Searchable abstracts of presentations at key conferences in endocrinology

ea0022p197 | Clinical case reports and clinical practice | ECE2010

Genetic pattern of sex development disorders: cases report

Andreescu Nicoleta , Belengeanu Valerica , Stoian Monica , Stoicanescu Dorina , Farcas Simona , Belengeanu Alina , Muresan Anca , Amzar Daniela

Objective: To study the spectrum of chromosomal anomalies in three cases as related to the phenotypic variability of patients with anomalies of disorder of sexual development.Female 18 years old with secondary amenorrhea, stigmata of Turner’s syndrome, Tanner stage II. Ultrasound showed streak gonads. Hormonal analysis revealed elevated levels of FSH, LH and a low plasma estradiol level. The chromosomal investigation showed gonosomal mosaicism 45,X(...

ea0016p330 | Endocrine tumours | ECE2008

Ovarian serous and mucinous tumors of low malignant potential: patterns of stromal invasion

Costi Simona , Dema Alis , Golu Ioana , Cornianu Marioara , Taban Sorina , Muresan Anca , Lazar Elena

Purpose: The purpose of this study was to evaluate the histologic spectrum of stromal–epithelial patterns of invasion in ovarian serous and mucinous tumors of low malignant potential.Materials and methods: We retrospectively analyzed 31 cases of borderline ovarian serous and mucinous tumors diagnosed of the Pathology Department of County Hospital Timisoara in a period of 5 years, between 2003 and 2007. Epithelial architecture, the patterns of stroma...

ea0099ep971 | Endocrine-Related Cancer | ECE2024

Secondary amenorrhea – an inconspicuous presentation of sporadic MEN1 syndrome

Monalisa Preda-Ivascu , Iorgulescu Radu , Schipor Sorina , Muresan Andrei , Braha Elena , Radian Serban , Poiana Catalina

Introduction: The MEN1 syndrome is caused by inactivating mutations of MEN1, a tumor suppressor gene encoding menin. A sporadic presentation is relatively rare (8-14%) and could be due to de novo mutations.Aim: To present an MEN1 case diagnosed following a routine consultation for amenorrheaCase presentation: A 44-year-old female presented with secondary amenorrhea and a history of complicated renal lithiasis requiring rep...

ea0090ep1035 | Thyroid | ECE2023

Graves’ Disease Hiding Metastatic Papillary Thyroid Carcinoma - case report-

Musat Madalina , Septar AIlin , Boanta Roxana , Goldstein Andrei , Terzea Dana , Ioachim Dumitru , Schipor Sorina , Muresan Andrei , Niculescu Dan , Elian Viviana

The coexistence of Graves disease (GD) and thyroid carcinoma used to be considered uncommon, but association between the two is being progressively acknowledged. Case report: We present the case of a 69-year-old woman with a 10 year history of GD who was referred to our clinic for fatigue, sweating, palpable cervical mass and weight loss. She was treated only in the previous 5 months with block and replace therapy. Laboratory workup at admission showed s...

ea0063p1133 | Reproductive Endocrinology 2 | ECE2019

Serum anti-Müllerian hormone is significantly associated with higher luteinizing hormone level in polycystic ovary syndrome

Baculescu Nicoleta , Leonte Laura , Radian Serban , Gheorghiu Monica , Muresan Andrei , Biban Bianca , Baleanu Maria , Grigorescu Florin , Poiana Catalina

Background: Recent data highlight the role of anti-Müllerian hormone (AMH) to trigger the neuroendocrine abnormalities involving GnRH and secretion of gonadotropins in polycystic ovary syndrome (PCOS).Aim: To study factors significantly correlated with neuroendocrine dysfunction in PCOS, with focus on AMH.Subjects and methods: We performed a cross-sectional study in 137 patients with PCOS selected by Rotterdam 2003 criteria an...

ea0032p1029 | Thyroid (non-cancer) | ECE2013

Vitamin E supplementation in the treatment of Graves' disease

Petrulea Mirela Sanda , Ilie Ioana , Valea Ana , Ghervan Cristina , Georgescu Carmen , Login Cezar , Muresan Adriana , Duncea Ileana

Hyperthyroidism in the course of Graves’ disease leads to intensification of oxidative processes resulting in increased oxidative stress.Objectives: The effect of supplementation with vitamin E was monitored on the speed of attaining euthyroidism and on the oxidative stress parameters in patients with Graves’ disease, treated with thiamazole.Patients and methods: We examined 43 hyperthyroid patients and 12 euthyroid healt...

ea0020p272 | Clinical case reports and clinical reports | ECE2009

The study of an immunohistochemical aggresivity marker in mammary carcinomas

Maria Muresan Anca , Elena Lazar , Alis Dema , Alexandra Faur , Remus Cornea , Diana Herman , Cristian Suciu , Izabella Sargan

Introduction: The mammary cancer is the most frequent malign tumor encountered in females, characterized by a high distant metastasis tendency. Among the potential prognosis factors, we mention the biomarkers that measure or are associated with biologic processes involved in the tumorous progression. The study analyzes the p53 protein’s positivity in correlation with the mammary cancer’s classical prognosis factors: the hystologic type, the histopathologic degree, th...

ea0020p313 | Clinical case reports and clinical reports | ECE2009

The study of an immunohistochemical aggresivity marker in mammary carcinomas

Maria Muresan Anca , Elena Lazar , Alis Dema , Sorina Taban , Marioara Cornianu , Simona Costi , Ramona Cioroboreanu , Izabella Sargan

Introduction: The mammary cancer is the most frequent malign tumor encountered in females, characterized by a high distant metastasis tendency. Among the potential prognosis factors, we mention the biomarkers that measure or are associated with biologic processes involved in the tumorous progression. The study analyzes the p53 protein’s positivity in correlation with the mammary cancer’s classical prognosis factors: the hystologic type, the histopathologic degree, th...

ea0093p3 | Guided Poster Tour 1: Adrenal and Neuroendocrine tumors | EYES2023

MEN 2 syndrome heterogeneity in a cohort of Romanian patients

Manole Tiberiu , Baciu Ionela , Galoiu Simona , Baculescu Nicoleta , Niculescu Dan , Radian Serban , Muresan Andrei , Braha Elena , Poiana Catalina

Background: Multiple endocrine neoplasms (MEN) are a rare hereditary syndrome, caused by an autosomal dominant mutation due to germline mutation in the rearranged during transfection (RET) proto-oncogene. According to the new WHO guidelines, MEN type 2 (formerly known as MEN 2A) is characterised by medullary thyroid cancer (MTC), paragangliomas, primary hyperparathyroidism (PHP) and cutaneous lichen amyloidosis.Objectives: To present the clinical and par...

ea0099rc3.7 | Rapid Communications 3: Adrenal and Cardiovascular Endocrinology | Part I | ECE2024

Factors that influence pheochromocytoma penetrance in MEN2A Syndrome

Lider-Burciulescu Sofia-Maria , Gheorghiu Monica Livia , Muresan Andrei , Laura-Semonia Stanescu , Dumitras¸cu Anda , Badiu Corin

Introduction: It is known that phaeochromocytoma penetrance in MEN2A syndrome steadily increases with age. In general, MEN2A related pheochromocytomas (PHEOs) have a benign evolution; however, some of them have an aggressive behaviour despite the same genetic background as the benign forms.Aim: To evaluate potential factors that may influence PHEO penetrance and tumor dimensions (age at diagnosis, MTC aggressiveness or genetic status).<p class="abste...