Searchable abstracts of presentations at key conferences in endocrinology

ea0049gp53 | Cardiovascular & Lipid Endocrinology | ECE2017

Clinical, laboratory and cardiac parameters in overt primary hypothyroidism versus overt central hypothyroidism

Balas Melania , Parv Florina , Vlad Mihaela , Golu Ioana , Amzar Daniela , Zosin Ioana

Background: Hypothyroidism affects cardiac function, leading to cardiomyopathy, pericarditis, lower left ventricular performance, etc. The present study investigates different parameters (clinical, hormonal, biochemical, echocardiographic) in overt primary hypothyroidism (OPHypo) and overt central hypothyroidism (OCHypo).Material and methods: The study included 33 untreated patients with OCHypo (5 with empty sella, 3 with idiopathic hypopituitarism, 7 wi...

ea0049ep306 | Calcium & Vitamin D metabolism | ECE2017

Hyperparathyroidism and cardiovascular risk

Amzar Daniela , Balas Melania , Golu Ioana , Vlad Mihaela , Sandu Ramona , Cornianu Maria

Background: Primary and secondary hyperparathyroidism (HP) are associated with increased risk for cardiovascular complications and high mortality. Risk factors correlated with hypertension in HP are hyperlipidemia, glucose intolerance, insulin resistance, vitamin D deficiency, etc. The aim of the study was to assess the incidence of cardiovascular complications in HP.Material and methods: The study included 45 patients (15 men, 30 women), with a mean age...

ea0049ep1068 | Pituitary - Clinical | ECE2017

Sheehan’s syndrome in clinical practice

Vlad Mihaela , Golu Ioana , Amzar Daniela , Balas Melania , Butaru Miruna , Milos Ioana , Zosin Ioana

Sheehan’s syndrome represents a rare cause of pituitary insufficiency, produced by an ischemic pituitary necrosis due to a severe haemorrhage at deliverance. Epidemiologic data indicate that, nowadays, this disease is quite rare in developed country.Aim: To determine and evaluate the clinical and hormonal characteristics of cases with Sheehan’s syndrome diagnosed and follow-up in our Clinic, during the last ten years.Subj...

ea0037ep869 | Thyroid cancer | ECE2015

A rare case of an off midline thyroglossal duct cyst papillary thyroid carcinoma

Balas Melania , Golu Ioana , Amzar Daniela , Vlad Mihaela , Ianes Emilia , Dema Alis , Zosin Ioana

Introduction: Papillary thyroid carcinoma can be found very rarely in a thyroglossal duct cyst (TDC) (1%), this cancer variant being the most common type. Although, most of the TDC develop in the midline of the thyroglossal duct (~70%), some cysts occur off midline, within 2 cm of the midline.Case presentation: The female patient of 34-year-old presented at the Maxillofacial Surgery Department in October 2014, with a right submandibular painless neck mas...

ea0037ep1138 | Endocrine tumours | ECE2015

Real-time shear wave elastography in the evaluation of parathyroid adenomas

Vlad Mihaela , Golu Ioana , Amzar Daniela , Balas Melania , Zosin Ioana , Sporea Ioan

Real-time shear wave ultrasound elastography (SWE) is a new technique, which evaluates elasticity and stiffness of the different structure.Aim: To determine the values of the elasticity index (EI) measured by SWE in parathyroid gland adenomas and to compare with those of normal thyroid tissue.Subjects and methods: We studied 50 cases (F/M=42/8), ten with primary or tertiary hyperparathyroidism, diagnosed by specific tests, and 40 h...

ea0035p543 | Endocrine tumours and neoplasia | ECE2014

The prevalence of malignancy in thyroid incidentalomas in an iodine-replete area

Balas Melania , Vlad Mihaela , Golu Ioana , Amzar Daniela , Urian Ananda , Gurban Camelia , Zosin Ioana

Background: Thyroid incidentalomas are reported with increasing incidence in the last decades. The rate of malignancy in these nodules may reach 9% or higher, depending on the patients selection.Material and methods: A retrospective study was done on 429 patients with nodular goiter (issued from an iodine-replete area), admitted in the Clinic of Endocrinology, Timisoara, Romania, from January 2011 to December 2013.Results: The prev...

ea0070ep335 | Pituitary and Neuroendocrinology | ECE2020

Complications of acromegaly regarding GH concentrations

Amzar Daniela-Georgiana , Melania Balas , Ioana Golu , Mihaela Vlad , Cotoi Laura

Introduction: Acromegaly is a rare disease caused by excess production of growth hormone (GH) and is associated with multiple complications. The prevalence of associated complications and the mortality rate are associated with the duration of exposure to elevated GH levels, early diagnosis being imperative. Diagnosis of acromegaly is most frequently late, after several years of evolution, with the development of cardiovascular, respiratory, metabolic complications. The presenc...

ea0070ep336 | Pituitary and Neuroendocrinology | ECE2020

GH-secreting adenoma in peripubertal period

Amzar Adaniela-Georgiana , Balas Melania , Ioana Golu , Mihaela Vlad , Corina Paul , Cotoi Laura

Introduction: Gigantism represents a rare pathology in children, characterized by growth hormone (GH) excess, before epiphyseal fusion. It associates significant morbidity and decreased life expectancy, in lack of appropriate treatment.Case presentation: O.D., a male patient, 16 years old now, has been followed in our clinic since 2016, being diagnosed with gigantism in Bega Pediatric Clinic, at the age of 12 years 9 months. In 2014, the patient presente...

ea0070ep365 | Pituitary and Neuroendocrinology | ECE2020

Acromegaly in young patients - treatment challenges, case presentation

Cotoi Laura , Melania Balas , Ioana Golu , Mihaela Vlad , Amzar Daniela-Georgiana

Introduction: Acromegaly is a debilitating, indolent disease that develops over several years due to extended exposure to elevated growth hormone (GH) levels. It is most commonly caused by somatotropinomas. It represents a rare pathology with an incidence of 3–14 cases per 1 million inhabitants and a prevalence of 40 to 90 cases per 1 million inhabitants. Pituitary adenomas respresent a challenging disease in young patients. Transphenoidal surgery is the best therapeutic...

ea0070ep514 | Thyroid | ECE2020

Management and evolution of papillary thyroid carcinoma in a patient with acromegaly

Vlad Mihaela , Cornianu Marioara , Balas Melania , Golu Ioana , Amzar Daniela-Georgiana , Varcus Flore

Background: Acromegaly is a chronic rare disease induced by persistent hypersecretion of growth hormone (GH) and insulin-like growth factor 1 (IGF-1) in adult patients. Several studies have associated acromegaly with an increased risk for developing different benign or malignant tumors.Case presentation: A 33-year old female patient was diagnosed with acromegaly due to a large pituitary macroadenoma, in 2009. In the same period, she was also diagnosed wi...