Searchable abstracts of presentations at key conferences in endocrinology

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...

ea0049ep45 | Adrenal cortex (to include Cushing's) | ECE2017

Adrenal involvement in MEN1 families

Ventura Mara , Melo Miguel , Gomes Leonor , Saraiva Joana , Barros Luisa , Rodrigues Dircea , Oliveira Diana , Martins Diana , Lages Adriana , Cunha Nelson , Carrilho Francisco

Introduction: MEN1 is a rare autosomal dominant syndrome typically characterized by neoplastic lesions of parathyroid glands, anterior pituitary gland and endocrine pancreas. Several other tumours are associated with this syndrome, including adrenal lesions, but their prevalence and clinical characteristics (endocrine secretion and aggressiveness) are largely unknown.Objective: To determine the prevalence, clinical characteristics and the possible genoty...

ea0049ep82 | Adrenal cortex (to include Cushing's) | ECE2017

Adrenocortical carcinoma - casuistic analysis

Ribeiro Catia , Lobo Joao , Mesquita Ana , Martins Pedro C , Peyroteo Mariana , Matos Maria Joao , Antunes Pedro , Sanches Cristina , Moreira Augusto , de Sousa Joaquim Abreu

Introduction: Adrenocortical carcinomas are rare neoplasms with an incidence of 0.7 to 1.5 per million/year. Diagnosis often requires a multidisciplinary approach. When the disease is confined to the adrenal gland, absolute criteria defining malignancy, do not exist, however a score of Weiss> or =a 3 is considered diagnosis. The prognosis is usually reserved and conventional chemotherapy is not curative.Material and Methods: Retrospective analysis of...

ea0049ep392 | Clinical case reports - Thyroid/Others | ECE2017

Continuous glucose monitoring in glycogen storage disease type Ia – a major improvement for patients

Martins Diana , Oliveira Diana , Baptista Carla , Paiva Sandra , Vicente Nuno , Cardoso Luis , Lages Adriana , Ventura Mara , Cunha Nelson , Moreira Sonia , Clemente Hugo , Esperto Helder , Carrilho Francisco

Introduction: Glycogen storage disease (GSD) type Ia (von Gierke’s disease) is an inherited metabolic disorder of glycogen metabolism, caused by defects in the glucose-6-phosphatase complex, with associated risk of severe hypoglycemia within 3–4 h after a meal.The aim of the present study was to evaluate the efficacy of continuous glucose monitoring (CGM) system in determining the magnitude of hypoglycemia in patients with GSD type Ia.<p cl...

ea0049ep394 | Clinical case reports - Thyroid/Others | ECE2017

Endocrine manifestations of Woodhouse-Sakati Syndrome – a Portuguese case

Oliveira Diana , Paiva Sandra , Louro Pedro , Macario M Carmo , Duraes Joao , Martins Diana , Ventura Mara , Lages Adriana , Cunha Nelson , Carrilho Francisco

Introduction: Woodhouse-Sakati Syndrome (WSS) is a very rare autossomic recessive disorder caused by mutations in DCAF17 gene that primarily affects the endocrine and the nervous systems. It is associated with hypogonadism, diabetes mellitus, hypothyroidism, sensorineural hearing loss, alopecia and extrapyramidal findings. Treatment is symptomatic and managed by multidisciplinary teams. Less than 80 cases are reported to date.Case repor...

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...

ea0049ep567 | Diabetes complications | ECE2017

Prevalence of distal symmetric polyneuropathy in diabetic patients in general medicine wards

Lopes Ana , Goncalves Helena , Fonseca Liliana , Branco Catarina Castelo , Goncalves Joao , Sousa Luisa , Calejo Margarida , Martins Sara , Neves Joao , Teixeira Sofia

Background: Distal symmetric polyneuropathy (DSPN) is one of the most prevalent chronic complications of diabetes and the most common cause in the pathway to diabetic foot ulceration. Screening for DSPN enables early intervention and prevention of complications. The Semmes-Weinstein Monofilament Examination (SWME) is currently the method of choice to screen DSPN, but ideally two neurologic tests should be used. The Michigan Neuropathy Screening Instrument (MNSI), which evaluat...

ea0049ep1269 | Thyroid (non-cancer) | ECE2017

Effectiveness of radioiodine treatment for autonomous toxic node

Osorio Ana Sofia , Martins Ana Filipa , Gomes Vania , de Castro Raquel Vaz , Nobre Ema , Ferreira Mickael Antoine , Cantinho Guilhermina , Bugalho Maria Joao

Objective: The aim of this study was to evaluate the treatment outcomes in patients with autonomous toxic nodule (ATN) that received a radioiodine treatment (RAIT) and to determine the influence of age, gender, nodule size and iodine activity.Methods: We performed a retrospective study of all RAIT done for hyperthyroidism (n=149) in our hospital during 2014 and 2015. Patients with ATN submitted to RAIT were selected to analysis. We studied 58 pa...

ea0049ep1465 | Thyroid (non-cancer) | ECE2017

Isolated bone metastases: a rare form of presentation of papillary thyroid carcinoma

Peyroteo Mariana , Ribeiro Catia , Martins Pedro C , Ferreira Ana , Giesteira Laurinda , Barbosa Rui , Carvalho Machado , Ramalho Antonio , Moreira Augusto , de Sousa Abreu

Background: Papillary thyroid cancer (PTC) is the most frequent type of well-differentiated thyroid cancer (WDTC) and frequently poses a management dilemma. Its indolent behavior associated with high long term survival support the trend towards a more conservative management approach. The authors present a case of isolated bone metastases as the form of presentation of papillary thyroid carcinoma. A 61-year-old man was admitted with complaints of lower back pain for the previo...

ea0041gp60 | Clinical Case Reports | ECE2016

Endoscopic ultrasound-guided ethanol ablation therapy for pancreatic insulinoma: an unusual strategy

Lages Adriana de Sousa , Oliveira Patricia , Paiva Isabel , Portela Francisco , Guelho Daniela , Cardoso Luis , Vicente Nuno , Oliveira Diana , Martins Diana , Ventura Mara , Carrilho Francisco

Introduction: Insulinomas are the most frequent cause of endogenous hypoglycaemia. 90 to 95% of these are benign. Surgical enucleation or resection is the standard treatment. Medical therapy focuses mainly on the use of diazoxide with few alternatives in patients with high surgical risk.Case-report: Female patient, 89 years-old, non-diabetic, with previous history of acute myocardial infarction, stroke with motor sequelae, pacemaker carrier and severe ao...