Searchable abstracts of presentations at key conferences in endocrinology

ea0081p755 | Thyroid | ECE2022

Graves′ disease and unilateral gynecomastia - An uncommon initial presentation of a common disease

Dias Daniela , Carolina Neves Ana , Sapinho Ines

Most cases of gynecomastia are idiopathic. Among the most frequently identified etiologies are: persistent pubertal gynecomastia, hypogonadism, anabolic steroids and other pharmaceutical drugs use. In the literature, ginecomastia is a well-recognized manifestation of thyrotoxicosis in male patients (in the range of 10% to 40%). However, it is extremely rare in clinical practice as the initial presentation of thyrotoxicosis. The two main factors that contribute to gynecomastia ...

ea0090p647 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

New onset diabetes mellitus and thyroid dysfunction following Prembolizumab – a case report

Matos Tania , Dias Daniela , Silvestre Catarina , Serra Filipa , Sapinho Ines

Introduction: Prembrolizumab, a programmed cell death protein 1 (PD-1) inhibitor, is one of the immune checkpoint inhibitors (ICI) that have revolutionized cancer therapy. However, ICIs can also trigger immune-related adverse events (irAEs) in different organ systems, including endocrine glands. While thyroid dysfunction is among the most common endocrinopathies reported, ICI-induced diabetes mellitus (DM) is extremely rare, with an overall incidence ranging from 0.9 to 2%.</p...

ea0081ep76 | Adrenal and Cardiovascular Endocrinology | ECE2022

Pulmonary thromboembolism as the initial presentation of ACTH-independent Cushing’s Syndrome

Dias Daniela , Damasio Ines , Simoes Helder , Serra Filipa , Fontes Luisa , Leichsenring Carlos , Pinheiro Nuno , Sapinho Ines

Cushing’s syndrome (CS) is associated with a considerable risk of complications including thromboembolic events (TE). They occur mostly within the first 2–3 months postoperatively. When present before surgery, CS has high rates of perioperative mortality and morbidity. The benefit of steroidogenesis inhibitors after TE is not fully known. Furthermore, little guidance is available regarding TE assessment/management in CS. We report a case of a 34-year-old male admitte...

ea0090p746 | Reproductive and Developmental Endocrinology | ECE2023

Falsely elevated estradiol levels in a young female with iatrogenic menopause

Dias Daniela , Matos Tania , Fontes-Sousa Mario , Silvestre Catarina , Serra Filipa , Sapinho Ines

False elevation of estradiol(E2) due to immunoassay interference is a rare but important phenomenon reported in the literature. It is most commonly related to cross-reactivity(CR) from drugs sharing structural similarity with E2, namely fulvestrant and exemestane. These laboratory interferences(LI) can lead to unnecessary investigation/inappropriate treatments. Therefore, in such instances, a more selective and sensitive method is required. We present the case of a young femal...

ea0073aep578 | Reproductive and Developmental Endocrinology | ECE2021

Turner Syndrome–An unusual presentation of normal stature and incomplete puberty

Dias Daniela , Serra FIlipa , Neves Carolina , Real Mendes Leonor , Nogueira Filomena , Sapinho Inês

IntroductionTurner syndrome(TS) is characterized by complete/partial monosomy or by a structural defect in one of X chromosomes. Despite clinical hallmarks of short stature(SS) and gonadal dysgenesis(GD), phenotype is variable and related to underlying chromosomal pattern. Loss of the distal segment of the short arm of x-chromosome(Xp-), including haploinsufficiency of short stature homeobox-containing (SHOX) gene, is thought to be the main factor for gr...

ea0081p276 | Adrenal and Cardiovascular Endocrinology | ECE2022

Adrenal lesions - the importance of a careful evaluation

Dias Daniela , Figueiredo Ines , Duarte Cristina , Serra FIlipa , Leichsenring Carlos , Tavora Isabel , Paulo Fernandes Joao , Sapinho Ines

Most differential diagnoses of unilateral adrenal lesions include non-functional adenoma, adrenocortical carcinoma or pheochromocytoma. Primary adrenal lymphoma(PAL) is an extremely uncommon type of primary extranodal non-Hodgkin’s lymphoma(<1%). Most cases are bilateral (~75%), being unilateral PAL scarcely reported. The apparent unilateral involvement of this entity at presentation, in the CT scan/MRI may difficult the diagnosis, delaying the start of chemotherapy. ...

ea0090ep1151 | Late Breaking | ECE2023

Non-functioning adenomas submitted to surgery: clinical characterization and outcomes

Dias Daniela , Matos Tania , Silvestre Catarina , Serra FIlipa , Palha Ana , Lucas Neto Lia , Tavares Ferreira Joana , Subtil Joao , Tortosa Francisco , Sagarribay Amets , Sapinho Ines

Introduction: Nonfunctioning pituitary adenomas (NFPAs) are a heterogeneous group of tumors with different presentations. Clinical management of these tumors is complex. Our aim was to evaluate the clinical characteristics/postsurgical outcomes of NFPAs and to identify predictive factors of good response to surgery.Methods: Retrospective analysis of NFPA, who underwent surgery and followed in our hospital, from 2015-2022.Results: W...

ea0073ep13 | Adrenal and Cardiovascular Endocrinology | ECE2021

Pheochromocytoma in pregnancy: the need for a multidisciplinary approach

Dias Daniela , Catarina Matos Ana , Inês Sapinho , Coelho Catarina , Borges Augusta , Baleiras Carla , Lima Jorge , Gomes Paulo , Morais Suzette , Cardoso Osvaldo , Lucas Mafalda , Leichsenring Carlos , Pinheiro Nuno

IntroductionPheochromocytoma(PHEO) occurs in pregnancy with an estimated incidence of 0.007%. Its rarity and overlapping presentation with other pregnancy-related hypertensive disorders make the diagnosis really challenging. If left unrecognized, may result in increased maternal and fetal mortality. There are no guidelines on approaching PHEO during pregnancy. This case highlights the difficulties encountered in managing this condition in pregnancy.<...

ea0070aep29 | Adrenal and Cardiovascular Endocrinology | ECE2020

Treatment outcomes in 198 patients of the portuguese adrenocortical carcinoma register

Nunes da Silva Tiago , Catarino Diana , Paiva Isabel , Chaves Carolina , Costa Claudia , Castro Raquel , Paula Marques Ana , Souteiro Pedro , Pereira Maria , Machado Catarina , Belo Carlos , Simões Helder , Cortes Luisa , Pereira Bernardo , Anselmo João , Sapinho Inês , Gonçalves Ferreira Ana , Teresa Pereira Maria , Fonseca Liliana , Fernandes Isabel , Rita Elvas Ana , Donato Sara , Martins Anabela , Fajar Laura , Martinho Mariana , Garrido Susana , Ferreira Marta

Introduction: Adrenocortical carcinoma (ACC) is a rare entity, usually associated with a poor prognosis. There are still many areas of uncertainty regarding its approach.Methods: A Portuguese ACC register was established in 2020, including information from 24 endocrine centres. Kaplan-Meier was used to calculate overall survival and recurrence; log- rank test to assess survival and progression free survival (PFS) differences between groups; cox-regressio...