolic syndrome parame...

ea0035p841 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

Demographical and clinical characteristics of 62 acromegalic patients

Evran Mehtap , Sariakcali Baris , Sert Murat , Tetiker Tamer

Background: Acromegaly is a relatively rare endocrine disorder which may result in morbidity and mortality. In this study, we report the demographical and clinical characteristics of 62 acromegalic patients who were followed-up at our Department of Endocrinology Clinic.Methods and results: In this retro-prospective study, medical files of the patients who were followed-up from 1984 to 2013 were examined. Data was obtained for age at the time of diagnosis...