Searchable abstracts of presentations at key conferences in endocrinology

ea0088018 | Abstracts | BES2022

A rare cause of Cushing syndrome

Bastiaan Sol , Marilyn Carpriaux , Leu Nico De

Introduction: Diagnosis of Cushing Syndrome (CS) is challenging due to its various non-specific symptoms, and multiple endogenous and exogenous causes. The incidence of endogenous CS is rare and estimated at 2 to 3 cases per million inhabitants per year in Europe (1). Primary bilateral macronodular adrenal hyperplasia (PBMAH) is an uncommon cause of endogenous ACTH-independent CS. It is a benign condition, characterized by the presence of bilateral macronodules (>1 cm), an...

ea0097025 | Section | BES2023

An extremely rare cause of psychosis, hypokalemia, and metabolic alkalosis

N. Mutebi , Leu N. De , D. Unuane

Cushing’s syndrome (CS) remains a diagnostic challenge due to an overlap with other clinical conditions such as pseudo-Cushing, which can be triggered by major depression, alcoholism, and metabolic syndrome. The most prevalent cause of CS is iatrogenic. When Cushing’s syndrome is caused by endogenous cortisol secretion, most often an ACTH-secreting pituitary adenoma is the culprit and the syndrome is hence referred to as Cushing’s disease. In very rare cases CS ...

ea0063p741 | Pituitary and Neuroendocrinology 2 | ECE2019

Ongoing challenges in treatment of cushing’s disease due to pituitary macroadenoma

Teuşan Teodora , Ciobotar Mihaela , Florescu Alexandru , Ungureanu Maria Christina , Mogoş Voichiţa , Leuştean Letiţia

Introduction: Cushing’s disease (CD) is five to six times more common than Cushing’s syndrome, with a peak incidence at 20–40 years. It is usually an ACTH-secreting microadenoma, the local invasion being associated with one third of macroadenomas. The treatment of choice is the transsphenoidal surgery, but nearly 50% of the patients with macroadenomas ultimately require additional treatment. Cabergoline appears to be an attractive treatment option for CD, consid...

ea0063p863 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

A rare case of primary hyperaldosteronism associated with chronic kidney disease-difficulties in diagnosis and treatment

Leuştean Letiţia , Bălineanu Ginuţa Marcela , Rimbu Cosmina , Hrişcă Anamaria , Luminiţa Voroneanu Elena , Ungureanu Maria-Christina

Introduction: Primary aldosteronism (PA) accounts for 20% of patients with resistant hypertension and is one of its leading causes. Options of treatment include adrenalectomy and mineralocorticoid receptor antagonists (MRAs). Latest studies suggest that both may paradoxically lead to a decline in estimated glomerular filtration rate (eGFR), explained by the masked glomerular hyperfiltration associated to PA before treatment.Case report: A 56 years old ma...

ea0057008 | Vegf-A mRNA transfection as a novel approach to improve mouse and human islet graft revascularization | BES2018

Vegf-A mRNA transfection as a novel approach to improve mouse and human islet graft revascularization

Willem Staels , Yannick Verdonck , Yves Heremans , Gunter Leuckx , Sofie De Groef , Carlo Heirman , Eelco de Koning , Conny Gysemans , Kris Thielemans , Luc Baeyens , Harry Heimberg , Nico De Leu

Aims/hypothesis: The initial avascular period following islet transplantation seriously compromises graft function and survival. Enhancing graft revascularization to improve engraftment has been attempted through virus-based delivery of angiogenic triggers, but risks associated with viral vectors have hampered clinical translation. In vitro transcribed mRNA transfection circumvents these risks and may be used for improving islet engraftment.Meth...