Searchable abstracts of presentations at key conferences in endocrinology

ea0029p399 | Clinical case reports - Pituitary/Adrenal | ICEECE2012

Unusual association between pheochromocytoma, adrenocortical nodular hyperplasia and empty sella: case report

Preda C. , Grigorovici A. , Ciobanu D. , Moisii L. , Vulpoi C. , Ungureanu M. , Leustean L. , Mogos V.

Introduction: Pheochromocytoma occasionally associates with pathological lesions of the adrenal cortex. We report a case of non-functional adrenocortical nodular hyperplasia with a concomitant pheochromocytoma in the controlateral adrenal and empty sella.Case report: We describe the case of a 52 year old women with a history of essential hypertension and type 2 diabetes mellitus. She complained of: nausea, abdominal pain, vomiting and constipation. The c...

ea0029p966 | Female Reproduction | ICEECE2012

Clinical, hormonal and metabolic profile in overweight and obese women with polycystic ovary syndrome

Leustean L. , Preda C. , Fica S. , Ungureanu M. , Cristea C. , Ungureanu D. , Mogos V. , Vulpoi C.

Polycystic ovary syndrome (PCOS) is a heterogeneous condition affecting 5–10% of reproductive -age female population.The aim of this study was to determine the clinical features, metabolic and hormonal profile in obese and overweight women with PCOS.Patients and method: A total of 102 women (age 31.28±6.05 and BMI 33.02±5.93) with PCOS and 110 (age 32.35±4.96 and BMI 33.05±5.87) matched controls were invest...

ea0011p209 | Clinical practise and governance | ECE2006

Does HT still have a place? The impact on menopausal-related symptoms

Cristea C , Vulpoi C , Ungureanu MC , Leustean L , Concita C , Mogos V , Zbranca E

Hormonal treatment (HT) represents the only complete therapy of the consequences of the postmenopausal estrogenic deficiency. Quality of life in postmenopausal women is often compromised. We evaluated the quality of life (appreciated with IQL questionnaire) in 80 postmenopausal women – 40 with intact uterus, treated with natural estrogens associated with progestin, and 40 non-treated women. Group selection (treated/not treated) was made function of the inform consent of t...

ea0029p389 | Clinical case reports - Pituitary/Adrenal | ICEECE2012

Hyponatremia and cytolysis as first signs of decompensated pituitary insufficiency: case report

Potorac I. , Preda C. , Cimpoesu D. , Stanciu R. , Idriceanu J. , Vasiliu I. , Leustean L. , Ungureanu M. , Mogos V. , Vulpoi C.

Introduction: Pituitary insufficiency of the adult is a rare pathology (~30–40/1 000 000 per year). Among the acquired causes, Sheehan syndrome (SS) is often characterized by an insidious evolution, which allows it to pass unnoticed for a long time.Case report: R Maria, 58 years-old, known with SS for 10 years, was hospitalized in the ER with severe asthenia, obnubilation, symptomatic arterial hypotension. Laboratory studies revealed severe hyponatr...

ea0026p117 | Female reproduction | ECE2011

Adiponectin and metabolic syndrome in PCOS patients – beyond obesity

Leustean L , Fica S , Preda C , Ungureanu M C , Cristea C , Mogos S , Mogos V , Vulpoi C

Introduction: Polycystic ovary syndrome (PCOS) have an increased rate of metabolic syndrome (MS). Many studies have proved that adiponectin is closely associated with MS and participate in the disturbances of gonadal axis. The aim of the study was to evaluate the association of adiponectin levels with MS in PCOS.Patients and methods: Study group included 38 patients with PCOS (Rotterdam criteria) compared to 30 healthy volunteers age and sex matched, all...

ea0026p630 | Clinical case reports | ECE2011

A rare variant of Wolfram syndrome with diabetic microvascular disease, hypergonadotropic hypogonadism and palmar fibromatosis: case report

Preda C , Gaspar I , Ungureanu M-C , Leustean L , Cristea C , Moisii L , Mogos V , Vulpoi C

Introduction: Wolfram syndrome, a very rare condition, is a neurodegenerative disorder characterized by diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) which appear in childhood, hampering diagnosis and treatment. Others less frequent features as hypergonadotropic hypogonadism, microvascular disease and local fibromatosis are reported in a male patient diagnosed at the age of 18 years.Case report: An 18-year-old male patient d...