Searchable abstracts of presentations at key conferences in endocrinology

ea0056gp98 | Diabetes Therapy | ECE2018

Adult-onset autoimmune diabetes: comparative analysis of classical and latent presentation

Fadiga Lucia , Saraiva Joana , Oliveira Diana , Lages Adriana , Ventura Mara , Cunha Nelson , Catarino Diana , Marques Bernardo , Frade Joao , Carrilho Francisco

Introduction: Adult-onset autoimmune diabetes (AID) has two different phenotypes: classic type 1 diabetes mellitus (T1DM), with insulin requirement just after diagnosis, and latent autoimmune diabetes in adults (LADA). According to the Immunology of Diabetes Society, LADA diagnostic criteria are: age of onset of 30 years or more, any islet autoantibody, absence of insulin requirement for at least 6 months. The purpose of this study is to characterize patients with AID followed...

ea0075d13 | Diabetes | EYES2021

Does diabetes and poor glycemic control increase the severity and mortality in patients with COVID-19?

Cunha Clara , Barradas Ana Rita , Silva Eugenia , Vasconcelos Joana , Saraiva Catarina , Duarte Sequeira , Mansinho Kamal , Madruga Isabel , Fonseca Candida

Background and Aims: Diabetes is often associated with an increased severity and mortality in COVID-19 patients. Possible mechanisms include hyperglycemia-induced impaired immune response, characterized by a state of chronic low-grade inflammation. Objectives: evaluate if diabetes and glycemic control were related to the severity of disease and mortality in hospitalized COVID-19 patients.Methods: We conducted a retrospective case control study that inclu...

ea0099p165 | Thyroid | ECE2024

Clinical and histopathological factors associated with the prognosis of medullary thyroid cancer in a tertiary center

Martins Ferreira Mafalda , Carvalho Tania , Madeira Joana , Lopes Sofia , Melo Miguel , Ribeiro Cristina , Saraiva Joana , Oliveira Patricia , Paiva Isabel

Introduction: Medullary thyroid cancer (MTC) is a rare tumour. Mostly sporadic, 25% are associated with multiple endocrine neoplasia (MEN2A/B) or isolated familial MTC. Surgery is the only curative option: its response is defined as complete (no evidence of biochemical or structural disease), incomplete (only structural response) and persistence of structural disease. We aimed to analyse the clinical and pathological factors associated with the prognosis of MTC.<p class="a...

ea0099ep796 | Calcium and Bone | ECE2024

Severe Hypercalcemia After Parathyroidectomy: When the Unexpected Happens

Carvalho Tania , Rodrigues Gustavo , Filipa Araujo Barbara , Saraiva Joana , Ventura Mara , Gouveia Sofia , Rodrigues Dircea , Paiva Isabel

Introduction: Severe hypercalcemia is defined as a total serum calcium level >14 mg/dl or ionized calcium >10 mg/dl . The most common causes are primary hyperparathyroidism (PHPT) and neoplasms (90% of cases). Vitamin D intoxication is an extremely rare cause. Case Report: A 56-year-old man presented to the emergency department with vomiting, generalized weakness and complaints of imbalance over one week. Upon physical examination, he displayed c...

ea0099ep795 | Thyroid | ECE2024

Medullary thyroid carcinoma – a 22-year case series from a tertiary hospital center

Carvalho Tania , Martins Ferreira Mafalda , Madeira Joana , Lopes Sofia , Saraiva Joana , Oliveira Patricia , Melo Miguel , Ribeiro Cristina , Paiva Isabel

Introduction: Medullary thyroid carcinoma (MTC) arises from thyroid parafollicular C cells and accounts for <5% of thyroid cancers. Nearly 25% occur in the context of multiple endocrine neoplasia type 2 syndrome (MEN2) or familial isolated MTC.Objectives: Evaluation of clinical characteristics and evolution of patients with MTC.Methods: Retrospective analysis of clinical records of patients with MTC diagnosed from 2001 to 2023....

ea0063ep104 | Pituitary and Neuroendocrinology | ECE2019

Corticotroph adenoma associated with a rare infection – case report

Catarino Diana , Ribeiro Cristina , Cunha Nelson , Fadia Lucia , Silva Diana , Guiomar Joana , Lavrador Mariana , Vieira Ines , Saraiva Joana , Rodrigues Dircea , Paiva Isabel , Gomes Leonor , Bastos Margarida

Introduction: Cushing Syndrome have long been recognised to predispose patients to infection diseases, a consequence of the immunosuppression induced by corticosteroids. There is a predisposition to viral, bacterial, parasitic and especially fungal diseases. Opportunistic infections, particularly invasive fungal infections, represent a serious complication associated with an increased risk of mortality.Clinical case: We represent a 55 years-old woman, po...

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...

ea0040p13 | (1) | ESEBEC2016

Multiple endocrine neoplasia type 1 – retrospective analysis of five families

Ventura Mara , Melo Miguel , Gomes Leonor , Saraiva Joana , Barros Luisa , Rodrigues Dircea , Guelho Daniela , Cardoso Luis , Vicente Nuno , Martins Diana , Oliveira Diana , Lages Adriana , Carrilho Francisco

Introduction: Multiple endocrine neoplasia type 1 (MEN 1) is a rare syndrome with autosomal dominant inheritance. It mainly involves the parathyroid glands (90%), the pancreas (60%) and the pituitary (40%). More than 300 different MEN1 germline mutations were already described.Objective: To characterize families with MEN1 followed at the Department of Endocrinology of the University and Hospital Center of Coimbra, Portugal, from 1990 until 2015.<p cl...

ea0035p327 | Clinical case reports Thyroid/Others | ECE2014

Hirata disease: a rare form of hyperinsulinemic hypoglycemia

Cardoso Luis , Church David , Rodrigues Dircea , Alves Marcia , Guelho Daniela , Saraiva Joana , Moreno Carolina , Dantas Rosa , Vicente Nuno , Semple Robert K. , Carrilho Francisco

Introduction: Insulin autoimmune syndrome or Hirata disease is a rare cause of hypoglycemia without prior insulin exposure. Approximately 400 cases were reported, mostly in Japan. ItÂ’s associated with other autoimmune diseases or exposure to sulfhydryl-containing drugs.Case report: A 56-year-old Caucasian woman presented with a 20-month history of hypoglycemia ameliorated by sugar intake. She had a past history of autoimmune thyroiditis, asthma and ...

ea0035p461 | Diabetes complications | ECE2014

Diabetes and end-stage renal disease: clinical evaluation of diabetic renal transplant candidates

Dantas Rosa , Bastos Margarida , Saraiva Joana , Moreno Carolina , Guelho Daniela , Vicente Nuno , Cardoso Luis Miguel , Simoes-Pereira Joana , Guimaraes Joana , Alves Rui , Carrilho Francisco

Introduction: Diabetes mellitus (DM) is one of the main causes of end-stage renal disease (ESRD). Renal transplantation is the most effective form or renal replacement.Methods: Retrospective, descriptive study of a sample of 108 diabetic patients admitted as candidates to renal transplant from January 1991 to December 2011, using the SPSS programme, version 20.0.Results: 11 women and 97 men were evaluated (medium age: 58±8.2 y...