Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep769 | Pituitary: clinical | ECE2015

Evolution of metabolic and psychiatric disorders after remission of Cushing's disease

Lau Eva , Oliveira Joana , Belo Sandra , Freitas Paula , Oliveira AnaIsabel , Vinha Eduardo , Castro Ligia , Pereira Josue , Carvaho Davide

Introduction: Cushing’s disease (CD) is a rare endocrine disorder characterized by endogenous hypercortisolism, which is associated with metabolic and psychiatric disorders. It is essential to understand the impact of normalization of serum cortisol in the evolution of these comorbidities.Aims: To evaluate the evolution of metabolic and psychiatric disorders after biochemical control of hypercortisolism in patients with CD.Met...

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...

ea0037ep939 | Thyroid (non-cancer) | ECE2015

Seasonality in paediatric Graves' disease compared to the general population: impact of month of birth: a national study

da Silva Tiago Nunes , Pereira Bernardo Dias , Luiz Henrique Vara , Matos Ana Catarina , Cordeiro Maria Carlos , Raimundo Luisa , Portugal Jorge

Paediatric Graves’ disease (PGD) is an uncommon autoimmune disorder with a multifactorial origin. Although, in some autoimmune endocrinophaties the seasonality of month of birth (MOB) distribution differed from the general population, this association has not been study in PGD. The aim of this work was to analyse the impact of seasonality of MOB on PGD incidence in Portugal.In 2013, the Portuguese Paediatric Society of Diabetes and Endocrinology und...

ea0035p247 | Clinical case reports Pituitary/Adrenal | ECE2014

Spindle cell oncocytoma: a new presentation of a rare disease

da Silva Tiago Nunes , Pereira Bernardo Dias , Luiz Henrique Vara , Veloza Andreia , Matos Ana Catarina , Portugal Jorge

Spindle cell oncocytoma (SCO) is a rare entity with just 18 cases reported in the literature. It was first described in 2002 and was codified as a separate diagnostic entity in the 2007 WHO classification of brain tumours. SCO is a nonadenomatous sellar neoplasm with rich vascularization and intra and supra-sellar infiltration. Usual clinical presentation consists of headache, visual field defects and pan-hypopituitarism. The preoperative diagnosis is difficult due to a lack o...

ea0035p945 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

Cushing's disease caused by atypical pituitary adenoma

Costa Maria Manuel , Nogueira Claudia , Oliveira Joana , Cunha Filipe , Castro Ligia , Pereira Josue , Vinha Eduardo , Carvalho Davide

Introduction: Cushing’s Disease results of corticotrophin (ACTH) hypersecretion from pituitary which increases cortisol production. WHO classified pituitary tumors as typical adenoma, atypical adenoma and carcinoma. Diagnostic criteria for an atypical adenoma include invasive growth, elevated mitotic index, Ki-67 labeling index greater than 3% and extensive p53 immunoreactivity.Case Report: Sixty-eight years-old man presented to our consult with his...

ea0070aep215 | Bone and Calcium | ECE2020

Progression of vertebral fractures in long-term controlled acromegaly: A 9-year follow-up study

Pelsma Iris , Claessen Kim , Pereira Alberto , van Furth Wouter , Appelman-Dijkstra Natasha , Kloppenburg Margreet , Kroon Herman , Biermasz Nienke

Objective: Growth hormone (GH) and insulin-like growth factor 1 (IGF-1) excess results in both reversible and irreversible damage to the skeleton, and includes increased vertebral fracture (VF) risk in the presence of normal BMD. The prevalence of VFs is approximately 60% in controlled acromegaly patients, and these VFs can progress during short-term follow-up. We aimed to identify the course of VFs and their associated risk factors in a cohort of acromegaly patients in long-t...

ea0070aep552 | General Endocrinology | ECE2020

The extent of variation in the reporting of clinical activity by reference centres in the field of rare pituitary and thyroid disorders within Endo-ERN, a new reference network for rare endocrine conditions in Europe

de Vries Friso , Bruin Mees , Cersosimo Angelica , Ahmed Faisal , Peeters Robin , Biermasz Nienke , Hiort Olaf , Pereira Alberto

Objective: Self-reported volume of patients and specific interventions is a specific network criterion that needs to be fulfilled by reference centres that are eligible for inclusion within Endo-ERN. The aim of the present study is to evaluate how self-reported volume data in the original applications were obtained, which data are retrievable, and which set is best suitable to use for future centre evaluations. This overview is provided for two Main Thematic Groups (MTGs) of E...

ea0070aep1101 | Hot topics (including COVID-19) | ECE2020

Measurement of calcitonin in nodular thyroid disease approach: The experience of a tertiary centre

Benido Silva Vânia , Teresa Pereira Maria , Carlos Oliveira José , Freitas Cláudia , Helena Cardoso Maria

Introduction: It is universally accepted that calcitonin (CT), a hormone secreted by the parafollicular cells of the thyroid, is a specific, sensitive and early marker of Medullary Thyroid Carcinoma (CMT), with higher diagnostic accuracy than fine needle aspiration biopsy(FNAB). However, the routine measurement of serum CT during assessment of nodular thyroid disease (NTD) remains controversial due to rarity of this cancer and possible false positive results.<p class="abst...

ea0070ep64 | Bone and Calcium | ECE2020

Malignant hypercalcemia – A rare case associated with abdominal liposarcoma

Figueiredo Ana , Damasio Ines , Cavaco Daniela , Simões Helder , Simões-Pereira Joana , Leite Valeriano

Background: Malignant hypercalcemia (MH) occurs in up to 30% of patients who are diagnosed with cancery, being associated with later stages of the disease and poor prognosis. The physiopathological mechanisms responsible for MH are the production of parathyroid hormone-related peptide by the tumor (PTHrp) (80% of cases), osteolytic cytokine production (20%) and excess of 1,25(OH)2vitamin D production (1%).Case report: We present the case of a ...

ea0032p243 | Clinical case reports – Pituitary/Adrenal | ECE2013

Osteoporotic fractures as manifestation of Cushing’s disease

Nogueira Claudia , Souto Selma , Quinaz Joao , Braga Daniel , Vinha Eduardo , Rios Elisabete , Bernardes Irene , Pereira Josue , Carvalho Davide

Introduction: Cushing’s syndrome (CS) is a well-known cause of bone loss and osteoporotic fractures, which may be the initial manifestation of the disease and may present 2 years before CS diagnosis. Trabecular bone is usually the most seriously affected, and vertebrae and ribs are the typical fracture locations.Case report: A 37-year-old man with dyslipidemia and obesity was observed due to uncontrolled hypertension and osteoporosis. He complained ...