Searchable abstracts of presentations at key conferences in endocrinology

ea0020p37 | Adrenal | ECE2009

Pheochromocytoma: a retrospective study on clinical presentation, management and outcomes

Martinho Mariana , Paiva Isabel , Carrilho Francisco , Fagulha Ana , Santos Jacinta , Vieira Alexandra , Rodrigues Fernando , Carvalheiro Manuela

Pheochromocytomas are rare, catecholamine-secreting, adrenal neoplasms. In about 25% of cases they arise in patients with germline mutations. Malignancy occurs in about 10%.We retrospectively analysed the records of patients with histological diagnosis of pheochromocytoma submitted to adrenal surgery between 1987–2008 and followed in the Endocrinology department.Thirteen patients were included. We evaluated age on diagnosis; c...

ea0020p333 | Diabetes and Cardiovascular | ECE2009

Characterization of a young population of type 1 diabetics

Vieira Alexandra , Fagulha Ana , Barros Luisa , Figueiredo Julia , Santos Jacinta , Martinho Mariana , Carrilho Francisco , Carvalheiro Manuela

Introduction: Type 1 diabetes is one the most common chronic diseases found in children and youngsters.Objectives: Characterization of a sample of young type 1 diabetic patients, treated with multiple daily injections of insulin.Patients and methods: Analysis of patients files with ages between 11 and 26 years observed on diabetology consultation during the first semester of 2008, with diagnosis of diabetes for at least 6 months. P...

ea0020p390 | Diabetes and Cardiovascular | ECE2009

Prevalence of cardiovascular risk polymorphisms and its association with microvascular complications in an adolescent type 1 diabetes population

Melo Miguel , Fagulha Ana , Barros Luisa , Santos Jacinta , Vieira Alexandra , Carvalheiro Manuela

Objectives: To determine the prevalence of several polymorphisms associated with increased cardiovascular risk in a group of adolescents with T1DM. To study the possible association of some polymorphisms with the occurrence of microvascular complications.Methods: Patients were randomly selected from our outpatient clinic. The following polymorphisms were studied:: ACE Ins/Del, Apo B R3500Q, Apo E2, 3, 4, MTHFR C677T and A1298C, PAI 4G/5G, ITGB3 PL(A1)/(A...

ea0014p464 | (1) | ECE2007

Cushing’s syndrome in paediatric age – casuistic, evolution of investigation tests and treatment options in our institution throughout the last 20 years

Melo Miguel , Fagulha Ana , Paiva Isabel , Guimaraes Joana , Baptista Carla , Gomes Fernando , Belo Francisco , Carvalheiro Manuela

Cushing’s syndrome is a rare disorder in children and adolescents. The diagnosis can be a challenge for the clinician, as its principal feature – obesity – is extremely common. We present three cases diagnosed in the last 20 years. The first one was a boy aged 17 that presented in 1984 with central obesity, acne, moon face with plethora, abdominal striae, easy bruising and skin atrophy. The investigations performed consisted in cortisol and ACTH plasma measureme...