Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep809 | Pituitary and Neuroendocrinology | ECE2022

Association between uncontrolled acromegaly and nasopharyngeal tumor-case presentation

Nicoleta Nastase Valeria , Iulia-Florentina Burcea , Ceausu Amalia Raluca , Cimpean Anca Maria , Raica Marius , Poiana Catalina

Introduction: Acromegaly is characterized by elevated levels of growth hormone (GH) and insulin-like growth factor 1 (IGF-1), most often due to a pituitary tumor. Persistent high levels of these hormones lead to a constellation of signs and symptoms and systemic complications associated with increased mortality. A potential association between acromegaly and cancer has been hypothesized regarding colorectal, thyroid, and prostate cancers, but there are few or no descriptions f...

ea0099ep921 | Calcium and Bone | ECE2024

Corticosteroid-associated osteonecrosis of the femoral head in young adolescents post-COVID 19 era - Two case reports

Anne-Marie Stefan Andreea , Iulia-Florentina Burcea , Ramona Dobre , Poiana Catalina

Background: Avascular necrosis of the femoral head (AVNFH) is a disorder caused mainly by chronic glucocorticoid use. Systemic corticosteroid (CS) therapy was widely used in patients with mild or moderate SARS-CoV 2 infection despite lack of clinical benefits. However, emerging evidence suggests that COVID-19 infection can cause long-term effects, affecting different body systems, known as ‘long COVID-19’1. One such sequela is AVNFH, although the link betw...

ea0081ep675 | Pituitary and Neuroendocrinology | ECE2022

Association between acromegaly and papillary thyroid cancer: A case series

Anne-Marie Stefan Andreea , Ioana Dumitriu Roxana , Iulia-Florentina Burcea , Raluca Trifănescu , Niculescu Dan Alexandru , Poiana Catalina

Background: Acromegaly is a rare disorder caused by hypersecretion of growth-hormone (GH) and insulin-like growth factor (IGF-1), the underlying lesion being most frequently a pituitary adenoma. This disease is associated with a higher risk of malignancy. We describe the clinical and biochemical particularities in a series of patients with acromegaly and papillary thyroid carcinoma (PTC).Case study: Out of 311 acromegalic patients, five cases that associ...

ea0099ep349 | Reproductive and Developmental Endocrinology | ECE2024

Early embryonic testicular regression syndrome: a rare case of primary amenorrhea

Elena Iftimie Mădălina , Dobre Ramona , Iulia-Florentina Burcea , Budulucă Larisa , Braha Emanuela , Poiana Catalina

Background: Normal sex development is warranted by a complex and coordinated interaction between mutually antagonistic activating and repressing genetic and hormonal factors that act in a strict spatio-temporal sequence. Deviations from this established pattern can result in heterogenous chromosomal, gonadal or phenotypic congenital abnormalities named disorders of sexual development (DSD). We present a rare case of early testicular regression syndrome.C...

ea0090ep795 | Pituitary and Neuroendocrinology | ECE2023

Coexistence of acromegaly and autoimmune disorders: Between hazard and causality – a case series

Iftimie Mădălina Elena , Iulia-Florentina Burcea , Dobre Ramona , Trifanescu Raluca , Niculescu Dan Alexandru , Baciu Ionela , Radian Serban , Capatana Cristina , Poiana Catalina

Introduction: Acromegaly is a rare, chronic endocrinopathy, that results from persistent hypersecretion of growth hormone (GH) and consequently of insulin-like growth factor 1 (IGF1). It is well known that GH excess has multisystemic effects throughout the body, but its interaction with the immune system has only been suggested in the last few decades. This prompted us to explore the frequency of autoimmune disorders in a retrospective acromegaly cohort....

ea0070ep363 | Pituitary and Neuroendocrinology | ECE2020

Metastatic neuroendocrine tumor of unknown primary site with associated carcinoid syndrome in a young patient–a case report

Antonia Sima , Iulia Florentina Burcea , Mădălina Cristina Sorohan , Roxana Dușceac , Cătălina Poiană

Background: Neuroendocrine tumors (NETs) are relatively uncommon, accounting for 10 to 14 percent of all neuroendocrine neoplasms. Twelve percent to 22% of patiens are metastatic at presentation. The most frequent primary sites are the gastrointestinal tract (62–67%) and the lung (22–27%).Case presentation: We report the case of a 36-year-old female patient diagnosed with metastatic disease, with liver, lung and lymph nodes metastasis with un...

ea0090p254 | Thyroid | ECE2023

Endocrine adverse events associated with immune checkpoint inhibitors - A case series

Anne-Marie Stefan Andreea , Iulia-Florentina Burcea , Roxana Ioana Dumitriu , Ramona Dobre , Nicoleta Baculescu , Ionela Baciu , Radian șerban , Cristina Căpățină , Trifanescu Raluca , Poiana Catalina

Background: Immune checkpoint inhibitors (ICIs) are a novel group of drugs, used for treatment of various types of malignancies. The receptors cytotoxic T-lymphocyte antigen-4 (CTLA-4) and programmed cell death protein-1 (PD-1) or its ligand (PDL-1) are targeted by those inhibitors. They are associated with immune-related adverse events (irAEs). Endocrinopathies are the most frequent irAEs with a prevalence of approximately 10%. Case study: We retrospect...