Searchable abstracts of presentations at key conferences in endocrinology

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 ...

ea0049ep88 | Adrenal medulla | ECE2017

Pheochromocytoma in neurofibromatosis type 1

Marengo Agustina Pia , Garcia-Sancho Paula , Guerrero Fernando , Peiro Inmaculada , Santacruz Elisa , Ortiz Andres , Diez Juan Jose , Iglesias Pedro , Villabona Carles

Background: Individuals with neurofibromatosis type-1 (NF1) carry an increased risk of pheochromocytoma (PHEO). Detection strategy is unknown but most experts recommend screening if hypertension develops.Objective: Report the characteristics of PHEO in patients with NF1 (NF1 group) and compare them with non-NF1-associated PHEO (non-NF1 group).Methods: Retrospective cohort study of patients undergoing PHEO resection in two Spanish t...

ea0049ep94 | Adrenal medulla | ECE2017

Pheochromocytoma: a clinical and pathological study

Santacruz Elisa , Marengo Agustina Pia , Ortiz Andres , Peiro Inma , Pian Hector , Diez Juan Jose , Garcia-Sancho Paula , Villabona Carles , Iglesias Pedro

Objective: To assess clinical features, diagnosis, treatment and outcome in patients with pheochromocytoma surgically treated in the past 3 decades in two tertiary referral hospitals.Methods: A retrospective study on clinical and pathological characteristics, treatment, and outcome in patients with pheochromocytoma followed up in specialized neuroendocrinology units who underwent surgery in the period 1981–2016 was performed.R...

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...

ea0049ep140 | Clinical case reports - Pituitary/Adrenal | ECE2017

Virilization – a non-negligible manifestation of an adrenal tumor

Magalhaes Daniela , Vinha Eduardo , Neves Joao Sergio , Souteiro Pedro , Neves Celestino , Freitas Paula , Maia Jose Costa , Rios Elisabete , Fernandes Ana Catarina , Rodrigues Elisabete , Carvalho Davide

Introduction: Adrenocortical carcinoma (ACC) is a rare and aggressive endocrine malignancy with a poor prognosis. Hormone-secreting ACC appear with manifestations of virilization, feminization or Cushing syndrome.Case Report: A 63-year-old woman with no pathological history of relief was referred to Endocrinology evaluation with an history of deepening of the voice since 1-year ago, as well as hair loss and facial and abdominal hirsutism with 6-month evo...

ea0049ep457 | Diabetes (to include epidemiology, pathophysiology) | ECE2017

The T allele of the rs1746661G/T polymorphism in FNDC5 (irisin) gene is associated with increased systolic blood pressure

Brondani Leticia A. , Boucas Ana Paula , Assmann Tais S. , Reichelt Angela J. , Martins-Costa Sergio , Weinert Leticia S. , Silveiro Sandra P. , de Souza Bianca M. , Crispim Daisy

Background: Gestational diabetes mellitus (GDM) is a risk factor for type 2 diabetes and both conditions are characterized by insulin resistance (IR) and decreased insulin production by pancreatic beta-cells. FNDC5 gene encodes a type I membrane protein that is proteolytically processed to form a hormone secreted into the blood, termed irisin. After induction by exercise, irisin activates profound changes in the subcutaneous adipose tissue, stimulating browning and UCP1 gene e...

ea0049ep468 | Diabetes (to include epidemiology, pathophysiology) | ECE2017

Hyperinter study: evaluation of glycemic values in acute inpatients from medical and surgical units. population without diabetes

Goncalves Helena Santos , Paixao Anusca Lopes , Lameirao Cristina , Rafael Ana , Gomes Marta , Silva Rita , Queiros Rita , Lopes Natalia , Rebelo Ana Filipa , Marques Paula Vaz

Introduction: Although inpatients hyperglycemia is a current uneasiness among the medical community, its prevalence in Portugal in unknown. We aim to identify ‘Stress hyperglycemia’ and ‘New onset diabetes’ cases in inpatients in a district hospital.Methods: We evaluated inpatients from Internal Medicine (IM), General Surgery (GS), Orthopedics and Traumatology (OT) and Stoke Unit (SU) departments, admitted from the emergency departmen...

ea0049ep576 | Diabetes complications | ECE2017

Severe diabetic gastroparesis – two cases of challenging treatment

Souteiro Pedro , Oliveira Sofia Castro , Neves Joao Sergio , Santos-Antunes Joao , Bettencourt-Silva Rita , Belo Sandra , Neves Celestino , Freitas Paula , Queiros Joana , Esteves Cesar , Carvalho Davide

Introduction: Gastroparesis is defined by a delayed gastric emptying without mechanical obstruction. It can be a debilitating complication of diabetes that is poorly understood and has limited therapeutic options.Case reports: 1st case - We report the case of a 34-year-old woman with type 1 diabetes mellitus (T1DM) with diabetic nephropathy and gastroparesis, and a reasonable glycaemic control...

ea0049ep599 | Diabetes therapy | ECE2017

Pancreas transplantation: experience in a central hospital

Martins Ana Claudia , Vasques Miguel , Bogalho Paula , Aires Ines , Ferreira Anibal , Remedio Francisco , Paulino Jorge , Nolasco Fernando , Martins Americo , Agapito Ana

Introduction: Pancreas transplantation is an established treatment for selected patients with type 1 diabetes mellitus (T1DM) and severe chronic kidney disease (CKD), reducing mortality and morbidity.Methods: We retrospectively reviewed the cases of pancreas transplantation performed at our centre from 1-January-2011 to 30-June-2016.Results: In this period, 53 transplants were performed: 48 simultaneous pancreas-kidney transplants ...