Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep630 | Obesity and cardiovascular endocrinology | ECE2015

Diet relationship with the metabolic syndrome's elements

Pop Raluca-Monica , Pascanu Ionela , Dogaru Grigore , Pop Marian

Background: Diet modification is an important part of the metabolic syndrome’s management but there is limited data regarding a direct relationship between food groups and the metabolic profile.Aim: Evaluation of the influence of food groups on the elements of metabolic syndrome in a group of subjects with abdominal obesity.Material and methods: A cross sectional study was conducted in the Endocrinology Outpatient Clinic betwe...

ea0022p850 | Thyroid | ECE2010

Lp(A) levels in thyroid disfunctions

Pop-Radu Cristina-Corina , Iazigian Ana

The aim of the study was to assess lipid status in subjects with hypothyroidism (overt and subclinical) and hyperthyroidism. Therefore, we analyzed the relationship between the levels of blood lipids (Lp(a), Apo AI, Apo B, Apo AI/B, total cholesterol (TC), triglyceride (TG), LDL, HDL, LDL) and TSH, FT4, T3, TPOAb concentration. The study groups included 38 subjects with overt hypothyroidism (mean±S.E.M., age 48.6±13.25 years), 30 ...

ea0083ercp5 | Endocrine-related Cancer | EYES2022

An exceptional case of a papillary thyroid carcinoma arising within an ovarian teratoma

D Pop Gjorceva , S Stojanoski , N Manevska , Lj Batkoska

Background: Papillary thyroid carcinoma (PTC) arising within an ovarian teratoma is an extremely rare condition that comes with certain difficulties in the preoperative diagnosis and postoperative treatment strategy. It is either asymptomatic (detected incidentally) or with nonspecific symptoms. Currently, no consensus exists on the surgical and postoperative treatment of patients with malignant struma ovarii.Case presentation: A 26-year-old female prese...

ea0029p860 | Endocrine tumours and neoplasia | ICEECE2012

A case of multiple endocrine neoplasia type 2a associated with rectal adenocarcinoma

Pop-Radu C. , Reti Z. , Radian S. , Al Hajjar N.

Multiple endocrine neoplasia type 2A (MEN2A) is an inherited syndrome caused by the mutation of RET gene. The classic variant of this syndrome includes the presence of medullary thyroid carcinoma (MTC), in association with pheochromocytoma and parathyroid neoplasia. MTC is usually the first presentation, with palpable neck mass and hypercalcitonemia, metastatic spread to local lymph nodes or distant sites.We report the case of a 41 year old Caucasian man...

ea0092op-01-04 | Oral Session 1: Highlights in Thyroidology: in Memory of Jacques Dumont | ETA2023

Should hypothyroxinaemia during early gestation be regarded as a condition of oxidative stress?

Pop Victor , Krabbe Hans , Broeren Maarten , Wiersinga Wilmar , Rayman Margaret

Background: Normal pregnancy is a state of physiological oxidative stress (OS) with oxidants facilitating the implantation of the embryo and optimal decidualisation but counterbalanced by antioxidants. Pro-oxidant processes exceeding the anti-oxidants capacity result in imbalanced OS, which has been associated with the ‘’big four’’ obstetric complications: pre-term birth, intra-uterine growth retardation, pre-eclampsia and diabetes gravidarum. Important OS ...

ea0050ep065 | Neuroendocrinology and Pituitary | SFEBES2017

A rare case of primary suprasellar meningeal melanocytoma associated with nonfunctional pituitary adenoma

Paveluc Oana Stefania , Dobrescu Ruxandra , Stancu Cristina , Dumitrascu Anda , Pop Doina , Badiu Corin

Introduction: Pituitary adenomas are the most common pituitary tumours, but in 18% of cases we can find other rare tumours like: Rathke’s cleft cyst, craniopharingyomas, chordomas, meningiomas, infiltrative or infectious disease. Meningeal melanocytoma is a benign neoplasm of central nervous system, commonly located in the base of the brain, cerebellopontine angle and the pineal body, difficult to differentiate from a nonfunctional p...

ea0050ep065 | Neuroendocrinology and Pituitary | SFEBES2017

A rare case of primary suprasellar meningeal melanocytoma associated with nonfunctional pituitary adenoma

Paveluc Oana Stefania , Dobrescu Ruxandra , Stancu Cristina , Dumitrascu Anda , Pop Doina , Badiu Corin

Introduction: Pituitary adenomas are the most common pituitary tumours, but in 18% of cases we can find other rare tumours like: Rathke’s cleft cyst, craniopharingyomas, chordomas, meningiomas, infiltrative or infectious disease. Meningeal melanocytoma is a benign neoplasm of central nervous system, commonly located in the base of the brain, cerebellopontine angle and the pineal body, difficult to differentiate from a nonfunctional p...

ea0063p666 | Interdisciplinary Endocrinology 1 | ECE2019

Pan-cancer analysis of thyroid hormone signaling pathway reveals new possible targets for combinations therapy

Hanusek Karolina , Popławski Piotr , Piekiełko-Witkowska Agnieszka

Introduction: Published studies suggest links between altered actions of thyroid hormones (TH) and cancer development and progression. It is not clear, however, whether these links are specific to cancer types or whether TH can globally affect cancerogenesis. Here, we performed PanCancer analysis of TH signaling pathway.Material/methods: 79 genes linked with TH signaling pathway, including genes encoding proteins involved in TH synthesis, transport, rece...

ea0049ep846 | Clinical case reports - Pituitary/Adrenal | ECE2017

Breast cancer and newly discovered non-secretor pituitary mass- as risk of metastases?

Valea Ana , Oprisor Iulia , Carsote Mara , Pop Dan Dumitru , Morar Andra , Ghervan Cristina , Georgescu Carmen Emanuela

Introduction: Even if breast cancer is rare cause of pituitary metastases, the diagnosis of a pituitary adenoma, shortly after surgery for breast cancer, raises suspicion of a possible secondary determinations.Material and method: This is a case report revealing the medical history and endocrine profile of a female with breast cancer and pituitary macroadenoma.Case data: A 64-year old non-smoking female (with menopause at age of 52...

ea0041ep49 | Adrenal cortex (to include Cushing's) | ECE2016

Cushing’ s disease, hasimoto’s thyroiditis and severe hyperandrogenemia

Valea Ana , Ciocan Irina , Carsote Mara , Morar Andra , Pop Dan Dumitru , Ghervan Cristina , Georgescu Carmen Emanuela

Introduction: Cushing’s disease (CD) is caused by high adrenocorticotropic hormone (ACTH), usually by a pituitary microadenoma.Material and method: This is a case report investigated in several Romanian centers by performing: morning plasma cortisol, circadian rhythm of plasma cortisol, plasma ACTH, dexamethasone (DXM) suppression tests.Case data: A 57-year female, known with hypertension and osteopenia, was ...