Searchable abstracts of presentations at key conferences in endocrinology

ea0090p665 | Endocrine-related Cancer | ECE2023

A rare cause of bilateral adrenal masses

Santos Sara , Calheiros Raquel , Souteiro Pedro , Oliveira Joana , Inacio Isabel , P Santos Ana , Torres Isabel

Introduction: Bilateral adrenal masses may appear in the context of metastatic disease, adrenal congenital hyperplasia, primary tumors or infections, among others. Primary adrenal lymphoma is rare, accounting for approximately 1% of cases of non-Hodgkin lymphoma. Clinical case: 47-year-old woman, with a history of erythema nodosum and left hemithyroidectomy in the context of benign nodular disease. She presented with persistent fever and tiredne...

ea0090ep828 | Pituitary and Neuroendocrinology | ECE2023

Panhypopituitarism of unknown aetiology in a young adult – a case report

Souteiro Pedro , Santos Sara , Oliveira Joana , Inacio Isabel , P Santos Ana , Torres Isabel

Introduction: Hypopituitarism is a rare diagnosis that is mainly due to primary pituitary neoplasms and their treatment. There are rarer causes such as hemorrhage/ischemia, traumatic brain injury, infections and infiltrative lesions. Clinical case: We herein present an 18-year-old male patient diagnosed with acute promyelocytic leukemia at the age of 14, with no evidence of central nervous system invasion in several lumbar punctures during his follow-up....

ea0011p720 | Reproduction | ECE2006

Screening for gene SRY by FISH in patients with Turner Syndrome

Guimarães J , Almeida Santos T , Barbosa A , Bastos M , Almeida Santos A , Carvalheiro M

Turner’s Syndrome is one of the most common chromosomal abnormalities found in 1 in 2500 live female births. Y chromosome material is detected in up to 6% of patients by karyotype, but with new technologies (DNA analysis), Y chrmosome sequences have been reported in 60% of patients. The presence of Y material has been associated with virilization and with the development of gonadal neoplasia.Aim: Determine the frequency of Y chromosome sequences in ...

ea0002p79 | Reproduction | SFE2001

IMPROVEMENT OF MALE HYPOGONADISM IN SEVERE OBESITY DURING WEIGHT LOSS AFTER BARIATRIC SURGERY

Monteiro M , Cardoso H , Vargas G , Mendes P , Sergio A , Santos M , Santos C , Ramos H

Objectives: To evaluate changes in gonadotrophins, total (TT) and free (FT) testosterone, SHBG, insulin and c-peptide levels during weight lost after bariatric surgery.Material and methods: Seven (n=7) patients submitted to bariatric surgery for treatment of severe obesity were followed-up over time. Before surgery mean age was 32,857 (19-56) years old, mean weight was 170,571 kg (± 37,362) and mean BMI was 58,824 kg per m2(± 14,...

ea0099ep344 | Endocrine-Related Cancer | ECE2024

Paediatric differentiated thyroid cancer: a single-centre retrospective study

Calheiros Raquel , Gil-Santos Sara , Souteiro Pedro , Oliveira Joana , Inacio Isabel , Paula Santos Ana , Torres Isabel

Introduction: Differentiated thyroid cancer (DTC) is rare in the paediatric population when compared to adults. Paediatric patients often present with advanced disease at diagnosis, characterized by multifocal disease, heightened lymph node involvement, and distant metastasis. Additionally, they face a higher risk of post-operative complications in comparison to adults. Despite that, paediatric DTC exhibits an excellent prognosis.Methods: A retrospective...

ea0099ep1013 | Endocrine-Related Cancer | ECE2024

Adrenocortical carcinoma with refractory cushing’s syndrome: could we have done better?

Calheiros Raquel , Gil-Santos Sara , Souteiro Pedro , Oliveira Joana , Inacio Isabel , Paula Santos Ana , Torres Isabel

Introduction: Adrenocortical carcinoma is a rare type of cancer that usually has a dismal prognosis. The concurrent hormonal excess of some of these tumours can have an additional negative impact on patients´ morbidity and mortality.Clinical Case: We present the case of a 57-year-old woman diagnosed with stage IV adrenocortical carcinoma, with liver and bone metastasis, and associated ACTH-independent Cushing syndrome and hyperandrogenism. The patie...

ea0099ep242 | Pituitary and Neuroendocrinology | ECE2024

Pancreatic neuroendocrine tumour: from glucagonoma to aggressive insulinoma

Santos Sara , Calheiros Raquel , Souteiro Pedro , Oliveira Joana , Inacio Isabel , Paula Santos Ana , Torres Isabel

Introduction: Pancreatic neuroendocrine tumors (PNETs) originate from neuroendocrine islet cells and can therefore secrete several neuropeptides. Multiple and secondary hormone secretion have been described in a minority of cases, mostly with advanced disease, and it has been hypothesized that this complex secretion pattern can serve as a marker for tumor behavior.Case report: Male patient, 69 years old, diagnosed with a glucagonoma with pulmonary and he...

ea0078p37 | Gonadal, DSD and Reproduction | BSPED2021

Primary hypogonadism: better not just think of klinefelter!

Rosinha Ines , Ramos Fabiana , Santos Lea , Mirante Alice

Background: Klinefelter syndrome is the most common sex chromosome abnormality causing primary hypogonadism and affects approximately 1 to 2.5 per 1000 males. However, other rarer sex chromosomal abnormalities have been associated to testicular dysfunction.Clinical Case: A thirteen-year-old male was referenced to Pediatric consultation due to obesity starting around age four. Perinatal background: maternal gestational diabetes controlled with diet and 10...

ea0081p187 | Reproductive and Developmental Endocrinology | ECE2022

Overall impact of gender affirming hormone therapy: the portuguese experience

Saraiva Miguel , Santos Rafael , Figueiredo Zelia , Lemos Carolina , Palma Isabel

Introduction: The prevalence of Transgender individuals seeking gender affirming hormone therapy (GAHT) has been increasing. This therapy has been known to be highly effective in the treatment of gender dysphoria and enhancing mental health in this population.Aim: To evaluate the overall impact of GAHT on self-esteem, well-being and social/familial relations in the Portuguese adult transgender populationMethods: Cross-sectional stu...

ea0049ep297 | Calcium & Vitamin D metabolism | ECE2017

Tc-99m sestamibi uptake by brown tumours in a patient with primary hyperparathyroidism

Dias Daniela , Macedo Daniel , Santos Rita , Leite Valeriano

Tc-99m sestamibi (MIBI) imaging is able to localize parathyroid adenomas/carcinomas in patients with primary hyperparathyroidism. Brown tumours are one of the skeletal manifestations of long standing hyperparathyroidism and its incidence has been reported to be 3%. Radiological features of these tumors may mimic bone metastasis. There are only a few reports showing brown tumours uptake in the whole-body Tc-sestamibi scan.We report a 72-year-old female wi...