Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep439 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Time restricted feeding 16/8 improves metabolic parameters and fatty liver in obese mice

Astudillo Camila , Acevedo Paula , Ceballo Karina , Julio Marcela , Dorfman Mauricio , Cruz Gonzalo

Obesity is a major health problem that is crucial in the pathogenesis of diabetes mellitus, cardiovascular diseases, and some types of cancer. Intermittent fasting is an eating pattern in which periods of fasting, lasting from 12 up to 36h, are alternated with periods of eating. Time restricted feeding (TRF) 16/8 is a type of intermittent fasting that is being used to lose weight and for treating metabolic disorders. Several studies in humans have shown a slight effect of TRF ...

ea00100wb4.3 | Workshop B: Disorders of the hypothalamus and pituitary (II) | SFEEU2024

Endocrine metabolic disorders secondary to acromegaly, description of a clinical case in a south american patient

Felipe Arias Ariza Anderson , Juliana Estevez Gomez Maria , Andrey Acevedo Pena Diego , Fernanda Castillo Goyeneche Silvia , Andres Dulcey Luis , Gomez Ayala Jaime , Camila Amaya Maria , Gutierrez Emily , Camila Gomez Contreras Maria , Alejandro Gomez Contreras Juan , Sebastian Theran Leon Juan , Sofia Ramos Caballero Gabriela , Sebastian Ramos Caballero Juan , Nathalia Gutierrez Laura , Lizcano Angie , Paula Ciliberti Maria , Blanco Camilo

Introduction: Acromegaly is caused by excessive secretion of growth hormone (GH), usually by a pituitary adenoma, and a concomitant excess of insulin-like growth factor 1 (IGF-1). Excess GH and IGF-1 exert many actions on the cardiovascular (CV) system and especially on cardiovascular disease (CVD) risk factors which are common, especially in active acromegaly, but often persist after adequate treatment in patients with controlled disease.Clinical case: ...

ea00100wc1.2 | Workshop C: Disorders of the thyroid gland | SFEEU2024

Primary hodgkin lymphoma of the thyroid: a case report

Camilo Blanco Pimiento Edgar , Paula Ciliberti Artavia Maria , Andres Dulcey Sarmiento Luis , Alberto Gomez Ayala Jaime , Sebastian Theran Leon Juan , Camila Amaya Munoz Maria , Paola Lizcano Manrique Angie , Fernanda Castillo Goyeneche Silvia , Juliana Estevez Gomez Maria , Andrey Acevedo Pena Diego , Felipe Arias Ariza Anderson , Camila Gomez Maria , Alejandro Gomez Juan

Introduction: The thyroid lymphoma (TL) is a rare disease, accounting for less than 2% of thyroid neoplasms. The majority of cases are of the non-Hodgkin (NHL) B-cell lineage and large cell type.Objective: To present a rare case documented in the literature of Primary Nodular Sclerosis Hodgkin Lymphoma (HL) of the thyroid, in a 20-year-old male patient.Methods: The clinical history and records of the case, biopsy reports, immunohis...

ea0092ps3-28-08 | Translational 2 | ETA2023

Understanding the putative role OF ACE2, TMPRSS2 and furin proteins on thyroid neoplastic transformation

Teresa Azevedo Maria , Macedo Sofia , Canberk Sule , Batista Rui , Soares Paula

Angiotensin-converting enzyme 2 (ACE2), Transmembrane serine protease 2 (TMPRSS2) and Furin were known to be key players for the SARS-CoV-2 infection. Thyroid gland was shown to be one of the relevant targets for SARS-CoV-2 infection allegedly due to the higher expression levels of these molecules in follicular cells. However, it remains to be fully determined the expression of ACE2, TMPRSS2 and Furin in normal follicular cell. In addition, the putative role of these molecules...

ea0028oc2.1 | Reproduction and bone | SFEBES2012

The expression of kisspeptin and kisspeptin receptor is altered in pre-eclampsia

Williams Paula

Background: Kisspeptins (KISS1) and their receptor, KISS-1R, are expressed at higher levels in first trimester placental trophoblast cells than in term gestation. Expression is localised to the trophoblast compartment. In contrast to KISS1 which is only expressed in the villous trophoblast, KISS-1R is also found in the extravillous trophoblast population. Kisspeptins produced by first trimester trophoblast cells inhibited migration. Pre-eclampsia is known to be caused due to d...

ea0049ep100 | Adrenal medulla | ECE2017

Lung adenocarcinoma in a 34-year-old female SDHB asynptomatic mutation carrier – case report

Matos Maria Joao , Costa Claudia , Santos Ana Paula , Teixeira Manuel , Franco Carlos , Bento Joao , Azevedo Isabel , Dias Susana , Sampaio Ines Lucena , Cunha Ana Luisa , Torres Isabel

Introduction: Patients with germline mutations in one of the succinate dehydrogenase (SDH) genes are at substantially increased risk of developing paragangliomas (PGL) and pheochromocytomas (PCC). Mutations in SDHB are the most commonly found gene mutations in PC/PGL and are associated with younger ages at presentation, higher rates of metastases and poorer prognosis. Although familial PGL syndromes were initially thought to predispose only for PCC and PGL, other tumor types s...

ea0081ep989 | Thyroid | ECE2022

King of the CASTLE? Immunohistochemistry in diagnosing rare thyroid carcinomas: a case report

Stanciu Mihaela , Ristea Ruxandra Paula

Introduction: Carcinoma showing thymus-like differentiation (CASTLE) is a rare, low-grade thyroid carcinoma, with indolent clinical course and usually a favorable prognosis. The clinical and imagistic features are not specific for CASTLE but similar to other malignant lesions of the thyroid, making diagnosis difficult and reliant on immunohistochemical examination. The conclusive diagnosis requires pathological examination and positive cluster of differentiation 5 (CD5) immuno...

ea0040l3 | Telomerase promoter mutations in cancer: beyond immortalization? | ESEBEC2016

Telomerase promoter mutations in cancer: beyond immortalization?

Soares Paula , Biology Group Cancer

Cell immortalization has been considered for a long time as a classic hallmark of cancer cells. Besides telomere maintenance due to the ‘alternative mechanism of telomere lengthening’ it was advanced that such immortalization could be due to telomerase reactivation, but the mechanisms underlying such reactivation remained elusive.Mutations in the coding region of telomerase gene are very rare in the cancer setting, despite being associated with...

ea0073aep845 | Late Breaking | ECE2021

Importance of proper diagnosis and treatment challenges in a 16-year-old patient with ectopic posterior pituitary and panhypopituitarism - a rare case report

Stanciu Mihaela , Paula Ristea Ruxandra

BackgroundPosterior pituitary ectopia is a rare congenital condition that consists of the abnormal position of the distinctly hyperintense signal suggestive of the posterior pituitary gland on magnetic resonance imaging. The classical features include the ectopic location of the posterior pituitary gland, pituitary stalk abnormalities and associated clinical manifestations related to isolated growth hormone deficiency. In rare cases, some patients suffer...

ea0056p652 | Endocrine tumours and neoplasia | ECE2018

Metformin and Simvastatin: a therapeutic combination to reduce the aggressiveness of glioblastoma multiforme

Fuentes-Fayos Antonio C , Vazquez-Borrego Mari C , Mansfield Beth , Blanco-Acevedo Cristobal , Solivera Juan , Castano Justo P , Luque Raul M

Gliomas constitute the most frequent type of brain tumors and are characterized by a rapid growth and high diffusion through the brain. In particular, astrocytomas are a subtype of malignant gliomas that are graded from low to high aggressiveness (i.e. grade I, II, III and IV), being grade IV (glioblastoma multiforme, GBM) the most malignant type, and one of the most common cancers in the brain and CNS. To date, surgery is the first-line therapy combined with chemotherapy or r...