Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep770 | Pituitary: clinical | ECE2015

Sex-related differences in clinical presentation and outcomes of Cushing's disease: a study from a referral centre

Lau Eva , Oliveira Joana , Belo Sandra , Freitas Paula , Oliveira Ana Isabel , Vinha Eduardo , Castro Ligia , Pereira Josue , Carvalho Davide

Introduction: Cushing’s disease (CD) presents a marked female preponderance, with a female-to-male ratio of 3–8:1, but whether this skewed gender distribution has any relevance to the presentation and outcomes of CD is not well understood.Aim: To evaluate sex-related differences in the presentation of CD, as regards: biochemical indices of hypercortisolism; complications of disease and outcomes.Methods: Observational, ret...

ea0090p708 | Pituitary and Neuroendocrinology | ECE2023

Congenital, isolated, and lifetime growth hormone deficiency provides superior cognitive performance in senescence

Batista Vanderlan O. , Kellner Michael , Salvatori Roberto , Oliveira Walter , Faro Andre , Santos Lucas B. , Melo Enaldo V. , Oliveira-Santos Alecia A. , Oliveira Carla R. P. , Almeida Viviane , Barros-Oliveira Cynthia S. , Santos Elenilde G. , Santana Nathalie O. , Villar-Gouy Keila R. , Leal Angela , Amorim Rivia S. , H. Aguiar-Oliveira Manuel

Mice with isolated GH deficiency (IGHD) due to GHRH receptor mutations live longer than their normal siblings with an extended healthspan, i.e., the period of life free from disabilities. Human IGHD individuals due to a mutation in the GHRH receptor gene from Itabaianinha, Brazil, has a normal lifespan with an extended healthspan (1). Our hypothesis is that their aging is accompanied by a delayed cognitive decline. Accordingly, we used the Literacy Independent Cognitive Assess...

ea0040p19 | (1) | ESEBEC2016

Recurrent adrenal pheochromocytoma – a benign condition?

Lages Adriana de Sousa , Oliveira Patricia , Rodrigues Dircea , Costa Gracinda , Martins Maria Joao , Furtado Emanuel , Oliveira Joao , Vicente Nuno , Cardoso Luis , Oliveira Diana , Martins Diana , Ventura Mara , Carrilho Francisco

Introduction: Pheochromocytomas are adrenomedullary catecholamine-secreting tumors. These account for <0.1% of all causes of hypertension and may be related to potentially fatal hypertensive crises. Can appear as sporadic tumors or associated with familial syndromes.Malignancy occurs in 15–20% of the cases and is characterized by local invasion or distant metastasis rather than capsular invasion. Tumor recurrence has been reported with a frequen...

ea0063gp76 | Thyroid Autoimmune Disorders | ECE2019

Cardiovascular risk factors, autoimmunity and insulin resistance in Graves disease

Ferreira Catia Tomas , Neves Celestino , Neves Joao Sergio , Oliveira Sofia Castro , Sokhatska Oksana , Pereira Miguel , Oliveira Ana , Medina Jose Luis , Delgado Luis , Carvalho Davide

Introduction: Graves’ disease is an autoimmune disease accounting for the majority of hyperthyroidism cases.Aim: We aimed to assess the interrelationships between cardiovascular risk factors, autoimmunity, insulin resistance and treatment in Graves’ disease.Material and methods: We measured free T3 (FT3), free T4 (FT4), TSH, thyrotropin receptor antibodies (TRAb), anti-thyroglobulin and anti-TPO antibodies, thyro...

ea0063gp77 | Thyroid Autoimmune Disorders | ECE2019

Lipid profile, insulin resistance and cytokines evaluation in autoimmune thyroiditis patients

Goncalves Juliana , Neves Celestino , Pego Francisco , Neves Joao Sergio , Oliveira Sofia Castro , Sokhatska Oksana , Pereira Miguel , Oliveira Ana , Medina Jose Luis , Delgado Luis , Carvalho Davide

Introduction: Thyroid dysfunction has been associated with cardiovascular events since it worsens atherogenesis, insulin resistance and dyslipidemia. Thyroid hormones and adipokines interact with each other to regulate metabolism. The impact of thyroid dysfunction on adipokines serum levels remains controversial.Objective: To evaluate the interrelations between thyroid function and cardiovascular risk factors as insulin resistance, lipid profile, inflamm...

ea0063gp78 | Thyroid Autoimmune Disorders | ECE2019

Autoimmune thyroiditis, Graves’ disease and adiponectin, resistin and plasminogen activator inhibitor-1 levels

Neves Celestino , Neves Joao Sergio , Oliveira Sofia Castro , Sokhatska Oksana , Pereira Miguel , Oliveira Ana , Medina Jose Luis , Delgado Luis , Carvalho Davide

Introduction: The interrelationship between autoimmune thyroiditis, Graves’ disease and plasma adipokines levels remains elusive.Aims: We aimed to compare the levels of adiponectin, resistin and PAI-1 levels in patients with autoimmune thyroiditis and Graves’ disease.Subjects and methods: We recorded thyroid function tests, BMI, the levels of total cholesterol (TC), HDL, LDL-cholesterol, triglycerides (TG), apolipoprotein...

ea0049ep44 | Adrenal cortex (to include Cushing's) | ECE2017

Late-night salivary cortisol: cut-off definition and diagnostic value in Cushing’s syndrome

Lages Adriana , Frade Joao , Paiva Isabel , Oliveira Patricia , Oliveira Diana , Martins Diana , Ventura Mara , Cunha Nelson , Rebelo-Marques Alexandre , Antunes Susana , Leitao Fatima , Carrilho Francisco

Background: The diagnosis of Cushing’s syndrome (CS) remains a challenge in clinical endocrinology. Several screening tests have been proposed to establish hypercortisolism. Late-night salivary cortisol (LNSC) is used as screening tool, however, individualized cut-off levels for each population must be defined.Methods: Three group of subjects were studied: healthy volunteers, suspected CS and proven CS. All patients collected saliva at 23.00 h using...

ea0049ep53 | Adrenal cortex (to include Cushing's) | ECE2017

Adrenal cushing’s syndrome surprisingly unveiling breast cancer

Neves Joao Sergio , Oliveira Ana Isabel , Souteiro Pedro , Oliveira Sofia Castro , Baldaia Helena , Melo Daniel , Neves Celestino , Freitas Paula , Carvalho Davide

Introduction: Cushing’s syndrome is an endocrinopathy characterized by glucocorticoids excess. Adrenalectomy is the recommend treatment for unilateral adrenal Cushing’s syndrome and is usually associated with resolution of the disease.Clinical Case: A 54-year old woman with central obesity (BMI 34.3 kg/m2), diabetes and hypertension had a left adrenal mass of 15 mm and characteristics suggestive of adenoma (Hounsfield unit of <10...

ea0049ep54 | Adrenal cortex (to include Cushing's) | ECE2017

Giant adrenal tumor in a patient admitted for fever

Neves Joao Sergio , Teles Luis , Souteiro Pedro , Oliveira Sofia Castro , Oliveira Ana Isabel , Fernandes Ana Catarina , Damasceno Margarida , Graca Luisa , Rodrigues Elisabete , Neves Celestino , Freitas Paula , Carvalho Davide

Introduction: Adrenal tumors are usually detected due to clinical manifestations of hormonal hypersecretion or incidental findings on imaging evaluation. Although most incidentalomas are non-functioning adenomas, it is important to appropriately evaluate such masses to exclude hormonal excess or malignancy.Case description: An 81-year old male was admitted to our hospital for fever with 15 days of evolution. The patient also presented chills and loss of ...

ea0041gp59 | Cardiovascular endocrinology | ECE2016

Familial partial lipodystrophy type 3 due to PPARgamma mutation: presentation with diabetes and severe hypertriglyceridemia

Oliveira Joana , Cunha Filipe , Rodrigues Elisabete , Menezes Joana , Saavedra Ana , Costa Maria Manuel , Magalhaes Daniela , Bettencourt-Silva Rita , Fernandes Susana , Oliveira Joao Paulo , Carvalho Davide , Freitas Paula

Introduction: Familial partial lipodystrophy (FPL) is an autosomal dominant disease characterized by selective loss of subcutaneous fat from the extremities and gluteal region, with lipohypertrophy of the face, neck and trunk. It is usually tightly linked with severe metabolic complications. FPL type 3 results from peroxisome proliferator-activated receptor gamma (PPARG) mutations.Case presentations: Fifty three-year-old woman, referred to endocrinology ...