Searchable abstracts of presentations at key conferences in endocrinology

ea0063p59 | Adrenal and Neuroendocrine Tumours 1 | ECE2019

Adrenal pheocromocytoma during childhood – a case report

Silva Eugenia , Cunha Clara , Ferrinho Catia , Ferreira Rute , Oliveira Manuela

Pheochromocytoma is a rare tumor made up of chromaffin cells from the adrenal medulla that secrete catecholamines. It can occur at any age, with a peak incidence between the fourth and fifth decade of life, and only 10% of cases occur in children. The majority of cases are sporadic and approximately 10% are malignant. The existence of familial syndrome, multiple or extra adrenal tumors is more common at younger ages. The clinic is very variable, and hypertension (HTA) is the m...

ea0063p888 | Diabetes, Obesity and Metabolism 3 | ECE2019

Maturity onset diabetes of the young type 5 – report of one phenotype

Roque Catarina , Ferrinho Catia , Cunha Clara , Oliveira Manuela

Introduction: MODYs are being identified more frequently but the rarity of some types still precludes in-dept knowledge of their natural course of disease. One of this rare forms is MODY 5, the result of a mutation on the hepatocyte nuclear factor 1 beta (HNF-1B) gene that associates with genitourinary and pancreatic malformations/dysfunction.Case report: A 24-year-old female was referred to the Endocrinology clinic due to hyperglycaemia identified on pr...

ea0063ep142 | Thyroid | ECE2019

Primary thyroid lymphoma: a differential diagnosis to be considered

Cunha Clara , Capitao Ricardo , Silva Eugenia , Saraiva Catarina , Oliveira Manuela

Introduction: Primary lymphoma of the thyroid (PTL) is a rare cause of malignancy, accounting for 5% of thyroid malignancies, with an annual estimated incidence of 2 per 1 million. Women are more commonly affected than men (2–8:1). Patients typically present in the sixth or seventh decade of life. Most thyroid lymphomas are non-Hodgkin’s lymphomas (NHLs) of B-cell origin. Patients with Hashimoto’s thyroiditis are at greater risk for developing PTL. Treatment and...

ea0090p495 | Thyroid | ECE2023

Weight Variability with the Treatment of Graves’ Disease in Adults

Lopes Leonor , Tavares Bello Carlos , Cunha Clara , Antunes Carolina , Limbert Clotilde , Manuel Sequeira Duarte Joao

Introduction: Graves disease (GD) is a frequent cause of primary hyperthyroidism and often presents with weight loss. Weight gain beyond the premorbid state is often reported and could be a challenge during patient’s management. Treatment modalities, disease remission and biochemical parameters at the diagnosis have been described as predictors of weight changes in patients with GD. Objectives: To evaluate the determinants of weight changes in GD tr...

ea0070ep506 | Thyroid | ECE2020

Hashimoto’s tiroiditis, quervain’s disease and a suspicious nodule

Roque Catarina , Cunha Clara , Bello Carlos , Saraiva Catarina , Sequeira Duarte João

Introduction: The Quervain’s disease is an infrequent subacute thyroiditis (ST) that results in granulomatous infiltration of the gland’s parenchyma. Is usually diagnosed clinically based on cervical pain, systemic symptoms, altered thyroid function tests (TFTs) and history of upper respiratory tract infection. It is a benign self-limited condition that may share US features with malignancy which may result in improper therapy, including lobectomy.<p class="abs...

ea0056p895 | Clinical case reports - Thyroid/Others | ECE2018

Hypergonadotropic hypogonadism secondary to vanishing testes syndrome newly diagnosed in a 42-year-old male patient

Sousa Santos Francisco , Capitao Ricardo , Ferrinho Catia , Cunha Clara , Limbert Clotilde , Vasconcelos Carlos

Introduction: Cryptorchidism is the most common abnormality of male sexual development. Approximately 5% of cases of cryptorchidism are associated with vanishing testes syndrome. This rare condition occurs when an initially normal testicle that existed in fetal life subsequently atrophies. Affected patients usually have normal male external genitalia and hypergonadotropic hypogonadism. This disease is usually diagnosed in early childhood allowing for normal sexual development ...

ea0067o38 | Oral Presentations | EYES2019

Non-functioning pituitary adenomas experience of a reference center

Cunha Clara , Ferrinho Catia , Silva Eugenia , Dias Lidia , Marques Conceicao , Chorao Martinha , Saraiva Catarina , Duarte Joao Sequeira

Objective: Describe clinical, laboratorial, imaging features, therapeutic management and the outcomes of patients with clinically non-functioning pituitary adenomas (NFPAs) presenting at our department.Methods: Retrospective review of electronic medical records of all patients with NFPAs evaluated at our department between 2010 and 2019.Results: We evaluated 160 patients, 51.3% female, with a median age of 56.6 years (18–89). ...

ea0067gp20 | Poster Presentations | EYES2019

Pheochromocytoma, unmasking the chameleon

Cunha Clara , Ferrinho Catia , Santos Francisco Sousa , Silva Eugenia , Fernandes Luis Viana , Saraiva Catarina , Oliveira Manuela , Duarte Joao Sequeira

Background: Pheochromocytoma is a rare catecholamine secreting tumor originating usually from adrenal medulla and representing approximately 5% of adrenal incidentalomas. Currently 10% of all pheochromocytomas are discovered incidentally during imaging studies for unrelated disorders.Case presentation: A thirty five year old woman with no relevant medical history presented at the emergency department with symptoms of left flank pain and vomiting. Abdomin...

ea0063p840 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

Adrenal incidentalomas – from diagnosis to follow-up

Cunha Clara , Capitao Ricardo , Bello Carlos Tavares , Santos Francisco Sousa , Roque Catarina , Saraiva Catarina , Duarte Joao Sequeira , Oliveira Manuela

Introduction: Adrenal incidentalomas (AIs) are defined as adrenal masses measuring 10 mm or more in diameter, incidentally discovered on imaging exams performed for a non-adrenal disorder. The aim of this study is to provide a clinical and imagiological characterization of patients diagnosed with AIs followed in our institution.Methods: We conducted an observational and retrospective study that included patients with AIs evaluated at our institution betw...

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...