Searchable abstracts of presentations at key conferences in endocrinology

ea0063gp115 | Calcium and Bone 2 | ECE2019

Different impact of marrow and visceral adipose tissue on bone phenotype

Paula Francisco de , Araujo Iana de , Carvalho Adriana , Elias Jorge , Salmon Carlos

Introduction: Central obesity and the consequent metabolic syndrome have global devastating effect on the health system due to their strong association with type 2 diabetes mellitus and cardiovascular disorder. There are contradictory results about the influence of insulin resistance and visceral adipose tissue on bone phenotype. The study was designed to evaluate the association between bone quality and bone mineral density (BMD) with bone marrow adipose tissue (MAT) as well ...

ea0063p186 | Diabetes, Obesity and Metabolism 1 | ECE2019

Relationship between cortisoluria and the presence of metabolic syndrome among HIV-infected patients

Guerreiro Vanessa , Sergio Joao , Serrao Rosario , Sarmento Antonio , Carvalho Davide , Freitas Paula

Introduction: People living with human immunodeficiency virus (HIV) are at increased risk of developing metabolic disorders, such as obesity, dyslipidemia, insulin resistance, diabetes and hypertension; which may also be associated with hypercortisolism. Due to the similarity between the metabolic changes present in these two clinical situations, several studies have evaluated whether HIV-infected patients have increased levels of cortisol, but the results are not consensual. ...

ea0063p493 | Calcium and Bone 2 | ECE2019

Hypocalcemic cardiomyopathy: a reversible entity?

Santos Tiago Da Silva , Carvalho Andre Couto de , Romao Raquel , Cruz Celia Maio , Cardoso Helena

Introduction: Hypocalcaemia is a rare and potentially reversible cause of cardiomyopathy. Restoration to normal serum calcium levels usually leads to rapid improvement of cardiac function.Case report: A 42-year-old woman with a history of total thyroidectomy, due to large nodular goiter in 2016, and acute pos-operative hypoparathyroidism, assumed to be transient, with no supplementation since early 2017. In September 2018 she was admitted due to acute ca...

ea0063p839 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

When MAX runs in the family

Duarte Diana Borges , Pereira Catarina A , Palma Isabel , Carvalho Rui , Cardoso Helena

Introduction: Recent advance of genetic testing has contributed to the diagnosis of hereditary pheochromocytoma and paraganglioma (PPGL). Germline mutations in MYC associated factor X(MAX) are responsible for 1.1% of these PPGL; the median age at onset is 33 years and no reliable penetrance estimation is available for MAX-carriers. The authors present the case of a synchronous bilateral pheochromocytoma that prompted the discovery of a proband of MAX mutation and three other r...

ea0063p855 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

Adrenal surgical series - radiologic-pathological correlation

Carvalho Ferreira Paulo , Castelo Diogo , Mota Filipe , Sanches Agostinho , Portugal Pedro

Introduction: Adrenal surgical series are scarce in the literature. We aim to present a single institution consecutive case series and to establish a radiologic-pathological correlation.Material and methods: A retrospective, observational and descriptive study was conducted by searching the Pathology database for surgically removed adrenal lesions. Cases were matched with the Imagiology database. Ultrasound, CT and MRI images were then reviewed by the sa...

ea0063p859 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

Phaeochromocytoma in pregnancy

Araujo Alexandra , Silvestre Catarina , Marcalo Jose , Gomes Ana Raquel , Carvalho Raquel

Phaeochromocytoma in pregnancy is an extremely rare condition. Early recognition can largely decrease maternal and fetal mortality rates. As symptoms of phaeochromocytoma are similar to those of other more common causes of hypertension during pregnancy, timely diagnosis is a challenge. There is no consensus in literature about the specific treatment nor about the optimal delivery timing or route. Case of a 32 years old woman with a single pregnancy of 30 weeks and 3 days admit...

ea0063p880 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

Cardiovascular and metabolic risk factors in children and adolescents with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Paredes Silvia , Alves Marta , Carvalho Fabia , Gomes Maria Miguel , Martins Sofia , Marques Olinda , Antunes Ana

Background: Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is associated with an increased cardiometabolic risk in adult life. Nevertheless, data regarding pediatric age is scarce. We aimed to evaluate cardiometabolic risk factors in patients with CAH due to 21-hydroxylase deficiency in pediatric age.Methods: We reviewed the clinical records of patients with CAH evaluated in a Pediatric Endocrinology Unit in a central hospital. Pat...

ea0049gp18 | Adrenal 2 | ECE2017

Effects of two mineralocorticoid receptor antagonists on the morphology of the adrenal cortex

Pereira Sofia S , Costa Madalena M , Moreira Angela , Carvalho Liliana , Monteiro Mariana , Vinson Gavin , Pignatelli Duarte

Arterial hypertension usually results from the deregulation and hyperactivity of the renin angiotensin-aldosterone system. One of the available therapeutic approaches for its treatment is the use of mineralocorticoid receptor (MR) antagonists, thus blocking aldosterone action.The aim of this study was to characterize the effects of spironolactone and eplerenone, on the morphology of the adrenal gland of spontaneously hypertensive (SHR) and normotensive (...

ea0049gp226 | Thyroid Cancer | ECE2017

Malignancy Rate in Thyroid Nodules: Cytology versus Histology in challenging categories

Silvestre Catarina , Luis Rita , Bugalho Maria Joao , de Almeida Margarida Mendes , Carvalho Raquel

Background: To stratify the risk of malignancy, thyroid fine-needle aspiration cytology (FNAC) is an important and cost-effective method to evaluate nodules. The Bethesda System for Reporting Thyroid Cytopathology III, IV and V categories are diagnostic challenges, falling between benign and malignant.Objective: Determinate the malignancy rates of thyroid nodules classified as Bethesda Categories III-V.Methods: Retrospective study ...

ea0049ep98 | Adrenal medulla | ECE2017

Pheochromocytoma – surgical outcomes

Martins Pedro Carvalho , Ribeiro Catia , Peyroteo Mariana , Pereira Helena , de Sousa Abreu

Objective: To retrospectively evaluate the results of the pheochromocytoma surgery in our institution assessing the surgical complications, perioperative hemodynamic instability and oncologic outcomes.Methods: The medical records of patients admitted for pathologically confirmed pheochromocytoma between 2000 and 2015 were reviewed. Patients with paragangliomas were excluded.Results: We identified 40 patients with 43 resected pheoch...