Searchable abstracts of presentations at key conferences in endocrinology

ea0056p1179 | Thyroid cancer | ECE2018

A rare case of mixed medullary and papillary thyroid carcinoma related with heterozygous VAL804MET mutationa rare case of mixed medullary and papillary thyroid carcinoma related with heterozygous VAL804MET mutation

Guler Bagdagul Yuksel , Faki Sevgul , Aydin Cevdet , Yalcin Abdussamed , Yavuz Huban Sibel Orhun , Ersoy Reyhan , Cakir Bekir

Introduction: Papillary thyroid carcinoma(PTC) and medullary thyroid carcinoma(MTC) have always been considered different tumors. Concomitant presence of MTC and PTC in the same patient is a rare clinical event.Case report: A 43 year-old woman admitted with fatigue, a serum thyrotropin of 4.6 uIU/ml and a 15×11 mm thyroid nodule in right lobe detected in another center. Fine needle aspiration(FNA) of the nodule was consistent with MTC. In family his...

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...

ea0073pep15.1 | Presented ePosters 15: Late Breaking | ECE2021

Diabetic euglycemic ketoacidosis in newly diagnosed type 1 diabetes mellitus during A ketogenic diet

Erdogan Beril Turan , Durmaz Himmet , Bestepe Nagihan , Ogmen Berna , Ozdemir Didem , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

BackgroundDiabetic ketoacidosis (DKA) is one of the most serious complications of diabetes. It is characterised by the triad of hyperglycemia (blood sugar >250 mg/dl), ketosis and metabolic acidosis (arterial pH CaseA 22-year-old female patient appl...

ea0073aep788 | Late Breaking | ECE2021

Significant regression of primary adrenal lymphoma after acute steroid replacement therapy: a case with an insufficient initial biopsy

Helvaci Burcak , Durmus Bugra , Ozcelik Ozgur , Narin Nasirogluİmga , Ali Sendur Mehmet , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

ObjectiveThere is limited clinical data available on bilateral adrenal masses (BAM). Here we present a case with BAC and adrenal insufficiency. The patient’s lesions disappeared after steroids, re-grew in the follow-up, allowing a biopsy.CaseA 60-year-old male patient presented with abdominal pain, nausea, and weakness to another hospital. Hyponatremia and hyperkalemia accompanied by hypotension were det...

ea0073aep795 | Late Breaking | ECE2021

Severe hypercholesterolemia with primary sclerosing cholangitis

Durmaz Himmet , Arifoglu Unzile , Keskin Caglar , Baser Husniye , Akdogan Kayhan Meral , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

IntroductionHypercholesterolemia may develop due to primary and secondary causes. Diabetes mellitus, hypothyroidism, nephrotic syndrome and liver diseases are among the most common causes of secondary hyperlipidemia. Here, we will present a case with severe hyperlipidemia due to primary sclerosing cholangitis(PSC).CaseA 36-year-old male patient was admitted to our outpatient clinic due to severe hypercholeste...

ea0073aep796 | Late Breaking | ECE2021

A case of non-familial pheochromocytoma presenting one of the identical twin at young age

Turan Kubra , Copuroglu Esra , Sacikara Muhammed , Nasiroglu Imga Narin , Tuncel Altug , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

BackgroundPheochromocytomas are rare tumors originating from chromaffin cells and characterized by excessive catecholamine synthesis. They are usually benign lesions. Hypertension(HT), tachycardia, sweating and headache are frequently observed. We aimed to present a high malignancy suspected pheochromocytoma case diagnosed in a young age female.Case presentationA 20-year-old female patient was admitted to the...

ea0073aep811 | Late Breaking | ECE2021

Post-transplant dyslipidemia in two cases

Ince Nurcan , Durmus Bugra , Ozcelik Ozgur , Dirikoc Ahmet , Cevdet Aydın , Topaloglu Oya , Ersoy Reyhan , Bekir Cakır

IntroductionLung transplantation was associated with a 32% prevalence of hypercholesterolemia and a 41% prevalence of hypertriglyceridemia. The prevalence of dyslipidemia in liver transplant recipients is 43% and 31% –51%. In this report, we present 2 cases who developed dyslipidemia after transplantation.Case 1The blood test of a 73-year-old male patient who had lung transplantation about 3 years ago re...

ea0073aep816 | Late Breaking | ECE2021

24-week impact of dapagliflozin treatment on body weight, body composition, and cardiac risk indicators of patients with type-2 diabetes mellitus

Akhanli Pinar , Hepsen Sema , Emre Arslan Ismail , Duger Hakan , Bostan Hayri , Kizilgul Muhammed , Ucan Bekir , Cakal Erman

AimsWe aimed to reveal the impacts of dapagliflozin, a sodium glucose transporter inhibitor (SGLT2i), on the body weight and body composition, cardiovascular risk indexes, and carotis intima-media thickness (CIMT).MethodsBody weights, body compositions measured by means of bioelectrical impedance, and CIMT in the baseline, the 12th, and the 24th week of 42 patients with type-2 diabetes mellitus receiving SGLT...

ea0073aep847 | Late Breaking | ECE2021

Two thyrotropin secreting pituitary adenoma cases diagnosed after response to the somatostatin analogue

Karahmetli Gulsum , Houssein Mehdi , Belma Ozlem Tural Balsak , Ogmen Berna , Topaloglu Oya , Ersoy Reyhan , Bekir Cakır

IntroductionPituitary adenomas secreting TSH (TSHoma) are a rare cause of hyperthyroidism. They account for approximately 0.5–3 % of functioning pituitary tumours and much less than 1% of all cases of hyperthyroidism. TSHoma should be considered in all hyperthyroid patients, especially those with diffuse goitre and no extrathyroidal signs of Graves’ disease.Case 1A 30-year-old female applied to the ...

ea0073aep850 | Late Breaking | ECE2021

A case of pituitary xanthogranuloma diagnosed with diabetes insipidus

Turan Kubra , Arifoglu Unzile , Nasiroglu Imga Narin , Tural Balsak Belma , Divanlioglu Denizhan , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

BackgroundPituitary xanthogranulomas are extremely rare tumors of the sellar region. A cystic mass lesion was found in the pituitary MRI of our patient diagnosed with central diabetes insipidus (DI). We aimed to present a case who was operated for a pituitary mass and diagnosed with sellar xanthogranuloma.Case presentation37-year-old female patient was applied to our outpatient clinic with complaints of polyd...